EFFECT OF PUTATIVE MELATONIN RECEPTOR ANTAGONISTS ON MELATONIN-INDUCED PIGMENT AGGREGATION IN ISOLATED XENOPUS-LAEVIS MELANOPHORES

被引:45
作者
SUGDEN, D
机构
[1] Physiology Group, Biomedical Sciences Division, King's College London, London, W8 7AH, Campden Hill Road
关键词
MELATONIN; MELATONIN RECEPTOR ANTAGONISTS; XENOPUS MELANOPHORES; PIGMENT AGGREGATION; LUZINDOLE;
D O I
10.1016/0014-2999(92)90629-I
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The ability of putative melatonin receptor antagonists to antagonise melatonin-induced aggregation of pigment granules in cultured neural crest Xenopus laevis melanophores was examined. Neither ML 23 (N-(2,4-dinitrophenyl)-5-methoxytryptamine) nor 6-methoxy-2-benzoxazolinone showed agonist or antagonist activity. N-Acetyltryptamine and N-butanoyltryptamine were partial agonists; both compounds aggregated pigment granules in some cells, but also reversed melatonin-induced pigment agregation in a fraction of the cells tested. In contrast, 2-benzyl N-acetyltryptamine (luzindole) did not show agonist activity (upto 10-mu-M) but did reverse the aggregating action of melatonin at 1 and 10-mu-M. Pretreatment of melanophores with luzindole shifted the melatonin concentration-response curve to the right.
引用
收藏
页码:405 / 408
页数:4
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