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在体外对一大系列人类促肾上腺皮质激素分泌垂体腺瘤进行促肾上腺皮质激素释放激素和地塞米松反应,揭示了多种促肾上腺皮质肿瘤表型。

Responses to corticotrophin-releasing hormone and dexamethasone in a large series of human adrenocorticotrophic hormone-secreting pituitary adenomas in vitro reveal manifold corticotroph tumoural phenotypes.

机构信息

Department of Medical Sciences, University of Milan, Milan, Italy.

出版信息

J Neuroendocrinol. 2011 Dec;23(12):1214-21. doi: 10.1111/j.1365-2826.2011.02213.x.

Abstract

Patients with Cushing's disease are known to present a variable secretory response to stimulatory and inhibitory challenges. Evaluation of the secretory behaviour of pituitary adrenocorticotrophic hormone (ACTH)-secreting adenomas in vitro aids in the comprehension of its behaviour in vivo; however, given the small size of these tumours and the consequent paucity of material available to in vitro studies, a comprehensive study on the secretory behaviour of human corticotroph tumours has not yet been performed. The present study aimed to assess the spectrum of responses to the two main corticotroph modulators, corticotrophin-releasing hormone (CRH) and dexamethasone, in a large series of human ACTH-secreting pituitary tumours. Seventy-two ACTH-secreting pituitary tumours were collected during surgery and established in culture. Specimens were incubated with 10 nm CRH and/or 10 nm dexamethasone for 4 h and 24 h. Secretion in unstimulated, control wells was set at 100% and changes in ACTH concentrations by at least 20% were considered as responses. Parallel experiments in 12 rat anterior pituitary primary cultures were evaluated. A marked ACTH increase was observed during incubation with CRH in 70% of tumoural specimens at 4 h (range 124-3500% of control wells) and in 57% at 24 h (range 122-3323%). Dexamethasone reduced ACTH secretion in almost 50% of tumours (range 78-2% of control at 4 h; 76-3% at 24 h), whereas it did not affect ACTH medium levels in 30% of specimens and induced a paradoxical ACTH increase in 20% of tumours (range 130-327% of control at 4 h; 156-348% at 24 h). By comparison, CRH uniformly increased ACTH levels in rat anterior pituitary primary cultures (mean 745 ± 84% at 4 h; 347 ± 25% at 24 h), whereas dexamethasone decreased ACTH levels by 40-50% in all experiments. In conclusion, the present study of a large series of human ACTH-secreting pituitary tumours in vitro revealed a considerable variability in the responses to CRH and dexamethasone. This finding indicates the existence of multiple corticotroph tumoural phenotypes and may account for the different responses to physiological and pharmacological modulators in vivo.

摘要

患有库欣病的患者已知其对刺激和抑制性挑战的分泌反应具有可变性。体外评估垂体促肾上腺皮质激素(ACTH)分泌腺瘤的分泌行为有助于理解其体内行为;然而,由于这些肿瘤体积小,并且可供体外研究的材料很少,因此尚未对人类促皮质素肿瘤的分泌行为进行全面研究。本研究旨在评估两大主要促皮质素调节剂促肾上腺皮质释放激素(CRH)和地塞米松对一系列人类 ACTH 分泌性垂体肿瘤的反应谱。在手术过程中收集了 72 例 ACTH 分泌性垂体肿瘤,并进行了培养。将标本用 10nm CRH 和/或 10nm 地塞米松孵育 4 小时和 24 小时。未刺激对照孔中的分泌设定为 100%,并且 ACTH 浓度变化至少 20%被认为是反应。评估了 12 例大鼠前垂体原代培养物中的平行实验。在 4 小时时,CRH 孵育时观察到 70%的肿瘤标本中 ACTH 明显增加(对照孔的范围为 124-3500%),而在 57%的标本中在 24 小时时(对照孔的范围为 122-3323%)。地塞米松在近 50%的肿瘤中降低了 ACTH 分泌(4 小时时对照孔的范围为 78-2%;24 小时时对照孔的范围为 76-3%),而在 30%的标本中不影响 ACTH 介质水平,并且在 20%的肿瘤中诱导了矛盾的 ACTH 增加(4 小时时对照孔的范围为 130-327%;24 小时时对照孔的范围为 156-348%)。相比之下,CRH 均匀地增加了大鼠前垂体原代培养物中的 ACTH 水平(4 小时时的平均值为 745±84%;24 小时时的平均值为 347±25%),而地塞米松在所有实验中使 ACTH 水平降低了 40-50%。总之,本研究对体外大量人类 ACTH 分泌性垂体肿瘤的研究揭示了对 CRH 和地塞米松的反应存在相当大的可变性。这一发现表明存在多种促皮质素肿瘤表型,可能解释了体内对生理和药理学调节剂的不同反应。

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