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Combined physical exercise reverses the reduced expression of Bmal1 in the liver of aged mice.
Pinto, Ana P; Muñoz, Vitor R; Tavares, Maria Eduarda A; Dos Santos, Jonathas R; Rebelo, Macario A; Alberici, Luciane C; Simabuco, Fernando M; Teixeira, Giovana R; Pauli, José R; de Moura, Leandro P; Cintra, Dennys E; Ropelle, Eduardo R; Freitas, Ellen C; Rivas, Donato A; da Silva, Adelino S R.
Afiliação
  • Pinto AP; School of Physical Education and Sport of Ribeirão Preto, University of São Paulo (USP), Ribeirão Preto, São Paulo, Brazil.
  • Muñoz VR; School of Physical Education and Sport of Ribeirão Preto, University of São Paulo (USP), Ribeirão Preto, São Paulo, Brazil.
  • Tavares MEA; Multicentric Program of Postgraduate in Physiological Sciences, São Paulo State University (UNESP), School of Dentistry of Araçatuba, Araçatuba, São Paulo, Brazil.
  • Dos Santos JR; Department of Biomolecular Sciences, School of Pharmaceutical Sciences of Ribeirao Preto, University of Sao Paulo-FCFRP USP, Ribeirao Preto, Sao Paulo, Brazil.
  • Rebelo MA; Department of Pharmacology, Faculty of Medicinal Sciences, University of Campinas, State University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.
  • Alberici LC; Department of Biomolecular Sciences, School of Pharmaceutical Sciences of Ribeirao Preto, University of Sao Paulo-FCFRP USP, Ribeirao Preto, Sao Paulo, Brazil.
  • Simabuco FM; Laboratory of Molecular Biology of Exercise (LaBMEx), School of Applied Sciences, University of Campinas (UNICAMP), Limeira, São Paulo, Brazil; Department of Biochemistry, Federal University of São Paulo (UNIFESP), Brazil.
  • Teixeira GR; Multicentric Program of Postgraduate in Physiological Sciences, São Paulo State University (UNESP), School of Dentistry of Araçatuba, Araçatuba, São Paulo, Brazil; Department of Physical Education, State University of São Paulo (UNESP), Presidente Prudente, São Paulo, Brazil.
  • Pauli JR; Laboratory of Molecular Biology of Exercise (LaBMEx), School of Applied Sciences, University of Campinas (UNICAMP), Limeira, São Paulo, Brazil.
  • de Moura LP; Laboratory of Molecular Biology of Exercise (LaBMEx), School of Applied Sciences, University of Campinas (UNICAMP), Limeira, São Paulo, Brazil.
  • Cintra DE; Laboratory of Molecular Biology of Exercise (LaBMEx), School of Applied Sciences, University of Campinas (UNICAMP), Limeira, São Paulo, Brazil.
  • Ropelle ER; Laboratory of Molecular Biology of Exercise (LaBMEx), School of Applied Sciences, University of Campinas (UNICAMP), Limeira, São Paulo, Brazil.
  • Freitas EC; School of Physical Education and Sport of Ribeirão Preto, University of São Paulo (USP), Ribeirão Preto, São Paulo, Brazil; Department of Health Sciences, Medical School, University of Sao Paulo, Ribeirao Preto, Sao Paulo, Brazil.
  • Rivas DA; Nutrition, Exercise, Physiology, and Sarcopenia Laboratory, Tufts University, Boston, MA 02111, United States of America.
  • da Silva ASR; School of Physical Education and Sport of Ribeirão Preto, University of São Paulo (USP), Ribeirão Preto, São Paulo, Brazil; Postgraduate Program in Rehabilitation and Functional Performance, Ribeirão Preto Medical School, University of São Paulo (USP), Ribeirão Preto, São Paulo, Brazil. Electronic a
Life Sci ; 312: 121175, 2023 Jan 01.
Article em En | MEDLINE | ID: mdl-36414092
Aging can modify the morphology and function of the liver, such as generating a decrease in the mitochondria content, autophagy, and cell senescence. Although exercise training has several beneficial effects on hepatic metabolism, its actions on autophagy processes, mitochondrial function, and cellular senescence need to be more widely explored. The present study verified the effects of aging and exercise on hepatic circadian markers, autophagy, and mitochondria activity in 24-month-old mice with a combined exercise training protocol. In addition, we used public datasets from human livers in several conditions and BMAL1 knockout mice. C57BL/6 mice were distributed into Control (CT, young, 6-month-old mice), sedentary old (Old Sed, sedentary, 24-month-old mice), and exercised old (Old Ex, 24-month-old mice submitted to a combined exercise training protocol). The exercise training protocol consisted of three days of endurance exercise - treadmill running, and two days of resistance exercise - climbing a ladder, for three weeks. At the end of the protocol, the liver was removed and prepared for histological analysis, reverse transcription-quantitative polymerase chain reaction (RT-qPCR), immunoblotting technique, and oxygen consumption. Heatmaps were built using a human dataset and Bmal1 knockout samples. In summary, the Old Sed had reduced strength, coordination, and balance, as well as a decrease in Bmal1 expression and the presence of degenerated liver cells. Still, this group upregulated the transcription factors related to mitochondrial biogenesis. The Old Ex group had increased strength, coordination, and balance, improved glucose sensitivity, as well as restored Bmal1 expression and the mitochondrial transcription factors. The human datasets indicated that mitochondrial markers and autophagy strongly correlate with specific liver diseases but not aging. We can speculate that mitochondrial and autophagy molecular markers alterations may depend on long-term training.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Condicionamento Físico Animal / Fatores de Transcrição ARNTL / Fígado Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Condicionamento Físico Animal / Fatores de Transcrição ARNTL / Fígado Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil