• 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

臭鼩:呕吐研究中的一种新实验模型。

Suncus murinus: a new experimental model in emesis research.

作者信息

Ueno S, Matsuki N, Saito H

出版信息

Life Sci. 1987 Jul 27;41(4):513-8. doi: 10.1016/0024-3205(87)90229-3.

DOI:10.1016/0024-3205(87)90229-3
PMID:3600192
Abstract

Effects of various emetic and antiemetic drugs were studied using Suncus murinus for its potential use as an experimental model in emetic research. Subcutaneous injection of nicotine bitartrate (10-15 mg/kg), veratrine sulfate (0.5-1.0 mg/kg), emetine dihydrochloride (40-80 mg/kg) and oral administration of copper sulfate (20-100 mg/kg) caused dose-dependent emesis in suncus. The ED50 of nicotine, veratrine, emetine and copper sulfate were 7.9, 0.4, 47.6 and 21.4 mg/kg, respectively. However, subcutaneously injected apomorphine hydrochloride (0.1-100 mg/kg), digitoxin (0.5-1.0 mg/kg) and orally administered emetine dihydrochloride (10-80 mg/kg) did not induce the vomiting. Chlorpromazine and promethazine decreased the emetic effect of nicotine, veratrine and copper sulfate, but scopolamine hydrobromide was not effective. These results indicate that the Suncus murinus is sensitive to various emetic and antiemetic drugs and can be used as a new experimental animal model for the emesis. Emetic behavior of suncus was discussed in comparison with other animals.

摘要

研究了各种催吐药和止吐药对麝鼩的作用,以探讨其作为催吐研究实验模型的潜在用途。皮下注射重酒石酸尼古丁(10 - 15毫克/千克)、硫酸藜芦碱(0.5 - 1.0毫克/千克)、盐酸依米丁(40 - 80毫克/千克)以及口服硫酸铜(20 - 100毫克/千克)可使麝鼩产生剂量依赖性呕吐。尼古丁、藜芦碱、依米丁和硫酸铜的半数有效量(ED50)分别为7.9、0.4、47.6和21.4毫克/千克。然而,皮下注射盐酸阿扑吗啡(0.1 - 100毫克/千克)、洋地黄毒苷(0.5 - 1.0毫克/千克)以及口服盐酸依米丁(10 - 80毫克/千克)未引发呕吐。氯丙嗪和异丙嗪可降低尼古丁、藜芦碱和硫酸铜的催吐作用,但氢溴酸东莨菪碱无效。这些结果表明,麝鼩对各种催吐药和止吐药敏感,可作为一种新的呕吐实验动物模型。并将麝鼩的呕吐行为与其他动物进行了比较。

相似文献

1
Suncus murinus: a new experimental model in emesis research.臭鼩:呕吐研究中的一种新实验模型。
Life Sci. 1987 Jul 27;41(4):513-8. doi: 10.1016/0024-3205(87)90229-3.
2
The evaluation of whole-body plethysmography as a semiautomated method for analysis of emesis in the house musk shrew (Suncus murinus).将全身体积描记法作为一种半自动方法用于分析家麝鼩(Suncus murinus)呕吐情况的评估。
J Am Assoc Lab Anim Sci. 2007 Mar;46(2):81-5.
3
Selective blockade of cytotoxic drug-induced emesis by 5-HT3 receptor antagonists in Suncus murinus.5-羟色胺3受体拮抗剂对麝香鼠细胞毒性药物诱发呕吐的选择性阻断作用
Jpn J Pharmacol. 1991 Jan;55(1):107-13. doi: 10.1254/jjp.55.107.
4
Emetic responses of Sorex unguiculatus.伶尾鼩鼱的催吐反应。
Jikken Dobutsu. 1993 Apr;42(2):225-8.
5
Action of anti-tussive drugs on the emetic reflex of Suncus murinus (house musk shrew).镇咳药对臭鼩(家麝鼩)呕吐反射的作用。
Eur J Pharmacol. 2007 Mar 22;559(2-3):196-201. doi: 10.1016/j.ejphar.2006.12.008. Epub 2006 Dec 29.
6
Emesis induced by cancer chemotherapeutic agents in the Suncus murinus: a new experimental model.
Jpn J Pharmacol. 1988 Oct;48(2):303-6. doi: 10.1254/jjp.48.303.
7
Suncus murinus as a new experimental model for motion sickness.小家鼠作为晕动病的一种新实验模型。
Life Sci. 1988;43(5):413-20. doi: 10.1016/0024-3205(88)90520-6.
8
Male/female differences in drug-induced emesis and motion sickness in Suncus murinus.臭鼩鼱药物性呕吐和晕动病的性别差异
Pharmacol Biochem Behav. 1997 Aug;57(4):721-5. doi: 10.1016/s0091-3057(96)00389-9.
9
Antiemetic activity of FK1052, a 5-HT3- and 5-HT4-receptor antagonist, in Suncus murinus and ferrets.5-羟色胺3型和5-羟色胺4型受体拮抗剂FK1052对臭鼩和雪貂的止吐活性
J Pharmacol Sci. 2005 Aug;98(4):396-403. doi: 10.1254/jphs.fpj05001x. Epub 2005 Jul 29.
10
Antiemetic effects of morphine on motion- and drug-induced emesis in Suncus murinus.吗啡对麝鼩运动和药物诱发呕吐的止吐作用。
Biol Pharm Bull. 1997 Jul;20(7):739-42. doi: 10.1248/bpb.20.739.

引用本文的文献

1
Hypophagia and body weight loss by tirzepatide are accompanied by fewer GI adverse events compared to semaglutide in preclinical models.在临床前模型中,与司美格鲁肽相比,替尔泊肽引起的摄食减少和体重减轻伴随着更少的胃肠道不良事件。
Sci Adv. 2025 Jun 20;11(25):eadu1589. doi: 10.1126/sciadv.adu1589. Epub 2025 Jun 18.
2
Rationale for phosphodiesterase-4 inhibition as a treatment strategy for interstitial lung diseases associated with rheumatic diseases.磷酸二酯酶-4抑制作为治疗风湿性疾病相关间质性肺疾病的策略的理论依据。
RMD Open. 2024 Dec 23;10(4):e004704. doi: 10.1136/rmdopen-2024-004704.
3
GIP receptor agonism blocks chemotherapy-induced nausea and vomiting.
GIP 受体激动剂可阻断化疗引起的恶心和呕吐。
Mol Metab. 2023 Jul;73:101743. doi: 10.1016/j.molmet.2023.101743. Epub 2023 May 26.
4
Phosphodiesterase 4B inhibition: a potential novel strategy for treating pulmonary fibrosis.磷酸二酯酶4B抑制:一种治疗肺纤维化的潜在新策略。
Eur Respir Rev. 2023 Feb 21;32(167). doi: 10.1183/16000617.0206-2022. Print 2023 Mar 31.
5
Insights Into Acute and Delayed Cisplatin-Induced Emesis From a Microelectrode Array, Radiotelemetry and Whole-Body Plethysmography Study of (House Musk Shrew).通过对家麝鼩进行微电极阵列、无线电遥测和全身体积描记法研究,深入了解顺铂诱导的急性和延迟性呕吐。
Front Pharmacol. 2021 Dec 3;12:746053. doi: 10.3389/fphar.2021.746053. eCollection 2021.
6
Motilin Comparative Study: Structure, Distribution, Receptors, and Gastrointestinal Motility.胃动素比较研究:结构、分布、受体与胃肠动力。
Front Endocrinol (Lausanne). 2021 Aug 23;12:700884. doi: 10.3389/fendo.2021.700884. eCollection 2021.
7
Glucagon-like peptide-1 in diabetes care: Can glycaemic control be achieved without nausea and vomiting?胰高血糖素样肽-1 在糖尿病治疗中的作用:能否在不引起恶心和呕吐的情况下实现血糖控制?
Br J Pharmacol. 2022 Feb;179(4):542-556. doi: 10.1111/bph.15647. Epub 2021 Sep 14.
8
The HCN Channel Blocker ZD7288 Induces Emesis in the Least Shrew ().超极化激活环核苷酸门控通道阻滞剂ZD7288在小鼠中诱发呕吐。 (注:原文中“Least Shrew”常见释义为“小鼠”,但也可能存在其他准确的物种名称,此处按常见理解翻译。你可根据实际的专业知识背景进一步确认。)
Front Pharmacol. 2021 Apr 29;12:647021. doi: 10.3389/fphar.2021.647021. eCollection 2021.
9
Synthesis, Optimization, and Biological Evaluation of Corrinated Conjugates of the GLP-1R Agonist Exendin-4.冠醚化 GLP-1R 激动剂 Exendin-4 类似物的合成、优化及生物学评价
J Med Chem. 2021 Mar 25;64(6):3479-3492. doi: 10.1021/acs.jmedchem.1c00185. Epub 2021 Mar 6.
10
Design and Evaluation of Peptide Dual-Agonists of GLP-1 and NPY2 Receptors for Glucoregulation and Weight Loss with Mitigated Nausea and Emesis.GLP-1 和 NPY2 受体肽双重激动剂的设计与评价,用于血糖调节和减肥,并减轻恶心和呕吐。
J Med Chem. 2021 Jan 28;64(2):1127-1138. doi: 10.1021/acs.jmedchem.0c01783. Epub 2021 Jan 15.