Losonczy G, Mucha I, DiPirro J, Sweeney J, Brown G, Brentjens J, Venuto R
Department of Medicine, School of Medicine and Biomedical Sciences, State University of New York at Buffalo 14215.
Am J Physiol. 1993 Oct;265(4 Pt 2):R772-80. doi: 10.1152/ajpregu.1993.265.4.R772.
We compared the hemodynamic actions of U-46619, a stable thromboxane A2 (TxA2) prostaglandin H2 (PGH2) analogue, in nonpregnant (NP) rabbits with those observed in late pregnant (P) rabbits. An intravenous injection of U-46619 (10 micrograms) to each of eight NP chronically instrumented rabbits (mean body weight 3.4 kg) induced an immediate (1 min) and reversible fall of cardiac output (CO, 66%) and mean arterial pressure (MAP, 41%, both P < 0.01). P rabbits (n = 6, mean body weight 3.8 kg), however, responded with an elevation of MAP (5%, P < 0.02) upon intravenous injection of the drug (10 micrograms), while CO remained unchanged. The fall of CO in NP rabbits was associated with the temporary disappearance of a fraction of circulating platelets between the superior vena cava and the aortic arch. The number of platelets at 30 and 60 s after U-46619 was reduced (P < 0.05) by 14 and 20% respectively in the aortic blood, whereas caval platelet counts were unchanged until 90 s (-6%, P < 0.05). In contrast, intraaortic administration of this drug (10 micrograms) to NP rabbits resulted in neither thrombocytopenia nor hypotension. U-46619 (10-30 micrograms i.v.) caused no decrease in platelet count in the aorta of P rabbits. In vitro, U-46619-induced aggregation of platelets harvested from P rabbits was also blunted (P < 0.001). This could not be attributed to reduced affinity or number of platelet thromboxane receptors. The data indicate that U-46619 induces a fall of arterial pressure simultaneous with intravascular platelet aggregation.(ABSTRACT TRUNCATED AT 250 WORDS)
我们比较了稳定的血栓素A2(TxA2)前列腺素H2(PGH2)类似物U - 46619在未孕(NP)兔和晚孕(P)兔中的血流动力学作用。给8只慢性植入仪器的NP兔(平均体重3.4千克)每只静脉注射U - 46619(10微克),导致心输出量(CO)立即(1分钟)且可逆性下降(66%),平均动脉压(MAP)下降(41%,两者P < 0.01)。然而,P兔(n = 6,平均体重3.8千克)静脉注射该药物(10微克)后,MAP升高(5%,P < 0.02),而CO保持不变。NP兔中CO的下降与上腔静脉和主动脉弓之间循环血小板的一部分暂时消失有关。U - 46619注射后30秒和60秒时,主动脉血中的血小板数量分别减少(P < 0.05)14%和20%,而腔静脉血小板计数直到90秒时才下降(-6%,P < 0.05)。相反,给NP兔主动脉内注射该药物(10微克)既未导致血小板减少,也未引起低血压。U - 46619(静脉注射10 - 30微克)未导致P兔主动脉内血小板计数下降。在体外,U - 46619诱导的从P兔采集的血小板聚集也受到抑制(P < 0.001)。这不能归因于血小板血栓素受体亲和力降低或数量减少。数据表明,U - 46619在诱导动脉压下降的同时会引起血管内血小板聚集。(摘要截短至250字)