[1例溃疡致残性肢端病的血浆、红细胞和脊髓液氨基酸水平]。

M Rasura, C Argentino, N Accornero, A Bondoli, M Manfredi
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引用次数: 0

摘要

在一个患有Thevenard病(脊髓神经节和后根的退行性疾病)的患者中,我们测量了红细胞内、血浆和脑脊液氨基酸的水平。在血浆中,我们发现牛磺酸和甘氨酸的浓度增加,高分解代谢的表达,这被游离红细胞内氨基酸水平下降的存在所证实。在脑脊液中,我们发现蛋氨酸、缬氨酸和赖氨酸的浓度增加,这表明存在一种酶抑制作用,这种酶抑制作用涉及氨基酸在屏障水平的全身运输。谷氨酸和精氨酸水平的升高表明α -鸟嘌呤丁酸的合成发生了变化。我们还发现缬氨酸、蛋氨酸、甘氨酸、酪氨酸水平的增加,这表明在生化进入克雷布斯循环的附带反应中存在酶的改变。因此,作者得出结论,这种疾病的基础可能是在生化合成的代谢缺陷中发现的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Plasma, intraerythrocytic and spinal fluid amino acid levels in a case of ulcero-mutilating acropathy].

In a patient affected by Thevenard's disease (degenerative disease of the spinal ganglia and posterior roots) we measured levels of intraerythrocytic, plasmatic and cerebrospinal fluid aminoacids. In the plasma we found an increased concentration of taurine and glycine, expression of hypercatabolism, which was confirmed by the presence of a decreased level of the free intraerythrocytic aminoacids. In the cerebrospinal fluid we found increased concentrations of methionine, valine and lysine which indicates the presence of an enzymatic inhibition that involves the systemic transport of aminoacids at the barrier level. The increased levels of glutamic acid and arginine suggests an alteration of the synthesis of alpha-guanino butyric acid. We have also found an increase in the levels of valine, methionine, glycine, tyrosine which suggests the presence of an enzymatic alteration in the collateral reactions that biochemically feed into the Krebs cycle. The authors therefore conclude that the basis of this disease may be found in a metabolic defect biochemical synthesis.

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