Hypometabolic Responses to Chronic Hypoxia: A Potential Role for Membrane Lipids

Metabolic suppression is an essential strategy to cope with chronic hypoxia. This review examines the physiological processes used to survive in low oxygen environments. It proposes a novel mechanism–the <i>remodeling of membrane lipids</i>–to suppress ATP use and production. Temperature...

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Main Authors: Elie Farhat, Jean-Michel Weber
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Metabolites
Subjects:
Online Access:https://www.mdpi.com/2218-1989/11/8/503
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spelling doaj-9c39630bb2e14ed9bde073c78ef5d4612021-08-26T14:03:45ZengMDPI AGMetabolites2218-19892021-07-011150350310.3390/metabo11080503Hypometabolic Responses to Chronic Hypoxia: A Potential Role for Membrane LipidsElie Farhat0Jean-Michel Weber1Biology Department, University of Ottawa, Ottawa, ON K1N 6N5, CanadaBiology Department, University of Ottawa, Ottawa, ON K1N 6N5, CanadaMetabolic suppression is an essential strategy to cope with chronic hypoxia. This review examines the physiological processes used to survive in low oxygen environments. It proposes a novel mechanism–the <i>remodeling of membrane lipids</i>–to suppress ATP use and production. Temperature (homeoviscous adaptation), diet (natural doping in migrant birds) and body mass (membrane pacemaker of metabolism) have an impact on the lipid composition of membranes, which, in turn, modulates metabolic capacity. Vertebrate champions of hypoxia tolerance show extensive changes in membrane lipids upon in vivo exposure to low oxygen. These changes and those observed in hibernating mammals can promote the downregulation of ion pumps (major ATP consumers), ion channels, mitochondrial respiration capacity (state 3, proton leak, cytochrome c oxidase), and energy metabolism (β-oxidation and glycolysis). A common membrane signal regulating the joint inhibition of ion pumps and channels could be an exquisite way to preserve the balance between ATP supply and demand in hypometabolic states. Membrane remodeling together with more traditional mechanisms could work in concert to cause metabolic suppression.https://www.mdpi.com/2218-1989/11/8/503metabolic suppressionhypometabolismhypoxia tolerancelow oxygen stressmembrane remodelingcholesterol
collection DOAJ
language English
format Article
sources DOAJ
author Elie Farhat
Jean-Michel Weber
spellingShingle Elie Farhat
Jean-Michel Weber
Hypometabolic Responses to Chronic Hypoxia: A Potential Role for Membrane Lipids
Metabolites
metabolic suppression
hypometabolism
hypoxia tolerance
low oxygen stress
membrane remodeling
cholesterol
author_facet Elie Farhat
Jean-Michel Weber
author_sort Elie Farhat
title Hypometabolic Responses to Chronic Hypoxia: A Potential Role for Membrane Lipids
title_short Hypometabolic Responses to Chronic Hypoxia: A Potential Role for Membrane Lipids
title_full Hypometabolic Responses to Chronic Hypoxia: A Potential Role for Membrane Lipids
title_fullStr Hypometabolic Responses to Chronic Hypoxia: A Potential Role for Membrane Lipids
title_full_unstemmed Hypometabolic Responses to Chronic Hypoxia: A Potential Role for Membrane Lipids
title_sort hypometabolic responses to chronic hypoxia: a potential role for membrane lipids
publisher MDPI AG
series Metabolites
issn 2218-1989
publishDate 2021-07-01
description Metabolic suppression is an essential strategy to cope with chronic hypoxia. This review examines the physiological processes used to survive in low oxygen environments. It proposes a novel mechanism–the <i>remodeling of membrane lipids</i>–to suppress ATP use and production. Temperature (homeoviscous adaptation), diet (natural doping in migrant birds) and body mass (membrane pacemaker of metabolism) have an impact on the lipid composition of membranes, which, in turn, modulates metabolic capacity. Vertebrate champions of hypoxia tolerance show extensive changes in membrane lipids upon in vivo exposure to low oxygen. These changes and those observed in hibernating mammals can promote the downregulation of ion pumps (major ATP consumers), ion channels, mitochondrial respiration capacity (state 3, proton leak, cytochrome c oxidase), and energy metabolism (β-oxidation and glycolysis). A common membrane signal regulating the joint inhibition of ion pumps and channels could be an exquisite way to preserve the balance between ATP supply and demand in hypometabolic states. Membrane remodeling together with more traditional mechanisms could work in concert to cause metabolic suppression.
topic metabolic suppression
hypometabolism
hypoxia tolerance
low oxygen stress
membrane remodeling
cholesterol
url https://www.mdpi.com/2218-1989/11/8/503
work_keys_str_mv AT eliefarhat hypometabolicresponsestochronichypoxiaapotentialroleformembranelipids
AT jeanmichelweber hypometabolicresponsestochronichypoxiaapotentialroleformembranelipids
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