Liu Qing-Shan, Zhang Wei-Wei, Yin Xiao-Ying, Li Xu
Key Lab of Education Department, National Research Center for Minority Traditional Medicine, Minzu University of China, Beijing 100081, China.
College of Pharmacy, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, China.
Zhongguo Zhong Yao Za Zhi. 2016 May;41(10):1910-1915. doi: 10.4268/cjcmm20161025.
To study the effect and possible molecular mechanisms of Terminalia chebula extract HZ4 on focal cerebral infarction in rats, 90 healthy male SD rats were randomly divided into sham-operation group, model group, T. chebula extract HZ4 high dose, middle dose and low dose groups (80, 40, 20 mg•kg ⁻¹•d ⁻¹, ig) and positive control group (Panax notoginseng saponins, PNS 30 mg•kg ⁻¹•d ⁻¹, ig). The focal cerebral infarction models were established by photochemical method. After the rats were administered for 7 consecutive days, neurogenic behavior rating of these rats was done by balance beam test and foot fault test. The cells morphological changes of penumbra in focal cerebral infarction were investigated by HE staining method; the infarct volume was detected by TTC staining. The expression levels of β-catenin and cyclin D1, the key node genes in Wnt signaling pathway of the focal penumbra tissues were detected via RT-PCR. The results showed that, as compared with the model group, behavioural indicators were improved significantly in the rats of administration groups, and the infarct volume and pathological changes of penumbra tissues were also improved at the same time. Compared with the model group, the expression levels of β-catenin and cyclin D1 in Wnt signaling pathway were significantly up-regulated in administration groups(P<0.01). This study first confirmed that T. chebula extract HZ4 can decrease infarct volume, improve the sport ability score, and promote rehabilitation of model animals. In addition, it could significant up-regulated the expression levels of β-catenin and cyclin D1, and the mechanism may be associated with Wnt signaling pathway. The study is innovative to a certain extent.
为研究诃子提取物HZ4对大鼠局灶性脑梗死的影响及其可能的分子机制,将90只健康雄性SD大鼠随机分为假手术组、模型组、诃子提取物HZ4高剂量组、中剂量组、低剂量组(80、40、20 mg•kg⁻¹•d⁻¹,灌胃)和阳性对照组(三七总皂苷,PNS 30 mg•kg⁻¹•d⁻¹,灌胃)。采用光化学法建立局灶性脑梗死模型。大鼠连续给药7天后,通过平衡木试验和足错误试验对这些大鼠进行神经行为评分。采用HE染色法观察局灶性脑梗死灶周边半暗带细胞形态变化;采用TTC染色法检测梗死体积。通过RT-PCR检测局灶性半暗带组织Wnt信号通路关键节点基因β-连环蛋白和细胞周期蛋白D1的表达水平。结果显示,与模型组相比,各给药组大鼠行为学指标显著改善,同时梗死体积及半暗带组织病理变化也得到改善。与模型组相比,各给药组Wnt信号通路中β-连环蛋白和细胞周期蛋白D1的表达水平显著上调(P<0.01)。本研究首次证实诃子提取物HZ4可减小梗死体积,提高运动能力评分,促进模型动物康复。此外,其可显著上调β-连环蛋白和细胞周期蛋白D1的表达水平,机制可能与Wnt信号通路有关。本研究具有一定创新性。