TY - JOUR
T1 - Mitochondrial dysfunction and oxidative stress in metabolic disorders — A step towards mitochondria based therapeutic strategies
AU - Bhatti, Jasvinder Singh
AU - Bhatti, Gurjit Kaur
AU - Reddy, P. Hemachandra
N1 - Funding Information:
Work presented in this article is supported by NIH grants AG042178, AG047812 and the Garrison Family Foundation. Dr. Jasvinder Singh Bhatti is financially supported by the University Grants Commission, India under Raman Post-Doctoral Research Fellowship in USA [F.No. 5-82/2016 (IC)].
Funding Information:
Work presented in this article is supported by NIH grants AG042178 , AG047812 and the Garrison Family Foundation . Dr. Jasvinder Singh Bhatti is financially supported by the University Grants Commission, India under Raman Post-Doctoral Research Fellowship in USA [F.No. 5-82/2016 (IC)].
Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2017/5/1
Y1 - 2017/5/1
N2 - Mitochondria are the powerhouses of the cell and are involved in essential functions of the cell, including ATP production, intracellular Ca2 + regulation, reactive oxygen species production & scavenging, regulation of apoptotic cell death and activation of the caspase family of proteases. Mitochondrial dysfunction and oxidative stress are largely involved in aging, cancer, age-related neurodegenerative and metabolic syndrome. In the last decade, tremendous progress has been made in understanding mitochondrial structure, function and their physiology in metabolic syndromes such as diabetes, obesity, stroke and hypertension, and heart disease. Further, progress has also been made in developing therapeutic strategies, including lifestyle interventions (healthy diet and regular exercise), pharmacological strategies and mitochondria-targeted approaches. These strategies were mainly focused to reduce mitochondrial dysfunction and oxidative stress and to maintain mitochondrial quality in metabolic syndromes. The purpose of our article is to highlight the recent progress on the mitochondrial role in metabolic syndromes and also summarize the progress of mitochondria-targeted molecules as therapeutic targets to treat metabolic syndromes. This article is part of a Special Issue entitled: Oxidative Stress and Mitochondrial Quality in Diabetes/Obesity and Critical Illness Spectrum of Diseases - edited by P. Hemachandra Reddy.
AB - Mitochondria are the powerhouses of the cell and are involved in essential functions of the cell, including ATP production, intracellular Ca2 + regulation, reactive oxygen species production & scavenging, regulation of apoptotic cell death and activation of the caspase family of proteases. Mitochondrial dysfunction and oxidative stress are largely involved in aging, cancer, age-related neurodegenerative and metabolic syndrome. In the last decade, tremendous progress has been made in understanding mitochondrial structure, function and their physiology in metabolic syndromes such as diabetes, obesity, stroke and hypertension, and heart disease. Further, progress has also been made in developing therapeutic strategies, including lifestyle interventions (healthy diet and regular exercise), pharmacological strategies and mitochondria-targeted approaches. These strategies were mainly focused to reduce mitochondrial dysfunction and oxidative stress and to maintain mitochondrial quality in metabolic syndromes. The purpose of our article is to highlight the recent progress on the mitochondrial role in metabolic syndromes and also summarize the progress of mitochondria-targeted molecules as therapeutic targets to treat metabolic syndromes. This article is part of a Special Issue entitled: Oxidative Stress and Mitochondrial Quality in Diabetes/Obesity and Critical Illness Spectrum of Diseases - edited by P. Hemachandra Reddy.
KW - Cardiovascular disease
KW - Metabolic syndrome
KW - Mitochondria
KW - Mitochondria-targeted antioxidants
KW - Obesity
KW - Oxidative stress
KW - Pre-diabetes
KW - Reactive oxygen species
KW - Type-2-diabetes
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U2 - 10.1016/j.bbadis.2016.11.010
DO - 10.1016/j.bbadis.2016.11.010
M3 - Review article
C2 - 27836629
AN - SCOPUS:85006809796
SN - 0925-4439
VL - 1863
SP - 1066
EP - 1077
JO - Biochimica et Biophysica Acta - Molecular Basis of Disease
JF - Biochimica et Biophysica Acta - Molecular Basis of Disease
IS - 5
ER -