Institute of Life Science and Bio-pharmaceutics, Shenyang Pharmaceutical University, Shenyang, Liaoning, China.
Biochem Biophys Res Commun. 2011 Nov 11;415(1):152-6. doi: 10.1016/j.bbrc.2011.10.039. Epub 2011 Oct 18.
Liver fibrosis represents a process of healing and scarring in response to chronic liver injury. Augmenter of liver regeneration (ALR) has been shown to protect hepatocytes from various toxins. The aim of this study was to investigate the effects of ALR gene therapy on liver injury and fibrosis induced by CCl(4) in rats and further explore the underlying mechanisms. Human ALR expression plasmid was delivered via the tail vein. ALR gene therapy might protect the liver from CCl(4)-induced injury and fibrogenesis by attenuating the mitochondrial dysfunction, suppressing oxidative stress, and inhibiting activation of HSCs. This report demonstrated that ALR gene therapy protected against the ATP loss, increased the activity of ATPase, decreased intrahepatic reactive oxygen species level, and down-regulated transforming growth factor-β1, platelet-derived growth factor-BB, and α-smooth muscle actin expression. Following gene transfer liver function tests were significantly improved. In brief, ALR gene therapy might be an effective therapeutic reagent for liver fibrosis with potential clinical applications.
肝纤维化是一种肝脏对慢性损伤的修复和瘢痕形成过程。肝再生增强因子(ALR)已被证明可保护肝细胞免受各种毒素的侵害。本研究旨在探讨 ALR 基因治疗对 CCl(4)诱导的大鼠肝损伤和纤维化的影响,并进一步探讨其潜在机制。通过尾静脉递送人 ALR 表达质粒。ALR 基因治疗可能通过减轻线粒体功能障碍、抑制氧化应激和抑制 HSCs 的激活来保护肝脏免受 CCl(4)诱导的损伤和纤维化。本报告表明,ALR 基因治疗可防止 ATP 丢失,增加 ATP 酶活性,降低肝内活性氧水平,并下调转化生长因子-β1、血小板衍生生长因子-BB 和α-平滑肌肌动蛋白的表达。基因转染后肝功能明显改善。总之,ALR 基因治疗可能是一种有效的肝纤维化治疗试剂,具有潜在的临床应用价值。