Selenium in combination with a tomato lipid extract as a therapy for benign prostatic hyperplasia and its alterations in rats with induced BPH

Author:

Arias‐Chávez David Julian1ORCID,Mailloux‐Salinas Patrick1,Ledesma Aparicio Jessica1,Campos‐Pérez Elihu23,Medina‐Campos Omar Noel4,Pedraza‐Chaverri José4,Bravo Guadalupe1

Affiliation:

1. Departmento de Farmacobiología Centro de Investigación y de Estudios Avanzados del IPN, Sede Sur Mexico City Mexico

2. Departamento de Patología, ISSSTE Hospital General Dra. Matilde Petra Montoya Lafragua Mexico City Mexico

3. Departamento de Patología Hospital Ángeles Lindavista Mexico City Mexico

4. Laboratorio F‐315, Departamento de Biología, Facultad de Química Universidad Nacional Autónoma de México Mexico City Mexico

Abstract

AbstractBenign prostatic hyperplasia (BPH) is the most common adenoma in old men. Tomatoes are a rich source of bioactive compounds that, as well as selenium (Se), possess antioxidant and antiproliferative activity. The aim was to evaluate the therapeutic effect of Se in combination with a tomato extract in aged rats with BPH. Aged male Wistar rats were divided in the following groups (n = 10 rats/group): Control (C), BPH, BPH + Finasteride (BPH + F), BPH + Tomato Lipidic Extract (BPH + E), BPH + Selenium (BPH + S) and BPH plus E plus S (BPH + E + S). After 4 weeks of treatment, prostate weight, diuresis, antioxidants enzymes, prooxidants and inflammatory markers, growth factors and androgens were determined. BPH + E + S reduced prostate weight by 59.29% and inhibited growth by 99.35% compared to BPH + F which only decreased weight and inhibited growth by 15.31% and 57.54%, respectively. Prooxidant markers were higher with BPH + F (49.4% higher vs. BPH), but BPH + E + S decreased these markers (94.27% vs. BPH) and increased antioxidant activity. Finally, diuresis was higher with the BPH + E + S combination and markers of inflammation and growth factors were significantly lower with respect to BPH + F. Our findings provide a beneficial and protective therapeutic option of E + S directed against androgens, oxidative stress and inflammation that regulates cell proliferation in the prostate gland.

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

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