School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University, No.103, Wenhua Road, Shenyang 110016, PR China; Beijing Key Laboratory of Drug Target Identification and Drug Screening, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, PR China.
Beijing Key Laboratory of Drug Target Identification and Drug Screening, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, PR China.
Pharmacol Res. 2022 Jan;175:105989. doi: 10.1016/j.phrs.2021.105989. Epub 2021 Nov 18.
Chronic cerebral ischemia (CCI) refers to long-term hypoperfusion of cerebral blood flow with the main clinical manifestations of progressive cognitive impairment. The pathological mechanism of CCI is complex, and there is a lack of effective treatments. Salvianolic acid A (SalA) is a neuroprotective extract of Salvia miltiorrhiza with the effects of anti-inflammation and anti-apoptosis. In this study, the effect of SalA on cognitive function and Drd2/Cryab/NF-κB signaling pathway in rats with CCI was investigated. Morris water maze and open field test were used to observe the effects of SalA on the cognitive function of CCI rats. The pathological changes in the brain were observed by HE, Nissl, and LFB staining. TUNEL staining, enzyme-linked immunosorbent assay, and western blot analysis were used to detect the inflammatory and apoptosis in the cortex and hippocampus. The expression of Drd2/Cryab/NF-κB pathway-related molecules and Drd2 localization were detected by western blotting and dual immunofluorescence, respectively. SH-SY5Y cells were exposed to chronic hypoglycemic and hypoxic injury in vitro, and Drd2 inhibitor haloperidol was used to verify the involved pathway. The results showed that SalA could improve the cognitive function of CCI rats, reduce pathological damage of cortex and hippocampus, inhibit neuroinflammation and apoptosis, and suppress the activation of NF-κB by regulating Drd2/Cryab pathway. And SalA inhibited NF-κB activation and nuclear translocation in SH-SY5Y cells by upregulating Drd2/Cryab pathway, which was reversed by haloperidol interference. In conclusion, SalA could relieve CCI-induced cognitive impairment in rats, at least partly through the Drd2/Cryab/NF-κB pathway.
慢性脑缺血(CCI)是指脑血流长期灌注不足,主要临床表现为进行性认知功能障碍。CCI 的病理机制复杂,缺乏有效的治疗方法。丹参酸 A(SalA)是丹参的一种神经保护提取物,具有抗炎和抗细胞凋亡作用。本研究探讨了 SalA 对 CCI 大鼠认知功能及 Drd2/Cryab/NF-κB 信号通路的影响。采用 Morris 水迷宫和旷场实验观察 SalA 对 CCI 大鼠认知功能的影响。HE、Nissl 和 LFB 染色观察脑组织病理变化。TUNEL 染色、酶联免疫吸附试验和 Western blot 分析检测皮质和海马区炎症和凋亡情况。Western blot 和双免疫荧光分别检测 Drd2/Cryab/NF-κB 通路相关分子的表达和 Drd2 定位。体外慢性低糖低氧损伤 SH-SY5Y 细胞,用多巴胺受体 D2(Drd2)抑制剂氟哌啶醇验证相关通路。结果表明,SalA 可改善 CCI 大鼠认知功能,减轻皮质和海马区病理损伤,抑制神经炎症和细胞凋亡,通过调节 Drd2/Cryab 通路抑制 NF-κB 激活。SalA 通过上调 Drd2/Cryab 通路抑制 NF-κB 的激活和核转位,在 SH-SY5Y 细胞中,该作用可被氟哌啶醇干扰所逆转。结论:SalA 可缓解 CCI 大鼠认知功能障碍,其作用机制至少部分与 Drd2/Cryab/NF-κB 通路有关。