» Articles » PMID: 27143418

Age- and Brain Region-specific Differences in Mitochondrial Bioenergetics in Brown Norway Rats

Overview
Journal Neurobiol Aging
Publisher Elsevier
Date 2016 May 5
PMID 27143418
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

Mitochondria are central regulators of energy homeostasis and play a pivotal role in mechanisms of cellular senescence. The objective of the present study was to evaluate mitochondrial bioenergetic parameters in 5 brain regions (brain stem [BS], frontal cortex, cerebellum, striatum, hippocampus [HIP]) of 4 diverse age groups (1 month [young], 4 months [adult], 12 months [middle-aged], 24 months [old age]) to understand age-related differences in selected brain regions and their possible contribution to age-related chemical sensitivity. Mitochondrial bioenergetic parameters and enzyme activities were measured under identical conditions across multiple age groups and brain regions in Brown Norway rats (n = 5/group). The results indicate age- and brain region-specific patterns in mitochondrial functional endpoints. For example, an age-specific decline in ATP synthesis (State III respiration) was observed in BS and HIP. Similarly, the maximal respiratory capacities (State V1 and V2) showed age-specific declines in all brain regions examined (young > adult > middle-aged > old age). Amongst all regions, HIP had the greatest change in mitochondrial bioenergetics, showing declines in the 4, 12, and 24-months age groups. Activities of mitochondrial pyruvate dehydrogenase complex and electron transport chain complexes I, II, and IV enzymes were also age and brain region specific. In general, changes associated with age were more pronounced with enzyme activities declining as the animals aged (young > adult > middle-aged > old age). These age- and brain region-specific observations may aid in evaluating brain bioenergetic impact on the age-related susceptibility to environmental chemical stressors.

Citing Articles

Intrinsic aerobic capacity modulates Alzheimer's disease pathological hallmarks, brain mitochondrial function and proteome during aging.

Kugler B, Lysaker C, Franczak E, Hauger B, Csikos V, Stopperan J Geroscience. 2024; 46(5):4955-4967.

PMID: 38867031 PMC: 11336007. DOI: 10.1007/s11357-024-01248-3.


Long-Term Region-Specific Mitochondrial Functionality Changes in Both Cerebral Hemispheres after fMCAo Model of Ischemic Stroke.

Bahire K, Maluhins R, Bello F, Upite J, Makarovs A, Jansone B Antioxidants (Basel). 2024; 13(4).

PMID: 38671864 PMC: 11047464. DOI: 10.3390/antiox13040416.


Daily fluctuations in blood glucose with normal aging are inversely related to hippocampal synaptic mitochondrial proteins.

Braunstein P, Horovitz D, Hampton A, Hollis F, Newman L, Enos R Aging Brain. 2024; 5:100116.

PMID: 38596458 PMC: 11002859. DOI: 10.1016/j.nbas.2024.100116.


A long-term ketogenic diet in young and aged rats has dissociable effects on prelimbic cortex and CA3 ensemble activity.

Hernandez A, Barrett M, Lubke K, Maurer A, Burke S Front Aging Neurosci. 2023; 15:1274624.

PMID: 38155737 PMC: 10753023. DOI: 10.3389/fnagi.2023.1274624.


Age-Dependent Alterations in Platelet Mitochondrial Respiration.

Fisar Z, Hroudova J, Zverova M, Jirak R, Raboch J, Kitzlerova E Biomedicines. 2023; 11(6).

PMID: 37371659 PMC: 10295145. DOI: 10.3390/biomedicines11061564.