Benner
اياد علي امين ( مدرس )
كلية الصيدلة - صيدلة عام ( عميد )
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Ameliorative Effect of L-Carnitine on Renal Function and Oxidative Stress in Cancer Patients with Cisplatin-Induced Nephrotoxicity.
بحث النوع:
صيدلة التخصص العام:
Adeeb A. Al-zubaidy1 اسم الناشر:
, Arif S. Malik2, Imad K. Alwan3, Abbas M. Al-sarraf4, Haider N. Salih5, Ayad A. Hussein اسماء المساعدين:
International Journal of Pharmaceutical Sciences Review and Research الجهة الناشرة:
International Journal of Pharmaceutical Sciences Review and Research (Int J Pharm Sci Rev Res) is an open access, bi-monthly published, peer-reviewed, international online journal. The journal will cover topics related to Pharmaceutical Sciences (Pharmaceutical Technology, Pharmaceutics, Biopharmaceutics, Pharmacokinetics, Novel Drug Delivery, Pharmaceutical/Medicinal Chemistry, formulation technology, pharmaceutical product development, nutraceutical product development, cosmetic product development, Pharmacognosy and Phytochemistry, Pharmacology, Pharmaceutical Analysis, Pharmacy Practice, Clinical and Hospital Pharmacy, Pharmacogenomics, Bioinformatics and Biotechnology of Pharmaceutical Interest, quality assurance, herbal technology, regulatory affairs, Pharmaceutical marketing, Biological sciences, Botany, Zoology, Biochemistry etc.). Index copernicus value: 5.19 (ICV 2011: 5.19) Our International Journal of Pharmaceutical Sciences Review and Research (IJPSRR) achieved a good index copernicus value in short span of time amongst International community with great impact. Calculated 3 years Impact factor (as of 31st December 2015) = 2.544 Elsevier's SCImago Impact factor = 0.65  
2014 سنة النشر:

الخلاصة

Nephrotoxicity is a major dose-limiting side effect facing cisplatin-based chemotherapy of a wide variety of cancers. Oxidative stress plays an important role in mechanisms responsible for nephrotoxicity. This study was to examine the antioxidant properties of Lcarnitine in protection from nephrotoxicity due to cisplatin. 32 patients were enrolled in the study and were randomized into two groups. Only 28 patients were eligible and successfully completed treatment cycles. In group I, (N=14) patients received six cycles of cisplatin based regimen with 21 days-intervals. In group II, (N=14) patients received L-carnitine plus cisplatin based regimen. Serum creatinine and cystatin C were measured at base line and 21 days after 1, 2, 4 and 6 cycles while urinary malondialdehyde was measured at base line and 1 day after 1, 2, 4 and 6 cycles of cisplatin based regimen. Group I, cisplatin caused significant (P<0.05) increment in serum creatinine, serum cystatin C and urinary malondialdehyde in comparison to base line levels. Serum creatinine and cystatin C and urinary malondialdehyde level of group II was significantly (P<0.05) lower than that of group I. L-carnitine significantly ameliorated nephrotoxicity in patients receiving cisplatin primarily by inhibiting renal oxidative stress.