Impact of chronic administration of anabolic androgenic steroids and taurine on blood pressure in rats

Supraphysiological administration of anabolic androgenic steroids has been linked to increased blood pressure. The widely distributed amino acid taurine seems to be an effective depressor agent in drug-induced hypertension. The purpose of this study was to assess the impact of chronic high dose administration of nandrolone decanoate (DECA) and taurine on blood pressure in rats and to verify the potentially involved mechanisms. The study was conducted in 4 groups of 8 adult male Wistar rats, aged 14 weeks, treated for 12 weeks with: DECA (A group); vehicle (C group); taurine (T group), or with both drugs (AT group). Systolic blood pressure (SBP) was measured at the beginning of the study (SBP1), 2 (SBP2) and 3 months (SBP3) later. Plasma angiotensin-converting enzyme (ACE) activity and plasma end products of nitric oxide metabolism (NOx) were also determined. SBP3 and SBP2 were significantly increased compared to SBP1 only in the A group (P<0.002 for both). SBP2, SBP3 and ACE activity showed a statistically significant increase in the A vs C (P<0.005), andvs AT groups (P<0.05), while NOx was significantly decreased in the A and AT groups vs controls (P=0.01). ACE activity was strongly correlated with SBP3 in the A group (r=0.71, P=0.04). These findings suggest that oral supplementation of taurine may prevent the increase in SBP induced by DECA, an effect potentially mediated by angiotensin-converting enzyme.

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Main Authors: Roşca,A.E., Stoian,I., Badiu,C., Gaman,L., Popescu,B.O., Iosif,L., Mirica,R., Tivig,I.C., Stancu,C.S., Căruntu,C., Voiculescu,S.E., Zăgrean,L.
Format: Digital revista
Language:English
Published: Associação Brasileira de Divulgação Científica 2016
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2016000600706
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spelling oai:scielo:S0100-879X20160006007062019-03-25Impact of chronic administration of anabolic androgenic steroids and taurine on blood pressure in ratsRoşca,A.E.Stoian,I.Badiu,C.Gaman,L.Popescu,B.O.Iosif,L.Mirica,R.Tivig,I.C.Stancu,C.S.Căruntu,C.Voiculescu,S.E.Zăgrean,L. Anabolic androgenic steroids Nandrolone decanoate Taurine Blood pressure Angiotensin-converting enzyme Nitric oxide Supraphysiological administration of anabolic androgenic steroids has been linked to increased blood pressure. The widely distributed amino acid taurine seems to be an effective depressor agent in drug-induced hypertension. The purpose of this study was to assess the impact of chronic high dose administration of nandrolone decanoate (DECA) and taurine on blood pressure in rats and to verify the potentially involved mechanisms. The study was conducted in 4 groups of 8 adult male Wistar rats, aged 14 weeks, treated for 12 weeks with: DECA (A group); vehicle (C group); taurine (T group), or with both drugs (AT group). Systolic blood pressure (SBP) was measured at the beginning of the study (SBP1), 2 (SBP2) and 3 months (SBP3) later. Plasma angiotensin-converting enzyme (ACE) activity and plasma end products of nitric oxide metabolism (NOx) were also determined. SBP3 and SBP2 were significantly increased compared to SBP1 only in the A group (P<0.002 for both). SBP2, SBP3 and ACE activity showed a statistically significant increase in the A vs C (P<0.005), andvs AT groups (P<0.05), while NOx was significantly decreased in the A and AT groups vs controls (P=0.01). ACE activity was strongly correlated with SBP3 in the A group (r=0.71, P=0.04). These findings suggest that oral supplementation of taurine may prevent the increase in SBP induced by DECA, an effect potentially mediated by angiotensin-converting enzyme.info:eu-repo/semantics/openAccessAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research v.49 n.6 20162016-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2016000600706en10.1590/1414-431x20165116
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language English
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author Roşca,A.E.
Stoian,I.
Badiu,C.
Gaman,L.
Popescu,B.O.
Iosif,L.
Mirica,R.
Tivig,I.C.
Stancu,C.S.
Căruntu,C.
Voiculescu,S.E.
Zăgrean,L.
spellingShingle Roşca,A.E.
Stoian,I.
Badiu,C.
Gaman,L.
Popescu,B.O.
Iosif,L.
Mirica,R.
Tivig,I.C.
Stancu,C.S.
Căruntu,C.
Voiculescu,S.E.
Zăgrean,L.
Impact of chronic administration of anabolic androgenic steroids and taurine on blood pressure in rats
author_facet Roşca,A.E.
Stoian,I.
Badiu,C.
Gaman,L.
Popescu,B.O.
Iosif,L.
Mirica,R.
Tivig,I.C.
Stancu,C.S.
Căruntu,C.
Voiculescu,S.E.
Zăgrean,L.
author_sort Roşca,A.E.
title Impact of chronic administration of anabolic androgenic steroids and taurine on blood pressure in rats
title_short Impact of chronic administration of anabolic androgenic steroids and taurine on blood pressure in rats
title_full Impact of chronic administration of anabolic androgenic steroids and taurine on blood pressure in rats
title_fullStr Impact of chronic administration of anabolic androgenic steroids and taurine on blood pressure in rats
title_full_unstemmed Impact of chronic administration of anabolic androgenic steroids and taurine on blood pressure in rats
title_sort impact of chronic administration of anabolic androgenic steroids and taurine on blood pressure in rats
description Supraphysiological administration of anabolic androgenic steroids has been linked to increased blood pressure. The widely distributed amino acid taurine seems to be an effective depressor agent in drug-induced hypertension. The purpose of this study was to assess the impact of chronic high dose administration of nandrolone decanoate (DECA) and taurine on blood pressure in rats and to verify the potentially involved mechanisms. The study was conducted in 4 groups of 8 adult male Wistar rats, aged 14 weeks, treated for 12 weeks with: DECA (A group); vehicle (C group); taurine (T group), or with both drugs (AT group). Systolic blood pressure (SBP) was measured at the beginning of the study (SBP1), 2 (SBP2) and 3 months (SBP3) later. Plasma angiotensin-converting enzyme (ACE) activity and plasma end products of nitric oxide metabolism (NOx) were also determined. SBP3 and SBP2 were significantly increased compared to SBP1 only in the A group (P<0.002 for both). SBP2, SBP3 and ACE activity showed a statistically significant increase in the A vs C (P<0.005), andvs AT groups (P<0.05), while NOx was significantly decreased in the A and AT groups vs controls (P=0.01). ACE activity was strongly correlated with SBP3 in the A group (r=0.71, P=0.04). These findings suggest that oral supplementation of taurine may prevent the increase in SBP induced by DECA, an effect potentially mediated by angiotensin-converting enzyme.
publisher Associação Brasileira de Divulgação Científica
publishDate 2016
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2016000600706
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