Prasad M R, Cinti D L
Arch Biochem Biophys. 1986 Aug 1;248(2):479-88. doi: 10.1016/0003-9861(86)90501-1.
The feeding of 2% di(2-ethylhexyl)phthalate (DEHP) to rats increased the hepatic microsomal elongation of palmitoyl-CoA by about twofold, while those of palmitoleoyl-CoA and gamma-linolenoyl-CoA decreased to 83 and 63%, respectively, of the control values. When component reactions of the elongation pathway were measured, it was observed that only the activity of condensing enzyme was increased by twofold, while those of beta-ketostearoyl-CoA reductase, beta-hydroxypalmitoyl-CoA dehydrase, and trans-2-hexadecenoyl-CoA reductases were not affected. Furthermore, the time course for induction of both condensation and elongation of palmitoyl-CoA was similar. In vitro addition of DEHP had no effect on either condensation or elongation. Thus, these results indicate that the peroxisomal proliferator induces only the condensing enzyme which is the regulatory and rate-limiting step of elongation sequence. The DEHP treatment also markedly enhanced the cytosolic NADPH-generating activities of glucose-6-PO4 dehydrogenase (2.2-fold) and malic enzyme (7.3-fold). Unexpectedly, the activities of fatty acid synthetase and citrate cleavage enzyme were unaffected. These results are discussed in light of the fact that these lipogenic enzymes are coordinately induced by diet or hormones.
给大鼠喂食2%的邻苯二甲酸二(2-乙基己基)酯(DEHP)可使肝微粒体中棕榈酰辅酶A的延长增加约两倍,而棕榈油酰辅酶A和γ-亚麻酰辅酶A的延长分别降至对照值的83%和63%。当测量延长途径的组成反应时,发现只有缩合酶的活性增加了两倍,而β-酮硬脂酰辅酶A还原酶、β-羟基棕榈酰辅酶A脱水酶和反式-2-十六碳烯酰辅酶A还原酶的活性未受影响。此外,棕榈酰辅酶A缩合和延长的诱导时间进程相似。体外添加DEHP对缩合或延长均无影响。因此,这些结果表明过氧化物酶体增殖剂仅诱导缩合酶,而缩合酶是延长序列的调节和限速步骤。DEHP处理还显著增强了葡萄糖-6-磷酸脱氢酶(2.2倍)和苹果酸酶(7.3倍)的胞质NADPH生成活性。出乎意料的是,脂肪酸合成酶和柠檬酸裂解酶的活性未受影响。鉴于这些生脂酶受饮食或激素协同诱导这一事实,对这些结果进行了讨论。