Department of Pathophysiology, Basic Medical College, Chongqing Medical University, Chongqing, China.
Laboratory of Stem Cell and Tissue Engineering, Chongqing Medical University, Chongqing, China.
Transplant Proc. 2022 Sep;54(7):1992-1997. doi: 10.1016/j.transproceed.2022.04.024. Epub 2022 Jul 25.
Hepatic ischemia-reperfusion injury (HIRI) is a serious situation with high morbidity and mortality, which is usually accompanied with hyperlactatemia due to impaired lactate clearance in liver. G-protein-coupled receptor 81 (GPR81) has recently been identified as the bioactive receptor of lactate. GPR81 is profoundly involved in the modulation of metabolism and inflammation, but its significance in HIRI remains unclear. The present study investigated the potential roles of GPR81 in HIRI by using the GPR81 agonist 3-chloro-5-hydroxybenzoic acid (CHBA). The results indicated that treatment with CHBA had no obvious effects on HIRI-induced histologic abnormalities and elevation of serum aspartate aminotransferase, alanine aminotransferase. However, CHBA significantly upregulated the serum level of tumor necrosis factor alpha and interleukin-6 in mice with HIRI. Administration of CHBA also exacerbated HIRI-induced histologic lesions in lung, increased the level of myeloperoxidase in lung tissue and the protein concentration in bronchoalveolar lavage fluid. In addition, the serum levels of brain natriuretic peptide and creatinine also increased in CHBA-treated mice. The results indicate that activation of GPR81 might aggravate HIRI-induced remote organ injury and result in serious outcomes.
肝缺血再灌注损伤(HIRI)是一种严重的情况,发病率和死亡率都很高,通常伴有高乳酸血症,因为肝脏清除乳酸的能力受损。G 蛋白偶联受体 81(GPR81)最近被确定为乳酸的生物活性受体。GPR81 深刻地参与了代谢和炎症的调节,但它在 HIRI 中的意义尚不清楚。本研究通过使用 GPR81 激动剂 3-氯-5-羟基苯甲酸(CHBA)来研究 GPR81 在 HIRI 中的潜在作用。结果表明,CHBA 处理对 HIRI 诱导的组织学异常和血清天冬氨酸转氨酶、丙氨酸转氨酶升高没有明显影响。然而,CHBA 显著上调了 HIRI 小鼠血清中肿瘤坏死因子-α和白细胞介素-6 的水平。CHBA 的给药还加重了 HIRI 诱导的肺组织学损伤,增加了肺组织髓过氧化物酶的水平和支气管肺泡灌洗液中的蛋白浓度。此外,CHBA 处理的小鼠血清中脑钠肽和肌酐的水平也升高了。结果表明,GPR81 的激活可能加重 HIRI 诱导的远隔器官损伤,并导致严重后果。