Wang Mengmeng, Liu Zhuqing, Hu Shoushan, Duan Xianchun, Zhang Yanyan, Peng Can, Peng Daiyin, Han Lan
Anhui University of Chinese Medicine, Hefei, China.
Anhui Province Key Laboratory of Chinese Medicinal Formula, Hefei, China.
Front Pharmacol. 2020 Dec 8;11:590453. doi: 10.3389/fphar.2020.590453. eCollection 2020.
Taohong Siwu decoction (THSWD) is one of the classic prescriptions for promoting blood circulation and removing blood stasis, and it has a good therapeutic effect on ischemic stroke. We sought to explore the therapeutic effects of THSWD on pyroptosis in rats with middle cerebral artery occlusion-reperfusion (MCAO/R). MCAO/R model of rats were established by suture-occluded method. MCAO/R rats were randomly divided into five groups, which were model group, nimodipine group, THSWD high, medium and low dose group (18, 9, and 4.5 g/kg, respectively), rats of sham group without thread embolus. All rats were treated by intragastric administration for 7 days. We detected the level of inflammatory factors. NLRP3 and Caspase-1 were detected by immunofluorescence. Western blot was used to detect NLRP3, Caspase-1, ASC, and GSDMD in penumbra. Also, the expression of TXNIP, HMGB1, toll-like receptors (TLR4), NF-κB, and MAPK were detected. THSWD treatment improved the behavioral function and brain pathological damage. These results showed that the levels of TNF-α, TGF-β, IL-2, IL-6, IL-1β, and IL-18 were significantly reduced in THSWD treatment groups. THSWD could significantly decrease the expression levels of NLRP3, Caspase-1, Caspase-1 p10, ASC, TXNIP, GSDMD, HMGB1, TLR4/NFκB, p38 MAPK, and JNK in penumbra. Our results showed that THSWD could reduce the activation level of NLRP3 inflammatory corpuscle, down-regulate GSDMD, and inhibit pyroptosis in MCAO/R rats. These may be affected by inhibiting HMGB1/TLR4/NFκB, MAPK signaling pathways.
桃红四物汤(THSWD)是活血化瘀的经典方剂之一,对缺血性中风有良好的治疗效果。我们旨在探讨THSWD对大脑中动脉闭塞-再灌注(MCAO/R)大鼠细胞焦亡的治疗作用。采用线栓法建立大鼠MCAO/R模型。将MCAO/R大鼠随机分为五组,即模型组、尼莫地平组、THSWD高、中、低剂量组(分别为18、9和4.5 g/kg),假手术组大鼠不栓线。所有大鼠均经灌胃给药7天。我们检测了炎症因子水平。通过免疫荧光检测NLRP3和半胱天冬酶-1。采用蛋白质免疫印迹法检测半暗带中NLRP3、半胱天冬酶-1、ASC和GSDMD的表达。此外,还检测了TXNIP、HMGB1、 Toll样受体(TLR4)、NF-κB和丝裂原活化蛋白激酶(MAPK)的表达。THSWD治疗改善了行为功能和脑病理损伤。这些结果表明,THSWD治疗组中肿瘤坏死因子-α、转化生长因子-β、白细胞介素-2、白细胞介素-6、白细胞介素-1β和白细胞介素-18水平显著降低。THSWD可显著降低半暗带中NLRP3、半胱天冬酶-1、半胱天冬酶-1 p10、ASC、TXNIP、GSDMD、HMGB1、TLR4/NFκB、p38 MAPK和JNK的表达水平。我们的结果表明,THSWD可降低MCAO/R大鼠中NLRP3炎性小体的激活水平,下调GSDMD,并抑制细胞焦亡。这些可能是通过抑制HMGB1/TLR4/NFκB、MAPK信号通路而受到影响。