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Article

The Effect of the Stress Induced by Hydrogen Peroxide and Corticosterone on Tryptophan Metabolism, Using Human Neuroblastoma Cell Line (SH-SY5Y)

by
Ana Salomé Correia
1,2,3,
Isabel Silva
4,
Henrique Reguengo
4,5,
José Carlos Oliveira
2,4,5,
Francisco Vasques-Nóvoa
6,7,
Armando Cardoso
3,8,9 and
Nuno Vale
1,3,10,*
1
OncoPharma Research Group, Center for Health Technology and Services Research (CINTESIS), Rua Doutor Plácido da Costa, 4200-450 Porto, Portugal
2
Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto, Rua de Jorge Viterbo Ferreira 228, 4050-313 Porto, Portugal
3
CINTESIS@RISE, Faculty of Medicine, University of Porto, Alameda Professor Hernâni Monteiro, 4200-319 Porto, Portugal
4
Clinical Chemistry, Department of Laboratory Pathology, Hospital Center of the University of Porto (CHUP), Largo Prof. Abel Salazar, 4099-313 Porto, Portugal
5
Unit for Multidisciplinary Research in Biomedicine (UMIB), University of Porto, Rua de Jorge Viterbo Ferreira 228, 4050-313 Porto, Portugal
6
Cardiovascular R and D Center, Faculty of Medicine, University of Porto, Rua Doutor Plácido da Costa, s/n, 4200-450 Porto, Portugal
7
Department of Surgery and Physiology, Faculty of Medicine, University of Porto, Rua Doutor Plácido da Costa, 4200-450 Porto, Portugal
8
NeuroGen Research Group, Center for Health Technology and Services Research (CINTESIS), Rua Doutor Plácido da Costa, 4200-450 Porto, Portugal
9
Unit of Anatomy, Department of Biomedicine, Faculty of Medicine, University of Porto, Alameda Professor Hernâni Monteiro, 4200-319 Porto, Portugal
10
Department of Community Medicine, Health Information and Decision (MEDCIDS), Faculty of Medicine, University of Porto, Rua Doutor Plácido da Costa, 4200-450 Porto, Portugal
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2023, 24(5), 4389; https://doi.org/10.3390/ijms24054389
Submission received: 11 February 2023 / Revised: 18 February 2023 / Accepted: 21 February 2023 / Published: 23 February 2023
(This article belongs to the Special Issue DNA Damage, Oxidative Stress and Related Metabolic By-Products in Cancer and Environmental Studies 2.0)
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Versions Notes

Abstract

:
L-tryptophan (L-Trp) is an important amino acid in several physiological mechanisms, being metabolized into two important pathways: the kynurenine and the serotonin (5-HT) pathways. It is important in processes such as mood and stress response, the 5-HT pathway begins with the conversion of L-Trp to 5-hydroxytryptophan (5-HTP), that is metabolized into 5-HT, converted to melatonin or to 5-hydroxyindoleacetic acid (5-HIAA). Disturbances in this pathway are reported to be connected with oxidative stress and glucocorticoid-induced stress, are important to explore. Thus, our study aimed to understand the role of hydrogen peroxide (H2O2) and corticosterone (CORT)-induced stress on the serotonergic pathway of L-Trp metabolism, and on SH-SY5Y cells, focusing on the study of L-Trp, 5-HTP, 5-HT, and 5-HIAA in combination with H2O2 or CORT. We evaluated the effect of these combinations on cellular viability, morphology, and on the extracellular levels of the metabolites. The data obtained highlighted the different ways that stress induction led to different extracellular medium concentration of the studied metabolites. These distinct chemical transformations did not lead to differences in cell morphology/viability. Additionally, serotonin may be the most sensitive metabolite to the exposure to the different stress inducers, being more promissory to study conditions associated with cellular stress.

1. Introduction

L-tryptophan (L-Trp) is an essential amino acid, and is important in several physiological mechanisms, such as gastrointestinal and nervous processes. The metabolism of this amino acid is divided mainly in two branches: the kynurenine and the serotonin (5-HT) pathways [1,2]. Nevertheless, the metabolism of this amino acid is complex. Indeed, other compounds may be formed in the metabolism of this compound by the cells, such as indole-3-acetonitrile [3].
The kynurenine pathway represents about 95% of the metabolism of L-Trp [1]. This pathway has a crucial role on processes, such as inflammation and immune response, being connected to diseases, such as depression, cancer, and diabetes [4,5]. The 5-HT pathway is also extremely relevant in several physiological mechanisms. Indeed, processes, such as mood, sexuality, memory, appetite, stress response, motor control, regulation of circadian rhythm, gastrointestinal regulation, nociception, regulation of heart rate, and platelet aggregation, are influenced by this pathway [6]. Focusing on the 5-HT pathway, L-Trp is converted to 5-hydroxytryptophan (5-HTP) by tryptophan hydroxylase 1 or 2 (TPH1 or 2), the rate-limiting step. 5-HTP forms 5-HT by decarboxylation carried out by aromatic acid decarboxylase (AADC). Then, 5-HT may be converted to melatonin by metabolization to N-acetylserotonin (NAS), or to form 5-hydroxyindoleacetic acid (5-HIAA), the major 5-HT metabolite, by the enzyme monoamine oxidase (MAO) [7].
The impairment of L-Trp/5-HT pathways and oxidative stress and glucocorticoid-induced stress is important to explore, being already reported in some studies [8,9,10,11,12]. Indeed, oxidative stress generates neurotoxic compounds by the oxidation of the L-Trp. It also known that L-Trp may be metabolized to kynurenine directly by high levels of reactive oxygen species (ROS). Then, kynurenine may be metabolized to the oxidant compounds 3-hydroxykynurenine and quinolinic acid, associated with diseases, such as depressive disorders [13,14]. A previous study also revealed that L-Trp counteracted the cellular stress induced by hydrogen peroxide (H2O2), highlighting the role of L-Trp metabolism in the context of oxidative stress [8,15]. High levels of glucocorticoids are also reported to increase the kynurenine production, decreasing the activity of the 5-HT branch of L-Trp metabolism [12]. In patients with suicidal attempts, high levels of cortisol correlate with lower levels of L-Trp in the plasma, and a higher kynurenine/L-Trp ratio were also previously reported [16]. The administration of crocin also reduced cortisol levels and increased 5-HT in mice [17], supporting the inverse relationship between the levels of glucocorticoids and 5-HT.
Thus, our study aimed to explore the role of H2O2 and corticosterone (CORT)-induced stress on the L-Trp/5-HT metabolism, on SH-SY5Y cells previously used [8,9,18]. These cells are originally derived from a metastatic bone tumor biopsy, being widely used in the research of neuropsychiatric and neurological disorders and mechanisms, mainly because they have several neuronal features. Indeed, these cells can have cholinergic, adrenergic, or dopaminergic phenotypes, being frequently used in the study of Parkinson’s disease and depressive disorders [19,20]. It is also reported that SH-SY5Y cells produce 5-HT and express major serotonergic proteins, including the serotonergic type 1A receptor (5-HT1A) [21]. H2O2 induces direct oxidative stress, whereas high levels of CORT mimic the stress induced by hypothalamus-pituitary-adrenal axis disturbances [8,9].
Thus, to study this induced stress on L-Trp metabolism, we focused on the study of L-Trp, 5-HTP, 5-HT, and 5-HIAA (Figure 1). These compounds were added in high concentrations to the cells, either alone or in combination with H2O2 or CORT aiming to evaluate the effect on cellular viability, morphology, and on the extracellular levels of the studied metabolites.
Our results highlighted that different ways of stress induction led to different extracellular medium concentration of L-Trp, 5-HTP, 5-HT, and 5-HIAA. We also observed that these different chemical transformations did not lead to differences in cell morphology/viability between these different metabolites. Additionally, we hypothesized that the 5-HT pathway is the most sensitive and suitable to modulating effects of the cellular environment, and, therefore, presents the best applicability to be used in conditions associated with cellular stress.
The most important abbreviations used in this manuscript are present on Table S1.

2. Results

2.1. Effect of H2O2 and CORT on SH-SY5Y Cellular Viability

In our previous works, we determined the effect of crescent concentrations of H2O2 and CORT on the viability of SH-SY5Y cells [8,9]. Just to confirm these results, we repeated this procedure from one independent culture preparation, adding H2O2 50–300 µM and CORT 100–500 µM to the cells for 48 h. After that, we evaluated the effect of these compounds on the morphology and viability of SH-SY5Y cells. Figure 2 represents the obtained results.
These results confirm that both H2O2 and CORT decreased cellular viability in a concentration-dependent manner. Cellular viability values were 52.84% and 25.05% with H2O2 300 µM and CORT 500 µM, respectively. Additionally, cell viability values are also concordant with the cellular morphology. Imagens demonstrate cell damage after application of H2O2 300 µM and CORT 500 µM, reflected by rounded morphology, shrinkage, and, overall, a lower number of cells, typical features of cell death [22].

2.2. Effect of L-Trp and Combinations of L-Trp with H2O2 or CORT on SH-SY5Y Cell Viability and Extracellular L-Trp Concentration

To evaluate the 48 h effect of L-Trp and combinations of this amino acid with H2O2 or CORT on SH-SY5Y cellular viability and extracellular L-Trp concentration, this compound was added to the cells in a concentration of 500 µM. In turn, H2O2 and CORT were added to the cells in a concentration of 300 µM and 500 µM, respectively. As mentioned above, the purpose of these high concentrations was to ensure that we could obtain a measurable response of the cells to these compounds, allowing a better interpretation and examination of the results, mainly on the HPLC. After exposing the cells to the different treatment conditions, we evaluated the effect on the morphology and viability of SH-SY5Y cells (Figure 3A–D). The extracellular media was also collected, aiming to understand the effect of these treatments on the L-Trp extracellular concentration (Figure 3E).
Our results revealed that L-Trp (single compound) increased cell viability (128.39% vs. vehicle). On the other hand, when combined with both H2O2 and CORT, cell viability decreased (57.12% vs. vehicle and 21.55% vs. vehicle, respectively). However, analyzing HPLC results, we observed the opposite. Indeed, after the 48 h exposure of the cells to L-Trp (single compound), the concentration of L-Trp in the extracellular medium decreased 26 µM. When combined with both H2O2 and CORT, L-Trp levels in the extracellular medium increased 137 µM and 44 µM, respectively. Viability values and morphology assessment were also concordant. Indeed, lower viability values were reflected in rounded morphology, shrinkage, and a lower number of cells.

2.3. Effect of 5-HTP and Combinations of 5-HTP with H2O2 or CORT on SH-SY5Y Cell Viability and Extracellular 5-HTP Concentration

To evaluate the 48 h effect of 5-HTP and combinations of this compound with H2O2 or CORT on the viability of SH-SY5Y cells and on extracellular 5-HTP concentration, this compound was added to the cells in a concentration of 500 µM. H2O2 and CORT were added to the cells in a concentration of 300 µM and 500 µM, respectively. After exposing the cells to the different treatment conditions, we assessed the effect on the morphology and viability of SH-SY5Y cells (Figure 4A–D). The extracellular media was also collected, with the aim to understand the effect of these treatments on the 5-HTP extracellular concentration (Figure 4E).
Our data demonstrated that, similar to what happened with L-Trp, 5-HTP single compound increased cell viability (116.81% vs. vehicle). When combined with H2O2 and CORT, cell viability decreased (70.51% vs. vehicle and 15.76% vs. vehicle, respectively). HPLC results revealed that after the 48 h exposition of the cells to 5-HTP alone, the concentration of this compound in the extracellular medium slightly increased (22 µM). When combined with both H2O2 and CORT, 5-HTP levels in the extracellular medium decreased 259 µM and 22 µM, respectively, following an opposite tendency compared to the L-Trp levels on the extracellular medium. Regarding morphological evaluation, once again, these images supported viability values.

2.4. Effect of 5-HT and Combinations of 5-HT with H2O2 or CORT on SH-SY5Y Cell Viability and Extracellular 5-HT Concentration

Continuing the study of L-Trp metabolic cascade, to study the 48 h effect of 5-HT and combinations of this compound with H2O2 or CORT on the viability of SH-SY5Y cells and on extracellular 5-HT concentration, this compound was also added to the cells in a concentration of 500 µM. H2O2 and CORT were added to the cells in a concentration of 300 µM and 500 µM, respectively. After exposing the cells to the different treatment conditions, we assessed the effect on the morphology and viability of SH-SY5Y cells (Figure 5A–D). Once again, the extracellular media was collected, with the aim to understand the effect of these treatments on the 5-HT extracellular concentration (Figure 5E).
The obtained results evidence that 5-HT isolated slightly increased cell viability (123.74% vs. vehicle). On the other hand, when combined with both stress inducers, decreased cell viability. Combined with H2O2, the cellular viability was only slightly different than the vehicle (94.21%). However, combined with CORT, cell viability decreased sharply (15.89% vs. vehicle). Regarding the HPLC results, after the 48 h exposure of the SH-SY5Y cells to 5-HTP alone, the concentration of this compound in the extracellular medium decreased (38 µM). However, and in a different way than what was observed with the other analyzed compounds, when 5-HT was combined with both H2O2 and CORT, an opposite tendency in the extracellular levels of this neurotransmitter was observed. Indeed, when combined with H2O2, 5-HT levels in the extracellular medium decreased (61 µM), and when combined with CORT, these values increased (62 µM). It is important to note that viability and morphology assessment are in concordance.

2.5. Effect of 5-HIAA and Combinations of 5-HIAA with H2O2 or CORT on SH-SY5Y Cell Viability and Extracellular 5-HIAA Concentration

Finally, to study the 48 h effect of 5-HIAA and combinations of this compound with H2O2 or CORT on the viability of SH-SY5Y cells and on extracellular 5-HIAA concentration, this compound was also added to the cells in a concentration of 500 µM. Again, H2O2 and CORT were added to the cells in a concentration of 300 µM and 500 µM, respectively. After exposing the cells to the different treatment conditions, we evaluated the effect on the morphology and viability of SH-SY5Y cells (Figure 6A–D). The extracellular media was also collected, aiming to understand the effect of these treatments on the extracellular concentration of 5-HIAA (Figure 6E).
Our results revealed that 5-HIAA (alone) increased cell viability (136.06% vs. vehicle). On the other hand, when combined with both H2O2 and CORT, cell viability decreased slightly with H2O2 (94.28% vs. vehicle) and decreased markedly with CORT (15.07% vs. vehicle). Analyzing HPLC results, we observed marked increase in the 5-HIAA extracellular levels after all the treatments. Indeed, after the 48 h exposure of the cells to 5-HIAA (single compound), the concentration of this compound in the extracellular medium increased 345 µM. When combined with both H2O2 and CORT, L-Trp levels in the extracellular medium increased 256 µM and 187 µM, respectively. Viability values and morphology assessment were also concordant. In fact, lower viability values were reflected in rounded morphology, shrinkage, and a lower number of cells.

2.6. Effect of H2O2 and CORT on Extracellular 5-HT Concentration

Based on the results obtained with 5-HT and the importance of this neurotransmitter on the study of neuropsychiatric diseases, we added H2O2 50–300 µM and CORT 100–500 µM to cells, for 48 h, aiming to understand the effect of these treatments on the extracellular concentration of 5-HT. In this study, we used an electrochemical method of HPLC, more sensitive to detect 5-HT concentrations produced by the cells. Figure 7 represents the obtained results.
These results demonstrate that after exposing SH-SY5Y cells for 48 h with crescent concentrations of H2O2, 5-HT levels on the extracellular medium decreased in a concentration-dependent way, varying between 11.12 nM (vehicle) and 1.19 nM (H2O2 300 µM). Regarding CORT, the exposition of this compound to the cells did not significantly alter 5-HT concentrations in the extracellular medium. Indeed, CORT 100 μM led to 5-HT values of 8.05 nM. This value increased with the concentration of CORT, being near the vehicle value (11.12 nM) with CORT 500 µM (10.51 nM).

3. Discussion

L-Trp is an important amino acid in numerous physiological mechanisms, being the precursor of 5-HT synthesis [1]. The role of oxidative stress and glucocorticoid-induced stress in the impairment of the serotonergic pathway of L-Trp metabolism is important to explore, being the aim of our study. The data obtained with the application of H2O2 and CORT to the cells is consistent with previous studies [8,9,23,24], despite some limitations with the use of these agents. Particularly, H2O2 is an unstable compound, rapidly decomposing to oxygen and water, demanding a careful handle [25]. It is also important to note that cortisol is the primary endogenous adrenal steroid in humans, whereas CORT is the primary adrenal corticosteroid in rodents [26]. However, both glucocorticoids have a high level of similarity, being widely reported the use of CORT on human cells [27,28]. Indeed, previously, we also tested the effect of the synthetic form of cortisol (hydrocortisone), obtaining no responses regarding cellular viability, morphology, or DNA damage [9].
Nevertheless, despite limitations, it is widely reported that these agents induce oxidative stress, known to trigger processes, such as inflammation, neurodegeneration, tissue damage and cell death, particularly relevant for depressive disorders [29]. Based in our data, we selected H2O2 300 µM and CORT 500 µM to proceed HPLC analyses, aiming to ensure that we could obtain a measurable response of the cells to these compounds, allowing a better interpretation and examination of the results. In this study, the combination of these agents with L-Trp, 5-HTP, 5-HT, and 5-HIAA did not alleviate the harmful effect of both stressors, demonstrating that these high concentrations of CORT and H2O2 influenced the observed cellular viability inducer effect of the isolated L-Trp metabolites. In our previous studies, we revealed that L-Trp and mirtazapine (an antidepressant that act on serotonergic-related pathways) alleviated cellular stress, demonstrating the importance of this pathway for cellular viability, and recovery from the harmful effects of high levels of oxidative stress [8,9]. Indeed, several studies demonstrate the importance of compounds that act on L-Trp/5-HT pathway in the relieve of glucocorticoid and oxidative stress [10,30,31,32].
After a period of 48 h, the extracellular concentration of each added metabolite markedly varied, independently of cellular viability values. In fact, the obtained values regarding cellular viability and morphology were similar among all metabolites. This did not happen with the results obtained through the determination of the concentration in the extracellular medium demonstrating that different chemical transformations occurred which, during the study period, did not lead to differences in cell morphology/viability.
It is particularly noteworthy that regarding cellular viability and morphology, the results obtained with the combination of each metabolite with CORT revealed greater cell damage than with H2O2. However, the results obtained through the determination of the concentration in the extracellular medium clearly demonstrated that there was a much more pronounced variation with the combinations of the metabolites with H2O2 than with CORT, which can be explained by the high oxidative character of the H2O2 [33]. Indeed, previously, we also demonstrated that regarding ROS production, overall, CORT led to low levels of production compared to H2O2 [8]. This highlights that the way of inducing stress in cells leads to different responses, being an important future topic of studies.
It is important to note that L-Trp, 5-HTP, and 5-HIAA had the same tendency to decrease/increase extracellular concentration when combined with both CORT and H2O2. Regarding 5-HT, this trend was opposite between both stress inducer agents, revealing an increase in the extracellular concentration of this neurotransmitter when combined with CORT and a decrease when combined with H2O2. The results obtained with the electrochemical method for the detection of 5-HT, precisely demonstrated this trend regarding to the extracellular levels of 5-HT only with the addition of CORT/ H2O2. These results may indicate that different forms of stress induction affect 5-HT levels differently, mainly in short periods of time. Indeed, 5-HT has a known protective effect on oxidation processes because it protects membrane lipids from oxidation [34]. Possibly this compound acts on the oxidative effect of H2O2, being more consumed. This antioxidant power of 5-HT makes this pathway attractive for the focus on the development of drugs aiming to interact with serotonergic receptors in the context of stress.
Regarding both L-Trp and 5-HIAA, it can be observed that there was an increase in their extracellular levels after being combined with CORT and especially with H2O2. In fact, it is known that L-Trp is easily oxidized by free radicals, leading to products, such as tryptophanyl (indolyl) radical (Trp) [35], easily masked with L-Trp in its non-oxidized form. Concerning to 5-HIAA, the very high extracellular concentration values are possibly due to the ease of conjugation of this metabolite with other compounds. For example, it is known that urine samples need to be hydrolyzed to release 5-HIAA from conjugates, demonstrating that this compound is easily conjugated with other compounds [36]. With 5-HTP, there is a decrease in the levels of this metabolite. Indeed, its hydroxyl group makes it highly susceptible to oxidation, especially by H2O2 [37].
Studying extracellular levels of L-Trp, 5-HTP, 5-HT, and 5-HIAA after exposition to different stress stimuli is also important to ensure the fine equilibrium between low/high levels of these metabolites and homeostatic levels, that may be maintained. For example, regarding 5-HT, low levels of this neurotransmitter are associated with several pathologies, such as depressive disorders [38]. High levels of this neurotransmitter are also associated with pathological conditions, such as the serotonin syndrome, a potentially life-threatening disease [39].

4. Materials and Methods

4.1. Materials

Dulbecco’s Modified Eagle’s Medium (DMEM, cat. no. FG0415) and Fetal Bovine Serum (FBS, cat. no. S0615) were purchased from Millipore Sigma (Merck KGaA, Darmstadt, Germany). Penicillin/streptomycin (cat. no. P4333), thiazolyl blue tetrazolium bromide (MTT, cat. no. M5655), CORT (cat. no. 27840), H2O2 30% (cat. no. 1.07209), L-Trp (cat. no. T0254-5G), 5-HTP (cat. no. H9772-1G), 5-HT (cat. no. H9523-25MG), and 5-HIAA (cat. no. H8876-100MG) were acquired from Sigma-Aldrich (Merck KGaA, Darmstadt, Germany).
For the HPLC procedure (electrochemical method), materials were previously described [40]. Ultra-high-performance liquid chromatograph (uHPLC; Flexar FX-10 Ultra High-Performance LC 10,000 PSI) was obtained from Perkin Elmer (Waltham, MA, USA). The column (C18 EQV-8986, 75 × 3.0 mm2 id) was obtained from ACE ® (Aberdeen, UK).

4.2. Cell Treatments

All the compounds, except CORT, were dissolved in sterilized water, maximum 1% in culture medium. CORT was dissolved in methanol, 0.1% in culture medium. L-Trp, 5-HT, 5-HTP, 5-HIAA, and CORT were added to the cells in a concentration of 500 µM. H2O2 was added to the cells in a concentration of 300 µM. Only for the performance of the electrochemical method of HPLC, CORT, and H2O2 were added to the cells in concentrations ranging 100–500 µM and 50–300 µM, respectively. All the compounds were added to the cells for 48 h.

4.3. Cell Culture

SH-SY5Y cell line (American Type Culture Collection, VA, USA) was cultured in DMEM (10% FBS, 1% penicillin (1000 U/mL)/streptomycin (10 mg/mL)), and incubated at 37 °C (5% CO2). Cells were seeded at a density of 1.0 × 105 cells/mL in 96-well plates (200 µL/well), after trypsinization (0.25% trypsin-EDTA), and centrifugation (1100 rpm for SH-SY5Y, 5 min; Hettich, Tuttlingen, Germany).

4.4. Thiazolyl Blue Tetrazolium Bromide Assay

Cell viability was obtained by thiazolyl blue tetrazolium bromide (MTT) assay, after 48 h of exposure to the compounds, as previously reported [8,9]. To perform that, the culture medium was removed, and MTT (0.5 mg/mL in PBS) was added to the cells (100 µL/well), following a 3 h period of incubation at 37 °C in a light protected manner. After that, MTT was discarded and DMSO (100 µL/well) was added to the cells. Finally, absorbance values (570 nm) were obtained with the automated microplate reader (Tecan Infinite M200, Zurich, Switzerland).

4.5. Cell Morphology Assessment

The cellular morphology of SH-SY5Y cell lines was assessed by using Leica DMI6000 B Automated Microscope (Wetzlar, Germany) after all the exposure to the different treatment conditions for 48 h.

4.6. HPLC Analysis

HPLC (electrochemical method) analysis was carried out as previously described [40]. Briefly, the analysis of 5-HT content in the samples was carried out using the 3030 Reagent kit for HPLC analysis of this compound in the urine. The calibration curve was generated with concentrations between 1–1000 nM of 5-HT (y = 493146x; R² = 0.9963). The decade electrochemical detector contained a glassy carbon electrode programmed to a potential of 50 mV. Empower Pro software 3 (Waters Corporation, Milford, MA, USA) was used for controlling the produced current For uHPLC procedure, samples (20 µL, 4 °C) were subjected to the uHPLC, and the separation was carried out at a flux of 2 mL/min. Optical density of all the tested compounds was recorded at 280 nm. Quantification was performed based on standard curves for L-Trp (y = 750,542x; R² = 0.9971), 5-HTP (y = 804,860x; R² = 0.9986), 5-HT (y = 782,455x; R² = 0.9977), and 5-HIAA (y = 595,569x; R² = 0.9919). Results were analyzed on using Chromera® software, version 3.2.0, Perkin Elmer (Waltham, MA, USA).

4.7. Statistical and Data Analysis

Statistical and data analysis was performed using the software GraphPad Prism 8 (San Diego, CA, USA). Statistical comparisons were performed between vehicle and treatment groups (one-way ANOVA and Dunnett’s multiple comparisons test), statistical significance when p < 0.05. Cell viability studies results represent the mean ± SEM of 3 independent experiments. HPLC results represent the analysis of the mixture of samples of three independent experiments.

5. Conclusions

Taken together, our results highlight that different ways of stress induction lead to different responses regarding SH-SY5Y extracellular medium concentration of L-Trp, 5-HTP, 5-HT, and 5-HIAA. Indeed, the different chemical transformations that occurred during the study period did not lead to differences in cell morphology/viability between the different metabolites. We believe that, based on the opposite results on the concentration of 5-HT in the extracellular medium after exposition to both CORT and H2O2, the 5-HT pathway is the one that is most sensitive to modulating effects of the cellular environment and, therefore, presents the best applicability to be used in conditions associated with cellular stress.
Future studies exploring L-Trp metabolism with a focus on 5-HT branch are important in the context of several diseases that are extremely influenced by stress conditions, such as depressive disorders [29,41].

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijms24054389/s1.

Author Contributions

Conceptualization, N.V.; methodology A.S.C., I.S., H.R., J.C.O., F.V.-N., A.C. and N.V.; formal analysis, A.S.C. and N.V.; investigation, A.S.C., I.S., H.R., J.C.O., F.V.-N., A.C. and N.V.; resources, N.V.; writing—original draft preparation, A.S.C.; writing—review and editing, N.V.; supervision, N.V.; project administration, N.V.; funding acquisition, N.V. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financed by FEDER—Fundo Europeu de Desenvolvimento Regional— through the COMPETE 2020—Operational Programme for Competitiveness and Internationalization (POCI), Portugal 2020—and by Portuguese funds through FCT—Fundação para a Ciência e a Tecnologia—in a framework of the projects in CINTESIS, R and D Unit (reference UIDB/4255/2020), and within the scope of the project “RISE–LA/P/0053/2020. Nuno Vale thanks support from FCT and FEDER (European Union), award number IF/00092/2014/CP1255/CT0004 and CHAIR in Onco-Innovation at FMUP.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

Ana Salomé Correia thanks FCT for the PhD Grant (SFRH/BD/146093/2019). Nuno Vale thanks FCT and FEDER (European Union), award number IF/00092/2014/CP1255/CT0004, and CHAIR in Onco-Innovation from FMUP.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Summary of serotonin (5-HT)’s branch of L-tryptophan (L-Trp) biotransformation. This amino acid is (a) metabolized into 5-hydroxytryptophan (5-HTP), that is (b) converted into 5-HT, and finally (c) metabolized into 5-hydroxyindoleacetic acid (5-HIAA).
Figure 1. Summary of serotonin (5-HT)’s branch of L-tryptophan (L-Trp) biotransformation. This amino acid is (a) metabolized into 5-hydroxytryptophan (5-HTP), that is (b) converted into 5-HT, and finally (c) metabolized into 5-hydroxyindoleacetic acid (5-HIAA).
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Figure 2. Representative images (100 × total magnification) of SH-SY5Y cells after incubation with (A) vehicle (H2O 1%), (B) hydrogen peroxide (H2O2) 300 µM, (C) corticosterone (CORT) 500 µM, and the effect of (D) H2O2 50 µM–300 µM and (E) CORT 100 µM–500 µM on cellular viability. All the compounds were exposed to the cells for 48 h. Cell viability results are expressed as the percentage of the vehicle (100%). Scale bar: 50 μm.
Figure 2. Representative images (100 × total magnification) of SH-SY5Y cells after incubation with (A) vehicle (H2O 1%), (B) hydrogen peroxide (H2O2) 300 µM, (C) corticosterone (CORT) 500 µM, and the effect of (D) H2O2 50 µM–300 µM and (E) CORT 100 µM–500 µM on cellular viability. All the compounds were exposed to the cells for 48 h. Cell viability results are expressed as the percentage of the vehicle (100%). Scale bar: 50 μm.
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Figure 3. Representative images (100 × total magnification) of SH-SY5Y cells exposed to (A) L-Trp 500 µM, (B) L-Trp 500 µM + H2O2 300 µM, (C) L-Trp 500 µM + CORT 500 µM, and the effect of L-Trp 500 µM, L-Trp 500 µM + H2O2 300 µM, L-Trp 500 µM + CORT 500 µM on (D) cellular viability, and on (E) the variation of L-Trp concentration, in which the baseline represents L-Trp 500 µM. All the compounds were exposed to the cells for 48 h. Cell viability results represent the mean ± SEM of three independent assays, expressed as the percentage of the vehicle (100%). HPLC results represent the analysis of the mixture of samples from three independent experiments. Statistically significant *** p < 0.001 and **** p < 0.0001 vs. vehicle. Scale bar: 50 µm.
Figure 3. Representative images (100 × total magnification) of SH-SY5Y cells exposed to (A) L-Trp 500 µM, (B) L-Trp 500 µM + H2O2 300 µM, (C) L-Trp 500 µM + CORT 500 µM, and the effect of L-Trp 500 µM, L-Trp 500 µM + H2O2 300 µM, L-Trp 500 µM + CORT 500 µM on (D) cellular viability, and on (E) the variation of L-Trp concentration, in which the baseline represents L-Trp 500 µM. All the compounds were exposed to the cells for 48 h. Cell viability results represent the mean ± SEM of three independent assays, expressed as the percentage of the vehicle (100%). HPLC results represent the analysis of the mixture of samples from three independent experiments. Statistically significant *** p < 0.001 and **** p < 0.0001 vs. vehicle. Scale bar: 50 µm.
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Figure 4. Representative images (100× total magnification) of SH-SY5Y cells exposed to (A) 5-HTP 500 µM, (B) 5-HTP 500 µM + H2O2 300 µM, (C) 5-HTP 500 µM + CORT 500 µM, and effect of 5-HTP 500 µM, 5-HTP 500 µM + H2O2 300 µM, 5-HTP 500 µM + CORT 500 µM on (D) cellular viability and on (E) the variation of 5-HTP concentration, in which the baseline represents 5-HTP 500 μM. All the compounds were exposed to the cells for 48 h. Cell viability results represent the mean ± SEM of three independent assays, expressed as the percentage of the vehicle (100%). HPLC results represent the analysis of the mixture of samples from three independent experiments. Statistically significant * p < 0.05, *** p < 0.001 and **** p < 0.0001 vs. vehicle. Scale bar: 50 μm.
Figure 4. Representative images (100× total magnification) of SH-SY5Y cells exposed to (A) 5-HTP 500 µM, (B) 5-HTP 500 µM + H2O2 300 µM, (C) 5-HTP 500 µM + CORT 500 µM, and effect of 5-HTP 500 µM, 5-HTP 500 µM + H2O2 300 µM, 5-HTP 500 µM + CORT 500 µM on (D) cellular viability and on (E) the variation of 5-HTP concentration, in which the baseline represents 5-HTP 500 μM. All the compounds were exposed to the cells for 48 h. Cell viability results represent the mean ± SEM of three independent assays, expressed as the percentage of the vehicle (100%). HPLC results represent the analysis of the mixture of samples from three independent experiments. Statistically significant * p < 0.05, *** p < 0.001 and **** p < 0.0001 vs. vehicle. Scale bar: 50 μm.
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Figure 5. Representative images (100× total magnification) of SH-SY5Y cells exposed to (A) 5-HT 500 µM, (B) 5-HT 500 µM + H2O2 300 µM, (C) 5-HT 500 µM + CORT 500 µM, and effect of 5-HT 500 µM, 5-HT 500 µM + H2O2 300 µM, 5-HT 500 µM + CORT 500 µM on (D) cellular viability, and on (E) the variation of 5-HT concentration, in which the baseline represents 5-HT 500 µM. All the compounds were exposed to the cells for 48 h. Cell viability results represent the mean ± SEM of three independent assays, expressed as the percentage of the vehicle (100%). HPLC results represent the analysis of the mixture of samples from three independent experiments. Statistically significant ** p < 0.01 and **** p < 0.0001 vs. vehicle. Scale bar: 50 µm.
Figure 5. Representative images (100× total magnification) of SH-SY5Y cells exposed to (A) 5-HT 500 µM, (B) 5-HT 500 µM + H2O2 300 µM, (C) 5-HT 500 µM + CORT 500 µM, and effect of 5-HT 500 µM, 5-HT 500 µM + H2O2 300 µM, 5-HT 500 µM + CORT 500 µM on (D) cellular viability, and on (E) the variation of 5-HT concentration, in which the baseline represents 5-HT 500 µM. All the compounds were exposed to the cells for 48 h. Cell viability results represent the mean ± SEM of three independent assays, expressed as the percentage of the vehicle (100%). HPLC results represent the analysis of the mixture of samples from three independent experiments. Statistically significant ** p < 0.01 and **** p < 0.0001 vs. vehicle. Scale bar: 50 µm.
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Figure 6. Representative images (100 × total magnification) of SH-SY5Y cells exposed to (A) 5-HIAA 500 µM, (B) 5-HIAA 500 µM + H2O2 300 µM, (C) 5-HIAA 500 µM + CORT 500 µM, and effect of 5-HIAA 500 µM, 5-HIAA 500 µM + H2O2 300 µM, 5-HIAA 500 µM + CORT 500 µM on (D) cellular viability, and on (E) the variation of 5-HIAA concentration, in which the baseline represents 5-HIAA 500 μM. All the compounds were exposed to the cells for 48 h. Cell viability results represent the mean ± SEM of three independent assays, expressed as the percentage of the vehicle (100%). HPLC results represent the analysis of the mixture of samples from three independent experiments. Statistically significant * p < 0.05, and **** p < 0.0001 vs. vehicle. Scale bar: 50 μm.
Figure 6. Representative images (100 × total magnification) of SH-SY5Y cells exposed to (A) 5-HIAA 500 µM, (B) 5-HIAA 500 µM + H2O2 300 µM, (C) 5-HIAA 500 µM + CORT 500 µM, and effect of 5-HIAA 500 µM, 5-HIAA 500 µM + H2O2 300 µM, 5-HIAA 500 µM + CORT 500 µM on (D) cellular viability, and on (E) the variation of 5-HIAA concentration, in which the baseline represents 5-HIAA 500 μM. All the compounds were exposed to the cells for 48 h. Cell viability results represent the mean ± SEM of three independent assays, expressed as the percentage of the vehicle (100%). HPLC results represent the analysis of the mixture of samples from three independent experiments. Statistically significant * p < 0.05, and **** p < 0.0001 vs. vehicle. Scale bar: 50 μm.
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Figure 7. Concentrations of 5-HT (nM) in the extracellular medium of SH-SY5Y cells treated with (A) H2O2 50–300 µM and (B) CORT 100–500 µM, determined by HPLC (electrochemical method). The results represent the analysis of the supernatant collected from the three independent experiments.
Figure 7. Concentrations of 5-HT (nM) in the extracellular medium of SH-SY5Y cells treated with (A) H2O2 50–300 µM and (B) CORT 100–500 µM, determined by HPLC (electrochemical method). The results represent the analysis of the supernatant collected from the three independent experiments.
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Correia, A.S.; Silva, I.; Reguengo, H.; Oliveira, J.C.; Vasques-Nóvoa, F.; Cardoso, A.; Vale, N. The Effect of the Stress Induced by Hydrogen Peroxide and Corticosterone on Tryptophan Metabolism, Using Human Neuroblastoma Cell Line (SH-SY5Y). Int. J. Mol. Sci. 2023, 24, 4389. https://doi.org/10.3390/ijms24054389

AMA Style

Correia AS, Silva I, Reguengo H, Oliveira JC, Vasques-Nóvoa F, Cardoso A, Vale N. The Effect of the Stress Induced by Hydrogen Peroxide and Corticosterone on Tryptophan Metabolism, Using Human Neuroblastoma Cell Line (SH-SY5Y). International Journal of Molecular Sciences. 2023; 24(5):4389. https://doi.org/10.3390/ijms24054389

Chicago/Turabian Style

Correia, Ana Salomé, Isabel Silva, Henrique Reguengo, José Carlos Oliveira, Francisco Vasques-Nóvoa, Armando Cardoso, and Nuno Vale. 2023. "The Effect of the Stress Induced by Hydrogen Peroxide and Corticosterone on Tryptophan Metabolism, Using Human Neuroblastoma Cell Line (SH-SY5Y)" International Journal of Molecular Sciences 24, no. 5: 4389. https://doi.org/10.3390/ijms24054389

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