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. 2021 Sep 1:14:11786469211039220.
doi: 10.1177/11786469211039220. eCollection 2021.

Neurotransmitter Precursor Amino Acid Ratios Show Differential, Inverse Correlations with Depression Severity in the Low and High Depression Score Range

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Neurotransmitter Precursor Amino Acid Ratios Show Differential, Inverse Correlations with Depression Severity in the Low and High Depression Score Range

Katharina Hüfner et al. Int J Tryptophan Res. .

Abstract

The immunomodulatory capacity of mental stress is one of the basic concepts of psychoneuroimmunology. The current prospective longitudinal study was designed to evaluate the effect of acute mental stress on neurotransmitter precursor amino acid levels in individuals with depression at 2 time points. Ten physically healthy patients with a diagnosis of major depressive episode and Montgomery-Åsberg Depression Rating Scale scores (MADRAS) ⩾20 points at inclusion were assessed on 2 study days (once with higher MADRAS scores, once with lower MADRAS scores; median 34.5 days apart) and subjected to a standardized acute mental stress test on each study day. Blood was collected at 4 time points: once prior to and at 3 time points (0, 30 minutes, 60 minutes) following mental stress. Neurotransmitter precursor amino acid levels, that is kynurenine/tryptophan (KYN/TRP) and phenylalanine/tyrosine (PHE/TYR), as well as neopterin and nitrite were analyzed in a total of 80 individual blood samples. Regression and correlation analyses were performed. Regression analyses of PHE/TYR (R 2 = .547) and KYN/TRP (R 2 = .440) in relation to MADRAS depression severity showed a quadratic curve fit. This was reflected by a negative linear correlation between MADRAS scores and PHE/TYR as well as KYN/TRP in the lower score range (r = -.805, P < .001 and r = -.586, P < .001 respectively) and a positive correlation in the higher MADRAS score range (r = .713, P < .001 and r = .379, P = .016 respectively). No effect of acute mental stress was found. This analysis exemplifies the implications of sampling as well as data distributions on results. The crosstalk of biological mechanisms that orchestrate metabolic and immunological signaling may vary depending on depression severity resulting in non-linear associations that may explain the heterogeneity of results found in the literature.

Keywords: Depression severity; kynurenine; neurotransmitter; phenylalanine; quadratic curve fit; tryptophan; tyrosine.

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Conflict of interest statement

Declaration Of Conflicting Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figure 1.
Figure 1.
Aromatic amino acid catabolism and related pathways. Immune activation is characterized by an oxidative milieu and release of inflammatory stimuli that for example during the cellular immune response activate indoleamine 2,3-dioxygenase (IDO-1), which catalyzes the rate-limiting reaction in the tryptophan catabolic route along the kynurenine axis. Notably, also tryptophan 2,3-dioxygenase and IDO-2 can catalyze tryptophan breakdown (not shown). GTP-cyclohydrolase 1 (GTP-CH-I) forms 7,8 trihydroneopterin triphosphate, the precursor of tetrahydrobiopterin (BH4), and neopterin. In immune activation, this biosynthetic route is shifted towards neopterin formation in human macrophages and dendritic cells, moreover, the oxidative milieu destabilizes BH4. In consequence, the activity of BH4-dependent monooxygenases such as of tryptophan 5-hydroxylases (TPH), phenylalanine 4-hydroxylase (PAH), and tyrosine 3-monooxygenase (TH) decreases, indicated by smaller symbols. Both, aromatic amino acid availability and the activity of biosynthetic enzymes are determinants of serotonergic and dopaminergic neurotransmitter levels. Abbreviation: ROS: reactive oxygen species.
Figure 2.
Figure 2.
Flowchart of study design (a) and patient recruitment (b). Abbreviations: MADRAS, Montgomery–Åsberg Depression Rating Scale.
Figure 3.
Figure 3.
Scatter plots with quadratic regression curves showing the association between the MADRAS (Montgomery–Åsberg Depression Rating Scale) score (x-axis) and the phenylalanine to tyrosine ratio (PHE/TYR) (y-axis, left figure a) and the kynurenine to tryptophan ratio (KYN/TRP) (y-axis, right figure b). Data points and quadratic regression curves are shown separately for the 4 study time points, that is for baseline after 30 minutes of rest (T0, blue), immediately after the acute mental stress test (T1, red), 30 minutes post-acute mental stress (T2, green), and 60 minutes post-acute mental stress (T3, orange).

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