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Alveolar air and oxidative metabolic demand during exercise in healthy adults: the role of single‐nucleotide polymorphisms of the β (2) AR gene

The predominating β‐adrenergic receptor subtype expressed on human alveolar tissue is the β (2) AR. The homozygous arginine (Arg16Arg) single‐nucleotide polymorphism (SNP) at codon 16 of the β (2) AR gene has been associated with abnormal β (2) AR function accompanied by decreased resting alveolar‐c...

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Autores principales: Van Iterson, Erik H., Snyder, Eric M., Johnson, Bruce D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661237/
https://www.ncbi.nlm.nih.gov/pubmed/29061864
http://dx.doi.org/10.14814/phy2.13476
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author Van Iterson, Erik H.
Snyder, Eric M.
Johnson, Bruce D.
author_facet Van Iterson, Erik H.
Snyder, Eric M.
Johnson, Bruce D.
author_sort Van Iterson, Erik H.
collection PubMed
description The predominating β‐adrenergic receptor subtype expressed on human alveolar tissue is the β (2) AR. The homozygous arginine (Arg16Arg) single‐nucleotide polymorphism (SNP) at codon 16 of the β (2) AR gene has been associated with abnormal β (2) AR function accompanied by decreased resting alveolar‐capillary membrane gas‐transfer in certain healthy adults. Although not previously studied in the context of the β (2) AR gene, pulmonary gas‐transfer is also influenced by alveolar volume (V (A)) and with it the availability of alveolar surface area, particularly during exercise. Small V (A) implies less alveolar surface area available for O(2) transport. We tested the following hypothesis in healthy adults during exercise: compared with Gly16Gly and Arg16Gly β2AR genotypes, Arg16Arg will demonstrate reduced V (A) and ventilation (V̇ (A)) relative to V̇ (E) and oxidative metabolic demand. Age‐ BMI‐ and gender‐matched groups of Arg16Arg (N = 16), Gly16Gly (N = 31), and Arg16Gly (N = 17) performed consecutive low (9‐min, 40%‐peak workload) and moderate (9‐min, 75%‐peak workload) intensity exercise. We derived V (A) and V̇ (A) using “ideal” alveolar equations via arterialized gases combined with breath‐by‐breath ventilation and gas‐exchange measurements; whereas steady‐state V̇O(2) was used in metabolic equations to derive exercise economy (EC = workload÷V̇O(2)). Variables at rest did not differ across β (2) AR genotype. Strongest β (2) AR genotype effects occurred during moderate exercise. Accordingly, while V̇ (E) did not differ across genotype (P > 0.05), decreased in Arg16Arg versus Arg16Gly and Gly16Gly were V̇O(2) (1110 ± 263, 1269 ± 221, 1300 ± 319 mL/(min·m(2)), respectively, both P < 0.05), V̇ (A) (59 ± 21, 70 ± 16, 70 ± 21 L/min, respectively, both P < 0.05), and V (A) (1.43 ± 0.37, 1.95 ± 0.61, 1.93 ± 0.65 L, respectively, both P < 0.05). Also reduced was EC in Arg16Arg versus Arg16Gly (P < 0.05) and Gly16Gly (P > 0.05) (1.81 ± 0.23, 1.99 ± 0.30, and 1.94 ± 0.26 kcal/(L·m(2)), respectively). Compared with Gly16Gly and Arg16Gly genotypes, these data suggest the Arg16Arg β (2) AR genotype plays a role in the loss of oxidative metabolic efficiency coupled with an inadaptive V (A) and, hence, smaller alveolar surface area available for O(2) transport during submaximal exercise in healthy adults.
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spelling pubmed-56612372017-11-01 Alveolar air and oxidative metabolic demand during exercise in healthy adults: the role of single‐nucleotide polymorphisms of the β (2) AR gene Van Iterson, Erik H. Snyder, Eric M. Johnson, Bruce D. Physiol Rep Original Research The predominating β‐adrenergic receptor subtype expressed on human alveolar tissue is the β (2) AR. The homozygous arginine (Arg16Arg) single‐nucleotide polymorphism (SNP) at codon 16 of the β (2) AR gene has been associated with abnormal β (2) AR function accompanied by decreased resting alveolar‐capillary membrane gas‐transfer in certain healthy adults. Although not previously studied in the context of the β (2) AR gene, pulmonary gas‐transfer is also influenced by alveolar volume (V (A)) and with it the availability of alveolar surface area, particularly during exercise. Small V (A) implies less alveolar surface area available for O(2) transport. We tested the following hypothesis in healthy adults during exercise: compared with Gly16Gly and Arg16Gly β2AR genotypes, Arg16Arg will demonstrate reduced V (A) and ventilation (V̇ (A)) relative to V̇ (E) and oxidative metabolic demand. Age‐ BMI‐ and gender‐matched groups of Arg16Arg (N = 16), Gly16Gly (N = 31), and Arg16Gly (N = 17) performed consecutive low (9‐min, 40%‐peak workload) and moderate (9‐min, 75%‐peak workload) intensity exercise. We derived V (A) and V̇ (A) using “ideal” alveolar equations via arterialized gases combined with breath‐by‐breath ventilation and gas‐exchange measurements; whereas steady‐state V̇O(2) was used in metabolic equations to derive exercise economy (EC = workload÷V̇O(2)). Variables at rest did not differ across β (2) AR genotype. Strongest β (2) AR genotype effects occurred during moderate exercise. Accordingly, while V̇ (E) did not differ across genotype (P > 0.05), decreased in Arg16Arg versus Arg16Gly and Gly16Gly were V̇O(2) (1110 ± 263, 1269 ± 221, 1300 ± 319 mL/(min·m(2)), respectively, both P < 0.05), V̇ (A) (59 ± 21, 70 ± 16, 70 ± 21 L/min, respectively, both P < 0.05), and V (A) (1.43 ± 0.37, 1.95 ± 0.61, 1.93 ± 0.65 L, respectively, both P < 0.05). Also reduced was EC in Arg16Arg versus Arg16Gly (P < 0.05) and Gly16Gly (P > 0.05) (1.81 ± 0.23, 1.99 ± 0.30, and 1.94 ± 0.26 kcal/(L·m(2)), respectively). Compared with Gly16Gly and Arg16Gly genotypes, these data suggest the Arg16Arg β (2) AR genotype plays a role in the loss of oxidative metabolic efficiency coupled with an inadaptive V (A) and, hence, smaller alveolar surface area available for O(2) transport during submaximal exercise in healthy adults. John Wiley and Sons Inc. 2017-10-23 /pmc/articles/PMC5661237/ /pubmed/29061864 http://dx.doi.org/10.14814/phy2.13476 Text en © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Van Iterson, Erik H.
Snyder, Eric M.
Johnson, Bruce D.
Alveolar air and oxidative metabolic demand during exercise in healthy adults: the role of single‐nucleotide polymorphisms of the β (2) AR gene
title Alveolar air and oxidative metabolic demand during exercise in healthy adults: the role of single‐nucleotide polymorphisms of the β (2) AR gene
title_full Alveolar air and oxidative metabolic demand during exercise in healthy adults: the role of single‐nucleotide polymorphisms of the β (2) AR gene
title_fullStr Alveolar air and oxidative metabolic demand during exercise in healthy adults: the role of single‐nucleotide polymorphisms of the β (2) AR gene
title_full_unstemmed Alveolar air and oxidative metabolic demand during exercise in healthy adults: the role of single‐nucleotide polymorphisms of the β (2) AR gene
title_short Alveolar air and oxidative metabolic demand during exercise in healthy adults: the role of single‐nucleotide polymorphisms of the β (2) AR gene
title_sort alveolar air and oxidative metabolic demand during exercise in healthy adults: the role of single‐nucleotide polymorphisms of the β (2) ar gene
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661237/
https://www.ncbi.nlm.nih.gov/pubmed/29061864
http://dx.doi.org/10.14814/phy2.13476
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