Fetal programming effects of pentaerythritol tetranitrate in a rat model of superimposed preeclampsia

dc.contributor.authorMan, Andy W. C.
dc.contributor.authorChen, Min
dc.contributor.authorZhou, Yawen
dc.contributor.authorWu, Zhixiong
dc.contributor.authorReifenberg, Gisela
dc.contributor.authorDaiber, Andreas
dc.contributor.authorMünzel, Thomas
dc.contributor.authorXia, Ning
dc.contributor.authorLi, Huige
dc.date.accessioned2021-06-11T08:06:19Z
dc.date.available2021-06-11T08:06:19Z
dc.date.issued2020
dc.description.abstractPreeclampsia is a common medical condition during pregnancy and a major cause of maternal and prenatal mortality. The present study was conducted to investigate the effects of maternal treatment with pentaerythritol tetranitrate (PETN) in Dahl salt-sensitive rats (DSSR), a model of superimposed preeclampsia. F0 parental DSSR were treated with PETN (50 mg/kg) from the time point of mating to the end of lactation. Maternal PETN treatment improved fetal growth and had no effect on blood pressure in DSSR offspring fed with normal chow or high-salt diet. Upon high-fat diet (HFD) feeding, offspring from PETN-treated mother showed improved glucose tolerance despite similar weight gain. Unexpectedly, maternal PETN treatment significantly potentiated the HFD-induced blood pressure elevation in male DSSR offspring. Endothelium-derived hyperpolarization factor (EDHF)-mediated vasodilation was similar between NCD-fed and HFD-fed control offspring but was markedly reduced in HFD-fed PETN offspring. EDHF genes were downregulated in the vasculature of HFD-fed PETN offspring, which was associated with epigenetic changes in histone modifications. In conclusion, maternal PETN treatment in DSSR shows both beneficial and unfavorable effects. It improves fetal growth and ameliorates glucose tolerance in the offspring. Although maternal PETN treatment has no effect on blood pressure in offspring fed with normal chow or high-salt diet, the offspring is at higher risk to develop HFD-induced hypertension. PETN may potentiate the blood pressure response to HFD by epigenetic modifications of EDHF genes.en_GB
dc.identifier.doihttp://doi.org/10.25358/openscience-6053
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/6062
dc.language.isoeng
dc.rightsCC-BY-4.0
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleFetal programming effects of pentaerythritol tetranitrate in a rat model of superimposed preeclampsiaen_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.apc.pricePAR-Fee
jgu.journal.titleJournal of molecular medicine
jgu.journal.volume98
jgu.organisation.departmentFB 04 Medizinde_DE
jgu.organisation.nameJohannes Gutenberg-Universität Mainzde_DE
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.end1299
jgu.pages.start1287
jgu.publisher.doi10.1007/s00109-020-01949-0
jgu.publisher.issn1432-1440
jgu.publisher.nameSpringer
jgu.publisher.placeBerlin u.a.
jgu.publisher.urihttps://doi.org/10.1007/s00109-020-01949-0
jgu.publisher.year2020
jgu.rights.accessrightsopenAccessen_GB
jgu.subject.ddccode610
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTexten_GB
jgu.type.versionPublished versionen_GB

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