Optimal intervention time of ADSCs for hepatic ischemia-reperfusion combined with partial resection injury in rats

• Published in: Life sciences (1973) 2021-11, Vol.285, p.119986-119986, Article 119986
• Main Authors: Piao, Chenxi, Zhang, Qianzhen, Xu, Jiayuan, Wang, Yue, Liu, Tao, Ma, Haiyang, Liu, Guodong, Wang, Hongbin
• Format: Article
• Language: English
• Subjects: ADSCs; Antioxidants; Cytokines; Gene expression; Hepatectomy; Hepatic ischemia reperfusion injury; Hepatocytes; IL-1β; Inflammation; Injuries; Interleukin 6; Intervention time; Ischemia; Liver; Liver transplantation; Microenvironments; mRNA; Oxidative stress; Paracrine signalling; Protein expression; Proteins; Rats; Recovery; Recovery of function; Reperfusion; Stem cell transplantation; Stem cells; Surgery; Tissues; Transplantation; Tumor necrosis factor-α; Western blotting; Windows (intervals)
• ISSN: 0024-3205; 1879-0631
• DOI: 10.1016/j.lfs.2021.119986

Hepatic ischemia reperfusion injury (HIRI) is a complication of liver surgery and liver transplantation. Adipose-derived stem cells (ADSCs) can inhibit oxidative stress and inflammation through a paracrine effect. This study aimed to determine the optimal time window of ADSCs transplantation to restore liver function after HIRI. A rat model of hepatic ischemia reperfusion combined with partial hepatectomy (HIR/PH) was established. The animals were injected intravenously with 2 × 106 rat ADSCs 2 h before, immediately after, or 6 h after surgery. Liver tissues and blood samples were collected for routine histological and biochemical assays. The molecular changes were analyzed by qRT-PCR and western blotting. ADSCs significantly improved liver tissue structure and decreased the levels of AST, ALT and ALP, which was indicative of functional recovery. In addition, transplantation of ADSCs immediately after operation decreased the levels of inflammation-related cytokines such as TNF-α, IL-1β and IL-6, and significantly increased the activity of antioxidant enzymes. At the same time, the expression of MDA was decreased. Mechanistically, ADSCs activated the Keap1/Nrf2 pathway in the injured liver. Transplantation of ADSCs pre- and 6 h post-operation did not significantly affect some indices such as mRNA and protein expression of HO-1, and protein expression of NQO1. Transplanting ADSCs immediately after surgery accelerated tissue repair and functional recovery of the liver by activating the Keap1/Nrf2 pathway, which inhibited hepatic inflammation and oxidative stress, and restored the hepatic microenvironment.