Won J G, Oki Y, Orth D N
Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee 37232.
Endocrinology. 1990 Feb;126(2):858-68. doi: 10.1210/endo-126-2-858.
We examined the effects of removing extracellular Ca2+ (Ca2+e), depleting intracellular Ca2+ (Ca2+i), inhibiting cAMP-dependent calmodulin, and blocking voltage-sensitive Ca2+ channels on the secretion of ACTH by perifused dispersed rat anterior pituitary cells. The cells were stimulated with synthetic arginine vasopressin (AVP), oxytocin (OT), and angiotensin-II (AII), all of which are thought to act via the Ca2+/inositol phosphate-dependent protein kinase-C pathway, with synthetic ovine CRF, which acts via the cAMP-dependent protein kinase-A pathway, and with dioctanoylglycerol, which directly activates protein kinase-C. All three secretagogues elicited an initial spike phase ACTH secretory response that peaked within 1 or 2 min and ended within 6 min. AVP and OT also elicited a sustained plateau phase response that lasted for as long as the cells were exposed to the secretagogue, but AII did not. Removal of Ca2+e diminished the initial spike phase by 30-50%, but depletion of Ca2+i virtually abolished it. In contrast, the sustained phase of the response to AVP and OT was abolished by removal of Ca2+e. The effect of dioctanoylglycerol, which elicits a sustained progressive increase in ACTH release, but no initial spike phase, was also greatly inhibited by Ca2+e removal; no greater effect was observed when Ca2+i was depleted. Blockade of L-type voltage-sensitive Ca2+ channels with nimodipine, a dihydropyridine drug, had the same effect as Ca2+e removal on both the initial spike and sustained plateau phases of the response to AVP. Inhibiting cAMP-dependent calmodulin with penfluridol had no effect on the initial spike phase, but reduced the sustained plateau phase of the response to AVP. Removal of Ca2+e or depletion of Ca2+i did not abolish the synergistic ACTH secretory response to the combination of AVP and CRF.(ABSTRACT TRUNCATED AT 400 WORDS)
我们研究了去除细胞外钙离子(Ca2+e)、耗尽细胞内钙离子(Ca2+i)、抑制环磷酸腺苷(cAMP)依赖性钙调蛋白以及阻断电压敏感性钙离子通道对经灌流的分散大鼠垂体前叶细胞促肾上腺皮质激素(ACTH)分泌的影响。用合成的精氨酸加压素(AVP)、催产素(OT)和血管紧张素II(AII)刺激细胞,这三种物质都被认为是通过Ca2+/肌醇磷酸依赖性蛋白激酶C途径发挥作用;用通过cAMP依赖性蛋白激酶A途径发挥作用的合成羊促肾上腺皮质激素释放因子(CRF)以及直接激活蛋白激酶C的二辛酰甘油刺激细胞。所有这三种促分泌素均引发了一个初始的尖峰期ACTH分泌反应,该反应在1或2分钟内达到峰值,并在6分钟内结束。AVP和OT还引发了一个持续的平台期反应,只要细胞暴露于促分泌素,该反应就会持续,但AII不会。去除Ca2+e使初始尖峰期减少了30 - 50%,但耗尽Ca2+i实际上消除了该反应。相反,去除Ca2+e消除了对AVP和OT反应的持续期。二辛酰甘油可引发ACTH释放持续渐进增加,但无初始尖峰期,其作用也因去除Ca2+e而受到极大抑制;耗尽Ca2+i时未观察到更大影响。用二氢吡啶类药物尼莫地平阻断L型电压敏感性钙离子通道,对AVP反应的初始尖峰期和持续平台期的作用与去除Ca2+e相同。用五氟利多抑制cAMP依赖性钙调蛋白对初始尖峰期无影响,但降低了对AVP反应的持续平台期。去除Ca2+e或耗尽Ca2+i并未消除对AVP和CRF联合作用的协同ACTH分泌反应。(摘要截短于400字)