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首页> 外文期刊>Amino acids >An investigation into possible xenobiotic-endobiotic inter-relationships involving the amino acid analogue drug, S-carboxymethyl-L-cysteine and plasma amino acids in humans
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An investigation into possible xenobiotic-endobiotic inter-relationships involving the amino acid analogue drug, S-carboxymethyl-L-cysteine and plasma amino acids in humans

机译:人体中涉及氨基酸类似药物,S-羧甲基-L-半胱氨酸和血浆氨基酸的可能的异种生物-内源性相互关系的研究

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The amino acid derivative, S-carboxymethyl-L-cysteine, is an anti-oxidant agent extensively employed as adjunctive therapy in the treatment of human pulmonary conditions. A major biotransformation route of this drug, which displays considerable variation in capacity in man, involves the oxidation of the sulfide moiety to the inactive S-oxide metabolite. Previous observations have indicated that fasted plasma L-cysteine concentrations and fasted plasma L-cysteine/free inorganic sulfate ratios were correlated with the degree of sulfoxidation of this drug and that these particular parameters may be used as endobiotic bio-markers for this xenobiotic metabolism. It has been proposed also that the enzyme, cysteine dioxygenase, was responsible for the drug sulfoxidation. Further in this theme, the degree of S-oxidation of S-carboxymethyl-L-cysteine in 100 human volunteers was investigated with respect to it potential correlation with fasted plasma amino acid concentrations. Extensive statistical analyses showed no significant associations or relationships between the degree of drug S-oxidation and fasted plasma amino acid concentrations, especially with respect to the sulfur-containing compounds, methionine, L-cysteine, L-cysteine sulfinic acid, taurine and free inorganic sulfate, also the derived ratios of L-cysteine/ L-cysteine sulfinic acid and L-cysteine/free inorganic sulfate. It was concluded that plasma amino acid levels or derived ratios cannot be employed to predict the degree of S-oxidation of S-carboxymethyl-L-cysteine (or vice versa) and that it is doubtful if the enzyme, cysteine dioxygenase, has any involvement in the metabolism of this drug.
机译:氨基酸衍生物S-羧甲基-L-半胱氨酸是一种抗氧化剂,广泛用于辅助治疗人类肺部疾病。该药物的主要生物转化途径在人体内表现出相当大的变化,其中涉及到硫化物部分氧化为惰性S-氧化物代谢产物。先前的观察结果表明,禁食的血浆L-半胱氨酸浓度和禁食的血浆L-半胱氨酸/游离无机硫酸盐比率与该药物的亚硫酸盐氧化程度相关,并且这些特定参数可用作该异生物代谢的内生生物标记。还已经提出,半胱氨酸双加氧酶是造成药物磺氧化的原因。进一步在该主题中,针对与空腹血浆氨基酸浓度的潜在相关性,研究了100名人类志愿者中S-羧甲基-L-半胱氨酸的S-氧化程度。广泛的统计分析表明,药物S氧化程度与禁食的血浆氨基酸浓度之间无显着关联或相关性,特别是对于含硫化合物,蛋氨酸,L-半胱氨酸,L-半胱氨酸亚磺酸,牛磺酸和游离无机盐而言硫酸盐,以及L-半胱氨酸/ L-半胱氨酸亚磺酸和L-半胱氨酸/游离无机硫酸盐的比率。结论是血浆氨基酸水平或衍生比例不能用于预测S-羧甲基-L-半胱氨酸的S-氧化程度(反之亦然),并且怀疑半胱氨酸双加氧酶是否参与其中在这种药物的代谢。

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