白藜芦醇延长脂多糖攻击小鼠存活时间并提高微血管反应性

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目的:观察白藜芦醇(Res)对脂多糖(LPS)攻击小鼠血管反应性的作用。方法:腹腔注射LPS(35 mg/kg)1 h后,肌肉注射白藜芦醇(30 mg/kg)或等体积的溶媒实施干预,记录存活时间;通过生物信号采集系统记录LPS攻击后6 h和12 h的平均动脉血压,同时经右侧颈静脉注射去甲肾上腺素(4.2μg/kg),以注射前后平均动脉血压的差值评价小鼠的整体升压反应;在LPS攻击后6 h留取肠系膜二级微动脉血管,制备离体微血管环,应用离体血管张力系统观察微血管对梯度去甲肾上腺素收缩反应性的变化。结果:白藜芦醇显著延长了LPS攻击小鼠的存活时间;LPS攻击引起了小鼠6 h和12 h的平均动脉血压降低、升压反应增加,但白藜芦醇对LPS攻击小鼠的平均动脉血压及其差值没有明显的作用;LPS攻击显著降低了小鼠离体微血管对去甲肾上腺素的反应性,白藜芦醇引起了血管反应曲线左移,在一定程度上提高了血管反应性。结论:白藜芦醇对腹腔注射LPS小鼠具有一定的保护作用,表现在延长存活时间、提高微血管的反应性。 Objective: To observe the effect of resveratrol on the vascular reactivity of mice induced by lipopolysaccharide (LPS). Methods: After intraperitoneal injection of LPS (35 mg / kg) for 1 h, intramuscular injection of resveratrol (30 mg / kg) or equal volume of vehicle was used for intervention and the survival time was recorded. The biological signal acquisition system was used to record the effect of LPS And mean arterial blood pressure of 12 h, norepinephrine (4.2 μg / kg) was injected through the right jugular vein at the same time, and the difference of mean arterial blood pressure before and after injection was evaluated in the whole blood pressure response of mice. After 6 h The secondary mesenteric artery of the mesentery was collected and the isolated microvascular rings were prepared. The changes of gradient norepinephrine contractility were observed by using the ex vivo vascular tone system. Results: Resveratrol significantly prolonged the survival time of mice challenged with LPS; LPS challenge caused a decrease in mean arterial blood pressure at 6 and 12 h, and an increase in blood pressure response. However, resveratrol had no effect on LPS-challenged mice Mean arterial blood pressure and its difference had no significant effect; LPS challenge significantly reduced the reactivity of isolated mouse microvascular to norepinephrine, resveratrol caused a left shift of the vascular response curve, to a certain extent, increased blood vessels Reactivity. CONCLUSION: Resveratrol has a protective effect on intraperitoneal injection of LPS in mice, which shows that it prolongs survival time and improves microvascular reactivity.
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