INHIBITORY-ACTION OF MCN-A-343 ON ACETYLCHOLINE-INDUCED CONTRACTION IN MOLLUSCAN SMOOTH-MUSCLE

被引:0
|
作者
KUSAMA, T [1 ]
KIZAWA, Y [1 ]
MURAKAMI, H [1 ]
机构
[1] NIHON UNIV, COLL PHARM, DEPT PHYSIOL & ANAT, FUNABASHI, CHIBA 274, JAPAN
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY | 1992年 / 102卷 / 03期
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中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
1. The effect of McN-A-343 (McN) on the contractile response to certain cholinergic agonists was investigated in the anterior byssus retractor muscle (ABRM) of Mytilus. 2. McN (3 x 10(-5) to 3 x 10(-4) M) dose-dependently inhibited the contractile response to acetylcholine (ACh), carbachol (CCh) and 1,1-dimethyl-4-phenyl-piperazinium (DMPP) in a noncompetitive manner. 3. McN (3 x 10(-5) to 3 x 10(-4)M) did not have any effect on the contractile response to KCl, caffeine or FMRF-NH2. 4. In the rectus abdominis muscle (RAM) of frog, McN produced a contractile response similar in potency to that produced by ACh, CCh and DMPP. 5. In the RAM, hexamethonium (C6) (3 x 10(-4)M) and d-tubocurarine (d-Tc) (3 x 10(-6)M) inhibited the contractile response to McN in a noncompetitive manner, and to CCh and DMPP in a competitive manner. 6. These findings indicate that McN, a selective M1 muscarinic agonist in mammalian tissues, acts as a nicotinic agonist in the PAM, and as a cholinergic antagonist in the ABRM.
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页码:489 / 493
页数:5
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