L-(+)-Ergothioneine Significantly Improves the Clinical Characteristics of Preeclampsia in the Reduced Uterine Perfusion Pressure Rat Model.


Journal

Hypertension (Dallas, Tex. : 1979)
ISSN: 1524-4563
Titre abrégé: Hypertension
Pays: United States
ID NLM: 7906255

Informations de publication

Date de publication:
02 2020
Historique:
pubmed: 24 12 2019
medline: 22 10 2020
entrez: 24 12 2019
Statut: ppublish

Résumé

Preeclampsia is a multifactorial hypertensive disorder of pregnancy founded on abnormal placentation, and the resultant placental ischemic microenvironment is thought to play a crucial role in its pathophysiology. Placental ischemia because of fluctuations in the delivery of oxygen results in oxidative stress, and recent evidence suggests that mitochondrial dysfunction may be a prime mediator. However, large clinical trials of therapeutic antioxidants such as vitamins C and E for the treatment of preeclampsia have been disappointing. L-(+)-ergothioneine (ERG)-an unusual amino acid betaine derived from histidine-has important cytoprotective and antioxidant properties under conditions of high oxidative stress. In this study, we investigated the potential therapeutic effects of administration of ERG in the reduced uterine perfusion pressure (RUPP) rat model of preeclampsia. ERG (25 mg/kg per day) was administered to rats on gestational day 11. On gestational day 14, RUPP surgery was performed, and on gestational day 19, blood pressure (mean arterial pressure) and fetal growth were measured. Production of mitochondria-specific H

Identifiants

pubmed: 31865793
doi: 10.1161/HYPERTENSIONAHA.119.13929
doi:

Substances chimiques

Antioxidants 0
Biomarkers 0
Ergothioneine BDZ3DQM98W
Flt1 protein, rat EC 2.7.10.1
Vascular Endothelial Growth Factor Receptor-1 EC 2.7.10.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

561-568

Auteurs

Rachel D Williamson (RD)

From the Irish Centre for Fetal and Neonatal Translational Research, Cork University Maternity Hospital, Ireland (R.D.W., F.P.M., S.M., C.M.).

Fergus P McCarthy (FP)

From the Irish Centre for Fetal and Neonatal Translational Research, Cork University Maternity Hospital, Ireland (R.D.W., F.P.M., S.M., C.M.).

Samprikta Manna (S)

From the Irish Centre for Fetal and Neonatal Translational Research, Cork University Maternity Hospital, Ireland (R.D.W., F.P.M., S.M., C.M.).

Emer Groarke (E)

Clinical Biochemistry, Cork University Hospital, Ireland (E.G.).

Douglas B Kell (DB)

Department of Biochemistry, Faculty of Health and Life Sciences, Institute of Integrative Biology, University of Liverpool, United Kingdom (D.B.K.).
Novo Nordisk Foundation Centre for Biosustainability, Technical University of Denmark, Lyngby (D.B.K.).

Louise C Kenny (LC)

Department of Women's and Children's Health, Institute of Translational Medicine, University of Liverpool, United Kingdom (L.C.K.).

Cathal M McCarthy (CM)

From the Irish Centre for Fetal and Neonatal Translational Research, Cork University Maternity Hospital, Ireland (R.D.W., F.P.M., S.M., C.M.).
Department of Pharmacology and Therapeutics, Western Gateway Building, University College Cork, Ireland (C.M.).

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Classifications MeSH