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D-004 ameliorates phenylephrine-induced urodynamic changes and increased prostate and bladder oxidative stress in rats

BACKGROUND: Lower urinary tract symptoms (LUTS) in patients with benign prostatic hyperplasia (BPH) mainly depend on alpha1-adrenoreceptors (α(1)-ADR) stimulation, but a link with oxidative stress (OS) is also involved. D-004, a lipid extract of Roystonea regia fruits, antagonizes ADR-induced respon...

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Autores principales: Oyarzábal, Ambar, Pérez, Yohani, Molina, Vivian, Mas, Rosa, Ravelo, Yazmin, Jiménez, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708592/
https://www.ncbi.nlm.nih.gov/pubmed/26816837
http://dx.doi.org/10.3978/j.issn.2223-4683.2014.03.05
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author Oyarzábal, Ambar
Pérez, Yohani
Molina, Vivian
Mas, Rosa
Ravelo, Yazmin
Jiménez, Sonia
author_facet Oyarzábal, Ambar
Pérez, Yohani
Molina, Vivian
Mas, Rosa
Ravelo, Yazmin
Jiménez, Sonia
author_sort Oyarzábal, Ambar
collection PubMed
description BACKGROUND: Lower urinary tract symptoms (LUTS) in patients with benign prostatic hyperplasia (BPH) mainly depend on alpha1-adrenoreceptors (α(1)-ADR) stimulation, but a link with oxidative stress (OS) is also involved. D-004, a lipid extract of Roystonea regia fruits, antagonizes ADR-induced responses and produces antioxidant effects. The objective of this study was to investigate whether D-004 produce antioxidant effects in rats with phenylephrine (PHE)-induced urodynamic changes. METHODS: Rats were randomized into eight groups (ten rats/group): a negative vehicle control and seven groups injected with PHE: a positive control, three treated with D-004 (200, 400 and 800 mg/kg) and three others with tamsulosin (0.4 mg/kg), grape seed extract (GSE) (250 mg/kg) and vitamin E (VE) (250 mg/kg), respectively. RESULTS: Effects on urinary total volume (UTV), volume voided per micturition (VM), malondialdehyde (MDA) and carbonyl groups (CG) concentrations in prostate and bladder homogenates were study outcomes. While VM and UTV lowered significantly in the positive control as compared to the negative control group, the opposite occurred with prostate and bladder MDA and CG values. D-004 (200-800 mg/kg) increased significantly both VM and UTV, lowered significantly MDA in prostate and bladder homogenates, and reduced GC levels only in the prostate. Tamsulosin increased significantly VM and UTV, but unchanged oxidative variables. GSE and VE unchanged the UTV, whereas VE, not GSE, modestly but significantly attenuated the PHE-induced decrease of VM. CONCLUSIONS: Single oral administration of D-004 (200-800 mg/kg) was the only treatment that ameliorated the urodynamic changes and reduced increased oxidative variables in the prostate of rats with PHE-induced prostate hyperplasia.
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spelling pubmed-47085922016-01-26 D-004 ameliorates phenylephrine-induced urodynamic changes and increased prostate and bladder oxidative stress in rats Oyarzábal, Ambar Pérez, Yohani Molina, Vivian Mas, Rosa Ravelo, Yazmin Jiménez, Sonia Transl Androl Urol Original Article BACKGROUND: Lower urinary tract symptoms (LUTS) in patients with benign prostatic hyperplasia (BPH) mainly depend on alpha1-adrenoreceptors (α(1)-ADR) stimulation, but a link with oxidative stress (OS) is also involved. D-004, a lipid extract of Roystonea regia fruits, antagonizes ADR-induced responses and produces antioxidant effects. The objective of this study was to investigate whether D-004 produce antioxidant effects in rats with phenylephrine (PHE)-induced urodynamic changes. METHODS: Rats were randomized into eight groups (ten rats/group): a negative vehicle control and seven groups injected with PHE: a positive control, three treated with D-004 (200, 400 and 800 mg/kg) and three others with tamsulosin (0.4 mg/kg), grape seed extract (GSE) (250 mg/kg) and vitamin E (VE) (250 mg/kg), respectively. RESULTS: Effects on urinary total volume (UTV), volume voided per micturition (VM), malondialdehyde (MDA) and carbonyl groups (CG) concentrations in prostate and bladder homogenates were study outcomes. While VM and UTV lowered significantly in the positive control as compared to the negative control group, the opposite occurred with prostate and bladder MDA and CG values. D-004 (200-800 mg/kg) increased significantly both VM and UTV, lowered significantly MDA in prostate and bladder homogenates, and reduced GC levels only in the prostate. Tamsulosin increased significantly VM and UTV, but unchanged oxidative variables. GSE and VE unchanged the UTV, whereas VE, not GSE, modestly but significantly attenuated the PHE-induced decrease of VM. CONCLUSIONS: Single oral administration of D-004 (200-800 mg/kg) was the only treatment that ameliorated the urodynamic changes and reduced increased oxidative variables in the prostate of rats with PHE-induced prostate hyperplasia. AME Publishing Company 2015-08 /pmc/articles/PMC4708592/ /pubmed/26816837 http://dx.doi.org/10.3978/j.issn.2223-4683.2014.03.05 Text en 2015 Translational Andrology and Urology. All rights reserved.
spellingShingle Original Article
Oyarzábal, Ambar
Pérez, Yohani
Molina, Vivian
Mas, Rosa
Ravelo, Yazmin
Jiménez, Sonia
D-004 ameliorates phenylephrine-induced urodynamic changes and increased prostate and bladder oxidative stress in rats
title D-004 ameliorates phenylephrine-induced urodynamic changes and increased prostate and bladder oxidative stress in rats
title_full D-004 ameliorates phenylephrine-induced urodynamic changes and increased prostate and bladder oxidative stress in rats
title_fullStr D-004 ameliorates phenylephrine-induced urodynamic changes and increased prostate and bladder oxidative stress in rats
title_full_unstemmed D-004 ameliorates phenylephrine-induced urodynamic changes and increased prostate and bladder oxidative stress in rats
title_short D-004 ameliorates phenylephrine-induced urodynamic changes and increased prostate and bladder oxidative stress in rats
title_sort d-004 ameliorates phenylephrine-induced urodynamic changes and increased prostate and bladder oxidative stress in rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708592/
https://www.ncbi.nlm.nih.gov/pubmed/26816837
http://dx.doi.org/10.3978/j.issn.2223-4683.2014.03.05
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