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Submitted: 17 Sep 2021
Accepted: 25 Nov 2021
ePublished: 09 Mar 2022
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J Renal Inj Prev. 2023;12(2): e31958.
doi: 10.34172/jrip.2022.31958

Scopus ID: 85159011929
  Abstract View: 1613
  PDF Download: 672

Original

Protective effects of pretreatment or concomitant treatment with Hypericum extract on renal function and renal toxicity in cisplatin-induced nephrotoxicity

Hori Ghaneialvar 1 ORCID logo, Mohammad Reza Kaffashian 2 ORCID logo, Amir Hussein Salimi 3 ORCID logo, Neda Moulaei 2 ORCID logo, Nastaran Afsordeh 2 ORCID logo, Shams Parvari 4 ORCID logo, Naser Abasi 1 ORCID logo, Azra Kenarkoohi 5 ORCID logo, Maryam Maleki 2,6* ORCID logo

1 Biotechnology and Medicinal Plants Research Center, Ilam University of Medical Sciences, Ilam, Iran
2 Department of Physiology, Faculty of Medicine, Ilam University of Medical Sciences, Ilam, Iran
3 Student Research Committee, Faculty of Medicine, Ilam University of Medical Sciences, Ilam, Iran
4 Pathology laboratory of Dr. Parvari, Eyvan, Ilam, Iran
5 Department of Microbiology, Faculty of Medicine, Ilam University of Medical Sciences, Ilam, Iran
6 Non-Communicable Diseases Research Center, Ilam University of Medical Sciences, Ilam, Iran
*Corresponding Author: Maryam Maleki, Email: Maryammaleki777@yahoo.com, , Email: maleki-m@medilam.ac.irom

Abstract

Introduction: Cisplatin is a strong anticancer medicine, but its use is limited due to the potential nephrotoxicity induction.

Objectives: The present study seeks to determine the impact of Hypericum hydroalcoholic extract on cisplatin-induced nephrotoxicity.

Materials and Methods: Thirty-two male rats were assigned to groups 1 to 4. Group 1, control (Cont); treated by saline (IP). Group 2, Cis; cisplatin [intraperitoneal (IP), 7.5 mg/kg]. Group 3, CisH; cisplatin + Hypericum (70 mg/kg, IP, for one week). Group 4, HCis; first treated with Hypericum for a week, followed by cisplatin. Renal tissue and blood samples were obtained a week after cisplatin injection for tissue assay and biochemical analysis. Kidney tissue damage score (KTDS), plasma creatinine (Cr), blood urea nitrogen (BUN), serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), malondialdehyde (MDA), superoxide dismutase (SOD), and catalase (CAT) were measured.

Results: Kidney weight showed significant differences between the treated groups and the Cont group (P<0.001). Serum BUN, Cr, SGOT, and SGPT increased significantly in Cont (P<0.01). BUN decreased in CisH and HCis groups compared to Cis group, although there was no significant difference. Serum Cr, SGOT, and SGPT decreased significantly in CisH and HCis groups compared to the Cis group (P<0.05). MDA and KTDS increased in the Cis group and decreased significantly in the CisH and HCis groups compared to the Cis group (P<0.05). Serum SOD and CAT decreased significantly in Cis compared to Cont (P<0.05) and increased in CisH and HCis groups compared to Cis. There was no significant difference between the CisH and HCis groups in any of the measured parameters.

Conclusion: This study reveals that pretreatment with Hypericum extract or its concomitant administration with cisplatin can moderate the side-effects of cisplatin, improve renal function and decrease lipid peroxidation, renal toxicity and the KTDS.


Implication for health policy/practice/research/medical education:

In the current study, 32 male rats were assigned to four groups to determine the impacts of Hypericum hydroalcoholic extract on cisplatin-induced nephrotoxicity. This study reveals that pretreatment with Hypericum extract or its concomitant administration with cisplatin can moderate the side effects of cisplatin, improve renal function and decrease lipid peroxidation, and also renal toxicity.

Please cite this paper as: Ghaneialvar H, Kaffashian MR, Salimi AH, Moulaei N, Afsordeh N, Parvari S, Abasi N, Kenarkoohi A, Maleki M. Protective effects of pretreatment or concomitant treatment with Hypericum extract on renal function and renal toxicity in cisplatin-induced nephrotoxicity. J Renal Inj Prev. 2023; 12(2): e31958. doi: 10.34172/jrip.2022.31958.

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