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荔枝核总黄酮通过调控视黄醇代谢抗 CCl4 诱导的大鼠肝纤维化

Anti-liver fibrosis effects of the total flavonoids of litchi semen on CCl-induced liver fibrosis in rats associated with the upregulation of retinol metabolism.

机构信息

College of Pharmacy, Guangxi University of Chinese Medicine, Nanning, China.

School of Health, Wuzhou Vocational College, Wuzhou, China.

出版信息

Pharm Biol. 2022 Dec;60(1):1264-1277. doi: 10.1080/13880209.2022.2086584.

Abstract

CONTEXT

The litchi semen are traditional medications for treating liver fibrosis (LF) in China. The mechanism remains unclear.

OBJECTIVE

This study investigates the anti-liver fibrotic mechanism of the total flavonoids of litchi semen (TFL).

MATERIALS AND METHODS

Sprague-Dawley rats with carbon tetrachloride-induced LF were treated with TFL (50 and 100 mg/kg) for 4 weeks. The anti-liver fibrotic effects of TFL were evaluated and the underlying mechanisms were investigated via histopathological analysis, proteomic analysis and molecular biology technology.

RESULTS

Significant anti-LF effects were observed in the high-TFL-dose group (TFL-H,  < 0.05). Five hundred and eighty-five and 95 differentially expressed proteins (DEPs) were identified in the LF rat model (M group) and TFL-H group, respectively. The DEPs were significantly enriched in the retinol metabolism pathway ( < 0.0001). The content of 9--retinoic acid (0.93 ± 0.13 vs. 0.66 ± 0.10,  < 0.05, vs. the M group) increased significantly in the TFL-H group. The upregulation of RXRα (0.50 ± 0.05 vs. 0.27 ± 0.13 protein,  < 0.05), ALDH2 (1.24 ± 0.09 vs. 1.04 ± 0.08 protein,  < 0.05), MMP3 (0.89 ± 0.02 vs. 0.61 ± 0.12 protein,  < 0.05), Aldh1a7 (0.20 ± 0.03 vs. 0.03 ± 0.00 mRNA,  < 0.05) and Aox3 (0.72 ± 0.14 vs. 0.05 ± 0.01 mRNA,  < 0.05) after TFL treatment was verified.

CONCLUSIONS

TFL exhibited good anti-liver fibrotic effects, which may be related to the upregulation of the retinol metabolism pathway. TFL may be promising anti-LF agents with potential clinical application prospects.

摘要

背景

荔枝核是中国传统治疗肝纤维化(LF)的药物。其作用机制尚不清楚。

目的

本研究旨在探讨荔枝核总黄酮(TFL)的抗肝纤维化机制。

材料和方法

采用四氯化碳诱导的 LF 大鼠模型,给予 TFL(50 和 100mg/kg)治疗 4 周。通过组织病理学分析、蛋白质组学分析和分子生物学技术评估 TFL 的抗肝纤维化作用,并探讨其作用机制。

结果

高剂量 TFL 组(TFL-H,<0.05)显示出显著的抗 LF 作用。LF 大鼠模型(M 组)和 TFL-H 组分别鉴定出 585 个和 95 个差异表达蛋白(DEPs)。DEPs 显著富集在视黄醇代谢途径中(<0.0001)。TFL-H 组 9--视黄酸(0.93±0.13 对 0.66±0.10,<0.05,与 M 组相比)含量显著增加。RXRα(0.50±0.05 对 0.27±0.13 蛋白,<0.05)、ALDH2(1.24±0.09 对 1.04±0.08 蛋白,<0.05)、MMP3(0.89±0.02 对 0.61±0.12 蛋白,<0.05)、Aldh1a7(0.20±0.03 对 0.03±0.00mRNA,<0.05)和 Aox3(0.72±0.14 对 0.05±0.01mRNA,<0.05)经 TFL 治疗后上调。

结论

TFL 表现出良好的抗肝纤维化作用,可能与视黄醇代谢途径的上调有关。TFL 可能是一种有前途的抗 LF 药物,具有潜在的临床应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39a/9262366/230e340eb898/IPHB_A_2086584_F0001_C.jpg

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