Human Prolactin Receptor and Dopamine Actions in Feminizing Adrenal Neoplastic Cells

N. Furuhashi, V. Fang
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Abstract

Estrogen production by feminizing adrenal neoplastic cells (Fang-8 cells) in culture was stimulated by human prolactin (hPRL). The existence of hPRL receptor in the cells was demonstrated. The stimulatory effect of hPRL was abolished by dopamine and CB-154 (2-bromo-α-ergocriptine), since CB-154, at 60 μg/dish, inhibited cell growth and estrogen production in the absence of hPRL and since dopamine may involve different mechanisms of action. The action of CB-154 was blocked by propranolol, not by phenoxybenzamine or pimozide. Since we could not demonstrate adrenergic or dopaminergic receptor in Fang-8 cells, the interaction between CB-154 and propranolol may not be explained by a pharmacological beta-adrenergic mechanism.
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人催乳素受体和多巴胺在肾上腺肿瘤细胞雌性化中的作用
人催乳素(hPRL)刺激培养的肾上腺肿瘤细胞雌性化(Fang-8细胞)产生雌激素。证实了hPRL受体在细胞内的存在。多巴胺和CB-154(2-溴-α-麦角隐碱)可以消除hPRL的刺激作用,因为CB-154 (60 μg/盘)可以抑制hPRL缺失时细胞的生长和雌激素的产生,而且多巴胺可能涉及不同的作用机制。苯萘洛尔可阻断CB-154的作用,而苯氧苄胺或吡莫齐不能。由于我们无法在Fang-8细胞中证明肾上腺素能受体或多巴胺能受体,因此CB-154与心得安之间的相互作用可能无法用药理学β -肾上腺素能机制来解释。
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