PT  - JOURNAL ARTICLE
AU  - Sawyer, Gregory W.
AU  - Ehlert, Frederick J.
TI  - Contractile Roles of the M<sub>2</sub> and M<sub>3</sub>Muscarinic Receptors in the Guinea Pig Colon
DP  - 1998 Jan 01
TA  - Journal of Pharmacology and Experimental Therapeutics
PG  - 269--277
VI  - 284
IP  - 1
4099  - http://jpet.aspetjournals.org/content/284/1/269.short
4100  - http://jpet.aspetjournals.org/content/284/1/269.full
SO  - J Pharmacol Exp Ther1998 Jan 01; 284
AB  - The contractile roles of the M2 and M3muscarinic receptors were investigated in guinea pig longitudinal colonic smooth muscle. Prior treatment of the colon with N-(2-chloroethyl)-4-piperidinyl diphenylacetate (4-DAMP mustard) (40 nM) in combination with [[2-[(diethylamino)methyl]-1-piperidinyl]acetyl]-5,11-dihydro-6H-pyrido[2,3b][1,4]benzodiazepine-6-one (AF-DX 116) (1.0 μM) caused a subsequent, irreversible inhibition of oxotremorine-M-induced contractions when measured after extensive washing. The estimate of the degree of receptor inactivation after 2 hr (97%) was not much greater than that measured after 1 hr (95%), which suggests that both 4-DAMP mustard-sensitive and -insensitive muscarinic subtypes contribute to the contractile response. Pertussis toxin treatment had no significant inhibitory effect on the control contractile response to oxotremorine-M, but caused an 8.8-fold increase in the EC50 value measured after a 2-hr treatment with 4-DAMP mustard. These results suggest that, after elimination of most of the M3 receptors with 4-DAMP mustard, the contractile response can be mediated by the pertussis toxin-sensitive M2 receptor. After pertussis toxin treatment, the kinetics of alkylation of muscarinic receptors in the colon were consistent with a single, 4-DAMP mustard-sensitive, M3 receptor subtype mediating the contractile response. When measured after a 2-hr treatment with 4-DAMP mustard and in the presence of histamine (0.30 μM) and either forskolin (10 μM) or isoproterenol (0.60 μM), the contractile responses to oxotremorine-M were pertussis toxin-sensitive and potently antagonized by the M2 selective antagonist, AF-DX 116. Collectively, our results indicate that the M2 receptor elicits contraction through two mechanisms, a direct contraction and an indirect contraction by preventing the relaxant effects of cAMP-generating agents. The American Society for Pharmacology and Experimental Therapeutics