THE ADENOSINE AGONIST NECA INHIBITS INTESTINAL SECRETION AND PERISTALSIS

被引:14
作者
COUPAR, IM
HANCOCK, DL
机构
[1] Unit of Addictive Drug Research, School of Pharmaceutical Pharmacology, Victorian College of Pharmacy, Monash University, Parkville, Victoria, 3052
关键词
D O I
10.1111/j.2042-7158.1994.tb03733.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study aimed to determine whether the antidiarrhoeal effect of the mixed A(1)/A(2) adenosine agonist NECA (5'-N-ethylcarboxamido adenosine) is due to inhibition of intestinal fluid transport or to contractility. Intestinal secretion was stimulated in anaesthetized rats by intra-arterial infusions of PGE(2) (4 mu g min(-1)) or vasoactive intestinal peptide (0.8 mu g min(-1)). NECA reversed PGE(2)-induced secretion in the jejunum (ED50 16 mu g kg(-1)) and ileum (ED50 21 mu g kg(-1), i.v.) and inhibited VIP-induced secretion in the jejunum (ED50 21.5 mu g kg(-1)). NECA inhibited twitch responses (0.1 Hz, 1 ms, IC50 11.2nM) but not tetanic contractions at 10 Hz of the transmurally stimulated guinea-pig ileum. Likewise, NECA (10 mu M) did not inhibit frequency-related contractions over the range of 2.5 to 40 Hz of rat jejunum or ileum. However, NECA was shown to be a potent inhibitor (30 nM) of the peristaltic reflex in the rat ileum. The results indicate that adenosine receptors are involved in modulating peristalsis as well as the secretory activity of the mucosa in the rat small intestine.
引用
收藏
页码:801 / 804
页数:4
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