دورية أكاديمية

Targeting SIRT1 Rescues Age- and Obesity-Induced Microvascular Dysfunction in Ex Vivo Human Vessels

التفاصيل البيبلوغرافية
العنوان: Targeting SIRT1 Rescues Age- and Obesity-Induced Microvascular Dysfunction in Ex Vivo Human Vessels
المؤلفون: Mengozzi, Alessandro, Costantino, Sarah, Paneni, Francesco, Duranti, Emiliano, Nannipieri, Monica, Mancini, Rudj, Lai, Michele, La Rocca, Veronica, Puxeddu, Ilaria, Antonioli, Luca, Fornai, Matteo, Ghionzoli, Marco, Georgiopoulos, Georgios, Ippolito, Chiara, Bernardini, Nunzia, Ruschitzka, Frank, Pugliese, Nicola Riccardo, Taddei, Stefano, Virdis, Agostino, Masi, Stefano
المصدر: Mengozzi, Alessandro; Costantino, Sarah; Paneni, Francesco; Duranti, Emiliano; Nannipieri, Monica; Mancini, Rudj; Lai, Michele; La Rocca, Veronica; Puxeddu, Ilaria; Antonioli, Luca; Fornai, Matteo; Ghionzoli, Marco; Georgiopoulos, Georgios; Ippolito, Chiara; Bernardini, Nunzia; Ruschitzka, Frank; Pugliese, Nicola Riccardo; Taddei, Stefano; Virdis, Agostino; Masi, Stefano (2022). Targeting SIRT1 Rescues Age- and Obesity-Induced Microvascular Dysfunction in Ex Vivo Human Vessels. Circulation Research, 131(6):476-491.
بيانات النشر: Lippincott Williams & Wilkins
سنة النشر: 2022
المجموعة: University of Zurich (UZH): ZORA (Zurich Open Repository and Archive
مصطلحات موضوعية: Clinic for Cardiology, 610 Medicine & health
الوصف: ackground: Experimental evidence suggests a key role of SIRT1 (silent information regulator 1) in age- and metabolic-related vascular dysfunction. Whether these effects hold true in the human microvasculature is unknown. We aimed to investigate the SIRT1 role in very early stages of age- and obesity-related microvascular dysfunction in humans. Methods: Ninety-five subjects undergoing elective laparoscopic surgery were recruited and stratified based on their body mass index status (above or below 30 kg/m2) and age (above or below 40 years) in 4 groups: Young Nonobese, Young Obese, Old Nonobese, and Old Obese. We measured small resistance arteries' endothelial function by pressurized micromyography before and after incubation with a SIRT1 agonist (SRT1720) and a mitochondria reactive oxygen species (mtROS) scavenger (MitoTEMPO). We assessed vascular levels of mtROS and nitric oxide availability by confocal microscopy and vascular gene expression of SIRT1 and mitochondrial proteins by qPCR. Chromatin immunoprecipitation assay was employed to investigate SIRT1-dependent epigenetic regulation of mitochondrial proteins. Results: Compared with Young Nonobese, obese and older patients showed lower vascular expression of SIRT1 and antioxidant proteins (FOXO3 [forkhead box protein O3] and SOD2) and higher expression of pro-oxidant and aging mitochondria proteins p66Shc and Arginase II. Old Obese, Young Obese and Old Nonobese groups endothelial dysfunction was rescued by SRT1720. The restoration was comparable to the one obtained with mitoTEMPO. These effects were explained by SIRT1-dependent chromatin changes leading to reduced p66Shc expression and upregulation of proteins involved in mitochondria respiratory chain. Conclusions: SIRT1 is a novel central modulator of the earliest microvascular damage induced by age and obesity. Through a complex epigenetic control mainly involving p66Shc and Arginase II, it influences mtROS levels, NO availability, and the expression of proteins of the mitochondria respiratory chain. ...
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
تدمد: 0009-7330
العلاقة: https://www.zora.uzh.ch/id/eprint/229345/1/CIRCRESAHA.122.320888.pdfTest; info:pmid/35968712; urn:issn:0009-7330
DOI: 10.5167/uzh-229345
DOI: 10.1161/CIRCRESAHA.122.320888
الإتاحة: https://doi.org/10.5167/uzh-22934510.1161/CIRCRESAHA.122.320888Test
https://www.zora.uzh.ch/id/eprint/229345Test/
https://www.zora.uzh.ch/id/eprint/229345/1/CIRCRESAHA.122.320888.pdfTest
حقوق: info:eu-repo/semantics/openAccess ; Creative Commons: Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) ; http://creativecommons.org/licenses/by-nc-nd/4.0Test/
رقم الانضمام: edsbas.6DC55582
قاعدة البيانات: BASE
الوصف
تدمد:00097330
DOI:10.5167/uzh-229345