• 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

相似文献

1
The use of occupation isoboles for analysis of a response mediated by two receptors: M2 and M3 muscarinic receptor subtype-induced mouse stomach contractions.使用职业等效线分析由两种受体介导的反应:M2和M3毒蕈碱受体亚型诱导的小鼠胃收缩。
J Pharmacol Exp Ther. 2008 Jun;325(3):954-60. doi: 10.1124/jpet.108.137018. Epub 2008 Mar 13.
2
Functional roles of muscarinic M2 and M3 receptors in mouse stomach motility: studies with muscarinic receptor knockout mice.毒蕈碱型M2和M3受体在小鼠胃动力中的功能作用:毒蕈碱受体基因敲除小鼠的研究
Eur J Pharmacol. 2007 Jan 12;554(2-3):212-22. doi: 10.1016/j.ejphar.2006.10.013. Epub 2006 Oct 17.
3
Muscarinic receptor subtypes involved in carbachol-induced contraction of mouse uterine smooth muscle.参与卡巴胆碱诱导的小鼠子宫平滑肌收缩的毒蕈碱受体亚型。
Naunyn Schmiedebergs Arch Pharmacol. 2008 Jun;377(4-6):503-13. doi: 10.1007/s00210-007-0223-1. Epub 2007 Dec 11.
4
M(2) and M(3) muscarinic receptor-mediated contractions in longitudinal smooth muscle of the ileum studied with receptor knockout mice.利用受体敲除小鼠研究M(2)和M(3)毒蕈碱受体介导的回肠纵行平滑肌收缩。
Br J Pharmacol. 2005 Sep;146(1):98-108. doi: 10.1038/sj.bjp.0706300.
5
A role for M(2) and M(3) muscarinic receptors in the contraction of rat and human small airways.M2 和 M3 毒蕈碱受体在大鼠和人小气道收缩中的作用。
Eur J Pharmacol. 2013 Feb 28;702(1-3):109-15. doi: 10.1016/j.ejphar.2013.01.054. Epub 2013 Feb 8.
6
Gastric body cholinergic contractile signal transduction in M2 and M3 receptor knockout mice.M2和M3受体基因敲除小鼠胃体胆碱能收缩信号转导
J Recept Signal Transduct Res. 2013 Aug;33(4):249-54. doi: 10.3109/10799893.2013.802803. Epub 2013 Jun 20.
7
M2 and M3 muscarinic receptor activation of urinary bladder contractile signal transduction. I. Normal rat bladder.毒蕈碱M2和M3受体激活膀胱收缩信号转导。I. 正常大鼠膀胱
J Pharmacol Exp Ther. 2006 Feb;316(2):869-74. doi: 10.1124/jpet.105.097303. Epub 2005 Oct 21.
8
M2 and M3 muscarinic receptor activation of urinary bladder contractile signal transduction. II. Denervated rat bladder.M2和M3毒蕈碱受体激活膀胱收缩信号转导。II. 去神经大鼠膀胱
J Pharmacol Exp Ther. 2006 Feb;316(2):875-80. doi: 10.1124/jpet.105.094961. Epub 2005 Oct 21.
9
The inhibitory effects of antimuscarinic autoantibodies in the sera of primary Sjogren syndrome patients on the gastrointestinal motility.原发性干燥综合征患者血清中抗毒蕈碱自身抗体对胃肠动力的抑制作用。
Mol Immunol. 2013 Dec;56(4):583-7. doi: 10.1016/j.molimm.2013.06.004. Epub 2013 Aug 1.
10
Roles of M2 and M3 muscarinic receptors in cholinergic nerve-induced contractions in mouse ileum studied with receptor knockout mice.利用受体敲除小鼠研究M2和M3毒蕈碱受体在胆碱能神经诱导的小鼠回肠收缩中的作用。
Br J Pharmacol. 2006 Dec;149(8):1022-30. doi: 10.1038/sj.bjp.0706955. Epub 2006 Nov 13.

引用本文的文献

1
Tramadol/paracetamol fixed-dose combination in the treatment of moderate to severe pain.曲马多/对乙酰氨基酚固定剂量复方制剂治疗中重度疼痛。
J Pain Res. 2012;5:327-46. doi: 10.2147/JPR.S33112. Epub 2012 Aug 29.
2
Synergistic interaction between the two mechanisms of action of tapentadol in analgesia.曲马多两种作用机制在镇痛中的协同作用。
J Pharmacol Exp Ther. 2011 Apr;337(1):312-20. doi: 10.1124/jpet.110.175042. Epub 2011 Jan 24.
3
Oxycodone combinations for pain relief.用于止痛的羟考酮复方制剂。
Drugs Today (Barc). 2010 Jun;46(6):379-98. doi: 10.1358/dot.2010.46.6.1470106.
4
The application of drug dose equivalence in the quantitative analysis of receptor occupation and drug combinations.药物剂量等效性在受体占有率和药物组合的定量分析中的应用。
Pharmacol Ther. 2010 Aug;127(2):165-74. doi: 10.1016/j.pharmthera.2010.04.011. Epub 2010 May 28.
5
Comparison of human and porcine gastric clasp and sling fiber contraction by M2 and M3 muscarinic receptors.比较 M2 和 M3 毒蕈碱受体对人胃扣和吊索纤维收缩的影响。
Am J Physiol Gastrointest Liver Physiol. 2010 Apr;298(4):G530-4. doi: 10.1152/ajpgi.00129.2009. Epub 2010 Feb 4.
6
Quantitation of the contractile response mediated by two receptors: M2 and M3 muscarinic receptor-mediated contractions of human gastroesophageal smooth muscle.两种受体介导的收缩反应的定量分析:M2和M3毒蕈碱受体介导的人胃食管平滑肌收缩
J Pharmacol Exp Ther. 2009 Apr;329(1):218-24. doi: 10.1124/jpet.108.148106. Epub 2009 Jan 6.

本文引用的文献

1
Neuronally released acetylcholine acts on the M2 muscarinic receptor to oppose the relaxant effect of isoproterenol on cholinergic contractions in mouse urinary bladder.神经元释放的乙酰胆碱作用于M2毒蕈碱受体,以对抗异丙肾上腺素对小鼠膀胱胆碱能收缩的舒张作用。
J Pharmacol Exp Ther. 2007 Aug;322(2):631-7. doi: 10.1124/jpet.107.121756. Epub 2007 May 1.
2
M2 mediated contractions of human bladder from organ donors is associated with an increase in urothelial muscarinic receptors.M2介导的来自器官捐献者的人膀胱收缩与尿路上皮毒蕈碱受体增加有关。
Neurourol Urodyn. 2007;26(1):63-70. doi: 10.1002/nau.20378.
3
Interactions between drugs and occupied receptors.药物与被占据受体之间的相互作用。
Pharmacol Ther. 2007 Jan;113(1):197-209. doi: 10.1016/j.pharmthera.2006.08.002. Epub 2006 Sep 7.
4
Comparison study of autonomous activity in bladders from normal and paraplegic rats.正常大鼠和截瘫大鼠膀胱自主活动的比较研究
Neurourol Urodyn. 2006;25(4):368-78; discussion 379-80. doi: 10.1002/nau.20206.
5
An overview of drug combination analysis with isobolograms.用等效线图进行药物联合分析概述。
J Pharmacol Exp Ther. 2006 Oct;319(1):1-7. doi: 10.1124/jpet.106.104117. Epub 2006 May 2.
6
Signal-transduction pathways that regulate visceral smooth muscle function. III. Coupling of muscarinic receptors to signaling kinases and effector proteins in gastrointestinal smooth muscles.调节内脏平滑肌功能的信号转导通路。III. 毒蕈碱受体与胃肠道平滑肌中信号激酶及效应蛋白的偶联
Am J Physiol Gastrointest Liver Physiol. 2005 May;288(5):G849-53. doi: 10.1152/ajpgi.00530.2004.
7
Isobolographic analysis for combinations of a full and partial agonist: curved isoboles.对完全激动剂和部分激动剂组合的等效线分析:曲线等效线
J Pharmacol Exp Ther. 2004 Sep;310(3):981-6. doi: 10.1124/jpet.104.067264. Epub 2004 Jun 2.
8
The M2 muscarinic receptor mediates in vitro bladder contractions from patients with neurogenic bladder dysfunction.M2毒蕈碱受体介导神经源性膀胱功能障碍患者的体外膀胱收缩。
Am J Physiol Regul Integr Comp Physiol. 2004 May;286(5):R874-80. doi: 10.1152/ajpregu.00391.2003. Epub 2004 Jan 29.
9
Role of muscarinic receptor subtypes in the constriction of peripheral airways: studies on receptor-deficient mice.毒蕈碱受体亚型在周围气道收缩中的作用:对受体缺陷小鼠的研究。
Mol Pharmacol. 2003 Dec;64(6):1444-51. doi: 10.1124/mol.64.6.1444.
10
The problem of synergism and antagonism of combined drugs.联合用药的协同和拮抗问题。
Arzneimittelforschung. 1953 Jun;3(6):285-90.

使用职业等效线分析由两种受体介导的反应:M2和M3毒蕈碱受体亚型诱导的小鼠胃收缩。

The use of occupation isoboles for analysis of a response mediated by two receptors: M2 and M3 muscarinic receptor subtype-induced mouse stomach contractions.

作者信息

Braverman Alan S, Tallarida Ronald J, Ruggieri Michael R

机构信息

Department of Urology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.

出版信息

J Pharmacol Exp Ther. 2008 Jun;325(3):954-60. doi: 10.1124/jpet.108.137018. Epub 2008 Mar 13.

DOI:10.1124/jpet.108.137018
PMID:18339971
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3277794/
Abstract

Smooth muscle contains multiple muscarinic receptor subtypes, including M2 and M3. M2 receptors outnumber M3 receptors. Based on the potency of subtype selective anticholinergics, contraction is mediated by the M3 subtype. However, results from knockout (KO) mice show that the M2 receptor mediates approximately 45% of the contractile response produced by the M3 receptor. The traditional theory of one receptor mediating a response does not allow assessment of interactions between receptors when more than one receptor participates in a response. Our study was performed using a novel analysis method based on dual receptor occupancy to determine how M2 and M3 receptor subtypes interact to mediate contraction in mouse stomach. Cumulative carbachol concentration contractile responses were determined for wild-type, M2-KO, and M3-KO stomach body smooth muscle. Using affinity constants for carbachol at M2 and M3 cholinergic receptors, the concentration values were converted to fractional receptor occupation. The resulting occupation-effect relations showed maximum effects for the M2 and M3 subtypes, respectively. These occupation-effect relations allow determination of the additive (expected) isobole based on this dual occupancy, thereby providing a curve (mathematically derived) for comparison against the experimentally derived value in wild type. The actual values determined experimentally in the wild type were not statistically significantly different from that predicted by the isobole. This confirms that the interaction between these mutually occupied receptors is additive. The new method of analysis also expands the traditional Schild theory that was based on a single receptor type to which the agonist and antagonist bind.

摘要

平滑肌含有多种毒蕈碱受体亚型,包括M2和M3。M2受体的数量超过M3受体。根据亚型选择性抗胆碱能药物的效力,收缩是由M3亚型介导的。然而,基因敲除(KO)小鼠的结果表明,M2受体介导了M3受体产生的约45%的收缩反应。当不止一种受体参与反应时,传统的一种受体介导一种反应的理论无法评估受体之间的相互作用。我们的研究采用了一种基于双受体占有率的新型分析方法,以确定M2和M3受体亚型如何相互作用来介导小鼠胃的收缩。测定了野生型、M2-KO和M3-KO胃体平滑肌对卡巴胆碱累积浓度的收缩反应。利用卡巴胆碱在M2和M3胆碱能受体上的亲和常数,将浓度值转换为受体占有率分数。所得的占有率-效应关系分别显示了M2和M3亚型的最大效应。这些占有率-效应关系允许根据这种双占有率确定相加性(预期)等效线,从而提供一条曲线(通过数学推导),以便与野生型实验得出的值进行比较。在野生型中实验测定的实际值与等效线预测的值在统计学上没有显著差异。这证实了这些相互占据的受体之间的相互作用是相加性的。这种新的分析方法也扩展了基于激动剂和拮抗剂结合的单一受体类型的传统希尔德理论。