89
Views
1
CrossRef citations to date
0
Altmetric
ORIGINAL RESEARCH

Long-Term Exposure to Morphine Induces Cross-Tolerance to Acute Antinociceptive Effect of Remifentanil on Somatic and Visceral Stimuli in Rats

, , , , , & ORCID Icon show all
Pages 4047-4054 | Received 14 Sep 2022, Accepted 15 Nov 2022, Published online: 22 Dec 2022

References

  • Al-Hasani R, Bruchas MR. Molecular mechanisms of opioid receptor-dependent signaling and behavior. Anesthesiology. 2011;115(6):1363–1381. doi:10.1097/ALN.0b013e318238bba6
  • Nersesyan H, Slavin KV. Current approach to cancer pain management: availability and implications of different treatment options. Ther Clin Risk Manag. 2007;3(3):381–400.
  • Williams JT, Ingram SL, Henderson G, et al. Regulation of μ-opioid receptors: desensitization, phosphorylation, internalization, and tolerance. Pharmacol Rev. 2013;65(1):223–254. doi:10.1124/pr.112.005942
  • Davis JJ, Johnson KB, Egan TD, Vezina DP, Snell TE, Swenson JD. Preoperative fentanyl infusion with pharmacokinetic simulation for anesthetic and perioperative management of an opioid-tolerant patient. Anesth Analg. 2003;97(6):1661–1662. doi:10.1213/01.ANE.0000090151.13573.42
  • Athanasos P, Smith CS, White JM, Somogyi AA, Bochner F, Ling W. Methadone maintenance patients are cross-tolerant to the antinociceptive effects of very high plasma morphine concentrations. Pain. 2006;120(3):267–275. doi:10.1016/j.pain.2005.11.005
  • de Aquino JP, Parida S, Avila-Quintero VJ, et al. Opioid-induced analgesia among persons with opioid use disorder receiving methadone or buprenorphine: a systematic review of experimental pain studies. Drug Alcohol Depend. 2021;228:109097. doi:10.1016/j.drugalcdep.2021.109097
  • Gemma M, Tommasino C, Cozzi S, et al. Remifentanil provides hemodynamic stability and faster awakening time in transsphenoidal surgery. Anesth Analg. 2002;94(1):163–168. doi:10.1213/00000539-200201000-00031
  • Kim SH, Stoicea N, Soghomonyan S, Bergese SD. Remifentanil-acute opioid tolerance and opioid-induced hyperalgesia: a systematic review. Am J Ther. 2015;22(3):e62–e74. doi:10.1097/MJT.0000000000000019
  • Vinik HR, Kissin I. Rapid development of tolerance to analgesia during remifentanil infusion in humans. Anesth Analg. 1998;86(6):1307–1311. doi:10.1213/00000539-199806000-00033
  • Chu LF, D’Arcy N, Brady C, et al. Analgesic tolerance without demonstrable opioid-induced hyperalgesia: a double-blinded, randomized, placebo-controlled trial of sustained-release morphine for treatment of chronic nonradicular low-back pain. Pain. 2012;153(8):1583–1592. doi:10.1016/j.pain.2012.02.028
  • Cervero F. Visceral versus somatic pain: similarities and differences. Dig Dis. 2009;27(suppl 1):3–10. doi:10.1159/000268115
  • Ness TJ, Follett KA. The development of tolerance to intrathecal morphine in rat models of visceral and cutaneous pain. Neurosci Lett. 1998;248(1):33–36. doi:10.1016/S0304-3940(98)00327-9
  • Parkitna JR, Obara I, Wawrzczak-Bargiela A, Makuch W, Przewlocka B, Przewlocki R. Effects of glycogen synthase kinase 3beta and cyclin-dependent kinase 5 inhibitors on morphine-induced analgesia and tolerance in rats. J Pharmacol Exp Ther. 2006;319(2):832–839. doi:10.1124/jpet.106.107581
  • Ishida R, Nikai T, Hashimoto T, Tsumori T, Saito Y. Intravenous infusion of remifentanil induces transient withdrawal hyperalgesia depending on administration duration in rats. Anesth Analg. 2012;114(1):224–229. doi:10.1213/ANE.0b013e318237f678
  • Miyamoto H, Saito Y, Kirihara Y, Hara K, Sakura S, Kosaka Y. Spinal coadministration of ketamine reduces the development of tolerance to visceral as well as somatic antinociception during spinal morphine infusion. Anesth Analg. 2000;90(1):136–141. doi:10.1097/00000539-200001000-00030
  • Kissin I, Brown PT, Robinson CA, Bradley EL. Acute tolerance in morphine analgesia: continuous infusion and single injection in rats. Anesthesiology. 1991;74(1):166–171. doi:10.1097/00000542-199101000-00025
  • Nowoczyn M, Marie N, Coulbault L, et al. Remifentanil produces cross-desensitization and tolerance with morphine on the mu-opioid receptor. Neuropharmacology. 2013;73:368–379. doi:10.1016/j.neuropharm.2013.06.010
  • Mercadante S, Arcuri E, Santoni A. Opioid-induced tolerance and hyperalgesia. CNS Drugs. 2019;33(10):943–955. doi:10.1007/s40263-019-00660-0
  • McMahon SB. Are there fundamental differences in the peripheral mechanisms of visceral and somatic pain? Behav Brain Sci. 1997;20(3):381–391. doi:10.1017/S0140525X97231481
  • Saito Y, Kaneko M, Kirihara Y, Sakura S, Kosaka Y. Interaction of intrathecally infused morphine and lidocaine in rats (part II): effects on the development of tolerance to morphine. Anesthesiology. 1998;89(6):1464–1470. doi:10.1097/00000542-199812000-00024
  • Eidson LN, Murphy AZ. Persistent peripheral inflammation attenuates morphine-induced periaqueductal gray glial cell activation and analgesic tolerance in the male rat. J Pain. 2013;14(4):393–404. doi:10.1016/j.jpain.2012.12.010
  • Coutinho SV, Meller ST, Gebhart GF. Intracolonic zymosan produces visceral hyperalgesia in the rat that is mediated by spinal NMDA and non-NMDA receptors. Brain Res. 1996;736(1–2):7–15. doi:10.1016/0006-8993(96)00661-0
  • Becker JB, Prendergast BJ, Liang JW. Female rats are not more variable than male rats: a meta-analysis of neuroscience studies. Biol Sex Differ. 2016;7:34. doi:10.1186/s13293-016-0087-5
  • Romanescu M, Buda V, Lombrea A, et al. Sex-related differences in pharmacological response to CNS drugs: a narrative review. J Pers Med. 2022;12(6):907. doi:10.3390/jpm12060907