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Volume 7, Issue 4 (Suppl)

J Clin Trial

ISSN: 2167-0870 JCTR, an open access journal

Global Pharmacovigilance 2017

July 06-07, 2017

JULY 06-07, 2017 KUALA LUMPUR, MALAYSIA

8

TH

GLOBAL

Pharmacovigilance &

Drug Safety Summit

J Clin Trial 2017, 7:4 (Suppl)

DOI: 10.4172/2167-0870-C1-017

Potential nephroprotective effects of L-carnitine against drug-induced nephropathy: A review of

literature

Atefeh Jafari

Guilan University of Medical Sciences, Iran

D

rug-induced nephrotoxicity (DIN) has been reported with a great number of medications. The significance of DIN lies

in its contribution to approximately 20% of the hospital admissions. Various therapeutic agents such as L-carnitine have

been proposed to reduce DIN. Antioxidant, anti-inflammatory and anti-apoptotic effects of L-carnitine make it a candidate for

nephro-protection against DIN. These benefits of L-carnitine necessitated the current review. The present review covered all

clinical and animal research published on the concept of nephroprotective effects of L-carnitine against DIN. L-carnitine was

significantly effective in amelioration of DIN in

in vitro

and animal studies, especially against cisplatin-induced renal damage.

Inhibitionof reactive oxygen species generation, lipidperoxidation, apoptosis,matrix remodeling, anti-inflammatoryproperties,

and improvement in carnitine deficiency has been suggested as probable nephroprotective mechanisms of L-carnitine. In

spite of the evidence support the nephroprotective effect of L-carnitine, the main problems in this area are the inadequacy of

reliable studies in humans and difficulty of translating the experimental results into clinical practice. Use of L-carnitine as a

prophylactic nephroprotective agent for nephrotoxic therapies is rarely possible except for contrast-induced nephrotoxicity.

Research on these nephroprotective effects in human population seems essential before generalization the results to human

subjects. The possible impact of L-carnitine on the therapeutic efficacy of nephrotoxic agents such as calcineurin inhibitors

and aminoglycosides remain as a question for further studies. Development of validated early biomarkers to detect DIN may

provide the opportunity to use prophylactic nephroprotective agents at the golden time.

atf.jafari@gmail.com