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Metabolism of an oral tryptophan load. I: Effects of dose and pretreatment with tryptophan.

机译:口服色氨酸负荷的代谢。 I:剂量和色氨酸预处理的影响。

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摘要

1 The metabolism of three oral doses of L-tryptophan (50, 25 and 10 mg/kg) in healthy young males has been investigated. 2 There was a linear relationship between both peak and area under curve of the total plasma tryptophan concentrations whilst the relationship between these parameters and plasma free tryptophan was hyperbolic. 3 Before the tryptophan load about 85% of plasma tryptophan was bound to albumin. As plasma tryptophan concentrations increased there was a hyperbolic increase in free tryptophan. Scatchard analysis revealed 1.4 binding sites/molecule albumin with a dissociation constant (Kd) of 57.9 microM. Following administration of L-tryptophan (50 mg/kg) twice daily for 7 days there was no alteration in the number of binding sites but the dissociation constant (Kd) had decreased to 30.9 microM. 4 L-Tryptophan (50 mg/kg twice daily for 7 days) markedly increased both basal plasma total and free tryptophan. However following a further load the total tryptophan curve was comparable to that seen after acute administration. The plasma free tryptophan curve was lowered relative to that seen after an acute dose. 5 Increasing the tryptophan dose shortened the plasma half-life and decreased the volume of distribution and the rate of clearance. Longer term tryptophan administration had no significant effect on plasma half-life or volume of distribution but did decrease the rate of plasma clearance. 6 The plasma kynurenine concentration increased with increasing tryptophan dose and basal concentrations increased markedly after longer term tryptophan administration. 7 Tryptophan administration either acutely or chronically produced little change in urinary tryptophan or 5-hydroxyindole acetic acid excretion. Urinary kynurenine and indole acetic acid excretion increased with increasing doses of tryptophan. 8 Data are discussed in relation to the administration of L-tryptophan for the treatment of depression.
机译:1研究了健康男性中三种口服剂量L-色氨酸(50、25和10 mg / kg)的代谢。 2总血浆色氨酸浓度的峰下面积与曲线下面积之间存在线性关系,而这些参数与血浆游离色氨酸之间的关系是双曲线的。 3在色氨酸负载之前,血浆色氨酸中约有85%与白蛋白结合。随着血浆色氨酸浓度的增加,游离色氨酸呈双曲线增加。斯卡查德分析显示1.4个结合位点/分子白蛋白的解离常数(Kd)为57.9 microM。每天两次给予L-色氨酸(50 mg / kg),连续7天后,结合位点的数量没有变化,但解离常数(Kd)已降至30.9 microM。 4 L-色氨酸(50 mg / kg每天两次,连续7天)显着增加基础血浆总量和游离色氨酸。然而,在进一步的负荷之后,总色氨酸曲线与急性给药后所见的曲线相当。血浆游离色氨酸曲线相对于急性剂量后降低。 5增加色氨酸剂量会缩短血浆半衰期并降低分布体积和清除率。长期服用色氨酸对血浆半衰期或分布体积没有明显影响,但确实降低了血浆清除率。 6长期服用色氨酸后,血浆犬尿氨酸浓度随色氨酸剂量的增加而增加,而基础浓度则显着增加。 7色氨酸的急性或慢性给药对尿中色氨酸或5-羟吲哚乙酸排泄几乎没有影响。尿色氨酸和吲哚乙酸的排泄随着色氨酸剂量的增加而增加。 8讨论了与L-色氨酸治疗抑郁症有关的数据。

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