首页> 外文期刊>Biochimica et biophysica acta: international journal of biochemistry and biophysics >Enzyme activities along the tryptophan-nicotinic acid pathway in alloxan diabetic rabbits.
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Enzyme activities along the tryptophan-nicotinic acid pathway in alloxan diabetic rabbits.

机译:四氧嘧啶糖尿病兔的色氨酸-烟酸途径中的酶活性。

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Recent data from our laboratory have indicated that the rabbit is a suitable animal model for the study of enzyme activities of the tryptophan-nicotinic acid pathway. We report here the pattern of tryptophan metabolism in rabbits made diabetic with alloxan treatment, and hypercholesterolemic with a high-cholesterol diet. A group of rabbits with only hypercholesterolemia was also considered. The enzymes assayed were: liver tryptophan 2,3-dioxygenase (TDO), intestine indoleamine 2,3-dioxygenase (IDO), liver and kidney kynurenine 3-monooxygenase, kynurenine-oxoglutarate transaminase, kynureninase, 3-hydroxyanthranilate 3,4-dioxygenase and aminocarboxymuconate-semialdehyde decarboxylase.TDO showed a reduction of specific activity in liver of diabetic-hyperlipidemic and hyperlipidemic rabbits compared to controls. Intestine IDO activities and liver and kidney kynurenine monooxygenase were unchanged with respect to controls.Kynurenine-oxoglutarate transaminase and kynureninase activities were reduced in the kidneys, but not in the liver, of diabetic-hyperlipidemic rabbits.The main finding was the reduction of 3-hydroxyanthranilate 3,4-dioxygenase activity (expressed as activity per g of fresh tissue) in the liver and kidneys of diabetic-hypercholesterolemic and hyperlipidemic rabbits compared to controls. Conversely, aminocarboxymuconate-semialdehyde decarboxylase activity was significantly higher in diabetic hypercholesterolemic rabbits in comparison with control and hypercholesterolemic rabbits.These data demonstrate that also in diabetic rabbits there is an alteration of tryptophan metabolism at the level of 3-hydroxyanthranilic acid-->nicotinic acid step. Also dyslipidemia seems to be involved in enzyme activity variations of the tryptophan metabolism along the kynurenine pathway.
机译:来自我们实验室的最新数据表明,该兔子是研究色氨酸-烟酸途径酶活性的合适动物模型。我们在这里报告了用四氧嘧啶治疗后患有糖尿病的兔和高胆固醇饮食的高胆固醇血症兔的色氨酸代谢模式。还考虑了一组只有高胆固醇血症的兔子。所检测的酶为:肝色氨酸2,3-二加氧酶(TDO),肠吲哚胺2,3-二加氧酶(IDO),肝和肾脏犬尿氨酸3-单加氧酶,犬尿氨酸-草酸谷氨酰胺转氨酶,犬尿氨酸,3-羟基邻氨基苯甲酸3,4-二加氧酶与对照相比,TDO显示糖尿病高脂血症和高脂血症兔子的肝脏比活性降低。与对照组相比,肠道IDO活性和肝肾肾上腺素单加氧酶没有变化,糖尿病高脂血症兔的肾脏中的尿嘧啶氧合谷氨酸转氨酶和犬尿素酶活性降低,但肝脏没有降低,主要发现是降低了3-与对照组相比,糖尿病-高胆固醇血症和高血脂兔的肝脏和肾脏中的羟基邻氨基苯甲酸3,4-双加氧酶活性(以每克新鲜组织的活性表示)。相反,糖尿病高胆固醇血症兔的氨基羧基粘康酸酯-半醛脱羧酶活性明显高于对照组和高胆固醇血症兔,这些数据表明,糖尿病兔的色氨酸代谢在3-羟基邻氨基苯甲酸->烟酸水平上也发生了改变。步。血脂异常似乎也与沿犬尿氨酸途径的色氨酸代谢的酶活性变化有关。

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