Literature DB >> 8822036

Selective muscarinic receptor agonists and antagonists.

R M Eglen1, N Watson.   

Abstract

Muscarinic receptors are composed of a family of four subtypes each of which can be distinguished pharmacologically and structurally. The physiological role of each subtype in the central and peripheral nervous systems remains to be clarified, due, in part, to a lack of agonists and antagonists with adequate subtype selectivity. Nonetheless, several agonists with functional selectivity for M1 receptors are now in advanced clinical evaluation for Alzheimer's disease, while selective M1/M3 antagonists may prove useful in the treatment of disorders of smooth muscle function. These novel compounds thus provide an advance over earlier therapeutics with which the clinical efficacy was compromised by the side effect profile. This review attempts to assess novel, selective agonists and antagonists, both in terms of their use in defining muscarinic receptor subtypes and their potential clinical utility.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8822036     DOI: 10.1111/j.1600-0773.1996.tb00181.x

Source DB:  PubMed          Journal:  Pharmacol Toxicol        ISSN: 0901-9928


  17 in total

1.  Absence of muscarinic cholinergic airway responses in mice deficient in the cyclic nucleotide phosphodiesterase PDE4D.

Authors:  G Hansen; S Jin; D T Umetsu; M Conti
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-06       Impact factor: 11.205

2.  Receptor binding studies of soft anticholinergic agents.

Authors:  F Huang; P Buchwald; C E Browne; H H Farag; W M Wu; F Ji; G Hochhaus; N Bodor
Journal:  AAPS PharmSci       Date:  2001

3.  Design, pharmacokinetic, and pharmacodynamic evaluation of a new class of soft anticholinergics.

Authors:  Fenglei Huang; Clinton E Browne; Whei-Mei Wu; Attila Juhász; Fubao Ji; Nicholas Bodor
Journal:  Pharm Res       Date:  2003-10       Impact factor: 4.200

Review 4.  Trospium chloride: a quaternary amine with unique pharmacologic properties.

Authors:  Raymond W Pak; Steven P Petrou; David R Staskin
Journal:  Curr Urol Rep       Date:  2003-12       Impact factor: 3.092

Review 5.  Functional M3 muscarinic acetylcholine receptors in mammalian hearts.

Authors:  Zhiguo Wang; Hong Shi; Huizhen Wang
Journal:  Br J Pharmacol       Date:  2004-05-17       Impact factor: 8.739

6.  Spontaneously hypertensive rats cholinergic hyper-responsiveness: central and peripheral pharmacological mechanisms.

Authors:  E Lazartigues; C Brefel-Courbon; M A Tran; J L Montastruc; O Rascol
Journal:  Br J Pharmacol       Date:  1999-08       Impact factor: 8.739

7.  Pharmacokinetic and pharmacodynamic evaluations of the zwitterionic metabolite of a new series of N-substituted soft anticholinergics.

Authors:  Whei-Mei Wu; Peter Buchwald; Nobuhiro Mori; Fubao Ji; JiaXiang Wu; Nicholas Bodor
Journal:  Pharm Res       Date:  2005-09-26       Impact factor: 4.200

8.  M3 subtype of muscarinic receptors mediate Ca2+ release from intracellular stores in rat prostate neuroendocrine cells.

Authors:  Jin Kyoung Kim; Soo Jung Kim; Ji Eun Lee; Kyeong Min Min; Sung Joon Kim
Journal:  J Korean Med Sci       Date:  2005-04       Impact factor: 2.153

9.  Cholinergic responses of ophthalmic arteries in M3 and M5 muscarinic acetylcholine receptor knockout mice.

Authors:  Adrian Gericke; Veronique G A Mayer; Andreas Steege; Andreas Patzak; Ulrike Neumann; Franz H Grus; Stephanie C Joachim; Lars Choritz; Jürgen Wess; Norbert Pfeiffer
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-04-30       Impact factor: 4.799

10.  Divergence of allosteric effects of rapacuronium on binding and function of muscarinic receptors.

Authors:  Jan Jakubík; Alena Randáková; Esam E El-Fakahany; Vladimír Dolezal
Journal:  BMC Pharmacol       Date:  2009-12-28
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.