Akpan J O, Hurley M C, Pek S, Lands W E
Can J Biochem. 1979 Jun;57(6):540-7. doi: 10.1139/o79-068.
The secretion of both glucagon and insulin by the isolated perfused rat pancreas was significantly stimulated by 10(-7) M PGH2. Experiments to show that the stimulated secretion was mediated by conversion of PGH2 to TXA2 or TXB2 revealed no correlation between the amount of secretion and the amount of thromboxane formed. Conversion of PGH2 with a crude platelet thromboxane synthase preparation caused a progressive loss of ability to secret insulin, whereas the capacity to stimulate release of glucagon remained at about one-half the maximal level. This relatively stable and selective secretagogue action on the alpha-cells appeared to be due to the formation of PGD2 by the platelet preparation. Direct administration of PGD2 confirmed this interpretation and showed clearly that this prostaglandin is a potent secretagogue for glucagon with little activity in stimulating the release of insulin. Our results have shown high and relatively equal stimulation of secretion by alpha- and beta-cells with exogenous PGE2, PGF2 alpha, and PGH2, little or no secretion by either cell type with TXA2, TXB2, or PGI2, and a unique selective stimulatory action of PGD2 upon the alpha-cell.
离体灌注大鼠胰腺分泌胰高血糖素和胰岛素均受到10⁻⁷ M前列环素H₂(PGH₂)的显著刺激。旨在表明受刺激分泌由PGH₂转化为血栓素A₂(TXA₂)或血栓素B₂(TXB₂)介导的实验显示,分泌量与形成的血栓素量之间无相关性。用粗制血小板血栓素合酶制剂使PGH₂转化导致胰岛素分泌能力逐渐丧失,而刺激胰高血糖素释放的能力则维持在最大水平的约一半。对α细胞这种相对稳定且具选择性的促分泌作用似乎是由于血小板制剂形成了前列腺素D₂(PGD₂)。直接给予PGD₂证实了这一解释,并清楚表明该前列腺素是胰高血糖素的有效促分泌剂,而刺激胰岛素释放的活性很小。我们的结果显示,外源性前列腺素E₂(PGE₂)、前列腺素F₂α(PGF₂α)和PGH₂对α细胞和β细胞的分泌有高度且相对等同的刺激作用,血栓素A₂、血栓素B₂或前列环素I₂(PGI₂)对任一细胞类型几乎无分泌刺激作用,以及PGD₂对α细胞有独特的选择性刺激作用。