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金雀异黄素补充对运动诱导的小鼠肝脏和骨骼肌炎症及氧化应激的影响。

Effect of Genistein Supplementation on Exercise-Induced Inflammation and Oxidative Stress in Mice Liver and Skeletal Muscle.

机构信息

Graduate School of Sport Sciences, Waseda University, Tokorozawa 359-1192, Japan.

Faculty of Sport Sciences, Waseda University, Tokorozawa 359-1192, Japan.

出版信息

Medicina (Kaunas). 2021 Sep 27;57(10):1028. doi: 10.3390/medicina57101028.

DOI:10.3390/medicina57101028
PMID:34684067
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8537361/
Abstract

: The purpose of this study was to investigate the influences of oral high-dose genistein (GE) administration on exercise-induced oxidative stress, inflammatory response and tissue damage. : Thirty-two mice were randomly divided into control group (Con; sedentary/0.5% CMC-Na), GE administrated group (GE; sedentary/GE dosed), exercise group (Ex; exercise/0.5% CMC-Na), or GE administrated plus exercise group (GE + Ex; exercise/GE dosed), mice in the GE and GE + Ex group were given GE orally at the dose of 200 mg/kg weight. : Plasma aspartate aminotransferase (AST), alanine aminotransferase (ALT) levels, liver interleukin (IL)-6, IL-1β, superoxide dismutase 1 (), catalase (), hemeoxygenase-1 () gene expression levels and skeletal muscle IL-6, nuclear factor erythroid 2-related factor (), and gene expression levels increased immediately after exhaustive exercise. GE supplementation increased liver protein carbonyl concentrations. On the other hand, GE supplementation significantly decreased , gene expression levels in the liver and , and gene expression levels in the skeletal muscles. : Acute exercise induced organ damage, inflammation, and oxidative stress in skeletal muscles and the liver. However, a single dose of GE supplementation before exercise did not lead to favorable antioxidant and anti-inflammatory effects in this study.

摘要

: 本研究旨在探讨口服高剂量金雀异黄素(GE)对运动诱导的氧化应激、炎症反应和组织损伤的影响。 : 32 只小鼠随机分为对照组(Con;静息/0.5% CMC-Na)、GE 给药组(GE;静息/GE 给药)、运动组(Ex;运动/0.5% CMC-Na)或 GE 给药加运动组(GE + Ex;运动/GE 给药),GE 和 GE + Ex 组小鼠口服给予 200mg/kg 体重的 GE。 : 运动后即刻,血浆天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)水平、肝脏白细胞介素(IL)-6、IL-1β、超氧化物歧化酶 1()、过氧化氢酶()、血红素加氧酶-1()基因表达水平以及骨骼肌白细胞介素(IL)-6、核因子红细胞 2 相关因子()和基因表达水平均升高。GE 补充剂增加了肝脏蛋白羰基浓度。另一方面,GE 补充剂显著降低了肝脏和骨骼肌中的、基因表达水平。 : 急性运动导致肌肉和肝脏的器官损伤、炎症和氧化应激。然而,在本研究中,运动前单次给予 GE 补充剂并没有产生有利的抗氧化和抗炎作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/2f9e28c9dca2/medicina-57-01028-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/f9f76a8d6e37/medicina-57-01028-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/090af48f0291/medicina-57-01028-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/88d3195c722c/medicina-57-01028-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/e9bf58f838cb/medicina-57-01028-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/b97aee9e6ea3/medicina-57-01028-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/9462cc3c1bb9/medicina-57-01028-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/2f9e28c9dca2/medicina-57-01028-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/f9f76a8d6e37/medicina-57-01028-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/090af48f0291/medicina-57-01028-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/0800076ce494/medicina-57-01028-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/dc36a275395f/medicina-57-01028-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/32c9c30a7b6c/medicina-57-01028-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/88d3195c722c/medicina-57-01028-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/e9bf58f838cb/medicina-57-01028-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/b97aee9e6ea3/medicina-57-01028-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/9462cc3c1bb9/medicina-57-01028-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fd/8537361/2f9e28c9dca2/medicina-57-01028-g010.jpg

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