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Metabolic and Energy Imbalance in Dysglycemia-Based Chronic Disease

Metabolic flexibility is the ability to efficiently adapt metabolism based on nutrient availability and requirement that is essential to maintain homeostasis in times of either caloric excess or restriction and during the energy-demanding state. This regulation is orchestrated in multiple organ syst...

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Autores principales: Kalra, Sanjay, Unnikrishnan, Ambika Gopalakrishnan, Baruah, Manash P, Sahay, Rakesh, Bantwal, Ganapathi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816219/
https://www.ncbi.nlm.nih.gov/pubmed/33488105
http://dx.doi.org/10.2147/DMSO.S286888
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author Kalra, Sanjay
Unnikrishnan, Ambika Gopalakrishnan
Baruah, Manash P
Sahay, Rakesh
Bantwal, Ganapathi
author_facet Kalra, Sanjay
Unnikrishnan, Ambika Gopalakrishnan
Baruah, Manash P
Sahay, Rakesh
Bantwal, Ganapathi
author_sort Kalra, Sanjay
collection PubMed
description Metabolic flexibility is the ability to efficiently adapt metabolism based on nutrient availability and requirement that is essential to maintain homeostasis in times of either caloric excess or restriction and during the energy-demanding state. This regulation is orchestrated in multiple organ systems by the alliance of numerous metabolic pathways under the master control of the insulin-glucagon-sympathetic neuro-endocrine axis. This, in turn, regulates key metabolic enzymes and transcription factors, many of which interact closely with and culminate in the mitochondrial energy generation machinery. Metabolic flexibility is compromised due to the continuous mismatch between availability and intake of calorie-dense foods and reduced metabolic demand due to sedentary lifestyle and age-related metabolic slowdown. The resultant nutrient overload leads to mitochondrial trafficking of substrates manifesting as mitochondrial dysfunction characterized by ineffective substrate switching and incomplete substrate utilization. At the systemic level, the manifestation of metabolic inflexibility comprises reduced skeletal muscle glucose disposal rate, impaired suppression of hepatic gluconeogenesis and adipose tissue lipolysis manifesting as insulin resistance. This is compounded by impaired β-cell function and progressively reduced β-cell mass. A consequence of insulin resistance is the upregulation of the mitogen-activated protein kinase pathway leading to a pro-hypertensive, atherogenic, and thrombogenic environment. This is further aggravated by oxidative stress, advanced glycation end products, and inflammation, which potentiates the risk of micro- and macro-vascular complications. This review aims to elucidate underlying mechanisms mediating the onset of metabolic inflexibility operating at the main target organs and to understand the progression of metabolic diseases. This could potentially translate into a pharmacological tool that can manage multiple interlinked conditions of dysglycemia, hypertension, and dyslipidemia by restoring metabolic flexibility. We discuss the breadth and depth of metabolic flexibility and its impact on health and disease.
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spelling pubmed-78162192021-01-21 Metabolic and Energy Imbalance in Dysglycemia-Based Chronic Disease Kalra, Sanjay Unnikrishnan, Ambika Gopalakrishnan Baruah, Manash P Sahay, Rakesh Bantwal, Ganapathi Diabetes Metab Syndr Obes Review Metabolic flexibility is the ability to efficiently adapt metabolism based on nutrient availability and requirement that is essential to maintain homeostasis in times of either caloric excess or restriction and during the energy-demanding state. This regulation is orchestrated in multiple organ systems by the alliance of numerous metabolic pathways under the master control of the insulin-glucagon-sympathetic neuro-endocrine axis. This, in turn, regulates key metabolic enzymes and transcription factors, many of which interact closely with and culminate in the mitochondrial energy generation machinery. Metabolic flexibility is compromised due to the continuous mismatch between availability and intake of calorie-dense foods and reduced metabolic demand due to sedentary lifestyle and age-related metabolic slowdown. The resultant nutrient overload leads to mitochondrial trafficking of substrates manifesting as mitochondrial dysfunction characterized by ineffective substrate switching and incomplete substrate utilization. At the systemic level, the manifestation of metabolic inflexibility comprises reduced skeletal muscle glucose disposal rate, impaired suppression of hepatic gluconeogenesis and adipose tissue lipolysis manifesting as insulin resistance. This is compounded by impaired β-cell function and progressively reduced β-cell mass. A consequence of insulin resistance is the upregulation of the mitogen-activated protein kinase pathway leading to a pro-hypertensive, atherogenic, and thrombogenic environment. This is further aggravated by oxidative stress, advanced glycation end products, and inflammation, which potentiates the risk of micro- and macro-vascular complications. This review aims to elucidate underlying mechanisms mediating the onset of metabolic inflexibility operating at the main target organs and to understand the progression of metabolic diseases. This could potentially translate into a pharmacological tool that can manage multiple interlinked conditions of dysglycemia, hypertension, and dyslipidemia by restoring metabolic flexibility. We discuss the breadth and depth of metabolic flexibility and its impact on health and disease. Dove 2021-01-15 /pmc/articles/PMC7816219/ /pubmed/33488105 http://dx.doi.org/10.2147/DMSO.S286888 Text en © 2021 Kalra et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Kalra, Sanjay
Unnikrishnan, Ambika Gopalakrishnan
Baruah, Manash P
Sahay, Rakesh
Bantwal, Ganapathi
Metabolic and Energy Imbalance in Dysglycemia-Based Chronic Disease
title Metabolic and Energy Imbalance in Dysglycemia-Based Chronic Disease
title_full Metabolic and Energy Imbalance in Dysglycemia-Based Chronic Disease
title_fullStr Metabolic and Energy Imbalance in Dysglycemia-Based Chronic Disease
title_full_unstemmed Metabolic and Energy Imbalance in Dysglycemia-Based Chronic Disease
title_short Metabolic and Energy Imbalance in Dysglycemia-Based Chronic Disease
title_sort metabolic and energy imbalance in dysglycemia-based chronic disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816219/
https://www.ncbi.nlm.nih.gov/pubmed/33488105
http://dx.doi.org/10.2147/DMSO.S286888
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