Link H, Dayanithi G, Föhr K J, Gratzl M
Abteilung Anatomie und Zellbiologie, Universität Ulm, Deutschland.
Endocrinology. 1992 Apr;130(4):2183-91. doi: 10.1210/endo.130.4.1312449.
The potency of oxytocin (OT) in evoking ACTH secretion by isolated, superfused rat adenohypophyseal corticotrophs and its enhancement by CRF and arginine vasopressin (AVP) were analyzed. Each secretagogue effectively released ACTH from adenohypophyseal cells when added separately in pulsatile fashion in physiological concentrations based on hypophyseal portal blood (OT, 10 nM; AVP, 0.5 nM; CRF, 0.1 nM). OT released ACTH at concentrations as low as 1 nM. Moreover, a dose-response relationship up to 10 microM was revealed. Combinations of a constant amount of CRF (0.1 nM) with increasing concentrations of OT exerted a synergistic effect on ACTH release. In contrast, OT given in various concentrations in combination with AVP (0.5 nM) produced an additive effect on ACTH release. To study the mechanism of action of OT on ACTH secretion, cytosolic free calcium levels in single pituitary cells exposed to OT or AVP were measured using the calcium-sensitive fluorescent indicator Fura-2. Corticotrophs among mixed adenohypophyseal cell types in the primary cultures were identified by immunocytochemistry. More than 500 cells were individually stimulated with OT or AVP. Basal cytosolic free calcium levels ranged between 80-130 nM free calcium. The addition of 100 nM OT or 1 microM AVP increased the cytosolic free calcium concentration within 3 sec to values ranging from 500-800 nM. An increase in intracellular calcium ranging from 200-500 nM due to OT could still be observed after extracellular calcium depletion. Taken together, our data demonstrate that physiological concentrations of OT stimulate ACTH secretion, independent of the other ACTH secretagogues, by mobilizing calcium mainly from intracellular stores.
分析了催产素(OT)在刺激离体、经超灌注的大鼠腺垂体促肾上腺皮质激素细胞分泌促肾上腺皮质激素(ACTH)方面的效能,以及促肾上腺皮质激素释放因子(CRF)和精氨酸加压素(AVP)对其的增强作用。当以基于垂体门脉血的生理浓度以脉冲方式分别添加时,每种促分泌素均能有效地从腺垂体细胞释放ACTH(OT,10 nM;AVP,0.5 nM;CRF,0.1 nM)。OT在低至1 nM的浓度下就能释放ACTH。此外,还揭示了高达10 μM的剂量反应关系。恒定剂量的CRF(0.1 nM)与浓度不断增加的OT联合使用,对ACTH释放产生协同作用。相反,不同浓度的OT与AVP(0.5 nM)联合使用时,对ACTH释放产生相加作用。为研究OT对ACTH分泌的作用机制,使用钙敏感荧光指示剂Fura-2测量了暴露于OT或AVP的单个垂体细胞中的胞质游离钙水平。通过免疫细胞化学鉴定原代培养物中混合腺垂体细胞类型中的促肾上腺皮质激素细胞。用OT或AVP分别刺激500多个细胞。基础胞质游离钙水平在80 - 130 nM游离钙之间。添加100 nM OT或1 μM AVP可在3秒内将胞质游离钙浓度提高到500 - 800 nM的范围。细胞外钙耗尽后,仍可观察到因OT导致的细胞内钙增加200 - 500 nM。综上所述,我们的数据表明,生理浓度的OT通过主要从细胞内储存库动员钙来刺激ACTH分泌,独立于其他ACTH促分泌素。