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

Citation
G. Re et al., Effects of mepartricin on estradiol and testosterone serum levels and on prostatic estrogen, androgen and adrenergic receptor concentrations in adultrats, PHARMAC RES, 44(2), 2001, pp. 141-147
Citations number
44
Categorie Soggetti
Pharmacology & Toxicology
Journal title
PHARMACOLOGICAL RESEARCH
ISSN journal
10436618 → ACNP
Volume
44
Issue
2
Year of publication
2001
Pages
141 - 147
Database
ISI
SICI code
1043-6618(200108)44:2<141:EOMOEA>2.0.ZU;2-R
Abstract
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 pro static estrogen, androgen, alpha (1)- and beta -adrenergic receptor concent rations and on estradiol and testosterone serum levels in adult male rats w ere studied. The effects produced by mepartricin treatments on the weight a nd dimension of the gland were investigated. Both mepartricin dosages induc ed significant decreases (P < 0.05) of the absolute and relative weights an d 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 fa r as prostatic steroid receptor concentrations were concerned, a significan t (P < 0.05) decrease in estrogen receptor number was observed in both trea ted groups, whilst a significant increase (P < 0.05) of androgen receptor c oncentrations 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 (mepartri cin treatment), therefore the combination of estrogen suppression (mepartri cin) and adrenergic suppression (alpha (1)-AR blockers) may be suggested as a possible pharmacotherapeutic strategy for the treatment of benign prosta tic hyperplasia. (C) 2001 Academic Press.