COMPARISON OF LONG-ACTING ANALOGS OF LUTEINIZING-HORMONE RELEASING HORMONE IN MAN

被引:19
作者
WASS, JAH
BESSER, GM
GOMEZPAN, A
SCANLON, MF
HALL, R
KASTIN, AJ
COY, DH
SCHALLY, AV
机构
[1] ST BARTHOLOMEWS HOSP,DEPT ENDOCRINOL,LONDON EC1A 7BE,ENGLAND
[2] ROYAL VICTORIA INFIRM,DEPT MED,ENDOCRINE UNIT,NEWCASTLE TYNE NE1 4LP,TYNE & WEAR,ENGLAND
[3] TULANE UNIV,ENDOCRINE LAB,NEW ORLEANS,LA 70118
[4] TULANE UNIV,POLYPEPTIDE LAB,NEW ORLEANS,LA 70118
[5] VET ADM HOSP,NEW ORLEANS,LA 70140
关键词
D O I
10.1111/j.1365-2265.1979.tb02098.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Currently, LHRH, when used therapeutically, is given by parenteral injection every 8 h. We have looked at the release of LH and FSH induced by five analogues of LHRH and compared this with gonadotrophin release after synthetic LHRH. The analogues were substituted in position 6 or in positions 6 and 10 and were given intravenously, intranasally or subcutaneously in three separate studies. After intravenous administration of 100μg, all analogues caused greater release of LH and FSH than did synthetic LHRH. Given intranasally in a dose of 500 μg, three of the four analogues tested caused greater LH and FSH release than did LHRH. With tryptophan substitution in position 6 (D‐TRP6‐LHRH), mean LH levels in five subjects were still above the normal range 24 h after a single intranasal dose. The intranasal administration of selected analogues of LHRH has great potential in the treatment of conditions associated with deficient gonadotrophin secretion, provided that pituitary overstimulation, which may eventually lead to a decrease in LH and FSH output by the anterior pituitary, is avoided. Copyright © 1979, Wiley Blackwell. All rights reserved
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收藏
页码:419 / 430
页数:12
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