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Quercetin upregulates CREM gene expression in cyanide-induced endocrine dysfunction

Cyanide is among the ubiquitous chemicals that humans are usually exposed to and it is well documented that cyanide induces infertility in humans and experimental rodents. However, the pathogenesis remains unknown. Likewise, quercetin is an important nutraceutical that detoxifies reactive oxygen spe...

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Autores principales: Oyewopo, Adeoye, Adeleke, Opeyemi, Johnson, Olawumi, Akingbade, Adebanji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8121865/
https://www.ncbi.nlm.nih.gov/pubmed/34027151
http://dx.doi.org/10.1016/j.heliyon.2021.e06901
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author Oyewopo, Adeoye
Adeleke, Opeyemi
Johnson, Olawumi
Akingbade, Adebanji
author_facet Oyewopo, Adeoye
Adeleke, Opeyemi
Johnson, Olawumi
Akingbade, Adebanji
author_sort Oyewopo, Adeoye
collection PubMed
description Cyanide is among the ubiquitous chemicals that humans are usually exposed to and it is well documented that cyanide induces infertility in humans and experimental rodents. However, the pathogenesis remains unknown. Likewise, quercetin is an important nutraceutical that detoxifies reactive oxygen species, but its effects on testicular damage is not clear. The present study investigated the role of nutraceutical, quercetin on cyanide-induced testicular toxicity and probable involvement of cAMP-response-element modulator (CREM) which is a transcription factor necessary for the process of spermatogenesis. Thus, this work hypothesized that quercetin will mitigate endocrine dysfunction induced by cyanide. Seventy-two adult male Wistar rats were divided into seven groups (A to G). Groups A, B, C, F and G comprised of eight (8) rats per group while groups D and E comprised of sixteen (16) rats per group. Group A was designated as control while Groups B and C were given 0.5 and 1 mg/kg of cyanide respectively for 56 days. Group D and E received 0.5 and 1 mg/kg body weight cyanide respectively for 30 days. At day 30, eight animals were sacrificed from Group D and E and the remaining eight (8) rats were subdivided into sub-groups (D1 and E1) and were given 20 and 40 mg/kg of quercetin respectively for twenty-six (26) days. Group F and G were given concurrent administration of cyanide and quercetin at a dose of 0.5 + 20 mg/kg and 1 + 40 mg/kg respectively for 56 days. Body and testicular weight were significantly reduced in cyanide treated groups while quercetin modulates the reduction. Significant down-regulation of CREM gene and reduction in serum level of follicle stimulating hormone (FSH), Luteinizing hormone (LH), testosterone, glutathione peroxidase (GPx) and zinc in cyanide-treated groups, whereas administration of quercetin concomitantly with cyanide exposure or post-treated significantly reversed the alterations.
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spelling pubmed-81218652021-05-20 Quercetin upregulates CREM gene expression in cyanide-induced endocrine dysfunction Oyewopo, Adeoye Adeleke, Opeyemi Johnson, Olawumi Akingbade, Adebanji Heliyon Research Article Cyanide is among the ubiquitous chemicals that humans are usually exposed to and it is well documented that cyanide induces infertility in humans and experimental rodents. However, the pathogenesis remains unknown. Likewise, quercetin is an important nutraceutical that detoxifies reactive oxygen species, but its effects on testicular damage is not clear. The present study investigated the role of nutraceutical, quercetin on cyanide-induced testicular toxicity and probable involvement of cAMP-response-element modulator (CREM) which is a transcription factor necessary for the process of spermatogenesis. Thus, this work hypothesized that quercetin will mitigate endocrine dysfunction induced by cyanide. Seventy-two adult male Wistar rats were divided into seven groups (A to G). Groups A, B, C, F and G comprised of eight (8) rats per group while groups D and E comprised of sixteen (16) rats per group. Group A was designated as control while Groups B and C were given 0.5 and 1 mg/kg of cyanide respectively for 56 days. Group D and E received 0.5 and 1 mg/kg body weight cyanide respectively for 30 days. At day 30, eight animals were sacrificed from Group D and E and the remaining eight (8) rats were subdivided into sub-groups (D1 and E1) and were given 20 and 40 mg/kg of quercetin respectively for twenty-six (26) days. Group F and G were given concurrent administration of cyanide and quercetin at a dose of 0.5 + 20 mg/kg and 1 + 40 mg/kg respectively for 56 days. Body and testicular weight were significantly reduced in cyanide treated groups while quercetin modulates the reduction. Significant down-regulation of CREM gene and reduction in serum level of follicle stimulating hormone (FSH), Luteinizing hormone (LH), testosterone, glutathione peroxidase (GPx) and zinc in cyanide-treated groups, whereas administration of quercetin concomitantly with cyanide exposure or post-treated significantly reversed the alterations. Elsevier 2021-05-06 /pmc/articles/PMC8121865/ /pubmed/34027151 http://dx.doi.org/10.1016/j.heliyon.2021.e06901 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Oyewopo, Adeoye
Adeleke, Opeyemi
Johnson, Olawumi
Akingbade, Adebanji
Quercetin upregulates CREM gene expression in cyanide-induced endocrine dysfunction
title Quercetin upregulates CREM gene expression in cyanide-induced endocrine dysfunction
title_full Quercetin upregulates CREM gene expression in cyanide-induced endocrine dysfunction
title_fullStr Quercetin upregulates CREM gene expression in cyanide-induced endocrine dysfunction
title_full_unstemmed Quercetin upregulates CREM gene expression in cyanide-induced endocrine dysfunction
title_short Quercetin upregulates CREM gene expression in cyanide-induced endocrine dysfunction
title_sort quercetin upregulates crem gene expression in cyanide-induced endocrine dysfunction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8121865/
https://www.ncbi.nlm.nih.gov/pubmed/34027151
http://dx.doi.org/10.1016/j.heliyon.2021.e06901
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