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Postoperative Pain Management and Proinflammatory Cytokines: Animal and Human Studies

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Abstract

The postoperative period is associated with neuroendocrine, metabolic, and immune alterations, which are the combined result of tissue damage, anesthesia, postoperative pain, and psychological stress. Limited evidence indicates that pain management in the postoperative period can affect the outcome of the surgery, reducing cardiac, pulmonary, and metabolic complications. Recent evidence indicates that pain and immune factors, especially proinflammatory cytokines, mutually interact and influence each other. A series of animal studies demonstrates that effective preemptive analgesia improved postoperative recovery, and this effect was enhanced by coadministration of IL-1ra together with the preemptive analgesics. Furthermore, preemptive analgesia attenuated surgery-induced PGE2 production in the amygdala and the activation of the HPA axis. IL-1 signaling is required for the production of amygdala PGE2 in response to surgical stress, and may thus affect the physiological and psychological aspects of surgical stress. These reports suggest that short-term effective analgesia can have long-lasting beneficial effects on surgery recovery. They further suggest that IL-1 blockade should be considered in the clinical management of pain associated with peripheral or nerve injury. Another series of human studies describes an interaction between the effectiveness of postoperative pain relief and surgery-associated immune alterations: In three separate studies, the more effective pain management technique was associated with diminished surgery-induced immune alterations, especially diminished elevation of IL-1. Reduced elevation of postoperative IL-1 and effective pain relief may both contribute to an attenuated illness response and a better surgery outcome.

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References

  • Baxevanis CN, Papilas K, Dedoussis GV, Pavlis T, Papamichail M (1994) Abnormal cytokine serum levels correlate with impaired cellular immune responses after surgery. Clin Immunol Immunopathol 71:82–88

    Article  PubMed  CAS  Google Scholar 

  • Beilin B, Bessler H, Mayburd E, Smirnov G, Dekel A, Yardeni I, Shavit Y (2003a) Effects of preemptive analgesia on pain and cytokine production in the postoperative period. Anesthesiology 98:151–155

    Article  PubMed  CAS  Google Scholar 

  • Beilin B, Bessler H, Papismedov L, Weinstock M, Shavit Y (2005) Continuous physostigmine combined with morphine-based patient-controlled analgesia in the postoperative period. Acta Anaesthesiol Scand 49:78–84

    Article  PubMed  CAS  Google Scholar 

  • Beilin B, Shavit Y, Dekeyser FG, Itzik A, Weidenfeld J (2006) The involvement of glucocorticoids and interleukin-1 in the regulation of brain prostaglandin production in response to surgical stress. Neuroimmunomodulation 13:36–42

    Article  PubMed  CAS  Google Scholar 

  • Beilin B, Shavit Y, Trabekin E, Mordashev B, Mayburd E, Zeidel A, Bessler H (2003b) The effects of postoperative pain management on immune response to surgery. Anesth Analg 97:822–827

    Article  PubMed  Google Scholar 

  • Besedovsky HO, del Rey A (1996) Immune-neuro-endocrine interactions: facts and hypotheses. Endocr Rev 17:64–102

    Article  PubMed  CAS  Google Scholar 

  • Borovikova LV, Ivanova S, Zhang M, Yang H, Botchkina GI, Watkins LR, Wang H, Abumrad N, Eaton JW, Tracey KJ (2000) Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin. Nature 405:458–462

    Article  PubMed  CAS  Google Scholar 

  • Buvanendran A, Kroin JS, Berger RA, Hallab NJ, Saha C, Negrescu C, Moric M, Caicedo MS, Tuman KJ (2006) Upregulation of prostaglandin E2 and interleukins in the central nervous system and peripheral tissue during and after surgery in humans. Anesthesiology 104:403–410

    Article  PubMed  CAS  Google Scholar 

  • Chacur M, Milligan ED, Gazda LS, Armstrong C, Wang H, Tracey KJ, Maier SF, Watkins LR (2001) A new model of sciatic inflammatory neuritis (SIN): induction of unilateral and bilateral mechanical allodynia following acute unilateral peri-sciatic immune activation in rats. Pain 94:231–244

    Article  PubMed  CAS  Google Scholar 

  • Christensen P, Brandt MR, Rem J, Kehlet H (1982) Influence of extradural morphine on the adrenocortical and hyperglycaemic response to surgery. Br J Anaesth 54:23–27

    PubMed  CAS  Google Scholar 

  • Coderre TJ, Katz J, Vaccarino AL, Melzack R (1993) Contribution of central neuroplasticity to pathological pain: review of clinical and experimental evidence. Pain 52:259–285

    Article  PubMed  CAS  Google Scholar 

  • Cui JG, Holmin S, Mathiesen T, Meyerson BA, Linderoth B (2000) Possible role of inflammatory mediators in tactile hypersensitivity in rat models of mononeuropathy. Pain 88:239–248

    Article  PubMed  CAS  Google Scholar 

  • Cunha JM, Cunha FQ, Poole S, Ferreira SH (2000) Cytokine-mediated inflammatory hyperalgesia limited by interleukin-1 receptor antagonist. Br J Pharmacol 130:1418–1424

    Article  PubMed  CAS  Google Scholar 

  • DeKeyser FG, Leker RR, Weidenfeld J (2000) Activation of the adrenocortical axis by surgical stress: involvement of central norepinephrine and interleukin-1. Neuroimmunomodulation 7:182–188

    Article  PubMed  CAS  Google Scholar 

  • DeLeo JA, Yezierski RP (2001) The role of neuroinflammation and neuroimmune activation in persistent pain. Pain 90:1–6

    Article  PubMed  CAS  Google Scholar 

  • Dunn AJ (1992) The role of interleukin-1 and tumor necrosis factor alpha in the neurochemical and neuroendocrine responses to endotoxin. Brain Res Bull 29:807–812

    Article  PubMed  CAS  Google Scholar 

  • Falchi M, Ferrara F, Gharib C, Dib B (2001) Hyperalgesic effect of intrathecally administered interleukin-1 in rats. Drugs Exp Clin Res 27:97–101

    PubMed  CAS  Google Scholar 

  • Ferreira SH, Lorenzetti BB, Bristow AF, Poole S (1988) Interleukin-1 beta as a potent hyperalgesic agent antagonized by a tripeptide analogue. Nature 334:698–700

    Article  PubMed  CAS  Google Scholar 

  • Flecknell PA, Liles JH (1991) The effects of surgical procedures, halothane anaesthesia and nalbuphine on locomotor activity and food and water consumption in rats. Lab Anim 25:50–60

    PubMed  CAS  Google Scholar 

  • Friedrich M, Rixecker D, Friedrich G (1999) Evaluation of stress-related hormones after surgery. Clin Exp Obstet Gynecol 26:71–75

    PubMed  CAS  Google Scholar 

  • Goshen I, Yirmiya R, Iverfeldt K, Weidenfeld J (2003) The role of endogenous interleukin-1 in stress-induced adrenal activation and adrenalectomy-induced adrenocorticotropic hormone hypersecretion. Endocrinology 144:4453–4458

    Article  PubMed  CAS  Google Scholar 

  • Hallak M, Giacobini E (1986) Relation of brain regional physostigmine concentration to cholinesterase activity and acetylcholine and choline levels in rat. Neurochem Res 11:1037–1048

    Article  PubMed  CAS  Google Scholar 

  • Hamra JG, Yaksh TL (1996) Equianalgesic doses of subcutaneous but not intrathecal morphine alter phenotypic expression of cell surface markers and mitogen-induced proliferation in rat lymphocytes. Anesthesiology 85:355–365

    Article  PubMed  CAS  Google Scholar 

  • Heinricher MM, Martenson ME, Neubert MJ (2004) Prostaglandin E2 in the midbrain periaqueductal gray produces hyperalgesia and activates pain-modulating circuitry in the rostral ventromedial medulla. Pain 110:419–426

    Article  PubMed  CAS  Google Scholar 

  • Hill AG, Jacobson L, Gonzalez J, Rounds J, Majzoub JA, Wilmore DW (1996) Chronic central nervous system exposure to interleukin-1 beta causes catabolism in the rat. Am J Physiol 271:R1142–R1148

    PubMed  CAS  Google Scholar 

  • Hollmann MW, Durieux ME (2000) Local anesthetics and the inflammatory response: a new therapeutic indication? Anesthesiology 93:858–875

    Article  PubMed  CAS  Google Scholar 

  • Hori T, Oka T, Hosoi M, Abe M, Oka K (2000) Hypothalamic mechanisms of pain modulatory actions of cytokines and prostaglandin E2. Ann NY Acad Sci 917:106–120

    Article  PubMed  CAS  Google Scholar 

  • Jiang CL, Xu D, Lu CL, Wang YX, You ZD, Liu XY (2000) Interleukin-2: structural and biological relatedness to opioid peptides. Neuroimmunomodulation 8:20–24

    Article  PubMed  CAS  Google Scholar 

  • Josephs MD, Solorzano CC, Taylor M, Rosenberg JJ, Topping D, Abouhamze A, Mackay SL, Hirsch E, Hirsh D, Labow M, Moldawer LL (2000) Modulation of the acute phase response by altered expression of the IL-1 type 1 receptor or IL-1ra. Am J Physiol Regul Integr Comp Physiol 278:R824–R830

    PubMed  CAS  Google Scholar 

  • Kalff JC, Turler A, Schwarz NT, Schraut WH, Lee KK, Tweardy DJ, Billiar TR, Simmons RL, Bauer AJ (2003) Intra-abdominal activation of a local inflammatory response within the human muscularis externa during laparotomy. Ann Surg 237:301–315

    Article  PubMed  Google Scholar 

  • Kehlet H, Holte K (2001) Effect of postoperative analgesia on surgical outcome. Br J Anaesth 87:62–72

    Article  PubMed  CAS  Google Scholar 

  • Kehlet H, Werner M, Perkins F (1999) Balanced analgesia: what is it and what are its advantages in postoperative pain? Drugs 58:793–797

    Article  PubMed  CAS  Google Scholar 

  • Kennedy BC, Hall GM (1999) Neuroendocrine and inflammatory aspects of surgery: do they affect outcome? Acta Anaesthesiol Belg 50:205–209

    PubMed  CAS  Google Scholar 

  • Kiecolt-Glaser JK, Page GG, Marucha PT, MacCallum RC, Glaser R (1998) Psychological influences on surgical recovery. Perspectives from psychoneuroimmunology. Am Psychol 53:1209–1218

    Article  PubMed  CAS  Google Scholar 

  • Kissin I (2000) Preemptive analgesia. Anesthesiology 93:1138–1143

    Article  PubMed  CAS  Google Scholar 

  • Kroin JS, Ling ZD, Buvanendran A, Tuman KJ (2004) Upregulation of spinal cyclooxygenase-2 in rats after surgical incision. Anesthesiology 100:364–369

    Article  PubMed  CAS  Google Scholar 

  • Liles JH, Flecknell PA (1993) The effects of surgical stimulus on the rat and the influence of analgesic treatment. Br Vet J 149:515–525

    PubMed  CAS  Google Scholar 

  • Liles JH, Flecknell PA (1994) A comparison of the effects of buprenorphine, carprofen and flunixin following laparotomy in rats. J Vet Pharmacol Ther 17:284–290

    PubMed  CAS  Google Scholar 

  • Liu SS, Allen HW, Olsson GL (1998) Patient-controlled epidural analgesia with bupivacaine and fentanyl on hospital wards: prospective experience with 1,030 surgical patients. Anesthesiology 88:688–695

    Article  PubMed  CAS  Google Scholar 

  • Lloyd CE, Palopoli M, Vary TC (2003) Effect of central administration of interleukin-1 receptor antagonist on protein synthesis in skeletal muscle, kidney, and liver during sepsis. Metabolism 52:1218–1225

    Article  PubMed  CAS  Google Scholar 

  • Lu CH, Chao PC, Borel CO, Yang CP, Yeh CC, Wong CS, Wu CT (2004) Preincisional intravenous pentoxifylline attenuating perioperative cytokine response, reducing morphine consumption, and improving recovery of bowel function in patients undergoing colorectal cancer surgery. Anesth Analg 99:1465–1471

    Article  PubMed  CAS  Google Scholar 

  • Machelska H, Stein C (2006) Leukocyte-derived opioid peptides and inhibition of pain. J Neuroimmune Pharmacol 1:90–97

    Article  PubMed  Google Scholar 

  • Maier SF, Wiertelak EP, Martin D, Watkins LR (1993) Interleukin-1 mediates the behavioral hyperalgesia produced by lithium chloride and endotoxin. Brain Res 623:321–324

    Article  PubMed  CAS  Google Scholar 

  • Marchand F, Perretti M, McMahon SB (2005) Role of the immune system in chronic pain. Nat Rev Neurosci 6:521–532

    Article  PubMed  CAS  Google Scholar 

  • McMahon SB, Cafferty WB, Marchand F (2005) Immune and glial cell factors as pain mediators and modulators. Exp Neurol 192:444–462

    Article  PubMed  CAS  Google Scholar 

  • Minami M, Kuraishi Y, Yamaguchi T, Nakai S, Hirai Y, Satoh M (1991) Immobilization stress induces interleukin-1 beta mRNA in the rat hypothalamus. Neurosci Lett 123:254–256

    Article  PubMed  CAS  Google Scholar 

  • Nakamura H, Nakanishi K, Kita A, Kadokawa T (1988) Interleukin-1 induces analgesia in mice by a central action. Eur J Pharmacol 149:49–54

    Article  PubMed  CAS  Google Scholar 

  • Nemirovsky A, Niv D (1997) Cholinergic mechanisms and antinociception. In: Raj P, Aronoff G, Pawl R, Parris W (eds) Current Review of Pain. Vol. 1, Psychiatric Management of Pain. Current Science, Philadelphia, PA, pp. 10–22

    Google Scholar 

  • Nilsson L, Nordberg A, Hardy J, Wester P, Winblad B (1986) Physostigmine restores 3H-acetylcholine efflux from Alzheimer brain slices to normal level. J Neural Transm 67:275–285

    Article  PubMed  CAS  Google Scholar 

  • Petersson J, Gordh TE, Hartvig P, Wiklund L (1986) A double-blind trial of the analgesic properties of physostigmine in postoperative patients. Acta Anaesthesiol Scand 30:283–288

    PubMed  CAS  Google Scholar 

  • Plaza MA, Fioramonti J, Bueno L (1997) Role of central interleukin-1 beta in gastrointestinal motor disturbances induced by lipopolysaccharide in sheep. Dig Dis Sci 42:242–250

    Article  PubMed  CAS  Google Scholar 

  • Raghavendra V, Tanga F, Rutkowski MD, DeLeo JA (2003) Anti-hyperalgesic and morphine-sparing actions of propentofylline following peripheral nerve injury in rats: mechanistic implications of spinal glia and proinflammatory cytokines. Pain 104:655–664

    Article  PubMed  CAS  Google Scholar 

  • Reeve AJ, Patel S, Fox A, Walker K, Urban L (2000) Intrathecally administered endotoxin or cytokines produce allodynia, hyperalgesia and changes in spinal cord neuronal responses to nociceptive stimuli in the rat. Eur J Pain 4:247–257

    Article  PubMed  CAS  Google Scholar 

  • Romano JA, Shih TM (1983) Cholinergic mechanisms of analgesia produced by physostigmine, morphine and cold water swimming. Neuropharmacology 22:827–833

    Article  PubMed  CAS  Google Scholar 

  • Rosenberg J, Kehlet H (1999) Does effective postoperative pain management influence surgical morbidity? Eur Surg Res 31:133–137

    Article  PubMed  CAS  Google Scholar 

  • Safieh-Garabedian B, Poole S, Allchorne A, Winter J, Woolf CJ (1995) Contribution of interleukin-1 beta to the inflammation-induced increase in nerve growth factor levels and inflammatory hyperalgesia. Br J Pharmacol 115:1265–1275

    PubMed  CAS  Google Scholar 

  • Salo M (1992) Effects of anaesthesia and surgery on the immune response. Acta Anaesthesiol Scand 36:201–220

    Article  PubMed  CAS  Google Scholar 

  • Samad TA, Moore KA, Sapirstein A, Billet S, Allchorne A, Poole S, Bonventre JV, Woolf CJ (2001) Interleukin-1beta-mediated induction of Cox-2 in the CNS contributes to inflammatory pain hypersensitivity. Nature 410:471–475

    Article  PubMed  CAS  Google Scholar 

  • Schafer M (2003) Cytokines and peripheral analgesia. Adv Exp Med Biol 521:40–50

    PubMed  Google Scholar 

  • Shamash S, Reichert F, Rotshenker S (2002) The cytokine network of Wallerian degeneration: tumor necrosis factor-alpha, interleukin-1alpha, and interleukin-1beta. J Neurosci 22:3052–3060

    PubMed  CAS  Google Scholar 

  • Shavit Y, Fish G, Wolf G, Mayburd E, Meerson Y, Yirmiya R, Beilin B (2005a) The effects of perioperative pain management techniques on food consumption and body weight after laparotomy in rats. Anesth Analg 101:1112–1116

    Article  PubMed  Google Scholar 

  • Shavit Y, Weidenfeld J, DeKeyser FG, Fish G, Wolf G, Mayburd E, Meerson Y, Beilin B (2005b) Effects of surgical stress on brain prostaglandin E(2) production and on the pituitary–adrenal axis: attenuation by preemptive analgesia and by central amygdala lesion. Brain Res 1047:10–17

    Article  PubMed  CAS  Google Scholar 

  • Shavit Y, Wolf G, Goshen I, Livshits D, Yirmiya R (2005c) Interleukin-1 antagonizes morphine analgesia and underlies morphine tolerance. Pain 115:50–59

    Article  PubMed  CAS  Google Scholar 

  • Shintani F, Nakaki T, Kanba S, Sato K, Yagi G, Shiozawa M, Aiso S, Kato R, Asai M (1995) Involvement of interleukin-1 in immobilization stress-induced increase in plasma adrenocorticotropic hormone and in release of hypothalamic monoamines in the rat. J Neurosci 15:1961–1970

    PubMed  CAS  Google Scholar 

  • Souter AJ, Garry MG, Tanelian DL (2000) Spinal interleukin-1beta reduces inflammatory pain. Pain 86:63–68

    Article  PubMed  CAS  Google Scholar 

  • Stein C, Hassan AH, Lehrberger K, Giefing J, Yassouridis A (1993) Local analgesic effect of endogenous opioid peptides. Lancet 342:321–324

    Article  PubMed  CAS  Google Scholar 

  • Suzuki E, Shintani F, Kanba S, Asai M, Nakaki T (1997) Immobilization stress increases mRNA levels of interleukin-1 receptor antagonist in various rat brain regions. Cell Mol Neurobiol 17:557–562

    Article  PubMed  CAS  Google Scholar 

  • Svensson CI, Yaksh TL (2002) The spinal phospholipase–cyclooxygenase–prostanoid cascade in nociceptive processing. Annu Rev Pharmacol Toxicol 42:553–583

    Article  PubMed  CAS  Google Scholar 

  • Sweitzer SM, Colburn RW, Rutkowski M, DeLeo JA (1999) Acute peripheral inflammation induces moderate glial activation and spinal IL-1beta expression that correlates with pain behavior in the rat. Brain Res 829:209–221

    Article  PubMed  CAS  Google Scholar 

  • Sweitzer S, Martin D, DeLeo JA (2001) Intrathecal interleukin-1 receptor antagonist in combination with soluble tumor necrosis factor receptor exhibits an anti-allodynic action in a rat model of neuropathic pain. Neuroscience 103:529–539

    Article  PubMed  CAS  Google Scholar 

  • Tadano T, Namioka M, Nakagawasai O, Tan-No K, Matsushima K, Endo Y, Kisara K (1999) Induction of nociceptive responses by intrathecal injection of interleukin-1 in mice. Life Sci 65:255–261

    Article  PubMed  CAS  Google Scholar 

  • Taylor BK, Akana SF, Peterson MA, Dallman MF, Basbaum AI (1998) Pituitary–adrenocortical responses to persistent noxious stimuli in the awake rat: endogenous corticosterone does not reduce nociception in the formalin test. Endocrinology 139:2407–2413

    Article  PubMed  CAS  Google Scholar 

  • Tonnesen E, Wahlgreen C (1988) Influence of extradural and general anaesthesia on natural killer cell activity and lymphocyte subpopulations in patients undergoing hysterectomy. Br J Anaesth 60:500–507

    PubMed  CAS  Google Scholar 

  • Turnbull AV, Rivier CL (1999) Regulation of the hypothalamic–pituitary–adrenal axis by cytokines: actions and mechanisms of action. Physiol Rev 79:1–71

    PubMed  CAS  Google Scholar 

  • Vanegas H, Schaible HG (2001) Prostaglandins and cyclooxygenases [correction of cycloxygenases] in the spinal cord. Prog Neurobiol 64:327–363

    Article  PubMed  CAS  Google Scholar 

  • Watkins LR, Maier SF (2000) The pain of being sick: implications of immune-to-brain communication for understanding pain. Annu Rev Psychol 51:29–57

    Article  PubMed  CAS  Google Scholar 

  • Watkins LR, Maier SF (2002) Beyond neurons: evidence that immune and glial cells contribute to pathological pain states. Physiol Rev 82:981–1011

    PubMed  CAS  Google Scholar 

  • Watkins LR, Maier SF, Goehler LE (1995) Immune activation: the role of pro-inflammatory cytokines in inflammation, illness responses and pathological pain states. Pain 63:289–302

    Article  PubMed  CAS  Google Scholar 

  • Watkins LR, Martin D, Ulrich P, Tracey KJ, Maier SF (1997) Evidence for the involvement of spinal cord glia in subcutaneous formalin induced hyperalgesia in the rat. Pain 71:225–235

    Article  PubMed  CAS  Google Scholar 

  • Watkins LR, Milligan ED, Maier SF (2001) Spinal cord glia: new players in pain. Pain 93:201–205

    Article  PubMed  CAS  Google Scholar 

  • Watkins LR, Wiertelak EP, Goehler LE, Smith KP, Martin D, Maier SF (1994) Characterization of cytokine-induced hyperalgesia. Brain Res 654:15–26

    Article  Google Scholar 

  • Winkelstein BA, Rutkowski MD, Sweitzer SM, Pahl JL, DeLeo JA (2001) Nerve injury proximal or distal to the DRG induces similar spinal glial activation and selective cytokine expression but differential behavioral responses to pharmacologic treatment. J Comp Neurol 439:127–139

    Article  PubMed  CAS  Google Scholar 

  • Wolf G, Gabay E, Tal M, Yirmiya R, Shavit Y (2006) Genetic impairment of interleukin-1 signaling attenuates neuropathic pain, autotomy, and spontaneous ectopic neuronal activity, following nerve injury in mice. Pain 120:315–324

    Article  PubMed  CAS  Google Scholar 

  • Wordliczek J, Szczepanik AM, Banach M, Turchan J, Zembala M, Siedlar M, Przewlocki R, Serednicki W, Przewlocka B (2000) The effect of pentoxifiline on post-injury hyperalgesia in rats and postoperative pain in patients. Life Sci 66:1155–1164

    Article  PubMed  CAS  Google Scholar 

  • Wu CT, Jao SW, Borel CO, Yeh CC, Li CY, Lu CH, Wong CS (2004) The effect of epidural clonidine on perioperative cytokine response, postoperative pain, and bowel function in patients undergoing colorectal surgery. Anesth Analg 99:502–509

    Article  PubMed  CAS  Google Scholar 

  • Yaksh TL, Dirksen R, Harty GJ (1985) Antinociceptive effects of intrathecally injected cholinomimetic drugs in the rat and cat. Eur J Pharmacol 117:81–88

    Article  PubMed  CAS  Google Scholar 

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Acknowledgements

This study was supported in part by a grant no. 3701 from the Chief Scientist’s Office of the Ministry of Health, and by a grant from the State Public Committee for the Designation of Estate Funds upon the recommendation of the Chief Scientist’s Office of the Ministry of Health, Jerusalem, Israel (Y.S. and B.B.); by a grant from the Hebrew University Intramural Research Fund—Basic Project Award (Y.S.); and was facilitated by the Leon and Clara Sznajderman Chair of Psychology (Y.S.).

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Shavit, Y., Fridel, K. & Beilin, B. Postoperative Pain Management and Proinflammatory Cytokines: Animal and Human Studies. Jrnl Neuroimmune Pharm 1, 443–451 (2006). https://doi.org/10.1007/s11481-006-9043-1

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