蒙药沏其日甘八味片对高脂血症模型金黄地鼠肠道菌群的影响OA
Effects of Mongolian medicine Qiqirigan-8 Tablets on the gut microbiota in a golden hamster model of hyperlipidemia
目的 基于肠道菌群探讨蒙药沏其日甘八味片对高脂血症模型金黄地鼠的调节作用,并比较其与传统丸剂及缺黑冰片方、缺大黄方的药效差异.方法 将60 只健康的雄性金黄地鼠随机分为空白对照组、模型组、缺黑冰片阴性对照组、缺大黄阴性对照组、沏其日甘八味片组和沏其日甘八味丸组共六组,每组10 只.空白对照组给予普通饲料喂养,其余各组给予高脂饲料喂养6 周建立高脂血症模型.造模成功后,各给药组分别给予相应药物灌胃:缺黑冰片阴性对照组、缺大黄阴性对照组及沏其日甘八味片组给药剂量为 36.68 mg/kg,沏其日甘八味丸组给药剂量为104.95 mg/kg,空白对照组与模型组给予等体积0.5%羧甲基纤维素钠溶液,每日 1 次,连续 12 周.末次给药后禁食12 小时,取血检测血清总胆固醇(total cholesterol,TC)、甘油三酯(triglyceride,TG)、低密度脂蛋白胆固醇(low-density lipoprotein cholesterol,LDL-C)、高密度脂蛋白胆固醇(high-density lipoprotein cholesterol,HDL-C)、谷草转氨酶(aspartate aminotransferase,AST)、谷丙转氨酶(alanine aminotransferase,ALT)水平,计算肝脏指数;采集盲肠内容物用于16S rRNA 基因高通量测序,分析肠道菌群多样性、物种组成、物种差异及功能.结果 与空白对照组比较,模型组血清 TC、TG、LDL-C水平及肝脏指数均显著升高(P<0.01),血清 AST、ALT 活性亦显著升高(P<0.01),肠道菌群 Chao1、Shannon、Simpson 指数显著降低(P<0.01),厚壁菌门/拟杆菌门比值升高,总 ASV 数目(2402)及特有 ASV 数目(988)显著减少.与模型组比较,沏其日甘八味片组血清 TC、TG、LDL-C 水平、肝脏指数显著降低(P<0.01),AST、ALT 活性显著改善(P<0.01);肠道菌群 Chao1、Shannon、Simpson 指数显著回升(P<0.01),厚壁菌门/拟杆菌门比值显著降低(P<0.05),总 ASV 数目(2933)接近空白对照组(2964),菌群结构向空白对照组方向趋近;PICRUSt2 功能预测显示,脂质代谢、碳水化合物代谢等紊乱通路显著回调.沏其日甘八味片组在上述指标的改善效果均优于沏其日甘八味丸组及两个阴性对照组.结论 蒙药沏其日甘八味片对由高脂饲料诱发的高脂血症金黄地鼠的肠道菌群起到正向调节作用,同时具有调脂保肝功效,剂型改良后效果更优.
Objective To investigate the regulatory effects of Mongolian medicine Qiqirigan-8 Tablets on intestinal microbiota in hyperlipidemic golden hamsters and to compare its efficacy with that of the traditional pill formulation and formula-deficient preparations.Methods Sixty healthy male golden hamsters were randomly divided into six groups(n=10 per group):the control group,the model group,the Black Borneol-deficient negative control group,Rhei Radix et Rhizoma-deficient negative control group,Qiqirigan-8 Tablets group,and the Qiqirigan-8 Pills group.The golclen hamsters in the control group received a normal diet,while the other groups were fed a high-fat diet for 6 weeks to establish a hyperlipidemic model.After successful modeling,the treatment groups were administered corresponding drugs by gavage:The Black Borneol-deficient negative control group,the Rhei Radix et Rhizoma-deficient negative control group,and the Qiqirigan-8 Tablets group at 36.68 mg/kg,the Qiqirigan-8 Pills group at 104.95 mg/kg,and the control and model groups received equal volumes of 0.5%sodium carboxymethyl-cellulose solution,once daily for 12 weeks.After the last administration,animals were fasted for 12 hours,and blood samples were collected to measure serum total cholesterol(TC),triglyceride(TG),low-density lipoprotein cholesterol(LDL-C),high-density lipoprotein cholesterol(HDL-C),aspartate aminotransferase(AST),and alanine aminotransferase(ALT)levels.Liver index was calculated.Cecal contents were collected for 16S rRNA gene high-throughput sequencing to analyze gut microbiota diversity,species composition,differential taxa and microbial function.Results Compared with the control group,the model group showed significantly elevated serum TC,TG,LDL-C,liver index,and AST and ALT activities(P<0.01).Intestinal microbiota Chao1,Shannon,and Simpson indices were significantly decreased(P<0.01),the Firmicutes/Bacteroidetes ratio was increased,and the total number of ASVs(2402)and unique ASVs(988)were markedly reduced.Compared with the model group,the Qiqirigan-8 Tablets group exhibited significantly decreased serum TC,TG,LDL-C(P<0.01),reduced liver index(P<0.01),and alleviated the abnormal increase of serum AST and ALT(P<0.01).Intestinal microbiota Chao1,Shannon,and Simpson indices were significantly restored(P<0.01),the Firmicutes/Bacteroidetes ratio was significantly decreased(P<0.05),total ASV number(2933)approached that of the control group(2964),and the microbial community structure recovered to the level of the control group.PICRUSt2 functional prediction indicated that disturbed pathways such as lipid metabolism and carbohydrate metabolism were notably reversed.The Qiqirigan-8 Tablets group showed superior improvements in all the above indices compared with the Qiqirigan-8 Pills group and the two negative control groups.Conclusion Qiqirigan-8 Tablets positively regulate intestinal microbiota in hyperlipidemic golden hamsters induced by a high-fat diet,concurrently exerting lipid-lowering and hepatoprotective effects,with the modified tablet for-mulation demonstrating superior efficacy.
包海萍;刘卫东;哈申图雅;金澈乐格尔;巴国政;乌云斯琴;孟根杜希
010110 呼和浩特,内蒙古医科大学蒙医药学院内蒙古奥特奇医药研发有限公司010110 呼和浩特,内蒙古医科大学蒙医药学院010110 呼和浩特,内蒙古医科大学蒙医药学院内蒙古溢多利生物科技有限公司010110 呼和浩特,内蒙古医科大学蒙医药学院010110 呼和浩特,内蒙古医科大学蒙医药学院
医药卫生
沏其日甘八味片高脂血症肠道菌群16S rRNA测序金黄地鼠菌群多样性调脂保肝剂型比较
Qiqirigan-8 Tabletshyperlipidemiagut microbiota16S rRNA sequencinggolden hamstermicrobial diversitylipid-lowering and hepatoprotective effectsformulation compari-son
《环球中医药》 2026 (5)
961-973,13
内蒙古自治区自然科学基金(2023LHMS08026)内蒙古自治区科技计划项目(2019GG161)2025中医学(蒙医学)"一流建设学科"建设项目(2025MYXYLXK012)
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