نتایج جستجو برای: muscarinic antagonists

تعداد نتایج: 58413  

Journal: :The Journal of pharmacology and experimental therapeutics 2000
H G Preiksaitis P S Krysiak T Chrones V Rajgopal L G Laurier

Esophageal peristalsis is dependent on activation of muscarinic receptors, but little is known about the roles of specific receptor subtypes in the human esophagus. We examined muscarinic receptor expression and function in human esophageal smooth muscle obtained from patients undergoing resection for cancer. [(3)H]Quinuclidinyl benzylate (QNB)-specific binding was similar in longitudinal muscl...

Journal: :Circulation research 1993
I L Buxton D J Cheek D Eckman D P Westfall K M Sanders K D Keef

Analogues of L-arginine with modifications at the terminal guanidino nitrogen and/or the carboxyl terminus of the molecule have been widely used for their ability to inhibit the production of nitric oxide and are thought to be competitive antagonists of nitric oxide synthase. The present studies were designed to test the possibility that these agents are also muscarinic receptor antagonists. Ac...

Journal: :Journal of neurochemistry 1999
Y S Lee Y S Park D J Chang J M Hwang C K Min B K Kaang N J Cho

We have isolated a cDNA clone from the nematode Caenorhabditis elegans that encodes a protein of greatest sequence similarity to muscarinic acetylcholine receptors. This gene codes for a polypeptide of 682 amino acids containing seven putative transmembrane domains. The amino acid identities, excluding a highly variable middle portion of the third intracellular loop, to the human m1-m5 receptor...

Journal: :Bioorganic & medicinal chemistry letters 2005
Yin-Yao Niu Li-Min Yang Hui-Zhong Liu Yong-Yao Cui Liang Zhu Ju-Mei Feng Jian-Hua Yao Hong-Zhuan Chen Bo-Tao Fan Ze-Nai Chen Yang Lu

Baogongteng A (BGT-A), a naturally occurring tropane muscarinic agonist isolated from Chinese medicinal plant, exhibits a bioactive effect different from those of many tropane alkaloids that are muscarinic antagonists. A series of racemic derivatives of BGT-A was synthesized to study the structure-activity relationships (SAR). To explore further the SAR in this series and to ultimately design m...

2009
Anders T. Ryberg Ondrej Soukup Gunnar Tobin

In the in vivo experiments on anaesthetized sheep, it was presently examined whether muscarinic receptor antagonists with diverse selectivity affect the release of VIP in response to electrical stimulation of the parasympathetic chorda tympanic nerve differently, and if the changes in the release could be associated to altered secretory and vasodilator responses. The location of the muscarinic ...

Journal: :The Journal of pharmacology and experimental therapeutics 1997
G D'Agostino A Barbieri E Chiossa M Tonini

A pharmacological analysis was carried out in the rat urinary bladder to assess the nature of muscarinic receptors subtypes functionally involved in the negative feedback mechanism regulating acetylcholine (ACh) secretion from postganglionic cholinergic nerve terminals and in smooth muscle contraction. Bladder strips were preincubated with 3H-choline, and the electrically evoked [3H]ACh release...

Journal: :The Journal of pharmacology and experimental therapeutics 2009
Paola Casarosa Thierry Bouyssou Sabine Germeyer Andreas Schnapp Florian Gantner Michael Pieper

Chronic obstructive pulmonary disease (COPD) is characterized by progressive airflow limitation caused by persistent inflammatory processes in the airways. An increased cholinergic tone mediates different pathophysiological features of COPD, such as bronchoconstriction and mucus hypersecretion, mostly through activation of the human muscarinic M(3) receptor (hM(3)) subtype. Tiotropium bromide (...

Journal: :The Biochemical journal 1985
S R Hootman T M Picado-Leonard

Muscarinic acetylcholine receptors in isolated rat pancreatic acinar cells have an apparent Mr of 88 000, which could be decreased to 46 000 by papain, as deduced by covalent binding of the specific alkylating agent [3H]propylbenzilylcholine mustard. Muscarinic receptors on papain-treated acinar cells retained the antagonist-binding site and both high- and low-affinity binding sites for the cho...

2013

Hypothesis / aims of study It is clinically known that anticholinergic agents, commonly used for treating overactive bladder, etc., act on the muscarinic receptor in salivary glands, causing dry mouth as an adverse effect. Not only the muscarinic receptor but also the α1-adrenergic receptor are present in human salivary glands, and are thought to accelerate saliva production. The common adverse...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1991
S Sugita N Uchimura Z G Jiang R A North

Intracellular recordings were made from neurons of rat lateral amygdala, nucleus accumbens, and striatum in vitro. Synaptic potentials mediated by gamma-aminobutyric acid and by excitatory amino acids were isolated pharmacologically by using receptor antagonists, and their amplitudes were used as a measure of transmitter release. Muscarine and acetylcholine inhibited the release of both gamma-a...

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