Dimitriadis G, Leighton B, Parry-Billings M, Newsholme E A
Department of Biochemistry, University of Oxford, UK.
Diabetologia. 1988 Jan;31(1):58-61. doi: 10.1007/BF00279135.
The diuretic furosemide (0.5 mmol/l) impaired glucose uptake in the soleus muscle of the rat by decreasing the sensitivity of glycolysis to insulin. In addition, at higher concentrations (1.0 mmol/l) the drug inhibited the basal rate of glycolysis. It did not, however, inhibit the rate of glycogen synthesis except at a concentration of 6.0 mmol/l. Since furosemide has some structural similarities to adenosine, the above effects on insulin sensitivity may be due to its ability to act as an adenosine receptor agonist in muscle. These effects of furosemide in skeletal muscle may contribute to the glucose intolerance following therapy with this and similar agents in man.
利尿剂呋塞米(0.5毫摩尔/升)通过降低糖酵解对胰岛素的敏感性,损害了大鼠比目鱼肌的葡萄糖摄取。此外,在较高浓度(1.0毫摩尔/升)时,该药物抑制了糖酵解的基础速率。然而,它并不抑制糖原合成速率,除非浓度达到6.0毫摩尔/升。由于呋塞米在结构上与腺苷有一些相似之处,上述对胰岛素敏感性的影响可能是由于其在肌肉中作为腺苷受体激动剂的能力。呋塞米在骨骼肌中的这些作用可能导致人体使用该药物及类似药物治疗后出现葡萄糖不耐受。