Effects of mepartricin on estradiol and testosterone serum levels and on prostatic estrogen, androgen and adrenergic receptor concentrations in adult rats

被引:7
作者
Re, G
Badino, P
Odore, R
Vigo, D
Bonabello, A
Rabino, S
Capello, F
Bruzzese, T
机构
[1] Univ Turin, Div Pharmacol & Toxicol, Dept Anim Pathol, I-10095 Grugliasco, TO, Italy
[2] Univ Milan, Dept Vet Sci & Technol Food Safety, I-20133 Milan, Italy
[3] SPA, I-20143 Milan, Italy
关键词
mepartricin; steroids; receptors; prostate; rat;
D O I
10.1006/phrs.2001.0846
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effects induced by oral administration of 0, 5 and 20 mg of meparticin kg(-1) of body weight for 28 days (group 1, 2 and 3, respectively) upon prostatic estrogen, androgen, alpha (1)- and beta -adrenergic receptor concentrations and on estradiol and testosterone serum levels in adult male rats were studied. The effects produced by mepartricin treatments on the weight and dimension of the gland were investigated. Both mepartricin dosages induced significant decreases (P < 0.05) of the absolute and relative weights and of the dimensions of the prostate. A significant dose-dependent decrease (P < 0.05) in estradiol serum levels was observed in treated rats, whereas no significant modifications were found in testosterone serum levels. As far as prostatic steroid receptor concentrations were concerned, a significant (P < 0.05) decrease in estrogen receptor number was observed in both treated groups, whilst a significant increase (P < 0.05) of androgen receptor concentrations was recorded only in rats treated with 20 mg mepartricin kg(-1). Conversely, a dose-dependent up-regulation of both prostatic alpha (1)- and beta -AR was found. Data obtained suggest that the prostatic alpha (1)-AR expression may be strongly influenced by estrogen deprivation (mepartricin treatment), therefore the combination of estrogen suppression (mepartricin) and adrenergic suppression (alpha (1)-AR blockers) may be suggested as a possible pharmacotherapeutic strategy for the treatment of benign prostatic hyperplasia. (C) 2001 Academic Press.
引用
收藏
页码:141 / 147
页数:7
相关论文
共 45 条
[1]   THE DEVELOPMENT OF HUMAN BENIGN PROSTATIC HYPERPLASIA WITH AGE [J].
BERRY, SJ ;
COFFEY, DS ;
WALSH, PC ;
EWING, LL .
JOURNAL OF UROLOGY, 1984, 132 (03) :474-479
[2]  
Boehm S, 1998, WIEN KLIN WOCHENSCHR, V110, P817
[3]  
CLARK JH, 1985, TXB ENDOCRINOLOGY, P33
[4]   ANDROGEN AND ESTROGEN RESPONSIVENESS OF STROMAL CELLS DERIVED FROM THE HUMAN HYPERPLASTIC PROSTATE - ESTROGEN REGULATION OF THE ANDROGEN RECEPTOR [J].
COLLINS, AT ;
ZHIMING, B ;
GILMORE, K ;
NEAL, DE .
JOURNAL OF ENDOCRINOLOGY, 1994, 143 (02) :269-277
[5]  
DAVIES P, 1991, J ENDOCRINOL, V139, P5
[6]  
DELVECCHIO S, 1990, J INT MED RES, V18, P468
[7]  
GHELFI R, 1978, THER ANTIBIOT CHEMOT, V28, P3
[8]   Comparison of adrenoceptor subtype expression in porcine and human bladder and prostate [J].
Goepel, M ;
Wittmann, A ;
Rubben, H ;
Michel, MC .
UROLOGICAL RESEARCH, 1997, 25 (03) :199-206
[9]  
GRIFFITHS K, 1991, EUR UROL, V20, P68
[10]   beta-adrenoceptor-mediated inhibition of alpha(1)-adrenoceptor-mediated and field stimulation-induced contractile responses in the prostate of the guinea pig [J].
Haynes, JM ;
Hill, SJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 122 (06) :1067-1074