Coupar I M, Hancock D L
Unit of Addictive Drug Research, School of Pharmaceutical Pharmacology, Victorian College of Pharmacy, Monash University, Parkville, Australia.
J Pharm Pharmacol. 1994 Oct;46(10):801-4. doi: 10.1111/j.2042-7158.1994.tb03733.x.
This study aimed to determine whether the antidiarrhoeal effect of the mixed A1/A2 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 PGE2 (4 micrograms min-1) or vasoactive intestinal peptide (0.8 micrograms min-1). NECA reversed PGE2-induced secretion in the jejunum (ED50 16 micrograms kg-1) and ileum (ED50 21 micrograms kg-1, i.v.) and inhibited VIP-induced secretion in the jejunum (ED50 21.5 micrograms kg-1). NECA inhibited twitch responses (0.1 Hz, 1 ms, IC50 11.2 nM) but not tetanic contractions at 10 Hz of the transmurally stimulated guinea-pig ileum. Likewise, NECA (10 microM) 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.
本研究旨在确定混合A1/A2腺苷激动剂NECA(5'-N-乙基羧酰胺腺苷)的止泻作用是由于抑制肠液转运还是由于收缩性。通过动脉内输注PGE2(4微克/分钟)或血管活性肠肽(0.8微克/分钟)刺激麻醉大鼠的肠分泌。NECA可逆转PGE2诱导的空肠(ED50 16微克/千克)和回肠(ED50 21微克/千克,静脉注射)分泌,并抑制血管活性肠肽诱导的空肠分泌(ED50 21.5微克/千克)。NECA抑制跨壁刺激的豚鼠回肠的抽搐反应(0.1赫兹,1毫秒,IC50 11.2纳摩尔),但不抑制10赫兹的强直收缩。同样,NECA(10微摩尔)在大鼠空肠或回肠2.5至40赫兹范围内不抑制频率相关的收缩。然而,NECA被证明是大鼠回肠蠕动反射的有效抑制剂(30纳摩尔)。结果表明,腺苷受体参与调节大鼠小肠的蠕动以及粘膜的分泌活性。