L-692,429, A NONPEPTIDE GROWTH-HORMONE (GH) SECRETAGOGUE, REVERSES GLUCOCORTICOID SUPPRESSION OF GH SECRETION

被引:29
作者
GERTZ, BJ [1 ]
SCIBERRAS, DG [1 ]
YOGENDRAN, L [1 ]
CHRISTIE, K [1 ]
BADOR, K [1 ]
KRUPA, D [1 ]
WITTREICH, JM [1 ]
JAMES, I [1 ]
机构
[1] ROYAL FREE HOSP, SCH MED, DEPT CLIN PHARMACOL & CHEM PATHOL, LONDON, ENGLAND
关键词
D O I
10.1210/jc.79.3.745
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The reversal of glucocorticoid-induced negative nitrogen balance by GH supports a possible therapeutic role for GH treatment in patients receiving these catabolic steroids. A GH secretagogue might be of similar utility. However, stimulated GH secretion is generally suppressed by glucocorticoids. To test whether L-692,429, a nonpeptide mimic of GH-releasing peptide-6, can overcome such suppression, a double blind, placebo-controlled, three-period, cross-over study was performed in nine healthy young men who received 0.2 mg/kg L692,429, iv, preceded by 4 days of prednisolone (20 mg, orally, three times daily) or placebo, and 0.75 mg/kg L-692,429 preceded by prednisolone only. The mean (se) GH peak and area under the curve between 0-240 min after administration of 0.2 mg/kg L-692,429 in the absence of steroid were 53.8 (7.2) mu g/L and 3481 (1005) mu g/min.L, which were reduced to 25.1 (3.4) mu g/L and 1342 (285) mu g/min.L (P less than or equal to 0.01) when treatment was preceded by 4 days of prednisolone. However, the suppressive influence of the steroid was attenuated by the high dose of L-692,429, which achieved a GH peak and area under the curve between 0-240 min of 42.6 (5.8) mu g/L and 2298 (425) mu g/min.L, respectively (P < 0.01 us. 0.2 mg/kg L-692,429 plus prednisolone). L-692,429 stimulates GH secretion even in the setting of short term, high dose, concomitant glucocorticoid treatment, suggesting that such compounds might provide an alternative means of increasing circulating GH and reversing the catabolic effects of these steroids.
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页码:745 / 749
页数:5
相关论文
共 31 条
[11]   EFFECTS OF RECOMBINANT HUMAN GROWTH-HORMONE ON DONOR-SITE HEALING IN SEVERELY BURNED CHILDREN [J].
HERNDON, DN ;
BARROW, RE ;
KUNKEL, KR ;
BROEMELING, L ;
RUTAN, RL .
ANNALS OF SURGERY, 1990, 212 (04) :424-431
[12]   EFFICACY AND SPECIFICITY OF L-692,429, A NOVEL NONPEPTIDYL GROWTH-HORMONE SECRETAGOGUE, IN BEAGLES [J].
HICKEY, G ;
JACKS, T ;
JUDITH, F ;
TAYLOR, J ;
SCHOEN, WR ;
KRUPA, D ;
CUNNINGHAM, P ;
CLARK, J ;
SMITH, RG .
ENDOCRINOLOGY, 1994, 134 (02) :695-701
[13]   HUMAN GROWTH-HORMONE PREVENTS THE PROTEIN CATABOLIC SIDE-EFFECTS OF PREDNISONE IN HUMANS [J].
HORBER, FF ;
HAYMOND, MW .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (01) :265-272
[14]   OVERESTIMATION OF RENAL-FUNCTION IN GLUCOCORTICOSTEROID TREATED PATIENTS [J].
HORBER, FF ;
SCHEIDEGGER, J ;
FREY, FJ .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1985, 28 (05) :537-541
[15]   EFFECT OF HUMAN GROWTH HORMONE-RELEASING HORMONE ON GH SECRETION IN CUSHINGS-SYNDROME AND NON-ENDOCRINE DISEASE PATIENTS TREATED WITH GLUCOCORTICOIDS [J].
HOTTA, M ;
SHIBASAKI, T ;
MASUDA, A ;
IMAKI, T ;
SUGINO, N ;
DEMURA, H ;
LING, N ;
SHIZUME, K .
LIFE SCIENCES, 1988, 42 (09) :979-984
[16]   EFFECT OF A NEW SYNTHETIC HEXAPEPTIDE TO SELECTIVELY STIMULATE GROWTH-HORMONE RELEASE IN HEALTHY-HUMAN SUBJECTS [J].
ILSON, BE ;
JORKASKY, DK ;
CURNOW, RT ;
STOTE, RM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 69 (01) :212-214
[17]  
JEFFRIES M K, 1992, Journal of Burn Care and Rehabilitation, V13, P391, DOI 10.1097/00004630-199207000-00001
[18]  
JORGENSEN JOL, 1989, LANCET, V1, P1221
[19]   INHIBITION BY PREDNISONE OF GROWTH-HORMONE (GH) RESPONSE TO GH-RELEASING HORMONE IN NORMAL MEN [J].
KAUFMANN, S ;
JONES, KL ;
WEHRENBERG, WB ;
CULLER, FL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1988, 67 (06) :1258-1261
[20]  
PONG SS, 1992, 74TH P ANN M END SOC, P255