Literature DB >> 14733410

Increased placental expression of tissue factor is associated with abnormal uterine and umbilical Doppler waveforms in severe preeclampsia with fetal growth restriction.

Salvatore Di Paolo1, Paolo Volpe, Giuseppe Grandaliano, Giovanni Stallone, Antonio Schena, Pantaleo Greco, Leonardo Resta, Luigi Selvaggi, Raffaele Cincione, F Paolo Schena, Loreto Gesualdo.   

Abstract

BACKGROUND: This study investigated whether modifications of placental expression of endothelin-1 (ET-1), nitric oxide synthase (NOS) and tissue factor (TF) are associated with abnormal Doppler waveforms.
METHODS: Fourteen pre-term severe preeclamptic (PE) women with fetal growth restriction (FGR) and 14 normal preg nant women underwent serial Doppler examination of the uterine and umbilical arteries (UA). Placental ET-1 and T expression was evaluated by in situ hybridization, NOS by NADPH-diaforase staining and in situ hybridization Doppler evaluation was extended to 11 female kidney transplant recipients (Tx), without FGR and/or PE, in wh we previously demonstrated a strong modification of placental ET-1/NOS vasoactive balance.
RESULTS: PE women showed a marked reduction of endothelial constitutive NOS (ecNOS) expression in the syncy tiotrophoblast layer of all villi, whereas ET-1 expression was unchanged. All cases showed abnormal uterine artery blood flow velocimetry, 13 out of 14 PE women showed abnormal UA Doppler waveforms. In contrast, all Tx women showed normal UA blood velocimetry, all but one woman displayed a normal uterine artery waveform pattern. The Doppler velocimetry abnormalities were significantly associated with only TF expression, which was markedly increased, exclusively, in the endothelial cells within the basal decidua of PE women.
CONCLUSIONS: The modification of ET-1/NOS vasoactive balance, per se, did not lead to Doppler impedance modifica tions in the UA and uterine arteries, observed in pre-term PE women with FGR. Instead, Doppler velocimetry modi fications appeared to correlate with endothelial cell activation, as revealed by increased TF expression.

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Year:  2003        PMID: 14733410

Source DB:  PubMed          Journal:  J Nephrol        ISSN: 1121-8428            Impact factor:   3.902


  9 in total

1.  Significance of platelet endothelial cell adhesion molecule-1 (PECAM-1) and intercellular adhesion molecule-1 (ICAM-1) expressions in preeclamptic placentae.

Authors:  Azize Yasemin Goksu Erol; Mumtaz Nazli; Sevda Elis Yildiz
Journal:  Endocrine       Date:  2012-03-07       Impact factor: 3.633

2.  Preeclampsia: the role of tissue factor and tissue factor pathway inhibitor.

Authors:  Lara Carvalho Godoi; Karina Braga Gomes; Patrícia Nessralla Alpoim; Maria das Graças Carvalho; Bashir A Lwaleed; Luci Maria Sant'Ana Dusse
Journal:  J Thromb Thrombolysis       Date:  2012-07       Impact factor: 2.300

3.  Expression of endothelial NO synthase, inducible NO synthase, and estrogen receptors alpha and beta in placental tissue of normal, preeclamptic, and intrauterine growth-restricted pregnancies.

Authors:  Barbara Schiessl; Ioannis Mylonas; Peer Hantschmann; Christina Kuhn; Sandra Schulze; Susi Kunze; Klaus Friese; Udo Jeschke
Journal:  J Histochem Cytochem       Date:  2005-06-27       Impact factor: 2.479

4.  Pravastatin prevents miscarriages in mice: role of tissue factor in placental and fetal injury.

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Journal:  J Matern Fetal Neonatal Med       Date:  2008-10

6.  Impaired A2A adenosine receptor/nitric oxide/VEGF signaling pathway in fetal endothelium during late- and early-onset preeclampsia.

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Authors:  Amir A Shamshirsaz; Michael Paidas; Graciela Krikun
Journal:  J Pregnancy       Date:  2011-12-11

8.  Potential role of A2B adenosine receptors on proliferation/migration of fetal endothelium derived from preeclamptic pregnancies.

Authors:  Jesenia Acurio; Felipe Troncoso; Patricio Bertoglia; Carlos Salomon; Claudio Aguayo; Luis Sobrevia; Carlos Escudero
Journal:  Biomed Res Int       Date:  2014-04-28       Impact factor: 3.411

Review 9.  Identification of key signaling pathways induced by SARS-CoV2 that underlie thrombosis and vascular injury in COVID-19 patients.

Authors:  Anthony J Maxwell; Jiahui Ding; Yuan You; Zhong Dong; Hussein Chehade; Ayesha Alvero; Yechiel Mor; Sorin Draghici; Gil Mor
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  9 in total

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