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积雪草苷通过 Toll 样受体 4 通路改善急性胰腺炎腺泡细胞坏死。

Asiaticoside ameliorates acinar cell necrosis in acute pancreatitis via toll-like receptor 4 pathway.

机构信息

Pancreatic Center, Department of Gastroenterology, Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, Jiangsu, 225009, PR China.

Department of Critical Care Medicine, PLA Key Laboratory of Emergency and Critical Care Research, Jinling Hospital, Medical School of Nanjing University, Nanjing, Jiangsu, 210000, PR China.

出版信息

Mol Immunol. 2021 Feb;130:122-132. doi: 10.1016/j.molimm.2020.11.018. Epub 2020 Dec 9.

Abstract

Acinar cell necrosis is one of the most prominent pathophysiological changes of acute pancreatitis (AP). Asiaticoside (AS) is a triterpene compound with confirmed apoptosis-and necrosis-related activities. However, the specific effects of AS on AP have not been determined. In this study, we aimed to investigate the protective effect of AS on AP using two mouse models. In the caerulein-induced mild acute pancreatitis (MAP) model, We found that AS administration reduced serum amylase levels and alleviated the histopathological manifestations of pancreatic tissue in a dose-dependent manner. And the levels of toll-like receptor 4 (TLR4) and necrotic related proteins (RIP3 and p-MLKL) of pancreatic tissue were reduced after AS administration. In addition, TLR4 deficiency eliminated the protective effect of AS on AP induced by caerulein in mice. Correspondingly, we elucidated the effect of AS in vitro and found that AS protected against pancreatic acinar cells necrosis and TAK-242 counteracted this protective effect. Meanwhile, we found that AS ameliorated the severity of pancreatic tissue injury and pancreatitis-associated lung injury in a severe acute pancreatitis model induced by l-arginine. Furthermore, Molecular docking results revealed interaction between AS and TLR4. Taken together, our data for the first time confirmed the protective effects of AS on AP in mice via TLR4 pathway.

摘要

腺泡细胞坏死是急性胰腺炎 (AP) 最显著的病理生理变化之一。积雪草苷 (AS) 是一种三萜化合物,已被证实具有凋亡和坏死相关活性。然而,AS 对 AP 的具体作用尚未确定。在本研究中,我们旨在使用两种小鼠模型研究 AS 对 AP 的保护作用。在胆酸钠诱导的轻度急性胰腺炎 (MAP) 模型中,我们发现 AS 给药可降低血清淀粉酶水平,并以剂量依赖性方式减轻胰腺组织的组织病理学表现。并且,AS 给药后胰腺组织中 Toll 样受体 4 (TLR4) 和坏死相关蛋白 (RIP3 和 p-MLKL) 的水平降低。此外,TLR4 缺乏消除了 AS 对胆酸钠诱导的小鼠 AP 的保护作用。相应地,我们阐明了 AS 在体外的作用,发现 AS 可防止胰腺腺泡细胞坏死,而 TAK-242 则拮抗这种保护作用。同时,我们发现 AS 可改善精氨酸诱导的严重急性胰腺炎模型中胰腺组织损伤和胰腺炎相关肺损伤的严重程度。此外,分子对接结果显示 AS 与 TLR4 之间存在相互作用。总之,我们的数据首次证实了 AS 通过 TLR4 通路对 AP 具有保护作用。

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