Age-Dependent Alterations in Platelet Mitochondrial Respiration

Mitochondrial dysfunction is an important cellular hallmark of aging and neurodegeneration. Platelets are a useful model to study the systemic manifestations of mitochondrial dysfunction. To evaluate the age dependence of mitochondrial parameters, citrate synthase activity, respiratory chain complex...

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Main Authors: Zdeněk Fišar, Jana Hroudová, Martina Zvěřová, Roman Jirák, Jiří Raboch, Eva Kitzlerová
Format: Article
Language:English
Published: MDPI AG 2023-05-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/11/6/1564
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author Zdeněk Fišar
Jana Hroudová
Martina Zvěřová
Roman Jirák
Jiří Raboch
Eva Kitzlerová
author_facet Zdeněk Fišar
Jana Hroudová
Martina Zvěřová
Roman Jirák
Jiří Raboch
Eva Kitzlerová
author_sort Zdeněk Fišar
collection DOAJ
description Mitochondrial dysfunction is an important cellular hallmark of aging and neurodegeneration. Platelets are a useful model to study the systemic manifestations of mitochondrial dysfunction. To evaluate the age dependence of mitochondrial parameters, citrate synthase activity, respiratory chain complex activity, and oxygen consumption kinetics were assessed. The effect of cognitive impairment was examined by comparing the age dependence of mitochondrial parameters in healthy individuals and those with neuropsychiatric disease. The study found a significant negative slope of age-dependence for both the activity of individual mitochondrial enzymes (citrate synthase and complex II) and parameters of mitochondrial respiration in intact platelets (routine respiration, maximum capacity of electron transport system, and respiratory rate after complex I inhibition). However, there was no significant difference in the age-related changes of mitochondrial parameters between individuals with and without cognitive impairment. These findings highlight the potential of measuring mitochondrial respiration in intact platelets as a means to assess age-related mitochondrial dysfunction. The results indicate that drugs and interventions targeting mitochondrial respiration may have the potential to slow down or eliminate certain aging and neurodegenerative processes. Mitochondrial respiration in platelets holds promise as a biomarker of aging, irrespective of the degree of cognitive impairment.
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spelling doaj.art-3d2fb26ba6394849b0a29661dda1730f2023-11-18T09:25:07ZengMDPI AGBiomedicines2227-90592023-05-01116156410.3390/biomedicines11061564Age-Dependent Alterations in Platelet Mitochondrial RespirationZdeněk Fišar0Jana Hroudová1Martina Zvěřová2Roman Jirák3Jiří Raboch4Eva Kitzlerová5Department of Psychiatry, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 11, 120 00 Prague, Czech RepublicDepartment of Psychiatry, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 11, 120 00 Prague, Czech RepublicDepartment of Psychiatry, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 11, 120 00 Prague, Czech RepublicDepartment of Psychiatry, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 11, 120 00 Prague, Czech RepublicDepartment of Psychiatry, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 11, 120 00 Prague, Czech RepublicDepartment of Psychiatry, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 11, 120 00 Prague, Czech RepublicMitochondrial dysfunction is an important cellular hallmark of aging and neurodegeneration. Platelets are a useful model to study the systemic manifestations of mitochondrial dysfunction. To evaluate the age dependence of mitochondrial parameters, citrate synthase activity, respiratory chain complex activity, and oxygen consumption kinetics were assessed. The effect of cognitive impairment was examined by comparing the age dependence of mitochondrial parameters in healthy individuals and those with neuropsychiatric disease. The study found a significant negative slope of age-dependence for both the activity of individual mitochondrial enzymes (citrate synthase and complex II) and parameters of mitochondrial respiration in intact platelets (routine respiration, maximum capacity of electron transport system, and respiratory rate after complex I inhibition). However, there was no significant difference in the age-related changes of mitochondrial parameters between individuals with and without cognitive impairment. These findings highlight the potential of measuring mitochondrial respiration in intact platelets as a means to assess age-related mitochondrial dysfunction. The results indicate that drugs and interventions targeting mitochondrial respiration may have the potential to slow down or eliminate certain aging and neurodegenerative processes. Mitochondrial respiration in platelets holds promise as a biomarker of aging, irrespective of the degree of cognitive impairment.https://www.mdpi.com/2227-9059/11/6/1564agingplateletmitochondriarespiratory chain complexmitochondrial respirationcognitive decline
spellingShingle Zdeněk Fišar
Jana Hroudová
Martina Zvěřová
Roman Jirák
Jiří Raboch
Eva Kitzlerová
Age-Dependent Alterations in Platelet Mitochondrial Respiration
Biomedicines
aging
platelet
mitochondria
respiratory chain complex
mitochondrial respiration
cognitive decline
title Age-Dependent Alterations in Platelet Mitochondrial Respiration
title_full Age-Dependent Alterations in Platelet Mitochondrial Respiration
title_fullStr Age-Dependent Alterations in Platelet Mitochondrial Respiration
title_full_unstemmed Age-Dependent Alterations in Platelet Mitochondrial Respiration
title_short Age-Dependent Alterations in Platelet Mitochondrial Respiration
title_sort age dependent alterations in platelet mitochondrial respiration
topic aging
platelet
mitochondria
respiratory chain complex
mitochondrial respiration
cognitive decline
url https://www.mdpi.com/2227-9059/11/6/1564
work_keys_str_mv AT zdenekfisar agedependentalterationsinplateletmitochondrialrespiration
AT janahroudova agedependentalterationsinplateletmitochondrialrespiration
AT martinazverova agedependentalterationsinplateletmitochondrialrespiration
AT romanjirak agedependentalterationsinplateletmitochondrialrespiration
AT jiriraboch agedependentalterationsinplateletmitochondrialrespiration
AT evakitzlerova agedependentalterationsinplateletmitochondrialrespiration