Qingda Granules alleviate brain damage in spontaneously hypertensive rats by modulating the miR-124/STAT3 signaling axis
- PMID: 39819708
- PMCID: PMC11744273
- DOI: 10.12122/j.issn.1673-4254.2025.01.03
Qingda Granules alleviate brain damage in spontaneously hypertensive rats by modulating the miR-124/STAT3 signaling axis
Abstract
Objectives: To explore the mechanism of Qingda Granules (QDG) for alleviating brain damage in spontaneously hypertensive rats (SHRs).
Methods: Twelve 5-week-old SHRs were randomized into SHR control group and SHR+QDG group treated with QDG by gavage at the daily dose of 0.9 g/kg for 12 weeks. The control rats, along with 6 age-matched WKY rats, were treated with saline only. Blood pressure changes of the rats were monitored, and pathologies and neuronal apoptosis in the cerebral cortex were examined with HE staining and TUNEL staining. Cerebral cortical expressions of miR-124 and STAT3 mRNA were detected using RT-qPCR, and the protein expressions of NeuN, STAT3, Bcl-2, Bax, and cleaved caspase-3 were detected with immunohistochemistry and Western blotting. In a HT22 cell model of oxygen and glucose deprivation/reoxygenation (OGD/R), the effects of QDG on cell viability and apoptosis, expressions of miR-124 and STAT3 mRNA, and protein expressions of STAT3, Bcl-2, Bax, and cleaved caspase-3 were evaluated using CCK8 assay, Hoechst 33342 staining, RT-qPCR, and Western blotting.
Results: Compared with WKY rats, SHRs had significantly elevated systolic blood pressure, diastolic blood pressure and mean arterial pressure with significantly increased neuronal apoptosis in the cerebral cortex, reduced expressions of NeuN, miR-124 and Bcl-2, and enhanced expressions of STAT3, Bax and cleaved caspase-3 (P<0.05). All these changes in the SHRs were significantly ameliorated by treatment with QDG (P<0.05). In the HT22 cell model, QDG treatment obviously reduced OGD/R-induced cell apoptosis, increased the expressions of miR-124 and Bcl-2, and suppressed the elevation of protein expressions of STAT3, Bax and cleaved caspase-3.
Conclusions: QDG inhibits cerebral cortical neuronal apoptosis and thereby attenuates brain damage in SHR rats by modulating the miR-124/STAT3 signaling axis.
目的: 探讨清达颗粒(QDG)对自发性高血压大鼠(SHR)脑损伤的保护作用及其对miR-124/STAT3信号轴的影响。方法: 6只5周龄WKY大鼠为WKY组,12只5周龄SHR大鼠分为SHR组、SHR+QDG组,6只/组。SHR+QDG组大鼠每天给予QDG灌胃,灌胃剂量为0.9 g/(kg·d),连续灌胃12周,其余组大鼠每天给予等体积生理盐水灌胃。利用鼠尾无创血压仪监测血压,HE染色观察脑皮质区病理,TUNEL染色检测皮质区凋亡,Q-PCR检测miR-124、STAT3 mRNA的表达,免疫组化和Western blotting检测NeuN、STAT3、Bcl-2、Bax、cleaved caspase-3的表达;利用氧糖剥夺/复氧(OGD/R)构建神经元HT22细胞损伤模型,分为Control组、QDG组、OGD/R组、OGD/R+QDG组。利用CCK-8法检测细胞活力,Hoechst 33342染色检测细胞凋亡,Q-PCR检测miR-124、STAT3、Bcl-2、Bax mRNA的表达,Western blotting检测STAT3、Bcl-2、Bax、cleaved caspase-3的表达。结果: 体内实验中,与WKY组比较,SHR组大鼠的收缩压、舒张压及平均动脉压均升高(P<0.05),脑皮质区神经元出现核固缩,数量减少,凋亡率升高(P<0.05),NeuN、miR-124、Bcl-2的表达降低,STAT3、Bax、cleaved caspase-3的表达升高(P<0.05)。与SHR组比较,清达颗粒能降低SHR大鼠的收缩压、舒张压及平均动脉压(P<0.05),改善SHR大鼠脑皮质区的病理损伤,降低皮质区的凋亡率(P<0.05),升高皮质区的NeuN、miR-124、Bcl-2的表达(P<0.05),降低STAT3、Bax、cleaved caspase-3的表达(P<0.05)。体外实验中,与Control组比较,OGD/R组凋亡率升高,miR-124、Bcl-2表达降低,STAT3、Bax、cleaved caspase-3表达升高(P<0.05);与OGD/R组比较,清达颗粒能降低OGD/R诱导的HT22细胞凋亡,升高miR-124、Bcl-2表达,降低STAT3、Bax、cleaved caspase-3表达(P<0.05)。结论: 清达颗粒可能通过调控miR-124/STAT3信号轴,抑制神经元的凋亡,从而减轻SHR大鼠的脑损伤。.
Keywords: Qingda Granules; brain damage; hypertension; miR-124/STAT3 signaling axis; neurons.
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