Comparison of the effects of melatonin and genistein on radiation-induced nephrotoxicity: Results of an experimental study

被引:29
作者
Canyilmaz, Emine [1 ]
Uslu, Gonca Hanedan [2 ]
Bahat, Zumrut [1 ]
Kandaz, Mustafa [1 ]
Mungan, Sevdegul [3 ]
Haciislamoglu, Emel [1 ]
Mentese, Ahmet [4 ]
Yoney, Adnan [1 ]
机构
[1] Karadeniz Tech Univ, Fac Med, Dept Radiat Oncol, 2 Farabi St, TR-61080 Trabzon, Turkey
[2] Kanuni Res & Educ Hosp, Fac Med, Dept Radiat Oncol, TR-60080 Trabzon, Turkey
[3] Karadeniz Tech Univ, Fac Med, Dept Med Pathol, TR-61080 Trabzon, Turkey
[4] Karadeniz Tech Univ, Fac Med, Dept Biochem Med, TR-61080 Trabzon, Turkey
关键词
genistein; nephrotoxicity; melatonin; mice; radiation; radioprotection;
D O I
10.3892/br.2015.547
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
The aim of the present study was to compare the effects of melatonin and genistein on radiation-induced nephrotoxicity (RIN). A total of 70 Swiss Albino mice were divided into 7 groups. Five control groups were defined, which were sham irradiation (C, G1), radiation therapy only (RT, G2), melatonin (M, G3), genistein (G, G4) and polyethylene glycol-400 (G5), respectively. The co-treatment groups were the RT plus melatonin (RT+M, G6) and RT plus genistein (RT+G, G7) groups. Irradiation was applied using a cobalt-60 teletherapy machine (80-cm fixed source-to-surface distance, 2.5-cm depth). Melatonin was administered (100 mg/kg, intraperitoneal injection) 30 min before the single dose of irradiation, whereas genistein was administered (200 mg/kg, subcutaneous injection) 1 day before the single dose of irradiation. All the mice were sacrificed 6 months after irradiation. As an end point, the extent of renal tubular atrophy for each mouse was quantified with image analysis of histological sections of the kidney. Tissue malondialdehyde (MDA) levels were also measured in each animal. In the histopathological examination of the mouse kidneys, there was a statistically significant reduction (P<0.05) in the presence of tubular atrophy between the RT+M and RT+G groups and the RT group. There was a statistically significant increase in MDA levels in the irradiated versus sham groups (RT vs. C; P<0.05); however, MDA levels were significantly decreased by co-treatment with melatonin or genistein vs. RT alone (RT+M and RT+G vs. RT; P<0.05). In conclusion, the present experimental study showed that melatonin and genistein supplementation prior to irradiation-protected mice against RIN, which may have therapeutic implications for radiation-induced injuries.
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页码:45 / 50
页数:6
相关论文
共 58 条
[1]
A phase II trial of subcutaneous Amifostine and radiation therapy in patients with head and neck cancer [J].
Anné, PR ;
Curran, WJ .
SEMINARS IN RADIATION ONCOLOGY, 2002, 12 (01) :18-19
[2]
The effect of melatonin on eye lens of rats exposed to ultraviolet radiation [J].
Anwar, MM ;
Moustafa, MA .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 2001, 129 (01) :57-63
[3]
Bolling T, 2006, STRAHLENTHER ONKOL, V182, P443, DOI 10.1007/s00066-006-1517-9
[4]
CLINICAL RADIATION NEPHROPATHY [J].
CASSADY, JR .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1995, 31 (05) :1249-1256
[5]
Radiation nephropathy [J].
Cohen, EP ;
Robbins, MEC .
SEMINARS IN NEPHROLOGY, 2003, 23 (05) :486-499
[6]
Radiation-induced chronic oxidative renal damage can be reduced by amifostine [J].
Cosar, Rusen ;
Yurut-Caloglu, Vuslat ;
Eskiocak, Sevgi ;
Ozen, Alaattin ;
Altaner, Semsi ;
Ibis, Kamuran ;
Turan, Nesrin ;
Denizli, Bengu ;
Uzal, Cem ;
Saynak, Mert ;
Parlar, Sule ;
Caloglu, Murat ;
Uregen, Burcu ;
Kocak, Zafer .
MEDICAL ONCOLOGY, 2012, 29 (02) :768-775
[7]
Genistein induces radioprotection by hematopoietic stem cell quiescence [J].
Davis, Thomas A. ;
Mungunsukh, Ognoon ;
Zins, Stephen ;
Day, Regina M. ;
Landauer, Michael R. .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 2008, 84 (09) :713-726
[8]
Influence of melatonin on proliferation and antioxidant system in Ehrlich ascites carcinoma cells [J].
El-Missiry, MA ;
Abd El-Aziz, AF .
CANCER LETTERS, 2000, 151 (02) :119-125
[9]
El-Missiry MA, 2000, J BIOCHEM MOL TOXIC, V14, P57, DOI 10.1002/(SICI)1099-0461(2000)14:1<57::AID-JBT8>3.0.CO
[10]
2-B