Kottegoda S R, Adaikan P G, Karim S M
Prostaglandins Leukot Med. 1982 Apr;8(4):343-8. doi: 10.1016/0262-1746(82)90057-9.
17 (S)methyl-omega-homo trans delta 2 PGE1 (ONO 1206) an analogue of PGE1 was studied on vasopressin-induced ECG changes in four male monkeys and three female baboons. Bolus intravenous doses of vasopressin (0.8 I.U. to 1.0 I.U./kg) produced flattening of the T wave (2 monkeys) elevation of ST segment (1 baboon and 1 monkey) and inversion of T wave (1 baboon). Inverted T waves were also present in one baboon and one monkey prior to any drug administration. In four out of seven animals, boLus intravenous doses (5 to 15 micrograms/kg) of ONO 1206 reversed the ECG changes produced by vasopressin and in one animal ONO 1206 reversed the existing inverted T wave. These findings indicate that vasopressin is a suitable agent for the induction of coronary vasoconstriction in primates and that ONO 1206 is able to reverse this effect.
研究了17(S)-甲基-ω-高反式δ2前列腺素E1(ONO 1206,一种前列腺素E1类似物)对4只雄性猴子和3只雌性狒狒血管加压素诱导的心电图变化的影响。静脉注射大剂量血管加压素(0.8国际单位至1.0国际单位/千克)导致T波平坦(2只猴子)、ST段抬高(1只狒狒和1只猴子)以及T波倒置(1只狒狒)。在任何药物给药前,1只狒狒和1只猴子也存在T波倒置。在7只动物中的4只,静脉注射大剂量(5至15微克/千克)的ONO 1206可逆转血管加压素引起的心电图变化,并且在1只动物中,ONO 1206逆转了现有的T波倒置。这些发现表明,血管加压素是诱导灵长类动物冠状动脉收缩的合适药物,并且ONO 1206能够逆转这种效应。