Akanda Md Rashedunnabi, Kim In-Shik, Ahn Dongchoon, Tae Hyun-Jin, Tian Weishun, Nam Hyeon-Hwa, Choo Byung-Kil, Park Byung-Yong
College of Veterinary Medicine and Biosafety Research Institute, Chonbuk National University, Iksan 54596, Republic of Korea.
Department of Pharmacology and Toxicology, Sylhet Agricultural University, Sylhet 3100, Bangladesh.
Evid Based Complement Alternat Med. 2017;2017:8137627. doi: 10.1155/2017/8137627. Epub 2017 Jul 5.
(GK) is an indigenous Chinese herbal medicine widely used for the treatment of various inflammation and liver disorders. However, the exact mechanism of action of GK remains unknown. This study aimed to investigate the protective effect and related molecular mechanism of GK on NaAsO-induced cytotoxicity in HepG2 cells and liver damage in mice. The cytoprotective role of GK was assessed on HepG2 cells using MTT assay. Oxidative stress and lactate dehydrogenase levels were measured with ROS and LDH assay. Histopathology and serum enzymes levels were estimated. The molecular mechanism was evaluated by qPCR and immunoblotting to ensure the hepatoprotective role of GK against NaAsO intoxication in mice. We found cotreatment with GK significantly attenuated NaAsO-induced cell viability loss, intracellular ROS, and LDH release. Hepatic histopathology and serum biochemical parameters, ALT, and AST were notably improved by cotreatment with GK. Beside, GK markedly altered both mRNA and protein expression level of MAPK. The proapoptotic and antiapoptotic protein Bax/Bcl-2 ratio was significantly regulated by GK. Moreover, GK remarkably suppressed the postapoptotic transcription protein cleaved caspase-3 expression. The present study reveals that GK possesses hepatoprotective activity which is probably involved in the modulation of the MAPK/caspase-3 pathway.
绞股蓝(GK)是一种中国本土草药,广泛用于治疗各种炎症和肝脏疾病。然而,GK的确切作用机制尚不清楚。本研究旨在探讨GK对NaAsO诱导的HepG2细胞毒性和小鼠肝损伤的保护作用及相关分子机制。采用MTT法评估GK对HepG2细胞的细胞保护作用。通过ROS和LDH测定法测量氧化应激和乳酸脱氢酶水平。评估组织病理学和血清酶水平。通过qPCR和免疫印迹评估分子机制,以确保GK对小鼠NaAsO中毒的肝脏保护作用。我们发现,与GK共同处理可显著减轻NaAsO诱导的细胞活力丧失、细胞内ROS和LDH释放。与GK共同处理可显著改善肝脏组织病理学和血清生化参数、ALT和AST。此外,GK显著改变了MAPK的mRNA和蛋白质表达水平。GK显著调节促凋亡和抗凋亡蛋白Bax/Bcl-2的比率。此外,GK显著抑制凋亡后转录蛋白裂解的caspase-3表达。本研究表明,GK具有肝脏保护活性,可能参与了MAPK/caspase-3途径的调节。