Mahmoud Ayman M, Abd El-Twab Sanaa M
Physiology Division, Zoology Department, Faculty of Science, Beni-Suef University, Egypt.
Physiology Division, Zoology Department, Faculty of Science, Beni-Suef University, Egypt.
Biomed Pharmacother. 2017 Jul;91:303-311. doi: 10.1016/j.biopha.2017.04.073. Epub 2017 May 2.
Hexavalent chromium [Cr(VI)] is commonly used in industry, and is a proven toxin and carcinogen. However, the information regarding its neurotoxic mechanism is not completely understood. The present study was designed to scrutinize the possible protective effects of caffeic acid phenethyl ester (CAPE), a bioactive phenolic of propolis extract, on Cr(VI)-induced brain injury in rats, with an emphasis on the JAK/STAT signaling pathway. Rats received 2mg/kgKCrO and concurrently treated with 20mg/kg CAPE for 30 days. Cr(VI)-induced rats showed a significant increase in cerebral lipid peroxidation, nitric oxide and pro-inflammatory cytokines, with concomitantly declined antioxidants and acetylcholinesterase. CAPE attenuated oxidative stress and inflammation and enhanced antioxidant defenses in the cerebrum of rats. Cr(VI) significantly up-regulated JAK2, STAT3 and SOCS3, an effect that was reversed by CAPE. In conclusion, CAPE protects the brain against Cr(VI) toxicity through abrogation of oxidative stress, inflammation and down-regulation of JAK2/STAT3 signaling in a SOCS3-independent mechanism.
六价铬[Cr(VI)]在工业中广泛使用,是一种已被证实的毒素和致癌物。然而,关于其神经毒性机制的信息尚未完全明确。本研究旨在探讨蜂胶提取物中的生物活性酚类成分咖啡酸苯乙酯(CAPE)对Cr(VI)诱导的大鼠脑损伤可能具有的保护作用,重点关注JAK/STAT信号通路。大鼠接受2mg/kg K₂CrO₄处理,并同时给予20mg/kg CAPE,持续30天。Cr(VI)诱导的大鼠脑内脂质过氧化、一氧化氮和促炎细胞因子显著增加,同时抗氧化剂和乙酰胆碱酯酶水平下降。CAPE减轻了大鼠大脑中的氧化应激和炎症反应,并增强了抗氧化防御能力。Cr(VI)显著上调JAK2、STAT3和SOCS3,而CAPE可逆转这一效应。总之,CAPE通过消除氧化应激、炎症反应以及以不依赖SOCS3的机制下调JAK2/STAT3信号通路,保护大脑免受Cr(VI)毒性的影响。