The activation of somatostatinergic receptors by either somatostatin-14 or cortistatin-17 often inhibits ACTH hypersecretion in patients with Cushing's disease

被引:26
作者
Giordano, R.
Picu, A.
Bonelli, L.
Broglio, F.
Prodam, F.
Grottoli, S.
Mucciolil, G.
Ghigo, E.
Arvat, E. [1 ]
机构
[1] Univ Turin, Dept Internal Med, Div Endocrinol & Metab, I-10126 Turin, Italy
[2] Univ Turin, Dipartimento Anat Pharmacol & Forensic Med, I-10125 Turin, Italy
关键词
D O I
10.1530/EJE-07-0147
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Object: Somatostatin (SS) is known to inhibit GH and insulin, while its effect on corticotrope secretion is controversial: inhibition of ACTH secretion by agonists activating somatostatinergic receptors (sst)-2 and sst-5 was reported in vitro. Cortistatin (CST) not only binds all sst receptor subtypes but also possesses central actions that are not shared by SS. Design: In nine patients with Cushing's disease (CD), ACTH, cortisol, GH, insulin, and glucose levels were studied during 120-min i.v. infusion of SS-14 (2.0 mu g/kg per h). CST-17 (2.0 mu g/kg per h) or saline. Results: Both SS or CST significantly affected the hypothalamic-pituitary-adrenal axis. Cortisol was decreased to the same extent by either SS or CST (P < 0.05). Both SS and CST decreased ACTH. although statistical difference was reached only during CST (P < 0.05). Analyzing the individual responses as Delta areas under curve (Delta AUCs), a clear and consensual inhibition of ACTH and cortisol under either SS or CST was recorded in five out of nine patients. Both SS or CST inhibited (P < 0.05) insulin, that even showed a rebound (P < 0.01.) at the end of infusion. GH was not modified by either peptide. Conclusion: SS and CST often display similar inhibitory effects on the HPA axis in CR The activation of sst receptors by both peptides is followed in almost 50% of patients by a remarkable inhibition of ACTH and cortisol hypersecretion. These findings reinforce the view that sst receptors are involved in the control of the secretory activity of tumoral corticotropic cells.
引用
收藏
页码:393 / 398
页数:6
相关论文
共 30 条
[1]   Expression of cortistatin and MrgX2, a specific cortistatin receptor, in human neuroendocrine tissues and related tumours [J].
Allia, E ;
Tarabra, E ;
Volante, M ;
Cerrato, M ;
Ghigo, E ;
Muccioli, G ;
Papotti, M .
JOURNAL OF PATHOLOGY, 2005, 207 (03) :336-345
[2]   FAILURE OF SOMATOSTATIN AND OCTREOTIDE TO ACUTELY AFFECT THE HYPOTHALAMIC-PITUITARY-ADRENAL FUNCTION IN PATIENTS WITH CORTICOTROPIN HYPERSECRETION [J].
AMBROSI, B ;
BOCHICCHIO, D ;
FADIN, C ;
COLOMBO, P ;
FAGLIA, G .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1990, 13 (03) :257-261
[3]  
American Diabetes Association, 2004, Diabetes Care, V27 Suppl 1, pS5, DOI 10.2337/diacare.27.2007.S5
[4]  
Arnaldi G, 2005, J Endocrinol Invest, V28, P106
[5]   Endocrine activities of cortistatin-14 and its interaction with GHRH and ghrelin in humans [J].
Broglio, F ;
Arvat, E ;
Benso, A ;
Gottero, C ;
Prodam, F ;
Grottoli, S ;
Papotti, M ;
Muccioli, G ;
van der Lely, AJ ;
Deghenghi, R ;
Ghigo, E .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (08) :3783-3790
[6]   CENTRAL NERVOUS-SYSTEM REGULATION OF ADRENOCORTICOTROPIN SECRETION - ROLE OF SOMATOSTATINS [J].
BROWN, MR ;
RIVIER, C ;
VALE, W .
ENDOCRINOLOGY, 1984, 114 (05) :1546-1549
[7]   ENHANCED SENSITIVITY GROWTH-HORMONE (GH) CHEMILUMINESCENCE ASSAY REVEALS LOWER POSTGLUCOSE NADIR GH CONCENTRATIONS IN MEN THAN WOMEN [J].
CHAPMAN, IM ;
HARTMAN, ML ;
STRAUME, M ;
JOHNSON, ML ;
VELDHUIS, JD ;
THORNER, MO .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (06) :1312-1319
[8]  
de Lecea L, 2005, J Endocrinol Invest, V28, P10
[9]   Cortistatin, but not somatostatin, binds to growth hormone secretagogue (GHS) receptors of human pituitary gland [J].
Deghenghi, R ;
Papotti, M ;
Ghigo, E ;
Muccioli, G .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2001, 24 (01) :RC1-RC3
[10]   A cortical neuropeptide with neuronal depressant and sleep-modulating properties [J].
deLecea, L ;
Criado, JR ;
ProsperoGarcia, O ;
Gautvik, KM ;
Schweitzer, P ;
Danielson, PE ;
Dunlop, CLM ;
Siggins, GR ;
Henriksen, SJ ;
Sutcliffe, JG .
NATURE, 1996, 381 (6579) :242-245