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Cellular assessment of muscle in COPD: case studies of two males

The objective of this paper is to provide an overview of the recent developments in muscle physiology and biochemistry in general, and with respect to chronic obstructive pulmonary disease (COPD) specifically. As a way of illustration, we have presented data on the remodeling that occurs in vastus l...

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Autores principales: Green, Howard J, Bombardier, Eric, Burnett, Margaret E, D’Arsigny, Christine L, Iqbal, Sobia, Webb, Katherine A, Ouyang, Jing, O’Donnell, Denis E
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2840564/
https://www.ncbi.nlm.nih.gov/pubmed/20360908
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author Green, Howard J
Bombardier, Eric
Burnett, Margaret E
D’Arsigny, Christine L
Iqbal, Sobia
Webb, Katherine A
Ouyang, Jing
O’Donnell, Denis E
author_facet Green, Howard J
Bombardier, Eric
Burnett, Margaret E
D’Arsigny, Christine L
Iqbal, Sobia
Webb, Katherine A
Ouyang, Jing
O’Donnell, Denis E
author_sort Green, Howard J
collection PubMed
description The objective of this paper is to provide an overview of the recent developments in muscle physiology and biochemistry in general, and with respect to chronic obstructive pulmonary disease (COPD) specifically. As a way of illustration, we have presented data on the remodeling that occurs in vastus lateralis in two patients with COPD (COPD #1, forced expiratory volume in one second/forced vital capacity [FEV(1)/FVC] = 63%; COPD #2, FEV(1)/FVC = 41%) exhibiting differences in muscle wasting as compared to healthy controls (CON; FEV(1)/FVC = 111 ± 2.2%, n = 4). Type I fibers percentages were lower in both COPD #1 (16.7) and COPD #2 (24.9) compared to CON (57.3 ± 5.2). Cross sectional area of the type I fibers of the patients ranged between 65%–68% of CON and for the type II subtypes (IIA, IIAX, IIX) between 74% and 89% (COPD #1) and 17%–32% (COPD #2). A lower number of capillary contacts were observed for all fiber types in COPD #1 but not COPD #2. Lower concentrations of adenosine triphosphate (ATP) (24%–26%) and phosphocreatine (18%–20%), but not lactate occurred in COPD. In contrast to COPD #1, who displayed normal glucose transporter content, GLUT1 and GLUT4 were only 71% and 54%, respectively of CON in COPD #2. Lower monocarboxylate contents were found for MCT1 in both COPD #1 (63%) and COPD #2 (41%) and for MCT4 (78%) in COPD #1. Maximal oxidative enzyme activities (V(max)) for COPD #2 ranged between 37% (succinic dehydrogenase) and 70% (cytochrome C oxidase) of CON. For the cytosolic enzymes, V(max) ranged between 89% (hexokinase) to 31% (pyruvate kinase) of CON. Depressions were also observed in V(max) of the Na(+)-K(+)-ATPase for COPD #1 (66% of CON) but not COPD #2 (92% of CON) while V(max) of the Ca(2+)-ATPase was near normal in COPD #1 (84% CON). It is concluded that disturbances can occur in muscle to a wide range of excitation, contraction and metabolic processes in COPD.
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spelling pubmed-28405642010-04-01 Cellular assessment of muscle in COPD: case studies of two males Green, Howard J Bombardier, Eric Burnett, Margaret E D’Arsigny, Christine L Iqbal, Sobia Webb, Katherine A Ouyang, Jing O’Donnell, Denis E Int J Gen Med Review The objective of this paper is to provide an overview of the recent developments in muscle physiology and biochemistry in general, and with respect to chronic obstructive pulmonary disease (COPD) specifically. As a way of illustration, we have presented data on the remodeling that occurs in vastus lateralis in two patients with COPD (COPD #1, forced expiratory volume in one second/forced vital capacity [FEV(1)/FVC] = 63%; COPD #2, FEV(1)/FVC = 41%) exhibiting differences in muscle wasting as compared to healthy controls (CON; FEV(1)/FVC = 111 ± 2.2%, n = 4). Type I fibers percentages were lower in both COPD #1 (16.7) and COPD #2 (24.9) compared to CON (57.3 ± 5.2). Cross sectional area of the type I fibers of the patients ranged between 65%–68% of CON and for the type II subtypes (IIA, IIAX, IIX) between 74% and 89% (COPD #1) and 17%–32% (COPD #2). A lower number of capillary contacts were observed for all fiber types in COPD #1 but not COPD #2. Lower concentrations of adenosine triphosphate (ATP) (24%–26%) and phosphocreatine (18%–20%), but not lactate occurred in COPD. In contrast to COPD #1, who displayed normal glucose transporter content, GLUT1 and GLUT4 were only 71% and 54%, respectively of CON in COPD #2. Lower monocarboxylate contents were found for MCT1 in both COPD #1 (63%) and COPD #2 (41%) and for MCT4 (78%) in COPD #1. Maximal oxidative enzyme activities (V(max)) for COPD #2 ranged between 37% (succinic dehydrogenase) and 70% (cytochrome C oxidase) of CON. For the cytosolic enzymes, V(max) ranged between 89% (hexokinase) to 31% (pyruvate kinase) of CON. Depressions were also observed in V(max) of the Na(+)-K(+)-ATPase for COPD #1 (66% of CON) but not COPD #2 (92% of CON) while V(max) of the Ca(2+)-ATPase was near normal in COPD #1 (84% CON). It is concluded that disturbances can occur in muscle to a wide range of excitation, contraction and metabolic processes in COPD. Dove Medical Press 2009-12-29 /pmc/articles/PMC2840564/ /pubmed/20360908 Text en © 2009 Green et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Green, Howard J
Bombardier, Eric
Burnett, Margaret E
D’Arsigny, Christine L
Iqbal, Sobia
Webb, Katherine A
Ouyang, Jing
O’Donnell, Denis E
Cellular assessment of muscle in COPD: case studies of two males
title Cellular assessment of muscle in COPD: case studies of two males
title_full Cellular assessment of muscle in COPD: case studies of two males
title_fullStr Cellular assessment of muscle in COPD: case studies of two males
title_full_unstemmed Cellular assessment of muscle in COPD: case studies of two males
title_short Cellular assessment of muscle in COPD: case studies of two males
title_sort cellular assessment of muscle in copd: case studies of two males
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2840564/
https://www.ncbi.nlm.nih.gov/pubmed/20360908
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