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1
Ligand binding to muscarinic receptors in intact longitudinal muscle strips from guinea-pig intestine.豚鼠肠道完整纵肌条中配体与毒蕈碱受体的结合
Br J Pharmacol. 1977 Oct;61(2):189-97. doi: 10.1111/j.1476-5381.1977.tb08404.x.
2
Changes in muscarinic ligand binding to intestinal muscle strips produced by pre-exposure to hypotonic conditions.预先暴露于低渗条件下对毒蕈碱配体与肠肌条结合产生的影响。
J Pharm Pharmacol. 1978 Jan;30(1):27-35. doi: 10.1111/j.2042-7158.1978.tb13148.x.
3
Persistent effects of high concentrations of chlorpromazine on 3H-propylbenzilylcholine mustard binding to muscarinic receptors in guinea-pig intestinal muscle strips.高浓度氯丙嗪对豚鼠肠肌条中3H-丙基苄基胆碱氮芥与毒蕈碱受体结合的持续影响。
Arch Int Pharmacodyn Ther. 1980 Sep;247(1):21-30.
4
Activation of propylbenzilylcholine mustard-sensitive muscarinic cholinoceptors more effectively utilizes cytosolic Ca2+ for contraction in guinea-pig intestinal smooth muscle.丙基苄基胆碱氮芥敏感的毒蕈碱型胆碱能受体的激活,能更有效地利用胞质Ca2+来引起豚鼠肠道平滑肌收缩。
Eur J Pharmacol. 1990 Oct 2;187(1):139-42. doi: 10.1016/0014-2999(90)90352-7.
5
Propylbenzilylcholine mustard discriminates between two subtypes of muscarinic cholinoceptors in guinea-pig taenia caecum.丙基苄基胆碱氮芥可区分豚鼠盲肠带中两种毒蕈碱型胆碱能受体亚型。
Arch Int Pharmacodyn Ther. 1989 Mar-Apr;298:210-9.
6
Muscarinic receptors in rat intestinal muscle: comparison with the guinea pig.大鼠肠肌中的毒蕈碱受体:与豚鼠的比较。
Eur J Pharmacol. 1975 Apr;31(2):319-26. doi: 10.1016/0014-2999(75)90055-2.
7
Guanosine 5'-triphosphate converts some populations of propylbenzilylcholine mustard-sensitive muscarinic cholinoceptor sites to sites resistant to the drug in intestinal smooth muscle.5'-三磷酸鸟苷可使肠道平滑肌中一些对丙基苄基胆碱芥子碱敏感的毒蕈碱型胆碱能受体位点转变为对该药物耐药的位点。
Jpn J Pharmacol. 1991 Mar;55(3):329-38. doi: 10.1254/jjp.55.329.
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The effect of propylbenzilylcholine mustard on contraction and radioligand binding parameters of muscarinic receptors in guinea pig ileum.丙基苄基胆碱氮芥对豚鼠回肠毒蕈碱受体收缩及放射性配体结合参数的影响。
Life Sci. 1987 Oct 26;41(17):2023-32. doi: 10.1016/0024-3205(87)90476-0.
9
Characterization of subtype of propylbenzilylcholine mustard (PrBCM)-sensitive and -resistant muscarinic cholinoceptors in guinea pig ileal muscle.豚鼠回肠肌中对丙基苄基胆碱氮芥(PrBCM)敏感和耐药的毒蕈碱胆碱能受体亚型的表征
Jpn J Pharmacol. 1992 Aug;59(4):485-7. doi: 10.1254/jjp.59.485.
10
Propylbenzilylcholine mustard-sensitive and -resistant muscarinic receptors in cardiac muscle.心肌中对丙基苄基胆碱氮芥敏感和耐药的毒蕈碱受体。
Gen Pharmacol. 1991;22(4):691-4. doi: 10.1016/0306-3623(91)90079-l.

引用本文的文献

1
The interaction of amine local anaesthetics with muscarinic receptors.胺类局部麻醉药与毒蕈碱受体的相互作用。
Br J Pharmacol. 1980;71(1):327-35. doi: 10.1111/j.1476-5381.1980.tb10943.x.
2
Proceedings of the British Pharmacological Society. 17th-19th December, 1979: University of London (Institute of Education).英国药理学会会议记录。1979年12月17日至19日:伦敦大学(教育学院)
Br J Pharmacol. 1980 Jun;69(2):265P-346P.
3
Pre- and postsynaptic effects of muscarinic agonists in the guinea-pig ileum.毒蕈碱激动剂对豚鼠回肠的突触前和突触后效应。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Nov;314(3):259-66. doi: 10.1007/BF00498547.
4
Actions of various muscarinic agonists on membrane potential, potassium efflux, and contraction of longitudinal muscle of guinea-pig intestine.各种毒蕈碱激动剂对豚鼠肠纵肌膜电位、钾外流和收缩的作用。
Br J Pharmacol. 1981 Feb;72(2):319-34. doi: 10.1111/j.1476-5381.1981.tb09131.x.
5
Influence of N-ethylmaleimide on cholinoceptors and responses in longitudinal muscles from guinea-pig ileum.N-乙基马来酰亚胺对豚鼠回肠纵行肌中胆碱能受体及反应的影响。
Br J Pharmacol. 1982 Sep;77(1):89-95. doi: 10.1111/j.1476-5381.1982.tb09273.x.
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The binding characteristics of [3H]-dihydroergocryptine on intact human platelets.[3H]-二氢麦角隐亭在完整人血小板上的结合特性
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7
Muscarinic cholinergic receptor binding in rat mast cells.大鼠肥大细胞中的毒蕈碱型胆碱能受体结合
Agents Actions. 1983 Jun;13(4):327-32. doi: 10.1007/BF01971484.
8
The effect of gallamine, gallopamil and nifedipine on responses to acetylcholine and carbachol in the taenia of the guinea-pig caecum.加拉明、加洛帕米和硝苯地平对豚鼠盲肠带对乙酰胆碱和卡巴胆碱反应的影响。
Br J Pharmacol. 1984 Sep;83(1):145-55. doi: 10.1111/j.1476-5381.1984.tb10129.x.
9
Muscarinic receptors in rat sympathetic ganglia.大鼠交感神经节中的毒蕈碱受体。
Br J Pharmacol. 1980 Dec;70(4):577-92. doi: 10.1111/j.1476-5381.1980.tb09777.x.
10
The relationship between muscarinic receptor binding and ion movements in rat parotid cells.大鼠腮腺细胞中毒蕈碱受体结合与离子运动之间的关系。
J Physiol. 1980 Feb;299:521-31. doi: 10.1113/jphysiol.1980.sp013140.

本文引用的文献

1
THE UPTAKE OF ATROPINE AND RELATED DRUGS BY INTESTINAL SMOOTH MUSCLE OF THE GUINEA-PIG IN RELATION TO ACETYLCHOLINE RECEPTORS.豚鼠肠道平滑肌对阿托品及相关药物的摄取与乙酰胆碱受体的关系
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Muscarinic receptors.毒蕈碱受体
Nature. 1961 Feb 25;189:671-3. doi: 10.1038/189671b0.
3
An alkylating derivative of benzilylcholine with specific and long-lasting parasympatholytic activity.一种具有特异性和长效副交感神经阻滞活性的苄基胆碱烷基化衍生物。
Mol Pharmacol. 1966 Jul;2(4):284-97.
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The rate of action of atropine.阿托品的作用速率。
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The properties of muscarinic receptors in mammalian cerebral cortex.哺乳动物大脑皮层中毒蕈碱受体的特性。
Br J Pharmacol. 1974 Jun;51(2):279-85. doi: 10.1111/j.1476-5381.1974.tb09658.x.
6
Proceedings: Two populations of acetylcholine receptors in guinea-pig ileum.论文:豚鼠回肠中的两类乙酰胆碱受体
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7
Seasonal variation in sensitivity of guinea pig tissues to agonists.豚鼠组织对激动剂敏感性的季节性变化。
Nature. 1974 Oct 4;251(5474):427-8. doi: 10.1038/251427a0.
8
Desensitisation and agonist binding to cholinergic receptors in intestinal smooth muscle.肠道平滑肌中胆碱能受体的脱敏作用及激动剂结合
FEBS Lett. 1974 Sep 15;46(1):354-6. doi: 10.1016/0014-5793(74)80405-9.
9
The kinetics of action of acetylcholine antagonists in smooth muscle.乙酰胆碱拮抗剂在平滑肌中的作用动力学。
Proc R Soc Lond B Biol Sci. 1966 Apr 19;164(996):488-510. doi: 10.1098/rspb.1966.0045.
10
The binding of (3H)-propylbenzilycholine mustard by longitudinal muscle strips from guinea-pig small intestine.豚鼠小肠纵行肌条对(3H)-丙基苯甲酰胆碱氮芥的结合
Br J Pharmacol. 1974 Jan;50(1):145-51. doi: 10.1111/j.1476-5381.1974.tb09602.x.

豚鼠肠道完整纵肌条中配体与毒蕈碱受体的结合

Ligand binding to muscarinic receptors in intact longitudinal muscle strips from guinea-pig intestine.

作者信息

Ward D, Young J M

出版信息

Br J Pharmacol. 1977 Oct;61(2):189-97. doi: 10.1111/j.1476-5381.1977.tb08404.x.

DOI:10.1111/j.1476-5381.1977.tb08404.x
PMID:922248
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1667513/
Abstract

1 The binding of ligands to muscarinic receptors in intact longitudinal muscle strips from guinea-pig small intestine has been determined by measuring the inhibition of the irreversible binding of [3H]-propylbenzilylcholine mustard ([3H]-PrBCM). 2 The IC50 values for inhibition of [3H]-PrBCM binding by a given ligand were generally higher in intact strips than those reported for broken-cell preparations. This effect is probably due, at least in part, to the presence of an access-limitation factor in the kinetics of the irreversible binding of [3H]-PrBCM to the intact tissue. 3 The mean Hill coefficients for antagonist binding approached unity, but those for strong agonists were significantly less than unity. There was, with the possible exceptions of hexyltrimethylammonium and oxotremorine, reasonably good agreement with the Hill coefficients reported for brain homogenates.

摘要

1 通过测量[3H]-丙基苄基胆碱氮芥([3H]-PrBCM)不可逆结合的抑制作用,已确定了配体与豚鼠小肠完整纵肌条中毒蕈碱受体的结合情况。2 给定配体对[3H]-PrBCM结合的抑制作用的IC50值在完整肌条中通常高于破碎细胞制剂中报道的值。这种效应至少部分可能是由于[3H]-PrBCM与完整组织不可逆结合动力学中存在进入限制因子。3 拮抗剂结合的平均希尔系数接近1,但强激动剂的希尔系数明显小于1。除己基三甲基铵和氧化震颤素可能例外,与脑匀浆中报道的希尔系数有较好的一致性。