Intrauterine exposure to chronic hypoxia in the rat leads to progressive diastolic function and increased aortic stiffness from early postnatal developmental stages

Abstract Aim We sought to explore whether fetal hypoxia exposure, an insult of placental insufficiency, is associated with left ventricular dysfunction and increased aortic stiffness at early postnatal ages. Methods Pregnant Sprague Dawley rats were exposed to hypoxic conditions (11.5% FiO2) from em...

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Main Authors: Praveen Kumar, Jude S. Morton, Amin Shah, Victor Do, Consolato Sergi, Jesus Serrano‐Lomelin, Sandra T. Davidge, Donna Beker, Jody Levasseur, Lisa K. Hornberger
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:Physiological Reports
Subjects:
Online Access:https://doi.org/10.14814/phy2.14327
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spelling doaj-0b4c4481a1dd426c8bbeeecfac41c5c12020-11-25T03:08:09ZengWileyPhysiological Reports2051-817X2020-01-0181n/an/a10.14814/phy2.14327Intrauterine exposure to chronic hypoxia in the rat leads to progressive diastolic function and increased aortic stiffness from early postnatal developmental stagesPraveen Kumar0Jude S. Morton1Amin Shah2Victor Do3Consolato Sergi4Jesus Serrano‐Lomelin5Sandra T. Davidge6Donna Beker7Jody Levasseur8Lisa K. Hornberger9Division of Cardiology Department of Pediatrics University of Alberta Edmonton AB CanadaWomen and Children’s Health Research Institute University of Alberta Edmonton AB CanadaWomen and Children’s Health Research Institute University of Alberta Edmonton AB CanadaDivision of Cardiology Department of Pediatrics University of Alberta Edmonton AB CanadaCardiovascular Research Institute and Mazankowski Alberta Heart Institute University of Alberta Edmonton AB CanadaWomen and Children’s Health Research Institute University of Alberta Edmonton AB CanadaWomen and Children’s Health Research Institute University of Alberta Edmonton AB CanadaCardiovascular Research Institute and Mazankowski Alberta Heart Institute University of Alberta Edmonton AB CanadaCardiovascular Research Institute and Mazankowski Alberta Heart Institute University of Alberta Edmonton AB CanadaDivision of Cardiology Department of Pediatrics University of Alberta Edmonton AB CanadaAbstract Aim We sought to explore whether fetal hypoxia exposure, an insult of placental insufficiency, is associated with left ventricular dysfunction and increased aortic stiffness at early postnatal ages. Methods Pregnant Sprague Dawley rats were exposed to hypoxic conditions (11.5% FiO2) from embryonic day E15‐21 or normoxic conditions (controls). After delivery, left ventricular function and aortic pulse wave velocity (measure of aortic stiffness) were assessed longitudinally by echocardiography from day 1 through week 8. A mixed ANOVA with repeated measures was performed to compare findings between groups across time. Myocardial hematoxylin and eosin and picro‐sirius staining were performed to evaluate myocyte nuclear shape and collagen fiber characteristics, respectively. Results Systolic function parameters transiently increased following hypoxia exposure primarily at week 2 (p < .008). In contrast, diastolic dysfunction progressed following fetal hypoxia exposure beginning weeks 1–2 with lower early inflow Doppler velocities, and less of an increase in early to late inflow velocity ratios and annular and septal E’/A’ tissue velocities compared to controls (p < .008). As further evidence of altered diastolic function, isovolumetric relaxation time was significantly shorter relative to the cardiac cycle following hypoxia exposure from week 1 onward (p < .008). Aortic stiffness was greater following hypoxia from day 1 through week 8 (p < .008, except week 4). Hypoxia exposure was also associated with altered nuclear shape at week 2 and increased collagen fiber thickness at week 4. Conclusion Chronic fetal hypoxia is associated with progressive LV diastolic dysfunction, which corresponds with changes in nuclear shape and collagen fiber thickness, and increased aortic stiffness from early postnatal stages.https://doi.org/10.14814/phy2.14327cardiovascular programmingdevelopmentdiastolic dysfunctionechocardiographyintrauterine growth restriction (IUGR)myocardial function
collection DOAJ
language English
format Article
sources DOAJ
author Praveen Kumar
Jude S. Morton
Amin Shah
Victor Do
Consolato Sergi
Jesus Serrano‐Lomelin
Sandra T. Davidge
Donna Beker
Jody Levasseur
Lisa K. Hornberger
spellingShingle Praveen Kumar
Jude S. Morton
Amin Shah
Victor Do
Consolato Sergi
Jesus Serrano‐Lomelin
Sandra T. Davidge
Donna Beker
Jody Levasseur
Lisa K. Hornberger
Intrauterine exposure to chronic hypoxia in the rat leads to progressive diastolic function and increased aortic stiffness from early postnatal developmental stages
Physiological Reports
cardiovascular programming
development
diastolic dysfunction
echocardiography
intrauterine growth restriction (IUGR)
myocardial function
author_facet Praveen Kumar
Jude S. Morton
Amin Shah
Victor Do
Consolato Sergi
Jesus Serrano‐Lomelin
Sandra T. Davidge
Donna Beker
Jody Levasseur
Lisa K. Hornberger
author_sort Praveen Kumar
title Intrauterine exposure to chronic hypoxia in the rat leads to progressive diastolic function and increased aortic stiffness from early postnatal developmental stages
title_short Intrauterine exposure to chronic hypoxia in the rat leads to progressive diastolic function and increased aortic stiffness from early postnatal developmental stages
title_full Intrauterine exposure to chronic hypoxia in the rat leads to progressive diastolic function and increased aortic stiffness from early postnatal developmental stages
title_fullStr Intrauterine exposure to chronic hypoxia in the rat leads to progressive diastolic function and increased aortic stiffness from early postnatal developmental stages
title_full_unstemmed Intrauterine exposure to chronic hypoxia in the rat leads to progressive diastolic function and increased aortic stiffness from early postnatal developmental stages
title_sort intrauterine exposure to chronic hypoxia in the rat leads to progressive diastolic function and increased aortic stiffness from early postnatal developmental stages
publisher Wiley
series Physiological Reports
issn 2051-817X
publishDate 2020-01-01
description Abstract Aim We sought to explore whether fetal hypoxia exposure, an insult of placental insufficiency, is associated with left ventricular dysfunction and increased aortic stiffness at early postnatal ages. Methods Pregnant Sprague Dawley rats were exposed to hypoxic conditions (11.5% FiO2) from embryonic day E15‐21 or normoxic conditions (controls). After delivery, left ventricular function and aortic pulse wave velocity (measure of aortic stiffness) were assessed longitudinally by echocardiography from day 1 through week 8. A mixed ANOVA with repeated measures was performed to compare findings between groups across time. Myocardial hematoxylin and eosin and picro‐sirius staining were performed to evaluate myocyte nuclear shape and collagen fiber characteristics, respectively. Results Systolic function parameters transiently increased following hypoxia exposure primarily at week 2 (p < .008). In contrast, diastolic dysfunction progressed following fetal hypoxia exposure beginning weeks 1–2 with lower early inflow Doppler velocities, and less of an increase in early to late inflow velocity ratios and annular and septal E’/A’ tissue velocities compared to controls (p < .008). As further evidence of altered diastolic function, isovolumetric relaxation time was significantly shorter relative to the cardiac cycle following hypoxia exposure from week 1 onward (p < .008). Aortic stiffness was greater following hypoxia from day 1 through week 8 (p < .008, except week 4). Hypoxia exposure was also associated with altered nuclear shape at week 2 and increased collagen fiber thickness at week 4. Conclusion Chronic fetal hypoxia is associated with progressive LV diastolic dysfunction, which corresponds with changes in nuclear shape and collagen fiber thickness, and increased aortic stiffness from early postnatal stages.
topic cardiovascular programming
development
diastolic dysfunction
echocardiography
intrauterine growth restriction (IUGR)
myocardial function
url https://doi.org/10.14814/phy2.14327
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