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The protective effect of Pentoxifylline on testopathy in male rats following Dimethyl Nitrosamine administration: An experimental study

BACKGROUND: Nitrosamines as a carcinogenic agent has unfavorable effects on some of the male reproductive parameters. Pentoxifylline (PX) is a xanthine derivative used as a drug inhibiting the inflammatory factors, reducing blood viscosity, improving peripheral blood flow, and so on. Objective: The...

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Autores principales: Reza Salahshoor, Mohammad, Faramarzi, Azita, Roshankhah, Shiva, Jalili, Cyrus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Knowledge E 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6844288/
https://www.ncbi.nlm.nih.gov/pubmed/31807721
http://dx.doi.org/10.18502/ijrm.v17i10.5292
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author Reza Salahshoor, Mohammad
Faramarzi, Azita
Roshankhah, Shiva
Jalili, Cyrus
author_facet Reza Salahshoor, Mohammad
Faramarzi, Azita
Roshankhah, Shiva
Jalili, Cyrus
author_sort Reza Salahshoor, Mohammad
collection PubMed
description BACKGROUND: Nitrosamines as a carcinogenic agent has unfavorable effects on some of the male reproductive parameters. Pentoxifylline (PX) is a xanthine derivative used as a drug inhibiting the inflammatory factors, reducing blood viscosity, improving peripheral blood flow, and so on. Objective: The aim of the present study is to evaluate the effects of PX against Dimethyl nitrosamine (DMN)-inducing the damage to the reproductive parameter of male rats. MATERIALS AND METHODS: In this experimental study, 48 male Wistar rats (8 wk, 220-250 gr) were randomly assigned to eight groups (n = 6/each): normal control and DMN control groups (40 mg/kg); PX groups (25, 50, 100 mg/kg), and DMN + PX groups (25, 50, 100 mg/kg). Treatments were administered intraperitoneally and the gavage applied daily for 28 days. The sperm parameters, spermatogenesis index, total antioxidant capacity, testosterone level, and seminiferous tube diameter were assessed. RESULTS: The values of all parameters reduced significantly in the DMN control group compared to the normal control group (p [Formula: see text] 0.001). The PX and PX + DMN treatments at all entirely doses improved all parameters significantly compared to the DMN control group (p [Formula: see text] 0.001). CONCLUSION: DMN caused detrimental effects on reproductive parameters. Also, no significant modifications were observed in PX treatments at all doses compared to the normal control group. PX compensated the toxic effect of DMN on reproductive parameters.
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spelling pubmed-68442882019-12-05 The protective effect of Pentoxifylline on testopathy in male rats following Dimethyl Nitrosamine administration: An experimental study Reza Salahshoor, Mohammad Faramarzi, Azita Roshankhah, Shiva Jalili, Cyrus Int J Reprod Biomed (Yazd) Research Article BACKGROUND: Nitrosamines as a carcinogenic agent has unfavorable effects on some of the male reproductive parameters. Pentoxifylline (PX) is a xanthine derivative used as a drug inhibiting the inflammatory factors, reducing blood viscosity, improving peripheral blood flow, and so on. Objective: The aim of the present study is to evaluate the effects of PX against Dimethyl nitrosamine (DMN)-inducing the damage to the reproductive parameter of male rats. MATERIALS AND METHODS: In this experimental study, 48 male Wistar rats (8 wk, 220-250 gr) were randomly assigned to eight groups (n = 6/each): normal control and DMN control groups (40 mg/kg); PX groups (25, 50, 100 mg/kg), and DMN + PX groups (25, 50, 100 mg/kg). Treatments were administered intraperitoneally and the gavage applied daily for 28 days. The sperm parameters, spermatogenesis index, total antioxidant capacity, testosterone level, and seminiferous tube diameter were assessed. RESULTS: The values of all parameters reduced significantly in the DMN control group compared to the normal control group (p [Formula: see text] 0.001). The PX and PX + DMN treatments at all entirely doses improved all parameters significantly compared to the DMN control group (p [Formula: see text] 0.001). CONCLUSION: DMN caused detrimental effects on reproductive parameters. Also, no significant modifications were observed in PX treatments at all doses compared to the normal control group. PX compensated the toxic effect of DMN on reproductive parameters. Knowledge E 2019-11-07 /pmc/articles/PMC6844288/ /pubmed/31807721 http://dx.doi.org/10.18502/ijrm.v17i10.5292 Text en Copyright © 2019 Mohammad Reza Salahshoor et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Article
Reza Salahshoor, Mohammad
Faramarzi, Azita
Roshankhah, Shiva
Jalili, Cyrus
The protective effect of Pentoxifylline on testopathy in male rats following Dimethyl Nitrosamine administration: An experimental study
title The protective effect of Pentoxifylline on testopathy in male rats following Dimethyl Nitrosamine administration: An experimental study
title_full The protective effect of Pentoxifylline on testopathy in male rats following Dimethyl Nitrosamine administration: An experimental study
title_fullStr The protective effect of Pentoxifylline on testopathy in male rats following Dimethyl Nitrosamine administration: An experimental study
title_full_unstemmed The protective effect of Pentoxifylline on testopathy in male rats following Dimethyl Nitrosamine administration: An experimental study
title_short The protective effect of Pentoxifylline on testopathy in male rats following Dimethyl Nitrosamine administration: An experimental study
title_sort protective effect of pentoxifylline on testopathy in male rats following dimethyl nitrosamine administration: an experimental study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6844288/
https://www.ncbi.nlm.nih.gov/pubmed/31807721
http://dx.doi.org/10.18502/ijrm.v17i10.5292
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