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Light and electron microscopic assessment of progressive atrophy following moderate traumatic brain injury in the rat

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Abstract

The presence of progressive white matter atrophy following traumatic brain injury (TBI) has been reported in humans as well as in animal models. However, a quantitative analysis of progressive alterations in myelinated axons and other cellular responses to trauma has not been conducted. This study examined quantitative differences in myelinated axons from several white and gray matter structures between non-traumatized and traumatized areas at several time points up to 1 year. We hypothesize that axonal numbers decrease over time within the structures analyzed, based on our previous work demonstrating shrinkage of tissue in these vulnerable areas. Intubated, anesthetized male Sprague-Dawley rats were subjected to moderate (1.8–2.2 atm) parasagittal fluid-percussion brain injury, and perfused at various intervals after surgery. Sections from the fimbria, external capsule, thalamus and cerebral cortex from the ipsilateral hemisphere of traumatized and sham-operated animals were prepared and. estimated total numbers of myelinated axons were determined by systematic random sampling. Electron micrographs were obtained for ultrastructural analysis. A significant (P<0.05) reduction in the number of myelinated axons in the traumatized hemisphere compared to control in all structures was observed. In addition, thalamic and cortical axonal counts decreased significantly (P<0.05) over time. Swollen axons and macrophage/microglia infiltration were present as late as 6 months post-TBI in various structures. This study is the first to describe quantitatively chronic axonal changes in vulnerable brains regions after injury. Based on these data, a time-dependent decrease in the number of myelinated axons is seen to occur in vulnerable gray matter regions including the cerebral cortex and thalamus along with distinct morphological changes within white matter tracts after TBI. Although this progressive axonal response to TBI may include Wallerian degeneration, other potential mechanisms underlying this progressive pathological response within the white matter are discussed.

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References

  1. Adams JH, Doyle D, Ford I, Gennarelli TA, Graham DI, McLellan DR (1989) Diffuse axonal injury in head injury: definition, diagnosis and grading. Histopathology 15:49–59

    Google Scholar 

  2. Adams JH, Graham DI, Gennarelli TA, Maxwell WL (1991) Diffuse axonal injury in non-missile head injury. J Neurol Neurosurg Psychiatry 54:481–483

    Google Scholar 

  3. Anderson CV, Bigler ED (1995) Ventricular dilation, cortical atrophy, and neuropsychological outcome following traumatic brain injury. J Neuropsychiatry Clin Neurosci 7:42–48

    Google Scholar 

  4. Arvin B, Neville LF, Barone FC, Feuerstein GZ (1996) The role of inflammation and cytokines in brain injury. Neurosci Biobehav Rev 20:445–452

    Google Scholar 

  5. Biagas KV, Uhl MW, Schiding JK, Nemoto EM, Kochanek PM (1992) Assessment of posttraumatic polymorphonuclear leukocyte accumulation in rat brain using tissue myeloperoxidase assay and vinblastine treatment. J Neurotrauma 9:363–371

    Google Scholar 

  6. Blumbergs PC, Scott G, Manavis J, Wainwright H, Simpson DA, McLean AJ (1994) Staining of amyloid precursor protein to study axonal damage in mild head injury. Lancet 344:1055–1066

    Google Scholar 

  7. Bramlett HM, Dietrich WD (2002) Quantitative structural changes in white and gray matter 1 year following traumatic brain injury in rats. Acta Neuropathol 103:607–614

    Google Scholar 

  8. Bramlett HM, Dietrich WD (2004) Pathophysiology of cerebral ischemia and brain trauma: similarities and differences. J Cereb Blood Flow Metab 24:133–150

    Google Scholar 

  9. Bramlett HM, Dietrich WD, Green EJ, Busto R (1997) Chronic histopathological consequences of fluid-percussion brain injury in rats: effects of post-traumatic hypothermia. Acta Neuropathol 93:190–199

    Google Scholar 

  10. Bramlett HM, Kraydieh S, Green EJ, Dietrich WD (1997) Temporal and regional patterns of axonal damage following traumatic brain injury: a beta-amyloid precursor protein immunocytochemical study in rats. J Neuropathol Exp Neurol 56:1132–1141

    Google Scholar 

  11. Braun H, Schafer K, Hollt V (2002) BetaIII tubulin-expressing neurons reveal enhanced neurogenesis in hippocampal and cortical structures after a contusion trauma in rats. J Neurotrauma 19:975–983

    Google Scholar 

  12. Bullock R, Maxwell WL, Graham DI, Teasdale GM, Adams JH (1991) Glial swelling following human cerebral contusion: an ultrastructural study. J Neurol Neurosurg Psychiatry 54:427–434

    Google Scholar 

  13. Carlos TM, Clark RS, Franicola-Higgins D, Schiding JK, Kochanek PM (1997) Expression of endothelial adhesion molecules and recruitment of neutrophils after traumatic brain injury in rats. J Leukoc Biol 61:279–285

    Google Scholar 

  14. Chatzipanteli K, Alonso OF, Kraydieh S, Dietrich WD (2000) Importance of posttraumatic hypothermia and hyperthermia on the inflammatory response after fluid percussion brain injury: biochemical and immunocytochemical studies. J Cereb Blood Flow Metab 20:531–542

    Google Scholar 

  15. Chen XH, Iwata A, Nonaka M, Browne KD, Smith DH (2003) Neurogenesis and glial proliferation persist for at least one year in the subventricular zone following brain trauma in rats. J Neurotrauma 20:623–631

    Google Scholar 

  16. Chirumamilla S, Sun D, Bullock MR, Colello RJ (2002) Traumatic brain injury induced cell proliferation in the adult mammalian central nervous system. J Neurotrauma 19:693–703

    Google Scholar 

  17. Chodobski A, Chung I, Kozniewska E, Ivanenko T, Chang W, Harrington JF, Duncan JA, Szmydynger-Chodobska J (2003) Early neutrophilic expression of vascular endothelial growth factor after traumatic brain injury. Neuroscience 122:853–867

    Google Scholar 

  18. Crutcher KA (1990) The regulation of axonal growth in the mature mammalian nervous system. Acta Neurobiol Exp (Wars) 50:115–124

    Google Scholar 

  19. Csuka E, Hans VH, Ammann E, Trentz O, Kossmann T, Morganti-Kossmann MC (2000) Cell activation and inflammatory response following traumatic axonal injury in the rat. Neuroreport 11:2587–2590

    Google Scholar 

  20. Cullum CM, Bigler ED (1986) Ventricle size, cortical atrophy and the relationship with neuropsychological status in closed head injury: a quantitative analysis. J Clin Exp Neuropsychol 8:437–452

    Google Scholar 

  21. Dixon CE, Kochanek PM, Yan HQ, Schiding JK, Griffith RG, Baum E, Marion DW, DeKosky ST (1999) One-year study of spatial memory performance, brain morphology, and cholinergic markers after moderate controlled cortical impact in rats. J Neurotrauma 16:109–122

    Google Scholar 

  22. Feuerstein GZ, Liu T, Barone FC (1994) Cytokines, inflammation, and brain injury: role of tumor necrosis factor-alpha. Cerebrovasc Brain Metab Rev 6:341–360

    Google Scholar 

  23. Furukawa S, Furukawa Y, Satoyoshi E, Hayashi K (1986) Synthesis and secretion of nerve growth factor by mouse astroglial cells in culture. Biochem Biophys Res Commun 136:57–63

    Google Scholar 

  24. Gahm C, Holmin S, Mathiesen T (2000) Temporal profiles and cellular sources of three nitric oxide synthase isoforms in the brain after experimental contusion. Neurosurgery 46:169–177

    Google Scholar 

  25. Gale SD, Johnson SC, Bigler ED, Blatter DD (1995) Nonspecific white matter degeneration following traumatic brain injury. J Int Neuropsychol Soc 1:17–28

    Google Scholar 

  26. Gennarelli TA, Thibault LE, Adams JH, Graham DI, Thompson CJ, Marcincin RP (1982) Diffuse axonal injury and traumatic coma in the primate. Ann Neurol 12:564–574

    Google Scholar 

  27. Gentleman SM, Roberts GW, Gennarelli TA, Maxwell WL, Adams JH, Kerr S, Graham DI (1995) Axonal injury: a universal consequence of fatal closed head injury? Acta Neuropathol 89:537–543

    Google Scholar 

  28. Gentleman SM, Leclercq PD, Moyes L, Graham DI, Smith C, Griffin WS, Nicoll JA (2004) Long-term intracerebral inflammatory response after traumatic brain injury. Forensic Sci Int 146:97–104

    Google Scholar 

  29. Goss JR, O’Malley ME, Zou L, Styren SD, Kochanek PM, DeKosky ST (1998) Astrocytes are the major source of nerve growth factor upregulation following traumatic brain injury in the rat. Exp Neurol 149:301–309

    Google Scholar 

  30. Grad S, Ertel W, Keel M, Infanger M, Vonderschmitt DJ, Maly FE (1998) Strongly enhanced serum levels of vascular endothelial growth factor (VEGF) after polytrauma and burn. Clin Chem Lab Med 36:379–383

    Google Scholar 

  31. Graham DI, Gentleman SM, Lynch A, Roberts GW (1995) Distribution of beta-amyloid protein in the brain following severe head injury. Neuropathol Appl Neurobiol 21:27–34

    Google Scholar 

  32. Graham DI, McIntosh TK, Maxwell WL, Nicoll JA (2000) Recent advances in neurotrauma. J Neuropathol Exp Neurol 59:641–651

    Google Scholar 

  33. Graham DI, Raghupathi R, Saatman KE, Meaney D, McIntosh TK (2000) Tissue tears in the white matter after lateral fluid percussion brain injury in the rat: relevance to human brain injury. Acta Neuropathol 99:117–124

    Google Scholar 

  34. Hamberger A, Huang YL, Zhu H, Bao F, Ding M, Blennow K, Olsson A, Hansson HA, Viano D, Haglid KG (2003) Redistribution of neurofilaments and accumulation of beta-amyloid protein after brain injury by rotational acceleration of the head. J Neurotrauma 20:169–178

    Google Scholar 

  35. Holmin S, Schalling M, Hojeberg B, Nordqvist AC, Skeftruna AK, Mathiesen T (1997) Delayed cytokine expression in rat brain following experimental contusion. J Neurosurg 86:493–504

    Google Scholar 

  36. Hughes CC, Lantos PL (1987) A morphometric study of blood vessel, neuron and glial cell distribution in young and old rat brain. J Neurol Sci 79:101–110

    Google Scholar 

  37. Jafari SS, Maxwell WL, Neilson M, Graham DI (1997) Axonal cytoskeletal changes after non-disruptive axonal injury. J Neurocytol 26:207–221

    Google Scholar 

  38. Jafari SS, Nielson M, Graham DI, Maxwell WL (1998) Axonal cytoskeletal changes after nondisruptive axonal injury. II. Intermediate sized axons. J Neurotrauma 15:955–966

    Google Scholar 

  39. Kimbelberg HK, Norenberg MD (1994) Astroglial response to CNS trauma. In: Salzman SK, Faden AI (eds) The neurobiology of central nervous system trauma. Oxford University Press, New York, pp 193–208

  40. Kinoshita K, Chatzipanteli K, Vitarbo E, Truettner JS, Alonso OF, Dietrich WD (2002) Interleukin-1beta messenger ribonucleic acid and protein levels after fluid-percussion brain injury in rats: importance of injury severity and brain temperature. Neurosurgery 51:195–203

    Google Scholar 

  41. Kunz T, Marklund N, Hillered L, Oliw EH (2002) Cyclooxygenase-2, prostaglandin synthases, and prostaglandin H2 metabolism in traumatic brain injury in the rat. J Neurotrauma 19:1051–1064

    Google Scholar 

  42. Leclercq PD, McKenzie JE, Graham DI, Gentleman SM (2001) Axonal injury is accentuated in the caudal corpus callosum of head-injured patients. J Neurotrauma 18:1–9

    Google Scholar 

  43. Leclercq PD, Stephenson MS, Murray LS, McIntosh TK, Graham DI, Gentleman SM (2002) Simple morphometry of axonal swellings cannot be used in isolation for dating lesions after traumatic brain injury. J Neurotrauma 19:1183–1192

    Google Scholar 

  44. Lewen A, Li GL, Nilsson P, Olsson Y, Hillered L (1995) Traumatic brain injury in rat produces changes of beta-amyloid precursor protein immunoreactivity. Neuroreport 6:357–360

    Google Scholar 

  45. Li S, Jiang Q, Stys PK (2000) Important role of reverse Na(+)-Ca(2+) exchange in spinal cord white matter injury at physiological temperature. J Neurophysiol 84:1116–1119

    Google Scholar 

  46. Liberto CM, Albrecht PJ, Herx LM, Yong VW, Levison SW (2004) Pro-regenerative properties of cytokine-activated astrocytes. J Neurochem 89:1092–1100

    Google Scholar 

  47. Liedtke W, Edelmann W, Bieri PL, Chiu FC, Cowan NJ, Kucherlapati R, Raine CS (1996) GFAP is necessary for the integrity of CNS white matter architecture and long-term maintenance of myelination. Neuron 17:607–615

    Google Scholar 

  48. Liu D, Smith CL, Barone FC, Ellison JA, Lysko PG, Li K, Simpson IA (1999) Astrocytic demise precedes delayed neuronal death in focal ischemic rat brain. Brain Res Mol Brain Res 68:29–41

    Google Scholar 

  49. LoPachin RM, Lehning EJ (1997) Mechanism of calcium entry during axon injury and degeneration. Toxicol Appl Pharmacol 143:233–244

    Google Scholar 

  50. Lu J, Moochhala S, Shirhan M, Ng KC, Tan MH, Teo AL, Ling EA (2003) Nitric oxide induces macrophage apoptosis following traumatic brain injury in rats. Neurosci Lett 339:147–150

    Google Scholar 

  51. Maxwell WL (1996) Histopathological changes at central nodes of Ranvier after stretch-injury. Microsc Res Tech 34:522–535

    Google Scholar 

  52. Maxwell WL, Graham DI (1997) Loss of axonal microtubules and neurofilaments after stretch-injury to guinea pig optic nerve fibers. J Neurotrauma 14:603–614

    Google Scholar 

  53. Maxwell WL, Irvine A, Graham, Adams JH, Gennarelli TA, Tipperman R, Sturatis M (1991) Focal axonal injury: the early axonal response to stretch. J Neurocytol 20:157–164

    Google Scholar 

  54. Maxwell WL, Watt C, Graham DI, Gennarelli TA (1993) Ultrastructural evidence of axonal shearing as a result of lateral acceleration of the head in non-human primates. Acta Neuropathol 86:136–144

    Google Scholar 

  55. Maxwell WL, Povlishock JT, Graham DL (1997) A mechanistic analysis of nondisruptive axonal injury: a review. J Neurotrauma 14:419–440

    Google Scholar 

  56. Maxwell WL, Kosanlavit R, McCreath BJ, Reid O, Graham DI (1999) Freeze-fracture and cytochemical evidence for structural and functional alteration in the axolemma and myelin sheath of adult guinea pig optic nerve fibers after stretch injury. J Neurotrauma 16:273–284

    Google Scholar 

  57. Maxwell WL, Domleo A, McColl G, Jafari SS, Graham DI (2003) Post-acute alterations in the axonal cytoskeleton after traumatic axonal injury. J Neurotrauma 20:151–168

    Google Scholar 

  58. McKenzie KJ, McLellan DR, Gentleman SM, Maxwell WL, Gennarelli TA, Graham DI (1996) Is beta-APP a marker of axonal damage in short-surviving head injury? Acta Neuropathol 92:608–613

    Google Scholar 

  59. Medana IM, Esiri MM (2003) Axonal damage: a key predictor of outcome in human CNS diseases. Brain 126:515–530

    Google Scholar 

  60. Morganti-Kossman MC, Lenzlinger PM, Hans V, Stahel P, Csuka E, Ammann E, Stocker R, Trentz O, Kossmann T (1997) Production of cytokines following brain injury: beneficial and deleterious for the damaged tissue. Mol Psychiatry 2:133–136

    Google Scholar 

  61. Morganti-Kossmann MC, Rancan M, Stahel PF, Kossmann T (2002) Inflammatory response in acute traumatic brain injury: a double-edged sword. Curr Opin Crit Care 8:101–105

    Google Scholar 

  62. Murphy S, Pearce B (1987) Functional receptors for neurotransmitters on astroglial cells. Neuroscience 22:381–394

    Google Scholar 

  63. 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 61:778–788

    Google Scholar 

  64. Nonaka M, Chen XH, Pierce JE, Leoni MJ, McIntosh TK, Wolf JA, Smith DH (1999) Prolonged activation of NF-kappaB following traumatic brain injury in rats. J Neurotrauma 16:1023–1034

    Google Scholar 

  65. Orihara Y, Ikematsu K, Tsuda R, Nakasono I (2001) Induction of nitric oxide synthase by traumatic brain injury. Forensic Sci Int 123:142–149

    Google Scholar 

  66. Paxinos G, Watson C (1982) The rat brain in stereotaxic coordinates. Academic Press, New York

  67. Peters A, Palay SL, Webster HdeF. (1976) The fine structure of the nervous system. Saunders, Philadelphia

  68. Pettus EH, Povlishock JT (1996) Characterization of a distinct set of intra-axonal ultrastructural changes associated with traumatically induced alteration in axolemmal permeability. Brain Res 722:1–11

    Google Scholar 

  69. Pierce JE, Trojanowski JQ, Graham DI, Smith DH, McIntosh TK (1996) Immunohistochemical characterization of alterations in the distribution of amyloid precursor proteins and beta-amyloid peptide after experimental brain injury in the rat. J Neurosci 16:1083–1090

    Google Scholar 

  70. Pierce JE, Smith DH, Trojanowski JQ, McIntosh TK (1998) Enduring cognitive, neurobehavioral and histopathological changes persist for up to one year following severe experimental brain injury in rats. Neuroscience 87:359–369

    Google Scholar 

  71. Povlishock JT, Christman CW (1995) The pathobiology of traumatically induced axonal injury in animals and humans: a review of current thoughts. J Neurotrauma 12:555–564

    Google Scholar 

  72. Povlishock JT, Jenkins LW (1995) Are the pathobiological changes evoked by traumatic brain injury immediate and irreversible? Brain Pathol 5:415–426

    Google Scholar 

  73. Povlishock JT, Pettus EH (1996) Traumatically induced axonal damage: evidence for enduring changes in axolemmal permeability with associated cytoskeletal change. Acta Neurochir (Wien) Suppl 66:81–86

    Google Scholar 

  74. Rosenberg LJ, Wrathall JR (1997) Quantitative analysis of acute axonal pathology in experimental spinal cord contusion. J Neurotrauma 14:823–838

    Google Scholar 

  75. Schwab JM, Seid K, Schluesener HJ (2001) Traumatic brain injury induces prolonged accumulation of cyclooxygenase-1 expressing microglia/brain macrophages in rats. J Neurotrauma 18:881–890

    Google Scholar 

  76. Sherriff FE, Bridges LR, Sivaloganathan S (1994) Early detection of axonal injury after human head trauma using immunocytochemistry for beta-amyloid precursor protein. Acta Neuropathol 87:55–62

    Google Scholar 

  77. Shohami E, Novikov M, Bass R, Yamin A, Gallily R (1994) Closed head injury triggers early production of TNF alpha and IL-6 by brain tissue. J Cereb Blood Flow Metab 14:615–619

    Google Scholar 

  78. Shore PM, Jackson EK, Wisniewski SR, Clark RS, Adelson PD, Kochanek PM (2004) Vascular endothelial growth factor is increased in cerebrospinal fluid after traumatic brain injury in infants and children. Neurosurgery 54:605–611; discussion 611–612

    Google Scholar 

  79. Smith DH, Chen XH, Pierce JE, Wolf JA, Trojanowski JQ, Graham DI, McIntosh TK (1997) Progressive atrophy and neuron death for one year following brain trauma in the rat. J Neurotrauma 14:715–727

    Google Scholar 

  80. Soares HD, Hicks RR, Smith D, McIntosh TK (1995) Inflammatory leukocytic recruitment and diffuse neuronal degeneration are separate pathological processes resulting from traumatic brain injury. J Neurosci 15:8223–8233

    Google Scholar 

  81. Strauss KI, Barbe MF, Marshall RM, Raghupathi R, Mehta S, Narayan RK (2000) Prolonged cyclooxygenase-2 induction in neurons and glia following traumatic brain injury in the rat. J Neurotrauma 17:695–711

    Google Scholar 

  82. Tanaka K, Nogawa S, Suzuki S, Dembo T, Kosakai A (2003) Upregulation of oligodendrocyte progenitor cells associated with restoration of mature oligodendrocytes and myelination in peri-infarct area in the rat brain. Brain Res 989:172–179

    Google Scholar 

  83. Van der Naalt J, Hew JM, Van Zomeren AH, Sluiter WJ, Minderhoud JM (1999) Computed tomography and magnetic resonance imaging in mild to moderate head injury: early and late imaging related to outcome. Ann Neurol 46:70–78

    Google Scholar 

  84. Vega JA, Del Valle M, Amenta F (1994) Expression of neurofilament proteins in the rat cerebellar cortex as a function of age: an immunohistochemical study. Mech Ageing Dev 73:9–16

    Google Scholar 

  85. Wada K, Chatzipanteli K, Kraydieh S, Busto R, Dietrich WD (1998) Inducible nitric oxide synthase expression after traumatic brain injury and neuroprotection with aminoguanidine treatment in rats. Neurosurgery 43:1427–1436

    Google Scholar 

  86. West MJ (1993) New stereological methods for counting neurons. Neurobiol Aging 14:275–285

    Google Scholar 

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Acknowledgements

We wish to thank the Electron Microscopy Core and the Image Analysis Core of the Miami Project to Cure Paralysis, especially Dr. Beata Frydel, for their support and facilities to accomplish this study. We wish to thank Robert Camarena for his assistance in photography, Ofelia Alonso for her excellent technical assistance and Dr. W. Dalton Dietrich for his helpful suggestions in preparing this manuscript. This research was supported by Army Grant DAMD17-02-1-0190.

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Correspondence to Helen M. Bramlett.

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Rodriguez-Paez, A.C., Brunschwig, J.P. & Bramlett, H.M. Light and electron microscopic assessment of progressive atrophy following moderate traumatic brain injury in the rat. Acta Neuropathol 109, 603–616 (2005). https://doi.org/10.1007/s00401-005-1010-z

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