Sanger G J, Bennett A
J Pharm Pharmacol. 1980 Oct;32(10):705-8. doi: 10.1111/j.2042-7158.1980.tb13043.x.
The effects of prostaglandins (PGs) D2, E2, F2 alpha, an epoxymethano analogue of PGH2 (U-46619), prostacyclin (PGI2), 6-keto-PGF1 alpha and thromboxane (TX) B2 were tested on spirally-cut strips of guinea-pig isolated ileum or colon. In the ileum no prostanoid exerted a marked effect on the resting tissue, but PGD2, PGE2 or PGI2 1 ug ml-1 inhibited submaximal contraction to KC1. U-46619 1 ug ml-1 either inhibited or increased contractions in KC1, but PGF2 alpha, 6-keto-PGF1 alpha or TXB2 1 ug ml-1 had no significant effect. PGE2 relaxed colonic strips whereas the other prostanoids caused contraction, except for TXB2 which had no effect. The PG antagonist SC-19220 blocked colonic contractions to the prostanoids, and the residual inhibitory effect of PGD2, U-46619 or PGI2 was demonstrated by the reduction of submaximal contractions to acetylcholine. Our results suggest that prostanoid receptors mediating inhibitory responses of circular muscle predominate in the ileum, whereas in the colon both excitatory and inhibitory prostanoid receptors occur.
研究了前列腺素(PGs)D2、E2、F2α、PGH2的环氧甲叉类似物(U-46619)、前列环素(PGI2)、6-酮-PGF1α和血栓素(TX)B2对豚鼠离体回肠或结肠螺旋形切片的作用。在回肠中,没有前列腺素对静息组织产生显著影响,但1μg/ml的PGD2、PGE2或PGI2可抑制对氯化钾的次最大收缩。1μg/ml的U-46619可抑制或增强对氯化钾的收缩,但1μg/ml的PGF2α、6-酮-PGF1α或TXB2无显著影响。PGE2可使结肠切片松弛,而其他前列腺素则引起收缩,但TXB2无作用。PG拮抗剂SC-19220可阻断结肠对前列腺素的收缩,PGD2、U-46619或PGI2的残余抑制作用通过对乙酰胆碱次最大收缩的降低得以证明。我们的结果表明,介导回肠环行肌抑制反应的前列腺素受体占主导地位,而在结肠中,既有兴奋性前列腺素受体,也有抑制性前列腺素受体。