S-Allyl-Cysteine Ameliorates Cirrhotic Portal Hypertension by Enhancing Lymphangiogenesis via a VEGF-C-Independent Manner.

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Tác giả: Min Chen, Qiang Fan, Haizhong Huo, Hongjie Li, Jiayun Lin, Guqing Luo, Meng Luo, Xiaoliang Qi, Guangbo Wu, Zhenghao Wu, Jiwei Yu, Chihao Zhang, Jinbo Zhao, Lei Zheng

Ngôn ngữ: eng

Ký hiệu phân loại: 553.453 Tin

Thông tin xuất bản: United States : Liver international : official journal of the International Association for the Study of the Liver , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 208855

BACKGROUND AND AIMS: Lymphangiogenesis is enhanced during the development of liver cirrhosis and portal hypertension (PHT). However, hepatic lymphatic vascular system is understudied in liver cirrhosis and PHT. Hydrogen sulfide (H METHODS: BDL rats with cholestatic liver cirrhosis and PHT were orally administrated with SAC at 100 or 200 mg/kg/day, as well as DL-propargylglycine (PAG) or MAZ-51 injections. Hemodynamic parameters were determined, and subsequent evaluations of liver fibrosis, intrahepatic vascular resistance (IHVR) and lymphangiogensis were performed. Human lymphatic endothelial cells (hLECs) were used for in vitro verification of prolymphangiogenic effects of SAC. RESULTS: SAC treatment significantly decreased PP and promoted endogenous H CONCLUSIONS: SAC significantly alleviated BDL-induced liver cirrhosis and PHT. Meanwhile, elevated H
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