Knepel W, Schöfl C, Götz D M
Department of Pharmacology, University of Freiburg im Breisgau, Federal Republic of Germany.
Naunyn Schmiedebergs Arch Pharmacol. 1988 Sep;338(3):303-9. doi: 10.1007/BF00173405.
Arachidonic acid is liberated from phospholipids by various hypothalamic releasing hormones and may be involved in stimulus-secretion coupling in rat adenohypophysis. In the present study, the effect of exogenous arachidonic acid on calcium homeostasis in rat anterior pituitary cells was investigated in vitro. Arachidonic acid markedly stimulated the release of various anterior pituitary hormones (beta-endorphin, luteinizing hormone, growth hormone). Arachidonic acid (10 mumol/l) decreased the initial rate of 45Ca2+ uptake. In cells prelabelled with 45Ca2+, arachidonic acid (10 mumol/l) decreased the exchangeable cell calcium content and increased the rate of 45Ca2+ extrusion. Cytosolic free calcium concentration [( Ca2+]i) was measured with the fluorescent indicator fura-2. Arachidonic acid markedly elevated [Ca2+]i. The concentration dependency of this effect (1 mumol/l and above) was similar to that on hormone secretion. Arachidonic acid (6 mumol/l) elevated [Ca2+]i by about 300 nmol/l, and arachidonic acid (10 mumol/l) raised [Ca2+]i into the micromolar range. The effect of arachidonic acid (3 mumol/l) on [Ca2+]i was not influenced by inhibitors of arachidonic acid metabolism (nordihydroguaiaretic acid, BW755C). In Ca2+-free media (Ca2+ omitted, EGTA 2 mmol/l), the effect of arachidonic acid (3 mumol/l) on [Ca2+]i was almost unimpaired, whereas the effect of arachidonic acid (10 mumol/l) was reduced. Thus, the secretagogue arachidonic acid induces calcium mobilization and an increase in cytosolic free calcium concentration. These actions further qualify arachidonic acid as a potential intracellular mediator of stimulus-induced hormone secretion from rat adenohypophysis.
花生四烯酸可被多种下丘脑释放激素从磷脂中释放出来,可能参与大鼠腺垂体的刺激 - 分泌偶联过程。在本研究中,体外研究了外源性花生四烯酸对大鼠垂体前叶细胞钙稳态的影响。花生四烯酸显著刺激了多种垂体前叶激素(β - 内啡肽、黄体生成素、生长激素)的释放。花生四烯酸(10 μmol/L)降低了45Ca2+摄取的初始速率。在用45Ca2+预标记的细胞中,花生四烯酸(10 μmol/L)降低了可交换的细胞钙含量,并增加了45Ca2+的外排速率。用荧光指示剂fura - 2测量胞质游离钙浓度[Ca2+]i。花生四烯酸显著升高了[Ca2+]i。这种效应(1 μmol/L及以上)的浓度依赖性与对激素分泌的依赖性相似。花生四烯酸(6 μmol/L)使[Ca2+]i升高约300 nmol/L,花生四烯酸(10 μmol/L)使[Ca2+]i升高到微摩尔范围。花生四烯酸(3 μmol/L)对[Ca2+]i的作用不受花生四烯酸代谢抑制剂(去甲二氢愈创木酸、BW755C)的影响。在无钙培养基(省略Ca2+,2 mmol/L EGTA)中,花生四烯酸(3 μmol/L)对[Ca2+]i的作用几乎未受损害,而花生四烯酸(10 μmol/L)的作用则减弱。因此,促分泌剂花生四烯酸诱导钙动员并增加胞质游离钙浓度。这些作用进一步证明花生四烯酸是大鼠腺垂体刺激诱导激素分泌的潜在细胞内介质。