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Leptin action in normal and pathological pregnancies

Authors :
Pérez Pérez, Antonio
Toro, Ayelén
Vilariño García, Teresa
Maymó, Julieta L.
Guadix, Pilar
Varone, C.
Sánchez Margalet, Víctor
Universidad de Sevilla. Departamento de Bioquímica Médica y Biología Molecular e Inmunología
Universidad de Sevilla. Departamento de Cirugía
Source :
idUS: Depósito de Investigación de la Universidad de Sevilla, Universidad de Sevilla (US), idUS. Depósito de Investigación de la Universidad de Sevilla, instname
Publication Year :
2018

Abstract

Leptin is now considered an important signalling molecule of the reproductive system, as it regulates the production of gonadotrophins, the blastocyst formation and implantation, the normal placentation, as well as the foeto-placental communication. Leptin is a peptide hormone secreted mainly by adipose tissue, and the placenta is the second leptin-producing tissue in humans. Placental leptin is an important cytokine which regulates placental functions in an autocrine or paracrine manner. Leptin seems to play a crucial role during the first stages of pregnancy as it modulates critical processes such as proliferation, protein synthesis, invasion and apoptosis in placental cells. Furthermore, deregulation of leptin levels has been correlated with the pathogenesis of various disorders associated with reproduction and gestation, including polycystic ovary syndrome, recurrent miscarriage, gestational diabetes mellitus, pre-eclampsia and intrauterine growth restriction. Due to the relevant incidence of the mentioned diseases and the importance of leptin, we decided to review the latest information available about leptin action in normal and pathological pregnancies to support the idea of leptin as an important factor and/or predictor of diverse disorders associated with reproduction and pregnancy

Details

Database :
OpenAIRE
Journal :
idUS: Depósito de Investigación de la Universidad de Sevilla, Universidad de Sevilla (US), idUS. Depósito de Investigación de la Universidad de Sevilla, instname
Accession number :
edsair.dedup.wf.001..38e6238e9623c3452c7e80424f9a1bda