Bryson J M, Cooney G J, Wensley V R, Blair S C, Caterson I D
Department of Endocrinology, Royal Prince Alfred Hospital, Sydney, N.S.W., Australia.
Biochem J. 1993 Nov 1;295 ( Pt 3)(Pt 3):731-4. doi: 10.1042/bj2950731.
The diurnal pattern of the activity of the pyruvate dehydrogenase complex (PDHC) was studied in the heart and liver of gold-thioglucose (GTG)-obese mice and age-matched controls. The diurnal pattern of lipogenesis was also measured in the liver. Both lean and obese mice had one main eating period, from 20:00 to 24:00 h. Eating produced no change in serum glucose of control mice but there was a significant rise in serum insulin and triacylglycerols. There was also a 3-fold increase in cardiac PDHC activity and a 3-fold increase in hepatic lipogenesis in the control mice, but little change in hepatic PDHC activity. GTG-obese mice were hyperglycaemic, hyperinsulinaemic and hypertriglyceridaemic at all times studied, with significant increases in these parameters being seen in response to eating. Eating produced little change in cardiac PDHC activity, but there was a 5-fold increase in hepatic PDHC activity, paralleled by a 10-fold increase in hepatic lipogenesis. Hepatic PDHC activity was significantly higher in GTG-obese mice at all times except 16:00 h. The simultaneous rise of hepatic PDHC activity, lipogenesis and serum triacylglycerols in GTG-obese mice suggests an increased utilization of glucose for lipogenesis. The lack of change in heart PDHC activity in GTG-obese mice over 24 h suggests that a general decrease in PDHC activity may contribute to the development of the glucose intolerance and insulin resistance of obesity and non-insulin-dependent diabetes. However, it appears that a different level of metabolic control allows hepatic PDHC activity of the same obese animals to increase in response to hyperinsulinaemia and contribute to the higher rates of lipogenesis seen in obese mice.
研究了硫代葡萄糖金(GTG)诱导的肥胖小鼠及年龄匹配的对照小鼠心脏和肝脏中丙酮酸脱氢酶复合体(PDHC)活性的昼夜模式。同时也测定了肝脏中脂肪生成的昼夜模式。瘦小鼠和肥胖小鼠都有一个主要进食期,从20:00至24:00时。进食对对照小鼠的血清葡萄糖没有影响,但血清胰岛素和三酰甘油显著升高。对照小鼠的心脏PDHC活性增加了3倍,肝脏脂肪生成增加了3倍,而肝脏PDHC活性变化不大。在所有研究时间点,GTG肥胖小鼠均出现高血糖、高胰岛素血症和高甘油三酯血症,进食后这些参数显著增加。进食对心脏PDHC活性影响不大,但肝脏PDHC活性增加了5倍,同时肝脏脂肪生成增加了10倍。除16:00时外,GTG肥胖小鼠肝脏PDHC活性在所有时间均显著较高。GTG肥胖小鼠肝脏PDHC活性、脂肪生成和血清三酰甘油同时升高,提示葡萄糖用于脂肪生成的利用率增加。GTG肥胖小鼠心脏PDHC活性在24小时内无变化,提示PDHC活性普遍降低可能导致肥胖和非胰岛素依赖型糖尿病的葡萄糖不耐受和胰岛素抵抗的发生。然而,似乎不同水平的代谢控制使得同一肥胖动物的肝脏PDHC活性能够对高胰岛素血症作出反应而增加,并导致肥胖小鼠脂肪生成率升高。