Literature DB >> 30119252

Reduction of cisplatin-induced renal and hepatic side effects in rat through antioxidative and anti-inflammatory properties of Malva sylvestris L. extract.

Zeynab Mohamadi Yarijani1, Aliashraf Godini1, Seyed Hamid Madani2, Houshang Najafi3.   

Abstract

BACKGROUND: Cisplatin is widely used in the chemotherapy of solid organ cancers. However, its application is associated with serious side effects in various organs including the kidneys and liver.
OBJECTIVES: The aim of this study was to investigate the effects of mallow extract on the side effects of cisplatin in the kidneys and liver.
METHODS: Hydroalcoholic extract of mallow, at doses of 200, 400, and 600 mg/kg BW, was administered to the animals for seven days intraperitoneally (ip). Animals in the Cis + Mallow group received a dose of cisplatin (8 mg/kg, ip) on the third day. Renal and hepatic functional disturbances were evaluated by measuring concentrations of creatinine, urea-nitrogen, aspartate aminotransferase (AST), and alanine aminotransferase (ALT) in the plasma. In order to assess oxidative stress, malondialdehyde (MDA) and ferric reducing antioxidant power (FRAP) levels were measured in the kidney tissue. Then, degree of mRNA expressions of TNF-α and ICAM-1 were measured to examine renal inflammation. Hematoxylin and Eosin (H & E) staining of kidney and liver tissues was performed to study tissue damage and leukocyte infiltration.
RESULTS: Cisplatin increased levels of plasma creatinine, urea-nitrogen, AST, and ALT; levels of tissue damage and leukocytes infiltration in the kidneys and liver; and MDA level and expression of pro-inflammatory factors in the kidney tissue. Meanwhile, it decreased FRAP level in the kidney tissue. Pretreatment by mallow extract resulted in significant improvement in all measured variables although 200-mg and 400-mg doses yielded better results.
CONCLUSION: Results showed that mallow supplement protects the kidneys and liver against side effects of cisplatin, and reduces the resultant oxidative stress and inflammation.
Copyright © 2018 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Cisplatin; Inflammation; Malva sylvestris; Nephrotoxicity; Oxidative stress

Mesh:

Substances:

Year:  2018        PMID: 30119252     DOI: 10.1016/j.biopha.2018.07.115

Source DB:  PubMed          Journal:  Biomed Pharmacother        ISSN: 0753-3322            Impact factor:   6.529


  4 in total

1.  Protective effect of piperine in ischemia-reperfusion induced acute kidney injury through inhibition of inflammation and oxidative stress.

Authors:  Maryam Mohammadi; Houshang Najafi; Zeynab Mohamadi Yarijani; Gholamhasan Vaezi; Vida Hojati
Journal:  J Tradit Complement Med       Date:  2019-07-26

2.  Piperine pretreatment attenuates renal ischemia-reperfusion induced liver injury.

Authors:  Maryam Mohammadi; Houshang Najafi; Zeynab Mohamadi Yarijani; Gholamhasan Vaezi; Vida Hojati
Journal:  Heliyon       Date:  2019-08-13

3.  A Combination of Rosa Canina Extracts and Gold Complex Favors Apoptosis of Caco-2 Cells by Increasing Oxidative Stress and Mitochondrial Dysfunction.

Authors:  Inés Mármol; Nerea Jiménez-Moreno; Carmen Ancín-Azpilicueta; Jesús Osada; Elena Cerrada; María Jesús Rodríguez-Yoldi
Journal:  Antioxidants (Basel)       Date:  2019-12-24

4.  Antioxidant and Anti-inflammatory Properties Mediate the Neuroprotective Effects of Hydro-ethanolic Extract of Tiliacora triandra Against Cisplatin-induced Neurotoxicity.

Authors:  Yanping Huang; Chunhong Liu; Xianbing Song; Mei An; Meimei Liu; Lei Yao; Ademola C Famurewa; Opeyemi Joshua Olatunji
Journal:  J Inflamm Res       Date:  2021-12-09
  4 in total

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