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Inhibitory Effects of Intranasal Administration of Insulin on Fat Oxidation during Exercise Are Diminished in Young Overweight Individuals
It remains unknown whether the high insulin (INS) levels in the brain affect fat oxidation during exercise. We examined the effects of the intranasal administration of INS, which increases the INS concentration in the cerebrospinal fluid when peripheral effects are lacking, on the maximum fat oxidat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6210388/ https://www.ncbi.nlm.nih.gov/pubmed/30274197 http://dx.doi.org/10.3390/jcm7100308 |
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author | Yokoyama, Hisayo Takeda, Ryosuke Kawai, Eriko Ota, Akemi Morita, Emiko Imai, Daiki Suzuki, Yuta Morioka, Tomoaki Emoto, Masanori Inaba, Masaaki Okazaki, Kazunobu |
author_facet | Yokoyama, Hisayo Takeda, Ryosuke Kawai, Eriko Ota, Akemi Morita, Emiko Imai, Daiki Suzuki, Yuta Morioka, Tomoaki Emoto, Masanori Inaba, Masaaki Okazaki, Kazunobu |
author_sort | Yokoyama, Hisayo |
collection | PubMed |
description | It remains unknown whether the high insulin (INS) levels in the brain affect fat oxidation during exercise. We examined the effects of the intranasal administration of INS, which increases the INS concentration in the cerebrospinal fluid when peripheral effects are lacking, on the maximum fat oxidation rate (maxFOR) and its intensity (FATmax) during exercise in 15 young normal-weight (N group) and eight young overweight (O group) individuals. On two separate days, either INS or placebo (PL) was randomly administered intranasally before a graded exercise test. Indirect calorimetry was used to assess maxFOR and FATmax during exercise. Blood INS and glucose levels did not change after INS administration. In the N group, maxFOR and FATmax were significantly smaller in the INS trial than in the PL trial. MaxFOR was significantly smaller in the O group than in the N group and was not influenced by INS administration. Exercise-induced elevation in blood epinephrine levels tended to be reduced by INS administration only in the N group. Intranasal INS administration reduces fat oxidation during exercise without any peripheral effects, possibly by suppressing sympathetic nerve activity. This inhibitory effect is diminished in overweight subjects, suggesting that cerebral insulin effects are attenuated in this population. |
format | Online Article Text |
id | pubmed-6210388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62103882018-11-02 Inhibitory Effects of Intranasal Administration of Insulin on Fat Oxidation during Exercise Are Diminished in Young Overweight Individuals Yokoyama, Hisayo Takeda, Ryosuke Kawai, Eriko Ota, Akemi Morita, Emiko Imai, Daiki Suzuki, Yuta Morioka, Tomoaki Emoto, Masanori Inaba, Masaaki Okazaki, Kazunobu J Clin Med Article It remains unknown whether the high insulin (INS) levels in the brain affect fat oxidation during exercise. We examined the effects of the intranasal administration of INS, which increases the INS concentration in the cerebrospinal fluid when peripheral effects are lacking, on the maximum fat oxidation rate (maxFOR) and its intensity (FATmax) during exercise in 15 young normal-weight (N group) and eight young overweight (O group) individuals. On two separate days, either INS or placebo (PL) was randomly administered intranasally before a graded exercise test. Indirect calorimetry was used to assess maxFOR and FATmax during exercise. Blood INS and glucose levels did not change after INS administration. In the N group, maxFOR and FATmax were significantly smaller in the INS trial than in the PL trial. MaxFOR was significantly smaller in the O group than in the N group and was not influenced by INS administration. Exercise-induced elevation in blood epinephrine levels tended to be reduced by INS administration only in the N group. Intranasal INS administration reduces fat oxidation during exercise without any peripheral effects, possibly by suppressing sympathetic nerve activity. This inhibitory effect is diminished in overweight subjects, suggesting that cerebral insulin effects are attenuated in this population. MDPI 2018-09-28 /pmc/articles/PMC6210388/ /pubmed/30274197 http://dx.doi.org/10.3390/jcm7100308 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yokoyama, Hisayo Takeda, Ryosuke Kawai, Eriko Ota, Akemi Morita, Emiko Imai, Daiki Suzuki, Yuta Morioka, Tomoaki Emoto, Masanori Inaba, Masaaki Okazaki, Kazunobu Inhibitory Effects of Intranasal Administration of Insulin on Fat Oxidation during Exercise Are Diminished in Young Overweight Individuals |
title | Inhibitory Effects of Intranasal Administration of Insulin on Fat Oxidation during Exercise Are Diminished in Young Overweight Individuals |
title_full | Inhibitory Effects of Intranasal Administration of Insulin on Fat Oxidation during Exercise Are Diminished in Young Overweight Individuals |
title_fullStr | Inhibitory Effects of Intranasal Administration of Insulin on Fat Oxidation during Exercise Are Diminished in Young Overweight Individuals |
title_full_unstemmed | Inhibitory Effects of Intranasal Administration of Insulin on Fat Oxidation during Exercise Are Diminished in Young Overweight Individuals |
title_short | Inhibitory Effects of Intranasal Administration of Insulin on Fat Oxidation during Exercise Are Diminished in Young Overweight Individuals |
title_sort | inhibitory effects of intranasal administration of insulin on fat oxidation during exercise are diminished in young overweight individuals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6210388/ https://www.ncbi.nlm.nih.gov/pubmed/30274197 http://dx.doi.org/10.3390/jcm7100308 |
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