%0 Journal Article %A Carl W White %A Jennifer L Short %A John M Haynes %A Minoru Matsui %A Sabatino Ventura %T Title: Contractions of the mouse prostate elicited by acetylcholine are mediated by M3 muscarinic receptors %D 2011 %R 10.1124/jpet.111.186841 %J Journal of Pharmacology and Experimental Therapeutics %P jpet.111.186841 %X Increased smooth muscle tone in the human prostate contributes to the symptoms associated with benign prostatic hyperplasia. In the mouse prostate gland, cholinergic innervation is responsible for a component of the nerve mediated contractile response. This study investigates the muscarinic receptor subtype responsible for the cholinergic contractile response in the mouse prostate gland. To characterise the muscarinic receptor subtype, mouse prostates taken from wild-type or M3 muscarinic receptor knockout mice were mounted in organ baths. The isometric force that tissues developed in response to, electrical field stimulation or exogenously applied cholinergic agonists in the presence or absence of a range of muscarinic receptor antagonists, was evaluated. Carbachol elicited reproducible and concentration dependent contractions of the isolated mouse prostate, which were antagonised by the presence of muscarinic receptor antagonists. Calculation of antagonist affinities (pA2-values) indicated a rank order of antagonist potencies in the mouse prostate of: darifenacin (9.08) = atropine (9.07) = 4-DAMP (9.02) > HHSiD (7.85) > p-F-HHSiD (7.39) > himbacine (7.19) > pirenzipine (6.88) > methoctramine (6.20). Furthermore, genetic deletion of the M3 muscarinic receptor inhibited prostatic contractions to electrical field stimulation or exogenous administration of acetylcholine. In this study we identified that the cholinergic component of contraction in the mouse prostate is mediated by the M3 muscarinic receptor subtype. Pharmacological antagonism of the M3 muscarinic receptor may be a beneficial additional target for the treatment of benign prostatic hyperplasia in the human prostate gland. %U https://jpet.aspetjournals.org/content/jpet/early/2011/09/01/jpet.111.186841.full.pdf