• 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

μ和κ阿片受体激动剂对马运动行为的相互作用评估。

Evaluation of the interaction of mu and kappa opioid agonists on locomotor behavior in the horse.

作者信息

Mama K R, Pascoe P J, Steffey E P

机构信息

Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California, Davis 95616.

出版信息

Can J Vet Res. 1993 Apr;57(2):106-9.

PMID:8490803
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1263602/
Abstract

This study was designed to determine the interactive effects of mu and kappa opioid agonists on locomotor behavior in the horse. Three doses of a mu agonist, fentanyl (5, 10, 20 micrograms/kg) and a kappa agonist U50,488H (30, 60, 120 micrograms/kg) were administered in a random order to six horses. Locomotor activity was measured using a two minute footstep count. Each dose of U50,488H was then combined with 20 micrograms/kg of fentanyl to determine the interactive effects of the drugs on locomotor activity. A significant increase in locomotor activity was seen with 20 micrograms/kg of fentanyl and all the drug combinations. The combination of U50,488H with fentanyl resulted in an earlier onset of locomotor activity. At the highest doses of the combination (U50,488H 120 micrograms/kg, fentanyl 20 micrograms/kg), the duration of locomotor activity was significantly increased when compared to the other doses. We conclude that locomotor activity is maintained or enhanced in horses when a receptor specific kappa agonist is combined with a mu receptor agonist.

摘要

本研究旨在确定μ和κ阿片类激动剂对马匹运动行为的交互作用。将三种剂量的μ激动剂芬太尼(5、10、20微克/千克)和κ激动剂U50,488H(30、60、120微克/千克)以随机顺序给予6匹马。使用两分钟的步数计数来测量运动活性。然后将每种剂量的U50,488H与20微克/千克的芬太尼联合使用,以确定药物对运动活性的交互作用。在给予20微克/千克芬太尼以及所有药物组合后,观察到运动活性显著增加。U50,488H与芬太尼联合使用导致运动活性更早出现。在联合使用的最高剂量(U50,488H 120微克/千克,芬太尼20微克/千克)下,与其他剂量相比,运动活性的持续时间显著增加。我们得出结论,当受体特异性κ激动剂与μ受体激动剂联合使用时,马匹的运动活性得以维持或增强。

相似文献

1
Evaluation of the interaction of mu and kappa opioid agonists on locomotor behavior in the horse.μ和κ阿片受体激动剂对马运动行为的相互作用评估。
Can J Vet Res. 1993 Apr;57(2):106-9.
2
Interactions between the discriminative stimulus effects of mu and kappa opioid agonists in the squirrel monkey.松鼠猴中μ和κ阿片类激动剂的辨别性刺激效应之间的相互作用。
J Pharmacol Exp Ther. 1991 Jan;256(1):149-58.
3
Functional effects of systemically administered agonists and antagonists of mu, delta, and kappa opioid receptor subtypes on body temperature in mice.全身给予μ、δ和κ阿片受体亚型激动剂和拮抗剂对小鼠体温的功能影响。
J Pharmacol Exp Ther. 2002 Sep;302(3):1253-64. doi: 10.1124/jpet.102.037655.
4
Effects of mu-, delta- and kappa-opioid receptor agonists on methamphetamine-induced self-injurious behavior in mice.μ-、δ-和κ-阿片受体激动剂对甲基苯丙胺诱导的小鼠自伤行为的影响。
Eur J Pharmacol. 2006 Feb 17;532(1-2):81-7. doi: 10.1016/j.ejphar.2005.12.035. Epub 2006 Feb 7.
5
kappa-Opioid agonist, U50,488H, stimulates ovine fetal pituitary-adrenal function via hypothalamic arginine-vasopressin and corticotrophin-releasing factor.κ-阿片受体激动剂U50,488H通过下丘脑精氨酸加压素和促肾上腺皮质激素释放因子刺激绵羊胎儿垂体-肾上腺功能。
J Pharmacol Exp Ther. 1996 May;277(2):877-84.
6
Interactions of NMDA antagonists and an alpha 2 agonist with mu, delta and kappa opioids in an acute nociception assay.在急性伤害感受试验中,NMDA拮抗剂和一种α2激动剂与μ、δ和κ阿片类药物的相互作用。
Acta Anaesthesiol Belg. 2002;53(3):203-12.
7
Activation of the cloned human kappa opioid receptor by agonists enhances [35S]GTPgammaS binding to membranes: determination of potencies and efficacies of ligands.激动剂对克隆的人κ阿片受体的激活增强了[35S]GTPγS与膜的结合:配体效力和效能的测定。
J Pharmacol Exp Ther. 1997 Aug;282(2):676-84.
8
Behavioural effect of pretreatment with opioid antagonists and sigma binding site ligands on the abnormal motor response produced by the kappa opioid agonist U50,488H in guinea pigs.阿片类拮抗剂和σ结合位点配体预处理对κ阿片激动剂U50,488H在豚鼠中产生的异常运动反应的行为学影响。
Neuropharmacology. 1993 Aug;32(8):751-60. doi: 10.1016/0028-3908(93)90183-4.
9
Differential influence of D1 and D2 dopamine receptors on acute opiate withdrawal in guinea-pig isolated ileum.D1和D2多巴胺受体对豚鼠离体回肠急性阿片戒断的不同影响。
Br J Pharmacol. 1997 Mar;120(6):1001-6. doi: 10.1038/sj.bjp.0700995.
10
The effect of mu and kappa opioid receptor agonists on cAMP level in hippocampus of kainic acid-treated rats.
Pol J Pharmacol. 1995 Mar-Apr;47(2):121-6.

引用本文的文献

1
High and Hyper: Fentanyl Induces Psychomotor Side-Effects in Healthy Pigs.高剂量与超剂量:芬太尼在健康猪身上诱发精神运动性副作用。
Animals (Basel). 2023 May 17;13(10):1671. doi: 10.3390/ani13101671.
2
Effect of Fentanyl Infusion on Heart Rate Variability and Anaesthetic Requirements in Isoflurane-Anaesthetized Horses.芬太尼输注对异氟烷麻醉马匹心率变异性和麻醉需求的影响。
Animals (Basel). 2021 Oct 9;11(10):2922. doi: 10.3390/ani11102922.
3
Metabolism, pharmacokinetics and selected pharmacodynamic effects of codeine following a single oral administration to horses.犬单次口服可待因后的代谢、药代动力学和部分药效学研究
Vet Anaesth Analg. 2020 Sep;47(5):694-704. doi: 10.1016/j.vaa.2020.04.004. Epub 2020 Apr 23.
4
Sedative and cardiopulmonary effects of buprenorphine and xylazine in horses.丁丙诺啡和赛拉嗪对马的镇静及心肺效应
Can J Vet Res. 2011 Jan;75(1):35-41.

本文引用的文献

1
Role of central dopaminergic receptors in manic response of cats to morphine.中枢多巴胺能受体在猫对吗啡的躁狂反应中的作用。
Psychopharmacologia. 1972;24(3):380-3. doi: 10.1007/BF00402532.
2
Comparative analgesia of xylazine, xylazine/morphine, xylazine/butorphanol, and xylazine/nalbuphine in the horse, using dental dolorimetry.使用牙科痛觉测量法比较赛拉嗪、赛拉嗪/吗啡、赛拉嗪/布托啡诺和赛拉嗪/纳布啡对马的镇痛效果。
Am J Vet Res. 1987 Jul;48(7):1087-91.
3
Dose related effects of the kappa agonist U-50, 488H on behaviour, nociception and autonomic response in the horse.κ激动剂U-50,488H对马的行为、痛觉感受和自主反应的剂量相关效应。
Equine Vet J. 1988 Mar;20(2):114-8. doi: 10.1111/j.2042-3306.1988.tb01471.x.
4
Sensitization occurs to the locomotor effects of morphine and the specific mu opioid receptor agonist, DAGO, administered repeatedly to the ventral tegmental area but not to the nucleus accumbens.对反复注射到腹侧被盖区而非伏隔核的吗啡及特异性μ阿片受体激动剂DAGO的运动效应会产生敏化作用。
Brain Res. 1987 Aug 4;417(1):51-8. doi: 10.1016/0006-8993(87)90178-8.
5
Place preference conditioning reveals the involvement of D1-dopamine receptors in the motivational properties of mu- and kappa-opioid agonists.位置偏爱条件反射揭示了D1-多巴胺受体参与μ-阿片受体激动剂和κ-阿片受体激动剂的动机特性。
Brain Res. 1987 Dec 8;436(1):169-72. doi: 10.1016/0006-8993(87)91571-x.
6
Dose-related effects of ethylketazocine on nociception, behaviour and autonomic responses in the horse.乙基酮唑辛对马的痛觉、行为和自主反应的剂量相关效应。
J Pharm Pharmacol. 1986 Jan;38(1):40-5. doi: 10.1111/j.2042-7158.1986.tb04464.x.
7
Bidirectional effects of opioids in motivational processes and the involvement of D1 dopamine receptors.阿片类药物在动机过程中的双向作用及D1多巴胺受体的参与
NIDA Res Monogr. 1988;90:17-26.
8
Opposite effects of mu and kappa opiate agonists on dopamine release in the nucleus accumbens and in the dorsal caudate of freely moving rats.μ和κ阿片受体激动剂对自由活动大鼠伏隔核和背侧尾状核中多巴胺释放的相反作用。
J Pharmacol Exp Ther. 1988 Mar;244(3):1067-80.
9
Motivational effects of opioids: influence of D-1 versus D-2 receptor antagonists.阿片类药物的动机效应:D-1与D-2受体拮抗剂的影响
Eur J Pharmacol. 1988 Jul 7;151(2):233-42. doi: 10.1016/0014-2999(88)90803-5.
10
Pharmacological studies on the interrelation between the dopaminergic, GABAergic and opioid peptidergic systems in the central nervous system of the rat.大鼠中枢神经系统中多巴胺能、γ-氨基丁酸能和阿片肽能系统之间相互关系的药理学研究
Jpn J Pharmacol. 1987 Dec;45(4):439-47. doi: 10.1254/jjp.45.439.