Researches on the influence of some pharmacological interferences of the metabolism of icosanoids on the glycemia in rats.

Physiologie (Bucarest) Pub Date : 1989-07-01
M Nechifor, A Busuioc, F Cocu, M Costuleanu, B Naghebaner
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Abstract

We studied the influence of cloprostenol (CIPG) 200 micrograms/Kg i.p. (a synthetic analogue of PGF2-alpha) and of imidazol 70 mg/Kg i.p. (a selective inhibitor of thromboxane synthetase) on fasting glycemia and on hypoglycemia induced by Actrapid insulin 0.5 UI/Kg i.p. to rats (male adults). The determinations of glycemia were made 60 minutes and 3 hours after the administration of the substances. The tests were made in groups of 20 animals which were not fed 14 hours before the experiment, but were not deprived of water. The results were interpreted statistically by means of the "t" test. The data obtained show that CIPG 200 micrograms/Kg i.p. is a significant hyperglycemic icosanoid (statistically p less than 0.01) both in the case of fasting glycemia and in the case of insulin hypoglycemia. The hyperglycemic effect was stronger at 60 min. Imidazol does not modify significantly either glycemia or insulin hypoglycemia, which pleads for a more reduced implication of thromboxanes in the regulation of glycemia in comparison to the prostaglandins.

二十烷酸代谢的一些药理干扰物对大鼠血糖影响的研究。
我们研究了氯前列腺醇(CIPG) 200微克/千克(pgf2 - α的合成类似物)和咪唑70毫克/千克(血栓素合成酶选择性抑制剂)对大鼠(雄性成年)空腹血糖和0.5 UI/千克胰岛素诱导的低血糖的影响。分别于给药后60分钟和3小时测定血糖。实验以20只动物为一组,在实验前14小时不喂食,但不剥夺水。结果用“t”检验进行统计学解释。结果表明,无论在空腹血糖还是胰岛素低血糖情况下,CIPG 200微克/Kg i.p.都是显著的高血糖类二十碳酸盐(p < 0.01)。高血糖作用在60分钟时更强。咪唑对血糖或胰岛素低血糖都没有明显的改变,这表明与前列腺素相比,血栓素对血糖的调节作用更低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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