Malinowska B, Pietraszek M, Chabielska E, Pawlak D, Buczko W
Department of Pharmacodynamics, Medical Academy, Białystok, Poland.
Pol J Pharmacol Pharm. 1990 Jul-Aug;42(4):333-42.
In in vitro conditions ethanol dose-dependently contracts the isolated tail artery and aorta of the rat. In concentration 0.03 M ethanol did not change the perfusing pressure in isolated vessels, but potentiated the contracting action of serotonin. In concentration of 0.1 M ethanol did not change the sensitivity of blood vessels to serotonin, and in concentration of 0.3 M inhibited it. Statistically significant changes were observed only in tail artery. The tail artery isolated from the rat receiving a single dose of ethanol (2 g/kg) displayed decreased sensitivity to action of serotonin. Chronic administration of ethanol (6 g/kg/day for 14 days) did not change the serotonin-induced contraction of the isolated tail artery of the rat. The present data indicate that ethanol modifies the sensitivity of rat blood vessels to serotonin.
在体外条件下,乙醇能使大鼠离体尾动脉和主动脉呈剂量依赖性收缩。浓度为0.03M时,乙醇不会改变离体血管的灌注压力,但会增强血清素的收缩作用。浓度为0.1M时,乙醇不会改变血管对血清素的敏感性,而浓度为0.3M时则会抑制这种敏感性。仅在尾动脉中观察到具有统计学意义的变化。从接受单剂量乙醇(2g/kg)的大鼠分离出的尾动脉对血清素作用的敏感性降低。长期给予乙醇(6g/kg/天,持续14天)不会改变血清素诱导的大鼠离体尾动脉收缩。目前的数据表明,乙醇会改变大鼠血管对血清素的敏感性。