Dopamine synthesis and dopamine receptor expression are disturbed in recurrent miscarriages

Objectives l-dopa decarboxylase (DDC) is responsible for the synthesis of dopamine. Dopamine, which binds to the D2-dopamine receptor (D2R), plays an important role in the maintenance of pregnancy. Aim of our study was the analysis of DDC and D2R expression in placentas of spontaneous miscarriages (...

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Published inEndocrine Connections Vol. 7; no. 5; pp. 727 - 738
Main Authors Gratz, Michael J, Stavrou, Stavroula, Kuhn, Christina, Hofmann, Simone, Hermelink, Kerstin, Heidegger, Helene, Hutter, Stefan, Mayr, Doris, Mahner, Sven, Jeschke, Udo, Vattai, Aurelia
Format Journal Article
LanguageEnglish
Published England Bioscientifica Ltd 01.05.2018
Bioscientifica
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Summary:Objectives l-dopa decarboxylase (DDC) is responsible for the synthesis of dopamine. Dopamine, which binds to the D2-dopamine receptor (D2R), plays an important role in the maintenance of pregnancy. Aim of our study was the analysis of DDC and D2R expression in placentas of spontaneous miscarriages (SMs) and recurrent miscarriages (RMs) in comparison to healthy controls. Methods Patients with SM (n = 15) and RM (n = 15) were compared with patients from healthy pregnancies (n = 15) (pregnancy weeks 7–13 each). Placental tissue has been collected from SMs and RMs from the first trimester (Department of Gynaecology and Obstetrics, LMU Munich) and from abruptions (private practice, Munich). Placental cell lines, BeWo- and JEG-3 cells, were stimulated with the trace amines T0AM and T1AM in vitro. Results Levels of DDC and D2R in trophoblasts and the decidua were lower in RMs in comparison to healthy controls. Stimulation of BeWo cells with T1AM significantly reduced DDC mRNA and protein levels. Via double-immunofluorescence, a DDC-positive cell type beneath decidual stromal cells and foetal EVT in the decidua could be detected. Conclusions Downregulation of DDC and D2R in trophoblasts of RMs reflects a reduced signal cascade of catecholamines on the foetal side.
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ISSN:2049-3614
2049-3614
DOI:10.1530/EC-18-0126