A Focus on the Effect of L-theanine on Improving Depression and Cognition in C 57 BL / J Male Mice Subjected For Chronic Stress Induced Neuroinflammation

A long term stressful event in life altering immune system is a major factor for the development of psychopathological conditions. By now it’s clear that stress induced neuroinflammatory cytokines are the key role in mediating neurochemical and neuroendocrine systems causing the behavioral disorders and cognitive impairment. Current anti depressants are unable to correct neurotransmitters levels directly or indirectly by inhibiting cytokines expression. Present study was conducted to elucidate the effect and mechanism of L-theanine on chronic restrainer stress (CRS) induced neuroinflammation, anxiety-like, depression, learning and memory impairment in C57BL/J male mice. Chronic restrain stress was induced by well ventilated 50ml conical tube for 6 hours/day 21 consecutive days. After stressor cessation behavioral and recognition tests were conducted, at the end of study mice were sacrificed, brain and blood was collected. Cytokines (TNF-á and IL-6), neurotransmitters were quantified in prefrontal cortex and estimated corticosterone levels in plasma. Histopathological examination of the hippocampus was performed. The results was implicated that L-theanine significantly (p<0.05) reversed the effect of CRS induced behavioral changes and memory impairment, reduced cytokines expression and restored neurotransmitter levels in prefrontal cortex. It also alleviated neuronal apoptosis and lowered the corticosterone levels in plasma of CRS mice. These results indicate that L-theanine exerted protective effect on chronic stress induced neuroinflammation, anxiety, depression and cognitive dysfunction. The mechanism of protective effect is by reducing cytokine expression in frontal cortex and preventing hippocampal apoptosis.


INTRODUCTION
One of the serious burden of society is stress which may be psychological, physiological o r e n v i r o n m e n t a l s t r e s s o r s r e s u l t i n g i n neuropsychological dysfunction like Major depressive disorder (MDD) with cognitive impairment. 1,2 ording to world health organization, 350 million people worldwide suffer with MDD.Repeated stressful events changes mood and cognitive decline altered by neurochemicals, of immune and stress hormones system. 3Evidences of chronic stress for functional and structural impairment in vital areas of brain such as prefrontal cortex PFC and hippocampus have increased abundantly. 4,5The PFC plays a major role in behavior, learning and memory, and also particularly hypersensitive to chronic stress. 5Preclinical and clinical studies on depression highlighted an increased cytokines expression in PFC. 6,710] Interestingly, these pathways implicate the path-physiology of chronic stress induced depression as explained below.3][14][15] Many researchers concluded that cytokines imbalance the kynurenine (KYN) pathway by the activation of indolamine-2, 3-Dioxgenase IDO, lead tryptophan depletion and reduction serotonin synaptic availability and also increases the activity of serotonin reuptake transporters in depressive condition. 16,17In animal study chronic stress model expressed cytokines and elevated IDO activity in PFC 18 and another study apoptosis was detected in mice hippocampus with depression and cognitive dysfunction induced by CRS model. 19,20These indications are an important pathogenesis of emotion, depression and associated with cognitive dysfunction in chronic stress.At present most common selective serotonin reuptake inhibitors and noradrenaline reuptake inhibitors as anti-depressants are enable to suppress the expression of cytokines.According to this hypothesis we urgently need novel compound with antiinflammatory and neuro-modulatory activities for chronic stress induced MDD.
Green Tea is freely available in nature and one of the most consumed beverages through worldwide.L-theanine is a major amino acid component (Gamma-glutamythylamide) in green tea 21 and it has been shown to exhibit neuroprotective effect in various animal experimental models.Examples: antidepressant activity, 22 prevent memory impairment induced by repeated cerebral ischemia in rodents. 23and anti inflammatory effect in peripheral system. 24Even it has been proven neuroprotective effect of L-theanine (2 and 4mg/kg) doses on CRS induced cognitive dysfunction with anti oxidant and anti stress activities. 25sed on recent reports we discussed above possible mechanism of stress induced neuroinflammation changes in behavior and memory impairment.In present study, we investigated the effect and underlying mechanism of L-theanine (4mg/kg) 25 on anxiety, depression and cognitive impairment induced by neuroinflammation in CRS model.In addition to that we quantified cytokines (TNF-á & IL-6) NE and 5-HT levels in PFC and morphology of hippocampus was observed.This work also suggests novel opportunities for preventing and treating depression by reducing neuroinflammation.

Animals
Adult C57BL/J male mice were housed in group on semi soft bedding with pellet, water and ad libitum.The animals are maintained under standard laboratory conditions at 25±1ºc temperature, relative humidity 50±10% and light dark cycle of 12:12h.All the animals allowed habituating to the housing facilities for at least one week prior to initiation of the procedure.The study was approved by the Institutional Animal Ethics Committee, Sri Ramachandra University (IAEC No: IAEC/XLVII/ SRU/497/2016).

Restrain protocol
In CRS procedure, mice were restrained in 50 ml (21D 2 cm x 8 cm) falcon tube inside wellventilated and 6h/day for three weeks (21 days) from age of 8 or 9 weeks.The mice were fitted tightly into restrainers and there is no possible to move or turn around.

Animal groups
Each group contains 8 animals.Group1.(Control) The mice were treated with vehicle (0.9%normal saline) from day 1 to day 21.Group2.(CRS) The mice were treated with restrain stress + vehicle was administrated 1 hour before restrain stress from day 1 to day 21.Group3.(L-theanine) The mice was treated with restrain stress + L-theanine was administrated 1 hour before restrain stress (4mg/kg/body weight, oral) from day 1 to day 21.

Chemicals
L-theanine (SRL chemicals India) was obtained from The I.L.E.Co, Chennai India.Neurotransmitter standards (HPLC sigma, st Louis, Mo.U.S.A) were obtained from bicorporals, Chennai, India.Primary and secondary antibodies (abcam) were obtained from Allied scientific products, Kolkata.

General condition
After the stress cessation all subjects were underwent behavioral test (from 22nd day to 25th).Each behavioral test was conducted by the same person between 9AM to 4PM and which was recorded by camera.All mice were allowed to experimental room for adaption, 1 hour before testing.Behavior

Behavioral test OFT
To measure the locomotor activity and anxiety like behavior of mice we used open field apparatus. 26The apparatus are wood in material and comprised of 15.74 x 15.74 inches square arena with 7.87 inches high wall.It was divided into 25 equal squares which was marked in floor of arena.Single mice gently placed into corner of floor in order to explore the arena for five minutes.The activity of mice was recorded by a camera; number of squares was crossed by each mice was scored.In addition to that time spent in central and peripheral squares, immobility period, rearing behavior and grooming activity were scored and analyzed.After finishing the test for each mouse, floor was cleaned with alcohol to exclude the intervention of odor signal.

FST
The test was performed as described previously with minor modifications. 18To measure the depressive like behavior, mice were placed into a glass tank (diameter 23 cm & high 30cm) up to 20 cm high filled with 25 ± 1ºc water so that mice cannot reaches the bottom with their tail.Behavior (struggling: the mouse was vertical in the water, scratching vigorously the walls of the beaker; floating: no movements of the mouse except for minor movements to keep balance; swimming: all other behavior i.e. activity movement) was recorded by a camera for 5 minutes.Thereafter mice was dried with towels and shifted into a fresh cage.Water was replaced after completing the procedure for each animal.

NORT
Mice were assessed using novel object recognition task similar to that described previously. 26uring habituation the mice were allowed to explore the empty apparatus for 15 minutes.During the acquisition trail (T1), apparatus contained two identical objects.A mice was taken from its home cage and placed into the apparatus, central from 2 objects facing the wall in front of the observer and time spent actively exploring (exploration was defined as the animal sniffing or touching) the objects during 5 minutes after T1, the mice was transferred into home cage.After 24 hours, the mice were again placed into the apparatus for the discrimination trail (T2).The time spent exploring the two objects during T1 and T2 was recorded and discrimination index (DI) was calculated based on the following formula: DI = RI / (Time spent in exploring novel object + Time spent in exploring familiar object) Recognition Index (RI) = Time spent in exploring novel object -Time spent in exploring familiar object.

Y maze
The Y maze test is less stressful and ethological more relevant to spatial memory test.Mice was assessed spatial memory function, as described previously with minor modifications. 27The maze consist of 3 arms appear as Y shape.The

Sample storage
After behavioral study (i.e.26th day), the mice was anesthetized and scarified using isoflurane, blood and brain was collected.Blood centrifuged at 3000 rpm for 10 minutes at 4ºC, plasma and brain samples were frozen at -80ºc until the analysis.

Detection of PFC tissue TNF-á and IL-6 by Immunohistochemistry
Paraffin section was pretreated by using heat mediated antigen retrieval with sodium citrate buffer (pH 6) for ½ hour.The sections were stained with one of the primary antibodies: Rabbit polyclonal to mouse IL-6 (ab6672, 1/200 dilution) or Rabbit polyclonal to mouse TNF alpha (ab6671, 1/200 dilution).The slides were washed with appropriate buffer and incubated with HRP conjugated secondary (ab 97023, 1/1000 dilution) for 1 hour at room temperature.Sections were washed and stained with DAP for 15mins.Counterstaining with hematoxylin was performed the slides were mounted with aqueous mounting media and visualized under light microscope.The percentage of positive cells in 5 random microscopic fields was measured by 2 independent pathologists who were blind to clinical data.

Neurotransmitters estimation by LCMS
PFC tissues were homogenized with ice cold methanol (1mg/10µl).After homogenization samples were centrifuged at 10,000 rpm for 10 minutes at 4ºc.

Histopathology Analysis
Hippocampus collected from the mice and fixed in 10% neutral buffered formalin.Representative tissue section of brain at the level of hippocampus region was trimmed and dehydrated in series of graded alcohol and embedded in paraffin wax.Tissue sections of 3-4 micron thickness was obtained, mounted on a clean glass slides and stained with haematoxylin and eosin (H&E).Morphology of hippocampus was observed by a light microscope.Affected neuron cells were identified by their pyknotic nuclei and acidophilic (esinophilic) cytoplasm, which are the suggestive of necrotic morphology. 20Semi quantitative scale used for affected cells counting (0-absent, 1-weak, 2-moderate and 3-high) in the hippocampus neuronal cells.

Corticosterone analysis
Plasma CORT levels were estimated using the fluorometric assay of matingly (1962) 28 , a corticosterone stock (sigma) solution 100mg/dl was prepared and diluted to a range of concentrations 10-100µg/dl.Plasma samples and corticosterone standards were mixed in 7.5mldichloromethane.Five milliliters of the dichloromethane extract phase was transferred and mixed with 2.5ml of fluorescent reagent congaing concentrated sulphuric acid: absolute ethanol at 70:30 ratio and the tubes were thoroughly mixed.An aliquot of the lower phase was removed and measured with fluorescence at excitation 470 nm & emission 530 nm using spectrophotofluorimeter.The results were expressed as µg/dl of plasma.

Statistical analysis
Data expressed as mean ± standard error of mean (SEM).The difference between time spent exploring the novel object versus familiar object during discrimination trail was calculated for each group and the level of significance was analyzed using two-side student's t test.For other parameters the difference between the groups were determined using one way ANOVA followed by Tukey's -post

RESULTS
Behavior Assessment OFT CRS induced mice were made significantly (p<0.001)decrease total number of squares crossed compared to control group (Figure : 1A).There was also significant increases time spent in peripheral squares and decrease in central squares (p<0.001) in CRS group compared to control group (Figure : 1B).Treatment of L-theanine increase the number of squares crossed, time spent in central squares and decrease the peripheral squares compared to CRS group.Administration of L-theanine treated mice significantly decreased immobility period and reversed effect of rearing and grooming compared to CRS group (p<0.001).

FST
In FST significantly increase the floating period and decrease the swimming time in CRS compared to controlled group (p<0.001).It has shown in figure: 2 the treated with L-theanine mice significantly (p<0.001) increase the swimming time and decrease the floating period compared to CRS group.

Y Maze
In Y maze test group-2 significantly decreased the novel arm entries and increased the open arm entries compared to control group (Figure : 4A).Treatment of L-theanine was increased novel arm entries and decreased open arm entries compared to group-2.Time spent in open arm significantly (p<0.001)increased in CRS group compared to control group, but there is no significance between L-theanine treated group and CRS group (Figure : 4B).

Immunohistochemistry analysis
Immunohistochemical analysis showed that inflammation in CRS mice PFC exhibited an increased expression of TNF-á and IL-6 when compared to the control group.However the protein expression of TNF-á and IL-6 in PFC were considerably decreased in the L-theanine treated group (Figure : 5A, 5B & 6).

Effect of L-theanine on neurotransmitters decreased in PFC
In CRS significantly (p<0.001)reduced levels of NA and 5-HT as compared to the control group (Figure : 7).However, treatment of L-theanine resulted significantly (p<0.001)increased NA and 5-HT levels in PFC as compared to the CRS group.

Effect of corticosterone elevated levels in plasma
The CORT levels in plasma were significantly (p<0.001) higher in CRS group than control group

Histopathological examination of Hippocampus
L-theanine reversed the CRS induced neuronal apoptosis in the hippocampus.The neuronal cells of hippocampus histopathological changes were observed by hematoxylin and eosin (H&E) staining.In control group, there were absent of neuronal abnormalities.However, in CRS degenerated neurons (esinophilic pyknotic neuron) were highly observed.L-theanine treated mice neuronal abnormality was absent and potentially reversed the neuronal degeneration (Figure : 9).

DISCUSSION
Based on the evidences explained in review literature of previous clinical and pre-clinical studies, the present study confirmed and expanded the information on chronic stress which produced changes in behavior and cognition status of C57BL6/J mice.Stress was induced by restrainer for 21 days (6hrs/day) and from 22nd to 25th day the animals were observed for behavioral changes and memory impairment.CRS group mice showed decrease in locomotor activity (decreased number of squares crossed), increased anxiety (decreased time spent center squares in OFT) and more depressive like behavior (increased floating time in FST).Impairment in recognition (NOR test on novel object exploration was less when compared to neither control group) and in spatial memory impairment (novel arm entries were decreased in Y maze) 26,27 These behavioral and cognitive changes were in parallel with neurotransmitters such as NE and 5-HT, pro-inflammatory cytokines such as TNF-á and IL-6 were evoked in PFC, 26,30 stress hormones (CORT) levels were elevated in plasma and apoptosis was found in hippocampus. 20Most abnormalities resulting from chronic restrain stress were reduced by oral administration of L-theanine.These findings support the present hypothesis that treatment with L -theanine on group 3 can counteract chronic stress induced depression, impairment in cognitive function and alterations in neurotransmitters by reducing cytokines expression.D e s p i t e f a c t s w e l l k n o w n t h a t neuroinflammation is a key factor in development of neuropsychiatric dysfunction, 31,32 there is increase in TNF-á and IL-6 protein expression after CRS. 33n this present experiment, L-theanine decreased the expression of TNF-á and IL-6 in PFC shown in 5 & 6, as reported already that anti inflammatory activity of L-theanine. 34Also GCs have potential anti-inflammatory activity, but previous findings by Shawn F Sorrells et al., 2009 suggested that chronic stress which increase GCs levels, can enhance cytokines transcription factor which varies in vital regions of brain. 12,15Even in present study L-theanine decreased CORT levels in plasma (anti inflammatory activity has proven in earlier preclinical studies). 25This activity may be potentiating the anti inflammatory activity in present study.
In brain neurotransmitters were easily affected by chronic stress.NE and 5-HT levels in PFC were decreased which might be the reason for behavioral changes caused by chronic stress induced neuroinflammation. 18,26 he present study L-theanine group significantly increased levels of 5-HT and NE in PFC comparatively to CRS group.Xia Tian et al., has suggested that L-theanine restored NE levels in brain which was altered by CRS. 25 Reduction of serotonin levels is a major role in etiology of MDD.Increasing serotonin levels at neuroeffector junction is the most common treatment which is currently advised in depression.The present study shows, restoration of 5-HT levels in PFC of L-theanine treated group, probably following mechanism may be involved for the restoring serotonin levels in PFC.,30 The present study L-theanine inhibited the expression of cytokines which may lead to increase bioavailability of 5-HT.Previous studies concluded that L-theanine has neuro protective activity by interacting with monoamino neurotransmitters. 25.linga et al. stated that CRS induced inflammation reduced the levels of 5-HT in PFC and recognition memory impairment determined by the object recognition test.26 In our present study, L-theanine restoration of 5-HT levels improved recognition performance in NOR test (Figure : 3A, 3B& 3C) and decreased the duration of immobility period in FST (Figure : 2).Previously Wakabayashi reported that L-theanine has antidepressant activity by increasing mobility period in FST.22 In present study treatment of L-theanine increased locomotor activity and time spent in central squares and decreased time spent in peripheral squares during OFT (Figure : 1A&B) indicating the anxiolytic and anti depressant activity.34 The hippocampus is an important region for learning and memory.In previous study spatial memory impairment in CRS model with neuronal apoptosis in hippocampus CA1 region was correlated with the activation of Akt/GSK-3 signaling pathways.19,20 In present study treatment of L-theanine prevented the spatial memory impairment shown in figure : 4A & 4b by alleviating CRS-induced neuronal apoptosis of hippocampus as shown in 9.In previous study L-theanine shown ameliorative role by inhibiting phosphorylations of GSK-3 in neuronal cells. 36Our present study result showed the effect of L-theanine as novel therapeutic compound in various long-term stress induced depression and cognitive impairment conditions.As well as these findings strongly support the possible mechanism behind the adjuvant action and present hypothesis.37

CONCLUSION
The group of mice kept under CRS showed features of behavioral abnormalities like anxiety, mental depression and impairment in cognition, also lowered neurotransmitter levels and expression of cytokines like TNF-á and IL-6 in PFC resulting elevated apoptosis in hippocampus.These effects are found to be reversed in the group of mice treated with L-theanine in addition to CRS mice.This may explain the possible mechanism of preventing the cytokines involvement in PFC neurotransmitters and apoptosis in hippocampus as well.Our findings strongly suggest that L-theanine is a potential compound to prevent anxiety, depression associated with cognitive impairment, protecting PFC and hippocampus from chronic stress.

Fig. 1A &Fig. 2 :
Fig. 1A & 1B: Effect of stress and L-theanine treatment on number of squares crossed (Figure: 1A) time spent in central, peripheral squares and immobility period (Figure: 1B) in the open field exploration test.Data expressed as mean ± SEM (n=8 per group).a P<0.001, as compared to the control group; b P<0.001, as compared to the CRS group

Fig. 4A &
Fig. 4A & 4B: Effect of stress and L-theanine treatment in the Y maze task and the data expressed as mean ± SEM (n=8 per group).Figure: 4A Number of entries in novel arm a P<0.001, as compared to the control group; b P<0.001, as compared to the CRS group and number of open arm entries a p<0.001, as compared to the control group; b P<0.01, as compared to the CRS group.Figure: 4B Time spent in open arm, as a P<0.001 compared to control group; b P >0.05 as compared to the CRS group

Fig. 7 :Fig. 8 :Fig. 9 :
Fig. 7: Effect of L-theanine on the CRS induced 5-HT and NE reduction in the PFC.Data are reported as mean ±SEM (n=8).a p<0.001, as compared to control group; b p<0.001, as compared to the CRS group 3 arms of the maze randomly assigned as open arm (which is left open during training and test duration) start arm (where mice was left first during training and test duration) novel arm (which is blocked during first training period).Ocular clues were hung on the maze during the trails and test.Mice were pre-trained keeping novel arm closed.After 1 hour break test was carried keeping the novel arm is open.Novel versus familiarity of the mice was assessed by comparing the behavior in all the 3 arms.Mice were placed in start arm during all assessment.Number of visits and time spent in each arm was recorded by camera for 5 minutes.