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Acta Physiologica 2011; Volume 203, Supplement 686
Joint Congress of FEPS and Turkish Society of Physiological Sciences
9/3/2011-9/7/2011
Istanbul, Turkey
PROTECTIVE EFFECT OF QUERCETIN ON ETHANOL-INDUCED TESTICULAR DAMAGE IN RATS
Abstract number: PC267
Uygur1 Ramazan, Yagmurca2 Murat, Alper Alkoc3 Ozan, Genc4 Abdurrahman, Songur5 Ahmet, Ucok4 Kagan, Aslan Ozen1 Oguz
1Namik Kemal University, School of Medicine, Department of Anatomy, Tekirdag, Turkey
2Fatih University, School of Medicine, Department of Histology&Embryology, Ankara, Turkey
3Duzce University, School of Medicine, Department of Anatomy, Duzce, Turkey
4Afyon Kocatepe University, School of Medicine, Department of Physiology, Afyonkarahisar, Turkey
5Afyon Kocatepe University, School of Medicine, Department of Anatomy, Afyonkarahisar, Turkey
Objective:
Ethanol exposure is known to suppress male reproductive activity in laboratory animals and humans. Quercetin is a natural antioxidant. In this study, the effects of quercetin on the testicular changes due to ethanol exposure in rats were investigated.
Methods:
The animals were divided into three groups. Group 1) Control (Saline 3 ml/kg/day, i.g.; n=9), Group 2) Ethanol (40% 3 g/kg/day, i.g.; n=9), Group 3) Ethanol + Quercetin (270 mg/kg/day, i.g.; n=9). After 8-weeks of treatment, all animals were sacrificed and the testes were removed for biochemical and histopathological investigation. Tissue sections from testes were stained with hematoxylin & eosin. Apoptotic cells were analyzed by using TUNEL assay. The activities of SOD, CAT, and GSH-Px as well as MDA and NO levels were measured by spectrophotometry.
Results:
It has been observed that the ethanol administered rats have retarded in terms of body weight gain, besides developing degenerative changes in morphologic analyses as well as showing decrease in seminiferous tubule diameters. TUNEL assay also showed an increase in apoptotic cell number. Biochemically, increases in MDA and NO levels were detected, whereas decreases in SOD, CAT, and GSH-Px activities were observed.
Histopathologic changes caused by ethanol have been recovered partly or completely by giving quercetin. It was also found that protection was provided by increasing SOD, CAT and GSH-Px activities and by decreasing the levels of NO in groups administered quercetin.
Conclusions:
In view of the present findings, it is suggested that quercetin treatment may prevent ethanol-induced oxidative damage and apoptosis in rat testes.
To cite this abstract, please use the following information:
Acta Physiologica 2011; Volume 203, Supplement 686 :PC267