首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Direct effects of catecholamines thyrotropin-releasing hormone and somatostatin on growth hormone and prolactin secretion from adenomatous and nonadenomatous human pituitary cells in culture.
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Direct effects of catecholamines thyrotropin-releasing hormone and somatostatin on growth hormone and prolactin secretion from adenomatous and nonadenomatous human pituitary cells in culture.

机译:儿茶酚胺促甲状腺素释放激素和生长抑素对培养的腺瘤和非腺瘤人垂体细胞生长激素和催乳激素分泌的直接影响。

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摘要

To determine the mechanism and the site of action of catecholamines as well as hormones including thyrotropin-releasing hormone (TRH)1 and somatostatin on pituitary hormone release in patients with acromegaly and in normal subjects, the effects of these substances on growth hormone (GH) and prolactin (PRL) secretion from adenomatous and nonadenomatous human pituitary cells in culture were examined. When dopamine (0.01-0.1 microM) or bromocriptine (0.01-0.1 microM) was added to the culture media, a significant inhibition of GH and PRL secretion from adenoma cells from acromegalic patients was observed. This inhibition was blocked by D2 receptor blockade with metoclopramide or sulpiride, but not by D1 receptor blockade. Similarly, dopamine suppressed GH and PRL release by nonadenomatous pituitary cells in a dose-dependent manner, which was again blocked by D2 receptor blockade. The minimum effective concentration of dopamine required for a significant inhibition of PRL secretion (0.01 microM) was lower than that for GH release (0.1 microM). Norepinephrine, likewise, caused a suppression of PRL secretion from adenomatous and nonadenomatous pituitary cells. This effect was blocked by sulpiride, phentolamine, however, was ineffective. When TRH was added to the media, both GH and PRL secretion were enhanced in adenoma cells, while only the stimulation of PRL release was observed in nonadenomatous pituitary cells. Coincubation of TRH and dopamine resulted in variable effects on GH and PRL secretion. Somatostatin consistently lowered GH and PRL secretion in both adenomatous and nonadenomatous pituitary cells and completely blocked the TRH-induced stimulation of GH and PRL secretion from adenoma cells. Opioid peptides (1 microM) failed to affect hormone release. These results suggest that no qualitative difference in GH and PRL responses to dopaminergic agonists or to somatostatin exists between adenoma cells of acromegalic patients and normal pituitary cells, and that the direct effect of catecholamines on GH and PRL secretion from human pituitary cells is mediated mainly through dopamine receptor activation.
机译:为了确定儿茶酚胺以及包括促甲状腺激素释放激素(TRH)1和生长抑素在内的激素对肢端肥大症患者和正常受试者垂体激素释放的作用机理和作用部位,这些物质对生长激素(GH)的作用检测了腺瘤和非腺瘤人垂体细胞分泌的催乳素(PRL)。当将多巴胺(0.01-0.1 microM)或溴隐亭(0.01-0.1 microM)添加到培养基中时,观察到了肢端肥大症患者腺瘤细胞对GH和PRL分泌的显着抑制作用。这种抑制作用是通过甲氧氯普胺或舒必利的D2受体阻滞来阻止的,而不是D1受体阻滞来阻止的。类似地,多巴胺以剂量依赖的方式抑制非腺瘤性垂体细胞释放GH和PRL,这又被D2受体阻断所阻断。显着抑制PRL分泌所需的最小多巴胺有效浓度(0.01 microM)低于GH释放的最低有效浓度(0.1 microM)。同样,去甲肾上腺素引起腺瘤和非腺瘤垂体细胞PRL分泌的抑制。舒必利,酚妥拉明可阻断该作用,但无效。当将TRH添加到培养基中时,腺瘤细胞中GH和PRL的分泌均增加,而在非腺瘤性垂体细胞中仅观察到PRL释放的刺激。 TRH和多巴胺的共同孵育对GH和PRL分泌产生不同的影响。生长抑素持续降低腺瘤和非腺瘤垂体细胞中GH和PRL的分泌,并完全阻断TRH诱导的腺瘤细胞GH和PRL分泌的刺激。阿片肽(1 microM)未能影响激素释放。这些结果表明,肢端肥大症患者的腺瘤细胞与正常垂体细胞之间对多巴胺能激动剂或生长抑素的GH和PRL反应没有质的差异,儿茶酚胺对人垂体细胞GH和PRL分泌的直接作用主要是通过介导的。多巴胺受体激活。

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