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呋塞米诱发的高血糖症:糖酵解激酶的作用

Furosemide-induced hyperglycaemia: the implication of glycolytic kinases.

作者信息

Dimitriadis G, Tegos C, Golfinopoulou L, Roboti C, Raptis S

机构信息

Clinical Research Unit, 401 Army General Hospital, Athens, Greece.

出版信息

Horm Metab Res. 1993 Nov;25(11):557-9. doi: 10.1055/s-2007-1002176.

Abstract

Hyperglycaemia is a well known adverse effect of therapy with diuretics. In adipose tissue, hydrochlorothiazide and furosemide inhibit the rate of glucose transport. In skeletal muscle, furosemide decreases the rate of glucose phosphorylation and glycolysis. However, whether furosemide has any direct effect on the activities of any of the glycolytic enzymes is not known. In the present study, the effects of furosemide on the activities of the hexokinase, phosphofructokinase and pyruvate kinase were examined. Pieces of skeletal muscle (quadriceps) and liver were obtained from 10 non-diabetic subjects during surgery. Tissues were homogenized and the activities of the enzymes were measured in the presence or absence of furosemide (0-1.5 mM). Furosemide inhibited the activity of all three key glycolytic enzymes. The concentration of furosemide required to inhibit phosphofructokinase in muscle was lower than that required to inhibit the activity of this enzyme in the liver or to inhibit the activities of hexokinase and pyruvate kinase in both muscle and liver. These direct effects of furosemide may contribute to the decrease in glucose utilisation following therapy with this and similar agents in man.

摘要

高血糖是利尿剂治疗众所周知的不良反应。在脂肪组织中,氢氯噻嗪和呋塞米会抑制葡萄糖转运速率。在骨骼肌中,呋塞米会降低葡萄糖磷酸化和糖酵解速率。然而,呋塞米是否对任何糖酵解酶的活性有直接影响尚不清楚。在本研究中,检测了呋塞米对己糖激酶、磷酸果糖激酶和丙酮酸激酶活性的影响。在手术过程中从10名非糖尿病受试者获取骨骼肌(股四头肌)和肝脏组织块。将组织匀浆,并在存在或不存在呋塞米(0 - 1.5 mM)的情况下测量酶的活性。呋塞米抑制了所有三种关键糖酵解酶的活性。抑制肌肉中磷酸果糖激酶活性所需的呋塞米浓度低于抑制肝脏中该酶活性或抑制肌肉和肝脏中己糖激酶及丙酮酸激酶活性所需的浓度。呋塞米的这些直接作用可能导致人类使用该药物及类似药物治疗后葡萄糖利用率降低。

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