Carmignani M, Marchetti P, Caprino L
Artery. 1980;8(1):90-5.
The atherosclerotic condition is associated with a reduction of PGI2 synthesis; moreover, in the presence of elevated serum cholesterol levels, pressor responses to norepinephrine are potentiated. In order to verify if a complete inhibition of PGI2 production affects the vascular reactivity, it was assayed two cycloxygenase inhibitors (lysine acetylsalicylate and indomethacin) in rats. The two drugs significantly potentiated the blood pressure responses to norepinephrine, and completely inhibited PGI2-like substances production by arterial rings. The prostacyclin infusion (15 ng/kg/min, i.v.) completely reversed such potentiation, without any major modification in the basal blood pressure values. These results show that PGI2 production is responsible for vascular tone modulation and may partially explain the altered vascular reactivity in the atherosclerotic condition.
动脉粥样硬化状态与前列环素(PGI2)合成减少有关;此外,在血清胆固醇水平升高的情况下,对去甲肾上腺素的升压反应会增强。为了验证完全抑制PGI2生成是否会影响血管反应性,在大鼠中对两种环氧化酶抑制剂(赖氨酸乙酰水杨酸酯和吲哚美辛)进行了测定。这两种药物显著增强了对去甲肾上腺素的血压反应,并完全抑制了动脉环产生的PGI2样物质。前列环素输注(15 ng/kg/min,静脉注射)完全逆转了这种增强作用,而基础血压值没有任何重大改变。这些结果表明,PGI2的产生负责血管张力调节,并且可能部分解释动脉粥样硬化状态下血管反应性的改变。