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血清生长激素和催乳素抑制期间大鼠乳腺癌的消退

Rat mammary carcinoma regressions during suppression of serum growth hormone and prolactin.

作者信息

Rose D P, Gottardis M, Noonan J J

出版信息

Anticancer Res. 1983 Sep-Oct;3(5):323-5.

PMID:6139974
Abstract

Female rats bearing N-nitrosomethylurea-induced mammary carcinomas were treated with pergolide mesylate to suppress serum prolactin. The drug was given alone, or with somatostatin, 20 micrograms/hr delivered by osmotic minipump for 7 days to suppress serum growth hormone. Tumour regressions did not occur with pergolide alone, but did so promptly in all of 5 rats when growth hormone levels were also suppressed by somatostatin. A potent long-acting agonistic analogue of somatostatin, L362,823 produced similar tumour regressions at a dose of 5 micrograms/hr when given with pergolide, but was ineffective alone. This dose completely prevented the episodic release of pituitary growth hormone.

摘要

用甲磺酸培高利特处理携带N-亚硝基甲基脲诱导的乳腺癌的雌性大鼠,以抑制血清催乳素。该药物单独给药,或与生长抑素联合给药,通过渗透微型泵以20微克/小时的速度给药7天,以抑制血清生长激素。单独使用培高利特时肿瘤未消退,但当生长抑素也抑制生长激素水平时,5只大鼠中有4只迅速出现肿瘤消退。生长抑素的一种强效长效激动剂类似物L362,823与培高利特联合给药时,以5微克/小时的剂量产生了类似的肿瘤消退,但单独使用时无效。该剂量完全阻止了垂体生长激素的间歇性释放。

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