Dynamic Variation in Hippocampal Metabolism after Acute Stress Exposure: An In Vivo Proton Magnetic Resonance Spectroscopy Study at 9.4 T

Hwang, Yoon Ho; Lee, Min-Hee; Yun, Chang-Soo; Kim, Yong-Tae; Baek, Hyeon-Man; Han, Bong Soo; Kim, Dong Youn

doi:https://doi.org/10.1155/2021/6533727

Journal of Spectroscopy

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Abstract Introduction Materials and Methods Results Discussion Conclusions Data Availability Conflicts of Interest Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2021 | Article ID 6533727 | https://doi.org/10.1155/2021/6533727

Dynamic Variation in Hippocampal Metabolism after Acute Stress Exposure: An In Vivo Proton Magnetic Resonance Spectroscopy Study at 9.4 T

Yoon Ho Hwang,¹Min-Hee Lee,²Chang-Soo Yun,³Yong-Tae Kim,⁴Hyeon-Man Baek,⁴Bong Soo Han,³and Dong Youn Kim¹

Academic Editor: Nives Galić

Received05 Jul 2021

Revised10 Sept 2021

Accepted25 Sept 2021

Published20 Oct 2021

Abstract

An acute stress response is a complex process that activates the neuroendocrine and metabolic systems for homeostasis. A study on acute stress is important to understand how an organism adapts to stress for survival. However, most studies have focused on chronic stress, and there are few studies on acute stress. They have analyzed the metabolic alterations in the brain at a particular time after acute stress. This study explored the temporal variations of the brain metabolites in the hippocampus after acute restraint stress using proton magnetic resonance spectroscopy. All mice in the acute stress group were physically restrained for two hours in a 50 mL conical tube. A 9.4 T animal MRI and MRS scanner was used with point-resolved spectroscopy technique for data acquisition, which was repeated four times without interscan interval. Metabolites were quantified from the data using LCModel with a simulated basis set. Based on the change in concentration of metabolites, the data were statistically analyzed using two-way repeated-measures analysis of variance between groups and a support vector machine for all time points and Student’s t-test with FDR correction for each time point. The present study found that the differences between groups are significantly () presented in alanine and glutamate. The effect of time of the two metabolites significantly exists (): the first, second, and third time points in alanine and the first and second time points in glutamate. A combination of stress-specific metabolites (alanine, glutamate, N-acetyl-aspartate) that best reflect the influence of acute stress was determined using a support vector machine. These findings may indicate the importance of the timing of analysis after acute stress and provide new insights into a deeper understanding of acute stress response, including the molecular mechanism of stress-related disorders and stress resilience or vulnerability.

1. Introduction

The stress response is defined as a neurochemical process, which is an adaptive or maladaptive reaction to alterations in the external environment (e.g., stressful situations or events) that threaten the physiological homeostasis of the brain for the survival of living organisms [1–5]. External stimuli triggering the stress response are characterized as different types of stressors (physical, pharmacological, psychological, and social) [6, 7]. Depending on the stress-induced time by one or more stressors, stress is classified as acute or chronic. As most of the previous studies have focused on chronic stress [8, 9], the importance of the effects of acute stress has not emerged and there are only a few related studies [10–13].

Acute stress is based on a single stressor that generates an intense stimulus once producing negative structural and functional changes in the brain [14–18]. The influence of acute stress in the brain may result in morphological changes such as hippocampal volume loss [19], apical dendritic retraction [20], reduced activity of antioxidant enzymes [12], neurotoxicity due to the overactivation of glutamate release [21–24], and diminished cell proliferation [7, 25]. The effects of acute stress in the brain are caused by atypical physiological responses leading to stress-related disorders. These results raise the necessity of investigation into the maladaptive pathways involved in the acute stress response [5, 26, 27]. In addition, as the acute stress response is the underlying response to chronic stress as well as nature’s fundamental mechanism for survival, the study of acute stress is essential to develop a deep understanding of the harmful effects caused by chronic stress and the basal mechanism of stress-related disorders [28].

In regard to stress, the hippocampus is considered an important region in the brain regulating the activation of the hypothalamic-pituitary-adrenal axis based on stress hormones such as glucocorticoids (e.g., corticosterone or cortisol) along with the medial prefrontal cortex [4]. The region is particularly vulnerable and susceptible to acute stress, which may lead to neurogenesis inhibition, neurochemistry alterations, neuron excitability changes, and/or neuron death [16]. Previous studies reported that acute stress in a rat brain induced changes in the concentration of metabolites [29, 30]. Gandhi et al. found that there are significant metabolic alterations in the urine due to acute cold stress with a 9.4 T NMR spectrometer [29]. Shi et al. found that trimellitic anhydride decreased in the FST-1d model compared with the control based on a 14.1 T NMR spectrometer [30]. The ex vivo experiments using high-field NMR may provide more accurate and reliable information on the concentrations of metabolites in the rat brain than in vivo experiments. However, ex vivo experiments are inappropriate to apply studies that analyze the effects of acute stress on living organisms because they sacrifice animals to prepare dissected brain samples of the regions of interest. Therefore, noninvasive in vivo experiments using proton magnetic resonance spectroscopy (¹H-MRS) are needed. Recent in vivo studies have investigated the metabolic changes in the rodent brain after exposure to acute stress using ¹H-MRS [11, 31]. Kim et al. found significantly increased glutamate levels in the cerebral cortex and hippocampus of the rat brain following acute restraint stress, and glutamate levels returned to the normal state in the hippocampus but not in the cerebral cortex after a 1-h recovery period from 1-h restraint stress [11]. Gapp et al. reported that a mouse exposed to acute cold swim stress during early life stages showed reduced concentrations of N-acetyl-aspartate, glutamate, and γ-aminobutyrate in the prefrontal cortex using 14.1 T ¹H-MRS [31].

While these ¹H-MRS studies provided evidence on metabolic alterations induced by acute stress in the brain using endpoint analysis [6], these cross-sectional studies could not investigate metabolic dynamics for the response to acute stress over time. Houtepen et al. [13] reported that (1) mean glutamate and γ-aminobutyric acid levels varied over time in the control group, (2) the difference between both groups after acute stress and the difference in glutamate levels before and after acute stress in the stress group were not similar [13]. These results support that comparing both groups only at any specific time point can lead to bias and by chance in the analyzed results. Therefore, metabolic dynamics over time are important for acute stress [32]. Physiological variations induced by acute stress in the brain occur over time, including hormonal changes, classified as short-term and long-term effects of acute stress. These prolonged changes may be relevant for stress-related disorders with structural (e.g., dendritic retraction) and functional (e.g., glutamate release) consequences. This finding raises the necessity for investigating the metabolic changes of the acute stress response over time [5].

Recently, machine learning (ML) techniques have been introduced that have been used in various fields to select the metabolites that better characterize the effects of acute stress. One of the methods of ML, a support vector machine (SVM), is a supervised learning technique that divides into two different classes using a hyperplane (or decision boundary) that maximizes the margin between data in a two-dimensional or more feature space [33]. It is a powerful tool for subtle pattern recognition and classification [34]. Moreover, the SVM has the advantage of being less error data impact and less overfitting by adjusting the cost (C) parameter. This elicits that using the SVM, metabolites that best describe the effects of acute stress by better classifying both groups can be selected from time-series in vivo data.

Our primary hypothesis is that acute stress impacts the metabolic dynamics of the brain; then stress-specific changes in the concentration of metabolites occur over time. Based on ¹H-MRS data acquired over time, the present study investigates (1) which metabolites differ in metabolic dynamics between control and acute stress groups, (2) the period that accurately reflects a variation in the characteristics of the metabolites in the hippocampus after acute stress exposure, and (3) the metabolites that are most influenced by acute stress through feature selection using the SVM. To our knowledge, this is the first study to investigate a dynamic variation in the metabolites after inflicting restraint stress in the mouse brain. Furthermore, our proposed noninvasive approach could help explore the effects of acute stress on metabolites in human research.

2. Materials and Methods

2.1. Experimental Animals

Male C57BL/6N mice (ORIENT BIO Inc., South Korea) with body weight over 18 g and below 25 g at 4 weeks of age were used as experimental animals. The mice were housed three per transparent plastic cage and allowed to acclimatize for 2 weeks before the ¹H-MRS experiment to adapt to the environment and minimize the stress resulting from an unfamiliar situation. The mice had unconstrained access to water and food and were maintained under controlled temperature (21–23°C) and humidity (50–60%) with a 12-h light/12-h dark cycle (light on from 06:00 to 18:00). The mice were randomly divided into a control group (N = 12) and a stress group (N = 12). All experiments were approved by the Institutional Animal Care and Use Committee and conducted at the Lee Gil Ya Cancer and Diabetes Institute accredited by the Association for Assessment and Accreditation of Laboratory Animal Care International that uses international standards for animal care and use globally. All procedures for experiments were in compliance with the Center of Animal Care and Use in Animal research (guidelines for animal users).

2.2. Restraint Stress Protocol

As shown in Figure 1(a), based on the stress protocol reported by previous studies [35, 36], 12 mice were exposed to acute restraint stress physically for 2 hours in a transparent 50 mL conical plastic centrifuge tube (3 cm in diameter and 10 cm in length) with openings toward the body (3 mm in diameter) and mouth (5 mm in diameter) of the mice to create airflow for ventilation with background noise in an air-conditioned room for the period of restraint. The residual space in the tube was filled to create pressure and minimize mouse movement for perfect immobility. The body and head were fixed to make the mice immovable and create an inescapable space. After completing the restraint procedure, the mice were used for in vivo¹H-MRS data acquisition. The mice in the control group were not exposed to restraint stress and maintained in the cage until the initiation of the ¹H-MRS experiment.

2.3. Proton Magnetic Resonance Spectroscopy

¹H-MRS experiment was performed using ParaVision 5.0 software under Red Hat Linux based on Bruker BioSpec Avance III 94/20 USR (Bruker BioSpin MRI GmbH, Ettlingen, Germany) with a 9.4 T horizontal 200 mm bore magnet (inner diameter: 114 mm) and 660 mT/m actively shielded gradient coil at cell to in vivo imaging core-facility research center as shown in Figure 1(b). Excitation resonating at 400 MHz was conducted using a volume transmit-only resonator. A receive-only surface coil (2 × 2 array coil) was used for the reception of signals from the mouse brain.

Each experiment in both groups was conducted alternatively, three mice at a day. Excluding other processes such as brain positioning in the center of the magnet, shimming, voxel positioning, and acquisition of unsuppressed water signal, ¹H-MRS data were acquired every 34 minutes at 4 consecutive time points in both groups. Spontaneously respiring mice were anesthetized with 4.0% isoflurane at the introduction and 1.0–2.0% isoflurane during the experiment in a 1 : 2 O₂ : air mixture. The mice were placed on a flat MR bed in a prone position. The mouse brain was tightly fixed with a glass bite bar and 2 plastic ear inserts. A water-heated body-warming system was applied to the mouse to prevent the risk of hypothermia during anesthesia [37]. The whole body of the mouse was maintained at a constant temperature via a cover connected to the water-circulating equipment that set the distilled water to 38°C [38]. The rate of respiration was monitored in real time with MR-compatible instruments (SA Instruments, Inc., Stony Brook, NY, USA) to adjust anesthetic concentrations and maintain a stable condition.

To localize the desired voxel of interest (VOI), T2-weighted images were acquired using rapid acquisition with relaxation enhancement (RARE) with the following acquisition parameters: TR = 5000 ms, TE_eff = 48 ms, RARE factor = 8, NA = 1, FOV = 3 × 3 cm², slice thickness = 1 mm, matrix size = 256 × 256, 36 slices (axial = 12, sagittal = 12, coronal = 12). The VOI (1.8 × 3.4 × 1.8 mm³, 11.016 μL) was placed to include most of the hippocampus, an area related to stress through the anatomical images as shown in Figure 1(b). For uniform homogeneity of the magnetic field inside the VOI, the shim (first and second order) was adjusted automatically using a fast and automatic shimming technique by mapping along with projections. The procedure for automated shim was repeated until the linewidth of the resulting water signal was below 14 Hz. A point-resolved spectroscopy (PRESS) was used for the acquisition of ¹H-MRS data from a single voxel with the following acquisition parameters: TR = 4000 ms, TE = 10 ms, NA = 512, complex points = 4096, spectral width = 5000 Hz, including that the bandwidth of the excitation/refocusing RF pulse is 5600 Hz to minimize the chemical shift displacement error in the higher magnetic field. The predominant water signal inside the VOI was suppressed by variable power RF pulses with optimized relation delays to detect metabolite signals [11, 39]. An outer volume suppression scheme was performed for the minimization of artifacts caused by the unwanted signals outside the VOI. The eight averaged unsuppressed water signals were acquired in the same manner and VOI as ¹H-MRS data [40]. Additionally, the compensation of eddy current [41] due to strong gradient fields and phase correction was applied during data acquisition [42] for distortion resulting from combining the RF signals with a different phase in the surface coil. When 512 scans were obtained and one averaged raw datum was computed with one, a procedure for frequency drift like the alignment of each scan was performed due to the long acquisition time.

2.4. Metabolite Quantification

As shown in Figure 1(c), the ¹H-MRS data corrected were analyzed with the linear combination analysis method (LCModel) [43, 44] to calculate the concentration of brain metabolites by fitting the experimentally obtained ¹H-MRS data based on eight averaged unsuppressed water signal and a simulated basis set provided by the LCModel. The simulated macromolecule signal and the following metabolites were included in the simulated basis set: alanine (Ala), aspartate (Asp), creatine (Cr), γ-aminobutyric acid (GABA), glucose (Glc), glutamine (Gln), glutamate (Glu), glycerophosphorylcholine (GPC), glutathione (GSH), myo-inositol (m-Ins), lactate (Lac), phosphorylcholine (PCh), phosphocreatine (PCr), scyllo-inositol (s-Ins), N-acetylaspartate (NAA), N-acetylaspartylglutamate (NAAG), and taurine (Tau). Among the basis spectra in the simulated basis set, s-Ins was excluded from the process of quantification using the LCModel because it had a smaller concentration (<1 mM) in the mouse brain and nothing to do with the acute stress [45]. Also, ascorbate (Asc), phosphorylethanolamine (PE), and glycine (Gly) were excluded from the analysis based on the LCModel because these metabolites were not related to acute stress and it was difficult to detect for the following reasons: (1) smaller concentration (Asc: about 1 mM [46]; PE: 1∼2 mM; Gly: <1 mM [46, 47]), (2) overlap with other metabolites (Asc: Glu, Gln, and GSH [48]; PE: other phospholipids with similar structures; Gly: m-Ins [47]), and (3) multiplicity (Asc: multiplet at 3.73 and 4.01 ppm [48]; PE: multiplet at 3.22 and 3.98 ppm [47]). Using the LCModel, the concentrations of metabolites were calculated from the ¹H-MRS data using a prior knowledge about the chemical shift of each metabolite (e.g., simulated basis set) and the unsuppressed water signal for water scaling. When the metabolites were quantified by the LCModel, the unsuppressed water signal was used as an internal reference and its attenuation by relaxation and other effects was applied by multiplying the gain correction factor (ATTH2O: 0.01094). The ¹H-MRS data were analyzed at a range between 0.2 ppm and 4.3 ppm for the most discriminating metabolites. Spectral fitting was evaluated by the signal-to-noise ratio (SNR) and Cramer–Rao lower bound (CRLB). CRLB was the estimated standard error in percent of the estimated concentration of metabolites through the spectral registration by the LCModel. If the SNR was below 10 [11], and the CRLB for metabolites and time points was over 20% as recommended by the LCModel [49], the ¹H-MRS data were excluded from the statistical analysis to minimize bias in the results of inaccurate quantification.

2.5. Feature Selection

SVM, one of the machine learning algorithms, is a powerful classifier that separates two distinguishable classes based on the support vectors and the optimal hyperplane divided with the maximum margin [50]. The SVM with a linear kernel was used to select the features that best explain the effect of acute stress by dividing the control group and stress group. Each of the metabolites quantified through the LCModel was considered one feature with each dimension and independent variable; the area under the concentration curve (AUC) of consecutive four time points for each metabolite was calculated with numerical integration via the trapezoidal method. The optimal number of features that best differentiated the stress group from the control group was determined based on the recursive feature elimination (RFE) with cross-validation using the linear SVM. To select the features corresponding to the optimum number, the shuffled stratified 4-fold cross-validation on the RFE was performed based on the linear SVM. It provided the information on the ranking of features, and the features were selected as the optimal number in the order of highest ranking. Through 100 iterations of this process, the feature importance was determined by calculating the number of times features were selected, and then the features as the optimum number were chosen in the order of high importance.

2.6. Statistical Analysis

All statistical analyses were performed with IBM SPSS Statistics 24 (IBM Corp., Armonk, NY, USA) except for the SVM using scikit learn module [51] in Python software, version 3.6.10 (Python Software Foundation, Wilmington, DE, USA). The concentration of brain metabolites are represented as mean ± standard deviation. Two-way repeated-measures ANOVA, one of the statistical methods for analyzing time-series data, was performed by comparing the time-dependent change in the concentrations of metabolites between control and stress groups to identify the metabolites that best reflect the acute stress effect. When there were metabolites with statistically significant () differences in the metabolic dynamics between both groups or significant () interactions between time and group, Student’s t-test for each time point about the metabolites was performed to determine the time point that accurately reflects the acute stress response. False discovery rate (FDR) correction was performed to avoid the multiple comparisons problem of both groups over time.

3. Results

To investigate the temporal effects of acute stress in the mouse hippocampus from a metabolic perspective, all mice in the stress group were under restraint stress for two hours. To objectively evaluate the influence of acute stress, all conditions except for the stress remained the same in both groups. As shown in Figure 2, the metabolites were quantified from ¹H-MRS data of both groups acquired in four consecutive time points (0.8 h: the first time point, 1.6 h: the second time point, 2.4 h: the third time point, 3.2 h: the fourth time point). Among the fifteen metabolites quantified except for Lac (CRLB: 999%), four metabolites were excluded from the statistical analysis based on the comparison of metabolite concentrations in both groups by using all mouse and time points because they did not meet the averaged CRLB criteria: Asp (166%), Glc (144%), GPC (88%), and NAAG (279%).

(a)

(b)

As shown in Table 1, a total of eleven metabolites were used for the statistical analysis between both groups. Before the analysis, Mauchly’s test of sphericity was performed for the time points (within-subject effect), and if the sphericity was violated, the Greenhouse–Geisser and Huynh–Feldt correction were executed using Epsilon. A two-way repeated-measures ANOVA demonstrated a significant difference () in the concentrations of Glu and Ala. The concentrations of Glu and Ala in the stress group were higher than those in the control group at all time points. The effect of time, which is a repetition factor, was statistically significant in most metabolites except for the following metabolites: PCh, Tau, tCr, and tNAA. The interactions between time and group significantly () existed only in Ala, but other metabolites did not.

To make multiple comparisons based on each time point between both groups for Ala and Glu, Student’s t-test and FDR correction [52, 53] were performed for each time point including NAA and Gln associated with stress: reduced apical dendrites (NAA) [5, 20] and glutamate-glutamine (Glu-Gln) cycle (Gln) [54]. Figure 3 illustrates the change in concentration over time for each of the four metabolites. First, Ala was represented in order of time as shown in Figure 3(a): 0.8 h (adjusted ), 1.6 h (adjusted ), 2.4 h (adjusted ), and 3.2 h (adjusted ); second, Glu in Figure 3(b): 0.8 h (adjusted ), 1.6 h (adjusted ), 2.4 h (adjusted ), and 3.2 h (adjusted ); third, NAA in Figure 3(c): 0.8 h (adjusted ), 1.6 h (adjusted ), 2.4 h (adjusted ), and 3.2 h (adjusted ); and finally, Gln in Figure 3(d): 0.8 h (adjusted ), 1.6 h (adjusted ), 2.4 h (adjusted ), and 3.2 h (adjusted ).

(a)

(b)

(c)

(d)

Figure 4 elucidates the optimal number of features, feature importance, and decision boundary in two- and three-dimensional space. Based on the RFE and the cross-validation score that was considered the ratio of correct classification from the linear SVM using repeated stratified 4-fold cross-validation (n = 100), the optimal number of features that best explain the effects of acute stress while classifying both groups was three as in Figure 4(a). To select three features among the eleven features, a stratified 4-fold cross-validation that randomly shuffled the data into 3 training sets and 1 test set was used to train the linear SVM and three features with the RFE were determined from the trained linear SVM. Through 100 iterations of this process, the feature importance (n_total = 300), which quantified the influence of each feature to indicate its importance in best distinguishing between both groups, was calculated and three features were selected in order of high ranking based on feature importance as follows: Ala = 30% (n_selected = 89), Glu = 18% (n_selected = 54), and NAA = 17% (n_selected = 51). The feature importance as in Figure 4(b) was indicated by the number of times, and the percentage above the rectangular bar for each feature was the ratio of the number of times to the total times. Figure 4(c) shows the decision boundary that best classified both groups. This was a three-dimensional analysis using Ala, Glu, and NAA identified by the linear SVM.

(a)

(b)

(c)

4. Discussion

The present study revealed that acute restraint stress significantly had a time-based effect on the levels of metabolites in the hippocampus of a mouse. There have been few studies on acute stress over the past decades [10–12, 55, 56] because chronic stress linked to neurological or physiological changes due to an abnormal regulation resulting from a multitude of adaptations to the stress response of the brain has been the focus of interest in stress studies [57, 58]. However, there have been differences in responses to chronic and acute stress [59], and hence, the necessity of studies on acute stress has recently emerged [5].

To our knowledge, the current study using ¹H-MRS was the first attempt to analyze the effect over time on acute restraint stress with the SVM technique providing the following information: (1) acute restraint stress was associated with neurotransmitter transmission through tripartite synapses [54] based on the changes in the concentrations of metabolites including Ala and Glu along with four consecutive time points; (2) the time points that best represented the effect of acute restraint stress were identified; and (3) the three metabolites (Ala, Glu, NAA) were used as an acute stress-specific biomarker, most affected by and vulnerable to acute restraint stress.

Based on the significant difference between both groups using the two-way repeated-measures ANOVA, Ala and Glu are selected for metabolites associated with acute restraint stress. Acute restraint stress is a single extreme stressor, and the acute stress response resulting from the stressor is an immediate neurochemical reaction to adapt for survival [7]. Acute restraint stress activates the hypothalamic-pituitary-adrenal axis. The hypothalamus releases the corticotropin-releasing hormone (CRH). CRH stimulates the pituitary secretion of adrenocorticotropic hormone (ACTH), which activates the release of glucocorticoids such as corticosterone (CORT) from the adrenal glands [60–62]. CORT enters the hippocampus via the bloodstream and combines with the glucocorticoid receptors to release an excitatory neurotransmitter, Glu, from the presynaptic membrane of the neuron [63]. Although Glu has been implicated in stress, the role of Ala in the stress response is unclear. The physiological characteristics of Ala associated with stress suggest that it may act as a regulator of the acute stress response [64]. First, L-alanine is mediated via the glycine receptor and glycine is considered an inhibitory neurotransmitter that inhibits the sensitivity of the neurons in the brain region with the highest CRH concentration. Second, L-alanine produces β-alanine, considered to have an antistress effect, as a by-product of the reaction to convert to pyruvate. β-alanine increases the amount of carnosine that enhances the resilience to stress and regulates the stress response in the mouse hypothalamus [55, 65]. Finally, using alanine transaminase and ammonium ions from α-ketoglutarate, L-alanine provides pyruvate and Glu through the Glu-Gln cycling during pyruvate conversion, and pyruvate is converted into glucose [66, 67]. The metabolism involved in converting L-alanine to glucose through pyruvate may be responsible for the sedative effects of L-alanine [64, 68]. Based on the above evidence, acute stress can increase the concentrations of Ala and Glu. This finding is consistent with the results of the present study, which show higher concentrations of Ala and Glu in the stress group than in the control group.

In the control group, the concentration of Glu decreases over time, the one of Ala shows a trend of decreasing and then recovering, and the one of Gln shows a constant trend. The brain is trying to reduce the Glu in the extracellular space (ECS) such as synaptic clefts as much as possible to the normal state [13, 69]. Conversely, the concentrations of Ala and Glu decrease over time in the stress group and the one of Gln increases over time. As a result of acute stress, more glutamate is produced and a pattern that decreases with time is like the one of the control group due to trying to reduce it as much as possible. Glu-Gln cycling in the hippocampus of the mouse brain can be described as the transport of Glu acting as the excitatory neurotransmitter and Gln forming through the amidation of glutamate in the tripartite synapses [54, 70–72]. Thus, Gln production and Glu decomposition occur in astrocytes, and the opposite effects occur in neurons via Glu-Gln cycling [67]. The tripartite synapses consist of presynaptic and postsynaptic neurons and astrocytes. Stress stimulates the presynaptic neuron to release Glu into the ECS. Subsequently, Glu is transported via glutamate transporter-1 (GLT-1) to neighboring astrocytes as a glial cell type adjacent to the neuron, where it is amidated to Gln using ammonium ions and converted into a nontoxic neutral amino acid. Elimination of Glu controls its ECS concentration, enables the maintenance of homeostasis in the tripartite synapses, and prevents excitotoxicity resulting from Glu accumulation in the ECS [54, 73]. Impaired astrocyte and GLT-1 function can produce symptoms of neurodegenerative diseases and mental disorders such as depression [54, 74–76]. Thus, the opposite effects of Glu and Gln over time can be attributed to the Glu-Gln cycle that is responsible for Glu removal and Glu synthesis in the ECS following acute stress. As the Ala cycle is associated with the Glu-Gln cycle [77], Ala may represent the same results as Glu. The continuous decrease in the concentration of Ala and Glu over time following acute stress can be explained as follows: (1) the estimate of astrocyte-to-neuron ratio in the hippocampus is 0.68 [78], and therefore, several hippocampal astrocytes decompose Ala into pyruvate and covert Glu to Gln compared to synthesis of Gln via Glu in neurons [67]; (2) the physiological responses during acute stress increase the energy demands for various neural activities, such as glutamatergic neurotransmission, including Glu-Gln cycling. The energy required for Glu cycling in Glu-Gln cycling between astrocytes and neurons can be estimated as three ATP molecules per glutamate molecule, approximately [63, 79, 80]. Thus, lactate dehydrogenase converts the pyruvate caused by Ala to Lac, which is used as a material for energy metabolism in astrocytes [63, 67, 81].

Although there is no statistically significant difference, Gln and NAA related to acute stress are added. Gln is directly related through the Glu-Gln cycle and NAA is associated with the effects of acute stress such as reduced neurons based on recent studies [5, 20, 27]. Comparing the concentrations of the above four metabolites between both groups at each time point, Ala differs in the first, second, and third time points, and Glu differs in the first time point after FDR correction, while NAA and Gln do not differ at every point in time. After acute stress is induced, Ala is found to have a time-dependent effect on acute stress for up to an hour and a half and Glu for half an hour. This observation demonstrates that the acute stress response and its effect varies over time, which can overcome the limitation of the existing end-point analysis methods due to several adaptive changes occurring during acute stress responses in many animal studies [10, 11, 13], and provides a deep understanding of the stress response for important time points and related metabolism with time after acute stress. Moreover, recent studies have shown that the effects of acute stress over time can be divided as short-term and long-term effects, necessitating a consideration of the stress response itself [5, 58, 82]. The time-lasting effects can cause morphological changes such as remodeling and atrophy of apical dendrites in the hippocampus [4, 18, 83–86]. An impaired physiological and functional response to stress may lead to the development of stress-related disorders in the brain [20]. These time-related short-term and long-term effects provide an understanding of acute stress response mechanisms in the brain from the metabolic viewpoint [5, 28, 87]. This observation may help us to identify turning points (recovery via adaption) [5, 58] and sensitivity (vulnerable vs. resilient) [88, 89] for stress response by evaluating the time-based effects of acute stress and monitoring maladaptive acute stress responses that may induce stress-related brain disorders.

Because of the small sample size, the AUC is used for the selection of features basing on the linear SVM to reduce the bias such as the difference between animals rather than using absolute concentrations at four time points. The AUC of each metabolite is calculated through the integration based on the trapezoidal method under the concentration curve of four time points, and it reflects the change over time and is similar to the averaged concentration of all time points. Using the cross-validation and RFE of the linear SVM based on the AUC in each feature as a metabolite, the three features (Ala, Glu, and NAA) are selected in the order of high importance in Figure 4(b). This indicates that the three metabolites as stress-specific metabolites are important for acute stress response and best represent the temporal effects of acute stress. Using the RFE and cross-validation with the linear SVM rather than the two-way repeated-measures ANOVA and Student’s t-test adds one additional metabolite (NAA) that differentiates the effects of acute stress. Based on the recent studies [5, 27], NAA is demonstrated to be a metabolite affecting the effects of acute stress as well as the third most important one as shown in Figure 4(b), although there is no statistically significant difference. The decision boundary that best classifies between both groups using three metabolites, one metabolite is one dimension, is shown in Figure 4(c). This can be obtained from a different perspective than the information obtained by comparing and analyzing the concentration itself and can be used as a biological indicator or stress-specific biomarker to characterize the effect of acute stress in the future.

There are a few limitations to the present study. First, the simulated lipid and macromolecule is used because it cannot be acquired under the same conditions as before due to breakdowns, repairs, and upgrades of the MRI machine. This indicates that the concentration of metabolites can be under- and overquantified rather than precisely quantified. Second, the sample size is too small, which may have resulted in bias due to various reasons, including differences between animals. Third, the time resolution is low. The current study takes 30 minutes to acquire a single point of time. As there is a 30-minute interval for each time point, we cannot evaluate the physiological responses occurring within the interval from a metabolic point of view. Fourth, the experimental animals are anesthetized for a prolonged period to acquire ¹H-MRS data. Prolonged administration of isoflurane to obtain all time points can influence several metabolites. Finally, the total acquisition time may have been short for analyzing the long-term effects of acute stress, which can only be assessed in part in the overall response. Despite these limitations, the current study can provide useful information such as stress-specific or stress-related metabolites and important time points after acute stress on the temporal effects of acute stress.

5. Conclusions

This study analyzes the effect of acute restraint stress on the metabolite levels in the mouse hippocampus over time. We found the following results: (1) there was a significant difference in Ala and Glu levels due to acute restraint stress; (2) among the four time points, the statistical difference between both groups occurred in the preceding three time points in Ala and the first time point in Glu after acute restraint stress; and (3) Ala, Glu, and NAA, which best classified the two groups, were selected with SVM as an optimal combination of metabolites. Our findings indicate the effects of acute stress over time, providing information on the timing of analysis after acute stress. Furthermore, the stress-specific biomarker, a combination of three metabolites (Ala, Glu, and NAA), best explains the influence of acute stress. Moreover, this study may provide a better understanding of the acute stress response mechanisms and present new insights into whether laboratory animals such as rodents are vulnerable or resilient to acute stress from a metabolic point of view.

Data Availability

The analyzed data for the metabolites used to support the findings of this study are available from the corresponding author upon reasonable request.

Conflicts of Interest

The authors declare no conflicts of interest.

Acknowledgments

This research was supported by the Brain Research Program of the National Research Foundation (NRF) funded by the Korean Government (MSIT) (2016M3C7A1905385).

Supplementary Materials

Figure S1: averaged proton MRS raw data, LCModel fit, and quantified metabolites at the first time point. Figure S2: averaged proton MRS raw data, LCModel fit, and quantified metabolites at the second time point. Figure S3: averaged proton MRS raw data, LCModel fit, and quantified metabolites at the third time point. Figure S4: averaged proton MRS raw data, LCModel fit, and quantified metabolites at the fourth time point. Table S1: statistical comparison (Wilcoxon rank sum test with FDR correction) by group of baselines per ppm (). (Supplementary Materials)

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