Mohan P F, Cleary M P
Hormel Institute, University of Minnesota, Austin 55912.
Am J Physiol. 1988 Jul;255(1 Pt 1):E1-8. doi: 10.1152/ajpendo.1988.255.1.E1.
Lean and obese Zucker rats, 7-8 wk of age, were treated with dehydroepiandrosterone (DHEA) for either 3 or 7 days to determine the initial cellular event(s) that might be responsible for the antiobesity activity of DHEA. Epididymal, retroperitoneal, and brown adipose tissue weights were unaltered by either 3 or 7 days of DHEA treatment. Liver weight was not affected by 3 days of treatment but was 13 and 18% higher in 7-day DHEA-treated lean and obese rats, respectively, compared with their corresponding control group. Mitochondrial state 3 respiration rates with glutamate-malate and succinate as substrates were elevated by an average of 35% in 3- and 7-day DHEA-treated obese rats and by 15-20% in 7-day DHEA-treated lean rats compared with rates obtained in the corresponding control groups. State 3 respiration was not affected in 3-day DHEA-treated lean rats compared with control lean rats. The specific activities of long-chain fatty acyl-coenzyme A synthase and hydrolase and the levels of free CoA were increased by severalfold in cellular fractions of both DHEA-treated lean and obese rats compared with their respective control group. Hepatic malic enzyme activity, which was shown earlier to be elevated with long-term DHEA treatment, was unaltered by either 3 or 7 days of DHEA administration. The above results suggest the involvement of mitochondrial respiration and fatty acid deacylation/reacylation in the antiobesity mechanism of action of DHEA.
7至8周龄的瘦型和肥胖型 Zucker 大鼠接受脱氢表雄酮(DHEA)治疗3天或7天,以确定可能导致 DHEA 抗肥胖活性的初始细胞事件。附睾、腹膜后和棕色脂肪组织的重量在 DHEA 治疗3天或7天后均未改变。肝重在治疗3天时不受影响,但在接受 DHEA 治疗7天的瘦型和肥胖型大鼠中,分别比相应对照组高13%和18%。以谷氨酸-苹果酸和琥珀酸为底物时,在接受 DHEA 治疗3天和7天的肥胖大鼠中,线粒体状态3呼吸速率平均提高35%,在接受 DHEA 治疗7天的瘦型大鼠中提高15%-20%,而在接受 DHEA 治疗3天的瘦型大鼠中,与对照瘦型大鼠相比,状态3呼吸不受影响。与各自对照组相比,在接受 DHEA 治疗的瘦型和肥胖型大鼠的细胞组分中,长链脂肪酰辅酶 A 合酶和水解酶的比活性以及游离辅酶 A 的水平均增加了几倍。肝脏苹果酸酶活性在长期 DHEA 治疗时会升高,但在 DHEA 给药3天或7天后均未改变。上述结果表明,线粒体呼吸以及脂肪酸去酰化/再酰化参与了 DHEA 的抗肥胖作用机制。