Henly D C, Berry M N
Department of Medical Biochemistry, Flinders University of South Australia, Bedford Park.
Biochim Biophys Acta. 1991 May 17;1092(3):277-83. doi: 10.1016/s0167-4889(97)90001-x.
Isolated hepatocytes from fasted rats were used to study the effects of lactate on palmitate metabolism. Lactate was found to stimulate fatty acid esterification and citric acid cycle oxidation and to inhibit ketone body synthesis. These effects of lactate were largely maintained when gluconeogenesis was inhibited with either quinolinate or perfluorosuccinate, but were overcome by alpha-cyano-4-hydroxycinnamate. However, the responses of hepatocytes to lactate could be restored in the presence of alpha-cyano-4-hydroxycinnamate by the further addition of propionate. The stimulation of triacylglycerol synthesis by lactate was not associated with an increase in the concentration of glycerol 3-phosphate. Rather, there was a correlation between flux through the citric acid cycle and the rate of triacylglycerol synthesis. In all instances reduction of ketone body formation in the presence of lactate was accompanied by a stimulation of citric acid cycle oxidation.
来自禁食大鼠的分离肝细胞被用于研究乳酸对棕榈酸代谢的影响。发现乳酸可刺激脂肪酸酯化和柠檬酸循环氧化,并抑制酮体合成。当用喹啉酸或全氟琥珀酸抑制糖异生时,乳酸的这些作用在很大程度上得以维持,但被α-氰基-4-羟基肉桂酸所克服。然而,在α-氰基-4-羟基肉桂酸存在的情况下,通过进一步添加丙酸可恢复肝细胞对乳酸的反应。乳酸对三酰甘油合成的刺激与3-磷酸甘油浓度的增加无关。相反,通过柠檬酸循环的通量与三酰甘油合成速率之间存在相关性。在所有情况下,乳酸存在时酮体生成的减少伴随着柠檬酸循环氧化的刺激。