番石榴果肉对胆汁淤积性肝损伤的保护作用。

ISRN hepatology Pub Date : 2013-11-17 eCollection Date: 2013-01-01 DOI:10.1155/2013/601071
Jian Peng, Chunyan Yue, Kai Qiu, Jie Chen, Maria-Angeles Aller, Kwang Suk Ko, Heping Yang
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引用次数: 3

摘要

背景。胆汁淤积性肝损伤是与氧化应激变化和炎症有关的慢性肝病的主要原因;因此,富含抗氧化和抗炎症化合物的番石榴可能在防止胆汁淤积性肝损伤中起关键作用。我们的目的是研究番石榴浆(GP)是否对胆汁淤积性肝损伤小鼠模型和白细胞介素-6 (IL-6)介导的QBC939胆管癌细胞增殖具有保护作用。方法。采用左、中胆管结扎术(LMBDL)诱导小鼠胆汁淤积性肝损伤,并给予GP治疗。采集血浆和肝脏标本进行生化和病理分析。采用5-溴-2'-脱氧尿苷(BrdU)法和Western blot检测QBC939细胞的增殖和基因表达。结果。与LMBDL组比较,gp处理小鼠的谷丙转氨酶(ALT)、胆红素水平降低,胆道上皮细胞增殖和肝纤维化受到抑制,Src/MEK/ erk1 /c-Myc通路及转化生长因子β1(TGF-β1)、金属蛋白酶组织抑制剂TIMP、前胶原1α1(COL1α1)表达明显下调。此外,GP提取物还降低了il -6增强的QBC939细胞增殖、p-ERK和c-Myc表达。结论。GP可能为胆汁淤积性肝损伤的治疗提供新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Protective Effects of Guava Pulp on Cholestatic Liver Injury.

Protective Effects of Guava Pulp on Cholestatic Liver Injury.

Protective Effects of Guava Pulp on Cholestatic Liver Injury.

Protective Effects of Guava Pulp on Cholestatic Liver Injury.

Background. Cholestatic liver injury is a leading cause of chronic liver diseases involved with oxidative stress changes and inflammation; thus, antioxidant and anti-inflammation compound-rich guava may play a pivotal role in protecting against the cholestatic liver damages. Our aims for this study are to determine whether guava pulp (GP) has protective effects on cholestatic liver injury-induced mouse model and on interleukin-6 (IL-6) mediated proliferation of QBC939 cholangiocarcinoma cell line. Methods. Mice were induced to cholestatic liver damage by left and median bile duct ligation (LMBDL) surgery and then treated with GP. Plasma and liver samples were collected for biochemical and pathological assays. 5-Bromo-2'-deoxyuridine (BrdU) assay and Western blots were used to detect proliferation and gene expression in QBC939 cells, respectively. Results. Compared with LMBDL only group, in GP-treated mice, the levels of alanine aminotransferase (ALT) and bilirubin decreased, biliary epithelial cell proliferation and liver fibrogenesis were suppressed, Src/MEK/ERK1/2/c-Myc pathway and expressions of transforming growth factor β1(TGF-β1), tissue inhibitor of metalloproteinases TIMP), and procollagen 1α1(COL1α1) were downregulated significantly. Moreover, the GP extract reduced IL-6-enhanced QBC939 cell proliferation, p-ERK, and c-Myc expression as well. Conclusions. GP may provide a new perspective for the treatment of cholestatic liver injury.

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