1. Academic Validation
  2. Escin Sodium Improves the Prognosis of Acute Pancreatitis via Promoting Cell Apoptosis by Suppression of the ERK/STAT3 Signaling Pathway

Escin Sodium Improves the Prognosis of Acute Pancreatitis via Promoting Cell Apoptosis by Suppression of the ERK/STAT3 Signaling Pathway

  • Oxid Med Cell Longev. 2021 Aug 12:2021:9921839. doi: 10.1155/2021/9921839.
Qian Zhang 1 Chen Zhao 2 Lei Zhang 3 Kai Sun 4 Linlin Yu 5 Xianming Wang 4 Lei Ren 4 Nan Zhang 3 Chengyu Chen 6 Ju Liu 7 Haimei Wang 3 Hu Tian 4
Affiliations

Affiliations

  • 1 Department of General Surgery, Shandong Provincial Qianfoshan Hospital, Shandong University of Traditional Chinese Medicine, China.
  • 2 Weihai Hospital Affiliated to Shandong University of Traditional Chinese Medicine, No. 29, Qingdao North Road, Huancui District, Weihai City Shandong Province, China.
  • 3 College of First Clinical Medicine, Shandong University of Traditional Chinese Medicine, 16369 Jingshi Road, Lixia District, Jinan City, Shandong Province, China.
  • 4 Department of General Surgery, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, No. 16766, Jingshi Road, Jinan City, Shandong Province, China.
  • 5 Shandong Hospital of Traditional Chinese Medicine Affiliated to Shandong University of Traditional Chinese Medicine, 16369 Jingshi Road, Lixia District, Jinan City, Shandong Province, China.
  • 6 Department of Thoracic Surgery, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, No. 16766, Jingshi Road, Jinan City, Shandong Province, China.
  • 7 Laboratory of Microvascular Medicine and Medical Research Center, Shandong Provincial Qianfoshan Hospital, The First Affiliated Hospital of Shandong First Medical University, No. 16766, Jingshi Road, Jinan City, Shandong Province, China.
Abstract

Acute pancreatitis (AP), an inflammatory disorder of the pancreas, can cause systemic inflammatory responses. Escin Sodium (ES), a natural mixture of triterpene saponins extracted from the dry ripe fruit of Fructus Aesculi or horse chestnut crude, has been demonstrated to have antiedematous, anti-inflammatory, and antiexudative effects. We here aim to investigate the effects of ES pretreatment on AP in vivo and in vitro and explore its potential molecular mechanism. In the present study, we demonstrated that ES pretreatment could apparently decrease amylase and Lipase, downregulate inflammatory cytokines, and attenuate pancreatic damage. Additionally, the increased expression of apoptotic-related proteins and the results of flow cytometry demonstrated the effects of ES on promoting Apoptosis in acinar cells. Moreover, ES could enhance mitochondrial membrane potential (MMP, ΔΨm) and Reactive Oxygen Species (ROS) level and reduce intracellular calcium concentration, which are closely related to mitochondrial-mediated death. The effect of ES pretreatment on acinar cell Apoptosis was furtherly confirmed by the regulatory pathway of the ERK/STAT3 axis. These results suggest that ES attenuates the severity of AP by enhancing cell Apoptosis via suppressing the ERK/STAT3 signaling pathway. These findings provide evidence for ES which is treated as a novel and potent therapeutic for the treatment of AP.

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