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Impact of HIF1-α/TGF-β/Smad-2/Bax/Bcl2 pathways on cobalt chloride-induced cardiac and hepatorenal dysfunction

BACKGROUND: Cobalt chloride (CoCl(2)) is a ferromagnetic ubiquitous trace element extensively dispersed in the environment. Nevertheless, it may merit human hazard. AIM: Excess cobalt can harm vital organs this paves the way to elucidate the toxic impact of CoCl(2) on the liver, kidney and heart. ME...

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Autores principales: Kadry, Mai O, Ali, Hanaa Mahmoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10445593/
https://www.ncbi.nlm.nih.gov/pubmed/37621844
http://dx.doi.org/10.2144/fsoa-2023-0050
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author Kadry, Mai O
Ali, Hanaa Mahmoud
author_facet Kadry, Mai O
Ali, Hanaa Mahmoud
author_sort Kadry, Mai O
collection PubMed
description BACKGROUND: Cobalt chloride (CoCl(2)) is a ferromagnetic ubiquitous trace element extensively dispersed in the environment. Nevertheless, it may merit human hazard. AIM: Excess cobalt can harm vital organs this paves the way to elucidate the toxic impact of CoCl(2) on the liver, kidney and heart. METHOD: CoCl(2) was injected in a dose of (60 mg/kg, S.C.) proceeded via Carnosine (200 mg/kg) and/or Arginine (200 mg/kg) treatment 1 month, 24 and 1 h, prior to CoCl(2)-intoxication. RESULTS: CoCl(2) significantly alleviated hemoglobin concentration and BCl2; meanwhile, protein expression of transforming growth factor (TGF-β), hypoxia-inducible factor (HIF-1α), Mothers against decapentaplegic (Smad-2), AKT protein expression and Bax/Bcl2 ratio was noticeably elevated. CONCLUSION: The combination of the aforementioned antioxidants exerted a synergistic anti-apoptotic impact in all target tissues.
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spelling pubmed-104455932023-08-24 Impact of HIF1-α/TGF-β/Smad-2/Bax/Bcl2 pathways on cobalt chloride-induced cardiac and hepatorenal dysfunction Kadry, Mai O Ali, Hanaa Mahmoud Future Sci OA Research Article BACKGROUND: Cobalt chloride (CoCl(2)) is a ferromagnetic ubiquitous trace element extensively dispersed in the environment. Nevertheless, it may merit human hazard. AIM: Excess cobalt can harm vital organs this paves the way to elucidate the toxic impact of CoCl(2) on the liver, kidney and heart. METHOD: CoCl(2) was injected in a dose of (60 mg/kg, S.C.) proceeded via Carnosine (200 mg/kg) and/or Arginine (200 mg/kg) treatment 1 month, 24 and 1 h, prior to CoCl(2)-intoxication. RESULTS: CoCl(2) significantly alleviated hemoglobin concentration and BCl2; meanwhile, protein expression of transforming growth factor (TGF-β), hypoxia-inducible factor (HIF-1α), Mothers against decapentaplegic (Smad-2), AKT protein expression and Bax/Bcl2 ratio was noticeably elevated. CONCLUSION: The combination of the aforementioned antioxidants exerted a synergistic anti-apoptotic impact in all target tissues. Future Science Ltd 2023-07-13 /pmc/articles/PMC10445593/ /pubmed/37621844 http://dx.doi.org/10.2144/fsoa-2023-0050 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Research Article
Kadry, Mai O
Ali, Hanaa Mahmoud
Impact of HIF1-α/TGF-β/Smad-2/Bax/Bcl2 pathways on cobalt chloride-induced cardiac and hepatorenal dysfunction
title Impact of HIF1-α/TGF-β/Smad-2/Bax/Bcl2 pathways on cobalt chloride-induced cardiac and hepatorenal dysfunction
title_full Impact of HIF1-α/TGF-β/Smad-2/Bax/Bcl2 pathways on cobalt chloride-induced cardiac and hepatorenal dysfunction
title_fullStr Impact of HIF1-α/TGF-β/Smad-2/Bax/Bcl2 pathways on cobalt chloride-induced cardiac and hepatorenal dysfunction
title_full_unstemmed Impact of HIF1-α/TGF-β/Smad-2/Bax/Bcl2 pathways on cobalt chloride-induced cardiac and hepatorenal dysfunction
title_short Impact of HIF1-α/TGF-β/Smad-2/Bax/Bcl2 pathways on cobalt chloride-induced cardiac and hepatorenal dysfunction
title_sort impact of hif1-α/tgf-β/smad-2/bax/bcl2 pathways on cobalt chloride-induced cardiac and hepatorenal dysfunction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10445593/
https://www.ncbi.nlm.nih.gov/pubmed/37621844
http://dx.doi.org/10.2144/fsoa-2023-0050
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