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1.广西中医药大学 研究生学院,南宁 530023;
2.广西中医药大学 第一附属医院,南宁 530001
汪顺贵,在读硕士,从事癫痫的基础与临床研究,E-mail:1191298244@qq.com
刁丽梅,博士,教授,主任医师,硕士生导师,从事癫痫的基础与临床研究,E-mail:dlm721226@163.com
收稿日期:2019-04-02,
网络出版日期:2019-07-18,
纸质出版日期:2019-11-20
移动端阅览
汪顺贵, 玉倩, 李华霞, 等. 加味柴胡疏肝汤调控miRNA-204对癫痫小鼠海马自噬的影响[J]. 中国实验方剂学杂志, 2019,25(22):1-7.
Shun-gui WANG, Qian YU, Hua-xia LI, et al. Effect of Modified Chaihu Shugantang Regulat miRNA-204 on Hippocampus Autophagy in Epileptic Mice[J]. Chinese journal of experimental traditional medical formulae, 2019, 25(22): 1-7.
汪顺贵, 玉倩, 李华霞, 等. 加味柴胡疏肝汤调控miRNA-204对癫痫小鼠海马自噬的影响[J]. 中国实验方剂学杂志, 2019,25(22):1-7. DOI: 10.13422/j.cnki.syfjx.20192137.
Shun-gui WANG, Qian YU, Hua-xia LI, et al. Effect of Modified Chaihu Shugantang Regulat miRNA-204 on Hippocampus Autophagy in Epileptic Mice[J]. Chinese journal of experimental traditional medical formulae, 2019, 25(22): 1-7. DOI: 10.13422/j.cnki.syfjx.20192137.
目的:
2
观察加味柴胡疏肝汤对癫痫小鼠海马微小非编码RNA 204(miRNA-204)的表达影响,探讨其发挥神经保护作用的机制。
方法:
2
将60只小鼠随机分为6组:正常组,模型组(盐酸匹罗卡品180 mg·kg
-1
),加味柴胡疏肝汤组(7 g·kg
-1
·d
-1
),加味柴胡疏肝汤+miRNA-204模拟物组(7 g·kg
-1
·d
-1
+2 μL),加味柴胡疏肝汤+miRNA-204抑制物组(7 g·kg
-1
·d
-1
+2 μL),卡马西平组(30 mg·kg
-1
·d
-1
),各灌胃2周;采用匹罗卡品使小鼠致痫,6组分别灌胃给药、抑制及过表达miRNA-204后,处死小鼠,取其海马组织,观察每组的指标情况,采用实时荧光定量聚合酶链式反应(Real-time PCR)检测小鼠海马miRNA-204的表达;蛋白免疫印迹法(Western blot)检测自噬相关蛋白微管相关蛋白轻链3(LC3),自噬相关标志性蛋白7(ATG7)的表达情况,苏木素-伊红(HE)染色观察每组小鼠海马病理学变化;透射电镜观察各组小鼠海马组织自噬情况。
结果:
2
与正常组比较,模型组小鼠miRNA-204表达显著降低(
P
<
0.01),海马C1区病理改变最明显,ATG7,LC3Ⅱ/LC3Ⅰ表达显著升高(
P
<
0.01),自噬小体数量最多;与模型组比较,加味柴胡疏肝组小鼠海马组织miRNA-204表达明显升高(
P
<
0.05),海马C1区病理改变减轻,ATG7,LC3Ⅱ/LC3Ⅰ表达明显降低(
P
<
0.05),自噬小体数量减少;加味柴胡疏肝汤+miRNA-204模拟物组小鼠海马组织miRNA-204表达显著升高(
P
<
0.01),海马C1区病理改变最轻,ATG7,LC3Ⅱ/LC3Ⅰ表达显著降低(
P
<
0.01),自噬小体数量最少;与加味柴胡疏肝汤比较,加味柴胡疏肝汤+miRNA-204抑制物组上述指标变化趋势相同,变化幅度明显减少(
P
<
0.05)。
结论:
2
加味柴胡疏肝汤可以改善癫痫小鼠海马组织病理改变,其作用机制可能是通过升高癫痫小鼠海马miRNA-204的表达,抑制神经元过度自噬,减少细胞凋亡。
Objective:
2
To observe the effect of modified Chaihu Shugantang on the expression of miRNA-204 in hippocampus of epileptic mice
and to explore its mechanism of neuroprotection.
Method:
2
The sixty mice were randomly divided into 6 groups: normal group
model group (pilocarpine 180 mg·kg
-1
)
and modified Chaihu Shugantang group (7 g·kg
-1
·d
-1
)
modified Chaihu Shugantang+ miRNA-204 mimic group (7 g·kg
-1
·d
-1
+ 2 μL)
modified Chaihu Shugantang+ miRNA-204 inhibitor group (7 g·kg
-1
·d
-1
+ 2 μL)
carbamazepine group (30 mg·kg
-1
·d
-1
)
each was given intragastric administration for 2 weeks
using pilocarpine to cause epilepsy in mice
respectively
add flavor to Bupleurum after intragastric administration
inhibition and overexpression of miRNA-204
the mice were sacrificed and their hippocampus tissues were harvested.The indicators of each group were observed
Real-time quantitative PCR detecting system (Real-time PCR) was used to detect mouse hippocampal miRNA-204 expression
Western blot analysis of autophagy-related protein microtubule-associated protein light chain 3 (LC3)
autophagy-associated marker protein 7 (ATG7) expression
hematoxylin pathological condition of hippocampus in each group was observed by hematoxylin-eosin(HE)staining.The autophagy of hippocampus in each group was observed by transmission electron microscopy.
Result:
2
Compared with normal group
the expression of miRNA-204 was significantly decreased in model group (
P
<
0.01)
the pathological changes in the hippocampal C1 area were the most obvious
the expression of ATG7
LC3Ⅱ/LC3Ⅰ was increased (
P
<
0.01)
and the autophagy was small. Compared with model group
the expression of miRNA-204 in the hippocampus of the modified Chaihu Shugantang group was increased (
P
<
0.05)
the pathological changes in the hippocampal C1 area were alleviated
the expression of ATG7
LC3Ⅱ/LC3Ⅰ was decreased (
P
<
0.05)
and the autophagy was small. The number of body decreased
the expression of miRNA-204 in hippocampus of modified Chaihu Shugantang+ miRNA-204 mimic group was significantly increased (
P
<
0.01)
the pathological changes in hippocampal C1 area were the lightest
and the expression of ATG7
LC3II/LC3I was decreased (
P
<
0.01)
the number of autophagosomes was the least.Compared with modified Chaihu Shugantang group
the above-mentioned indicators of modified Chaihu Shugantang+ miRNA-204 inhibitor group had the same change trend and the change range decreased (
P
<
0.05).
Conclusion:
2
Modified Chaihu Shugantang can improve the pathological changes of hippocampus in mice with epilepsy and play a neuroprotective role. The mechanism may be to increase the expression of miRNA-204 in hippocampus of mice with epilepsy
inhibit excessive autophagy of neurons and reduce apoptosis.
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