{"title":"鸡胸肌和大腿肌中铁中毒相关基因表达及氧化应激水平的差异。","authors":"Tomonori Nakanishi , Jun Wakamatsu , Saki Nemoto , Akihiro Yamamoto , Laurie Erickson , Satoshi Kawahara","doi":"10.1016/j.cbpa.2025.111919","DOIUrl":null,"url":null,"abstract":"<div><div>Ferroptosis is an iron-dependent regulated cell death characterized by lipid peroxidation. In the skeletal muscle of mammals, where oxidative stress plays an important role in lipid peroxidation, ferroptosis is involved in various diseases and aging. However, the role of ferroptosis in avian skeletal muscle remains underexplored. This study investigated the gene expression of glutathione peroxidase 4 (<em>GPX4</em>) and other ferroptosis-related genes, along with oxidative stress markers in chicken skeletal muscles, focusing on the breast (pectoralis major) and thigh (iliotibialis lateralis) muscles. Gene expression was analyzed using quantitative reverse transcription polymerase chain reaction. Lipid peroxidation and oxidative stress were evaluated by measuring malondialdehyde (MDA), a lipid peroxidation byproduct, and by evaluating the ratio of reduced glutathione (GSH) to oxidized glutathione (GSSG). Our results showed that <em>GPX4</em> gene expression was significantly higher in the thigh muscle compared to the breast muscle. Ferroptosis suppressor protein 1 (<em>FSP1</em>) expression was also higher in the thigh muscle, while ferritin heavy chain 1 (<em>FTH1</em>) expression was lower in the thigh muscle than in the breast muscle. In contrast, lipid peroxidation, indicated by MDA levels, was higher in the breast muscle, correlating with a lower GSH/GSSG ratio, indicating that the breast muscle is more susceptible to ferroptosis than the thigh muscle. Additionally, the expression of <em>FSP1</em> and <em>FTH1</em> showed significant correlations with oxidative stress markers, highlighting their roles in regulating ferroptosis in avian skeletal muscle. This study provides insights into the molecular mechanisms of ferroptosis in avian skeletal muscle, suggesting that regulatory processes may vary between muscle types.</div></div>","PeriodicalId":55237,"journal":{"name":"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology","volume":"309 ","pages":"Article 111919"},"PeriodicalIF":2.2000,"publicationDate":"2025-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Differences in expression of ferroptosis-related genes and oxidative stress level between chicken breast and thigh muscles\",\"authors\":\"Tomonori Nakanishi , Jun Wakamatsu , Saki Nemoto , Akihiro Yamamoto , Laurie Erickson , Satoshi Kawahara\",\"doi\":\"10.1016/j.cbpa.2025.111919\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Ferroptosis is an iron-dependent regulated cell death characterized by lipid peroxidation. In the skeletal muscle of mammals, where oxidative stress plays an important role in lipid peroxidation, ferroptosis is involved in various diseases and aging. However, the role of ferroptosis in avian skeletal muscle remains underexplored. This study investigated the gene expression of glutathione peroxidase 4 (<em>GPX4</em>) and other ferroptosis-related genes, along with oxidative stress markers in chicken skeletal muscles, focusing on the breast (pectoralis major) and thigh (iliotibialis lateralis) muscles. Gene expression was analyzed using quantitative reverse transcription polymerase chain reaction. Lipid peroxidation and oxidative stress were evaluated by measuring malondialdehyde (MDA), a lipid peroxidation byproduct, and by evaluating the ratio of reduced glutathione (GSH) to oxidized glutathione (GSSG). Our results showed that <em>GPX4</em> gene expression was significantly higher in the thigh muscle compared to the breast muscle. Ferroptosis suppressor protein 1 (<em>FSP1</em>) expression was also higher in the thigh muscle, while ferritin heavy chain 1 (<em>FTH1</em>) expression was lower in the thigh muscle than in the breast muscle. In contrast, lipid peroxidation, indicated by MDA levels, was higher in the breast muscle, correlating with a lower GSH/GSSG ratio, indicating that the breast muscle is more susceptible to ferroptosis than the thigh muscle. Additionally, the expression of <em>FSP1</em> and <em>FTH1</em> showed significant correlations with oxidative stress markers, highlighting their roles in regulating ferroptosis in avian skeletal muscle. This study provides insights into the molecular mechanisms of ferroptosis in avian skeletal muscle, suggesting that regulatory processes may vary between muscle types.</div></div>\",\"PeriodicalId\":55237,\"journal\":{\"name\":\"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology\",\"volume\":\"309 \",\"pages\":\"Article 111919\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-08-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1095643325001187\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1095643325001187","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Differences in expression of ferroptosis-related genes and oxidative stress level between chicken breast and thigh muscles
Ferroptosis is an iron-dependent regulated cell death characterized by lipid peroxidation. In the skeletal muscle of mammals, where oxidative stress plays an important role in lipid peroxidation, ferroptosis is involved in various diseases and aging. However, the role of ferroptosis in avian skeletal muscle remains underexplored. This study investigated the gene expression of glutathione peroxidase 4 (GPX4) and other ferroptosis-related genes, along with oxidative stress markers in chicken skeletal muscles, focusing on the breast (pectoralis major) and thigh (iliotibialis lateralis) muscles. Gene expression was analyzed using quantitative reverse transcription polymerase chain reaction. Lipid peroxidation and oxidative stress were evaluated by measuring malondialdehyde (MDA), a lipid peroxidation byproduct, and by evaluating the ratio of reduced glutathione (GSH) to oxidized glutathione (GSSG). Our results showed that GPX4 gene expression was significantly higher in the thigh muscle compared to the breast muscle. Ferroptosis suppressor protein 1 (FSP1) expression was also higher in the thigh muscle, while ferritin heavy chain 1 (FTH1) expression was lower in the thigh muscle than in the breast muscle. In contrast, lipid peroxidation, indicated by MDA levels, was higher in the breast muscle, correlating with a lower GSH/GSSG ratio, indicating that the breast muscle is more susceptible to ferroptosis than the thigh muscle. Additionally, the expression of FSP1 and FTH1 showed significant correlations with oxidative stress markers, highlighting their roles in regulating ferroptosis in avian skeletal muscle. This study provides insights into the molecular mechanisms of ferroptosis in avian skeletal muscle, suggesting that regulatory processes may vary between muscle types.
期刊介绍:
Part A: Molecular & Integrative Physiology of Comparative Biochemistry and Physiology. This journal covers molecular, cellular, integrative, and ecological physiology. Topics include bioenergetics, circulation, development, excretion, ion regulation, endocrinology, neurobiology, nutrition, respiration, and thermal biology. Study on regulatory mechanisms at any level of organization such as signal transduction and cellular interaction and control of behavior are also published.