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老鼠簕生物碱A对大鼠非酒精性脂肪肝的改善作用及其机制研

        究  Δ


        徐万鹏 ,梁英琴,韦秀桂,王红园,张 华,周焕芳,林 兴,林 军(广西医科大学药学院,南宁 530021)
                                                                   #
              *
        中图分类号      R965    文献标志码 A           文章编号 1001-0408(2020)16-1955-06
        DOI  10.6039/j.issn.1001-0408.2020.16.07

        摘  要   目的:研究老鼠簕生物碱A(HBOA)对大鼠非酒精性脂肪肝的改善作用及其机制。方法:将SD大鼠随机分为空白对照
        组、模型组、水飞蓟宾胶囊组(阳性对照,26.25 mg/kg)和HBOA高、中、低剂量组(100、50、25 mg/kg),每组10只。除空白对照组喂
        养普通饲料外,其余各组大鼠连续喂养高脂饲料8周以复制非酒精性脂肪肝模型。于第9周起,空白对照组和模型组大鼠灌胃等
        体积0.6%羟甲基纤维素钠溶液,各给药组大鼠灌胃相应药物,每日1次,连续4周。观察各组大鼠一般情况并计算其体质量增量、
        脏器(肝、肾、脾)指数;检测肝组织中天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)、总胆固醇(TC)、三酰甘油(TG)、游离脂肪酸
       (NEFA)含量,以及血清中超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)活性和丙二醛(MDA)含量;采用免疫组织化学
        法检测肝组织中过氧化物酶体增殖物激活受体α(PPARα)蛋白的表达情况。结果:与空白对照组比较,模型组大鼠体质量增量和
        肝指数均显著升高(P<0.01);肝内可见脂肪沉积现象,血清中 SOD、GSH-Px 活性均显著降低,MDA 含量以及肝组织中 AST、
        ALT、TC、TG、NEFA含量均显著升高,PPARα蛋白表达水平显著降低(P<0.01)。与模型组比较,各给药组大鼠体质量增加量和肝
        指数均显著降低(P<0.05 或 P<0.01),肝内脂肪沉积现象改善,血清中 SOD、GSH-Px 活性(除 HBOA 低剂量组外)均显著升高,
        MDA含量以及肝组织中AST、ALT、TC(除HBOA低剂量组外)、TG(除HBOA低剂量组外)、NEFA含量均显著降低,PPARα蛋白
        表达水平(除 HBOA 低剂量组外)均显著升高(P<0.05 或 P<0.01),且高剂量组上述部分指标显著优于中、低剂量组(P<0.05)。
        结论:老鼠簕生物碱A对高脂饮食致大鼠非酒精性脂肪肝有一定的改善作用,其机制可能与改善脂质代谢紊乱、抗氧化应激及上
        调PPARα表达有关。
        关键词 老鼠簕生物碱A;大鼠;非酒精性脂肪肝;氧化应激;脂代谢紊乱

        Study on the Improvement Effect and Mechanism of Ilicifoliosids Alkaloid A on Non-alcoholic Fatty Liver
        Disease in Rats
        XU Wanpeng,LIANG Yingqin,WEI Xiugui,WANG Hongyuan,ZHANG Hua,ZHOU Huanfang,LIN Xing,LIN
        Jun(College of Pharmacy,Guangxi Medical University,Nanning 530021,China)

        ABSTRACT    OBJECTIVE:To study improvement effect and mechanism of ilicifoliosids alkaloid A(HBOA)on non-alcoholic
        fatty liver disease in rats. METHODS:SD rats were randomly divided into blank control group,model group,Silybin capsule
        group(positive control,26.25 mg/kg),HBOA high-dose,medium-dose and low-dose groups(100,50,25 mg/kg),with 10 rats
        in each group. Except that blank control group fed normal feed,the other groups were continuously fed with high-fat diet for 8
        weeks to induce non-alcoholic fatty liver disease model. Form the 9th week,blank control group and model group were given
        constant volume of 0.6% CMC-Na solution,and administration groups were given corresponding drugs by intragastric admini-
        stration,once a day,for consecutive 4 weeks. The general information of rats were observed and the body weight increase,organ
       (liver,kidney and spleen)indexes were calculated;the contents of AST,ALT,TC,TG and NEFA in liver tissue were detected,
        and SOD,GSH-Px activities and MDA content in the serum were also determined. The protein expression of PPARα in liver tissue
        was detected by immunohistochemistry. RESULTS:Compared with blank control group,the body mass increase and liver index of
        rats in model group were increased significantly(P<0.01);fat deposition could be observed in the liver;the activities of SOD and
        GSH-Px in serum were reduced significantly,and the contents of MDA,the contents of AST,ALT,TC,TG and NEFA in liver
        tissue were significantly increased,and the protein expression of PPARα was decreased significantly(P<0.01). Compared with
        model group,the body mass increase and liver index of the rats were decreased significantly in administration groups(P<0.05 or
        P<0.01),liver fat deposition was improved,the activity of SOD and GSH-Px in serum(except for HBOA low-dose group)were
        increased significantly while MDA content,the contents of AST,ALT,TC(except for HBOA low-dose group),TG(except for
                                                           HBOA low-dose group) and NEFA in liver tissue were
           Δ 基金项目:国家自然科学基金资助项目(No.81660106)
                                                           decreased significantly,while protein expression of PPAR α
           * 药 师 ,硕 士 研 究 生 。 研 究 方 向 :中 药 药 理 学 。 E-mail:
        15177460685@163.com                                was increased significantly (P<0.05 or P<0.01). Some of
           # 通信作者:教授,硕士生导师,博士。研究方向:中药药理学。                  the  above  indexes  of  HBOA  high-dose  group  were
        电话:0771-5302433。E-mail:junlin898@126.com           significantly better than HBOA medium- and low-dose group


        中国药房    2020年第31卷第16期                                            China Pharmacy 2020 Vol. 31 No. 16  ·1955 ·
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