Cargando…

Ameliorating potency of Chenopodium album Linn. and vitamin C against mercuric chloride-induced oxidative stress in testes of Sprague Dawley rats

BACKGROUND: Mercury has been documented as an industrial risk that posed a serious danger to human health. Mercury exposure results in oxidative stress that may lead to the pathogenesis of male reproductive dysfunction. The present study investigated the ameliorating potential of Chenopodium album L...

Descripción completa

Detalles Bibliográficos
Autores principales: Jahan, Sarwat, Azad, Tayyaba, Ayub, Amina, Ullah, Asad, Afsar, Tayyaba, Almajwal, Ali, Razak, Suhail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875164/
https://www.ncbi.nlm.nih.gov/pubmed/31759394
http://dx.doi.org/10.1186/s12199-019-0820-x
_version_ 1783472967245627392
author Jahan, Sarwat
Azad, Tayyaba
Ayub, Amina
Ullah, Asad
Afsar, Tayyaba
Almajwal, Ali
Razak, Suhail
author_facet Jahan, Sarwat
Azad, Tayyaba
Ayub, Amina
Ullah, Asad
Afsar, Tayyaba
Almajwal, Ali
Razak, Suhail
author_sort Jahan, Sarwat
collection PubMed
description BACKGROUND: Mercury has been documented as an industrial risk that posed a serious danger to human health. Mercury exposure results in oxidative stress that may lead to the pathogenesis of male reproductive dysfunction. The present study investigated the ameliorating potential of Chenopodium album L. and vitamin C against mercuric chloride-induced oxidative deterioration of reproductive functions in adult male rats. METHODS: Group 1 (control) received saline. Group 2 received Mercury (0.15 mg/kg b.w, i.p) dissolved in distilled water. Groups 3 and 4 were given oral gavage of vitamin C (200 mg/kg b.w) and the ethanolic extract of C. album (200 mg/kg b.w) respectively, along with Mercury (0.15 mg/kg b.w, i.p). Group 5 was treated only with C. album (200 mg/kg b.w). After 30 days of the treatment, the rats were dissected and their testicular tissue and the cauda epididymis were used for biochemical analysis while blood plasma was used for protein determination. RESULTS: The applied dose-treatment of Mercury-induced oxidative stress in the testis and cauda epididymis tissues of the rats was apparent by a noteworthy decrease in total protein, CAT, SOD, POD, and GST values while there was increase in ROS and TBARS levels. Furthermore, Mercury decreases daily sperm production and enhanced sperm DNA damage as noticeable by an increase in the head and tail length of comets and decrease in intact DNA. There was no significant effect on the body weight and the weight of the reproductive tissues. Treatment with C. album significantly ameliorated the total protein, ROS, and TBARS content. Similarly, the level of CAT, SOD, POD, and GST was significantly improved and the daily sperm production was significantly increased. Furthermore, C. album administration significantly protected Mercury-induced sperm DNA damage. The results of the extract treatment group were compared with those of vitamin C in detoxifying the oxidative stress and restoring the sperm parameters. CONCLUSION: C. album showed protection against Mercury-induced oxidative stress by ameliorating antioxidant enzyme activity, daily sperm production, and DNA damage in rat testes. This suggests that C. album could be beneficial against toxicity induced by an environmental toxicant.
format Online
Article
Text
id pubmed-6875164
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-68751642019-11-29 Ameliorating potency of Chenopodium album Linn. and vitamin C against mercuric chloride-induced oxidative stress in testes of Sprague Dawley rats Jahan, Sarwat Azad, Tayyaba Ayub, Amina Ullah, Asad Afsar, Tayyaba Almajwal, Ali Razak, Suhail Environ Health Prev Med Research Article BACKGROUND: Mercury has been documented as an industrial risk that posed a serious danger to human health. Mercury exposure results in oxidative stress that may lead to the pathogenesis of male reproductive dysfunction. The present study investigated the ameliorating potential of Chenopodium album L. and vitamin C against mercuric chloride-induced oxidative deterioration of reproductive functions in adult male rats. METHODS: Group 1 (control) received saline. Group 2 received Mercury (0.15 mg/kg b.w, i.p) dissolved in distilled water. Groups 3 and 4 were given oral gavage of vitamin C (200 mg/kg b.w) and the ethanolic extract of C. album (200 mg/kg b.w) respectively, along with Mercury (0.15 mg/kg b.w, i.p). Group 5 was treated only with C. album (200 mg/kg b.w). After 30 days of the treatment, the rats were dissected and their testicular tissue and the cauda epididymis were used for biochemical analysis while blood plasma was used for protein determination. RESULTS: The applied dose-treatment of Mercury-induced oxidative stress in the testis and cauda epididymis tissues of the rats was apparent by a noteworthy decrease in total protein, CAT, SOD, POD, and GST values while there was increase in ROS and TBARS levels. Furthermore, Mercury decreases daily sperm production and enhanced sperm DNA damage as noticeable by an increase in the head and tail length of comets and decrease in intact DNA. There was no significant effect on the body weight and the weight of the reproductive tissues. Treatment with C. album significantly ameliorated the total protein, ROS, and TBARS content. Similarly, the level of CAT, SOD, POD, and GST was significantly improved and the daily sperm production was significantly increased. Furthermore, C. album administration significantly protected Mercury-induced sperm DNA damage. The results of the extract treatment group were compared with those of vitamin C in detoxifying the oxidative stress and restoring the sperm parameters. CONCLUSION: C. album showed protection against Mercury-induced oxidative stress by ameliorating antioxidant enzyme activity, daily sperm production, and DNA damage in rat testes. This suggests that C. album could be beneficial against toxicity induced by an environmental toxicant. BioMed Central 2019-11-23 2019 /pmc/articles/PMC6875164/ /pubmed/31759394 http://dx.doi.org/10.1186/s12199-019-0820-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Jahan, Sarwat
Azad, Tayyaba
Ayub, Amina
Ullah, Asad
Afsar, Tayyaba
Almajwal, Ali
Razak, Suhail
Ameliorating potency of Chenopodium album Linn. and vitamin C against mercuric chloride-induced oxidative stress in testes of Sprague Dawley rats
title Ameliorating potency of Chenopodium album Linn. and vitamin C against mercuric chloride-induced oxidative stress in testes of Sprague Dawley rats
title_full Ameliorating potency of Chenopodium album Linn. and vitamin C against mercuric chloride-induced oxidative stress in testes of Sprague Dawley rats
title_fullStr Ameliorating potency of Chenopodium album Linn. and vitamin C against mercuric chloride-induced oxidative stress in testes of Sprague Dawley rats
title_full_unstemmed Ameliorating potency of Chenopodium album Linn. and vitamin C against mercuric chloride-induced oxidative stress in testes of Sprague Dawley rats
title_short Ameliorating potency of Chenopodium album Linn. and vitamin C against mercuric chloride-induced oxidative stress in testes of Sprague Dawley rats
title_sort ameliorating potency of chenopodium album linn. and vitamin c against mercuric chloride-induced oxidative stress in testes of sprague dawley rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875164/
https://www.ncbi.nlm.nih.gov/pubmed/31759394
http://dx.doi.org/10.1186/s12199-019-0820-x
work_keys_str_mv AT jahansarwat amelioratingpotencyofchenopodiumalbumlinnandvitamincagainstmercuricchlorideinducedoxidativestressintestesofspraguedawleyrats
AT azadtayyaba amelioratingpotencyofchenopodiumalbumlinnandvitamincagainstmercuricchlorideinducedoxidativestressintestesofspraguedawleyrats
AT ayubamina amelioratingpotencyofchenopodiumalbumlinnandvitamincagainstmercuricchlorideinducedoxidativestressintestesofspraguedawleyrats
AT ullahasad amelioratingpotencyofchenopodiumalbumlinnandvitamincagainstmercuricchlorideinducedoxidativestressintestesofspraguedawleyrats
AT afsartayyaba amelioratingpotencyofchenopodiumalbumlinnandvitamincagainstmercuricchlorideinducedoxidativestressintestesofspraguedawleyrats
AT almajwalali amelioratingpotencyofchenopodiumalbumlinnandvitamincagainstmercuricchlorideinducedoxidativestressintestesofspraguedawleyrats
AT razaksuhail amelioratingpotencyofchenopodiumalbumlinnandvitamincagainstmercuricchlorideinducedoxidativestressintestesofspraguedawleyrats