Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Fahim, Thanaa M., Mohamed, Marwa Abd EL-Hameed, Abdelrahman, Sahar S. M., Lotfy, Dina M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
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
_version_ 1785050553676464128
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
work_keys_str_mv AT fahimthanaam beneficialeffectofrosuvastatintherapyonspleeninjuryinducedbygammairradiationinratstargetingnrf2eprepathway
AT mohamedmarwaabdelhameed beneficialeffectofrosuvastatintherapyonspleeninjuryinducedbygammairradiationinratstargetingnrf2eprepathway
AT abdelrahmansaharsm beneficialeffectofrosuvastatintherapyonspleeninjuryinducedbygammairradiationinratstargetingnrf2eprepathway
AT lotfydinam beneficialeffectofrosuvastatintherapyonspleeninjuryinducedbygammairradiationinratstargetingnrf2eprepathway