山东大学学报(医学版) ›› 2017, Vol. 55 ›› Issue (2): 61-67.doi: 10.6040/j.issn.1671-7554.0.2016.995
张钰,韩琛,王朝霞,王兆朋,张月英,周淑萍,马冉冉,王恒孝
ZHANG Yu, HAN Chen, WANG Zhaoxia, WANG Zhaopeng, ZHANG Yueying, ZHOU Shuping, MA Ranran, WANG Hengxiao
摘要: 目的 观察柽柳乙醇提取物对小鼠酒精性肝损伤的保护作用,并对其分子机制进行初步探讨。 方法 采用慢性乙醇喂养加急性乙醇灌胃法诱导小鼠酒精性肝损伤。将80只雄性C57BL/6J小鼠随机分为5组:正常对照组、模型组、阳性对照组、柽柳低剂量组和柽柳高剂量组,每组16只。比较各组小鼠体质量、肝质量和肝指数之间的差别;通过HE染色和油红O染色观察肝组织的脂肪蓄积和损伤情况;检测外周血谷丙转氨酶(ALT)和甘油三酯(TG)以及肝脏中谷草转氨酶(AST)、超氧化物歧化酶(SOD)和丙二醛(MDA)水平;免疫组化法检测核苷酸结合寡聚化结构域样受体家族pyrin结构域蛋白3(NLRP3)炎性小体组成成份[NLRP3、凋亡相关微粒蛋白(ASC)、半胱氨酸蛋白酶-1(caspase-1)]和相关炎性因子IL-1β的蛋白表达水平。 结果 与模型组相比,柽柳高、低剂量组小鼠肝脏指数显著降低(P<0.05),肝脏脂肪蓄积和炎症情况明显减轻,血清中ALT和肝脏中AST水平显著降低(P<0.01);柽柳高剂量组肝脏MDA含量显著降低(P<0.05),SOD活性显著升高(P<0.05),肝脏中NLRP3、ASC、caspase-1和IL-1β的表达均显著减少(P<0.05)。 结论 柽柳可以在一定程度上抑制小鼠酒精性肝损伤的发生发展,其机制可能与抑制NLRP3-caspase-1-IL-1β通路活化有关。
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