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通过特异性放射免疫测定法测定肝脏和肾脏中果糖-1,6-二磷酸酶的浓度。

Concentration of liver and kidney fructose-1,6-diphosphatase determined by specific radioimmunoassay.

作者信息

Mazzotta M Y, Veneziale C M

出版信息

Biochim Biophys Acta. 1980 Jan 11;611(1):156-67. doi: 10.1016/0005-2744(80)90051-0.

Abstract

A radioimmunoassay for liver fructose-1,6-diphosphatase (D-fructose-1,6-bisphosphate 1-phosphohydrlase, EC 3.1.3.11) has been developed based on maintenance of its tetrameric structure and immunologic integrity after iodination by the Bolton-Hunter technique. The assay detected as little as 2 ng of standard enzyme. Nonspecific interference by tissue components did not occur. Enzyme concentration (mumol/1000 g tissue wet weight) was measured in tissue extracts of 49 rabbits subjected to a variety of conditions. In animals fed a 'balanced' diet containing 50--60% carbohydrate (by weight), the concentration in liver was 3.4 microM +/- 0.3. After fasts of 48, 72, or 96 h, the concentration in liver increased approximately 1.4-fold. A high-fat diet did not alter the concentration significantly but a high-protein diet caused an increase of 2.1-fold to 7.2 microM +/- 1.4. The greatest concentrations, 8.7 microM +/- 1.9, were observed in the livers of severely diabetic rabbits. The increase paralleled the increasing severity of diabetes and provides one explanation for the augmented gluconeogenesis which occurs in the diabetic state. Changes were less marked in kidney. The greatest apparent incrase, from 2.6 microM +/- 1.1 in the normal fed rabbit to 4.7 microM +/- 2.8, occurred in the severely diabetic animal. However, variation was sufficiently great in kidney to render apparent increases during fasting, protein feefing and diabetes statistically insignificant. For the most part changes in assayable activity followed changes in enzyme concentration except in the rabbits maintained on high-protein diets. In these, liver enzyme concentration increased by 2.4-fold whereas activity increased by only 1.3-fold, and the kidney enzyme concentration increased 1.3-fold whereas activity decreased by 20%.

摘要

基于采用博尔顿-亨特技术碘化后维持其四级结构和免疫完整性,已开发出一种用于检测肝脏果糖-1,6-二磷酸酶(D-果糖-1,6-二磷酸1-磷酸水解酶,EC 3.1.3.11)的放射免疫测定法。该测定法可检测低至2 ng的标准酶。未出现组织成分的非特异性干扰。在49只处于各种条件下的兔子的组织提取物中测量了酶浓度(微摩尔/1000克组织湿重)。在喂食含50 - 60%碳水化合物(按重量计)的“均衡”饮食的动物中,肝脏中的浓度为3.4微摩尔/升±0.3。在禁食48、72或96小时后,肝脏中的浓度大约增加了1.4倍。高脂饮食并未显著改变该浓度,但高蛋白饮食导致浓度增加2.1倍至7.2微摩尔/升±1.4。在严重糖尿病兔子的肝脏中观察到最高浓度,为8.7微摩尔/升±1.9。这种增加与糖尿病严重程度的增加平行,并为糖尿病状态下发生的糖异生增强提供了一种解释。肾脏中的变化不太明显。在严重糖尿病动物中出现了最明显的增加,从正常喂食兔子的2.6微摩尔/升±1.1增加到4.7微摩尔/升±2.8。然而,肾脏中的变化幅度足够大,以至于在禁食、蛋白质喂养和糖尿病期间的明显增加在统计学上不显著。在大多数情况下,可测定活性的变化跟随酶浓度的变化,但在维持高蛋白饮食的兔子中除外。在这些兔子中,肝脏酶浓度增加了2.4倍,而活性仅增加了1.3倍,肾脏酶浓度增加了1.3倍,而活性下降了20%。

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