Abstract

Tryptophan (TRP) is to an essential amino acid and its catabolites are significant to human health. By using ultra-high-performance liquid chromatography coupled to electrospray ionization triple quadrupole mass spectrometry (UHPLC-ESI-MS/MS), levels of three major components of kynurenic pathway namely tryptophan (TRP), kynurenic acid (KYNA) and kynurenine (KYN) in fluid from the anterior chamber of the eye were determined. The analysis was carried out on a Synergi 4 μ Fusion-RP column using gradient elution mode. For quantitative determination, l-tryptophan-amino-15N, 99 ATOM % 15N was used as an internal standard. The method was linear in the concentration range 4–2000 ng mL−1 for TRP, KYNA and KYN. The mean recoveries measured at four concentration levels for TRP, KYN and KYNA included the following ranges 94.3–96.1; 91.0–95.0; and 96.0–97.6%, respectively. The intra-day precision parameters were smaller than 4.4, 6.4 and 5% respectively. The developed method was applied to study the level of TRP, KYNA and KYN in eye fluid for the retrospective case series which included 28 patients suffering from cataracts and diabetes (n = 8). The experimental data was subjected to statistical analysis. The Mann-Whitney U-test revealed clear differences in the level of TRP catabolites and the ratios of TRP/KYN representing the activities of specific enzyme of kynurenine pathway in examined groups of patients. A level of probability p < 0.05 was used throughout a paper to denote statistically significant differences between the groups.

Highlights

  • The main route of tryptophan (TRP) degradation is through kynurenine pathway (KP) accounting for ~ 95% of its overall degradation

  • The KP leads to production of metabolites, such as kynurenic acid (KYNA), kynurenine (KYN), anthranilic acid (AA), 3-OH kynurenine (3-OH KYN), xanthurenic acid (XA), 3-hydroxybutyrate anthranilic acid (3-HAA), quinolinic acid (QA) subsequently denoted as kynurenines and, to biosynthesis of a crucial cofactor, namely, nicotinamide adenine dinucleotide (NAD+) [1]

  • Experiments on the fluid from the anterior chamber of the eye suggest that neuroactive metabolites of the tryptophan (TRP) in the kynurenine pathway (KP) may play a significant role in cataract formation in patients suffering from diabetes

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Summary

Introduction

The main route of tryptophan (TRP) degradation is through kynurenine pathway (KP) accounting for ~ 95% of its overall degradation. The process of metabolizing TRP into KYN takes place in different locations mostly in the liver, kidneys and the brain with the help of three enzymes: TRP-2,3-dioxygenase, Molecules 2018, 23, 3012; doi:10.3390/molecules23113012 www.mdpi.com/journal/molecules. TRP-2,3-dioxygenase, indoleamine-2,3-dioxygenase-1 and indoleamine dioxygenase—2 [1,2]. It indoleamine-2,3-dioxygenase-1 and indoleamine [1,2].byItthemselves, should be emphasized should be emphasized that humans are not abledioxygenase—2 to synthesize TRP it that humans are not able to synthesize. TRP by themselves, it comes only from comes only from the diet.

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