老鼠簕生物碱A对小鼠药物性肝损伤的保护作用

韦秀桂; 王红园; 黄秀昆; 孙雪梅; 梁英琴; 徐万鹏; 林兴; 林军

doi:10.13422/j.cnki.syfjx.20191503

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老鼠簕生物碱A对小鼠药物性肝损伤的保护作用

药理 | 更新时间：2021-02-09

- 老鼠簕生物碱A对小鼠药物性肝损伤的保护作用
- Protective Effect of Alkaloid A from Acanthi Ilicifolii Herba seu Radix on Drug-induced Liver Injury in Mice
- 中国实验方剂学杂志 2019年25卷第15期页码：103-107
- 作者机构：
  
  广西医科大学　药学院，南宁　 530021
- 作者简介：
  
  韦秀桂，在读硕士，从事中药药理学研究，E-mail：mijiss69@foxmail.com
  林军，博士，教授，从事中药药理学研究，Tel: 0771-5358272，E-mail: junlin989@sina.com
- 基金信息：
  
  国家自然科学基金项目(81660106)
- DOI：10.13422/j.cnki.syfjx.20191503
  中图分类号： R2-0; R22; R285.5
- 收稿日期：2019-01-06，
  
  网络出版日期：2019-04-18，
  
  纸质出版日期：2019-08-05
- 稿件说明：
移动端阅览
韦秀桂, 王红园, 黄秀昆, 等. 老鼠簕生物碱A对小鼠药物性肝损伤的保护作用[J]. 中国实验方剂学杂志, 2019,25(15):103-107.

Xiu-gui WEI, Hong-yuan WANG, Xiu-kun HUANG, et al. Protective Effect of Alkaloid A from Acanthi Ilicifolii Herba seu Radix on Drug-induced Liver Injury in Mice[J]. Chinese journal of experimental traditional medical formulae, 2019, 25(15): 103-107.
韦秀桂, 王红园, 黄秀昆, 等. 老鼠簕生物碱A对小鼠药物性肝损伤的保护作用[J]. 中国实验方剂学杂志, 2019,25(15):103-107. DOI： 10.13422/j.cnki.syfjx.20191503.

Xiu-gui WEI, Hong-yuan WANG, Xiu-kun HUANG, et al. Protective Effect of Alkaloid A from Acanthi Ilicifolii Herba seu Radix on Drug-induced Liver Injury in Mice[J]. Chinese journal of experimental traditional medical formulae, 2019, 25(15): 103-107. DOI： 10.13422/j.cnki.syfjx.20191503.

摘要

目的：

观察老鼠簕生物碱A(AAIA)对对乙酰氨基酚引起肝损伤模型的影响。

方法：

将小鼠随机分成正常组、模型组、联苯双酯组(联苯双酯，150 mg·kg

－1

)及AAIA高、中、低剂量(200，100，50 mg·kg

－1

)组，每组10只，连续灌胃给药10 d，末次给药后禁食不禁水8 h，除正常组外，其余各组给予腹腔注射275 mg·kg

－1

对乙酰氨基酚，诱导小鼠急性肝损伤模型。6 h后，进行眼球取血，称量小鼠体质量、肝脏、脾脏、肾脏、胸腺质量，计算相应脏器指数，使用试剂盒检测血清中丙氨酸氨基转移酶(ALT)，天冬氨酸氨基转移酶(AST)的含量，紫外分光光度法测定肝匀浆中一氧化氮(NO)，诱导型一氧化氮合酶(iNOS)的含量，蛋白免疫印迹法(Western blot)测定细胞外调节蛋白激酶(ERK1/2)，磷酸化细胞外调节蛋白激酶(p-ERK1/2)的表达。

结果：

与正常组比较，模型组的肝脏指数，血清中AST，ALT，肝组织匀浆NO，iNOS水平及p-ERK1/2在肝脏中的蛋白表达显著增高(

0.01)；与模型组比较，各给药组均能降低对乙酰氨基酚急性肝损伤小鼠肝脏指数，血清AST，ALT水平，肝组织匀浆中NO，iNOS的产生，肝脏p-ERK1/2蛋白表达(

0.01)；所有注射对乙酰氨基酚组的脾脏、肾脏及胸腺无明显变化，差异无统计学意义。

结论：

AAIA可能通过降低AST，ALT的水平，下调NO，iNOS的表达，减少p-ERK1/2的表达，对小鼠药物性肝损伤起到保护作用。

Abstract

Objective:

To observe the effect of alkaloid A from Acanthi Ilicifolii Herba seu Radix(AAIA) on liver injury model caused by acetaminophen.

Method:

Mice were randomly divided into normal group

model group

positive drug group (bifendate

150 mg·kg

-1

) and high

medium and low-dose AAIA groups (200

100

50 mg·kg

-1

)

with 10 in each group. They were given drugs by gavage for 10 days

and fasted for 8 hours after the last administration. Except the normal group

the other groups were intraperitoneally injected with 275 mg·kg

-1

acetaminophen to induce acute liver injury model in mice. Six hours later

blood was taken from the eyeball. The body

liver

spleen

kidney and thymus were weighed

and then the corresponding organ indexes were calculated. The kits were used to detect the contents of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) in serum. The contents of nitric oxide (NO) and inducible nitric oxide synthase (iNOS) in liver homogenate were determined by ultraviolet spectrophotometry

and the expressions of extracellular regulated protein kinases (ERK1/2) and phosphorylated extracellular regulatory protein kinase (p-ERK1/2) were determined by Western blot.

Result:

Compared with the normal group

the liver index

serum AST and ALT levels

the production of NO and iNOS in liver homogenate

the expression of p-ERK1/2 protein in liver of the model group increased significantly (

0.01). Compared with the model group

all of drug groups could reduce the liver index of mice with acute liver injury induced by acetaminophen

the levels of serum AST and ALT

the production of NO and iNOS in liver and homogenate and the expression of p-ERK1/2 protein in liver (

0.01). however

it had no significant effect on spleen

kidney and thymus of all acetaminophen injection groups.

Conclusion:

AAIA may protect mice from drug-induced liver injury by reducing AST and ALT levels

down-regulating the expressions of NO and iNOS

and reducing the expression of protein p-ERK1/2.

关键词

Keywords

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