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Neuronal mitochondrial amelioration by feeding acetyl-L-carnitine and lipoic acid to aged rats

Brain function declines with age and is associated with diminishing mitochondrial integrity. The neuronal mitochondrial ultrastructural changes of young (4 months) and old (21 months) F344 rats supplemented with two mitochondrial metabolites, acetyl-L-carnitine (ALCAR, 0.2%[wt/vol] in the drinking w...

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Autores principales: Aliev, Gjumrakch, Liu, Jiankang, Shenk, Justin C, Fischbach, Kathryn, Pacheco, Gerardo J, Chen, Shu G, Obrenovich, Mark E, Ward, Walter F, Richardson, Arlan G, Smith, Mark A, Gasimov, Eldar, Perry, George, Ames, Bruce N
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2790425/
https://www.ncbi.nlm.nih.gov/pubmed/18373733
http://dx.doi.org/10.1111/j.1582-4934.2008.00324.x
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author Aliev, Gjumrakch
Liu, Jiankang
Shenk, Justin C
Fischbach, Kathryn
Pacheco, Gerardo J
Chen, Shu G
Obrenovich, Mark E
Ward, Walter F
Richardson, Arlan G
Smith, Mark A
Gasimov, Eldar
Perry, George
Ames, Bruce N
author_facet Aliev, Gjumrakch
Liu, Jiankang
Shenk, Justin C
Fischbach, Kathryn
Pacheco, Gerardo J
Chen, Shu G
Obrenovich, Mark E
Ward, Walter F
Richardson, Arlan G
Smith, Mark A
Gasimov, Eldar
Perry, George
Ames, Bruce N
author_sort Aliev, Gjumrakch
collection PubMed
description Brain function declines with age and is associated with diminishing mitochondrial integrity. The neuronal mitochondrial ultrastructural changes of young (4 months) and old (21 months) F344 rats supplemented with two mitochondrial metabolites, acetyl-L-carnitine (ALCAR, 0.2%[wt/vol] in the drinking water) and R-α-lipoic acid (LA, 0.1%[wt/wt] in the chow), were analysed using qualitative and quantitative electron microscopy techniques. Two independent morphologists blinded to sample identity examined and scored all electron micrographs. Mitochondria were examined in each micrograph, and each structure was scored according to the degree of injury. Controls displayed an age-associated significant decrease in the number of intact mitochondria (P = 0.026) as well as an increase in mitochondria with broken cristae (P < 0.001) in the hippocampus as demonstrated by electron microscopic observations. Neuronal mitochondrial damage was associated with damage in vessel wall cells, especially vascular endothelial cells. Dietary supplementation of young and aged animals increased the proliferation of intact mitochondria and reduced the density of mitochondria associated with vacuoles and lipofuscin. Feeding old rats ALCAR and LA significantly reduced the number of severely damaged mitochondria (P = 0.02) and increased the number of intact mitochondria (P < 0.001) in the hippocampus. These results suggest that feeding ALCAR with LA may ameliorate age-associated mitochondrial ultrastructural decay and are consistent with previous studies showing improved brain function.
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spelling pubmed-27904252009-12-08 Neuronal mitochondrial amelioration by feeding acetyl-L-carnitine and lipoic acid to aged rats Aliev, Gjumrakch Liu, Jiankang Shenk, Justin C Fischbach, Kathryn Pacheco, Gerardo J Chen, Shu G Obrenovich, Mark E Ward, Walter F Richardson, Arlan G Smith, Mark A Gasimov, Eldar Perry, George Ames, Bruce N J Cell Mol Med Articles Brain function declines with age and is associated with diminishing mitochondrial integrity. The neuronal mitochondrial ultrastructural changes of young (4 months) and old (21 months) F344 rats supplemented with two mitochondrial metabolites, acetyl-L-carnitine (ALCAR, 0.2%[wt/vol] in the drinking water) and R-α-lipoic acid (LA, 0.1%[wt/wt] in the chow), were analysed using qualitative and quantitative electron microscopy techniques. Two independent morphologists blinded to sample identity examined and scored all electron micrographs. Mitochondria were examined in each micrograph, and each structure was scored according to the degree of injury. Controls displayed an age-associated significant decrease in the number of intact mitochondria (P = 0.026) as well as an increase in mitochondria with broken cristae (P < 0.001) in the hippocampus as demonstrated by electron microscopic observations. Neuronal mitochondrial damage was associated with damage in vessel wall cells, especially vascular endothelial cells. Dietary supplementation of young and aged animals increased the proliferation of intact mitochondria and reduced the density of mitochondria associated with vacuoles and lipofuscin. Feeding old rats ALCAR and LA significantly reduced the number of severely damaged mitochondria (P = 0.02) and increased the number of intact mitochondria (P < 0.001) in the hippocampus. These results suggest that feeding ALCAR with LA may ameliorate age-associated mitochondrial ultrastructural decay and are consistent with previous studies showing improved brain function. Blackwell Publishing Ltd 2009-02 2008-03-29 /pmc/articles/PMC2790425/ /pubmed/18373733 http://dx.doi.org/10.1111/j.1582-4934.2008.00324.x Text en © 2009 The Authors Journal compilation © 2009 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Articles
Aliev, Gjumrakch
Liu, Jiankang
Shenk, Justin C
Fischbach, Kathryn
Pacheco, Gerardo J
Chen, Shu G
Obrenovich, Mark E
Ward, Walter F
Richardson, Arlan G
Smith, Mark A
Gasimov, Eldar
Perry, George
Ames, Bruce N
Neuronal mitochondrial amelioration by feeding acetyl-L-carnitine and lipoic acid to aged rats
title Neuronal mitochondrial amelioration by feeding acetyl-L-carnitine and lipoic acid to aged rats
title_full Neuronal mitochondrial amelioration by feeding acetyl-L-carnitine and lipoic acid to aged rats
title_fullStr Neuronal mitochondrial amelioration by feeding acetyl-L-carnitine and lipoic acid to aged rats
title_full_unstemmed Neuronal mitochondrial amelioration by feeding acetyl-L-carnitine and lipoic acid to aged rats
title_short Neuronal mitochondrial amelioration by feeding acetyl-L-carnitine and lipoic acid to aged rats
title_sort neuronal mitochondrial amelioration by feeding acetyl-l-carnitine and lipoic acid to aged rats
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2790425/
https://www.ncbi.nlm.nih.gov/pubmed/18373733
http://dx.doi.org/10.1111/j.1582-4934.2008.00324.x
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