Chiba S, Malik K U
J Pharmacol Exp Ther. 1980 May;213(2):261-6.
The cardiovascular effects of prostaglandin (PG) I2 and E2 were investigated in the anesthetized dog and in the isolated blood perfused canine atrial preparation cross-circulated by the donor dog. When small doses of PGI2 (less than .01 microgram/kg) or PGE2 (1 microgram/kg) were injected into the jugular vein of the donor dog, there was a slight fall in blood pressure (5-10 mm Hg) and a slight degree of tachycardia (2-6 beats/min). However, larger doses of PGI2 (1-10 microgram/kg) or PGE2 (3-10 microgram/kg) produced hypotension that was associated with marked bradycardia. The bradycardia produced by both PGE2 and PGI2 in the donor dog was blocked by either atropine pretreatment or vagotomy and was inverted to tachycardia. The tachycardia was significantly suppressed by propranolol. Administration of PGI2 either to the donor dog or directly into the sinus node arterial cannula did not alter the atrial rate or developed tension in the isolated blood perfused atrial preparation. In contrast, when PGE2 was given in larger doses (10 microgram/kg) to the donor dog, the sinus rate and developed tension in the isolated atria were increased. This effect was markedly diminished after propranolol treatment. Administration of PGE2 (1-30 microgram) close-arterially into the sinus node artery produced positive chronotropic and inotropic effect which was not statistically significant. We conclude that PGI2 and PGE2 produce a negative chronotropic effect which is due to increased vagal activity and that these agents have no direct cardiac stimulatory effects in the anesthetized dog.
在麻醉犬以及由供血犬交叉循环的离体血液灌注犬心房制备物中研究了前列腺素(PG)I2和E2的心血管效应。当向供血犬的颈静脉注射小剂量的PGI2(小于0.01微克/千克)或PGE2(1微克/千克)时,血压略有下降(5 - 10毫米汞柱),心率略有加快(2 - 6次/分钟)。然而,较大剂量的PGI2(1 - 10微克/千克)或PGE2(3 - 10微克/千克)会导致低血压,并伴有明显的心动过缓。PGE2和PGI2在供血犬中引起的心动过缓可被阿托品预处理或迷走神经切断术阻断,并转变为心动过速。心动过速被普萘洛尔显著抑制。向供血犬或直接向窦房结动脉插管给予PGI2,并不会改变离体血液灌注心房制备物中的心房率或张力发展。相反,当向供血犬给予较大剂量(10微克/千克)的PGE2时,离体心房中的窦性心率和张力发展增加。普萘洛尔治疗后,这种效应明显减弱。向窦房结动脉近动脉处给予PGE2(1 - 30微克)产生正性变时和变力作用,但无统计学意义。我们得出结论,PGI2和PGE2产生负性变时作用是由于迷走神经活动增加,并且这些药物在麻醉犬中没有直接的心脏刺激作用。