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In this study we made use of the Reverse transcription-polymerase chain reaction to analyze the expression of mRNA for the five subtypes of muscarinic acetylcholine receptors in human blood mononuclear cells. mRNA for m3, m4 and m5 subtypes was detected,
Costa, L. G. +3 more
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M3 and nonselective muscarinic receptor antagonists on gastrointes-tinal transit and bowel habits in humans. Am J Physiol Gastrointest Liver Physiol 299: G215–G219, 2010.
Karthik Ravi +2 more
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Muscarinic receptor subtypes in the alimentary tract
Acetylcholine is a transmitter in preganglionic autonomic and postganglionic parasympathetic nerves and a non-neuronal paracrine mediator in the alimentary tract. Acetylcholine is involved in the control of almost any function within these organ systems,
Tobin, Gunnar, +2 more
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Muscarinic acetylcholine receptor M3 (CHRM3; HM3) [PDF]
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Muscarinic acetylcholine receptor M3 (CHRM3; HM3) [PDF]
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Physiological Significance of Endothelial M3 Muscarinic Receptors During Exercise
Gareth L. Ackland +12 more
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Muscarinic M3 receptor coupling and regulation
Life Sciences, 1997Current concepts regarding the regulation and coupling of muscarinic m3 receptors to G-proteins and various effectors are discussed. The last few years have provided much evidence that although muscarinic m1, m3 and m5 subtypes couple predominantly via pertussis toxin-insensitive G-proteins (Gq/11) to activate phosphoinositidase C (PIC), interactions ...
S R, Nahorski, A B, Tobin, G B, Willars
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m3 Muscarinic Acetylcholine Receptor Regulation in the Airway
American Journal of Respiratory Cell and Molecular Biology, 2002The m3 muscarinic acetylcholine receptor (m3 mAChR) plays an important role in airway function by mediating the effects of acetylcholine on multiple airway cell types. m3 mAChRs expressed in airway smooth muscle (ASM) cells promote increased ASM tension, and, therefore, airway narrowing, in response to acetylcholine release from postganglionic ...
Charlotte K, Billington, Raymond B, Penn
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M1 and M3 muscarinic receptors
NeuroReport, 1992P-fluoro-hexahydro-sila-difenidol hydrochloride (p-F-HHSiD) (15, 30 micrograms) and pirenzepine (7.5, 15, 30 micrograms), which are highly selective M3 and M1 muscarinic antagonists, respectively, were injected intracerebroventricularly into freely moving rats.
L. IMERI +3 more
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Synthesis of antagonists of muscarinic (M3) receptors
Collection of Czechoslovak Chemical Communications, 2011Several α-hydroxyamides with (2,6-dialkoxyphenoxy)methyl substituents have been prepared and their activities as antagonists of the M3 muscarinic receptor in guinea pig ileum have been evaluated. N-{1-[(Phenyl)methyl]piperidin-4-yl}-2-{2-[(2,6-dimethoxyphenoxy)-methyl]phenyl}-2-hydroxypropanamide and N-(1-[{6-amino-4-[(1-propylpiperidin-4-yl)methyl ...
Broadley, Kenneth J. +5 more
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