Göttlicher M, Demoz A, Svensson D, Tollet P, Berge R K, Gustafsson J A
Department of Medical Nutrition, Karolinska Institute, Huddinge Hospital, NOVUM, Sweden.
Biochem Pharmacol. 1993 Dec 14;46(12):2177-84. doi: 10.1016/0006-2952(93)90607-x.
Fatty acids have recently been demonstrated to activate peroxisome proliferator-activated receptors (PPARs) but specific structural requirements of fatty acids to produce this response have not yet been determined. Importantly, it has hitherto not been possible to show specific binding of these compounds to PPAR. To test whether a common PPAR binding metabolite might be formed, we tested the effects of long-chain omega-3 polyunsaturated fatty acids, differentially beta-oxidizable fatty acids and inhibitors of fatty acid metabolism. We determined the activation of a reporter gene by a chimaeric receptor encompassing the DNA binding domain of the glucocorticoid receptor and the ligand binding domain of PPAR. The omega-3 unsaturated fatty acids were slightly more potent PPAR activators in vitro than saturated fatty acids. The peroxisomal proliferation-inducing, non-beta-oxidizable, tetradecylthioacetic acid activated PPAR to the same extent as the strong peroxisomal proliferator WY 14,643, whereas the homologous beta-oxidizable tetradecylthiopropionic acid was only as potent as a non-substituted fatty acid. Cyclooxygenase inhibitors, radical scavengers or cytochrome P450 inhibitors did not affect activation of PPAR. In conclusion, beta-oxidation is apparently not required for the formation of the PPAR-activating molecule and this moiety might be a fatty acid, its ester with CoA, or a further derivative of the activated fatty acid prior to beta-oxidation of the acyl-CoA ester. These data should aid understanding of signal transduction via PPAR and the identification of a receptor ligand.
最近有研究表明脂肪酸可激活过氧化物酶体增殖物激活受体(PPARs),但尚未确定产生该反应的脂肪酸具体结构要求。重要的是,迄今为止还无法证明这些化合物与PPAR有特异性结合。为了测试是否可能形成一种常见的PPAR结合代谢物,我们检测了长链ω-3多不饱和脂肪酸、不同β-氧化能力的脂肪酸以及脂肪酸代谢抑制剂的作用。我们通过一种嵌合受体来测定报告基因的激活情况,该嵌合受体包含糖皮质激素受体的DNA结合结构域和PPAR的配体结合结构域。在体外,ω-3不饱和脂肪酸作为PPAR激活剂的效力略高于饱和脂肪酸。过氧化物酶体增殖诱导剂、非β-氧化的十四烷基硫代乙酸激活PPAR的程度与强效过氧化物酶体增殖剂WY 14,643相同,而同源的可β-氧化的十四烷基硫代丙酸的效力仅与未取代的脂肪酸相当。环氧化酶抑制剂、自由基清除剂或细胞色素P450抑制剂均不影响PPAR的激活。总之,PPAR激活分子的形成显然不需要β-氧化,该部分可能是脂肪酸、其与辅酶A的酯,或者是酰基辅酶A酯β-氧化之前活化脂肪酸的进一步衍生物。这些数据将有助于理解通过PPAR的信号转导以及受体配体的鉴定。