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多巴胺与雌二醇对培养的正常人垂体细胞和肿瘤垂体细胞催乳素释放的相互作用差异。

Differences in the interaction between dopamine and estradiol on prolactin release by cultured normal and tumorous human pituitary cells.

作者信息

Lamberts S W, Verleun T, Hofland L, Oosterom R

出版信息

J Clin Endocrinol Metab. 1986 Dec;63(6):1342-7. doi: 10.1210/jcem-63-6-1342.

Abstract

We studied the interaction between dopamine and estradiol on PRL release by cultured normal and tumorous PRL-secreting cells prepared from human pituitaries. If pituitary glands were obtained within 3 h after sudden death of previously normal individuals, the viability of isolated pituitary cells prepared by dispersion with dispase was more than 75%. After 4 days of culture, dopamine (500 nM) inhibited PRL release by cells prepared from four normal pituitaries by 24 +/- 3% (+/- SEM). Pretreatment of the cells with 100 nM estradiol did not alter dopamine-mediated inhibition of PRL release. Estradiol alone increased basal PRL release and cell PRL content. Cultured PRL-secreting pituitary tumor cells, obtained by transsphenoidal operation from four patients, were similarly sensitive to dopamine. Estradiol stimulated tumor cell PRL release and content, but significantly diminished the inhibitory effect of dopamine. The estrogen receptor blocker tamoxifen did not alter PRL release, but it did reverse the estradiol-induced insensitivity of the prolactinoma cells to the dopamine agonist bromocriptine. In conclusion, these in vitro results indicate that estrogens do not antagonize the effect of dopamine on normal human PRL-secreting pituitary cells. In human pituitary tumor cells, however, estradiol decreased the sensitivity of PRL release to dopamine (agonists), and the estrogen action can be acutely reversed by tamoxifen.

摘要

我们研究了多巴胺与雌二醇对从人垂体中制备的培养正常及肿瘤性催乳素分泌细胞催乳素释放的相互作用。如果垂体是在先前正常个体突然死亡后3小时内获取的,用dispase分散制备的分离垂体细胞的活力超过75%。培养4天后,多巴胺(500 nM)抑制了来自四个正常垂体的细胞的催乳素释放,抑制率为24±3%(±SEM)。用100 nM雌二醇预处理细胞并没有改变多巴胺介导的催乳素释放抑制作用。单独使用雌二醇增加了基础催乳素释放和细胞催乳素含量。通过经蝶窦手术从四名患者获取的培养催乳素分泌垂体肿瘤细胞对多巴胺同样敏感。雌二醇刺激肿瘤细胞催乳素释放和含量,但显著减弱了多巴胺的抑制作用。雌激素受体阻断剂他莫昔芬没有改变催乳素释放,但它确实逆转了雌二醇诱导的催乳素瘤细胞对多巴胺激动剂溴隐亭的不敏感性。总之,这些体外研究结果表明,雌激素并不拮抗多巴胺对正常人催乳素分泌垂体细胞的作用。然而,在人垂体肿瘤细胞中,雌二醇降低了催乳素释放对多巴胺(激动剂)的敏感性,并且他莫昔芬可以急性逆转雌激素的作用。

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