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Subclasses of muscarinic receptors and pirenzepine. Further experimental evidence.

作者信息

Hammer R

出版信息

Scand J Gastroenterol Suppl. 1982;72:59-67.

PMID:6957998
Abstract
摘要

相似文献

1
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.
2
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.
3
Does pirenzepine distinguish between 'subtypes' of muscarinic receptors?哌仑西平能否区分毒蕈碱受体的“亚型”？
Br J Pharmacol. 1982 Dec;77(4):567-9. doi: 10.1111/j.1476-5381.1982.tb09332.x.
4
Muscarinic receptors in the stomach.胃中的毒蕈碱受体
Scand J Gastroenterol Suppl. 1980;66:5-11.
5
Muscarinic cholinergic receptors in a rat phaeochromocytoma cell line.大鼠嗜铬细胞瘤细胞系中的毒蕈碱型胆碱能受体
Biochem Biophys Res Commun. 1984 Feb 29;119(1):163-7. doi: 10.1016/0006-291x(84)91633-4.
6
[Pirenzepine--an anticholinergic agent with selective antimuscarinic properties].哌仑西平——一种具有选择性抗毒蕈碱特性的抗胆碱能药物
Lakartidningen. 1982 Oct 13;79(41):3671-3.
7
Pirenzepine and exocrine secretions: a selective agent for gastric glands?哌仑西平和外分泌：一种针对胃腺的选择性药物？
Hepatogastroenterology. 1983 Dec;30(6):246-8.
8
Pharmacological evidence for cardiac muscarinic receptor subtypes.心脏毒蕈碱受体亚型的药理学证据。
Life Sci. 1984 Oct 22;35(17):1739-45. doi: 10.1016/0024-3205(84)90270-4.
9
Apparent noncompetitive antagonism of muscarinic receptor mediated Ca2+ mobilization by some muscarinic antagonists.
Biochem Biophys Res Commun. 1992 Dec 15;189(2):919-24. doi: 10.1016/0006-291x(92)92291-5.
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
Subclassification of muscarinic receptors in the heart, urinary bladder and sympathetic ganglia in the pithed rat. Selectivity of some classical agonists.
Naunyn Schmiedebergs Arch Pharmacol. 1985 Dec;331(4):301-6. doi: 10.1007/BF00500810.
2
Solubilization and characterization of high and low affinity pirenzepine binding sites from rat cerebral cortex.大鼠大脑皮层中高亲和力和低亲和力哌仑西平结合位点的增溶及特性研究
Br J Pharmacol. 1985 Jul;85(3):697-703. doi: 10.1111/j.1476-5381.1985.tb10566.x.
3
Pirenzepine. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic efficacy in peptic ulcer disease and other allied diseases.哌仑西平。其药效学和药代动力学特性以及在消化性溃疡疾病和其他相关疾病中的治疗效果综述。
Drugs. 1985 Aug;30(2):85-126. doi: 10.2165/00003495-198530020-00001.
4
Two types of muscarinic response to acetylcholine in mammalian cortical neurons.哺乳动物皮层神经元中对乙酰胆碱的两种毒蕈碱样反应。
Proc Natl Acad Sci U S A. 1985 Sep;82(18):6344-8. doi: 10.1073/pnas.82.18.6344.
5
Identification of muscarinic receptor subtype mediating colonic response to eating.介导结肠对进食反应的毒蕈碱受体亚型的鉴定。
Dig Dis Sci. 1985 Feb;30(2):124-8. doi: 10.1007/BF01308197.
6
The binding of pirenzepine to digitonin-solubilized muscarinic acetylcholine receptors from the rat myocardium.哌仑西平与大鼠心肌中洋地黄皂苷增溶的毒蕈碱型乙酰胆碱受体的结合。
Br J Pharmacol. 1986 Feb;87(2):307-16. doi: 10.1111/j.1476-5381.1986.tb10819.x.
7
Possible mechanisms of anti-cholinergic drug-induced bradycardia.抗胆碱能药物诱发心动过缓的可能机制。
Eur J Clin Pharmacol. 1988;35(5):503-6. doi: 10.1007/BF00558245.
8
AFDX-116 discriminates between muscarinic M2 receptors of the heart and the iris smooth muscle.AFDX - 116 可区分心脏的毒蕈碱型 M2 受体和虹膜平滑肌的毒蕈碱型 M2 受体。
Mol Cell Biochem. 1988 Jul-Aug;82(1-2):131-5. doi: 10.1007/BF00242528.
9
Subtypes of muscarinic receptors in vagal inhibitory pathway to the lower esophageal sphincter of the opossum.
Dig Dis Sci. 1987 Oct;32(10):1130-5. doi: 10.1007/BF01300200.
10
Receptors for neurotransmitters in opossum oesophagus muscularis mucosa.负鼠食管黏膜肌层中神经递质的受体
Br J Pharmacol. 1986 Jul;88(3):707-14. doi: 10.1111/j.1476-5381.1986.tb10254.x.