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链脲佐菌素诱导的非酮症糖尿病大鼠与四氧嘧啶诱导的酮症糖尿病大鼠肝脏中的糖异生-糖酵解能力及代谢分区

Gluconeogenic-glycolytic capacities and metabolic zonation in liver of rats with streptozotocin, non-ketotic as compared to alloxan, ketotic diabetes.

作者信息

Miethke H, Wittig B, Nath A, Jungermann K

出版信息

Histochemistry. 1986;85(6):483-9. doi: 10.1007/BF00508430.

Abstract

Activities (mumol X min-1 X g liver) and zonal distributions of key enzymes of carbohydrate metabolism were studied in livers of streptozotocin-diabetic rats and compared to the values in alloxan-diabetes. Streptozotocin led to a non-ketotic diabetes with blood glucose being increased by more than fivefold but ketone bodies being in the normal range, while alloxan produced a ketotic diabetes with blood glucose, acetoacetate and beta-hydroxybutyrate being elevated by more than fivefold. Portal insulin was decreased to about 20% in streptozotocin- and more drastically to about 7% in alloxan-diabetes. Conversely, portal glucagon was increased in the two states to about 250% and 180%, respectively. The glucogenic key enzyme phosphoenolpyruvate carboxykinase (PEPCK) was enhanced in streptozotocin- and alloxan-diabetes to over 300%, while the glycolytic pyruvate kinase L (PKL) was lowered to 65% and 80%, respectively. The normal periportal to perivenous gradient of PEPCK of about 3:1, as measured in microdissected tissue samples, was maintained with elevated activities in the two zones. The normal periportal to perivenous gradient of PKL of 1:1.7 was diminished with lowered activities in the two zones. The glucogenic glucose-6-phosphatase (G6Pase) was increased in streptozotocin- and alloxan-diabetes to 130% and 140%, respectively, while the glucose utilizing glucokinase (GK) was decreased to 60% and 50%, respectively. The normal periportal to perivenous gradient of G6Pase, demonstrated histochemically, remained unaffected. Carnitine palmitoyltransferase (CPT) was increased to over 190% and acetyl-CoA carboxylase (ACC) was decreased to 60% in streptozotocin, non-ketotic diabetes, while the two enzymes were altered more drastically to 400% and 50%, respectively, in alloxan, ketotic diabetes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了链脲佐菌素诱导糖尿病大鼠肝脏中碳水化合物代谢关键酶的活性(μmol×min⁻¹×g肝脏)及区域分布,并与四氧嘧啶糖尿病大鼠肝脏中的值进行比较。链脲佐菌素导致非酮症糖尿病,血糖升高超过五倍,但酮体在正常范围内;而四氧嘧啶导致酮症糖尿病,血糖、乙酰乙酸和β-羟基丁酸升高超过五倍。链脲佐菌素诱导糖尿病时门静脉胰岛素降至约20%,四氧嘧啶糖尿病时则更急剧地降至约7%。相反,两种状态下门静脉胰高血糖素分别升高至约250%和180%。生糖关键酶磷酸烯醇式丙酮酸羧激酶(PEPCK)在链脲佐菌素和四氧嘧啶糖尿病中均增强至超过300%,而糖酵解丙酮酸激酶L(PKL)分别降至65%和80%。在显微解剖的组织样本中测得的PEPCK正常的门静脉到肝静脉梯度约为3:1,在两个区域中活性升高的情况下得以维持。PKL正常的门静脉到肝静脉梯度为1:1.7,在两个区域中活性降低的情况下减小。生糖葡萄糖-6-磷酸酶(G6Pase)在链脲佐菌素和四氧嘧啶糖尿病中分别升高至130%和140%,而利用葡萄糖的葡萄糖激酶(GK)分别降至60%和50%。通过组织化学方法证实的G6Pase正常的门静脉到肝静脉梯度未受影响。肉碱棕榈酰转移酶(CPT)在链脲佐菌素诱导的非酮症糖尿病中升高至超过190%,乙酰辅酶A羧化酶(ACC)降至60%;而在四氧嘧啶诱导的酮症糖尿病中,这两种酶分别更急剧地改变至400%和50%。(摘要截选至250字)

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