A muscarinic mechanism inhibiting the release of noradrenaline from peripheral adrenergic nerve fibres by nicotinic agents.
作者信息
Lindmar R, Löffelholz K, Muscholl E
出版信息
Br J Pharmacol Chemother. 1968 Feb;32(2):280-94. doi: 10.1111/j.1476-5381.1968.tb00972.x.
Abstract
摘要
相似文献
1
A muscarinic mechanism inhibiting the release of noradrenaline from peripheral adrenergic nerve fibres by nicotinic agents.一种毒蕈碱机制，通过烟碱样物质抑制外周肾上腺素能神经纤维释放去甲肾上腺素。
Br J Pharmacol Chemother. 1968 Feb;32(2):280-94. doi: 10.1111/j.1476-5381.1968.tb00972.x.
2
The interferance of muscarinic receptors with the noradrenaline release from sympathetic nerve endings caused by nicotinic agents.毒蕈碱受体对烟碱样药物引起的交感神经末梢去甲肾上腺素释放的干扰。
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1968;259(2):181-2. doi: 10.1007/BF00537773.
3
Atropine-resistant effects of the muscarinic agonists McN-A-343 and AHR 602 on cardiac performance and the release of noradrenaline from sympathetic nerves of the perfused rabbit heart.毒蕈碱激动剂 McN - A - 343 和 AHR 602 对灌注兔心脏的心脏功能及交感神经去甲肾上腺素释放的抗阿托品作用。
Br J Pharmacol. 1974 Apr;50(4):531-41. doi: 10.1111/j.1476-5381.1974.tb08586.x.
4
Effects of several muscarinic agonists on cardiac performance and the release of noradrenaline from sympathetic nerves of the perfused rabbit heart.几种毒蕈碱激动剂对灌注兔心脏的心脏功能及交感神经去甲肾上腺素释放的影响。
Br J Pharmacol. 1972 Aug;45(4):616-29. doi: 10.1111/j.1476-5381.1972.tb08119.x.
5
A muscarinic inhibition of the noradrenaline release evoked by postganglionic sympathetic nerve stimulation.节后交感神经刺激诱发的去甲肾上腺素释放的毒蕈碱样抑制作用。
Naunyn Schmiedebergs Arch Pharmakol. 1969;265(1):1-15. doi: 10.1007/BF01417206.
6
The effects of DMPP on adrenergic nerves in perfused hearts.
Eur J Pharmacol. 1970 Jul 1;11(1):1-12. doi: 10.1016/0014-2999(70)90247-5.
7
Muscarinic inhibition of the release of the adrenergic transmitter from peripheral sympathetic fibres.
Acta Physiol Pol. 1973 Jan-Feb;24(1):177-84.
8
Effects of the muscarinic agonist McN-A-343 on the release by sympathetic nerve stimulation of (3H)-noradrenaline from rabbit isolated ear arteries and guinea-pig atria.毒蕈碱激动剂 McN - A - 343 对兔离体耳动脉和豚鼠心房交感神经刺激释放（3H）-去甲肾上腺素的影响。
Br J Pharmacol. 1974 May;51(1):29-34. doi: 10.1111/j.1476-5381.1974.tb09628.x.
9
Studies of cholinergic inhibition using the guinea-pig ileum.
Arch Int Pharmacodyn Ther. 1969 Dec;182(2):269-78.
10
Cardiostimulatory effects of oxyfedrine, DMPP and sympathomimetics in relation to their 3H-noradrenaline-releasing properties.奥昔非君、二甲基苯哌嗪和拟交感神经药的心脏刺激作用与其释放3H-去甲肾上腺素的特性的关系。
Naunyn Schmiedebergs Arch Pharmakol. 1971;268(1):59-70. doi: 10.1007/BF00997173.
引用本文的文献
1
Circulating noradrenaline leads to release of neuropeptide Y from cardiac sympathetic nerve terminals via activation of β-adrenergic receptors.循环中的去甲肾上腺素通过激活β-肾上腺素能受体，导致心脏交感神经末梢释放神经肽Y。
J Physiol. 2025 Mar;603(7):1911-1921. doi: 10.1113/JP285945. Epub 2024 Feb 14.
2
Acute sub-diaphragmatic anterior vagus nerve stimulation increases peripheral glucose uptake in anaesthetized rats.急性膈下前迷走神经刺激可增加麻醉大鼠的外周葡萄糖摄取。
IBRO Neurosci Rep. 2023 Jun 17;15:50-56. doi: 10.1016/j.ibneur.2023.06.005. eCollection 2023 Dec.
3
Serotonin and beyond-a tribute to Manfred Göthert (1939-2019).血清素与超越——纪念曼弗雷德·格特（1939-2019）。
Naunyn Schmiedebergs Arch Pharmacol. 2021 Sep;394(9):1829-1867. doi: 10.1007/s00210-021-02083-5. Epub 2021 May 15.
4
Muscarinic Receptor Type-3 in Hypertension and Cholinergic-Adrenergic Crosstalk: Genetic Insights and Potential for New Antihypertensive Targets.高血压与胆碱能-肾上腺素能相互作用中的M3型毒蕈碱受体：遗传学见解及新型抗高血压靶点的潜力
Can J Cardiol. 2019 May;35(5):555-557. doi: 10.1016/j.cjca.2019.02.003. Epub 2019 Feb 13.
5
Complex and interacting influences of the autonomic nervous system on cardiac electrophysiology in conscious mice.自主神经系统对清醒小鼠心脏电生理的复杂相互作用影响。
Auton Neurosci. 2016 Dec;201:24-31. doi: 10.1016/j.autneu.2016.08.017. Epub 2016 Aug 29.
6
Persistent sympathoexcitation long after submaximal exercise in subjects with and without coronary artery disease.在有和没有冠状动脉疾病的受试者中，亚最大运动后持续的交感兴奋。
Am J Physiol Heart Circ Physiol. 2011 Sep;301(3):H912-20. doi: 10.1152/ajpheart.00148.2011. Epub 2011 Jun 10.
7
Inhibition of transmitter release from rat sympathetic neurons via presynaptic M(1) muscarinic acetylcholine receptors.通过突触前 M1 毒蕈碱型乙酰胆碱受体抑制大鼠交感神经元递质释放。
Br J Pharmacol. 2009 Apr;156(8):1342-52. doi: 10.1111/j.1476-5381.2009.00136.x. Epub 2009 Mar 20.
8
Activation of M1 muscarinic receptors triggers transmitter release from rat sympathetic neurons through an inhibition of M-type K+ channels.M1毒蕈碱受体的激活通过抑制M型钾通道触发大鼠交感神经元释放神经递质。
J Physiol. 2003 Dec 15;553(Pt 3):789-802. doi: 10.1113/jphysiol.2003.052449. Epub 2003 Oct 10.
9
Heterogeneity of presynaptic muscarinic receptors mediating inhibition of sympathetic transmitter release: a study with M2- and M4-receptor-deficient mice.介导交感神经递质释放抑制的突触前毒蕈碱受体的异质性：对M2和M4受体缺陷小鼠的研究
Br J Pharmacol. 2003 Feb;138(3):469-80. doi: 10.1038/sj.bjp.0705053.
10
Calcium channel subtypes for the sympathetic and parasympathetic nerves of guinea-pig atria.豚鼠心房交感神经和副交感神经的钙通道亚型
Br J Pharmacol. 1995 Sep;116(1):1577-82. doi: 10.1111/j.1476-5381.1995.tb16375.x.
本文引用的文献
1
Pharmacology of 1,1-dimethyl-4-phenylpiperazinium iodide, a ganglion stimulating agent.神经节刺激剂1,1 - 二甲基 - 4 - 苯基哌嗪碘化物的药理学
J Pharmacol Exp Ther. 1951 Nov;103(3):330-6.
2
[The effect of cocaine, guanethidine, reserpine, hexamethonium, tetracaine and psicaine on noradrenalin liberation from the heart].[可卡因、胍乙啶、利血平、六甲铵、丁卡因和地布卡因对心脏去甲肾上腺素释放的影响]
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1961;242:214-27.
3
[The concentration of noradrenalin and adrenalin in isolated sections of the heart].[心脏离体切片中去甲肾上腺素和肾上腺素的浓度]
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1959;237:350-64.
4
[THE UPTAKE OF ALPHA-METHYLNORADRENALIN INTO THE ISOLATED RABBIT HEART AND ITS LIBERATION BY RESERPINE AND GUANETHIDINE IN VIVO].[α-甲基去甲肾上腺素在离体兔心脏中的摄取及其在体内被利血平和胍乙啶释放的情况]
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1965 Jan 8;249:529-48. doi: 10.1007/BF00246559.
5
[THE EFFECT OF DRUGS ON THE ELIMINATION OF NORADRENALIN FROM PERFUSION FLUID AND NORADRENALIN UPTAKE IN THE ISOLATED HEART].[药物对灌注液中去甲肾上腺素清除及离体心脏摄取去甲肾上腺素的影响]
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1964 Jul 28;247:469-92. doi: 10.1007/BF00329896.
6
A COMPARISON OF THE GANGLION POTENTIALS AND BLOCK PRODUCED BY ACETYLCHOLINE AND TETRAMETHYLAMMONIUM.乙酰胆碱和四甲铵产生的神经节电位及阻断作用的比较
Br J Pharmacol Chemother. 1964 Aug;23(1):80-9. doi: 10.1111/j.1476-5381.1964.tb01568.x.
7
GANGLIONIC BLOCKADE PRODUCED IN SYMPATHETIC GANGLIA BY CHOLINOMIMETIC DRUGS.拟胆碱药在交感神经节中产生的神经节阻断作用。
J Pharmacol Exp Ther. 1963 Sep;141:333-42.
8
The synpathomimetic effect of acetylcholine on the spleen of the cat.乙酰胆碱对猫脾脏的拟交感神经效应。
J Physiol. 1963 Jul;167(3):487-504. doi: 10.1113/jphysiol.1963.sp007164.
9
[On the effect of choline esters and biogenic amines on the isolated heart auricle].[胆碱酯类和生物胺对离体心耳的作用]
Acta Neuroveg (Wien). 1960;21:445-60. doi: 10.1007/BF01228273.
10
The action of acetylcholine and some related substances on conduction in mammalian non-myelinated nerve fibres.乙酰胆碱及某些相关物质对哺乳动物无髓神经纤维传导的作用。
J Physiol. 1961 Feb;155(2):372-84. doi: 10.1113/jphysiol.1961.sp006634.
Zotero 插件