Modulation of NRF2/KEAP1 Signaling in Preeclampsia

Author:

Tossetta Giovanni1ORCID,Fantone Sonia1ORCID,Piani Federica23ORCID,Crescimanno Caterina4,Ciavattini Andrea5,Giannubilo Stefano Raffaele5ORCID,Marzioni Daniela1

Affiliation:

1. Department of Experimental and Clinical Medicine, Università Politecnica delle Marche, 60126 Ancona, Italy

2. Cardiovascular Internal Medicine, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40128 Bologna, Italy

3. Department of Medical and Surgical Sciences, University of Bologna, 40138 Bologna, Italy

4. School of Human and Social Science, University “Kore” of Enna, 94100 Enna, Italy

5. Clinic of Obstetrics and Gynaecology, Department of Clinical Sciences, Università Politecnica delle Marche, Salesi Hospital, 60123 Ancona, Italy

Abstract

Placentation is a key and tightly regulated process that ensures the normal development of the placenta and fetal growth. Preeclampsia (PE) is a hypertensive pregnancy-related disorder involving about 5–8% of all pregnancies and clinically characterized by de novo maternal hypertension and proteinuria. In addition, PE pregnancies are also characterized by increased oxidative stress and inflammation. The NRF2/KEAP1 signaling pathway plays an important role in protecting cells against oxidative damage due to increased reactive oxygen species (ROS) levels. ROS activate NRF2, allowing its binding to the antioxidant response element (ARE) region present in the promoter of several antioxidant genes such as heme oxygenase, catalase, glutathione peroxidase and superoxide dismutase that neutralize ROS, protecting cells against oxidative stress damages. In this review, we analyze the current literature regarding the role of the NRF2/KEAP1 pathway in preeclamptic pregnancies, discussing the main cellular modulators of this pathway. Moreover, we also discuss the main natural and synthetic compounds that can regulate this pathway in in vivo and in vitro models.

Publisher

MDPI AG

Subject

General Medicine

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