Department of Health Laboratory Technology, School of Public Health, China Medical University, Shenyang, Liaoning, People's Republic of China.
Department of Health Laboratory Technology, School of Public Health, China Medical University, Shenyang, Liaoning, People's Republic of China; The Key Laboratory of Liaoning Province on Toxic and Biological Effects of Arsenic, Shenyang, Liaoning, People's Republic of China.
Biomed Pharmacother. 2022 Jun;150:112964. doi: 10.1016/j.biopha.2022.112964. Epub 2022 Apr 21.
Realgar, as a commonly used traditional Chinese medicine, exerts both pharmacological and biological effects. However, the mechanism by which it causes nervous system injury remains unclear. This study aimed to elucidate the specific mechanism underlying the hippocampal neurotoxicity caused by realgar. Nrf2 is an important receptor of exogenous toxic substances and oxidative stress. We utilized a p38-specific inhibitor (SB20358), ERK1/2-specific inhibitor (PD98059), JNK-specific inhibitor (SP600125) and AKT-specific inhibitor (LY249002) to establish the corresponding animal models and explore how realgar activates Nrf2. We established an Nrf2-shRNA gene silencing model in rats and an autophagy-specific inhibitor treatment model to further explore realgar-induced neurotoxicity and the role of Nrf2 in realgar-induced damage to the hippocampus. The results showed that realgar passed through the blood-brain barrier and accumulated in brain tissue to induce central nervous system toxicity. The specific mechanism was that realgar activated MAPKs and AKT signaling molecules to activate the Nrf2-Keap1-p62 positive feedback signaling axis, induced abnormal autophagy initiation and degradation, and promoted oxidative damage and apoptosis in neurons. Effective measures should be taken to prevent and control the arsenic poisoning caused by realgar in the early stage, and this study provides a theoretical and practical basis for the rational use of drugs in the clinic.
雄黄作为一种常用的中药,具有药理和生物学作用。然而,其引起神经系统损伤的机制尚不清楚。本研究旨在阐明雄黄引起海马神经毒性的具体机制。Nrf2 是外源性毒物和氧化应激的重要受体。我们利用 p38 特异性抑制剂(SB20358)、ERK1/2 特异性抑制剂(PD98059)、JNK 特异性抑制剂(SP600125)和 AKT 特异性抑制剂(LY249002)建立相应的动物模型,探讨雄黄如何激活 Nrf2。我们在大鼠中建立了 Nrf2-shRNA 基因沉默模型和自噬特异性抑制剂处理模型,以进一步探讨雄黄诱导的神经毒性以及 Nrf2 在雄黄诱导的海马损伤中的作用。结果表明,雄黄通过血脑屏障进入脑组织,引起中枢神经系统毒性。具体机制是雄黄激活 MAPKs 和 AKT 信号分子,激活 Nrf2-Keap1-p62 正反馈信号轴,诱导异常自噬起始和降解,促进神经元的氧化损伤和凋亡。应采取有效措施预防和控制雄黄引起的砷中毒,本研究为临床合理用药提供了理论和实践基础。