Back to Search Start Over

Impacts of dose and length of exposure to boldenone and stanazolol on enzymatic antioxidant systems, myeloperoxidase and NAGase activities, and glycogen and lactate levels in rat liver.

Authors :
Carvalho FB
Bueno A
Lhamas CL
Gutierres JM
Carvalho MB
Brusco I
Oliveira SM
Bottari NB
Silva AD
Miron VV
Alves MS
Leitemperger JW
Loro VL
Schetinger MRC
Morsch VM
de Andrade CM
Source :
Steroids [Steroids] 2020 Sep; Vol. 161, pp. 108670. Date of Electronic Publication: 2020 May 27.
Publication Year :
2020

Abstract

We investigated the adverse effects of the anabolic androgenic steroids (AAS) boldenone (BOL) and stanazolol (ST) on the enzymatic antioxidant systems of the rat liver. Male Wistar rats were divided in three protocols (P): PI, 5 mg/kg BOL or ST once a week for 4 weeks; PII, 2.5 mg/kg BOL or ST once a week for 8 weeks; PIII, 1.25 mg/kg BOL or ST once a week for 12 weeks. AAS were administered intramuscularly (0.2 ml, olive oil vehicle) once a week in all protocols. Activities of the enzymes glutathione peroxidase (GPx), glutathione S-transferase (GST), and glutathione reductase (GR), superoxide dismutase (SOD), catalase (CAT), were investigated. We assessed the content of hydrogen peroxide (H <subscript>2</subscript> O <subscript>2</subscript> ), glycogen and lactate; and enzyme markers of neutrophils (myeloperoxidase, MPO) and macrophages (NAGase). PI and PII altered the SOD and CAT activities and increased the H <subscript>2</subscript> O <subscript>2</subscript> content. PI led to increases in the MPO and NAGase activities. In contrast, changes in GPx, GST and, GR were observed under PII and, to a greater extend, under PIII. Following PIII, GPx, GR, and GST exhibited reduced activities. All protocols altered the glycogen and lactate content. The use of high doses of AAS for a short duration first alters SOD/CAT activity. In contrast, at lower doses of AAS for long periods is associated with changes in the glutathione system. Protocols with high doses of AAS for a short duration exert the most deleterious effects on redox status, markers of cellular infiltration, and the metabolic functioning of hepatic tissues.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1878-5867
Volume :
161
Database :
MEDLINE
Journal :
Steroids
Publication Type :
Academic Journal
Accession number :
32473164
Full Text :
https://doi.org/10.1016/j.steroids.2020.108670