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健康对照者和精神分裂症患者的色氨酸激发试验:对犬尿氨酸、犬尿喹啉酸和5-羟吲哚乙酸血浆水平的急性影响。

Tryptophan Challenge in Healthy Controls and People with Schizophrenia: Acute Effects on Plasma Levels of Kynurenine, Kynurenic Acid and 5-Hydroxyindoleacetic Acid.

作者信息

Sathyasaikumar Korrapati V, Notarangelo Francesca M, Kelly Deanna L, Rowland Laura M, Hare Stephanie M, Chen Shuo, Mo Chen, Buchanan Robert W, Schwarcz Robert

机构信息

Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD 21228, USA.

出版信息

Pharmaceuticals (Basel). 2022 Aug 15;15(8):1003. doi: 10.3390/ph15081003.

Abstract

The pivotal tryptophan (TRP) metabolite kynurenine is converted to several neuroactive compounds, including kynurenic acid (KYNA), which is elevated in the brain and cerebrospinal fluid of people with schizophrenia (SZ) and may contribute to cognitive abnormalities in patients. A small proportion of TRP is metabolized to serotonin and further to 5-hydroxyindoleacetic acid (5-HIAA). Notably, KP metabolism is readily affected by immune stimulation. Here, we assessed the acute effects of an oral TRP challenge (6 g) on peripheral concentrations of kynurenine, KYNA and 5-HIAA, as well as the cytokines interferon-γ, TNF-α and interleukin-6, in 22 participants with SZ and 16 healthy controls (HCs) using a double-blind, placebo-controlled, crossover design. TRP raised the levels of kynurenine, KYNA and 5-HIAA in a time-dependent manner, causing >20-fold, >130-fold and 1.5-fold increases in kynurenine, KYNA and 5-HIAA concentrations, respectively, after 240 min. According to multivariate analyses, neither baseline levels nor the stimulating effects of TRP differed between participants with SZ and HC. Basal cytokine levels did not vary between groups, and remained unaffected by TRP. Although unlikely to be useful diagnostically, measurements of circulating metabolites following an acute TRP challenge may be informative for assessing the in vivo efficacy of drugs that modulate the neosynthesis of KYNA and other products of TRP degradation.

摘要

关键的色氨酸(TRP)代谢产物犬尿氨酸可转化为多种神经活性化合物,包括犬尿喹啉酸(KYNA),在精神分裂症(SZ)患者的大脑和脑脊液中其水平升高,可能导致患者认知异常。一小部分TRP代谢为血清素,进而代谢为5-羟吲哚乙酸(5-HIAA)。值得注意的是,犬尿氨酸途径(KP)代谢很容易受到免疫刺激的影响。在此,我们采用双盲、安慰剂对照、交叉设计,评估了口服TRP激发试验(6克)对22名SZ患者和16名健康对照者(HCs)外周血中犬尿氨酸、KYNA和5-HIAA浓度以及细胞因子干扰素-γ、肿瘤坏死因子-α和白细胞介素-6的急性影响。TRP以时间依赖性方式提高了犬尿氨酸、KYNA和5-HIAA的水平,240分钟后,犬尿氨酸、KYNA和5-HIAA浓度分别增加了20倍以上、130倍以上和1.5倍。根据多变量分析,SZ患者和HCs之间的基线水平和TRP的刺激作用均无差异。各组间基础细胞因子水平无变化,且不受TRP影响。尽管急性TRP激发试验后循环代谢产物的测量不太可能用于诊断,但可能有助于评估调节KYNA新合成及TRP降解其他产物的药物的体内疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f588/9416551/c8cc83e02ae2/pharmaceuticals-15-01003-g001.jpg

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