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Beneficial Effect of Rosuvastatin Therapy on Spleen Injury Induced by Gamma Irradiation in Rats: Targeting Nrf2/EPRE Pathway
PURPOSE: The present study investigates the new approach of rosuvastatin (RUV) administration as a drug for the management of spleen injury induced by gamma irradiation. MAIN METHODS: Forty rats were used and divided equally into 4 groups: control group, irradiated group, IRR + rosuvastatin group (1...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226320/ https://www.ncbi.nlm.nih.gov/pubmed/37255693 http://dx.doi.org/10.1177/15593258231179900 |
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author | Fahim, Thanaa M. Mohamed, Marwa Abd EL-Hameed Abdelrahman, Sahar S. M. Lotfy, Dina M. |
author_facet | Fahim, Thanaa M. Mohamed, Marwa Abd EL-Hameed Abdelrahman, Sahar S. M. Lotfy, Dina M. |
author_sort | Fahim, Thanaa M. |
collection | PubMed |
description | PURPOSE: The present study investigates the new approach of rosuvastatin (RUV) administration as a drug for the management of spleen injury induced by gamma irradiation. MAIN METHODS: Forty rats were used and divided equally into 4 groups: control group, irradiated group, IRR + rosuvastatin group (10 mg/Kg b. wt), and IRR + rosuvastatin group (20 mg/kg b. wt) for 7 days orally. RESULTS: The possible curative effect can be illustrated via the improvement of hematopoietic cell count (Hb, RBCs, and WBCs) and oxidative stress markers (MDA and GST) in addition to biochemical parameters including [heme oxigenase-1 (HO-1), nuclear erythroid 2-related factor (Nrf2), NOD-, LRR- and pyrin domain- containing protein 3 (NLRP3) inflammasome] and immune assay of nuclear factor kappa beta (NF-kB P65) and inducible nitric oxide synthase (iNOS). Histological pictures emphasize the biochemical findings. Rosuvastatin treatments by using two different doses improve the tested parameters. High-dose administration of RUV (20 mg/kg p.o.) recorded better results than the low dose (10 mg/kg p.o.). CONCLUSION: Our results suggested that rosuvastatin reversed the radiation-induced spleen-damaging effects. So, RUV can be introduced to the market as a new therapy for the management of spleen damages. |
format | Online Article Text |
id | pubmed-10226320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-102263202023-05-30 Beneficial Effect of Rosuvastatin Therapy on Spleen Injury Induced by Gamma Irradiation in Rats: Targeting Nrf2/EPRE Pathway Fahim, Thanaa M. Mohamed, Marwa Abd EL-Hameed Abdelrahman, Sahar S. M. Lotfy, Dina M. Dose Response Original Article PURPOSE: The present study investigates the new approach of rosuvastatin (RUV) administration as a drug for the management of spleen injury induced by gamma irradiation. MAIN METHODS: Forty rats were used and divided equally into 4 groups: control group, irradiated group, IRR + rosuvastatin group (10 mg/Kg b. wt), and IRR + rosuvastatin group (20 mg/kg b. wt) for 7 days orally. RESULTS: The possible curative effect can be illustrated via the improvement of hematopoietic cell count (Hb, RBCs, and WBCs) and oxidative stress markers (MDA and GST) in addition to biochemical parameters including [heme oxigenase-1 (HO-1), nuclear erythroid 2-related factor (Nrf2), NOD-, LRR- and pyrin domain- containing protein 3 (NLRP3) inflammasome] and immune assay of nuclear factor kappa beta (NF-kB P65) and inducible nitric oxide synthase (iNOS). Histological pictures emphasize the biochemical findings. Rosuvastatin treatments by using two different doses improve the tested parameters. High-dose administration of RUV (20 mg/kg p.o.) recorded better results than the low dose (10 mg/kg p.o.). CONCLUSION: Our results suggested that rosuvastatin reversed the radiation-induced spleen-damaging effects. So, RUV can be introduced to the market as a new therapy for the management of spleen damages. SAGE Publications 2023-05-27 /pmc/articles/PMC10226320/ /pubmed/37255693 http://dx.doi.org/10.1177/15593258231179900 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Fahim, Thanaa M. Mohamed, Marwa Abd EL-Hameed Abdelrahman, Sahar S. M. Lotfy, Dina M. Beneficial Effect of Rosuvastatin Therapy on Spleen Injury Induced by Gamma Irradiation in Rats: Targeting Nrf2/EPRE Pathway |
title | Beneficial Effect of Rosuvastatin Therapy on Spleen Injury Induced by Gamma
Irradiation in Rats: Targeting Nrf2/EPRE Pathway |
title_full | Beneficial Effect of Rosuvastatin Therapy on Spleen Injury Induced by Gamma
Irradiation in Rats: Targeting Nrf2/EPRE Pathway |
title_fullStr | Beneficial Effect of Rosuvastatin Therapy on Spleen Injury Induced by Gamma
Irradiation in Rats: Targeting Nrf2/EPRE Pathway |
title_full_unstemmed | Beneficial Effect of Rosuvastatin Therapy on Spleen Injury Induced by Gamma
Irradiation in Rats: Targeting Nrf2/EPRE Pathway |
title_short | Beneficial Effect of Rosuvastatin Therapy on Spleen Injury Induced by Gamma
Irradiation in Rats: Targeting Nrf2/EPRE Pathway |
title_sort | beneficial effect of rosuvastatin therapy on spleen injury induced by gamma
irradiation in rats: targeting nrf2/epre pathway |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226320/ https://www.ncbi.nlm.nih.gov/pubmed/37255693 http://dx.doi.org/10.1177/15593258231179900 |
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