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Egyptian Journal of Histology
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Volume Volume 48 (2025)
Volume Volume 47 (2024)
Volume Volume 46 (2023)
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Badr, S., Sharaf Eldin, H., Ibrahim, M. (2023). The Possible Protective Role of Vitamin E Against Deferasirox-Induced Injury of Renal Cortical Tubules in Adult Male Albino Rat: A Histological and Immunohistochemical Study. Egyptian Journal of Histology, 46(4), 1741-1751. doi: 10.21608/ejh.2022.143261.1699
Shimaa M Badr; Heba EM Sharaf Eldin; Marwa A.A. Ibrahim. "The Possible Protective Role of Vitamin E Against Deferasirox-Induced Injury of Renal Cortical Tubules in Adult Male Albino Rat: A Histological and Immunohistochemical Study". Egyptian Journal of Histology, 46, 4, 2023, 1741-1751. doi: 10.21608/ejh.2022.143261.1699
Badr, S., Sharaf Eldin, H., Ibrahim, M. (2023). 'The Possible Protective Role of Vitamin E Against Deferasirox-Induced Injury of Renal Cortical Tubules in Adult Male Albino Rat: A Histological and Immunohistochemical Study', Egyptian Journal of Histology, 46(4), pp. 1741-1751. doi: 10.21608/ejh.2022.143261.1699
Badr, S., Sharaf Eldin, H., Ibrahim, M. The Possible Protective Role of Vitamin E Against Deferasirox-Induced Injury of Renal Cortical Tubules in Adult Male Albino Rat: A Histological and Immunohistochemical Study. Egyptian Journal of Histology, 2023; 46(4): 1741-1751. doi: 10.21608/ejh.2022.143261.1699

The Possible Protective Role of Vitamin E Against Deferasirox-Induced Injury of Renal Cortical Tubules in Adult Male Albino Rat: A Histological and Immunohistochemical Study

Article 14, Volume 46, Issue 4, December 2023, Page 1741-1751  XML PDF (5.96 MB)
Document Type: Original Article
DOI: 10.21608/ejh.2022.143261.1699
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Authors
Shimaa M Badrorcid 1; Heba EM Sharaf Eldinorcid 2; Marwa A.A. Ibrahim email orcid 3
1Histology and Cell Biology department, Faculty of Medicine, Tanta University, Egypt
2Histology and cell biology, Faculty of Medicine, Tanta University
3Histology department, Faculty of Medicine, Tanta University, Gharbia, Egypt
Abstract
Introduction: Deferasirox, as an oral iron chelator, is presently the first-choice medication for iron overload caused by repeated blood transfusions due to its ease of use, efficacy, and high bioavailability, yet deferasirox has been also reported with the occurrence of acute kidney injury and tubular dysfunction. Vitamin E is a potent antioxidant and anti-inflammatory agent.
Aim of the Work: To study the effect of deferasirox on the oxidative status, histological structure, apoptosis, proliferation, and inflammation of the renal cortical tubules and examine the potential protective role of vitamin E against such effect in adult male albino rat.
Material and Methods: Twenty-four adult male albino rats were subdivided into four equal groups; control, vitamin E-treated (100 mg/kg/day vitamin E orally for 4weeks), deferasirox-treated group (100 mg/kg/day deferasirox orally for 4weeks), and vitamin E&deferasirox-treated group (concomitantly administered vitamin E and deferasirox). Kidney specimens were processed for different biochemical, histological, and immunohistochemical studies.
Results: Deferasirox-treated group revealed loss of the normal histological architecture of the renal cortex involving numerous nuclear and cytoplasmic alterations of renal cortical tubules with inflammatory signs. Tissue malonaldehyde level was significantly surged. A significant increase in caspase-3, Ki67, and iNOS immunohistochemical expression was recorded, whereas a significant drop in the histochemical expression of PAS was detected. Results from the group concomitantly administered with vitamin E and deferasirox exhibited an apparently normal histology of the renal cortex with a non-significant difference in all studied parameters compared to the control group.
Conclusion: Deferasirox administration led to histological alterations in the renal cortical tubules through inducing oxidative stress, apoptosis, proliferation, and inflammation. Concomitant supplementation with vitamin E exerted a protective action against deferasirox harmful effects most probably through its antioxidative, antiapoptotic, and anti-inflammatory properties.
Keywords
Deferasirox; immunohistochemistry; renal cortex; vitamin E
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