참고문헌
- Siddall PJ, Molloy AR, Walker S, Mather LE, Rutkowski SB, Cousins MJ. The efficacy of intrathecal morphine and clonidine in the treatment of pain after spinal cord injury. Anesth Analg. 2000;91:1493-1498. https://doi.org/10.1097/00000539-200012000-00037
- Hulsebosch CE, Hains BC, Crown ED, Carlton SM. Mechanisms of chronic central neuropathic pain after spinal cord injury. Brain Res Rev. 2009;60:202-213. https://doi.org/10.1016/j.brainresrev.2008.12.010
- Portenoy RK, Foley KM, Inturrisi CE. The nature of opioid responsiveness and its implications for neuropathic pain: new hypotheses derived from studies of opioid infusions. Pain. 1990;43:273-286. https://doi.org/10.1016/0304-3959(90)90025-9
- Finnerup NB, Sindrup SH, Jensen TS. The evidence for pharmacological treatment of neuropathic pain. Pain. 2010; 150:573-581. https://doi.org/10.1016/j.pain.2010.06.019
- Rowbotham MC, Hansson PT, Fields HL, Hill RG, Marchettini P. Efficacy of opioids. In: Hansson PT, editor. Neuropathic pain: Pathophysiology and treatment. Seattle: ISAP Press; 2001. p.203-213.
- Brewer KL, McMillan D, Nolan T, Shum K. Cortical changes in cholecystokinin mRNA are related to spontaneous pain behaviors following excitotoxic spinal cord injury in the rat. Brain Res Mol Brain Res. 2003;118:171-174. https://doi.org/10.1016/j.molbrainres.2003.08.006
- Xu XJ, Puke MJ, Verge VM, Wiesenfeld-Hallin Z, Hughes J, Hokfelt T. Up-regulation of cholecystokinin in primary sensory neurons is associated with morphine insensitivity in experimental neuropathic pain in the rat. Neurosci Lett. 1993;152: 129-132. https://doi.org/10.1016/0304-3940(93)90500-K
- Kim J, Kim JH, Kim Y, Cho HY, Hong SK, Yoon YW. Role of spinal cholecystokinin in neuropathic pain after spinal cord hemisection in rats. Neurosci Lett. 2009;462:303-307. https://doi.org/10.1016/j.neulet.2009.07.042
- Xu XJ, Hao JX, Seiger A, Hughes J, Hokfelt T, Wiesenfeld-Hallin Z. Chronic pain-related behaviors in spinally injured rats: evidence for functional alterations of the endogenous cholecystokinin and opioid systems. Pain. 1994;56:271-277. https://doi.org/10.1016/0304-3959(94)90165-1
- Coudore-Civiale MA, Courteix C, Fialip J, Boucher M, Eschalier A. Spinal effect of the cholecystokinin-B receptor antagonist CI-988 on hyperalgesia, allodynia and morphineinduced analgesia in diabetic and mononeuropathic rats. Pain. 2000;88:15-22. https://doi.org/10.1016/S0304-3959(00)00304-3
- Torres-Lopez JE, Juarez-Rojop IE, Granados-Soto V, Diaz-Zagoya JC, Flores-Murrieta FJ, Ortiz-Lopez JU, Cruz-Vera J. Peripheral participation of cholecystokinin in the morphineinduced peripheral antinociceptive effect in non-diabetic and diabetic rats. Neuropharmacology. 2007;52:788-795. https://doi.org/10.1016/j.neuropharm.2006.09.015
- Idanpaan-Heikkila JJ, Perrot S, Guilbaud G, Kayser V. In mononeuropathic rats, the enhancement of morphine antinociception by L-365,260, a selective CCK(B) receptor antagonist, depends on the dose of systemic morphine and stimulus characteristics. Eur J Pharmacol. 1997;325:155-164. https://doi.org/10.1016/S0014-2999(97)00123-4
- Agnes RS, Ying J, Kover KE, Lee YS, Davis P, Ma SW, Badghisi H, Porreca F, Lai J, Hruby VJ. Structure-activity relationships of bifunctional cyclic disulfide peptides based on overlapping pharmacophores at opioid and cholecystokinin receptors. Peptides. 2008;29:1413-1423. https://doi.org/10.1016/j.peptides.2008.03.022
- Dixon WJ. Efficient analysis of experimental observations. Annu Rev Pharmacol Toxicol. 1980;20:441-462. https://doi.org/10.1146/annurev.pa.20.040180.002301
- Gale K, Kerasidis H, Wrathall JR. Spinal cord contusion in the rat: behavioral analysis of functional neurologic impairment. Exp Neurol. 1985;88:123-134. https://doi.org/10.1016/0014-4886(85)90118-9
- Kim J, Jung JI, Na HS, Hong SK, Yoon YW. Effects of morphine on mechanical allodynia in a rat model of central neuropathic pain. Neuroreport. 2003;14:1017-1020. https://doi.org/10.1097/01.wnr.0000070190.28954.ec
- Tallarida RJ. Drug synergism: its detection and applications. J Pharmacol Exp Ther. 2001;298:865-872.
- Tallarida RJ, Stone DJ Jr, Raffa RB. Efficient designs for studying synergistic drug combinations. Life Sci. 1997;61:PL 417-425.
- Kim J, Yoon YW, Hong SK, Na HS. Cold and mechanical allodynia in both hindpaws and tail following thoracic spinal cord hemisection in rats: time courses and their correlates. Neurosci Lett. 2003;343:200-204. https://doi.org/10.1016/S0304-3940(03)00377-X
- Kohno T, Ji RR, Ito N, Allchorne AJ, Befort K, Karchewski LA, Woolf CJ. Peripheral axonal injury results in reduced mu opioid receptor pre- and post-synaptic action in the spinal cord. Pain. 2005;117:77-87. https://doi.org/10.1016/j.pain.2005.05.035
- Hebb AL, Poulin JF, Roach SP, Zacharko RM, Drolet G. Cholecystokinin and endogenous opioid peptides: interactive influence on pain, cognition, and emotion. Prog Neuropsychopharmacol Biol Psychiatry. 2005;29:1225-1238. https://doi.org/10.1016/j.pnpbp.2005.08.008
- Wu HE, Schwasinger ET, Hong JS, Tseng LF. Pretreatment with antiserum against dynorphin, substance P, or cholecystokinin enhances the morphine-produced anti-allodynia in the sciatic nerve ligated mice. Neurosci Lett. 2005;386:46-51. https://doi.org/10.1016/j.neulet.2005.05.052
- Xu XJ, Alster P, Wu WP, Hao JX, Wiesenfeld-Hallin Z. Increased level of cholecystokinin in cerebrospinal fluid is associated with chronic pain-like behavior in spinally injured rats. Peptides. 2001;22:1305-1308. https://doi.org/10.1016/S0196-9781(01)00456-9
- Wiesenfeld-Hallin Z, Xu XJ. The role of cholecystokinin in nociception, neuropathic pain and opiate tolerance. Regul Pept. 1996;65:23-28. https://doi.org/10.1016/0167-0115(96)00068-7
- Kovelowski CJ, Ossipov MH, Sun H, Lai J, Malan TP, Porreca F. Supraspinal cholecystokinin may drive tonic descending facilitation mechanisms to maintain neuropathic pain in the rat. Pain. 2000;87:265-273. https://doi.org/10.1016/S0304-3959(00)00290-6
- Verge VM, Wiesenfeld-Hallin Z, Hokfelt T. Cholecystokinin in mammalian primary sensory neurons and spinal cord: in situ hybridization studies in rat and monkey. Eur J Neurosci. 1993;5:240-250. https://doi.org/10.1111/j.1460-9568.1993.tb00490.x
- Cesselin F. Opioid and anti-opioid peptides. Fundam Clin Pharmacol. 1995;9:409-433. https://doi.org/10.1111/j.1472-8206.1995.tb00517.x
- Mollereau C, Roumy M, Zajac JM. Opioid-modulating peptides: mechanisms of action. Curr Top Med Chem. 2005;5:341-355. https://doi.org/10.2174/1568026053544515
- Zhou Y, Sun YH, Zhang ZW, Han JS. Increased release of immunoreactive cholecystokinin octapeptide by morphine and potentiation of mu-opioid analgesia by CCKB receptor antagonist L-365,260 in rat spinal cord. Eur J Pharmacol. 1993; 234:147-154. https://doi.org/10.1016/0014-2999(93)90948-H
- Stanfa LC, Dickenson AH. Cholecystokinin as a factor in the enhanced potency of spinal morphine following carrageenin inflammation. Br J Pharmacol. 1993;108:967-973. https://doi.org/10.1111/j.1476-5381.1993.tb13493.x
- Chaparro LE, Wiffen PJ, Moore RA, Gilron I. Combination pharmacotherapy for the treatment of neuropathic pain in adults. Cochrane Database Syst Rev. 2012;7:CD008943.
- Hanlon KE, Herman DS, Agnes RS, Largent-Milnes TM, Kumarasinghe IR, Ma SW, Guo W, Lee YS, Ossipov MH, Hruby VJ, Lai J, Porreca F, Vanderah TW. Novel peptide ligands with dual acting pharmacophores designed for the pathophysiology of neuropathic pain. Brain Res. 2011;1395:1-11. https://doi.org/10.1016/j.brainres.2011.04.024
- McCleane G. The cholecystokinin antagonist proglumide has an analgesic effect when used alone in human neuropathic pain: A case report. Pain Clinic. 2003;15:71-73. https://doi.org/10.1163/156856903321196537
- McCleane GJ. The cholecystokinin antagonist proglumide enhances the analgesic efficacy of morphine in humans with chronic benign pain. Anesth Analg. 1998;87:1117-1120.
- McCleane GJ. A randomised, double blind, placebo controlled crossover study of the cholecystokinin 2 antagonist L-365,260 as an adjunct to strong opioids in chronic human neuropathic pain. Neurosci Lett. 2003;338:151-154. https://doi.org/10.1016/S0304-3940(02)01388-5