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[溶血磷脂酰胆碱对心脏对乙酰胆碱敏感性及奎宁环基苯甲酸酯与心肌膜结合的影响]

[Effect of lysophasphatidylcholine on sensitivity of the heart to acetylcholine and binding of quinuclidinyl benzilate to myocardial membranes].

作者信息

Prokazova N V, Zvezdina N D, Suslova I V, Korotaeva A A, Turpaev T M

机构信息

Cardiology Research Centre, Moscow, Russia.

出版信息

Ross Fiziol Zh Im I M Sechenova. 1998 Oct;84(10):969-78.

PMID:10097264
Abstract

Chemical nature of the blood serum factor exerting cholinolytic effect on the animal heart, was determined. The effect is due to the serum lipid component: lysophosphatidylcholine. The latter in concentration 1-25 microM suppresses the sensitivity of the frog perfused heart ventricle to acetylcholine. Phosphatidylcholine was found to protect the heart from the lysophosphatidylcholine effect. Lysophosphatidylcholine also affected the binding of the acetylcholine high affinity antagonist [3H]-quinuclidinylbenzilate to the rabbit atria cell membranes. The mechanism of this effect is related to an increased ability of muscarinic receptors to form oligomeric complexes in presence of lysophosphatidylcholine, the latter manifesting a positive cooperativity on binding to ligand.

摘要

已确定对动物心脏发挥胆碱溶解作用的血清因子的化学性质。该作用归因于血清脂质成分:溶血磷脂酰胆碱。后者浓度为1 - 25微摩尔时可抑制蛙类离体灌流心室对乙酰胆碱的敏感性。发现磷脂酰胆碱可保护心脏免受溶血磷脂酰胆碱的影响。溶血磷脂酰胆碱还影响乙酰胆碱高亲和力拮抗剂[3H] - 喹核醇基苯甲酸酯与兔心房细胞膜的结合。这种作用机制与在溶血磷脂酰胆碱存在下毒蕈碱受体形成寡聚复合物的能力增强有关,溶血磷脂酰胆碱在与配体结合时表现出正协同性。

相似文献

1
[Effect of lysophasphatidylcholine on sensitivity of the heart to acetylcholine and binding of quinuclidinyl benzilate to myocardial membranes].[溶血磷脂酰胆碱对心脏对乙酰胆碱敏感性及奎宁环基苯甲酸酯与心肌膜结合的影响]
Ross Fiziol Zh Im I M Sechenova. 1998 Oct;84(10):969-78.
2
[Change in the equilibrium binding parameters of (3H)-quinuclidinylbenzilate in rabbit atrial membranes exposed to lysophosphatidylcholine].[暴露于溶血磷脂酰胆碱的兔心房膜中(3H)-奎宁环基苯甲酸酯平衡结合参数的变化]
Dokl Akad Nauk. 1995 May;342(2):273-6.
3
The distribution of the muscarinic acetylcholine receptor antagonists, quinuclidinyl benzilate and quinuclidinyl benzilate methiodide (both tritiated), in rat, guinea pig, and rabbit.毒蕈碱型乙酰胆碱受体拮抗剂——苯甲托品和甲碘化苯甲托品(均为氚标记)在大鼠、豚鼠和兔体内的分布。
J Nucl Med. 1979 Aug;20(8):865-70.
4
[3H]tricyclopinate binding to brain muscarinic acetylcholine receptors: a comparison with [3H]quinuclidinyl benzilate.[3H]三环哌酯与脑毒蕈碱型乙酰胆碱受体的结合:与[3H]喹核醇基苯甲酸酯的比较。
Pharmacol Res. 1996 Apr-May;33(4-5):283-9. doi: 10.1006/phrs.1996.0040.
5
Irreversible binding of acetylethylcholine mustard to cardiac cholinergic muscarinic receptors.乙酰乙基胆碱氮芥与心脏胆碱能毒蕈碱受体的不可逆结合。
Mol Pharmacol. 1986 Nov;30(5):411-8.
6
Positive and negative allosteric interactions on muscarinic receptors.毒蕈碱受体上的正变构和负变构相互作用。
Eur J Pharmacol. 1995 Nov 30;291(3):427-30. doi: 10.1016/0922-4106(95)90085-3.
7
Characterization of high affinity [3H]pirenzepine and (-)-[3H] quinuclidinyl benzilate binding to muscarinic cholinergic receptors in rabbit peripheral lung.高亲和力[3H]哌仑西平和(-)-[3H]东莨菪碱与兔外周肺毒蕈碱胆碱能受体结合的特性研究
J Pharmacol Exp Ther. 1987 Jan;240(1):51-8.
8
[3H]pirenzepine and (-)-[3H]quinuclidinyl benzilate binding to rat cerebral cortical and cardiac muscarinic cholinergic sites. I. Characterization and regulation of agonist binding to putative muscarinic subtypes.[3H]哌仑西平和(-)-[3H]奎宁环基苯甲酸酯与大鼠大脑皮质和心脏毒蕈碱胆碱能位点的结合。I. 激动剂与假定毒蕈碱亚型结合的特性及调节
J Pharmacol Exp Ther. 1986 May;237(2):411-8.
9
Cholinergic muscarinic receptors in rat myocardium: properties of [3H]quinuclidinyl benzilate [QNB] binding sites.
Indian J Exp Biol. 1985 Jun;23(6):300-5.
10
Positive cooperativity in the binding of alcuronium and N-methylscopolamine to muscarinic acetylcholine receptors.阿库氯铵和N-甲基东莨菪碱与毒蕈碱型乙酰胆碱受体结合中的正协同性。
Mol Pharmacol. 1990 Nov;38(5):674-80.

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