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清络通痹方通过改善脂肪酸 β-氧化和线粒体生物合成对 诱导的小鼠肝损伤的保护作用。

Protective effect of Qingluotongbi formula against induced liver injury in mice by improving fatty acid β-oxidation and mitochondrial biosynthesis.

机构信息

The First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, China.

The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, China.

出版信息

Pharm Biol. 2023 Dec;61(1):80-88. doi: 10.1080/13880209.2022.2157842.

Abstract

CONTEXT

Qingluotongbi formula (QLT) is a Chinese medicine compound consisting of Hook. f. (Celastraceae, TW), (Burkill) F.H.Chen (Araliaceae, PN), (Gaertn.) DC. (Orobanchaceae, RG), (Thunb.) Rehder & E.H. Wilson (Menispermaceae, SA), and L. (Bombycidae, BM).

OBJECTIVE

This study investigated the protective effect and possible mechanism of QLT against TW-induced liver injury in mice.

MATERIALS AND METHODS

To establish the model of TW-induced liver injury in mice, C57BL/6J mice were randomly divided into 4 groups: control group, low-dose TW group, middle-dose TW group, and high-dose TW group. To observe the effects of QLT and its individual ingredients against TW-induced liver injury, C57BL/6J mice were randomly divided into 7 groups: control group, TW group, QLT group, PN group, RG group, SA group, BM group.After administration for 7 days, C57BL/6J mice were tested for biochemical indicators and liver pathological changes. Then, we evaluated the mitochondrial function and analysed the gene and protein expression related to the peroxisome proliferator-activated receptor alpha (PPARα)/peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1α) pathway by quantitative real-time PCR (qRT-PCR) and Western blotting.

RESULTS

Compared with the control group (0.30 ± 0.35), TW significantly increased mice liver histological score (L, 0.95 ± 1.14; M, 1.25 ± 1.16; H, 4.00 ± 1.13). QLT and its ingredients significantly improved the pathology scores (CON, 0.63 ± 0.74; TW, 4.19 ± 1.53; QLT, 1.56 ± 0.62; PN, 1.94 ± 0.68; RG, 2.75 ± 1.39; SA, 4.13 ± 0.99; BM, 4.13 ± 0.99). Western blot and qRT-PCR analysis revealed that QLT and its ingredients reversed TW-induced suppression of PPARα/PGC1-α pathway.Discussion and conclusions: These findings provide valuable information for compound compatibility studies and TW clinical applications.

摘要

背景

青藤碱配方(QLT)是一种中药复方,由钩藤(Celastraceae,TW)、两面针(Burkill)F.H.Chen(Araliaceae,PN)、徐长卿(Gaertn.)DC.(Orobanchaceae,RG)、鸡血藤(Thunb.)Rehder & E.H. Wilson(Menispermaceae,SA)和甘草(L.)(Bombycidae,BM)组成。

目的

本研究旨在探讨 QLT 对 TW 诱导的小鼠肝损伤的保护作用及其可能机制。

材料和方法

为建立 TW 诱导的小鼠肝损伤模型,将 C57BL/6J 小鼠随机分为 4 组:对照组、低剂量 TW 组、中剂量 TW 组和高剂量 TW 组。为观察 QLT 及其单体成分对 TW 诱导的肝损伤的影响,将 C57BL/6J 小鼠随机分为 7 组:对照组、TW 组、QLT 组、PN 组、RG 组、SA 组、BM 组。给药 7 天后,检测 C57BL/6J 小鼠的生化指标和肝组织病理学变化。然后,通过实时定量 PCR(qRT-PCR)和 Western blot 评估线粒体功能,并分析与过氧化物酶体增殖物激活受体α(PPARα)/过氧化物酶体增殖物激活受体γ共激活因子 1α(PGC-1α)通路相关的基因和蛋白表达。

结果

与对照组(0.30±0.35)相比,TW 显著增加了小鼠肝组织学评分(L,0.95±1.14;M,1.25±1.16;H,4.00±1.13)。QLT 及其成分显著改善了病理评分(CON,0.63±0.74;TW,4.19±1.53;QLT,1.56±0.62;PN,1.94±0.68;RG,2.75±1.39;SA,4.13±0.99;BM,4.13±0.99)。Western blot 和 qRT-PCR 分析显示,QLT 及其成分逆转了 TW 诱导的 PPARα/PGC1-α 通路抑制。

讨论与结论

这些发现为复方配伍研究和 TW 的临床应用提供了有价值的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb6/9788700/e5730ec730aa/IPHB_A_2157842_F0001_C.jpg

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