• 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

食蟹猴睫状体毒蕈碱受体的结合特性及激动剂亚敏感性诱导反应

The binding properties of the muscarinic receptors of the cynomolgus monkey ciliary body and the response to the induction of agonist subsensitivity.

作者信息

Bárány E, Berrie C P, Birdsall N J, Burgen A S, Hulme E C

出版信息

Br J Pharmacol. 1982 Dec;77(4):731-9. doi: 10.1111/j.1476-5381.1982.tb09353.x.

DOI:10.1111/j.1476-5381.1982.tb09353.x
PMID:6897523
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2044665/
Abstract

1 The binding properties of the muscarinic receptors in the ciliary muscle of cynomolgus monkeys have been evaluated. 2 The concentration of receptor binding sites is the highest yet reported. As found in many species and tissues, there are subclasses of agonist binding sites. Agonist binding is not affected by the non-hydrolysable guanosine triphosphate (GTP) analogue, GppNHp, suggesting that these receptors are not linked to adenylate cyclase. 3 Ciliary muscles made subsensitive by treatment with muscarinic agonists have a decreased receptor concentration but no other changes in the binding properties of the receptors could be detected.

摘要

1 已经评估了食蟹猴睫状肌中毒蕈碱受体的结合特性。2 受体结合位点的浓度是迄今报道的最高值。正如在许多物种和组织中所发现的那样,存在激动剂结合位点的亚类。激动剂结合不受不可水解的鸟苷三磷酸(GTP)类似物GppNHp的影响,这表明这些受体不与腺苷酸环化酶相连。3 用毒蕈碱激动剂处理后变得不敏感的睫状肌,其受体浓度降低,但未检测到受体结合特性的其他变化。

相似文献

1
The binding properties of the muscarinic receptors of the cynomolgus monkey ciliary body and the response to the induction of agonist subsensitivity.食蟹猴睫状体毒蕈碱受体的结合特性及激动剂亚敏感性诱导反应
Br J Pharmacol. 1982 Dec;77(4):731-9. doi: 10.1111/j.1476-5381.1982.tb09353.x.
2
Subclasses of muscarinic receptors and pirenzepine. Further experimental evidence.毒蕈碱受体亚型与哌仑西平。更多实验证据。
Scand J Gastroenterol Suppl. 1982;72:59-67.
3
Muscarinic responses and binding in a murine neuroblastoma clone (N1E-115). Mediation of separate responses by high affinity and low affinity agonist-receptor conformations.小鼠神经母细胞瘤克隆株(N1E-115)中的毒蕈碱反应与结合。高亲和力和低亲和力激动剂-受体构象对不同反应的介导作用。
Mol Pharmacol. 1985 Feb;27(2):223-35.
4
The effects of agonists on the components of the cardiac muscarinic receptor.激动剂对心脏毒蕈碱受体各组分的影响。
Br J Pharmacol. 1987 Oct;92(2):327-32. doi: 10.1111/j.1476-5381.1987.tb11327.x.
5
Short-term desensitization of muscarinic cholinergic receptors in mouse neuroblastoma cells: selective loss of agonist low-affinity and pirenzepine high-affinity binding sites.小鼠神经母细胞瘤细胞中毒蕈碱型胆碱能受体的短期脱敏:激动剂低亲和力和哌仑西平高亲和力结合位点的选择性丧失。
J Pharmacol Exp Ther. 1986 Sep;238(3):916-23.
6
Muscarinic subsensitivity without receptor change in monkey ciliary muscle.猴睫状肌中无受体改变的毒蕈碱敏感性降低
Br J Pharmacol. 1985 Jan;84(1):193-8.
7
Muscarinic receptors in the stomach.胃中的毒蕈碱受体
Scand J Gastroenterol Suppl. 1980;66:5-11.
8
Reconstitution of solubilized atrial cholinergic muscarinic receptors in liposomes.脂质体中溶解的心房胆碱能毒蕈碱受体的重组。
Neurochem Res. 1987 Jan;12(1):83-91. doi: 10.1007/BF00971369.
9
Agonist binding to M1 muscarinic receptors is sensitive to guanine nucleotides.激动剂与M1毒蕈碱受体的结合对鸟嘌呤核苷酸敏感。
Eur J Pharmacol. 1989 Oct 17;172(4-5):363-72. doi: 10.1016/0922-4106(89)90017-5.
10
Agonist regulation of the muscarinic cholinergic receptor in embryonic chick heart.胚胎期鸡心脏中毒蕈碱型胆碱能受体的激动剂调节
Adv Exp Med Biol. 1983;161:113-42. doi: 10.1007/978-1-4684-4472-8_7.

引用本文的文献

1
Examination of signalling pathways involved in muscarinic responses in bovine ciliary muscle using YM-254890, an inhibitor of the Gq/11 protein.使用Gq/11蛋白抑制剂YM-254890对牛睫状肌中参与毒蕈碱反应的信号通路进行研究。
Br J Pharmacol. 2008 Jun;154(4):890-900. doi: 10.1038/bjp.2008.140. Epub 2008 Apr 21.
2
Muscarinic receptor M1 and M2 subtypes in the human eye: QNB, pirenzipine, oxotremorine, and AFDX-116 in vitro autoradiography.人眼中毒蕈碱受体M1和M2亚型:体外放射自显影中的QNB、哌仑西平、氧化震颤素和AFDX-116
Br J Ophthalmol. 1994 Jul;78(7):555-9. doi: 10.1136/bjo.78.7.555.
3
Muscarinic subsensitivity without receptor change in monkey ciliary muscle.猴睫状肌中无受体改变的毒蕈碱敏感性降低
Br J Pharmacol. 1985 Jan;84(1):193-8.
4
Measurements of intracellular calcium and contractility in human ciliary muscle.人睫状肌细胞内钙和收缩性的测量
Pflugers Arch. 1991 Jul;418(6):531-7. doi: 10.1007/BF00370567.

本文引用的文献

1
Fine structure of the human cillary muscle.人类睫状肌的精细结构。
Invest Ophthalmol. 1962 Oct;1:587-608.
2
Muscarinic receptor: regulation by guanine nucleotides, ions, and N-ethylmaleimide.毒蕈碱受体:受鸟嘌呤核苷酸、离子和N-乙基马来酰亚胺的调节。
Fed Proc. 1981 Feb;40(2):153-9.
3
Agonist and guanine nucleotide modulation of muscarinic cholinergic receptors in cultured heart cells.培养心肌细胞中毒蕈碱型胆碱能受体的激动剂和鸟嘌呤核苷酸调节
J Biol Chem. 1980 Oct 25;255(20):9571-9.
4
Altered [3H]quinuclidinyl benzilate binding in the striatum of rats following chronic cholinesterase inhibition with diisopropylfluorophosphate.用二异丙基氟磷酸酯对大鼠进行慢性胆碱酯酶抑制后,其纹状体中[3H]奎宁环基苯甲酸酯结合发生改变。
Mol Pharmacol. 1980 Jan;17(1):24-30.
5
Regulation of muscarinic acetylcholine receptor concentration in cloned neuroblastoma cells.克隆化神经母细胞瘤细胞中毒蕈碱型乙酰胆碱受体浓度的调节
J Neurochem. 1980 Apr;34(4):993-9. doi: 10.1111/j.1471-4159.1980.tb09676.x.
6
Cardiac muscarinic cholinergic receptor binding is regulated by Na+ and guanyl nucleotides.心肌毒蕈碱胆碱能受体结合受钠离子和鸟苷核苷酸调节。
J Biol Chem. 1980 Feb 10;255(3):820-3.
7
Pirenzepine distinguishes between different subclasses of muscarinic receptors.哌仑西平可区分毒蕈碱受体的不同亚类。
Nature. 1980 Jan 3;283(5742):90-2. doi: 10.1038/283090a0.
8
In vivo modulation of the number of muscarinic receptors in rat brain by cholinergic ligands.胆碱能配体对大鼠脑内毒蕈碱受体数量的体内调节
Eur J Pharmacol. 1981 Aug 27;74(1):73-81. doi: 10.1016/0014-2999(81)90325-3.
9
Two populations of binding sites for muscarinic antagonists in the rat heart.大鼠心脏中毒蕈碱拮抗剂的两类结合位点
Eur J Pharmacol. 1981 Jul 17;73(2-3):137-42. doi: 10.1016/0014-2999(81)90085-6.
10
Cholinergic adaptations to chronic oxotremorine infusion.对慢性输注氧化震颤素的胆碱能适应性
J Pharmacol Exp Ther. 1981 Aug;218(2):337-43.