Protective action of Cuminum cyminum against cisplatin induced nephrotoxicity in rats
الكلمات المفتاحية:
Cisplatin، Nephrotoxicity، Antioxidants، Cuminum cyminumالملخص
Objective: The nephroprotective activity of aqueous extract of Cuminum cyminum (AEC) was evaluated on cisplatin (CP) induced nephrotoxicity in rats.
Methods: The rats were divided into four groups of six animals each. Group I treated with normal saline (2 ml/kg, p.o.). The group II treated with cisplatin (12 mg/kg i.p), group III and IV were treated with AEC (100 & 200 m/kg, p.o.). for 10 days, After 24 hrs of last dose of AEC treatment, blood was collected and serum was separated and subjected to serum creatinine and urea analysis. The kidneys were removed and homogenate for estimation of lipid peroxidation, reduced glutathione, superoxide dismutase (SOD) and catalase.
Results: CP treated rats caused nephrotoxicity as evidenced by marked elevation of serum urea, creatinine and lipid peroxidation levels and decreased levels of glutathione, SOD, catalase. Treatment of rats with different doses of AEC (100 and 200 mg/kg) significantly (P<0.001) altered serum urea, creatinine enzymes, lipid peroxidation and antioxidant levels to near normal against cisplatin treated rats. The results shown AEC produce nephroprotective effect on dose dependent manner.
Conclusion: The Cuminum cyminum showed the protective effect against CP induced nephrotoxicity in rats.
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Al-Majed AA, Abd-Allah ARA, Al-Rikabi AC, Al-Shabanah OA, Mostafa AM. Effect of oral administration of Arabic gum on cisplatin induced nephrotoxicity in rats. J Biochem Mol Toxicol. 2003; 17: 146-53.
Sayed AAR. Proanthocyanidin protects against cisplatin induced nephrotoxicity. Phytotherapy Res. 2009; 23: 1738–41.
Dubey NK, Kumar R, Tripathi P. Global promotion of herbal medicine: India’s opportunity. Current Sci. 2004; 86: 37-41.
Lado CM, Then, Varga IES, Szentminalyi K. Antioxidant Property of Volatile Oils Determined by the Ferric Reducing Ability. Z. Naturforsch 2004; 59c, 354-358.
Indian medicinal plants, Vol. II. A compendium of 500 species. Orient Longman, Chennai.2005; p.241.
Iacobellis NS, Cantore PL, Capasso F, Senatore F. Antibacterial activity of Cuminum cyminum L. and Carum carvi L. essential oils. J. Agri. Food Chem. 2005; 53: 57-61.
Aruna K, Sivaramakrishnan VM. Anticarcinogenic effects of some Indian plant products. Food Chem. Toxicol. 1992; 30: 953-956.
Sayyah M, Mahboubi A, Kamalinejad M. Anticonvulsant effect of the fruit essential oil of Cuminum cyminum in rat. Pharm. Biol. 2002; 40: 478-480.
Dhandapani S, Subramanian VR, Rajagopal S, Namasivayam N. Hypolipidemic effect of Cuminum cyminum L. on alloxan induced diabetic rats. Pharmacol Res. 2002; 46: 251-255.
Willatgamuwa SA, Patel K, Saraswathi G, Srinivasan K. Antidiabetic influence of dietary cumin seeds in streptozotocin induced diabetic rats. Nutrition Res. 1998; 18: 131-142.
Gachkar L, Yadegari D, Rezaei MB, Taghizadeh M, Astaneh SA, Rasooli I. Chemical and biological characteristics of Cuminum cyminum and Rosmarinus officinalis essential oils. Food Chem. 2007; 102: 898-904.
Hosseinzadeh H, Mohammad R, Basirat FM. Anticonvulsant effects of Cuminium cyminum L.seeds extracts and essential oil in micet. J . Med. Plants., 2002;1, 28-30.
Devasagayam, T.P.A., Tarachand, U., 1987. Decreased lipid peroxidation in the rat kidney during gestation. Biochemical and Biophysical Research Communication 56, 836 – 842.
Marklund, S., Marklund, G., 1974. Involvement of superoxide anion radical in the auto oxidation of pyrogallol and a convenient assay for superoxide dismutase. European Journal of Biochemistry 47, 469-474.
Sinha, A.K., 1972. Colorimetric assay of catalase. Analytical Biochemistry 47, 389-394.
Griffith OW. Determination of glutathione and glutathione disulfide using glutathione reductase and 2-vinylpyridine. Anal. Biochem. 1980; 106: 207–12.
Baldew GS, McVie JG, van der Valk MA, Los G, de Goeij JJ, Vermeulen NP. Selective reduction of cis-diamminedichloroplatinum(II) nephrotoxicity by ebselen. Cancer Res 1990; 50: 7031-7036
Kim YH, Kim YW, Oh YJ, Back NI, Chung SA, Chung HG. Protective effect of the ethanolic extract of the roots of Brassica rapa on cisplatin induce nephrotoxicity in LLC-PK1 cells and rats. Biol Pharm Bull 2006; 29: 2436-2441.
Naziroglu M, Karaogl A, Aksoy AO. Selenium and high dose vitamin E administration protects cisplatin induced oxidative damage to renal, liver and lens tissues in rats. Toxicology 2004; 195: 221-
Safirstein R, Miller P, Guttenplan JB. Uptake and metabolism of cisplatin by rat kidney. Kidney Int 1984; 25: 753-758.
Trakshel GM, Maines MD. Characterization of glutathione S-transferases in rat kidney: Alteration of composition by cisplatinum. Biochem J 1988; 252: 127-136
Ishikawa M, Takayanagi Y, Sasaki K. Enhancement of cisplatin toxicity by buthionine sulfoximine, a glutathione depleting agent in rat. Res Commun Chem Pathol Pharmacol 1990; 67: 131-141
Uslu R, Bonavida B. Involvment of the mitochondrion respiratory chain in the synergy achieved by treatment of human ovarian carcinoma cell lines with both tumor necrosis factor-alpha and cisdiamminedichloroplatinum. Cancer 1996; 77: 725-732
Sharma RP. Interactions of cisplatin with cellular zinc and copper in liver and kidney tissues. Pharmacol Res Commun 1985; 17: 197-206
Maliakel DM, Kagiya TV, Nair CK. Prevention of cisplatin-induced nephrotoxicity by glucosides of ascorbic acid and alpha-tocopherol. Exp Toxicol Pathol 2008; 60: 521-527.
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نُشر هذا المقال بالوصول المفتوح بموجب رخصة المشاع الإبداعي: نَسب المُصنَّف – غير تجاري – الترخيص بالمثل 4.0 دولي (CC BY-NC-SA 4.0). يجوز نسخه وإعادة توزيعه وتعديله والبناء عليه لأغراض غير تجارية، شريطة نسبته إلى مؤلفيه، والإشارة إلى نشره الأول في مجلة العلوم الطبية مع رقم المعرّف الرقمي (DOI)، وبيان أي تعديلات، وتوزيع أي عمل مشتق بموجب الرخصة نفسها. حقوق التأليف والنشر محفوظة للمؤلفين. لطلبات الاستخدام التجاري يُرجى التواصل مع المؤلف المراسل. الشروط الكاملة: https://sebhau.edu.ly/journal/joms/copyright-licensing



















