Park Haejoe, Kaushik Virendar K, Constant Scarlet, Prentki Marc, Przybytkowski Ewa, Ruderman Neil B, Saha Asish K
Diabetes Unit, Section of Endocrinology and Department of Medicine, Boston Medical Center, Boston, Massachusetts 02118, USA.
J Biol Chem. 2002 Sep 6;277(36):32571-7. doi: 10.1074/jbc.M201692200. Epub 2002 Jun 13.
Changes in the concentration of malonyl-CoA in many tissues have been related to alterations in the activity of acetyl-CoA carboxylase (ACC), the rate-limiting enzyme in its formation. In contrast, little is known about the physiological role of malonyl-CoA decarboxylase (MCD), an enzyme responsible for malonyl-CoA catabolism. In this study, we examined the effects of voluntary exercise on MCD activity in rat liver, skeletal muscle, and adipose tissue. In addition, the activity of sn-glycerol-3-phosphate acyltransferase (GPAT), which like MCD and ACC can be regulated by AMP-activated protein kinase (AMPK), was assayed. Thirty min after the completion of a treadmill run, MCD activity was increased approximately 2-fold, malonyl-CoA levels were reduced, and ACC and GPAT activities were diminished by 50% in muscle and liver. These events appeared to be mediated via activation of AMPK since: 1) AMPK activity was concurrently increased by exercise in both tissues; 2) similar findings were observed after the injection of 5-amino 4 imidazole carboxamide, an AMPK activator; 3) changes in the activity of GPAT and ACC paralleled that of MCD; and 4) the increase in MCD activity in muscle was reversed in vitro by incubating immunoprecipitated enzyme from the exercised muscle with protein phosphatase 2A, and it was reproduced by incubating immunopurified MCD from resting muscle with purified AMPK. An unexpected finding was that exercise caused similar changes in the activities of ACC, MCD, GPAT, and AMPK and the concentration of malonyl-CoA in adipose tissue.
MCD, GPAT, and ACC are coordinately regulated by AMPK in liver and adipose tissue in response to exercise, and except for GPAT, also in muscle. The results suggest that AMPK activation plays a major role in regulating lipid metabolism in many cells following exercise. They also suggest that in each of them, it acts to increase fatty acid oxidation and decrease its esterification.
许多组织中丙二酰辅酶A浓度的变化与乙酰辅酶A羧化酶(ACC)活性的改变有关,ACC是其形成过程中的限速酶。相比之下,人们对丙二酰辅酶A脱羧酶(MCD)的生理作用知之甚少,MCD是一种负责丙二酰辅酶A分解代谢的酶。在本研究中,我们检测了自愿运动对大鼠肝脏、骨骼肌和脂肪组织中MCD活性的影响。此外,还检测了与MCD和ACC一样可受AMP激活的蛋白激酶(AMPK)调节的甘油-3-磷酸酰基转移酶(GPAT)的活性。在跑步机跑步结束30分钟后,MCD活性增加了约2倍,丙二酰辅酶A水平降低,肌肉和肝脏中的ACC和GPAT活性降低了50%。这些变化似乎是通过AMPK的激活介导的,因为:1)运动同时增加了两个组织中的AMPK活性;2)注射AMPK激活剂5-氨基-4-咪唑甲酰胺后观察到类似的结果;3)GPAT和ACC活性的变化与MCD平行;4)通过将运动肌肉的免疫沉淀酶与蛋白磷酸酶2A在体外孵育,可逆转肌肉中MCD活性的增加,而通过将静息肌肉的免疫纯化MCD与纯化的AMPK孵育可重现这种增加。一个意外的发现是,运动在脂肪组织中引起了ACC、MCD、GPAT和AMPK活性以及丙二酰辅酶A浓度的类似变化。
在肝脏和脂肪组织中,MCD、GPAT和ACC在运动时受AMPK的协同调节,除GPAT外,在肌肉中也是如此。结果表明,AMPK激活在运动后许多细胞的脂质代谢调节中起主要作用。它们还表明,在每个细胞中,AMPK的作用是增加脂肪酸氧化并减少其酯化。