Reductive stress in mitochondria isolated from the carotid body of type 1 diabetic male Wistar rats.

IF 2.2 Q3 PHYSIOLOGY Physiological Reports Pub Date : 2024-09-01 DOI:10.14814/phy2.70016
Hector R Tejeda-Chavez, Sergio Montero, Alfredo Saavedra-Molina, Monica Lemus, Julio B Tejeda-Luna, Elena Roces de Alvarez-Buylla
{"title":"Reductive stress in mitochondria isolated from the carotid body of type 1 diabetic male Wistar rats.","authors":"Hector R Tejeda-Chavez, Sergio Montero, Alfredo Saavedra-Molina, Monica Lemus, Julio B Tejeda-Luna, Elena Roces de Alvarez-Buylla","doi":"10.14814/phy2.70016","DOIUrl":null,"url":null,"abstract":"<p><p>The carotid body (CB) senses changes in arterial O<sub>2</sub> partial pressure (pO<sub>2</sub>) and glucose levels; therefore, it is key for the detection of hypoxia and hypoglycemia. The CB has been suggested to detect pO<sub>2</sub> through an increase in reactive oxygen species (ROS) in the mitochondria. However, the mechanism protecting the chemoreceptor cells and their mitochondria from ROS and hyperglycemia is poorly understood. Here we measured glutathione levels in CB mitochondria of control and in streptozotocin (STZ)-induced type 1 diabetic male Wistar rats. We found a dramatic reduction in total glutathione from 11.45 ± 1.30 μmol/mg protein in control rats to 1.45 ± 0.31 μmol/mg protein in diabetic rats. However, the ratio of reduced to oxidized glutathione, a measure of the redox index, was increased in diabetic rats compared to controls. We conclude that the mitochondria of CB chemoreceptor cells in type 1 diabetic male Wistar rats were likely under glutathione-reducing stress.</p>","PeriodicalId":20083,"journal":{"name":"Physiological Reports","volume":"12 18","pages":"e70016"},"PeriodicalIF":2.2000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11410552/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiological Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14814/phy2.70016","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The carotid body (CB) senses changes in arterial O2 partial pressure (pO2) and glucose levels; therefore, it is key for the detection of hypoxia and hypoglycemia. The CB has been suggested to detect pO2 through an increase in reactive oxygen species (ROS) in the mitochondria. However, the mechanism protecting the chemoreceptor cells and their mitochondria from ROS and hyperglycemia is poorly understood. Here we measured glutathione levels in CB mitochondria of control and in streptozotocin (STZ)-induced type 1 diabetic male Wistar rats. We found a dramatic reduction in total glutathione from 11.45 ± 1.30 μmol/mg protein in control rats to 1.45 ± 0.31 μmol/mg protein in diabetic rats. However, the ratio of reduced to oxidized glutathione, a measure of the redox index, was increased in diabetic rats compared to controls. We conclude that the mitochondria of CB chemoreceptor cells in type 1 diabetic male Wistar rats were likely under glutathione-reducing stress.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
从 1 型糖尿病雄性 Wistar 大鼠颈动脉体中分离的线粒体中的还原应激。
颈动脉体(CB)能感知动脉血氧分压(pO2)和葡萄糖水平的变化,因此是检测缺氧和低血糖的关键。有人认为,CB 是通过线粒体中活性氧(ROS)的增加来检测 pO2 的。然而,保护化学感受器细胞及其线粒体免受 ROS 和高血糖影响的机制却鲜为人知。在这里,我们测量了对照组和链脲佐菌素(STZ)诱导的 1 型糖尿病雄性 Wistar 大鼠 CB 线粒体中的谷胱甘肽水平。我们发现总谷胱甘肽从对照组大鼠的 11.45 ± 1.30 μmol/mg 蛋白质急剧下降到糖尿病大鼠的 1.45 ± 0.31 μmol/mg 蛋白质。然而,与对照组相比,糖尿病大鼠还原型谷胱甘肽与氧化型谷胱甘肽的比率(衡量氧化还原指数的指标)有所增加。我们的结论是,1 型糖尿病雄性 Wistar 大鼠 CB 化学感受器细胞的线粒体很可能处于谷胱甘肽还原压力下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Physiological Reports
Physiological Reports PHYSIOLOGY-
CiteScore
4.20
自引率
4.00%
发文量
374
审稿时长
9 weeks
期刊介绍: Physiological Reports is an online only, open access journal that will publish peer reviewed research across all areas of basic, translational, and clinical physiology and allied disciplines. Physiological Reports is a collaboration between The Physiological Society and the American Physiological Society, and is therefore in a unique position to serve the international physiology community through quick time to publication while upholding a quality standard of sound research that constitutes a useful contribution to the field.
期刊最新文献
Exercise stress echocardiography shows impaired left ventricular function after hospitalization with COVID-19 without overt myocarditis: A pilot study. Diastolic dysfunction evaluation by cardiovascular magnetic resonance derived E, a, e': Comparison to echocardiography. Exploring the impact of occupational exposure: A study on cardiovascular autonomic functions of male gas station attendants in Sri Lanka. Physiologists as medical scientists: An early warning from the German academic system. Examining the effect of salbutamol use in ozone air pollution by people with exercise-induced bronchoconstriction.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1