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皮质类固醇对在无血清培养基中培养的垂体前叶细胞聚集体催乳素释放的影响。对多巴胺诱导的抑制、多巴胺后反弹以及促甲状腺激素释放激素(TRH)、血管活性肠肽(VIP)、血管紧张素II和异丙肾上腺素刺激的不同作用。

Influence of corticosteroids on prolactin release from anterior pituitary cell aggregates cultured in serum-free medium. Differential effects on dopamine-induced inhibition, post-dopamine rebound and stimulation by TRH, vasoactive intestinal peptide (VIP), angiotensin II and isoproterenol.

作者信息

Denef C, Schramme C, Baes M

出版信息

J Steroid Biochem. 1984 Jan;20(1):197-202. doi: 10.1016/0022-4731(84)90206-1.

Abstract

Dispersed rat anterior pituitary cells were allowed to reassociate into spherical aggregates by gyrotory shaking in serum-free chemically defined culture medium. When aggregates were superfused after being cultured for 5 days in this medium, stimulation of PRL release by TRH, VIP, angiotensin II and the beta-adrenergic agonist isoproterenol was comparable to that of aggregates cultured in serum-supplemented culture medium. Addition to the serum-free medium of 80 nM dexamethasone (Dex) resulted in a significant enhancement of the stimulation of PRL release by TRH, VIP and angiotensin II but not of the stimulation of PRL release by isoproterenol. Dex also failed to influence the inhibition of PRL release by 10 min exposure to 10 nM dopamine (DA). However, Dex significantly enhanced the post-DA rebound secretion of PRL. After 3 weeks in culture Dex provoked a similar potentiation of the response to angiotensin as at 5 days in culture but it abolished almost completely the stimulatory effect of isoproterenol. It is concluded that pituitary cell aggregates cultured in defined serum-free medium are a reliable system to study the multifactorial control of PRL release. The data show that peptidergic, dopaminergic and beta-adrenergic control at the pituitary level is differentially modulated by corticosteroids.

摘要

将分散的大鼠垂体前叶细胞在无血清化学限定培养基中通过旋转振荡使其重新聚集成球形聚集体。当聚集体在该培养基中培养5天后进行灌流时,促甲状腺激素释放激素(TRH)、血管活性肠肽(VIP)、血管紧张素II和β-肾上腺素能激动剂异丙肾上腺素对催乳素(PRL)释放的刺激作用与在补充血清的培养基中培养的聚集体相当。向无血清培养基中添加80 nM地塞米松(Dex)可显著增强TRH、VIP和血管紧张素II对PRL释放的刺激作用,但对异丙肾上腺素刺激PRL释放的作用无影响。Dex也未能影响10 nM多巴胺(DA)作用10分钟对PRL释放的抑制作用。然而,Dex显著增强了DA作用后PRL的反弹分泌。培养3周后,Dex对血管紧张素反应的增强作用与培养5天时相似,但几乎完全消除了异丙肾上腺素的刺激作用。得出的结论是,在限定的无血清培养基中培养的垂体细胞聚集体是研究PRL释放多因素控制的可靠系统。数据表明,垂体水平的肽能、多巴胺能和β-肾上腺素能控制受到皮质类固醇的不同调节。

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