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  4. Dysregulation of mitochondrial function and biogenesis modulators in adipose tissue of obese children
 
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Dysregulation of mitochondrial function and biogenesis modulators in adipose tissue of obese children

Journal
International Journal of Obesity
ISSN
0307-0565
1476-5497
Date Issued
2017
Author(s)
Zamora-Mendoza, R.
Rosas-Vargas, H.
Ramos-Cervantes, M. T.
García-Zúñiga, P.
Pérez-Lorenzana, H.
Mendoza-Lorenzo, Patricia
Miliar-García, A.
Facultad de Ciencias de la Salud - CampCM  
Lara-Padilla, E.
Estrada Mena, Francisco Javier  
Ceballos, Guillermo
Facultad de Ciencias de la Salud - CampCM  
Rodríguez, Alonso
Villarreal, Francisco J.
Ramírez-Sánchez, Israel
Type
Resource Types::text::journal::journal article
DOI
10.1038/ijo.2017.274
URL
https://scripta.up.edu.mx/handle/20.500.12552/2248
Abstract
Background/Objectives: We aimed to evaluate mitochondrial biogenesis (MB), structure, metabolism and dysfunction in abdominal adipose tissue from male pediatric patients with obesity. Subjects/Methods: Samples were collected from five children with obesity (percentile ⩾95) and five eutrophic boys (percentile ⩾5/⩽85) (8–12 years old) following parental informed consent. We analyzed the expression of key genes involved in MB (sirtuin-1 (SIRT1), peroxisome proliferator-activated receptor-γ (PPARγ), PPARγ coactivator-1α (PGC1α), nuclear respiratory factors 1 and 2 (NRF1, NRF2) and mitochondrial transcription factor A (TFAM) and surrogates for mitochondrial function/structure/metabolism (porin, TOMM20, complex I and V, UCP1, UCP2, SIRT3, SOD2) by western blot. Citrate synthase (CS), complex I (CI) activity, adenosine triphosphate (ATP) levels, mitochondrial DNA (mtDNA) content and oxidative stress end points were also determined.

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