Effects of Intermittent Hypoxia on Pulmonary Vascular and Systemic Diseases

Obstructive sleep apnea (OSA) causes many systemic disorders via mechanisms related to sympathetic nerve activation, systemic inflammation, and oxidative stress. OSA typically shows repeated sleep apnea followed by hyperventilation, which results in intermittent hypoxia (IH). IH is associated with a...

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Main Authors: Hiroshi Kimura, Hiroyo Ota, Yuya Kimura, Shin Takasawa
Format: Article
Language:English
Published: MDPI AG 2019-08-01
Series:International Journal of Environmental Research and Public Health
Subjects:
Online Access:https://www.mdpi.com/1660-4601/16/17/3101
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spelling doaj-07787cfe8287409193916a9f498a53212020-11-25T02:47:44ZengMDPI AGInternational Journal of Environmental Research and Public Health1660-46012019-08-011617310110.3390/ijerph16173101ijerph16173101Effects of Intermittent Hypoxia on Pulmonary Vascular and Systemic DiseasesHiroshi Kimura0Hiroyo Ota1Yuya Kimura2Shin Takasawa3Department of Advanced Medicine for Pulmonary Circulation and Respiratory Failure, Graduate School of Medicine, Nippon Medical School, Bunkyo, Tokyo 113-8603, JapanDepartment of Respiratory Medicine, Nara Medical University, Kashihara, Nara 634-8522, JapanCenter for Pulmonary Diseases, NHO Tokyo National Hospital, Kiyose, Tokyo 204-0023, JapanDepartment of Biochemistry, Nara Medical University, Kashihara, Nara 634-8521, JapanObstructive sleep apnea (OSA) causes many systemic disorders via mechanisms related to sympathetic nerve activation, systemic inflammation, and oxidative stress. OSA typically shows repeated sleep apnea followed by hyperventilation, which results in intermittent hypoxia (IH). IH is associated with an increase in sympathetic activity, which is a well-known pathophysiological mechanism in hypertension and insulin resistance. In this review, we show the basic and clinical significance of IH from the viewpoint of not only systemic regulatory mechanisms focusing on pulmonary circulation, but also cellular mechanisms causing lifestyle-related diseases. First, we demonstrate how IH influences pulmonary circulation to cause pulmonary hypertension during sleep in association with sleep state-specific change in OSA. We also clarify how nocturnal IH activates circulating monocytes to accelerate the infiltration ability to vascular wall in OSA. Finally, the effects of IH on insulin secretion and insulin resistance are elucidated by using an in vitro chamber system that can mimic and manipulate IH. The obtained data implies that glucose-induced insulin secretion (GIS) in pancreatic β cells is significantly attenuated by IH, and that IH increases selenoprotein P, which is one of the hepatokines, as well as TNF-α, CCL-2, and resistin, members of adipokines, to induce insulin resistance via direct cellular mechanisms. Clinical and experimental findings concerning IH give us productive new knowledge of how lifestyle-related diseases and pulmonary hypertension develop during sleep.https://www.mdpi.com/1660-4601/16/17/3101sleep apneaintermittent hypoxiasympathetic nervepulmonary hypertensionREM sleeplifestyle-related diseasesinsulin secretioninsulin resistance
collection DOAJ
language English
format Article
sources DOAJ
author Hiroshi Kimura
Hiroyo Ota
Yuya Kimura
Shin Takasawa
spellingShingle Hiroshi Kimura
Hiroyo Ota
Yuya Kimura
Shin Takasawa
Effects of Intermittent Hypoxia on Pulmonary Vascular and Systemic Diseases
International Journal of Environmental Research and Public Health
sleep apnea
intermittent hypoxia
sympathetic nerve
pulmonary hypertension
REM sleep
lifestyle-related diseases
insulin secretion
insulin resistance
author_facet Hiroshi Kimura
Hiroyo Ota
Yuya Kimura
Shin Takasawa
author_sort Hiroshi Kimura
title Effects of Intermittent Hypoxia on Pulmonary Vascular and Systemic Diseases
title_short Effects of Intermittent Hypoxia on Pulmonary Vascular and Systemic Diseases
title_full Effects of Intermittent Hypoxia on Pulmonary Vascular and Systemic Diseases
title_fullStr Effects of Intermittent Hypoxia on Pulmonary Vascular and Systemic Diseases
title_full_unstemmed Effects of Intermittent Hypoxia on Pulmonary Vascular and Systemic Diseases
title_sort effects of intermittent hypoxia on pulmonary vascular and systemic diseases
publisher MDPI AG
series International Journal of Environmental Research and Public Health
issn 1660-4601
publishDate 2019-08-01
description Obstructive sleep apnea (OSA) causes many systemic disorders via mechanisms related to sympathetic nerve activation, systemic inflammation, and oxidative stress. OSA typically shows repeated sleep apnea followed by hyperventilation, which results in intermittent hypoxia (IH). IH is associated with an increase in sympathetic activity, which is a well-known pathophysiological mechanism in hypertension and insulin resistance. In this review, we show the basic and clinical significance of IH from the viewpoint of not only systemic regulatory mechanisms focusing on pulmonary circulation, but also cellular mechanisms causing lifestyle-related diseases. First, we demonstrate how IH influences pulmonary circulation to cause pulmonary hypertension during sleep in association with sleep state-specific change in OSA. We also clarify how nocturnal IH activates circulating monocytes to accelerate the infiltration ability to vascular wall in OSA. Finally, the effects of IH on insulin secretion and insulin resistance are elucidated by using an in vitro chamber system that can mimic and manipulate IH. The obtained data implies that glucose-induced insulin secretion (GIS) in pancreatic β cells is significantly attenuated by IH, and that IH increases selenoprotein P, which is one of the hepatokines, as well as TNF-α, CCL-2, and resistin, members of adipokines, to induce insulin resistance via direct cellular mechanisms. Clinical and experimental findings concerning IH give us productive new knowledge of how lifestyle-related diseases and pulmonary hypertension develop during sleep.
topic sleep apnea
intermittent hypoxia
sympathetic nerve
pulmonary hypertension
REM sleep
lifestyle-related diseases
insulin secretion
insulin resistance
url https://www.mdpi.com/1660-4601/16/17/3101
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