Role of the indoleamine-2,3-dioxygenase/kynurenine pathway of tryptophan metabolism in behavioral alterations in a hepatic encephalopathy rat model
- Xi Jiang†1, 3Email author,
- Lexing Xu†1,
- Lin Tang†1,
- Fuhe Liu1,
- Ziwei Chen1,
- Jiajia Zhang1,
- Lei Chen1,
- Cong Pang2Email author and
- Xuefeng Yu1Email author
© The Author(s). 2018
Received: 23 June 2017
Accepted: 12 December 2017
Published: 4 January 2018
This study aims to explore the role of indoleamine-2,3-dioxygenase (IDO)/kynurenine (KYN) pathway of tryptophan (TRY) metabolism in behavioral alterations observed in hepatic encephalopathy (HE) rats.
Expression levels of proinflammatory cytokines were tested by QT-PCR and ELISA, levels of IDOs were tested by QT-PCR and Western blot, and levels of 5-hydroxytryptamine (5-HT), KYN, TRY, 3-hydroxykynurenine (3-HK), and kynurenic acid (KA) in different brain regions were estimated using HPLC. Effects of the IDO direct inhibitor 1-methyl-l-tryptophan (1-MT) on cognitive, anxiety, and depressive-like behavior were evaluated in bile duct ligation (BDL) rats.
Increased serum TNF-α, IL-1β, and IL-6 levels were shown in rats 7 days after BDL, and these increases were observed earlier than those in the brain, indicating peripheral immune activation may result in central upregulation of proinflammatory cytokines. Moreover, BDL rats showed a progressive decline in memory formation, as well as anxiety and depressive-like behavior. Further study revealed that IDO expression increased after BDL, accompanied by a decrease of 5-HT and an increase of KYN, as well as abnormal expression of 3-HK and KA. The above results affected by BDL surgery were reversed by IDO inhibitor 1-MT treatment.
Taken together, these findings indicate that (1) behavioral impairment in BDL rats is correlated with proinflammatory cytokines; (2) TRY pathway of KYN metabolism, activated by inflammation, may play an important role in HE development; and (3) 1-MT may serve as a therapeutic agent for HE.
Hepatic encephalopathy (HE) is a neuropsychiatric abnormality in patients with acute or chronic liver disease. It is characterized by personality mood change, cognitive impairment, decreased consciousness, and coma [1, 2]. The development of HE negatively impacts patient survival, and the survival reports of patients with HE showed a survival rate of 42% after 1 year and 23% after 3 years [3, 4]. Such high mortality in HE patients is due to the lack of effective treatment method in clinic. Therefore, it is urgent to identify potential therapeutic target for HE.
Neurological alteration in HE was affected by both hyperammonemia and inflammation [5, 6]. The serum and brain levels of proinflammatory cytokines, such as IL-1β, IL-6, and TNF-α, are higher in HE patients than those in patients only suffer from liver disease [6, 7]. Hyperammonemia and inflammation act synergistically to induce depression, anxiety, and cognitive impairment, as shown in the research analyzing neurological impairment in HE patients with different degrees of inflammation and hyperammonemia . Furthermore, it was found that the inflammation induced by HE is most obvious in the hippocampus and cerebral cortex, two important brain regions regulating executive functioning, working memory, and motor planning [9–11].
Recently, kynurenine (KYN) pathway, which regulates tryptophan (TRY) metabolism and the serotonergic system, was hypothesized to be important in mediating the effects of proinflammatory cytokines on the brain [12–14]. Normally, TRY is metabolized to KYN by indoleamine-2,3-dioxygenase (IDO)1, IDO-like enzyme, IDO2, and tryptophan-2,3-dioxygenase (TDO), then KYN is metabolized to kynurenic acid (KA, Fig. 11), an N-methyl-d-aspartate receptor (NMDAR) antagonist [15, 16]. TRY also can be metabolized to serotonin or 5-hydroxytryptamine (5-HT), which is further broken down by monoamine oxidase (MAO) to 5-hydroxyindoleacetic acid (5-HIAA). However, proinflammatory cytokines upregulate the expression of IDO with inflammation status, resulting in the activation of another metabolic pathway of KYN. In this circumstance, KYN is more likely to be metabolized to quinolinic acid (QA), a neurotoxic metabolite [17, 18]. Moreover, activation of IDO shifts TRY metabolism from serotonin synthesis to KYN formation, inducing an imbalance of the serotonergic system . This disorder of KYN pathway is hypothesized to underlie inflammation-associated depression and anxiety behaviors . Previous studies have proved that activation of IDO and high QA expression were found in an animal model of depression, and treatment with an IDO inhibitor prevented the development of inflammation-induced depressive-like behaviors in rodents [21–23]. High levels of QA were also observed in the brain and serum of HE animal model by Basile et al. .
Although inflammation-induced changes in KYN metabolism have been largely studied in depression and anxiety, pathogenesis of HE regarding the KYN pathway of TRY metabolism was never investigated. Therefore, the present study aims to assess whether inflammation-induced changes of KYN pathway contribute to depressive-like symptoms, anxiety-like symptoms, and cognitive impairment in rats with HE to seek possible therapeutic target for HE.
Male Wistar rats (220–240 g) were obtained from the Animal Center of Shanghai Branch, Chinese Academy of Sciences. Upon arrival, the rats were housed six per cage (54 × 39.5 × 20 cm) and acclimatized to a colony room with controlled ambient temperature (22 ± 1 °C), humidity (50 ± 10%), and a 12-h natural light/dark cycle. They were acclimatized to the local vivarium for a week prior to experiment. All the procedures were approved by the Wenzhou Medical University Committee on Animal Care and Use and were conducted in accordance with the guidelines for humane use and care of laboratory animals. The experiments were designed for a duration of 4 weeks, and rats were randomly segregated into five groups (0, 7, 14, 21, and 28 days). Each group contains five subgroups (n = 16 in each subgroup): sham (rats received identical laparotomy without bile duct ligation (BDL), used as control), BDL (rats underwent BDL surgery, model set), and BDL + 1-methyl-l-tryptophan (1-MT) (dose in 1, 3, and 9 mg/kg) groups. In this study, some rats died during the surgical process; a total of 450 rats were used to ensure that each subgroup contains at least 16 rats in data analysis.
Animals were anesthetized by intraperitoneal (i.p.) injection of mixed solution of ketamine hydrochloride (50 mg/kg) plus xylazine (5 mg/kg). Ketamine hydrochloride and xylazine powder were firstly dissolved in alkaline water (vehicle) (pH 11.0) to prepare 2.5 and 1.25 mg/ml solutions, respectively. Proper volume of each solution was extracted according to the exact body weight of each rat and then mixed with another solution before injection. The surgical procedure was performed aseptically according to the study reported by Kountouras (1984).  The sham operation consisted of laparotomy and bile duct identification and manipulation without ligation. For rats in the BDL group, the main bile duct was first ligated using two ligatures approximately 0.5 cm apart and then transected at the midpoint between the two ligatures. Immediately after the operation, each animal was placed alone in a cage for 4 h to avoid wound dehiscence and then moved to its original cage. Operative mortality was less than 5%.
Sucrose preference test
The sucrose preference test (SPT) was carried out as previously described . Before the test, rats were exposed to both test solution (1% sucrose) and tap water for a period of 24 h. During the test, sucrose preference was evaluated for 1 h by utilizing two bottles of 1% sucrose and tap water. The sucrose preference was calculated as the ratio of consumed sucrose solution to the consumed total amount of liquid.
Forced swimming test
The forced swimming test (FST) has been widely used to identify depressive-like behavior in animals [27, 28]. Briefly, rats firstly underwent a swimming stress session for 15 min (pre-test) in a glass cylinder (height 40 cm; diameter 18 cm; containing 23 cm of water at 24 ± 1 °C). Twenty-four hours later, the rats were placed in the cylinder again for 5 min (test session). The duration that rats remained immobile during a 5-min observation period was recorded. A rat was considered to be immobile when it ceased struggling and remained floating motionless in the water, or made only small movements necessarily to keep its head above the water.
The marble-burying test was carried out as previously described . In brief, each rat was placed individually in a polypropylene cage (40 × 24 × 20 cm) containing nine clean glass marbles (diameter 2.3 cm), which were evenly spaced on sawdust of 5 cm deep. Ten minutes later, rats were removed, and the number of marbles at least one half buried in the sawdust was recorded.
Elevated plus maze test
The elevated plus maze test was carried out as previously described . In brief, the rat was placed on the apparatus of an elevated platform, which consists of two open arms, two closed arms, and a central platform. At the beginning of the test, the rat was located on the central platform facing open arm. The number of entries and the total time spent in the closed and open arms, respectively, were quantified during a 10-min period using video tracking software (JZZ98; Institute of Materia Medica, Chinese Academy of Medical Sciences, China).
Morris water maze test
The Morris water maze test was carried out as previously described . The apparatus contains a circular plastic pool (diameter 140 cm; high 60 cm) located in a well-illuminated room with external cues visible from the inside of the pool, which was filled with opaque water (21 ± 1 °C). A hidden circular platform was submerged 2 cm under the water in one of four quadrants.
The acquisition trials (training to escape to the hidden platform) were carried out for six blocks consisting of three trials separated by 20-min inter-block intervals during which the platform remained in the same location relative to the distal cues in the room. On each trial, the rats were placed in the water at different start locations (E, S, W, and N), which were equally spaced from each other and offset from the goal location by 45°. One hour following the sixth block, the hidden platform was removed and the rats were scored during a 60-s probe trial for latency to reach, and crossings over, the previous platform location (memory recall). Another probe trial was run 24 h after training to assess consolidation and retrieval of memory. The escape latency and the number of crossing target quadrant were recorded 0, 7, 14, 21, and 28 days after BDL surgery using video tracking software (JZZ98; Institute of Materia Medica, Chinese Academy of Medical Sciences, China).
The locomotor activity was monitored using an actophotometer . The rat was placed in a square chamber (40 × 40 × 40 cm) which is connected to photoelectric cells with light beams passing through the chamber for 10 min. During this period, the number of light beam breaks was recorded.
Liver function test
Blood samples were taken from the orbital sinus of animals in each group (7, 14, 21, and 28 days) under light ether anesthesia. Blood was collected and kept for 1 h at room temperature for clotting. Serum was separated by centrifuging the blood sample at 3000 rpm for 20 min. The biochemical parameters, serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), ammonia, bilirubin, and total protein content in the serum of each rat, were evaluated using enzyme-linked immunosorbent assay according to the kit protocols (Nanjing Jiancheng Bioengineering Institute, Nanjing, China).
Brain levels of KYN and TRP were determined as previously described . Hippocampus and cerebral cortex tissues of each animal were weighed respectively, and then each tissue sample was mechanically homogenized in 0.1 N HClO4 + 25 μM ascorbate (50 μL lysate was added to every 10 mg tissue) using an ultrasonic tissue disruptor. Supernatants were extracted and loaded into a Costar Spin-X centrifuge tube filter (0.22 μM) and centrifuged at 12,000 rpm for 5 min. KYN and TRP were determined by HPLC. Mobile phase (pH = 4.6) consists of 75 mM NaH2PO4, 25 μM EDTA (disodium salt), and 100 μL/L triethylamine diluted in acetonitrile/water (6:94 v/v) solution.
The contents of 5-HT, 5-HIAA, 3-hydroxykynurenine (3-HK), QA, and KA in samples were analyzed by HPLC. Frozen brain tissue samples (cerebral cortex and hippocampus) of each animal were homogenized by ultrasonication in 200 μL of 0.4 M perchloric acid (50 μL lysate was added to every 10 mg tissue) and then centrifuged at 12,000 rpm (4 °C) for 20 min. An aliquot of 160 μL supernatant was added to 80 μL solution containing 0.2 M potassium citrate, 0.3 M dipotassium hydrogen phosphate, and 0.2 M EDTA and then centrifuged at 12,000 rpm for 20 min. The mobile phase (pH = 3.0) consists of 75 mM NaH2PO4, 25 μM EDTA, 0.45 mM octanesulfonic acid, and 100 μL/L triethylamine diluted in acetonitrile/water (6:94 v/v) solution.
Quantitative real-time RT-PCR
IL-1β, IL-6, and TNF-α expression levels in the hippocampus, cerebral cortex, hypothalamus, and striatum, and IDO expression in the hippocampus and cerebral cortex of each rat were measured by QT-PCR. Total cellular RNA was isolated using TRIzol reagent (Invitrogen) according to the manufacturer’s protocol, and RNA (1 mg) was reverse transcribed using an MJ Mini™ Gradient Thermal Cycler (Bio-Rad, Hercules CA, USA). RNA concentration was determined at 260 nm using a spectrophotometer (Bio-Rad Labs). The PCR reaction was performed using an iCycler Real-Time PCR machine (Bio-Rad, Hercules CA, USA). Each sample was added with SYBR Green (iQ SYBR Green Supermix reagent, Bio-Rad) at a concentration of 50 nmol/L. The primer sequences were as follows: IL-1β (forward: 5′-TGG ACT TCG CAG CAC AAA ATG-3′; reverse: 5′-GTT CAC TTC ACG CTC TTG GAT-3′), IL-6 (forward: 5′-CCA GAA ACC GCT ATG AAG TTC CT-3′; reverse: 5′-CAC CAG CAT CAG TCC CAA GA-3′), TNF-α (forward: 5′-GCT GGA TCT TCA AAG TCG GGT GTA-3′; reverse: 5′-TGT GAG TCT CAG CAC ACT TCC ATC-3′), IDO (forward: 5′-AGA AGT GGG CTT TGC TCT GC-3′; reverse: 5′-TGG CAA GAC CTT ACG GAC ATC TC-3′), IDO2 (forward: 5′-AAG CTT ATG GAG CCT CAA AGT CAG AGC-3′; reverse: 5′-CTC GAG CTA AGC ACC AGG ACA CAG G-3′), TDO (forward: 5′-TGG GAA CTA GAT TCT GTT CG-3′; reverse: 5′-TCG CTG CTG AAG TAA GAG CT-3′), and β-actin (forward: 5′-TGG AAT CCT GTG GCATCC ATG AAA C-3′; reverse: 5′-AA AAC GCA GCT CAG TAA CAGTCC G-3′). Amplification was performed by initial denaturation at 95 °C for 10 min, followed by 40 cycles at 95 °C for 10 s, 58 °C for 30 s, and 72 °C for 50 s. At the end of the PCR reaction, a melting curve was obtained by holding at 95 °C for 15 s, cooling to 60 °C for 1 min, and then heating slowly at 0.5 °C/s to 95 °C. Melt curve analysis and gel electrophoresis were then conducted to verify the specificity and purity of the PCR products. All the data were normalized to β-actin.
Western blot analysis
Protein levels of IDO in the hippocampus and cerebral cortex of each rat were measured by Western blot. The tissue samples were firstly weighed and then added with RIPA lysis buffer (Upstate Chemicon, Temecula, CA, USA) (50 μL lysate was added to every 10 mg tissue) and centrifuged at 13,000 rpm for 30 min at 4 °C. Total protein concentrations of the supernatants were assessed using a BCA assay kit (Thermo Scientific, Rockford, IL, USA). Proteins in lysate (40 μg per lane) were resolved using 10% sodium dodecyl sulfate polyacrylamide gel and transferred onto polyvinylidene difluoride membranes. Blots were then incubated in blocking buffer for 2 h at room temperature, washed in Tris-buffered saline with 0.1% Tween 20 (TBST), and incubated with the appropriate primary antibodies over night at 4 °C (anti-IDO, 1:1000, ab106134; anti-TDO2, 1:1000, ab123403; anti-β-actin, 1:1000, ab8227). After washing with TBST, the blots were incubated with the secondary antibodies (1:10,000) for 1 h at room temperature. The detection quantification of specific bands was carried out using a fluorescence scanner (Odyssey Infrared Imaging System, LI-COR Biotechnology, South San Francisco, CA, USA) at 700 and 800 nm wavelengths.
Protein levels of IL-1β, IL-6, and TNF-α in the hippocampus, cerebral cortex, hypothalamus, striatum, and serum were measured by an ELISA kit (R&D Systems China Co., Ltd.). Briefly, serial dilutions of protein standards and samples of each rat were added to ELISA plates, followed by biotinylated anti-IL-1β, IL-6, and TNF-α antibody addition. Then, the prepared solution of avidin, horseradish peroxidase-conjugated complex was added after rinsing with wash buffer. The reaction was stopped by the stopping solution, and absorbance was read at 450 nm [33, 34].
Results were presented as mean ± SEM. All data were statistically analyzed with SPSS software (International Business Machines Corporation, IBM, USA), and carried out by two-way or one-way analysis of variance (ANOVA). For two-way ANOVA, the procedure (sham or BDL surgery) and the treatment (saline vs. 1-MT treatment) were taken as between-group factors. When needed, the time of measurement (0, 7, 14, 21, and 28 days after BDL) was taken as a within-subject factor. The Newman-Keuls test was used for post hoc comparisons. For one-way ANOVA, Dunnett’s test was used for multiple comparisons to determine whether the means differed significantly between two groups. A value of p < 0.05 was considered statistically significant.
Induction of BDL
Liver function tests in sham and BDL rats
Sham (0 day)
112.4 ± 7.2
217.4 ± 9.1*
274.2 ± 10.2**
289.4 ± 11.2**
327.5 ± 12.8**
42.5 ± 4.3
79.4 ± 5.2*
91.5 ± 6.4*
97.5 ± 7.4**
110.7 ± 8.7**
120.5 ± 10.1
227.7 ± 11.1*
257.5 ± 12.5*
268.4 ± 11.4*
294.5 ± 15.4**
21.4 ± 3.2
68.1 ± 5.2*
134.7 ± 8.7**
157.8 ± 9.1**
187.4 ± 10.2***
Total bilirubin (mg/dL)
0.41 ± 0.01
2.5 ± 0.1*
4.6 ± 0.15**
5.2 ± 0.13**
5.9 ± 0.31***
Direct bilirubin (mg/dL)
0.20 ± 0.01
1.4 ± 0.1*
2.1 ± 0.12**
2.4 ± 0.14**
2.7 ± 0.21***
Indirect bilirubin (mg/dL)
0.18 ± 0.02
1.1 ± 0.1*
2.2 ± 0.13**
2.3 ± 0.15**
2.4 ± 0.18**
Expression of proinflammatory cytokines in the brain and blood of BDL rats
Likewise, we measured the protein level of proinflammatory cytokines in the blood of each rats by ELISA and found that the expression of IL-1β, IL-6, and TNF-α obviously increased 7 days after BDL [F(5,29) = 10.32, p < 0.001, for IL-1β; F(5,29) = 6.437, p < 0.01, for IL-6; F(5,29) = 14.31, p < 0.001, for TNF-α]. These increases were more obvious as time went on (Fig. 3e).
IDO expression in the brain of BDL rats
Effect of 1-MT on depressive-like behavior in BDL rats
As illustrated in Fig. 6, significant difference was found between groups in the FST (p < 0.001). Seven days after BDL surgery, the immobility time of these rats significantly increased when compared with the corresponding sham groups in the FST (p < 0.01, p < 0.001). However, treatment with 1-MT (dose of 9 mg/kg) abolished this adverse effect of BDL (p < 0.01, Fig. 6b).
Effect of 1-MT on anxiety-like behavior in BDL rats
Effect of 1-MT on anxiety-like behavior in BDL rats was assessed by the marble-burying test and elevated plus maze test. BDL rats exhibited anxiety-like behavior compared with the sham rats (Fig. 6). In the marble-burying test, the increased number of buried marbles was observed in the BDL group (p < 0.001). Chronic administration with 1-MT prevented this increase, and this effect was found significant 21 days after 1-MT treatment (p < 0.01, Fig. 6c).
In the elevated plus maze test, BDL rats spent more time in the closed arms (p < 0.001, Fig. 6d) and less time in the open arms (p < 0.001, Fig. 6e). A significantly increased number of entries were observed in BDL group in the closed arms at the 7th day after surgery as compared with the sham group (p < 0.05, Fig. 6f). However, 1-MT prevented this adverse effect of BDL (p < 0.01).
Effect of 1-MT on learning and memory function in BDL rats
The memory retention for the platform location of rats was tested in the second probe trial (24 h after training). BDL rats showed significantly longer latency to reach the platform (p < 0.001 for the 14 days group) and fewer platform crossings compared with sham rats (p < 0.01 for the 14 days group). 1-MT treatment for 21 days reversed these phenomena (p < 0.01, Fig. 7b).
Effect of 1-MT on spontaneous locomotor activity in BDL rats
Locomotor activity was assessed in terms of the number of photo beam counts recorded for 10 min. As shown in Fig. 7, BDL rats showed impairment in locomotor activity (48%) starting from day 7 till day 28 after BDL surgery when compared with sham rats. No significant difference was observed between BDL rats and BDL + 1-MT rats, when compared with sham rats [Fig. 7c, Additional file 1: Figure S1 for 1-MT (1 and 3 mg/kg) treatment].
Effects of 1-MT on BDL surgery-induced expression changes in the neurotoxic kynurenine pathway of tryptophan metabolism
The main findings of this study are as follows: BDL rats present the increases of anxiety-like and depressive-like behaviors, as well as memory deficits, and these behavioral changes are associated with the increased proinflammatory cytokine expression levels in the hippocampus and cerebral cortex, not in the hypothalamus and striatum; the KYN pathway of TRY metabolism may play an important role in inflammation-induced behavioral changes in HE; indoleamine-2,3-dioxygenase (IDO) inhibitor 1-methyl-l-tryptophan (1-MT) can reverse BDL-induced behavioral changes in rats, indicating that 1-MT may serve as a therapeutic agent for HE.
The BDL rat model is considered as a good experimental model for chronic HE [36, 37]. Seven days after biliary obstruction, the activity of liver marker enzymes (ALP, ALT, AST) and the levels of ammonia and bilirubin were significantly enhanced. We also observed significant increases of proinflammatory cytokines (TNF-α, IL-1β, and IL-6) in the hippocampus and cerebral cortex of BDL rats 3 weeks after biliary obstruction, which is similar to the results obtained by Hernandez-Rabaza et al. . Curiously, increases of proinflammatory cytokines in the blood were observed 2 weeks after surgery, earlier than those in the brain. In agreement with the present data, Dadsetan’s research found that a high level of inflammation first appeared in the peripheral system in a HE animal model . In fact, most of neuroinflammation was induced by peripheral inflammation [39, 40]. Initial neuroinflammatory response may be part of an adaptive beneficial process. However, chronic neuroinflammation results in adverse neurological consequences, such as disruption of neurotransmission and alteration of metabolic pathways [41–43], leading to many central nervous system diseases (depression, anxiety, and Alzheimer’s disease). Taken together, it seems plausible to hypothesize that these proinflammatory cytokines can be described as important features in HE development.
In the present study, l type 1-MT, not 1-methyl-d-tryptophan (d type 1-MT), was employed to further explore the role of IDO1 activity in the change of behavior. In the present BDL model, depressive-like and anxiety-like behaviors were seen to accompany the increase of proinflammatory cytokines. Clinical depressive behavior results from a perceived absence of control over the outcome of a situation, which has been described as the learned helplessness theory . Force swimming test, which was used to study animals with depression, was established based on this theory since helpless behaviors are frequently observed in depressed patients [49, 50]. Our data showed that the immobility times of BDL rats increased significantly when compared with the sham group. However, 1-MT treatment in the rats reversed these deficits. Another main symptom of depression is anhedonia, the inability to perform rewarded behaviors. The sucrose preference test is established based on this theory . We observed that BDL surgery induced a significantly reduced sucrose preference in rats, while the IDO inhibitor 1-MT treatment reversed this decrease, indicating IDO may play an important role in depression accompanied by HE.
The elevated plus maze test and marble-burying test have been reported to be the most widely used tests for determining anxiety in animals. In the present study, BDL rats exhibited a decrease in the time spent and the number of open arm entries in the elevated plus maze test and also showed behavioral deficits in the marble-burying test. However, these symptoms were reversed by 1-MT treatment, indicating that anxiety behavior of BDL rats may be related to IDO upregulation. Some earlier researches confirmed our results: BDL rats spent less time in the open arms and more time in the closed arms of the maze as compared to the control animals [52, 53]. Furthermore, Souza et al.’s study had shown that 1-MT may process anti-anxiety-like action in neurodegenerative disorder .
Memory dysfunction is one of the main symptoms of HE patient. In the present study, this symptom was confirmed in BDL rats in the Morris water maze test. BDL rats needed longer latency to reach the platform and a decreased number of crossings over the previous platform from day 7 till the end of the experiment. Huang and his team had also shown that the latency to reach the platform which is used as a measure of spatial memory was longer in the case of BDL rats as compared to sham rats . Furthermore, a recent study found that BDL rats took more time to locate the hidden platform than the control rats . Our results also showed that 1-MT-treated BDL rats had restored memory performance and learned faster than non-treated rats, suggesting IDO regulation may be related to the memory deficits induced by BDL surgery. Corroborating our results, 1-MT treatment can ameliorate the memory deficit induced by amyloid-β1-42 peptide in mice .
Locomotor activity has been considered to be an index of wakefulness or alertness of mental activity, and the decrease of this activity may lead to sedation as a result of inhibition of the central nervous system . Our data showed a significant decline in the locomotor activity from day 7 after rats received BDL surgery, and this effect continued till day 28. A similar result was also found in Leke et al.’s study . In our data, no significant difference of locomotor activity was found between the BDL + 1-MT group and BDL group when compared with the sham group, suggesting 1-MT did not influence the accuracy of behavioral results.
To examine the role of IDO1 activity in TRY metabolism in the pathogenesis of HE, we measured the levels of TRY, 5-HT, and KYN in the hippocampus and cerebral cortex using HPLC. 5-HT and KYN are two major TRY metabolites produced through the regulation of metabolic enzymes, including IDO. 5-HT, one of the neurotransmitters, is thought to produce feelings of calmness, relaxation, and contentment. According to the monoamine hypothesis of depression and anxiety, if the amount of 5-HT is reduced, depleted, or dysfunctional for some reason, as in the case of decreased concentrations of TRY, these disorders will ensue. Recently, the low TRY level, as well as abnormal IDO expression, was observed in depression and anxiety animal models [13, 58]. Furthermore, IDO activation is associated with decreased 5-HT content and increased KYN content. Contemporary research also reveals that the relative balance of these opposing metabolic branches, rather than simply changes in the levels of individual metabolites, constitutes the pathogenic potential of kynurenine metabolism . Curiously, the increased KYN/TRY ratio and decreased 5-HT/TRY ratio were observed in our study, indicating the balance of TRY metabolites was shifted from 5-HT synthesis to KYN formation in the brain of BDL rats. Moreover, 1-MT treatment reversed this imbalance of TRY metabolites and increased the 5-HT/5-HIAA ratio, which partly explained the antidepressant and anxiolytic-like effects of 1-MT in BDL rats.
The metabolism of KYN is physically compartmentalized within the brain [20, 51]. Normally, KYN is mainly metabolized to KA, not to 3-HK. During inflammation state, KYN is more likely to be metabolized to 3-HK, leading to the potential formation of several neurotoxic metabolites [60, 61]. Our data found that 3-HK increased, KA decreased, and the 3-HK/KA ratio increased in the brain of BDL rats, and these changes were normalized by 1-MT treatment. Furthermore, BDL treatment caused a significant change of QA, one of 3-HK’s neurotoxic metabolites and also an NMDA receptor agonist which is often used to induce memory impairment in animal models.
Despite the interesting findings, our study contains limitation. For these animals were weak after BDL surgery, additional intracerebral injection may cause high operative mortality. Thus, 1-MT was intraperitoneally injected in this study. However, it brings the issue that the neuroprotective effects observed after 1-MT injection may also be due to an indirect effect whereby the IDO1 inhibitor 1-MT alleviated the liver damage in addition to the direct action of IDO1 in the brain. We tested liver enzymes in serum after 1-MT treatment as a supplementary measurement. Data in Additional file 7: Table S1 indicated that 1-MT improved the liver function damaged by BDL surgery. Thus, in this study, 1-MT presented a hepatoprotective effect and this effect may influence the behavioral changes in HE rats. Nevertheless, it is reasonable to speculate that 1-MT exerted its protective effect mainly in the brain. Among the homologs of IDO, TDO is mainly expressed in the liver and IDO1 is mainly expressed in extrahepatic tissues, and 1-MT is specific for IDO1. Furthermore, previous studies reporting the potential therapeutic effect of 1-MT on diseases of the central nervous system administrated this inhibitor via i.p. injection or s.c. injection, because 1-MT can penetrate the blood-brain barrier [14, 62]. Detailed mechanism regarding how was the central nervous system affected by peripheral cytokines and to what extent it was affected remains to be explored in our future study.
In summary, we found that behavioral impairment in BDL rats is associated with the increased proinflammatory cytokines in the brain. The current study firstly explored the role of the KYN pathway of TRY metabolism in the behavioral changes in BDL rats. We also demonstrated that the IDO1 inhibitor 1-MT can effectively alleviate BDL-induced behavioral changes in HE rats, suggesting that 1-MT was a possible candidate for the treatment of HE.
This work was funded by the scientific research project of Zhejiang Pharmaceutical College (ZPCSR2016003), Natural Science Foundation of Ningbo (2016A610239), and Zhejiang Provincial Natural Science Foundation of China (LGF18H090014) for Xuefeng Yu; the science and technology project of Zhejiang Medical and Health Department (2017182371) and Natural Science Foundation of Ningbo (2017A610175) for Xi Jiang; Scientific Research Fund of Zhejiang Provincial Education Department(Y201636660) and Ningbo natural scientific foundation committee (2016A610238) for Ziwei Chen; and the scientific research project of Zhejiang Pharmaceutical College (ZPCSR2014009) for Lei Chen.
Availability of data and materials
All the data supporting the results are included in this manuscript.
XJ and XY designed the study. CP, LX, XJ, XY, JZ, LT, FL, and LC conducted the experiments and analyzed the data. LT, LX, and ZC wrote the manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
All the procedures were approved by the Wenzhou Medical University Committee on Animal Care and Use and were conducted in accordance with the guidelines for humane use and care of laboratory animals. Consent to participate was not required.
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