Lewis G P, Piper P J, Vigo C
Br J Pharmacol. 1979 Nov;67(3):393-400.
1 The prostaglandin synthesizing enzymes were found to be present in fat cell ghosts isolated from rabbit adipose tissue. 2 Prostaglandin E2 (PGE2) and PGF2, were synthesized by ghosts after stimulation with adrenocorticotrophic hormone (ACTH). 3 Indomethacin was found to inhibit this synthesis but not the synthesis of lipoxygenase products. 4 When fat cell ghosts were stimulated by ACTH, fatty acid release was observed from both neutral lipids and phospholipids. 5 The arachidonic acid (AA) pool within the ghosts and identified: approximately 90% was present in the phospholipid fraction, 8.5% in the neutral lipids and 1.5% unbound. 6 The glucocorticoids were found to stimulate incorporation of [14C]-AA into neutral lipids and inhibit its incorporation into phospholipids. 7 When fatty acid release was stimulated with ACTH, the glucocorticoids were found to inhibit the mobilisation of [14C]-AA from the phospholipids and enhance its release from the neutral lipids. 8 The glucocorticoids inhibit prostaglandin formation in fat cell ghosts.
发现前列腺素合成酶存在于从兔脂肪组织分离出的脂肪细胞空壳中。
促肾上腺皮质激素(ACTH)刺激后,脂肪细胞空壳合成了前列腺素E2(PGE2)和前列腺素F2α。
发现吲哚美辛可抑制这种合成,但不抑制脂氧合酶产物的合成。
当脂肪细胞空壳受到ACTH刺激时,观察到中性脂质和磷脂均有脂肪酸释放。
确定了脂肪细胞空壳内的花生四烯酸(AA)池:约90%存在于磷脂部分,8.5%存在于中性脂质中,1.5%为游离状态。
发现糖皮质激素可刺激[14C]-AA掺入中性脂质,并抑制其掺入磷脂。
当用ACTH刺激脂肪酸释放时,发现糖皮质激素可抑制[14C]-AA从磷脂中的动员,并增强其从中性脂质中的释放。
糖皮质激素抑制脂肪细胞空壳中前列腺素的形成。