EFFECT OF 2-METHOXYESTRADIOL ON GONADOTROPIN SECRETION AND OXIDATIVE STATUS OF PORCINE PITUITARY CELLS IN VITRO

被引:0
作者
Kosior-Korzecka, Urszula [1 ]
Radwanska, Paulina [1 ]
Wojcik, Marta [1 ]
机构
[1] Univ Life Sci Lublin, Dept Pathophysiol, Chair Preclin Vet Sci, Fac Vet Med, PL-20033 Lublin, Poland
关键词
swine; 2-methoxyestradiol; pituitary cells; FSH; LH; ENDOGENOUS ESTRADIOL METABOLITE; TUMOR-GROWTH; SUPEROXIDE-DISMUTASE; GRANULOSA-CELLS; CANCER-CELLS; GNRH; ANGIOGENESIS; APOPTOSIS; LEPTIN; BETA;
D O I
暂无
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The aim of the study was to investigate the effect of 2-methoxyestradiol (2-ME) on GnRH-induced LH and FSH secretion by porcine pituitary cells in vitro. Moreover, the concentrations of superoxide anion radical (O-2(-)), as a possible mediator of 2-ME action, and malonyldialdehyde (MDA), as an oxidative stress indicator, were estimated. Pituitary cells were cultured in McCoy 5A medium with GnRH (positive control), with GnRH and 3.3x10(-11)-3.3x10(-7)M/L of 2-ME, or with GnRH and 2.7x 10(-9)-2.7x10(-s) M/L of 17 beta-estradiol. The secretion of gonadotropins, as well as concentrations of superoxide anion and MDA were analysed after 2-72 h of the experiment. A positive correlation between 2-ME dose and FSH secretion from anterior pituitary cells (r=0.72, 0.95, 0.92, 0.90, 0.85, and 0.82 after 2, 6, 18, 24, 48, and 72 h, respectively) was demonstrated. In contrast, a negative correlation between 2-ME concentration and LH secretion was observed (r=-0.82, -0.72, -0.85, -0.89, -0.93, and -0.79 after 2, 6, 18, 24, 48, and 72 h, respectively). The concentration of O-2(-) was increasing under the influence of the rising doses of 2-ME, whereas the mean level of MDA was not changing significantly.
引用
收藏
页码:373 / 378
页数:6
相关论文
共 22 条
[1]  
Banerjee SK, 2000, ANTICANCER RES, V20, P2641
[2]   2-Methoxyestradiol inhibits superoxide anion generation while it enhances superoxide dismutase activity in swine granulosa cells [J].
Basini, Giuseppina ;
Santini, Sujen Eleonora ;
Grasselli, Francesca .
SIGNAL TRANSDUCTION PATHWAYS, PT B: STRESS SIGNALING AND TRANSCRIPTIONAL CONTROL, 2006, 1091 :34-40
[3]   Antiangiogenesis in swine ovarian follicle: A potential role for 2-methoxyestradiol [J].
Basini, Giuseppina ;
Bussolati, Simona ;
Santini, Sujen Eleonora ;
Bianchi, Federica ;
Careri, Maria ;
Mangia, Alessandro ;
Musci, Marilena ;
Grasselli, Francesca .
STEROIDS, 2007, 72 (08) :660-665
[4]   An SPME-GC-MS method using an octadecyl silica fibre for the determination of the potential angiogenesis modulators 17β-estradiol and 2-methoxyestradiol in culture media [J].
Bianchi, Federica ;
Mattarozzi, Monica ;
Careri, Maria ;
Mangia, Alessandro ;
Musci, Marilena ;
Grasselli, Francesca ;
Bussolati, Simona ;
Basini, Giuseppina .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2010, 396 (07) :2639-2645
[5]   The influence of GnRH, oxytocin and vasoactive intestinal peptide on the secretion of β-endorphin and production of cAMP and cGMP by porcine pituitary cells in vitro [J].
Bogacka, I ;
Siawrys, G ;
Okrasa, S ;
Kaminski, T ;
Przala, J .
ANIMAL REPRODUCTION SCIENCE, 2002, 69 (1-2) :125-137
[6]   The endogenous estradiol metabolite 2-methoxyestradiol reduces atherosclerotic lesion formation in female apolipoprotein E-deficient mice [J].
Bourghardt, Johan ;
Bergstrom, Goran ;
Krettek, Alexandra ;
Sjoberg, Sara ;
Boren, Jan ;
Tivesten, Asa .
ENDOCRINOLOGY, 2007, 148 (09) :4128-4132
[7]  
Das U.N., 2002, MED SCI MONIT, V8, P79
[8]   Acute effects of 2-methoxyestradiol on endothelial aortic No release in male and ovariectomized female rats [J].
Fenoy, Francisco J. ;
Hernandez, Maria E. ;
Hernandez, Moises ;
Quesada, Tomas ;
Salom, Miguel G. ;
Hernandez, Isabel .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2010, 23 (01) :12-19
[9]   Inhibition of mitochondrial respiration by the anticancer agent 2-methoxyestradiol [J].
Hagen, T ;
D'Amico, G ;
Quintero, M ;
Palacios-Callender, M ;
Hollis, V ;
Lam, F ;
Moncada, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 322 (03) :923-929
[10]   Superoxide dismutase as a target for the selective killing of cancer cells [J].
Huang, P ;
Feng, L ;
Oldham, EA ;
Keating, MJ ;
Plunkett, W .
NATURE, 2000, 407 (6802) :390-395