Cargando…

Diabetic pregnancy as a novel risk factor for cardiac dysfunction in the offspring—the heart as a target for fetal programming in rats

AIMS/HYPOTHESIS: The impact of diabetic pregnancy has been investigated extensively regarding offspring metabolism; however, little is known about the influence on the heart. We aimed to characterise the effects of a diabetic pregnancy on male adult offspring cardiac health after feeding a high-fat...

Descripción completa

Detalles Bibliográficos
Autores principales: Schütte, Till, Kedziora, Sarah M., Haase, Nadine, Herse, Florian, Alenina, Natalia, Müller, Dominik N., Bader, Michael, Schupp, Michael, Dechend, Ralf, Golic, Michaela, Kräker, Kristin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563640/
https://www.ncbi.nlm.nih.gov/pubmed/34537857
http://dx.doi.org/10.1007/s00125-021-05566-5
_version_ 1784593446942539776
author Schütte, Till
Kedziora, Sarah M.
Haase, Nadine
Herse, Florian
Alenina, Natalia
Müller, Dominik N.
Bader, Michael
Schupp, Michael
Dechend, Ralf
Golic, Michaela
Kräker, Kristin
author_facet Schütte, Till
Kedziora, Sarah M.
Haase, Nadine
Herse, Florian
Alenina, Natalia
Müller, Dominik N.
Bader, Michael
Schupp, Michael
Dechend, Ralf
Golic, Michaela
Kräker, Kristin
author_sort Schütte, Till
collection PubMed
description AIMS/HYPOTHESIS: The impact of diabetic pregnancy has been investigated extensively regarding offspring metabolism; however, little is known about the influence on the heart. We aimed to characterise the effects of a diabetic pregnancy on male adult offspring cardiac health after feeding a high-fat diet in an established transgenic rat model. METHODS: We applied our rat model for maternal type 2 diabetes characterised by maternal insulin resistance with hyperglycaemia and hyperinsulinaemia. Diabetes was induced preconceptionally via doxycycline-induced knock down of the insulin receptor in transgenic rats. Male wild-type offspring of diabetic and normoglycaemic pregnancies were raised by foster mothers, followed up into adulthood and subgroups were challenged by a high-fat diet. Cardiac phenotype was assessed by innovative speckle tracking echocardiography, circulating factors, immunohistochemistry and gene expression in the heart. RESULTS: When feeding normal chow, we did not observe differences in cardiac function, gene expression and plasma brain natriuretic peptide between adult diabetic or normoglycaemic offspring. Interestingly, when being fed a high-fat diet, adult offspring of diabetic pregnancy demonstrated decreased global longitudinal (−14.82 ± 0.59 vs −16.60 ± 0.48%) and circumferential strain (−23.40 ± 0.57 vs −26.74 ± 0.34%), increased relative wall thickness (0.53 ± 0.06 vs 0.37 ± 0.02), altered cardiac gene expression, enlarged cardiomyocytes (106.60 ± 4.14 vs 87.94 ± 1.67 μm), an accumulation of immune cells in the heart (10.27 ± 0.30 vs 6.48 ± 0.48 per fov) and higher plasma brain natriuretic peptide levels (0.50 ± 0.12 vs 0.12 ± 0.03 ng/ml) compared with normoglycaemic offspring on a high-fat diet. Blood pressure, urinary albumin, blood glucose and body weight were unaltered between groups on a high-fat diet. CONCLUSIONS/INTERPRETATION: Diabetic pregnancy in rats induces cardiac dysfunction, left ventricular hypertrophy and altered proinflammatory status in adult offspring only after a high-fat diet. A diabetic pregnancy itself was not sufficient to impair myocardial function and gene expression in male offspring later in life. This suggests that a postnatal high-fat diet is important for the development of cardiac dysfunction in rat offspring after diabetic pregnancy. Our data provide evidence that a diabetic pregnancy is a novel cardiac risk factor that becomes relevant when other challenges, such as a high-fat diet, are present. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s00125-021-05566-5) contains peer-reviewed but unedited supplementary material.
format Online
Article
Text
id pubmed-8563640
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-85636402021-11-04 Diabetic pregnancy as a novel risk factor for cardiac dysfunction in the offspring—the heart as a target for fetal programming in rats Schütte, Till Kedziora, Sarah M. Haase, Nadine Herse, Florian Alenina, Natalia Müller, Dominik N. Bader, Michael Schupp, Michael Dechend, Ralf Golic, Michaela Kräker, Kristin Diabetologia Article AIMS/HYPOTHESIS: The impact of diabetic pregnancy has been investigated extensively regarding offspring metabolism; however, little is known about the influence on the heart. We aimed to characterise the effects of a diabetic pregnancy on male adult offspring cardiac health after feeding a high-fat diet in an established transgenic rat model. METHODS: We applied our rat model for maternal type 2 diabetes characterised by maternal insulin resistance with hyperglycaemia and hyperinsulinaemia. Diabetes was induced preconceptionally via doxycycline-induced knock down of the insulin receptor in transgenic rats. Male wild-type offspring of diabetic and normoglycaemic pregnancies were raised by foster mothers, followed up into adulthood and subgroups were challenged by a high-fat diet. Cardiac phenotype was assessed by innovative speckle tracking echocardiography, circulating factors, immunohistochemistry and gene expression in the heart. RESULTS: When feeding normal chow, we did not observe differences in cardiac function, gene expression and plasma brain natriuretic peptide between adult diabetic or normoglycaemic offspring. Interestingly, when being fed a high-fat diet, adult offspring of diabetic pregnancy demonstrated decreased global longitudinal (−14.82 ± 0.59 vs −16.60 ± 0.48%) and circumferential strain (−23.40 ± 0.57 vs −26.74 ± 0.34%), increased relative wall thickness (0.53 ± 0.06 vs 0.37 ± 0.02), altered cardiac gene expression, enlarged cardiomyocytes (106.60 ± 4.14 vs 87.94 ± 1.67 μm), an accumulation of immune cells in the heart (10.27 ± 0.30 vs 6.48 ± 0.48 per fov) and higher plasma brain natriuretic peptide levels (0.50 ± 0.12 vs 0.12 ± 0.03 ng/ml) compared with normoglycaemic offspring on a high-fat diet. Blood pressure, urinary albumin, blood glucose and body weight were unaltered between groups on a high-fat diet. CONCLUSIONS/INTERPRETATION: Diabetic pregnancy in rats induces cardiac dysfunction, left ventricular hypertrophy and altered proinflammatory status in adult offspring only after a high-fat diet. A diabetic pregnancy itself was not sufficient to impair myocardial function and gene expression in male offspring later in life. This suggests that a postnatal high-fat diet is important for the development of cardiac dysfunction in rat offspring after diabetic pregnancy. Our data provide evidence that a diabetic pregnancy is a novel cardiac risk factor that becomes relevant when other challenges, such as a high-fat diet, are present. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s00125-021-05566-5) contains peer-reviewed but unedited supplementary material. Springer Berlin Heidelberg 2021-09-18 2021 /pmc/articles/PMC8563640/ /pubmed/34537857 http://dx.doi.org/10.1007/s00125-021-05566-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Schütte, Till
Kedziora, Sarah M.
Haase, Nadine
Herse, Florian
Alenina, Natalia
Müller, Dominik N.
Bader, Michael
Schupp, Michael
Dechend, Ralf
Golic, Michaela
Kräker, Kristin
Diabetic pregnancy as a novel risk factor for cardiac dysfunction in the offspring—the heart as a target for fetal programming in rats
title Diabetic pregnancy as a novel risk factor for cardiac dysfunction in the offspring—the heart as a target for fetal programming in rats
title_full Diabetic pregnancy as a novel risk factor for cardiac dysfunction in the offspring—the heart as a target for fetal programming in rats
title_fullStr Diabetic pregnancy as a novel risk factor for cardiac dysfunction in the offspring—the heart as a target for fetal programming in rats
title_full_unstemmed Diabetic pregnancy as a novel risk factor for cardiac dysfunction in the offspring—the heart as a target for fetal programming in rats
title_short Diabetic pregnancy as a novel risk factor for cardiac dysfunction in the offspring—the heart as a target for fetal programming in rats
title_sort diabetic pregnancy as a novel risk factor for cardiac dysfunction in the offspring—the heart as a target for fetal programming in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563640/
https://www.ncbi.nlm.nih.gov/pubmed/34537857
http://dx.doi.org/10.1007/s00125-021-05566-5
work_keys_str_mv AT schuttetill diabeticpregnancyasanovelriskfactorforcardiacdysfunctionintheoffspringtheheartasatargetforfetalprogramminginrats
AT kedziorasarahm diabeticpregnancyasanovelriskfactorforcardiacdysfunctionintheoffspringtheheartasatargetforfetalprogramminginrats
AT haasenadine diabeticpregnancyasanovelriskfactorforcardiacdysfunctionintheoffspringtheheartasatargetforfetalprogramminginrats
AT herseflorian diabeticpregnancyasanovelriskfactorforcardiacdysfunctionintheoffspringtheheartasatargetforfetalprogramminginrats
AT aleninanatalia diabeticpregnancyasanovelriskfactorforcardiacdysfunctionintheoffspringtheheartasatargetforfetalprogramminginrats
AT mullerdominikn diabeticpregnancyasanovelriskfactorforcardiacdysfunctionintheoffspringtheheartasatargetforfetalprogramminginrats
AT badermichael diabeticpregnancyasanovelriskfactorforcardiacdysfunctionintheoffspringtheheartasatargetforfetalprogramminginrats
AT schuppmichael diabeticpregnancyasanovelriskfactorforcardiacdysfunctionintheoffspringtheheartasatargetforfetalprogramminginrats
AT dechendralf diabeticpregnancyasanovelriskfactorforcardiacdysfunctionintheoffspringtheheartasatargetforfetalprogramminginrats
AT golicmichaela diabeticpregnancyasanovelriskfactorforcardiacdysfunctionintheoffspringtheheartasatargetforfetalprogramminginrats
AT krakerkristin diabeticpregnancyasanovelriskfactorforcardiacdysfunctionintheoffspringtheheartasatargetforfetalprogramminginrats