Blood–Central Nervous System Barriers: The Gateway to Neurodegeneration, Neuroprotection and Neuroregeneration
Abstract:
The microenvironment of the central nervous system (CNS) is precisely and meticulously maintained by a set of dynamic physiological barriers located within the cerebral microvessels of the brain (blood–brain barrier, BBB) and the spinal cord (blood–spinal cord barrier, BSCB), as well as within the epithelial cells of the choroid plexus separating the blood and cerebrospinal fluid (CSF) interface (blood–CSF barrier, BCSFB). The physicochemical properties of these cellular barriers are quite comparable to that of an extended plasma membrane. The BBB and the BSCB are quite tight to small molecules (12 Å, Lanthanum ion), whereas BCSFB is less restrictive in nature. On the other hand, the ependymal cell linings of the cerebral ventricles and spinal canal referred to as CSF–brain barrier do not normally restrict passage of several molecules of small sizes. However, protein transport across these blood–CNS barriers (BCNSB) is severely restricted. Entry of proteins into the CNS microenvironment induces vasogenic edema formation that is primarily responsible for cell and tissue injury. These BCNSB are often compromised under a wide variety of psychological, traumatic, metabolic, ischemic, environmental, or chemical insults leading to neuronal, glial, and axonal damage. Opening of the BCSNB to various endogenous or exogenous substances and proteins alters the molecular, cellular, biochemical, immunological, and metabolic environment of the CNS leading to abnormal neuronal function and/or brain pathology. This review is focused on current status of the BCSNB breakdown in experimental models of emotional stress, traumatic injuries, psychostimulants as well as key environmental health hazards, i.e., nanoparticles and heat exposure. Breakdown of the BCNSB in these conditions altered gene expression and induced brain pathology leading to neurodegeneration. Attenuation of the BCNSB disruption with drugs or antibodies affecting neurochemical metabolism and/or neurotrophic factors markedly reduced the development of brain pathology. Taken together, these novel observations strongly point out the role of BCNSB as a “gateway” to the neurodegeneration, neuroprotection, and/or neuroregeneration in neurological diseases.
List of Abbreviations:
- BBB
Blood–brain barrier
- BCNSB
blood–central nervous system barrier
- BCSFB
blood–CSF barrier
- BDNF
brain derived neurotrophic factor
- CBF
cerebral blood flow
- CHI
closed head injury
- CNS
central nervous system
- CSF
cerebrospinal fluid
- GFAP
glial fibrillary acidic protein
- HS
heat stress
- HSP
heat shock protein
- HVSA
high voltage slow activity
- IGF-1
insulin like growth factor-1
- LHRF
lutenizing hormone-releasing factor
- LVFA
low voltage fast activity
- MBP
myelin basic protein
- SCI
spinal cord injury
- TBI
traumatic brain injury
- TRH
thyrotropin-releasing hormone
- WBH
whole body hyperthermia
Notes
Acknowledgement
Author's research is supported by Grants from Swedish Medical Research Council, Stockholm Sweden; Alexander von Humboldt Foundation, Germany; European Office of Aerospace Research and Development (EOARD), London Office, UK. Secretarial Assistance of Aruna Sharma and Graphics support of Suraj Sharma is highly appreciated.
References
- Albert EN. 1979. Current status of microwave effects on the blood–brain barrier. J Microw Power 14(3): 281–285.PubMedGoogle Scholar
- Angel C. 1966. Adrenalectomy, stress and the blood–brain barrier. Dis Nerv Syst 27: 389–393.PubMedGoogle Scholar
- Angel C. 1969. Starvation, stress and the blood–brain barrier. Dis Nerv Syst 30: 94–97.PubMedGoogle Scholar
- Aukland K. 1973. Autoregulation of interstitial fluid volume: Edema-preventing mechanisms. Scand J Clin Lab Invest 31: 247–254.PubMedGoogle Scholar
- Baethmann A, Van A. Harreveld 1973. Water and electrolyte distribution in gray matter rendered edematous with a metabolic inhibitor. J Neuropathol Exp Neurol 32: 408–423.PubMedGoogle Scholar
- Bakay L, Lee JC. 1965. Cerebral Edema. Springfield, IL: Charles C Thomas.Google Scholar
- Balentine JD. 1988. Spinal cord trauma: In search of the meaning of granular axoplasm and vesicular myelin. J Neuropathol Exp Neurol 47: 77–92.PubMedGoogle Scholar
- Ballok DA. 2007. Neuroimmunopathology in a murine model of neuropsychiatric lupus. Brain Res Rev 54(1): 67–79.PubMedGoogle Scholar
- Banik NL, Hogan EL, Hsu CY. 1985. Molecular and anatomical correlates of spinal cord injury. Cent Nerv Syst Trauma 2(2): 99–107.PubMedGoogle Scholar
- Banik NL, Hogan EL, Hsu CY. 1987. The multimolecular cascade of spinal cord injury. Studies on prostanoids, calcium, and proteinases. Neurochem Pathol 7(1): 57–77.PubMedGoogle Scholar
- Barber AJ, Antonetti DA, Gardner TW, The Penn State Retina Research Group, 2000. Altered expression of retinal occludin and glial fibrillary acidic protein in experimental diabetes. Invest Ophthalmol Vis Sci 41: 3561–3568.PubMedGoogle Scholar
- Barbeito LH, Pehar M, Cassina P, Vargas MR, Peluffo H, et al. 2004. A role for astrocytes in motor neuron loss in amyotrophic lateral sclerosis. Brain Res Brain Res Rev 47(1–3): 263–274 (Review).PubMedGoogle Scholar
- Brightman MW, Hori M, Rapoport SI, Reese TS, Westergaard E. 1973. Osmotic opening of tight junctions in cerebral endothelium. J Comp Neurol 152(4): 317–325.PubMedGoogle Scholar
- Basch A, Fazekas G. 1970. Increased permeability of the blood–brain barrier following experimental thermal injury of the skin. Angiologica 7: 357–364.PubMedGoogle Scholar
- Batson OV. 1942. The vertebral vein system as a mechanism for the spread of metastases. Am J Roentgenol Rad Ther 48: 715–718.Google Scholar
- Beggs JL, Waggener JD. 1975. Vasogenic edema in the injured spinal cord: A method of evaluating the extent of blood–brain barrier alteration to horseradish peroxidase. Exp Neurol49(1 Pt 1): 86–96.PubMedGoogle Scholar
- Beggs JL, Waggener JD. 1976. Transendothelial vesicular transport of protein following compression injury to the spinal cord. Lab Invest 34(4): 428–439.PubMedGoogle Scholar
- Belova I, Jonsson G. 1982. Blood–brain barrier permeability and immobilization stress. Acta Physiol Scand 116: 21–29.PubMedGoogle Scholar
- Ben-Nathan D, Kobiler D, Loria RM, Lustig S. 1998. Stress-induced central nervous system penetration by non-invasive attenuated encephalitis viruses. New Frontiers in Stress Research, Modulation of Brain Function. Levy A, Grauer E, Ben-Nathan D, de Kloet ER, editors. The Netherlands: Harwood Academic Publishers; pp. 277–2283.Google Scholar
- Ben-Nathan D, Lustig S, Danenberg H. 1991. Stress-induced neuroinvasiveness of a neurovirulent non invasive Sindbis virus in cold or isolation subjected mice. Life Sci 48: 1493–1500.PubMedGoogle Scholar
- Ben-Nathan D, Lustig S, Kobiler D. 1996. Cold stress-induced neuroinvasiveness of attenuated arboviruses is not solely mediated by corticosterone. Arch Virol 141: 459–469.PubMedGoogle Scholar
- Blackwell RP, Saunders RD. 1986. The effects of low-level radiofrequency and microwave radiation on brain tissue and animal behaviour. Int J Radiat Biol Relat Stud Phys Chem Med 50(5): 761–787.PubMedGoogle Scholar
- Bonate PL. 1988. Quantification of albumin in cerebrospinal fluid. Anal Biochem 175(1): 300–304.PubMedGoogle Scholar
- Bondy SC, Purdy JL. 1974. Selective regulation of the blood–brain barrier by sensory input. Brain Res 76: 542–545.PubMedGoogle Scholar
- Borm PJ, Robbins D, Haubold S, Kuhlbusch T, Fissan H, et al. 2006. The potential risks of nanomaterials: A review carried out for ECETOC. Part Fibre Toxicol 3: 11 .PubMedGoogle Scholar
- Bouchama A, Knochel JP. 2002. Heat stroke. N Engl J Med 346(25): 1978–1988.PubMedGoogle Scholar
- Bradbury MWB. 1979. The Concept of a Blood–Brain Barrier. Chicester, London: John Wiley & sons.Google Scholar
- Bradbury MWB. 1992. Physiology and Pharmacology of the Blood–Brain Barrier. Handbook of Experimental Pharmacology, Vol. 103. Heidelberg: Springer-Verlag; pp. 1–450.Google Scholar
- Brightman MW, Klatzo I, Olsson Y, Reese TS. 1970. The blood–brain barrier to proteins under normal and pathological conditions. J Neurol Sci 10(3): 215–239.PubMedGoogle Scholar
- Brightman MW, Reese TS. 1969. Junctions between intimately apposed cell membranes in the vertebrate brain. J Cell Biol 40: 648–677.PubMedGoogle Scholar
- Butt AM, Jones HC. 1992. Effect of histamine and antagonists on electrical resistance across the blood–brain barrier in rat brain-surface microvessels. Brain Res 569: 100–105.PubMedGoogle Scholar
- Castel M, Sahar A, Erlij D. 1974. The movement of lanthanum across diffusion barriers in the choroid plexus of the cat. Brain Res 67(1): 178–184.PubMedGoogle Scholar
- Cervós-Navarro J, Ferszt R. 1980. Brain edema: Pathology, diagnosis, and therapy. Adv Neurol 28: 1–450.Google Scholar
- Cervós-Navarro J, Kannuki S, Nakagawa Y. 1988. Blood–brain barrier (BBB): Review from morphological aspect. Histol Histopathol 3: 203–213.PubMedGoogle Scholar
- Cervós-Navarro J, Sharma HS, Westman J, Bongcam-Rudloff E. 1998. Glial reactions in the central nervous system following heat stress. Prog Brain Res 115: 241–274.PubMedGoogle Scholar
- Chisari M, Salomone S, Laureanti F, Copani A, Sortino MA. 2004. Modulation of cerebral vascular tone by activated glia: Involvement of nitric oxide. J Neurochem 91(5): 1171–1179.PubMedGoogle Scholar
- Christensen TG, Diemer NH, Laursen H, Gjedde A. 1981. Starvation accelerates blood-brain glucose transfer. Acta Physiol Scand 112: 221–223.PubMedGoogle Scholar
- Cohen S. 1968. The immune response in relation to the nervous system. Biochemical Aspects of Neurological Disorders, Third series. Cumings JN, Kremer M, editors. Oxford: Blackwell; pp. 10–22.Google Scholar
- Cohen S, Williamson GM. 1991. Stress and infectious disease in human. Psychol Bull 109: 5–24.PubMedGoogle Scholar
- Connolly JH, Allen IV, Hurwitz LJ, Millar JH. 1968. Subacute sclerosing panencephalitis. Clinical, pathological, epidemiological, and virological findings in three patients. Q J Med 37(148): 625–644.PubMedGoogle Scholar
- Conrad S, Schluesener HJ, Adibzahdeh M, Schwab JM. 2005. Spinal cord injury induction of lesional expression of profibrotic and angiogenic connective tissue growth factor confined to reactive astrocytes, invading fibroblasts and endothelial cells. J Neurosurg Spine 2(3): 319–326.PubMedGoogle Scholar
- Cserr HF. 1971. Physiology of the choroid plexus. Physiol Rev 51(2): 273–311.PubMedGoogle Scholar
- Cserr HF, Ostrach LH. 1975. Bulk flow of interstitial fluid after intracranial injection of Blue Dextran 2000. Exp Neurol 45: 50–60.Google Scholar
- Cutler RW, Murray JE, Cornick LR. 1970. Variations in protein permeability in different regions of the cerebrospinal fluid. Exp Neurol 28(2): 257–265.PubMedGoogle Scholar
- Cutler RW, Lorenzo AV, Barlow CF. 1968. Changes in blood–brain barrier permeability during pharmacologically induced convulsions. Prog Brain Res 29: 367–384.PubMedGoogle Scholar
- Dantzer R, Kelley KW. 1989. Stress and immunity: An integrated view of the relationships between the brain and immune system. Life Sci 44: 1995–2008.PubMedGoogle Scholar
- Davson H. 1967. Physiology of the Cerebrospinal Fluid. London: Churchill.Google Scholar
- Davson H. 1976. Physiology of the Cerebrospinal Fluid. London: Churchill.Google Scholar
- Dawson CA, Horvath SM. 1970. Swimming in small laboratory animals. Med Sci Sports 2(2): 51–78.PubMedGoogle Scholar
- Demediuk P, Faden AI, Vink R, Romhanyi R, McIntosh TK. 1989. Effects of traumatic brain injury on arachidonic acid metabolism and brain water content in the rat. Ann N Y Acad Sci 559: 431–432.Google Scholar
- Dey PK, Sharma HS. 1983. Ambient temperature and development of traumatic brain oedema in anaesthetized animals. Indian J Med Res 77: 554–563.PubMedGoogle Scholar
- Dey PK, Sharma HS. 1984. Influence of ambient temperature and drug treatments on brain oedema induced by impact injury on skull in rat. Indian J Physiol Pharmacol 28: 177–186.PubMedGoogle Scholar
- Dohrmann GJ, Wagner FC Jr, Wick KM, Bucy PC. 1971. Fine structural alterations in transitory traumatic paraplegia. Proc Veterans Adm Spinal Cord Inj Conf 18: 6–8.PubMedGoogle Scholar
- Dubois M, Coppola R, Buchsbaum MS, Lees DE. 1981. Somatosensory evoked potentials during whole body hyperthermia in humans. Electroencephalogr Clin Neurophysiol 52(2): 157–162.PubMedGoogle Scholar
- Dubois M, Sato S, Lees DE, Bull JM, Smith R, et al. 1980. Electroencephalographic changes during whole body hyperthermia in humans. Electroencephalogr Clin Neurophysiol 50(5–6): 486–495.PubMedGoogle Scholar
- Dvorská I, Brust P, Hrbas P, Rühle HJ, Barth T, et al. 1992. On the blood–brain barrier to peptides: Effects of immobilization stress on regional blood supply and accumulation of labelled peptides in the rat brain. Endocr Regul 26(2): 77–82.PubMedGoogle Scholar
- Edvinsson E, McKenzie ET. 1977. Amine mechanisms in the cerebral circulation. Pharmacol Rev 28: 275–348.Google Scholar
- Esposito P, Chandler N, Kandere K, Basu S, Jacobson S, et al. 2002. Corticotropin-releasing hormone and brain mast cells regulate blood–brain barrier permeability by acute stress. J Pharmacol Exp Ther 303: 1061–1066.PubMedGoogle Scholar
- Esposito P, Gheorghe D, Kandere K, Pang X, Conally R, et al. 2001. Acute stress increase permeability of the blood–brain barrier through activation of mast cells. Brain Res 888: 117–127.PubMedGoogle Scholar
- Essman W. 1978. Serotonin in Health and Disease. The Central Nervous System, Vol. 3. New York: Spectrum.Google Scholar
- Faden AI. 1990. Opioid and non-opioid mechanisms may contribute to dynorphin's pathophysiological actions in the spinal cord injury. Ann Neurol 27: 64–74.Google Scholar
- Febbraio MA, Snow RJ, Stathis CG, Hargreaves M, Carey MF. 1994. Effect of heat stress on muscle energy metabolism during exercise. J Appl Physiol 77(6): 2827–2831.PubMedGoogle Scholar
- Feng N, Pagniano R, Tovar CA, Bonneaue RH, Glasser R, et al. 1991. The effect of restraint stress on the kinetics, magnitude, and isotype of the humoral immune response to influenza virus infection. Brain Behav Immun 5: 370–382.PubMedGoogle Scholar
- Fenstermacher JD. 1970. Extracellular space of the cerebral cortex of normothermic and hypothermic cats. Exp Neurol 27(1): 101–114.PubMedGoogle Scholar
- Fenstermacher JD, Rall DP. 1983. Physiology and pharmacology of cerebrospinal fluid. Pharmacology of Cerebral Circulation, Vol. 1. Oxford: Pergamon Press; pp. 35–79.Google Scholar
- Feringa ER, Wendt JS, Johnson RD. 1974. Immunosuppressive treatment to enhance spinal cord regeneration in rats. Neurology 24(3): 287–293.PubMedGoogle Scholar
- Frey AH, Feld SR, Frey B. 1975. Neural function and behavior: Defining the relationship. Ann N Y Acad Sci 247: 433–439.PubMedGoogle Scholar
- Frick E, Scheid-Seydel L. 1960. [Research with I 131-labelled gamma-globupin on the problem of the origin of cerebrospinal fluid proteins.] Klin Wochenschr 38: 1240–1243.PubMedGoogle Scholar
- Friedman SB, Glasgow LA, Ader R. 1970. Differential susceptibility to viral agent in mice housed alone or in group. Psychosom Med 32: 285–299.PubMedGoogle Scholar
- Gardner TW, Lieth E, Khin SA, Barber AJ, Bonsall DJ, et al. 1997. Astrocytes increase barrier properties and ZO-1 expression in retinal vascular endothelial cells. Invest Ophthalmol Vis Sci 38(11): 2423–2427.PubMedGoogle Scholar
- Ghersi-Egea JF, Strazielle N, Murat A, Edwards J, Belin MF. 2001. Are blood–brain interfaces efficient in protecting the brain from reactive molecules? Adv Exp Med Biol 500: 359–364.PubMedGoogle Scholar
- Gilbert GJ. 1965. Focal breakdown of the blood–brain barrier by specific sensory stimulation. Trans Am Neurol Assoc 90: 246–248.PubMedGoogle Scholar
- Griffiths HJ, Bushueff B, Zimmerman RE. 1976. Investigation of the loss of bone mineral in patients with spinal cord injury. Paraplegia 14(3): 207–212.PubMedGoogle Scholar
- Gonzalez-Alonso J, Teller C, Andersen SL, Jensen FB, Hyldig T, et al. 1999. Influence of body temperature on the development of fatigue during prolonged exercise in the heat. J Appl Physiol 86(3): 1032–1039.PubMedGoogle Scholar
- Goodman JH, Bingham WG Jr, Hunt WE. 1976. Ultrastructural blood–brain barrier alterations and edema formation in acute spinal cord trauma. J Neurosurg 44(4): 418–424.PubMedGoogle Scholar
- Gordh T, Chu H, Sharma HS. 2006. Spinal nerve lesion alters blood–spinal cord barrier function and activates astrocytes in the rat. Pain 124(1–2): 211–221.PubMedGoogle Scholar
- Gordh T, Sharma HS. 2006. Chronic spinal nerve ligation induces microvascular permeability disturbances, astrocytic reaction, and structural changes in the rat spinal cord. Acta Neurochir Suppl 96: 335–340.PubMedGoogle Scholar
- Gordh T, Sharma HS, Alm P, Westman J. 1998. Spinal nerve lesion induces upregulation of neuronal nitric oxide synthase in the spinal cord. An immunohistochemical investigation in the rat. Amino Acids 14(1–3): 105–112.PubMedGoogle Scholar
- Gordh T, Sharma HS, Azizi M, Alm P, Westman J. 2000. Spinal nerve lesion induces upregulation of constitutive isoform of heme oxygenase in the spinal cord. An immunohistochemical investigation in the rat. Amino Acids 19(1): 373–381.PubMedGoogle Scholar
- Govrin-Lippmann R, Devor M. 1978: Ongoing activity in severed nerves: Source and variation with time. Brain Res 159: 406–410.PubMedGoogle Scholar
- Griffiths IR. 1975. Vasogenic edema following acute and chronic spinal cord compression in the dog. J Neurosurg 42(2): 155–165.PubMedGoogle Scholar
- Griffiths IR. 1976. Spinal cord blood flow after acute experimental cord injury in dogs. J Neurol Sci 27(2): 247–259.PubMedGoogle Scholar
- Griffiths IR. 1978. Spinal cord injuries: A pathological study of naturally occurring lesions in the dog and cat. J Comp Pathol 88(2): 303–315.PubMedGoogle Scholar
- Griffiths IR. 1980. Trauma of the spinal cord. Vet Clin North Am Small Anim Pract 10(1): 131–146.PubMedGoogle Scholar
- Griffiths IR, Burns N, Crawford AR. 1978b. Early vascular changes in the spinal grey matter following impact injury. Acta Neuropathol (Berl) 41(1): 33–39.Google Scholar
- Griffiths IR, McCulloch MC. 1983. Nerve fibres in spinal cord impact injuries, Part 1. Changes in the myelin sheath during the initial 5 weeks. J Neurol Sci 58(3): 335–349.PubMedGoogle Scholar
- Griffiths IR, McCulloch M, Crawford RA. 1978a. Ultrastructural appearances of the spinal microvasculature between 12 hours and 5 days after impact injury. Acta Neuropathol (Berl) 43(3): 205–211.Google Scholar
- Groves PM, Thompson RF. 1970. Habituation: A dual-process theory. Psychol Rev 77(5): 419–450.PubMedGoogle Scholar
- Gruner JA, Altman J. 1980. Swimming in the rat: Analysis of locomotor performance in comparison to stepping. Exp Brain Res 40(4): 374–382.PubMedGoogle Scholar
- Guyton AC. 1963. A concept of negative interstitial pressure based on pressures in implanted perforated capsules. Circ Res 12: 399–412.PubMedGoogle Scholar
- Harri M, Kuusela P. 1986. Is swimming exercise or cold exposure for rats? Acta Physiol Scand 126(2): 189–197.PubMedGoogle Scholar
- Heins N, Malatesta P, Cecconi F, Nakafuku M, Tucker KL, et al. 2002. Glial cells generate neurons: The role of the transcription factor Pax6. Nat Neurosci 5(4): 308–315.PubMedGoogle Scholar
- Hermann G, Tovar CA, Beck FM, Sheridan JF. 1994. Kinetics of glucocorticoid response to restraint stress and/or experimental influenza viral infection in two inbred strains of mice. J Neuroimmunol 49: 25–33.PubMedGoogle Scholar
- Himmelsbach CK. 1943. With reference to physical dependence. Fed Proc 2: 201–203.Google Scholar
- Hirano A, Levine S, Zimmerman HM. 1967. Experimental cyanide encephalopathy: Electron microscopic observations of early lesions in white matter. J Neuropathol Exp Neurol 26(2): 200–213.PubMedGoogle Scholar
- Hirano A. 1971. Edema damage. Neurosci Res Prog Bull 9: 493–496.Google Scholar
- Hochwald GM, Wallenstein MC. 1967a. Exchange of gamma-globulin between blood, cerebrospinal fluid and brain in the cat. Exp Neurol 19(1): 115–126.Google Scholar
- Hochwald GM, Wallenstein M. 1967b. Exchange of albumin between blood, cerebrospinal fluid, and brain in the cat. Am J Physiol 212(5): 1199–1204.Google Scholar
- Hökfelt T, Ceccatelli S, Gustafsson L, Hulting AL, Verge V, et al. 1994. Plasticity of NO synthase expression in the nervous and endocrine systems. Neuropharmacology 33(11): 1221–1227.PubMedGoogle Scholar
- Houshyar H, Cooper ZD, Woods JH. 2001b. Paradoxical effects of chronic morphine treatment on the temperature and pituitary–adrenal responses to acute restraint stress: A chronic stress paradigm. J Neuroendocrinol 13(10): 862–874.Google Scholar
- Houshyar H, Galigniana MD, Pratt WB, Woods JH. 2001a. Differential responsivity of the hypothalamic–pituitary–adrenal axis to glucocorticoid negative-feedback and corticotropin releasing hormone in rats undergoing morphine withdrawal: Possible mechanisms involved in facilitated and attenuated stress responses. J Neuroendocrinol 13(10): 875–886.Google Scholar
- Inoue K, Tsuda M, Koizumi S. 2004. Chronic pain and microglia: The role of ATP. Novartis Found Symp 261:55–64; discussion 64–67: 149–154.PubMedGoogle Scholar
- Johansson BB, Owman Ch, Widner H. 1990. Pathophysiology of the blood–brain barrier. Fernström Foundation Series 14, Amsterdam: Elsevier; pp. 1–340.Google Scholar
- Johanson CE, Palm DE, Primiano MJ, McMillan PN, Chan P, et al. 2000. Choroid plexus recovery after transient forebrain ischemia: Role of growth factors and other repair mechanisms. Cell Mol Neurobiol 20(2): 197–216.PubMedGoogle Scholar
- Jones HC, Keep RF, Butt AM. 1992. The development of ion regulation at the blood–brain barrier. Prog Brain Res 91: 123–131.PubMedGoogle Scholar
- Joó F. 1987. A unifying concept on the pathogenesis of brain oedemas. Neuropathol Appl Neurobiol 13: 161–167.PubMedGoogle Scholar
- Katschinski DM, Wiedemann GJ, Longo W, d'Oleire FR, Spriggs D, et al. 1999. Whole body hyperthermia cytokine induction: A review, and unifying hypothesis for myeloprotection in the setting of cytotoxic therapy. Cytokine Growth Factor Rev 10(2): 93–97.PubMedGoogle Scholar
- Kiyatkin E, Brown L, Sharma HS. 2007. Brain edema and breakdown of the blood–brain barrier during methamphetamine intoxication: Critical Role of brain hyperthermia. Eur J Neurosci 26(5): 1242-1253.Google Scholar
- Klatzo I. 1967. Presidential address. Neuropathological aspects of brain edema. J Neuropathol Exp Neurol 26: 1–14.PubMedGoogle Scholar
- Klatzo I. 1972. Pathophysiological aspects of brain edema. Steroids and Brain Edema. Reulen H, Schurmann K, editors. Berlin: Springer-Verlag; pp. 1–8.Google Scholar
- Klatzo I. 1987. Pathophysiological aspects of brain edema. Acta Neuropathol (Berl) 72: 236–239.Google Scholar
- Klatzo I, Piraux A, Laskowski EJ. 1958. The relationship between edema, blood–brain barrier and tissue elements in local brain injury. J Neuropathol Exp Neurol 17: 548–564.PubMedGoogle Scholar
- Klatzo I, Seitelberger F. 1967. Brain Edema. Berlin: Springer-Verlag; pp. 1–350.Google Scholar
- Klatzo I, Wisniewski H, Smith DE. 1965. Observations on penetration of serum proteins into the central nervous system. Prog Brain Res 15: 73–88.PubMedGoogle Scholar
- Knigge KM, Joseph SA. 1974. Thyrotrophin releasing factor (TRF) in cerebrospinal fluid of the 3rd ventricle of rat. Acta Endocrinol (Copenh) 76(2): 209–213.Google Scholar
- Knigge KM, Silverman AJ. 1972. Transport capacity of the median eminence. Brain Endocrine Interaction, Median Eminence: Structure and Function. Knigge KM, Scott DE, Weindl A, editors. Basel: Karger; pp. 350–363.Google Scholar
- Kofman O, Levin U, Alpert C. 1995. Lithium attenuates hypokinesia induced by immobilization stress in rats. Prog Neuropsychopharmacol Biol Psychiatry 19(6): 1081–1090.PubMedGoogle Scholar
- Kristensson K, Olsson Y. 1973. Uptake and retrograde axonal transport of protein tracers in hypoglossal neurons. Fate of the tracer and reaction of the nerve cell bodies. Acta Neuropathol (Berl) 23(1): 43–47.Google Scholar
- Krum JM. 1994. Experimental gliopathy in the adult rat CNS: Effect on the blood–spinal cord barrier. Glia 11(4): 354–366.PubMedGoogle Scholar
- Kvetnansky R, Mikulaj L. 1970. Adrenal and urinary catecholamines in rats during adaptation to repeated immobilization stress. Endocrinology 87(4): 738–743.PubMedGoogle Scholar
- Lalonde R. 1986. Acquired immobility response in weaver mutant mice. Exp Neurol 94(3): 808–811.PubMedGoogle Scholar
- Lam CW, James JT, McCluskey R, Arepalli S, Hunter RL. 2006. A review of carbon nanotube toxicity and assessment of potential occupational and environmental health risks. Crit Rev Toxicol 36(3): 189–217.PubMedGoogle Scholar
- Leaf A. 1973. Cell swelling: A factor in ischemic tisuue injury. Circulation 48: 455–458.PubMedGoogle Scholar
- Leusen I. 1972. Regulation of cerebrospinal fluid composition with reference to breathing. Physiol Rev 52(1): 1–56.PubMedGoogle Scholar
- Levin VA, Fenstermacher JD, Patlak CS. 1970. Sucrose and inulin space measurements of cerebral cortex in four mammalian species. Am J Physiol 219(5): 1528–1533.PubMedGoogle Scholar
- Li YQ, Ballinger JR, Nordal RA, Su Zi-Fen, Wong CS. 2001. Hypoxia in radiation-induced blood–spinal cord barrier breakdown. Cancer Res 61: 3348–3354.PubMedGoogle Scholar
- Lieb WR, Stein WD. 1971. The molecular basis of simple diffusion within biological membranes. Curr Top Membr Transp 2: 1–39.Google Scholar
- Lorenzo AV, Fernandez C, Roth LJ. 1965. Physiologically induced alterations of sulfate penetration into brain. Arch Neurol 12: 128–132.PubMedGoogle Scholar
- Lossinsky AS, Shivers RR. 2004. Structural pathways for macromolecular and cellular transport across the blood–brain barrier during inflammatory conditions. Histol Histopathol 19(2): 535–564.PubMedGoogle Scholar
- Lowenthal A. 1972. Chemical physiopathology of the cerebrospinal fluid. Handbook of Neurochemistry, Vol. 7. Lajtha A, editor. New York: Plenum Press; pp. 429–464.Google Scholar
- Majno G, Palade GE. 1961. Studies on inflammation. I. The effect of histamine and serotonin on vascular permeability: An electron microscopic study. J Biophys Biochem Cytol 11: 571–605.PubMedGoogle Scholar
- Maloney KJ, Mainville L, Jones BE. 1999. Differential c-Fos expression in cholinergic, monoaminergic, and GABAergic cell groups of the pontomesencephalic tegmentum after paradoxical sleep deprivation and recovery. J Neurosci 19(8): 3057–3072.PubMedGoogle Scholar
- Maloney KJ, Mainville L, Jones BE. 2000. c-Fos expression in GABAergic, serotonergic, and other neurons of the pontomedullary reticular formation and raphe after paradoxical sleep deprivation and recovery. J Neurosci 20(12): 4669–4679.PubMedGoogle Scholar
- Marti O, Garcia A, Velles A, Harbuz MS, Armario A. 2001. Evidence that a single exposure to aversive stimuli triggers long-lasting effects in the hypothalamus–pituitary–adrenal axis that consolidate with time. Eur J Neurosci 13(1): 129–136.PubMedGoogle Scholar
- Martin R, Wallace BG, Fuch PA, Nicholls JG, editors. 2001. From Neuron to Brain: A Cellular and Molecular Approach to the Function of the Nervous System, Fourth edition (Hardcover). New York, USA: Sinauer Associates; pp. 1–617.Google Scholar
- Martinez AJ, Alderman JL, Kagan RS, Osterholm JL. 1981. Spatial distribution of edema in the cat spinal cord after impact injury. Neurosurgery 8: 450–453.PubMedGoogle Scholar
- Mautes AE, Bergeron M, Sharp FR, Panter SS, Weinzierl M, et al. 2000. Sustained induction of heme oxygenase-1 in the traumatized spinal cord. Exp Neurol 166(2): 254–265.PubMedGoogle Scholar
- Mautes AE, Noble LJ. 2000. Co-induction of HSP70 and heme oxygenase-1 in macrophages and glia after spinal cord contusion in the rat. Brain Res 883(2): 233–237.PubMedGoogle Scholar
- Mayhan WG, Heistad DD. 1985. Permeability of blood–brain barrier to various sized molecules. Am J Physiol 248: H712–H718.PubMedGoogle Scholar
- Mendelson WB, Guthrie RD, Frederick G, Wyatt RJ. 1974. The flower pot technique of rapid eye movement (REM) sleep deprivation. Pharmacol Biochem Behav 2(4): 553–556.PubMedGoogle Scholar
- Merritt JH, Chamness AF, Allen SJ. 1978. Studies on blood–brain barrier permeability after microwave-radiation. Radiat Environ Biophys 15(4): 367–377.PubMedGoogle Scholar
- Miller JD. 1976. Pressure-volume response-clinical aspects. Chicago Conference on Neural Trauma. McLaurin R, editor. New York: Grunne & Stratton; pp. 35–46.Google Scholar
- Mills NL, Amin N, Robinson SD, Anand A, Davies J, et al. 2006. Do inhaled carbon nanoparticles translocate directly into the circulation in humans? Am J Respir Crit Care Med 173(4): 426–431.PubMedGoogle Scholar
- Miyazato H, Skinner RD, Garcia-Rill E. 2000. Locus coeruleus involvement in the effects of immobilization stress on the p13 midlatency auditory evoked potential in the rat. Prog Neuropsychopharmacol Biol Psychiatry 24(7): 1177–1201.PubMedGoogle Scholar
- Mohanty S, Dey PK, Sharma HS, Ray AK. 1985. Experimental brain edema: Role of 5-HT. Brain Edema. Mohanty S, Dey PK, editors. India: Varanasi; Banaras Hindu University, Bhargava Bhushan Press; pp. 19–27.Google Scholar
- Mohanty S, Dey PK, Sharma HS, Singh S, Chansouria JP, et al. 1989. Role of histamine in traumatic brain edema. An experimental study in the rat. J Neurol Sci 90: 87–97.PubMedGoogle Scholar
- Moon L, Bunge MB. 2005. From animal models to humans: Strategies for promoting CNS axon regeneration and recovery of limb function after spinal cord injury. J Neurol Phys Ther 29(2): 55–69.PubMedGoogle Scholar
- Nag S, Eskandarian MR, Davis J, Eubanks JH. 2002. Differential expression of vascular endothelial growth factor-A (VEGF-A) and VEGF-B after brain injury. J Neuropathol Exp Neurol 61(9): 778–788.PubMedGoogle Scholar
- Nemecek S. 1978. Morphological evidence of microcirculatory disturbances in experimental spinal cord trauma. Adv Neurol 20: 395–405.PubMedGoogle Scholar
- Nemecek S, Petr R, Sube P, Rozseval V, Melka O. 1977. Longitudinal extension of edema in experimental spinal cord injury: Evidence for two types of post-traumatic edema. Acta Neurochir (Wien) 37: 7–16.Google Scholar
- Nevis AH, Collins GH. 1967. Electrical impedance and volume changes in brain during preparation for electon microscopy. Brain Res 5(1): 57–85.PubMedGoogle Scholar
- Nielsen B, Hyldig T, Bidstrup F, Gonzalez-Alonso J, Christoffersen GR. 2001. Brain activity and fatigue during prolonged exercise in the heat. Pflugers Arch 442(1): 41–48.PubMedGoogle Scholar
- Noble LJ, Donovan F, Igarashi T, Goussev S, Werb Z. 2002. Matrix metalloproteinases limit functional recovery after spinal cord injury by modulation of early vascular events. J Neurosci 22(17): 7526–7535.PubMedGoogle Scholar
- Noble LJ, Wrathall JR. 1987. The blood–spinal cord barrier after injury: Pattern of vascular events proximal and distal to a transection in the rat. Brain Res 424(1): 177–188.PubMedGoogle Scholar
- Noble LJ, Wrathall JR. 1988. Blood–spinal cord barrier disruption proximal to a spinal cord transection in the rat: Time course and pathways associated with protein leakage. Exp Neurol 99(3): 567–578.PubMedGoogle Scholar
- Noble LJ, Wrathall JR. 1989. Distribution and time course of protein extravasation in the rat spinal cord after contusive injury. Brain Res 482(1): 57–66.PubMedGoogle Scholar
- Nolan RT. 1969. Traumatic oedema of the spinal cord. Br Med J 1: 710PubMedGoogle Scholar
- Novikoff AB. 1960. Biochemical and staining reactions of cytoplasmic constituents. Developing Cell System and Their Control. Rudnic D, editor. New York: Ronald Press; pp. 167–203.Google Scholar
- Oberdörster E. 2004. Manufactured nanomaterials (fullerenes, C60) induce oxidative stress in brain of juvenile largemouth bass. Environ Health Perspect 112: 1058–1062.PubMedGoogle Scholar
- Oberdörster G. 1996. Significance of particle parameters in the evaluation of exposure-dose-response relationships of inhaled particles. Inhal Toxicol 8 Suppl: 73–89.PubMedGoogle Scholar
- Oberdörster G, Finkelstein JN, Johnston C, Gelein R, Cox C, et al. 2000. Acute pulmonary effects of ultrafine particles in rats and mice. Res Rep Health Eff Inst 96: 5–74; disc. 75–86PubMedGoogle Scholar
- Oberdorster G, Maynard A, Donaldson K, Castranova V, Fitzpatrick J, et al. 2005a. ILSI Research Foundation/Risk Science Institute Nanomaterial Toxicity Screening Working Group. Principles for characterizing the potential human health effects from exposure to nanomaterials: Elements of a screening strategy. Part Fibre Toxicol 6; 2: 8.Google Scholar
- Oberdorster G, Oberdorster E, Oberdorster J. 2005b. Nanotoxicology: An emerging discipline evolving from studies of ultrafine particles. Environ Health Perspect 113(7): 823–839.Google Scholar
- Ohata M, Fredericks WR, Sundaram U, Rapoport SI. 1981. Effects of immobilization stress on regional cerebral blood flow in the conscious rat. J Cereb Blood Flow Metab 1(2): 187–194.PubMedGoogle Scholar
- Ohata M, Takei H, Fredericks WR, Rapoport SI. 1982. Effects of immobilization stress on cerebral blood flow and cerebrovascular permeability in spontaneously hypertensive rats. J Cereb Blood Flow Metab 2(3): 373–379.PubMedGoogle Scholar
- Olesen SP. 1989. An electrophysiological study of microvascular permeability and its modulation by chemical mediators. Acta Physiol Scand Suppl 579: 1–28.PubMedGoogle Scholar
- Olsson Y, Sharma HS, Nyberg F, Westman J. 1995. The opioid receptor antagonist naloxone influences the pathophysiology of spinal cord injury. Progress in Brain Research Spinal Cord Monitoring: Basic Principles, Regeneration, Pathophysiology and Clinical Aspects, Vol. 104. Nyberg F, Sharma HS, Wissenfeld-Halin Z, editors. Amsterdam: Elsevier; pp. 381–399.Google Scholar
- Olsson Y, Sharma HS, Pettersson Å, Cervós-Navarro J. 1992. Endogenous release of neurochemicals may increase vascular permeability, induce edema and influence on cell changes in trauma to the spinal cord. Circumventricular organs and brain fluid environment. Prog Brain Res 91: 197–203.PubMedGoogle Scholar
- Olsson Y, Sharma HS, Pettersson CÅV. 1990. Effects of p-chlorophenylalanine on microvascular permeability changes in spinal cord trauma. An experimental study in the rat using 131I-sodium and lanthanum tracers. Acta Neuropathol (Berl) 79: 595–603.Google Scholar
- Osterholm JL. 1978. The Pathophysiology of Spinal Cord Trauma. Springfield, IL: Thomas.Google Scholar
- Osterholm JL. 1974. The pathophysiological response to spinal cord injury. The current status of related research. J Neurosurg 40(1): 5–33.PubMedGoogle Scholar
- Osterholm JL, Alderman JL, Northrup BE. 1987. Acute spinal cord injury. Spinal cord Injury Medical Engineering. Ghista DN, Frankel HL, Charles C, editors. Illinois: Charles C. Thomas Inc; pp. 5–46.Google Scholar
- Pappius HM. 1970. The chemistry and fine structure in various types of cerebral edema. Riv Patol Nerv Ment 91: 311–322.PubMedGoogle Scholar
- Parandoosh Z, Johanson CE. 1982. Ontogeny of blood–brain barrier permeability to, and cerebrospinal fluid sink action on, [14C]urea. Am J Physiol 243(3): R400–R407.PubMedGoogle Scholar
- Parker AJ, Park RD. Stowater JL. 1973. Reduction of trauma induced edema of spinal cord in dogs given mannitol. Am J Vet Res 34: 1355–1357.PubMedGoogle Scholar
- Porter JC. 1973. Neuroendocrine system. The need for precise identification and rigorous description of their operation. Prog Brain Res 92: 1–6.Google Scholar
- Porsolt RD, Anton G, Blavet N, Jalfre M. 1978. Behavioural despair in rats: A new model sensitive to antidepressant treatments. Eur J Pharmacol 47(4): 379–391.PubMedGoogle Scholar
- Porsolt RD, Bertin A, Blavet N, Deniel M, Jalfre M. 1979. Immobility induced by forced swimming in rats: Effects of agents which modify central catecholamine and serotonin activity. Eur J Pharmacol 57(2–3): 201–210.PubMedGoogle Scholar
- Porsolt RD, Bertin A, Jalfre M. 1977. Behavioral despair in mice: A primary screening test for antidepressants. Arch Int Pharmacodyn Ther 229(2): 327–336.PubMedGoogle Scholar
- Raichle ME, Hartmann BK, Eichling JO, Sharpe LG. 1975. Central noradrenergic regulation of cerebral blood flow and vascular permeability. Proc Natl Acad Sci USA 72: 3726–3730.PubMedGoogle Scholar
- Rapoport SI. 1976. Blood–brain barrier in physiology and medicine. New York: Raven Press; pp. 1–272.Google Scholar
- Rasmussen AF, March JT, Brill NQ. 1957. Increased susceptibility to herpes simplex in mice subjected to avoidance-learning stress or restrain. Proc Soc Exp Biol Med 96: 183–189.PubMedGoogle Scholar
- Rawson RA. 1943. The binding of T-1824 and structurally related diazo dyes by plasma proteins. Am J Physiol 138: 708–717.Google Scholar
- Reulen HJ. 1977a. Vasogenic brain oedema. New aspects in its formation, resolution and therapy. Br J Anaesth 48(8): 741–752.Google Scholar
- Reulen HJ. 1977b. [Development and correction of water-electrolyte and acid base equilibrium disorders in brain edema (proceedings)] [Article in German] Klin Anasthesiol Intensivther (15): 109-122.Google Scholar
- Reulen HJ, Baethmann A, Fenstermacher J, Marmarou A, Spatz M. 1990. Brain Edema VIII, Acta Neurochir (Wien) Suppl 51:1–414, Wien: Springer-Verlag.Google Scholar
- Reulen HJ, Graham R, Spatz M, Klatzo I. 1977. Role of pressure gradients and bulk flow in dynamics of vasogenic brain edema. J Neurosurg 46(1): 24–35.PubMedGoogle Scholar
- Reulen HJ, Kreysch HG. 1973. Measurement of brain tissue pressure in cold induced cerebral oedema. Acta Neurochir (Wien) 29: 29–40.Google Scholar
- Rexed BA. 1952. The cytoarchitectonic organization of the spinal cord in the cat. J Comp Neurol 96: 415–496.Google Scholar
- Rexed BA. 1954. Cytoarchitectonic atlas of the spinal cord of the cat. J Comp Neurol 100: 297–379.PubMedGoogle Scholar
- Rhodin JA. 1968. Ultrastructure of mammalian venous capillaries, venules, and small collecting veins. J Ultratstruct Res 25(5): 452–500.Google Scholar
- Rinder L. 1968. Artefactitious extravasation of fluorescent indicators in the investigation of vascular permeability in brain and spinal cord. Acta Pathol Microbiol Scand 74(3): 333–339.PubMedGoogle Scholar
- Robins HI, Kutz M, Wiedemann GJ, Katschinski DM, Paul D, et al. 1995. Cytokine induction by 41.8 degrees C whole body hyperthermia. Cancer Lett 97(2): 195–201.PubMedGoogle Scholar
- Robins HI, Rushing D, Kutz M, Tutsch KD, Tiggelaar CL, et al. 1997. Phase I clinical trial of melphalan and 41.8 degrees C whole-body hyperthermia in cancer patients. J Clin Oncol 15(1): 158–164.PubMedGoogle Scholar
- Rosomoff HL, Zugibe FT. 1963. Distribution of intracranial contents in experimental edema. Arch Neurol 9: 26–34.PubMedGoogle Scholar
- Rymer MM, Fishman RA. 1973. Protective adaptation of brain to water intoxication Arch Neurol 28: 49–54.PubMedGoogle Scholar
- Scott GS, Kean RB, Fabis MJ, Mikheeva T, Brimer CM, et al. 2004. ICAM-1 upregulation in the spinal cords of PLSJL mice with experimental allergic encephalomyelitis is dependent upon TNF-alpha production triggered by the loss of blood–brain barrier integrity. J Neuroimmunol 155(1–2): 32–42.PubMedGoogle Scholar
- Selye H. 1976. Stress in Health and Disease. London: Butterworths.Google Scholar
- Shapiro K, Shulman K, Marmarou A, Poll W. 1977. Tissue pressure gradients in spinal cord injury. Surg Neurol 7(5): 275–279.PubMedGoogle Scholar
- Sharma HS. 1982. Blood–Brain Barrier in Stress, PhD Thesis. Varanasi, India: Banaras Hindu University; pp. 1-85.Google Scholar
- Sharma HS, Westman J, Nyberg F. 1998a. Pathophysiology of brain edema and cell changes following hyperthermic brain injury. Prog Brain Res 115: 351–412 (Review).Google Scholar
- Sharma HS. 1999. Pathophysiology of blood–brain barrier, brain edema and cell injury following hyperthermia: New role of heat shock protein, nitric oxide and carbon monoxide. An experimental study in the rat using light and electron microscopy. Acta Univ Ups 830: 1–94.Google Scholar
- Sharma HS. 2000a. A bradykinin BK2 receptor antagonist HOE-140 attenuates blood–spinal cord barrier permeability following a focal trauma to the rat spinal cord. An experimental study using Evans blue, [131]I-sodium and lanthanum tracers. Acta Neurochir Suppl 76: 159–163.Google Scholar
- Sharma HS. 2000b. Degeneration and regeneration in the CNS. New roles of heat shock proteins, nitric oxide and carbon monoxide. Amino Acids 19: 335–337.Google Scholar
- Sharma HS. 2003. Neurotrophic factors attenuate microvascular permeability disturbances and axonal injury following trauma to the rat spinal cord. Acta Neurochir Suppl 86: 383–388.PubMedGoogle Scholar
- Sharma HS. 2004a. Pathophysiology of the blood–spinal cord barrier in traumatic injury. The Blood–Spinal Cord and Brain Barriers in Health and Disease. Sharma HS, Westman J, editors. San Diego: Elsevier Academic Press; pp. 437–518.Google Scholar
- Sharma HS. 2004b. Blood–brain and spinal cord barriers in stress. The Blood–Spinal Cord and Brain Barriers in Health and Disease. Sharma HS, Westman J, editors. San Diego: Elsevier Academic Press; pp. 231–298.Google Scholar
- Sharma HS. 2004c. Int J Neuropotec Neuroregen 1(1): 8 (Editorial).Google Scholar
- Sharma HS. 2004d. Influence of serotonin on the blood-brain and blood–spinal cord barriers. The Blood–Spinal Cord and Brain Barriers in Health and Disease. Sharma HS, Westman J, editors. San Diego: Elsevier Academic Press; pp. 117–158.Google Scholar
- Sharma HS. 2004e. Histamine influences the blood–spinal cord and brain barriers following injuries to the central nervous system. The Blood–Spinal Cord and Brain Barriers in Health and Disease. Sharma HS, Westman J, editors. San Diego: Elsevier Academic Press; pp. 159–190.Google Scholar
- Sharma HS. 2005a. Pathophysiology of blood–spinal cord barrier in traumatic injury and repair. Curr Pharm Des 11(11): 1353–1389.Google Scholar
- Sharma HS. 2005b. Selective neuronal vulnerability, blood–brain barrier disruption and heat shock protein expression in stress induced neurodegeneration. Invited Review: Depression and Dementia: Progress in Brain Research, Clinical Applications and Future Trends. Sarbadhikari SN, editor. NY: Nova Science Publishers; pp. 97–152.Google Scholar
- Sharma HS. 2005c. Heat-related deaths are largely due to brain damage. Indian J Med Res 121(5): 621–623.Google Scholar
- Sharma HS. 2005d. Neuroprotective effects of neurotrophins and melanocortins in spinal cord injury: An experimental study in the rat using pharmacological and morphological approaches. Ann NY Acad Sci 1053: 407–421.Google Scholar
- Sharma HS. 2005e. Methods to induce brain hyperthermia. Current Protocols in Toxicology, Suppl 23, Unit 11.14: 1–26.Google Scholar
- Sharma HS. 2006a. Hyperthermia induced brain oedema: Current status and future perspectives. Indian J Med Res 123(5): 629–652.Google Scholar
- Sharma HS. 2006b. Post-traumatic application of brain–derived neurotrophic factor and glia-derived neurotrophic factor on the rat spinal cord enhances neuroprotection and improves motor function. Acta Neurochir Suppl 96: 329–334.Google Scholar
- Sharma HS. 2006c. Hyperthermia influences excitatory and inhibitory amino acid neurotransmitters in the central nervous system. An experimental study in the rat using behavioural, biochemical, pharmacological, and morphological approaches. J Neural Transm 113(4): 497–519.Google Scholar
- Sharma HS, Sjöquist PO, Mohanty S, Wiklund L. 2006d. Post-injury treatment with a new antioxidant compound H-290/51 attenuates spinal cord trauma-induced c-fos expression, motor dysfunction, edema formation, and cell injury in the rat. Acta Neurochir Suppl 96: 322–328.Google Scholar
- Sharma HS, Patnaik R, Patnaik S, Mohanty S, Sharma A, et al. 2007. Antibodies to serotonin attenuate closed head injury induced blood–brain barrier disruption and brain pathology. Ann N Y Acad Sci 1122: 295–312.PubMedGoogle Scholar
- Sharma HS. 2007a. Neurodegeneration and neuroregeneration: Recent advancements and future perspectives. Curr Pharm Des 13(18): 1325–1327.Google Scholar
- Sharma HS. 2007b. Neurotrophic factors in combination: A possible new therapeutic strategy to influence pathophysiology of spinal cord injury and repair mechanisms. Curr Pharm Des 13(18): 1841–1874.Google Scholar
- Sharma HS. 2007c. Methods to produce hyperthermia-induced brain dysfunction. Prog Brain Res 162: 173–200.Google Scholar
- Sharma HS. 2007d. Interaction between amino acid neurotransmitters and opiod receptors in hyperthermia induced brain pathology. Prog Brain Res 162: 295–320.Google Scholar
- Sharma HS (editor). 2007e. Neurobiology of hyperthermia. Progress in Brain Research. Elsevier Amsterdam, North Hotland. Vol. 162. pp. 1–510.Google Scholar
- Sharma HS, Ali SF. 2006. Alterations in blood–brain barrier function by morphine and methamphetamine. Ann NY Acad Sci 1074: 198–224.PubMedGoogle Scholar
- Sharma HS, Ali SF. 2007. MDMA (ecstasy) induces blood–brain barrier disruption, brain edema formation and cell injury. An experimental study in rats and mice. Ann NY Acad Sci (in press).Google Scholar
- Sharma HS, Ali SF, Schlager J, Hussain S. 2006b. Effect of nanoparticles on the blood–brain barrier. Int J Neuroprotec Neuroregen 2(3): 78.Google Scholar
- Sharma HS, Alm P. 2004. Role of nitric oxide on the blood–brain and the spinal cord barriers. The Blood–Spinal Cord and Brain Barriers in Health and Disease. Sharma HS, Westman J, editors. San Diego: Elsevier Academic Press; pp. 191–230.Google Scholar
- Sharma HS, Alm P, Westman. 1998d. Nitric oxide and carbon monoxide in the pathophysiology of brain functions in heat stress. Brain Functions in Hot Environment. Sharma HS, Westman J, editors. Prog Brain Res 115: 297–333.Google Scholar
- Sharma HS, Cervós-Navarro J, Dey PK. 1991a. Increased blood–brain barrier permeability following acute short-term forced-swimming exercise in conscious normotensive young rats. Neurosci Res 10: 211–221.Google Scholar
- Sharma HS, Cervós-Navarro J, Gosztonyi G, Dey PK. 1992b. Role of serotonin in traumatic brain injury. An experimental study in the rat. The Role of Neurotransmitters in Brain Injury. Globus M, Dietrich WD, editors. New York: Plenum Press; pp. 147–152.Google Scholar
- Sharma HS, Dey PK. 1978. Influence of heat and immobilization stressors on the permeability of blood–brain and blood–CSF barriers. Indian J Physiol Pharmacol 22 (Suppl2): 59–60.Google Scholar
- Sharma HS, Dey PK. 1980. Increased permeability of blood–brain barrier (BBB) in stress: Blockade by p-CPA pretreatment. Indian J Physiol Pharmacol 24 (Suppl 1): 423–424.Google Scholar
- Sharma HS, Dey PK. 1981. Impairment of blood–brain barrier (BBB) in rat by immobilization stress: Role of serotonin (5-HT). Indian J Physiol Pharmacol 25(2): 111–122.PubMedGoogle Scholar
- Sharma HS, Dey PK. 1984. Role of 5-HT on increased permeability of blood–brain barrier under heat stress. Indian J Physiol Pharmacol 28: 259–267.PubMedGoogle Scholar
- Sharma HS, Dey PK. 1986a. Influence of long-term immobilization stress on regional blood–brain barrier permeability, cerebral blood flow and 5-HT level in conscious normotensive young rats. J Neurol Sci 72: 61–76.Google Scholar
- Sharma HS, Dey PK. 1986b. Probable involvement of 5-hydroxytryptamine in increased permeability of blood–brain barrier under heat stress. Neuropharmacology 25: 161–167.Google Scholar
- Sharma HS, Dey PK. 1987a. Increased blood–brain and blood-CSF barrier permeability following long-term immobilization stress in conscious rats. Wissenschaftliche Zeitschrift Karl-Marx Universität Leipzig, Mathematisch-Naturwissenschaftliche Reihe 36: 104–106.Google Scholar
- Sharma HS, Dey PK. 1987b. Influence of long-term acute heat exposure on regional blood–brain barrier permeability, cerebral blood flow and 5-HT level in conscious normotensive young rats. Brain Res 424: 153–162.Google Scholar
- Sharma HS, Dey PK. 1988. EEG changes following increased blood–brain barrier permeability under long-term immobilization stress in young rats. Neurosci Res 5(3): 224–239.PubMedGoogle Scholar
- Sharma HS, Dey PK, Kumar A. 1986. Role of circulating 5-HT and lung MAO activity in physiological processes of heat adaptation in conscious young rats. Biomedicine 6: 31–40.Google Scholar
- Sharma HS, Dey PK, Olsson Y. 1989. Brain edema, blood–brain barrier permeability and cerebral blood flow changes following intracarotid infusion of serotonin: Modification with cyproheptadine and indomethacin. Pharmacology of Cerebral Ischemia 1988. Krieglstein J, editor. Boca Raton, Florida: CRC Press; pp. 317–323.Google Scholar
- Sharma HS, Hoopes PJ. 2003. Hyperthermia induced pathophysiology of the central nervous system. Int J Hypertherm 19: 325–354.Google Scholar
- Sharma HS, Johanson CE. 2007. Blood–cerebrospinal fluid barrier in hyperthermia. Prog Brain Res 162: 459–480.PubMedGoogle Scholar
- Sharma HS, Kretzschmar R, Cervós-Navarro J, Ermisch A, Rühle H-J, et al. 1992c. Age-related pathophysiology of the blood–brain barrier in heat stress. Prog Brain Res 91: 189–196.Google Scholar
- Sharma HS, Lundstedt T, Boman A, Lek P, Seifert E, et al. 2006a. A potent serotonin-modulating compound AP-267 attenuates morphine withdrawal-induced blood–brain barrier dysfunction in rats. Ann NY Acad Sci 1074: 482–496.Google Scholar
- Sharma HS, Lundstedt T, Flardh M, Westman J, Post C, et al. 2003c. Low molecular weight compounds with affinity to melanocortin receptors exert neuroprotection in spinal cord injury – an experimental study in the rat. Acta Neurochir Suppl 86: 399–405.Google Scholar
- Sharma HS, Nyberg F, Cervós-Navarro J, Dey PK. 1992a. Histamine modulates heat stress induced changes in blood–brain barrier permeability, cerebral blood flow, brain oedema and serotonin levels: An experimental study in conscious young rats. Neuroscience 50: 445–454.Google Scholar
- Sharma HS, Nyberg F, Gordh T, Alm P, Westman J. 1998c. Neurotrophic factors attenuate neuronal nitric oxide synthase upregulation, microvascular permeability disturbances, edema formation and cell injury in the spinal cord following trauma. Spinal Cord Monitoring. Basic Principles, Regeneration, Pathophysiology and Clinical Aspects. Stålberg E, Sharma HS, Olsson Y, editors. New York: Springer Wien; pp. 118–148.Google Scholar
- Sharma HS, Nyberg F, Westman J, Alm P, Gordh T, et al. 1998b. Brain derived neurotrophic factor and insulin like growth factor-1 attenuate upregulation of nitric oxide synthase and cell injury following trauma to the spinal cord. Amino Acids 14: 121–130.Google Scholar
- Sharma HS, Olsson Y. 1990. Edema formation and cellular alteration in spinal cord injury in the rat and their modification with p-chlorophenylalanine. Acta Neuropathol (Berl) 79: 604–610.Google Scholar
- Sharma HS, Olsson Y, Cervós-Navarro J. 1993b. p-Chlorophenylalanine, a serotonin synthesis inhibitor, reduces the response of glial fibrillary acidic protein induced by trauma to the spinal cord. Acta Neuropathol (Berl) 86: 422–427.Google Scholar
- Sharma HS, Olsson Y, Dey PK. 1990a. Blood–brain barrier permeability and cerebral blood flow following elevation of circulating serotonin level in the anaesthetized rats. Brain Res 517: 215–223.Google Scholar
- Sharma HS, Olsson Y, Dey PK. 1990b. Early accumulation of serotonin in rat spinal cord subjected to traumatic injury. Relation to edema and blood flow changes. Neuroscience 36: 725–730.Google Scholar
- Sharma HS, Olsson Y, Dey PK. 1995b. Serotonin as a mediator of increased microvascular permeability of the brain and spinal cord. Experimental observations in anaesthetised rats and mice. New Concepts of a Blood–Brain Barrier. Greenwood J, Begley D, Segal M, Lightman S, editors. New York: Plenum Press; pp. 75–80.Google Scholar
- Sharma HS, Olsson Y, Nyberg F. 1995d. Influence of dynorphin-A antibodies on the formation of edema and cell changes in spinal cord trauma. Progress in Brain Research, Vol. 104. Nyberg F, Sharma HS, Wissenfeld-Halin Z, editors. Amsterdam: Elsevier; pp. 401–416.Google Scholar
- Sharma HS, Olsson Y, Nyberg F, Dey PK. 1993a. Prostaglandins modulate alterations of microvascular permeability, blood flow, edema and serotonin levels following spinal cord injury. An experimental study in the rat. Neuroscience 57: 443–449.Google Scholar
- Sharma HS, Olsson Y, Pearsson S, Nyberg F. 1995a. Trauma induced opening of the blood–spinal cord barrier is reduced by indomethacin, an inhibitor of prostaglandin synthesis. Experimental observations in the rat using 131I-sodium, Evans blue and lanthanum as tracers. Restor Neurol Neurosci 7: 207–215.Google Scholar
- Sharma HS, Patnaik R, Ray AK, Dey PK. 2004. Blood–central nervous system barriers in morphine dependence and withdrawal. The Blood-Spinal Cord and Brain Barriers in Health and Disease. Sharma HS, Westman J, editors. San Diego: Elsevier Academic Press; pp. 299–328.Google Scholar
- Sharma HS, Sharma A. 2007. Nanoparticles aggravate heat stress induced cognitive deficits, blood–brain barrier disruption, edema formation and brain pathology. Prog Brain Res 162: 245–276.PubMedGoogle Scholar
- Sharma HS, Sjöquist PO. 2002. A new antioxidant compound H-290/51 modulates glutamate and GABA immunoreactivity in the rat spinal cord following trauma. Amino Acids 23: 261–272.PubMedGoogle Scholar
- Sharma HS, Sjöquist PO, Ali SF. 2007. Drugs of abuse-induced hyperthermia, blood–brain barrier dysfunction and neurotoxicity: Neuroprotective effects of a new antioxidant compound H-290/51. Curr Pharm Des 13(18): 1903–1923.PubMedGoogle Scholar
- Sharma HS, Sjoquist PO, Alm P. 2003a. A new antioxidant compound H-290151 attenuates spinal cord injury induced expression of constitutive and inducible isoforms of nitric oxide synthase and edema formation in the rat. Acta Neurochir Suppl 86: 415–420.Google Scholar
- Sharma HS, Sjöquist PO, Westman J. 2001. Pathophysiology of the blood–spinal cord barrier in spinal cord injury. Influence of a new antioxidant compound H-290/51. Blood–Brain Barrier: Drug Delivery and Brain Pathology. Kobiler D, Lustig S, Shapra S, editors. New York: Kluwer Academic/Plenum Publishers; pp. 401–416.Google Scholar
- Sharma HS, Westman J. 1998. Brain function in hot environment. Prog Brain Res 115: 1–617.Google Scholar
- Sharma HS, Westman J. 2000. Pathophysiology of hyperthermic brain injury. Current concepts, molecular mechanisms and pharmacological strategies. Research in Legal Medicine. Hyperthermia, Burning and Carbon Monoxide, Vol. 21. Oehmichen M, editor. Lübeck, Germany: Lübeck Medical University Publications, Schmidt-Römhild Verlag; pp. 79–120.Google Scholar
- Sharma HS, Westman J. 2004. The Blood–Spinal Cord and Brain Barriers in Health and Disease. San Diego: Academic Press; pp. 1–617.Google Scholar
- Sharma HS, Westman J, Cervós-Navarro J, Dey PK, Nyberg F. 1995c. Probable involvement of serotonin in the increased permeability of the blood–brain barrier by forced swimming. An experimental study using Evans blue and 131I-sodium tracers in the rat. Behav Brain Res 72: 189–196.Google Scholar
- Sharma HS, Westman J, Cervós-Navarro J, Nyberg F. 1996b. A 5-HT2 receptor mediated breakdown of the blood–brain barrier permeability and brain pathology in heat stress. An experimental study using cyproheptadine and ketanserin in young rats. Biology and Physiology of the Blood–Brain Barrier. Couraud P, Scherman A, editors. New York: Plenum Press; pp. 117–124.Google Scholar
- Sharma HS, Westman J, Gordh T, Alm P. 2000b. Topical application of brain derived neurotrophic factor influences upregulation of constitutive isoform of heme oxygenase in the spinal cord following trauma. An experimental study using immunohistochemistry in the rat. Acta Neurochir Suppl 76: 365–369.Google Scholar
- Sharma HS, Westman J, Nyberg F. 1997a. Topical application of 5-HT antibodies reduces edema and cell changes following trauma to the rat spinal cord. Acta Neurochir Suppl (Wien) 70: 155–158.Google Scholar
- Sharma HS, Westman J, Nyberg F. 1998a. Pathophysiology of brain edema and cell changes following hyperthermic brain injury. Brain functions in hot environment. Sharma HS, Westman J, editors. Progress in Brain Research. 115: 351-412.Google Scholar
- Sharma HS, Westman J, Olsson Y, Alm P. 1996a. Involvement of nitric oxide in acute spinal cord injury: An immunohistochemical study using light and electron microscopy in the rat. Neurosci Res 24: 373–384.Google Scholar
- Sharma HS, Wiklund L, Badgaiyan RD, Mohanty S, Alm P. 2006c. Intracerebral administration of neuronal nitric oxide synthase antiserum attenuates traumatic brain injury-induced blood–brain barrier permeability, brain edema formation, and sensory motor disturbances in the rat. Acta Neurochir Suppl 96: 288–294.Google Scholar
- Sharma HS, Winkler T, Stalberg E, Gordh T, Alm P, et al. 2003b.Topical application of TNF-alpha antiserum attenuates spinal cord trauma induced edema formation, microvascular permeability disturbances and cell injury in the rat. Acta Neurochir Suppl 86: 407–413.Google Scholar
- Sharma HS, Winkler T, Stålberg E, Mohanty S, Westman J. 2000a. p-Chlorophenylalanine, an inhibitor of serotonin synthesis reduces blood–brain barrier permeability, cerebral blood flow, edema formation and cell injury following trauma to the rat brain. Acta Neurochir Suppl 76: 91–95.Google Scholar
- Sharma HS, Winkler T, Stålberg E, Olsson Y, Dey PK. 1991b. Evaluation of traumatic spinal cord edema using evoked potentials recorded from the spinal epidural space. An experimental study in the rat. J Neurol Sci 102: 150–162.Google Scholar
- Sharma HS, Zimmer C, Westman J, Cervós-Navarro J. 1992d. Acute systemic heat stress increases glial fibrillary acidic protein immunoreactivity in brain. An experimental study in the conscious normotensive young rats. Neuroscience 48: 889–901.Google Scholar
- Sheridan JF, Dobbs C, Brown D, Swilling B. 1994. Psychoneuroimmunology: Stress effects on pathogenesis and immunity during infection. Clin Microbiol Rev 7: 202–212.Google Scholar
- Sherman DG, Hart RG, Easton JD. 1981. Abrupt change in head position and cerebral infarction. Stroke 12(1): 2–6.PubMedGoogle Scholar
- Shu C, Shen H, Keep RF, Smith DE. 2002. Role of PEPT2 in peptide/mimetic trafficking at the blood-CSF barrier: Studies in rat choroid plexus epithelial cells in primary culture. J Pharmacol Exp Ther 301: 820–829.PubMedGoogle Scholar
- Shvedova AA, Kisin ER, Mercer R, Murray AR, Johnson VJ, et al. 2005. Unusual inflammatory and fibrogenic pulmonary responses to single-walled carbon nanotubes in mice. Am J Physiol Lung Cell Mol Physiol 289(5): L698–L708.PubMedGoogle Scholar
- Simonsen AH, Sheykhzade M, Berg Nyborg NC. 2004. Age- and endothelium-dependent changes in coronary artery reactivity to serotonin and calcium. Vascul Pharmacol 41(2): 43–49.PubMedGoogle Scholar
- Sminia P, Zee J, van der Wondergem J, Haveman J. 1994. Effect of hyperthermia on the central nervous system: A review. Int J Hyperthermia 10(1): 1–30.PubMedGoogle Scholar
- Smith QR, Rapoport SI. 1986. Cerebrovascular permeability coefficients to sodium, potassium, and chloride. J Neurochem 46: 1732–1742.PubMedGoogle Scholar
- Sofroniew MV. 2005. Reactive astrocytes in neural repair and protection. Neuroscientist 11(5): 400–407.PubMedGoogle Scholar
- Spector R, Johanson C. 1989. The mammalian choroid plexus. Sci Am 261(5): 68–74.PubMedGoogle Scholar
- Starling EH. 1896. On the absorption of fluids from the connective tissue spaces. J Physiol 19: 312–326.PubMedGoogle Scholar
- Staub NC. 1974. Pulmonary edema. Physiol Rev 54: 678–811.PubMedGoogle Scholar
- Stern JR, Eggleston LV, Hems R, Krebs HA. 1949. Accumulation of glutamic acid in isolated brain tissue. Biochem J 44: 410–418.Google Scholar
- Stern WE. 1959. Studies in experimental brain swelling and brain compression. J Neurosurg 16: 676–704.PubMedGoogle Scholar
- Stokes BT, Somerson SK. 1987. Spinal cord extracellular microenvironment: Can the changes resulting from trauma be graded? Neurochem Pathol 7: 47–55.PubMedGoogle Scholar
- Strazielle N, Ghersi-Egea JF. 1999. Demonstration of a coupled metabolism-efflux process at the choroid plexus as a mechanism of protection toward xenobiotics. J Neurosci 19: 6275–6289.PubMedGoogle Scholar
- Sutton CH, Carroll FB. 1979. Effects of microwave-induced hyperthermia on the blood–brain barrier of the rat. Radio Sci 14: 329–334.Google Scholar
- Sypert GW. 1990a. Thoracolumbar fusion techniques. Clin Neurosurg 36: 186–216.Google Scholar
- Sypert GW. 1990b. Stabilization and management of cervical injuries. Pitt LH, Wagner FC, editors. Craniospinal Trauma. Thieme; New York: pp. 363–370.Google Scholar
- Taub E, Uswatte G. 2005. Use of CI therapy for improving motor ability after chronic CNS damage: A development prefigured by paul Bach-y-Rita. J Integr Neurosci 4(4): 465–477.PubMedGoogle Scholar
- Toole JF, Tucker SH. 1960. Influence of head position upon cerebral circulation. Arch Neurol 2: 42–49.Google Scholar
- Tramo MJ, Hainline B, Petito F, Lee B, Caronna J. 1985. Vertebral artery injury and cerebellar stroke while swimming: Case report. Stroke 16(6): 1039–1042.PubMedGoogle Scholar
- Tsuda M, Mizokoshi A, Shigemoto-Mogami Y, Koizumi S, Inoue K. 2004. Activation of p38 mitogen-activated protein kinase in spinal hyperactive microglia contributes to pain hypersensitivity following peripheral nerve injury. Glia 45(1): 89–95.PubMedGoogle Scholar
- A. van Harreveld 1966. Extracellular space in the central nervous system. Proc K Ned Akad Wet C 69(1): 17–21.Google Scholar
- A, van Harreveld Dubrovsky BO. 1967. Water and electrolytes in hydrated gray and white matter. Brain Res 4: 81–86.PubMedGoogle Scholar
- Vannemreddy P, Ray AK, Patnaik R, Patnaik S, Mohanty S, et al. 2006. Zinc protoporphyrin IX attenuates closed head injury-induced edema formation, blood–brain barrier disruption, and serotonin levels in the rat. Acta Neurochir Suppl 96: 151–156.PubMedGoogle Scholar
- Vigh-Teichmann I, Vigh B. 1970. Structure and function of the liquor contacting neurosecretory system. Aspects of Neuroendocrinology. Bargmann W, Scharrer B, editors. Berlin: Springer-Verlag; pp. 329–337.Google Scholar
- Wagner FC, Green BA, Bucy PC. 1971. Spinal cord edema associated with paraplegia. Proc Veterans Adm Spinal Cord Inj Conf 18: 9–10.PubMedGoogle Scholar
- Wagner FC Jr, Stewart WB. 1981. Effect of trauma dose on spinal cord edema. J Neurosurg 54: 802–806.PubMedGoogle Scholar
- Wahl M, Unterberg A, Baethmann A, Schilling L. 1988. Mediators of blood–brain barrier dysfunction and formation of vasogenic brain edema. J Cereb Blood Flow Metab 8: 621–634.PubMedGoogle Scholar
- Whetstone WD, Hsu JY, Eisenberg M, Werb Z, Noble-Haeusslein LJ. 2003. Blood–spinal cord barrier after spinal cord injury: Relation to revascularization and wound healing. J Neurosci Res 74(2): 227–239.PubMedGoogle Scholar
- Warheit DB, Laurence BR, Reed KL, Roach DH, Reynolds GA, Webb TR. et al. 2004. Comparative pulmonary toxicity assessment of single-wall carbon nanotubes in rats. Toxicol Sci 77(1): 117–125.PubMedGoogle Scholar
- Wiederhielm CA. 1968. Dynamics of transcapillary fluid exchange. J Gen Physiol 52: 29S–63S.Google Scholar
- Williams WM, Hoss W, Formaniak M, Michaelson SM. 1984. Effect of 2450 MHz microwave energy on the blood–brain barrier to hydrophilic molecules. A. Effect on the permeability to sodium fluorescein. Brain Res 319(2): 165–170.PubMedGoogle Scholar
- Windle WF. 1980. The spinal cord and its reaction to traumatic injury. Anatomy-physiology-pharmacology-therapeutics. Modern Pharmacology-Toxicology, Vol. 18. New York, Basel: Marcel Dekker.Google Scholar
- Winkelstein BA, De Leo JA. 2002. Nerve root injury severity differentially modulates spinal glial activation in a rat lumbar radiculopathy model: Considerations for persistent pain. Brain Res 956(2): 294–301.PubMedGoogle Scholar
- Winkler T, Sharma HS, Stålberg E, Olsson Y, Dey PK. 1995. Impairment of blood–brain barrier function by serotonin induces desynchronisation of spontaneous cerebral cortical activity. Experimental observations in the anaesthetised rat. Neuroscience 68: 1097–1104.PubMedGoogle Scholar
- Winkler T, Sharma HS, Stålberg E, Westman. 1998. Spinal cord bioelectrical activity, edema and cell injury following a focal trauma to the spinal cord. An experimental study using pharmacological and morphological approach. Spinal Cord Monitoring. Basic Principles, Regeneration, Pathophysiology and Clinical Aspects. Stålberg E, Sharma HS, Olsson Y, editors. New York: Springer Wien; pp. 283–363.Google Scholar
- Woodbury DM. 1974. Maturation of the blood–brain barrier and blood–CSF barrier. Drugs and Developing Brain. Vernadakis A, Weiner N, editors. New York: Plenum Press; pp. 259–280.Google Scholar
- Woolf CJ. 1983. Evidence for a central component of post-injury pain hypersensitivity. Nature 306: 686–688.PubMedGoogle Scholar
- Woolf CJ, Shortland P, Coggeshall RE. 1992. Peripheral nerve injury triggers central sprouting of myelinated afferents. Nature 355: 75–78.PubMedGoogle Scholar
- Xia T, Kovochich M, Brant J, Hotze M, Sempf J, et al. 2006. Comparison of the abilities of ambient and manufactured nanoparticles to induce cellular toxicity according to an oxidative stress paradigm. Nano Lett 6(8): 1794–1807.PubMedGoogle Scholar
- Yashon D, Bingham WG Jr, Faddoul EM, Hunt WE. 1973. Edema of the spinal cord following experimental impact trauma. J Neurosurg 38(6): 693–697.PubMedGoogle Scholar
- Yeo JD. 1976. A review of experimental research in spinal cord injury. Paraplegia 14(1): 1–11.PubMedGoogle Scholar
- Zai LJ, Wrathall JR. 2005. Cell proliferation and replacement following contusive spinal cord injury. Glia 50(3): 247–257.PubMedGoogle Scholar
- Zebrowska-Lupina I, Stelmasiak M, Porowska A. 1990. Stress-induced depression of basal motility: Effects of antidepressant drugs. Pol J Pharmacol Pharm 42(2): 97–104.PubMedGoogle Scholar
- Zenker D, Begley D, Bratzke H, Rubsamen-Waigmann H, Briesen H. von 2003. Human blood-derived macrophages enhance barrier function of cultured primary bovine and human brain capillary endothelial cells. J Physiol 551(Pt 3): 1023–1032.PubMedGoogle Scholar
- Zhu S, Oberdorster E, Haasch ML. 2006.Toxicity of an engineered nanoparticle (fullerene, C60) in two aquatic species, Daphnia and fathead minnow. Mar Environ Res 62 (Suppl): S5–S9. Epub 2006 Apr 22.PubMedGoogle Scholar