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      Plant-Derived Agents for Counteracting Cisplatin-Induced Nephrotoxicity

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          Abstract

          Cisplatin (CSP) is a chemotherapeutic agent commonly used to treat a variety of malignancies. The major setback with CSP treatment is that its clinical efficacy is compromised by its induction of organ toxicity, particular to the kidneys and ears. Despite the significant strides that have been made in understanding the mechanisms underlying CSP-induced renal toxicity, advances in developing renoprotective strategies are still lacking. In addition, the renoprotective approaches described in the literature reveal partial amelioration of CSP-induced renal toxicity, stressing the need to develop potent combinatorial/synergistic agents for the mitigation of renal toxicity. However, the ideal renoprotective adjuvant should not interfere with the anticancer efficacy of CSP. In this review, we have discussed the progress made in utilizing plant-derived agents (phytochemicals) to combat CSP-induced nephrotoxicity in preclinical studies. Furthermore, we have also presented strategies to utilize phytochemicals as prototypes for the development of novel renoprotective agents for counteracting chemotherapy-induced renal damage.

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          Mechanisms of Cisplatin Nephrotoxicity

          Cisplatin is a widely used and highly effective cancer chemotherapeutic agent. One of the limiting side effects of cisplatin use is nephrotoxicity. Research over the past 10 years has uncovered many of the cellular mechanisms which underlie cisplatin-induced renal cell death. It has also become apparent that inflammation provoked by injury to renal epithelial cells serves to amplify kidney injury and dysfunction in vivo. This review summarizes recent advances in our understanding of cisplatin nephrotoxicity and discusses how these advances might lead to more effective prevention.
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            Vanilloid (Capsaicin) receptors and mechanisms.

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              Rosmarinic acid

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                Author and article information

                Journal
                Oxid Med Cell Longev
                Oxid Med Cell Longev
                OMCL
                Oxidative Medicine and Cellular Longevity
                Hindawi Publishing Corporation
                1942-0900
                1942-0994
                2016
                27 September 2016
                : 2016
                : 4320374
                Affiliations
                1Department of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain 17666, UAE
                2Department of Pharmacology and Therapeutics, Beirut Arab University, Beirut, Lebanon
                Author notes
                *Mohanraj Rajesh: rajm@ 123456uaeu.ac.ae

                Academic Editor: Renata Szymanska

                Author information
                http://orcid.org/0000-0001-7801-2966
                http://orcid.org/0000-0003-2660-2184
                Article
                10.1155/2016/4320374
                5059613
                27774117
                693e64fc-cdae-4214-8e88-b3f0d5946a66
                Copyright © 2016 Shreesh Ojha et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 8 June 2016
                : 23 August 2016
                Funding
                Funded by: United Arab Emirates University
                Categories
                Review Article

                Molecular medicine
                Molecular medicine

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