Effects of endothelin-1 on the rat pituitary-adrenocortical axis under basal and stressful conditions

被引:10
作者
Malendowicz, LK [1 ]
Nussdorfer, GG
Meneghelli, V
Nowak, M
Markowska, A
Majchrzak, M
机构
[1] Sch Med, Dept Histol & Embryol, Poznan, Poland
[2] Univ Padua, Dept Anat, I-35121 Padua, Italy
关键词
D O I
10.1080/07435809709031862
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Endothelins (ETs) and their receptor subtypes A and B (ETA and ETB) are expressed in the various components of the mammalian hypothalamo-pituitary-adrenal (HPA) axis, but their involvement in the functional regulation of HPA is controversial. To gain insight into this topic, we have investigated the effects of ET-1 and/or the specific antagonists of ETA and ETB receptors (BQ-123 and BQ-788, respectively) on the plasma concentrations of ACTH, corticosterone and aldosterone of non-stressed (control) and ether- or cold-stressed rats. The study of the effects of the administration of the two ET-receptor antagonists alone could provide informations about the possible action of endogenous ETs on the HPA axis. Exogenous ET-1 increased ACTH, corticosterone and aldosterone blood levels in control rats, as well as evoked a sizable enhancement of the HPA axis response to ether stress and a marked depression of the response to cold stress. BQ-123 and BQ-788 did not prevent the stimulatory effect of exogenous ET-1 in control rats, but when administered alone, raised the plasma concentrations of ACTH, corticosterone and aldosterone. Both ET-receptor antagonists magnified the HPA axis response to ether and cold stresses, but their effect was not counteracted by exogenous ET-1. Although very difficult to interpret, our present findings allow us to conclude that endogenous ETs play a role in the maintenance of the basal activity of rat HPA axis acting through ETA and ETB receptor subtypes, which are partially insensitive to BQ-123 and BQ-788. Conversely, the involvement of ETs in the modulation of the HPA axis responses to various stresses is very doubtful.
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页码:349 / 364
页数:16
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共 71 条
[2]   Distribution and functional significance of the endothelin receptor subtypes in the rat adrenal gland [J].
Belloni, AS ;
Pacheco, YG ;
Markowska, A ;
Andreis, PG ;
Meneghelli, V ;
Malendowicz, LK ;
Nussdorfer, GG .
CELL AND TISSUE RESEARCH, 1997, 288 (02) :345-352
[3]   ENDOTHELIN-1 (ET-1) AND CYCLOSPORINE-A (CSA) STIMULATE STEROID-SECRETION FROM RAT ADRENAL-CORTEX - EVIDENCE THAT BOTH ET-1 AND CSA SECRETAGOGUE EFFECTS ARE MEDIATED BY THE B-SUBTYPE OF ET-1 RECEPTORS [J].
BELLONI, AS ;
ANDREIS, PG ;
NERI, G ;
NUSSDORFER, GG .
BIOMEDICAL RESEARCH-TOKYO, 1995, 16 (05) :287-294
[4]   Mediated by the B receptor in rats [J].
Belloni, AS ;
Rossi, GP ;
Andreis, PG ;
Neri, G ;
Albertin, G ;
Pessina, AC ;
Nussdorfer, GG .
HYPERTENSION, 1996, 27 (05) :1153-1159
[5]   IN-VITRO AUTORADIOGRAPHIC DEMONSTRATION OF ENDOTHELIN-1 BINDING-SITES IN THE HUMAN ADRENAL-CORTEX [J].
BELLONI, AS ;
ROSSI, GP ;
ZANIN, L ;
PRAYERGALETTI, T ;
PESSINA, AC ;
NUSSDORFER, GG .
BIOMEDICAL RESEARCH-TOKYO, 1994, 15 (02) :95-99
[6]   EFFECTS OF ENDOTHELIN-1 AND ENDOTHELIN-3 ON RAT HYPOTHALAMIC CORTICOTROPIN-RELEASING HORMONE AND PITUITARY ACTH RELEASE IN-VITRO [J].
CALOGERO, AE ;
RAITI, F ;
NICOLOSI, G ;
BURRELLO, N ;
DAGATA, R ;
MANTERO, F .
JOURNAL OF ENDOCRINOLOGY, 1994, 140 (03) :419-424
[7]   ENDOTHELIN-1 RELEASE FROM THE ISOLATED-PERFUSED RAT ADRENAL-GLAND IS ELEVATED ACUTELY IN RESPONSE TO INCREASING FLOW-RATES AND ACTH(1-24) [J].
CAMERON, L ;
KAPAS, S ;
HINSON, JP .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 202 (02) :873-879
[8]   CARDIORENAL ACTIONS OF ENDOTHELIN .1. EFFECTS OF CONVERTING ENZYME-INHIBITION [J].
CAO, LQ ;
BANKS, RO .
LIFE SCIENCES, 1990, 46 (08) :577-583
[9]   ENDOTHELIN-1 POTENTIATION OF ANGIOTENSIN-II STIMULATION OF ALDOSTERONE PRODUCTION [J].
COZZA, EN ;
CHIOU, S ;
GOMEZSANCHEZ, CE .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (01) :R85-R89
[10]   ENDOTHELIN BINDING TO CULTURED CALF ADRENAL ZONA GLOMERULOSA CELLS AND STIMULATION OF ALDOSTERONE SECRETION [J].
COZZA, EN ;
GOMEZSANCHEZ, CE ;
FOECKING, MF ;
CHIOU, S .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (03) :1032-1035