• 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

雪貂催吐敏感性的行为学研究。

Behavioral studies of emetic sensitivity in the ferret.

作者信息

Knox A P, Strominger N L, Battles A H, Carpenter D O

机构信息

Department of Anatomy, Cell Biology and Neurobiology, Albany Medical College, NY 12208.

出版信息

Brain Res Bull. 1993;31(5):477-84. doi: 10.1016/0361-9230(93)90112-o.

DOI:10.1016/0361-9230(93)90112-o
PMID:8495372
Abstract

The ferrets' responsiveness to several known and putative emetic agents was evaluated using a variety of agents that were injected subcutaneously and/or intravenously. Apomorphine was consistently emetic at relatively high doses (100 micrograms/kg) when injected subcutaneously in large male ferrets (> or = 1.4 kg). The responsiveness to apomorphine was anomalous in that subcutaneous injections produced a more consistent response than intravenous ones. In addition, ferrets rapidly become tolerant or tachyphylactic to subcutaneously administered apomorphine. Area postrema ablation, but not abdominal vagotomy, rendered ferrets refractory to the emetic effects of apomorphine. This species, relative to dog and humans, proved to be insensitive to a variety of pharmacologic agents including angiotensin II, gastrin, histamine, Leu-enkephalin, neurotensin, serotonin, and vasopressin. Cisplatin elicited forceful retching and emesis. Emetic responses were obtained with substance P and Met-enkephalin in individual animals but were inconsistent. Sensitivity to DAGO [D-Ala2,MePhe4,Gly-ol5 enkephalin] was variable. Results of this study indicate that the ferret is not an optimal model for all forms of emesis.

摘要

使用多种经皮下和/或静脉注射的药剂评估雪貂对几种已知和假定催吐剂的反应性。阿扑吗啡在相对高剂量(100微克/千克)时,皮下注射给大型雄性雪貂(≥1.4千克)时始终会引起呕吐。雪貂对阿扑吗啡的反应异常,皮下注射产生的反应比静脉注射更一致。此外,雪貂对皮下注射的阿扑吗啡会迅速产生耐受性或快速耐受性。最后区损毁而非腹部迷走神经切断术使雪貂对阿扑吗啡的催吐作用产生抗性。相对于狗和人类,该物种对包括血管紧张素II、胃泌素、组胺、亮氨酸脑啡肽、神经降压素、血清素和加压素在内的多种药理剂不敏感。顺铂引发强烈干呕和呕吐。个别动物对P物质和甲硫氨酸脑啡肽有催吐反应,但不一致。对DAGO [D-丙氨酸2,甲基苯丙氨酸4,甘氨酸醇5脑啡肽]的敏感性各不相同。本研究结果表明,雪貂并非所有形式呕吐的最佳模型。

相似文献

1
Behavioral studies of emetic sensitivity in the ferret.雪貂催吐敏感性的行为学研究。
Brain Res Bull. 1993;31(5):477-84. doi: 10.1016/0361-9230(93)90112-o.
2
Enkephalin receptors in the emetic chemoreceptor trigger zone of the dog.狗催吐化学感受区中的脑啡肽受体。
Br J Pharmacol. 1981 Mar;72(3):471-5. doi: 10.1111/j.1476-5381.1981.tb10998.x.
3
Characterization of radiation-induced emesis in the ferret.雪貂辐射诱发呕吐的特征描述。
Radiat Res. 1988 Jun;114(3):599-612.
4
Comparison of three preclinical models for nausea and vomiting assessment.三种用于恶心和呕吐评估的临床前模型的比较。
J Pharmacol Toxicol Methods. 2016 Nov-Dec;82:45-53. doi: 10.1016/j.vascn.2016.07.006. Epub 2016 Jul 28.
5
Emetic effects of centrally administered angiotensin II, arginine vasopressin and neurotensin in the dog.中枢给予血管紧张素II、精氨酸加压素和神经降压素对犬的催吐作用。
Peptides. 1985;6 Suppl 1:173-5. doi: 10.1016/0196-9781(85)90028-2.
6
Peptide-induced emesis in dogs.肽诱导犬呕吐
Behav Brain Res. 1984 Mar;11(3):277-81. doi: 10.1016/0166-4328(84)90220-1.
7
Action of metyrapone and tetracosactrin to modify cisplatin-induced acute and delayed emesis in the ferret.甲吡酮和二十四肽促皮质素对雪貂顺铂诱导的急性和迟发性呕吐的作用。
Eur J Pharmacol. 2003 Apr 11;466(1-2):163-8. doi: 10.1016/s0014-2999(03)01550-4.
8
Morphine 6-glucuronide: a metabolite of morphine with greater emetic potency than morphine in the ferret.吗啡6-葡萄糖醛酸苷:吗啡的一种代谢产物,在雪貂中致吐效力比吗啡更强。
Br J Pharmacol. 1992 May;106(1):3-8. doi: 10.1111/j.1476-5381.1992.tb14284.x.
9
Area postrema mediates gastric motor response induced by apomorphine in rats.最后区介导阿扑吗啡诱导的大鼠胃运动反应。
Brain Res. 2003 Jan 17;960(1-2):122-31. doi: 10.1016/s0006-8993(02)03801-5.
10
Imiquimod-elicited emesis is mediated by the area postrema, but not by direct neuronal activation.咪喹莫特引发的呕吐是由最后区介导的,而非直接的神经元激活所介导。
Brain Res Bull. 2001 Jun;55(3):445-51. doi: 10.1016/s0361-9230(01)00539-1.

引用本文的文献

1
The efficacy of aprepitant for the prevention of postoperative nausea and vomiting: A meta-analysis.阿瑞匹坦预防术后恶心呕吐的疗效:一项荟萃分析。
Medicine (Baltimore). 2023 Jul 21;102(29):e34385. doi: 10.1097/MD.0000000000034385.
2
RNA sequencing least shrew () brainstem and gut transcripts following administration of a selective substance P neurokinin NK receptor agonist and antagonist expands genomics resources for emesis research.给予选择性P物质神经激肽NK受体激动剂和拮抗剂后,对伶鼬鼩的脑干和肠道转录本进行RNA测序,扩展了呕吐研究的基因组学资源。
Front Genet. 2023 Feb 14;14:975087. doi: 10.3389/fgene.2023.975087. eCollection 2023.
3
Neurokinin-1 Antagonists for Postoperative Nausea and Vomiting.
用于术后恶心和呕吐的神经激肽-1拮抗剂
Drugs. 2021 Jul;81(10):1171-1179. doi: 10.1007/s40265-021-01532-y. Epub 2021 Jun 9.
4
Why can't rodents vomit? A comparative behavioral, anatomical, and physiological study.为什么啮齿动物不会呕吐?一项比较行为学、解剖学和生理学的研究。
PLoS One. 2013 Apr 10;8(4):e60537. doi: 10.1371/journal.pone.0060537. Print 2013.
5
Investigating the effect of emetic compounds on chemotaxis in Dictyostelium identifies a non-sentient model for bitter and hot tastant research.研究呕吐化合物对变形虫趋化性的影响,为苦味和辣味味觉研究提供了一种无感知模型。
PLoS One. 2011;6(9):e24439. doi: 10.1371/journal.pone.0024439. Epub 2011 Sep 8.
6
Chemotherapy-induced kaolin intake is increased by lesion of the lateral parabrachial nucleus of the rat.大鼠臂旁外侧核损伤会增加化疗诱导的高岭土摄入量。
Am J Physiol Regul Integr Comp Physiol. 2009 Nov;297(5):R1375-82. doi: 10.1152/ajpregu.00284.2009. Epub 2009 Aug 26.
7
Utilization of the least shrew as a rapid and selective screening model for the antiemetic potential and brain penetration of substance P and NK1 receptor antagonists.利用小麝鼩作为快速且具选择性的筛选模型,用于评估P物质和NK1受体拮抗剂的止吐潜力及脑渗透性。
Brain Res. 2008 Jun 12;1214:58-72. doi: 10.1016/j.brainres.2008.03.077. Epub 2008 Apr 9.
8
The anti-emetic effects of CP-99,994 in the ferret and the dog: role of the NK1 receptor.CP-99,994对雪貂和犬的止吐作用:NK1受体的作用
Br J Pharmacol. 1995 May;115(1):84-94. doi: 10.1111/j.1476-5381.1995.tb16324.x.