کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5816739 | 1116155 | 2013 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Hesperidin attenuates cisplatin-induced acute renal injury by decreasing oxidative stress, inflammation and DNA damage
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
MDANEDDCFH-DADTNBCATDNPHGPXGSTNADPH2,7-dichlorofluorescein diacetate - 2،7-دی کرول فلوئورسین دی سکتهAc-DEVD-AMC - Ac- DEVD-AMCMPO - DFOPeriodic Acid Schiff - اسید فسفریکinflammation - التهاب( توروم) Oxidative stress - تنش اکسیداتیوtumor necrosis factor-α - تومور نکروز عامل αApoptosis - خزان یاختهایBUN - خوبDinitrophenyl hydrazine - دینیتروفنیل هیدرازینSOD - سدSuperoxide dismutase - سوکسوکس دیسموتازcisplatin - سیس پلاتینTNF-α - فاکتور نکروز توموری آلفاmalondialdehyde - مالون دی آلدهیدmyeloperoxidase - میلوپراکسیداز Nephrotoxicity - نفخ سمیPAS - نهblood urea nitrogen - نیتروژن اوره خونNitric oxide - نیتریک اکسیدHesperidin - هسپریدینbody weight - وزن بدنCatalase - کاتالازglutathione-S-transferase - گلوتاتیون S-ترانسفرازglutathione reductase - گلوتاتیون ردوکتازglutathione peroxidase - گلوتاتیون پراکسیداز
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
بیوشیمی بالینی
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
Nephrotoxicity is an important complication in cancer patients undergoing cisplatin therapy. Oxidative stress, inflammation and apoptosis/necrosis are the major patho-mechanisms of cisplatin induced nephrotoxicity. In the present study, hesperidin, a naturally-occurring bioflavonoid has been demonstrated to have protective effect on cisplatin-induced renal injury in rats. Cisplatin intoxication resulted in structural and functional renal impairment which was revealed by massive histopathological changes and elevated blood urea nitrogen and serum creatinine levels, respectively. Renal injury was associated with oxidative stress/lipid peroxidation as evident by increased reactive oxygen species (ROS) and malondialdehyde (MDA) formation with decreased levels of antioxidants such as reduced glutathione, vitamin C, catalase, superoxide dismutase, glutathione reductase, glutathione peroxidase and glutathione-S-transferase. Cisplatin administration also triggered inflammatory response in rat kidneys by inducing pro-inflammatory cytokine, TNF-α, with the increased expression of myeloperoxidase (MPO). Furthermore, cisplatin increased the activity of caspase-3 and DNA damage with decreased tissue nitric oxide levels. Hesperidin treatment significantly attenuated the cisplatin-induced oxidative stress/lipid peroxidation, inflammation (infiltration of leukocytes and pro-inflammatory cytokine), apoptosis/necrosis (caspase-3 activity with DNA damage) as well as increased expression of nitric oxide in the kidney and improved renal function. Thus, our results suggest that hesperidin co-administration may serve as a novel and promising preventive strategy against cisplatin-induced nephrotoxicity.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Phytomedicine - Volume 20, Issue 5, 15 March 2013, Pages 453-460
Journal: Phytomedicine - Volume 20, Issue 5, 15 March 2013, Pages 453-460
نویسندگان
Bidya Dhar Sahu, Madhusudana Kuncha, G. Jeevana Sindhura, Ramakrishna Sistla,