Chihara K, Iwasaki J, Minamitani N, Kaji H, Kodama H, Fujita T, Shirataki K, Tamaki N, Matsumoto S
Acta Endocrinol (Copenh). 1984 Jan;105(1):6-13. doi: 10.1530/acta.0.1050006.
To clarify the functional characteristics of prolactin (Prl)-producing adenoma cells, the effect of TRH, prostaglandin E1 (PGE1), theophylline, dopamine and dopaminergic antagonists on Prl secretion was examined in vitro in perifused pituitary adenoma tissues obtained at surgery from 8 patients with prolactinoma. Perifusion with TRH at a concentration of 10(-6) to 10(-5) M resulted in a significant increase in effluent Prl levels in 3 of the 8 adenoma tissues. In the remaining 5 adenomas, TRH produced no effect on Prl release in vitro. On the other hand, PGE1 (10(-5) M) stimulated Prl secretion in 2 of the 4 adenomas examined. Addition of theophylline (5.5 mM) caused a marked increase of effluent Prl levels in all 8 prolactinomas regardless of the reactivity to TRH or PGE1. Dopamine (5 X 10(-7) M) suppressed Prl secretion from adenoma tissue in 5 of 7 patients tested but had no effect in the remaining two adenomas. When perifused simultaneously with dopamine, sulpiride (D2-selective dopamine receptor blocker, 5 X 10(-7) M) blocked the inhibitory effect of dopamine on Prl release in 3 of the 4 dopamine-sensitive prolactinomas. In one adenoma responsive to dopamine but resistant to sulpiride, YM-09151-2 (relatively specific D1-dopamine receptor blocker, 5 X 10(-7) M) antagonized the dopaminergic inhibition of Prl release. When perifused alone, neither sulpiride nor YM-09151-2 affected Prl release from any of the adenoma tissues tested.(ABSTRACT TRUNCATED AT 250 WORDS)
为阐明催乳素(Prl)分泌性腺瘤细胞的功能特性,在体外对8例催乳素瘤患者手术获取的垂体腺瘤组织进行灌流,检测促甲状腺激素释放激素(TRH)、前列腺素E1(PGE1)、茶碱、多巴胺及多巴胺能拮抗剂对Prl分泌的影响。用浓度为10⁻⁶至10⁻⁵M的TRH灌流时,8例腺瘤组织中有3例流出液中Prl水平显著升高。其余5例腺瘤中,TRH在体外对Prl释放无影响。另一方面,在所检测的4例腺瘤中,2例对PGE1(10⁻⁵M)刺激Prl分泌有反应。添加茶碱(5.5mM)后,所有8例催乳素瘤流出液中Prl水平均显著升高,无论其对TRH或PGE1的反应性如何。多巴胺(5×10⁻⁷M)抑制了7例受试患者中5例腺瘤组织的Prl分泌,但对其余2例腺瘤无影响。当与多巴胺同时灌流时,舒必利(D2选择性多巴胺受体阻滞剂,5×10⁻⁷M)在4例对多巴胺敏感的催乳素瘤中的3例中阻断了多巴胺对Prl释放的抑制作用。在1例对多巴胺有反应但对舒必利耐药的腺瘤中,YM-09151-2(相对特异性的D1多巴胺受体阻滞剂,5×10⁻⁷M)拮抗了多巴胺对Prl释放的抑制作用。单独灌流时,舒必利和YM-09151-2均未影响所检测的任何腺瘤组织的Prl释放。(摘要截短于250字)