Rubin R P, Kelly K L, Halenda S P, Laychock S G
Prostaglandins. 1982 Aug;24(2):179-93. doi: 10.1016/0090-6980(82)90144-7.
Isolated rat pancreatic acini were employed to demonstrate that the exocrine pancreas can metabolize [14C]-arachidonic acid by way of the lipoxygenase pathway as well as the cyclooxygenase pathway. Analysis by high performance liquid chromatography delineated a monohydroxy acid, presumably 12-L-hydroxy-5,8-10,14-eicosatetraenoic acid (12-HETE) as the major lipoxygenase product. The formation of this hydroxy arachidonate derivative was stimulated by the calcium ionophore ionomycin. Stimulation of the lipoxygenase pathway by ionomycin was confirmed by thin layer chromatography. In addition, 6-keto-PGF1 alpha, PGF2 alpha, and PGE2 were identified; and ionomycin, carbamylcholine, and caerulein enhanced the formation of these metabolites of the cyclooxygenase pathway. Ionomycin induced stimulation of HETE formation was inhibited by ETYA and nordihydroguaiaretic acid, but spontaneous and evoked enzyme secretion was unaffected. Thus, although ionomycin, a pancreatic secretagogue, stimulates the lipoxygenase pathway, the precise role of these arachidonate metabolites in the physiology of the exocrine pancreas is still obscure.
采用分离的大鼠胰腺腺泡来证明外分泌胰腺能够通过脂氧合酶途径以及环氧化酶途径代谢[14C] - 花生四烯酸。通过高效液相色谱分析确定一种单羟基酸,推测为12 - L - 羟基 - 5,8,10,14 - 二十碳四烯酸(12 - HETE)是主要的脂氧合酶产物。钙离子载体离子霉素刺激了这种羟基花生四烯酸衍生物的形成。离子霉素对脂氧合酶途径的刺激通过薄层色谱得到证实。此外,还鉴定出了6 - 酮 - PGF1α、PGF2α和PGE2;离子霉素、氨甲酰胆碱和雨蛙肽增强了环氧化酶途径这些代谢产物的形成。离子霉素诱导的HETE形成刺激被ETYA和去甲二氢愈创木酸抑制,但自发和诱发的酶分泌不受影响。因此,尽管胰腺促分泌剂离子霉素刺激了脂氧合酶途径,但这些花生四烯酸代谢产物在外分泌胰腺生理学中的精确作用仍不清楚。