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黄芩对大鼠肝硬化内毒素血症肠黏膜损伤的保护性机制研究
引用本文:刘昳,叶峰,邹文静,邱根全,刘小静,蔺淑梅,杨雪亮. 黄芩对大鼠肝硬化内毒素血症肠黏膜损伤的保护性机制研究[J]. 中华实验和临床感染病杂志(电子版), 2013, 0(6): 5-10
作者姓名:刘昳  叶峰  邹文静  邱根全  刘小静  蔺淑梅  杨雪亮
作者单位:[1]西安交通大学医学院第一附属医院中医科,西安市710061 [2]西安交通大学医学院第一附属医院传染科,西安市710061
基金项目:陕西省中医药管理局科研课题项目(No.jc30)
摘    要:目的:探讨黄芩对大鼠肝硬化内毒素血症肠黏膜损伤的保护性机制。方法复合因素造模法建立肝硬化内毒素血症大鼠模型。模型确立后将大鼠随机分为3个实验组,即模型组、黄芩组治疗组和谷氨酰胺治疗组,每组各20只;另设正常对照组大鼠10只。各组大鼠给予灌胃治疗,共2周。实验结束后,采用ELISA法检测大鼠血清内毒素水平,TUNEL法检测各组大鼠肠黏膜细胞凋亡并计算凋亡率,采用RT-PCR检测肠黏膜细胞凋亡相关基因Bcl-2 RNA和Bax RNA的表达水平。结果3个实验组较正常对照组大鼠内毒素组水平均显著升高(F =3.31,P <0.05);其中模型组显著高于黄芩治疗组(q =5.12,P =0.0000);黄芩治疗组显著低于谷氨酰胺组(q =3.74,P =0.0123)。3个实验组与正常对照组比较,肠黏膜细胞的凋亡率均显著升高(F =4.77,P <0.01);其中模型组显著高于黄芩治疗组和谷氨酰胺组(q =4.56、4.35,P均<0.01);黄芩治疗组显著低于谷氨酰胺组(q =3.78,P =0.012)。3个实验组与正常对照组比较,肠黏膜组织Bcl-2 mRNA水平显著下降(F =3.55, P <0.05);其中模型组显著低于黄芩治疗组和谷氨酰胺治疗组(q =3.89、3.40,P <0.05);黄芩治疗组显著高于谷氨酰胺组(q =2.77,P <0.05)。3个实验组大鼠肠黏膜Bax mRNA水平则显著高于正常对照组(F =3.67,P <0.05);模型组显著高于黄芩治疗组和谷氨酰胺治疗组(q =3.62、2.91,P <0.05);黄芩治疗组显著低于谷氨酰胺组(q =2.85,P <0.05)。结论黄芩能够通过降低肠黏膜细胞的凋亡而减少肝硬化内毒素血症的发生。

关 键 词:黄芩  肝硬化  内毒素血症  肠黏膜  凋亡

Protective mechanism of Scutellaria baicalensis georgi on the intestinal mucosal injury of endotoxemia in rats with liver cirrhosis
LIU Yi,YE Feng,ZOU Wen-jing,QIU Gen-quan,LIU Xiao-jing,LIN Shu-mei,YANG Xue-liang. Protective mechanism of Scutellaria baicalensis georgi on the intestinal mucosal injury of endotoxemia in rats with liver cirrhosis[J]. Chinese Journal of Experimental and Clinical Infectious Diseases(Electronic Version), 2013, 0(6): 5-10
Authors:LIU Yi  YE Feng  ZOU Wen-jing  QIU Gen-quan  LIU Xiao-jing  LIN Shu-mei  YANG Xue-liang
Affiliation:(Department of Traditional Chinese Medicine, Xi'an Jiaotong University, Xi'an 710061, China)
Abstract:Objective To explore the protective mechanism of Scutellaria baicalensis georgi on the intestinal mucosal injury of endotoxemia in rats with liver cirrhosis. Methods Compound factors modeling was used to establish endotoxemia rat model with liver cirrhosis. The rats were randomly divided into 3 experimental groups: model group, the scutellaria treatment group and glutamine treatment group with 20 in each group. There were 10 rats in normal control group. Gavage was conducted to each group for 2 weeks. At the end of the experiment, serum endotoxin levels of rats and intestinal mucosa apoptosis of rats in each group were detected by ELISA and TUNEL, respectively. And the expression levels of gene Bcl-2 RNA and Bax RNA related to intestinal mucosa apoptosis were detected by RT-PCR. Results The endotoxin level of the three experimental groups was significantly elevated compared with that of the normal control group (F = 3.31, P 〈 0.05). The endotoxin level of the model group was significantly higher than that of the scutellaria treatment group (q = 5.12, P = 0.0000 ). The endotoxin level of the scutellaria treatment group was significantly lower than that of the glutamine group (q = 3.74, P = 0.0123). The increase of intestinal mucosal apoptosis rate in the three experimental groups was significantly higher than that of the normal control group (F = 4.77, P 〈 0.01). The intestinal mucosal apoptosis rate of the model group was significantly higher than that of the scutellaria treatment group and the glutamine group (q = 4.56, 4.35; P = 0.0000). The rate of intestinal mucosal apoptosis in the scutellaria treatment group was significantly lower than that of the glutamine group (q = 3.78, P = 0.012). The intestinal mucosal Bcl-2 mRNA level of the three experimental groups significantly decreased than that of the normal control group (F = 3.55, P 〈 0.05). The intestinal mucosal Bcl-2 mRNA levels of the model group were significantly lower than that of the scutellaria treatment group and the glutamine treatment group (q = 3.89, 3.40; P 〈 0.05). The intestinal mucosal Bcl-2 mRNA level of the scutellaria treatment group was significantly higher than that of the glutamine group (q = 2.77, P 〈0.05). The intestinal mucosal Bax mRNA level of the three experimental groups was significantly higher than that of the normal control group (F = 3.67, P 〈 0.05). The intestinal mucosal Bax mRNA level of the model group was significantly higher than that of the scutellaria treatment group and the glutamine treatment group (q = 3.62, 2.91; P 〈 0.05 ). The intestinal mucosal Bax mRNA level of the scutellaria treatment group was significantly lower than that of the glutamine group (q = 2.85,P 〈 0.05). Conclusions Scutellaria baicalensis georgi could reduce the occurrence of liver cirrhosis endotoxemia by reducing intestinal mucosal apoptosis.
Keywords:Scutellaria baicalensis georgi  Liver cirrhosis  Endotoxemia  Intestinal mucosa  Apoptosis
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