Effect of Buyang Huanwu Tang on Axonal Regeneration of Rats After Ischemic Stroke Injury
10.13422/j.cnki.syfjx.20202141
- VernacularTitle:补阳还五汤对大鼠缺血性脑中风损伤后轴突再生的影响
- Author:
Ai-ming YU
1
;
Xiang-li YAN
1
;
Hao-zhen ZHENG
1
;
Ying-ying HE
1
;
Ni-jun ZHONG
1
;
Li-sheng WANG
1
Author Information
1. School of Pharmaceutical Sciences， Guangzhou University of Chinese Medicine， Guangzhou 510006， China
- Publication Type:Research Article
- Keywords:
Buyang Huanwu Tang;
ischemic stroke;
axonal regeneration;
axon growth-related protein;
neurological rehabilitation
- From:
Chinese Journal of Experimental Traditional Medical Formulae
2020;26(21):15-20
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To investigate the effects of Buyang Huanwu Tang （BHT） on axonal regeneration and neurological rehabilitation of the rats suffering ischemic stroke （IS）. Method:A total of 180 SD rats were used to establish a middle cerebral artery infarction （MCAO） model. The animals that were successfully modeled were randomly divided into model group， BHT group （12 g·kg-1） and nimodipine group （20 mg·kg-1）， and a sham group was established， with 28 rats in each group. After seven-days intragastric administration of BHT， the animals were sacrificed. TTC staining was used to test cerebral infarction. Brain water content was measured to observe cerebral edema. Bielschowsky's silver staining and immunofluorescence were performed to observe axonal degeneration and the protein expression of neurofilament protein-200（NF-200）. Quantitative real-time polymerase chain reaction （PCR） was used to analyze the mRNA expression of repulsion oriented molecule a （RGMa）， Ras homologous enzyme （Rho）， Rho kinase （ROCK）， and collapsion response regulatory protein 2 （CRMP2）. Neurological function scores assay was used to examine neurological recovery. Result:Compared with sham group， the cerebral infarction volume and brain water content increased significantly（P<0.01）， and motor function was markablely decreased in the model group. Axonal degeneration and nerve fiber damage were obviously observed. Also， gene expression of axon growth-related protein was deviation from normal （P<0.01）. Compared with model group， the cerebral infarction rate （P<0.01）， brain water content （P<0.01） and axonal degeneration of BHT group and nimodipine group were significantly reduced. The expression of NF-200 was increased. Also， the mRNA expression of RGMa， Rho and ROCK was lower （P<0.05） while the mRNA expression of CRMP2 was higher （P<0.01）. And the neurological function was significantly improved （P<0.05）. Conclusion:BHT can promote axon regeneration after ischemic stroke injury by regulating the mRNA expression of axon growth-related protein， thereby improving nerve function.
