• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Additive effect of dextromethorphan on the inhibitory effect of anti-NT4 on morphine tolerance.

作者信息

Hatami Homeira, Oryan Shahrbanoo, Semnanian Saeed, Kazemi Bahram, Ahmadiani Abolhassan

机构信息

Department of Biology, Teacher Training University, Tehran, Iran.

出版信息

Pharmacology. 2006;78(3):105-12. doi: 10.1159/000095886. Epub 2006 Sep 22.

DOI:10.1159/000095886
PMID:17003573
Abstract

It has been proposed that opioid tolerance is a model of neuronal plasticity similar to learning and memory. Recent evidence suggests that neurotrophins may be involved in synaptic development and plasticity. Observations indicate that neurotrophin 4 (NT4) is required for the synaptic plasticity mediating both tolerance and memory. Also there are lines of evidence to indicate that NMDA receptors are involved in the neural plasticity underlying the development of opiate tolerance. Neurotrophins affect central transmission postsynaptically by enhancing NMDA receptor responsiveness. So we used the clinically available NMDA receptor antagonist, dextromethorphan, and the neurotrophin 4 antibody, anti-NT4, concomitantly and alone to investigate their effects on morphine tolerance. Tolerance was induced by injecting morphine (7 and 10 mg/kg i.p.) once per day for 4 days. Anti-NT4 (1 microg/rat i.c.v.) was administered 15 min before morphine. Results showed that chronic concomitant treatment of anti-NT4 with morphine in both doses inhibited the development of morphine tolerance. Also acute treatment of anti-NT4 significantly reversed the tolerance that was induced by morphine 7 mg/kg but failed to reverse the tolerance of morphine 10 mg/kg. Dextromethorphan in both doses (10 or 30 mg/kg) has an additive effect on the inhibitory effect of anti-NT4 on the reversal of morphine tolerance (7 mg/kg). These findings provide additional support for the hypothesis that NMDA receptor and NT4 may be involved in neural plasticity underlying opiate tolerance.

摘要

相似文献

1
Additive effect of dextromethorphan on the inhibitory effect of anti-NT4 on morphine tolerance.
Pharmacology. 2006;78(3):105-12. doi: 10.1159/000095886. Epub 2006 Sep 22.
2
Clinically available NMDA receptor antagonists memantine and dextromethorphan reverse existing tolerance to the antinociceptive effects of morphine in mice.临床上可用的N-甲基-D-天冬氨酸(NMDA)受体拮抗剂美金刚和右美沙芬可逆转小鼠对吗啡镇痛作用的现有耐受性。
Naunyn Schmiedebergs Arch Pharmacol. 2000 Apr;361(4):425-32. doi: 10.1007/s002109900205.
3
Dextromethorphan potentiates morphine antinociception, but does not reverse tolerance in rats.右美沙芬可增强吗啡的镇痛作用,但不能逆转大鼠的耐受性。
Neuroreport. 1996 Feb 29;7(3):838-40. doi: 10.1097/00001756-199602290-00037.
4
Differential antinociception by morphine and methadone in two sub-strains of Sprague-Dawley rats and its potentiation by dextromethorphan.吗啡和美沙酮在两种斯普拉格-道利大鼠亚系中的差异抗伤害感受作用及其被右美沙芬增强的作用
Brain Res. 2002 Jun 28;942(1-2):95-100. doi: 10.1016/s0006-8993(02)02701-4.
5
Attenuation of tolerance to opioid-induced antinociception and protection against morphine-induced decrease of neurofilament proteins by idazoxan and other I2-imidazoline ligands.咪唑克生及其他I2-咪唑啉配体对阿片类药物诱导的抗伤害感受耐受性的减弱作用以及对吗啡诱导的神经丝蛋白减少的保护作用。
Br J Pharmacol. 1998 Sep;125(1):175-85. doi: 10.1038/sj.bjp.0702031.
6
Dextromethorphan potentiates morphine antinociception at the spinal level in rats.右美沙芬增强大鼠脊髓水平的吗啡镇痛作用。
Can J Anaesth. 2004 Nov;51(9):905-10. doi: 10.1007/BF03018888.
7
Co-administration of dextromethorphan during pregnancy and throughout lactation significantly decreases the adverse effects associated with chronic morphine administration in rat offspring.孕期及整个哺乳期联合使用右美沙芬可显著降低大鼠后代因长期给予吗啡而产生的不良反应。
Life Sci. 2001 Oct 5;69(20):2439-50. doi: 10.1016/s0024-3205(01)01316-9.
8
Effects of N-methyl-D-aspartate receptor antagonists on acute morphine-induced and l-methadone-induced antinociception in mice.N-甲基-D-天冬氨酸受体拮抗剂对小鼠急性吗啡诱导及左旋美沙酮诱导的抗伤害感受的影响。
J Pain. 2005 Jul;6(7):425-33. doi: 10.1016/j.jpain.2005.02.003.
9
Comparison of ketamine and dextromethorphan in potentiating the antinociceptive effect of morphine in rats.氯胺酮与右美沙芬对大鼠吗啡镇痛作用增强效果的比较。
Anesth Analg. 1998 Apr;86(4):825-9. doi: 10.1097/00000539-199804000-00027.
10
NMDA antagonist modulation of morphine antinociception in female vs. male rats.NMDA拮抗剂对雌性和雄性大鼠吗啡镇痛作用的调节
Pharmacol Biochem Behav. 2005 Apr;80(4):639-49. doi: 10.1016/j.pbb.2005.02.003.

引用本文的文献

1
Endogenous opiates and behavior: 2006.内源性阿片类物质与行为:2006年
Peptides. 2007 Dec;28(12):2435-513. doi: 10.1016/j.peptides.2007.09.002. Epub 2007 Sep 11.