Laouari D, Jurkovitz C, Burtin M, Bois B, Vassault A, Kleinknecht C
INSERM U.192, Hôpital des Enfants Malades, Paris, France.
Metabolism. 1994 Apr;43(4):403-12. doi: 10.1016/0026-0495(94)90067-1.
A high-sucrose (S) diet accentuates anorexia and stunts growth in uremic (U) rats, and an oral S load induces a greater hyperfructosemia in U rats than in control (C) rats. Four studies were performed to determine the roles of S feeding and an acute S load on liver carbohydrate (CHO) metabolism in U and C rats (eight to 10 rats per group). We also examined the plasma responses to either water or a S load. Levels of the main metabolites of glycolysis, gluconeogenesis, and glycogenesis were measured under basal conditions (7 hours' postmeal) in U and C rats fed either a cornstarch diet (study I) or S diet (study II) and at 30 and 60 minutes after an intragastric S load (studies III and IV) in s-fed U and C rats. The weight gain, food intake, and plasma creatinine and urea levels of the rats in the four studies were comparable. Weight gain and liver weight (g/100 g body weight) were lower in U than in C rats. In the plasma, baseline levels of lactate were decreased by uremia and S feeding and those of glucose (G) were increased by S feeding. The increases in plasma G and fructose (F) levels after a S load were greater in U rats than in C rats, whereas those of plasma lactate were comparable. In the liver under basal conditions, uremia markedly decreased levels of glycogen, F-1,6-diphosphate (F-1,6-diP), F-2,6-diP, 3-glycero-phosphate (3-glycero-P), dihydroxyacetone phosphate (DHAP), pyruvate, lactate, and adenosine triphosphate (ATP), and the phosphorylation state (ATP/adenosine diphosphate [ADP] x inorganic phosphorus [PI]), increased phosphoenolpyruvate (PEP), ADP, and Pi levels, but did not affect the cytosolic redox state (pyruvate/lactate). In addition to uremia, S feeding further decreased levels of glycogen, F-2,6-diP, 3-glycero-P, and ATP. After S loading, liver F levels increased more in U than in C rats, but glycogen and 3-glycero-P levels increased less in U than in C rats. Liver lactate and pyruvate levels increased more in U than in C rats, and the pyruvate/lactate and DHAP/3-glycero-P ratios were higher in U than in C rats after a S load. The ATP level and the phosphorylation state in U rats increased 30 minutes later in U than in C rats. Our findings indicate that uremia causes a depletion in liver glycogen, which is enhanced by S feeding and could be partially attributed to decreased glycogen synthesis.(ABSTRACT TRUNCATED AT 400 WORDS)
高蔗糖(S)饮食会加重尿毒症(U)大鼠的厌食症状并阻碍其生长,且口服蔗糖负荷在U大鼠中诱导产生的高果糖血症比对照(C)大鼠更严重。进行了四项研究以确定S喂养和急性蔗糖负荷对U和C大鼠肝脏碳水化合物(CHO)代谢的作用(每组8至10只大鼠)。我们还检测了对水或蔗糖负荷的血浆反应。在基础条件下(餐后7小时),对喂食玉米淀粉饮食(研究I)或S饮食(研究II)的U和C大鼠,以及在喂食S的U和C大鼠中进行胃内蔗糖负荷后30和60分钟(研究III和IV),测量糖酵解、糖异生和糖原生成的主要代谢物水平。四项研究中大鼠的体重增加、食物摄入量以及血浆肌酐和尿素水平具有可比性。U大鼠的体重增加和肝脏重量(克/100克体重)低于C大鼠。在血浆中,尿毒症和S喂养降低了乳酸的基线水平,而S喂养增加了葡萄糖(G)的基线水平。蔗糖负荷后,U大鼠血浆G和果糖(F)水平的升高幅度大于C大鼠,而血浆乳酸水平相当。在基础条件下的肝脏中,尿毒症显著降低了糖原、F-1,6-二磷酸(F-1,6-diP)、F-2,6-二磷酸、3-磷酸甘油(3-甘油-P)、磷酸二羟丙酮(DHAP)、丙酮酸、乳酸和三磷酸腺苷(ATP)的水平,以及磷酸化状态(ATP/二磷酸腺苷[ADP]×无机磷[PI]),增加了磷酸烯醇丙酮酸(PEP)、ADP和Pi水平,但不影响胞质氧化还原状态(丙酮酸/乳酸)。除尿毒症外,S喂养进一步降低了糖原、F-2,6-二磷酸、3-甘油-P和ATP的水平。蔗糖负荷后,U大鼠肝脏F水平的增加幅度大于C大鼠,但糖原和3-甘油-P水平的增加幅度小于C大鼠。U大鼠肝脏乳酸和丙酮酸水平的增加幅度大于C大鼠,蔗糖负荷后U大鼠的丙酮酸/乳酸和DHAP/3-甘油-P比值高于C大鼠。30分钟后,U大鼠的ATP水平和磷酸化状态的增加幅度大于C大鼠。我们的研究结果表明,尿毒症导致肝脏糖原耗竭,S喂养会加剧这种情况,这可能部分归因于糖原合成减少。(摘要截取自400字)