Protective effects of sildenafil citrate administration on cisplatin-induced ovarian damage in rats

被引:33
作者
Taskin, Mine Islimye [1 ]
Yay, Arzu [2 ]
Adali, Ertan [1 ]
Balcioglu, Esra [2 ]
Inceboz, Umit [1 ]
机构
[1] Balikesir Univ, Sch Med, Dept Obstet & Gynecol, TR-10145 Balikesir, Turkey
[2] Erciyes Univ, Sch Med, Dept Histol & Embryol, Kayseri, Turkey
关键词
AMH; cisplatin; primordial follicle; sildenafil citrate; MULLERIAN-INHIBITING SUBSTANCE; PRIMORDIAL FOLLICULAR RESERVE; GNRH ANTAGONIST; CHEMOTHERAPY; HORMONE; TORSION/DETORSION; FERTILITY; CYCLOPHOSPHAMIDE; SELENIUM; INJURY;
D O I
10.3109/09513590.2014.984679
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this study is to evaluate the effects of sildenafil citrate on cisplatin-induced ovarian toxicity. Thirty-two female rats were divided into four groups. Group 1: saline control; group 2: cisplatin; group 3: sildenafil citrate; and group 4: cisplatin plus sildenafil citrate group. In groups 2 and 4, the rats were injected with 5 mg/kg cisplatin intraperitoneally (i.p.). In groups 3 and 4, the rats were injected with 1.4 mg/kg sildenafil citrate i.p. The ovaries were removed two weeks later in all groups. Histopathologic examination, follicle counting and classification were performed. The expression of anti-Mullerian hormone (AMH) was detected immunohistochemically in the ovarian tissues. Sildenafil alleviated cisplatin-induced histopathological changes in the ovarian tissue. Primordial, secondary and tertiary follicles were diminished in group 2 compared with group 1 (p <0.05). Pretreatment with sildenafil citrate preserved primordial follicle count in group 4 compared with group 2, and the difference was statistically significant (p <0.05). According to our results, immunoreactivity intensity of AMH was lower in group 2 compared with group 1 (92.4 +/- 3.97 versus 88.8 +/- 1.77) but not significantly, whereas immunoreactivity intensity of AMH was higher in group 4 compared with group 2 (88.8 +/- 1.77 versus 94.1 +/- 2.36; p<0.05). Our results demonstrated that pretreatment with sildenafil citrate is beneficial for protecting the ovaries from cisplatin-induced damage. Sildenafil citrate can be a choice for fertility preservation.
引用
收藏
页码:272 / 277
页数:6
相关论文
共 32 条
[1]   The Effect of Sildenafil on Cisplatin Nephrotoxicity in Rats [J].
Ali, Badreldin H. ;
Abdelrahman, Aly M. ;
Al-Salam, Suhail ;
Sudhadevi, Munjusha ;
AlMahruqi, Ahmed S. ;
Al-Husseni, Ishaq S. ;
Beegam, Sumiya ;
Dhanasekaran, Subramanian ;
Nemmar, Abderrahim ;
Al-Moundhri, Mansour .
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2011, 109 (04) :300-308
[2]   The Effect of Mirtazapine on Cisplatin-Induced Oxidative Damage and Infertility in Rat Ovaries [J].
Altuner, Durdu ;
Gulaboglu, Mine ;
Yapca, Omer Erkan ;
Cetin, Nihal .
SCIENTIFIC WORLD JOURNAL, 2013,
[3]   New Platinum and Ruthenium Complexes - the Latest Class of Potential Chemotherapeutic Drugs - a Review of Recent Developments in the Field [J].
Amin, Amr ;
Buratovich, Michael A. .
MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2009, 9 (13) :1489-1503
[4]   Protective effects of sildenafil administration on testicular torsion/detorsion damage in rats [J].
Beheshtian, Azadeh ;
Salmasi, Amirali Hassanzadeh ;
Payabvash, Seyedmehdi ;
Kiumehr, Saman ;
Ghazinezami, Behtash ;
Rahimpour, Sina ;
Tavangar, Seyed Mohammad ;
Dehpour, Ahmad Reza .
WORLD JOURNAL OF UROLOGY, 2008, 26 (02) :197-202
[5]   How to preserve fertility in young women exposed to chemotherapy? The role of GnRH agonist cotreatment in addition to Cryopreservation of embrya, oocytes, or ovaries [J].
Blumenfeld, Zeev .
ONCOLOGIST, 2007, 12 (09) :1044-1054
[6]   Morphological and functional state of rat ovaries in early and late periods after administration of platinum cytostatics [J].
Borovskaya, TG ;
Goldberg, VE ;
Fomina, TI ;
Pakhomova, AV ;
Kseneva, SI ;
Poluektova, ME ;
Goldberg, ED .
BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE, 2004, 137 (04) :331-335
[7]   Serum anti-Mullerian hormone is more strongly related to ovarian follicular status than serum inhibin B, estradiol, FSH and LH on day 3 [J].
Fanchin, R ;
Schonäuer, LM ;
Righini, C ;
Guibourdenche, J ;
Frydman, R ;
Taieb, J .
HUMAN REPRODUCTION, 2003, 18 (02) :323-327
[8]   The GnRH antagonist reduces chemotherapy-induced ovarian damage in rats by suppressing the apoptosis [J].
Huang, Yan-hong ;
Zhao, Xue-jing ;
Zhang, Qing-hong ;
Xin, Xiao-yan .
GYNECOLOGIC ONCOLOGY, 2009, 112 (02) :409-414
[9]  
Iwase A, 2014, REPROD SCI
[10]   Reduced ovarian function in long-term survivors of radiation- and chemotherapy-treated childhood cancer [J].
Larsen, EC ;
Müller, J ;
Schmiegelow, K ;
Rechnitzer, C ;
Andersen, AN .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (11) :5307-5314