CV-205-502 IN ACROMEGALY

被引:29
作者
CHIODINI, PG
ATTANASIO, R
COZZI, R
DALLABONZANA, D
OPPIZZI, G
ORLANDI, P
STRADA, S
LIUZZI, A
机构
[1] Divisione di Endocrinologia, Ospedale Niguarda, I-20162 Milan
来源
ACTA ENDOCRINOLOGICA | 1993年 / 128卷 / 05期
关键词
D O I
10.1530/acta.0.1280389
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In a series of acromegalic patients the effects of CV 205-502, a new long-acting dopamine-agonist drug, on growth hormone (GH), insulin-like growth factor I (IGF-I) and prolactin (PRL) levels were evaluated in an open study. After acute administration of CV 205-502 (0.03 75 mg, po) in 12 patients, GH levels did not change, whereas PRL values significantly decreased and remained suppressed for 24 h. In the 14 patients who underwent chronic CV 205-502 treatment (at daily doses of 0.150-0.600 mg/day given at bedtime or b.i.d. for up to 12 months), GH and IGF-I levels fell significantly from 60 +/- 17 (mean +/- SEM) mug/l to 28 +/- 10 mug/l and from 1127 +/- 84 mug/l to 738 +/- 57 mug/l, respectively (p < 0.05). A retrospective comparison with the results obtained for the same patients during a previous chronic bromocriptine treatment (at daily doses of 5-20 mg given t.i.d. or q.i.d.) did not show any significant difference in the suppression of GH levels between the two treatments; no bromocriptine-resistant patient was CV 205-502 sensitive, even at the highest CV 205-502 dose used. We conclude that in acromegaly chronic treatment with this new dopaminergic drug has a GH- and PRL-lowering effect that is similar to but more prolonged than that of bromocriptine, and normal or near-normal GH and IGF-I levels may be obtained in a few patients with b.i.d. administration. However, no GH-lowering effect is observed in bromocriptine-resistant patients.
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页码:389 / 393
页数:5
相关论文
共 9 条
[1]   STABLE REDUCTION OF PLASMA GROWTH-HORMONE (HGH) LEVELS DURING CHRONIC ADMINISTRATION OF 2-BR-ALPHA-ERGOCRYPTINE (CB-154) IN ACROMEGALIC PATIENTS [J].
CHIODINI, PG ;
LIUZZI, A ;
BOTALLA, L ;
OPPIZZI, G ;
MULLER, EE ;
SILVESTRINI, F .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1975, 40 (04) :705-708
[2]  
CHIODINI PG, 1989, ADV GROWTH HORMONE G, P423
[3]  
COZZI R, 1991, J ENDOCRINOL INVES S, V14, P54
[4]   EFFECT OF THE NEW DOPAMINERGIC AGONIST CV 205-502 ON PLASMA PROLACTIN LEVELS AND TUMOR SIZE IN BROMOCRIPTINE-RESISTANT PROLACTINOMAS [J].
DURANTEAU, L ;
CHANSON, P ;
LAVOINNE, A ;
HORLAIT, S ;
LUBETZKI, J ;
KUHN, JM .
CLINICAL ENDOCRINOLOGY, 1991, 34 (01) :25-29
[5]  
GAILLARD R, 1986, P INT C ENDOCRINOLOG, P305
[7]  
QUABBE HJ, 1981, ACTA ENDOCR-COP S, V240, P66
[8]   CV 205-502 - A NEW LONG-ACTING DRUG FOR INHIBITION OF PROLACTIN HYPERSECRETION [J].
RASMUSSEN, C ;
BERGH, T ;
WIDE, L ;
BROWNELL, J .
CLINICAL ENDOCRINOLOGY, 1987, 26 (03) :321-326
[9]   EFFECTS OF 2 NOVEL DOPAMINERGIC DRUGS, CV-205-502 AND CQP-201-403, ON PROLACTIN AND GROWTH-HORMONE SECRETION BY HUMAN PITUITARY-TUMORS INVITRO [J].
VENETIKOU, MS ;
BURRIN, JM ;
WOODS, CA ;
YEO, TH ;
BROWNELL, J ;
ADAMS, EF .
ACTA ENDOCRINOLOGICA, 1987, 116 (02) :287-292