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青稞多糖对糖尿病模型小鼠的降血糖作用及机制研究                                                            Δ


        王生亚 ,薛 洁 ,徐乃玉 ,张真庆 ,吕 栋 (1.南京医科大学附属无锡儿童医院药学部,江苏 无锡
                                                    3 #
               1*
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        214023;2.苏州大学医学部药学院,江苏 苏州 215123;3.南京医科大学附属无锡人民医院药学部,江苏 无锡
        214023)
        中图分类号 R285.5         文献标志码 A           文章编号 1001-0408(2021)07-0807-05
        DOI  10.6039/j.issn.1001-0408.2021.07.07

        摘  要   目的:研究青稞多糖(HVP)对糖尿病模型小鼠的降血糖作用及机制。方法:对小鼠腹腔注射链脲佐菌素(120 mg/kg)以
        复制糖尿病模型。将造模成功的小鼠随机分为模型组、二甲双胍组(阳性对照,200 mg/kg)和HVP高、中、低剂量组(300、150、75
        mg/kg),另设空白对照组,每组10只。各给药组灌胃相应药物,空白对照组和模型组小鼠灌胃等量水,每天1次,连续30 天。给药
        10、20、30 天时测定小鼠的空腹血糖(FBG);末次FBG测定后,小鼠腹腔注射10%葡萄糖溶液(2 g/kg),于注射后30、120 min时测
        定糖耐受量(GTT)曲线下面积;测定小鼠血清中胰岛素水平和肝组织中超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)、
        丙二醛(MDA)的含量;采用苏木精-伊红染色法观察小鼠胰腺组织病理学变化。结果:与空白对照组比较,模型组小鼠FBG、GTT
        曲线下面积和肝组织中 MDA 含量均显著升高或增加(P<0.01);血清中胰岛素水平和肝组织中 SOD、GSH-Px 含量均显著降低
       (P<0.01);胰腺组织损伤严重,形态不完整,有明显的空泡。与模型组比较,HVP高剂量组小鼠FBG、GTT曲线下面积和肝组织
        中MDA含量均显著降低或减少(P<0.05或P<0.01),血清中胰岛素含量和肝组织中SOD、GSH-Px含量均显著升高(P<0.05或
        P<0.01),HVP低、中剂量组上述指标部分改善,差异具有统计学意义(P<0.05或P<0.01);胰腺组织损伤有所减轻,形态较为完
        整,胰岛细胞排列紧密,空泡减少。结论:HVP可降低糖尿病模型小鼠的血糖水平,升高胰岛素水平并减轻胰腺组织损伤;该作用
        机制可能与其抗氧化作用有关。
        关键词 青稞多糖;糖尿病;抗氧化;小鼠

        Study on Hypoglycemic Effect of Hordeum vulgare Polysaccharide on Diabetes Mellitus Model Mice and
        Its Mechanism
        WANG Shengya ,XUE Jie ,XU Naiyu ,ZHANG Zhenqing ,LYU Dong(1. Dept. of Pharmacy,Wuxi Children’s
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        Hospital Affiliated to Nanjing Medical University,Jiangsu Wuxi 214023,China;2. College of Pharmaceutical
        Sciences, Health Science Center of Soochow University, Jiangsu Suzhou 215123, China; 3. Dept. of
        Pharmacy,Wuxi People’s Hospital Affiliated to Nanjing Medical University,Jiangsu Wuxi 214023,China)
        ABSTRACT    OBJECTIVE:To study the hypoglycemic effect of Hordeum vulgare polysaccharide(HVP)on diabetes mellitus
        model mice and its mechanism. METHODS:The mice were given intraperitoneal injection of streptozotocin(120 mg/kg)to induce
        diabetes mellitus model. After modeling,the mice were randomly divided into model group,metformin group(positive control,
        200 mg/kg),HVP high-dose,medium-dose and low-dose groups(300,150 and 75 mg/kg),with 10 mice in each group. Blank
        control group was established additionally. Administration groups were given relevant medicine intragastrically;blank control group
        and model group were given constant volume of water intragastrically,once a day,for consecutive 30 days. The levels of fasting
        blood glucose(FBG)were determined after 10,20,30 days of administration. After last FBG test,mice were intraperitoneally
        injected with 10% glucose solution(2 g/kg),then the area under the glucose tolerance(GTT)curve was measured at 30 and 120
        min after injection. The serum levels of insulin,the content of superoxide dismutase(SOD),glutathione peroxidase(GSH-Px),
        malondialdehyde(MDA)in liver tissue were detected. Pancreatic morphology of mice were detected by HE staining. RESULTS:
        Compared with blank control group,the FBG,area under GTT curve and MDA contnet in liver tissue were increased significantly
        in model group(P<0.01),while serum levels of insulin,SOD and GSH-Px contents in liver tissue were decreased significantly
       (P<0.01);the pancreatic tissue was seriously damaged with incomplete morphology and obvious vacuoles. Compared with model
                                                           group,FBG,area under GTT curve,MDA content in liver
           Δ 基金项目:国家自然科学基金资助项目(No.81473179)                tissue were decreased significantly in HVP high-dose group
           *主管药师。研究方向:临床药学。电话:0510-85351490。E-
                                                           (P<0.05 or P<0.01),serum content of insulin,the content
        mail:Wangshengya_helen@126.com
            # 通信作者:副主任药师。研究方向:医院药学。电话:0510-                of  SOD  and  GSH-Px  in  liver  tissue  were  increased
        85351490。E-mail:3103221944@qq.com                  significantly (P<0.05 or P<0.01);above indexes of HVP


        中国药房    2021年第32卷第7期                                               China Pharmacy 2021 Vol. 32 No. 7  ·807 ·
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