Spatial Memory Test Research Articles

Theta/gamma Co-modulation Disruption After NMDAr Blockade by MK-801 Is Associated with Spatial Working Memory Deficits in Mice

Abnormal N-methyl-D-aspartate receptor (NMDAr) function has been linked to oscillopathies, psychosis, and cognitive dysfunction in schizophrenia (SCZ). Here, we investigate the role of NMDAr hypofunction in pathological oscillations and behavior. We implanted mice with tetrodes in the dorsal/intermediate hippocampus and medial prefrontal cortex (mPFC), administered the NMDAr antagonist MK-801, and recorded oscillations during spontaneous exploration in an open field and in the y-maze spatial working memory test. Our results show that NMDAr blockade disrupted the correlation between oscillations and speed of movement, crucial for internal representations of distance. In the hippocampus, MK-801 increased gamma oscillations and disrupted theta/gamma coupling during spatial working memory. In the mPFC, MK-801 increased the power of theta and gamma, generated high-frequency oscillations (HFO 155–185 Hz), and disrupted theta/gamma coupling. Moreover, the performance of mice in the spatial working memory version of the y-maze was strongly correlated with CA1-PFC theta/gamma co-modulation. Thus, theta/gamma mediated by NMDAr function might explain several of SCZ’s cognitive symptoms and might be crucial to explaining hippocampal-PFC interaction.

THE EFFECT OF KAFFIR LIME PEEL EXTRACT (Citrus hystrix) ON SPATIAL MEMORY OF MICE WITH DEMENTIA USING MORRIS WATER MAZE

Background: Antioxidants are a group of chemicals that protect biological systems against the potential harmful effects of oxidation processes or its reactions. Kaffir lime peel (Citrus hystrix) contains various potential antioxidants substances those are able to protect neurons from free radical-induced damage. Objective: To evaluate the effect of kaffir lime peel extract (Citrus hystrix) on the spatial memory of mice induced by Scopolamine (SCM). Methods: This research was a true experimental study with a post-test-only controlled group design. Thirty mice were randomly divided into 5 groups. SCM was injected intraperitoneally on day 1-7 and kaffir lime peel extract was given orally on day 2-7, the spatial memory testing of mice using Morris Water Maze on day 8. Data analysis used One-Way ANOVA test (α = 0.05) and continued with Post Hoc LSD test (α = 0.05). Results: The mean spatial memory of K+, K-, P1, P2,P3 were 16,33 ± 7,42; 70,00 ± 32,24; 25,66 ± 24,43; 23,00 ± 19,39; 25,00 ± 19,50 seconds respectively. There were significant differences in spatial memory in P1, P2, dan P3 to the negative control group, but there is no significant differences between treatment grups. Conclusion: Kaffir lime peel extract (Citrus hystrix) can improve the spatial memory of scopolamine-induced dementia (SCM) mice. There is no dose effect relationship between the treatment groups

Stress degrades working memory-related frontostriatal circuit function.

Goal-directed behavior is dependent on neuronal activity in the prefrontal cortex (PFC) and extended frontostriatal circuitry. Stress and stress-related disorders are associated with impaired frontostriatal-dependent cognition. Our understanding of the neural mechanisms that underlie stress-related cognitive impairment is limited, with the majority of prior research focused on the PFC. To date, the actions of stress across cognition-related frontostriatal circuitry are unknown. To address this gap, the current studies examined the effects of acute noise-stress on the spiking activity of neurons and local field potential oscillatory activity within the dorsomedial PFC (dmPFC) and dorsomedial striatum (dmSTR) in rats engaged in a test of spatial working memory. Stress robustly suppressed responses of both dmPFC and dmSTR neurons strongly tuned to key task events (delay, reward). Additionally, stress strongly suppressed delay-related, but not reward-related, theta and alpha spectral power within, and synchrony between, the dmPFC and dmSTR. These observations provide the first demonstration that stress disrupts the neural coding and functional connectivity of key task events, particularly delay, within cognition-supporting dorsomedial frontostriatal circuitry. These results suggest that stress-related degradation of neural coding within both the PFC and striatum likely contributes to the cognition-impairing effects of stress.

A Comparative Study of the Impact of NO-Related Agents on MK-801- or Scopolamine-Induced Cognitive Impairments in the Morris Water Maze

Learning and memory deficits accompany numerous brain dysfunctions, including schizophrenia and Alzheimer's disease (AD), and many studies point to the role of nitric oxide (NO) in these processes. The present investigations constitute the follow-up of our previous research, in which we investigated the activity of NO releasers and a selective inhibitor of neuronal NO synthase (nNOS) to prevent short-term memory deficits in novel object recognition and T-maze. Here, the ability of the compounds to prevent the induction of long-term memory deficits by MK-801 or scopolamine administration was investigated. The Morris Water Maze test, a reliable and valid test of spatial learning and memory, was used, in which escape latency in the acquisition phase and nine different parameters in the retention phase were measured. A fast NO releaser (spermine NONOate), a slow NO releaser (DETA NONOate), and a nNOS inhibitor, N(ω)-propyl-L-arginine (NPLA), were used. The compounds were administered i.p. at a dose range of 0.05-0.5 mg/kg. All compounds prevented learning deficits in the acquisition phase and reversed reference memory deficits in the retention phase of the scopolamine-treated mice. Spermine NONOate was the least effective. In contrast, the drugs poorly antagonised MK-801-induced deficits, and only the administration of DETA NONOate induced some improvements in the retention trial.

Sex-specific effects of high-fat diet on rat brain glucose metabolism and early-onset dementia symptoms

Peripheral metabolic disturbances are associated with a variety of clinical health consequences and may contribute to the development of neurocognitive disorders. This study investigates whether long-term high-fat diet (HFD) consumption changes the brain glucose metabolism and impairs memory performance in a sex-dependent manner. Male and female rats, after weaning, were fed HFD or normal chow diet (NCD) for 16 weeks. Behavioral tests for spatial memory and an 18 F-FDG-PET scan were performed. Also, the expression of brain insulin resistance markers and Alzheimer’s pathology-related genes was assessed by qPCR. The Morris water maze and Y-maze results showed, respectively, that memory retrieval and spatial working memory were impaired only in HFD male rats compared to NCD controls. In addition, measuring whole brain 18 F-FDG uptake indicated a significant reduction in glucose metabolism in male but not female HFD rats. Analysis of 15 genes related to glucose metabolism and Alzheimer's pathology, in the hippocampus, showed that expression of GLUT3, IRS2, and IDE is significantly reduced in HFD male rats. Our results suggest that sex affects the HFD-induced dysregulation of brain glucose metabolism and cognitive performance.

Sequential order spatial memory in male rats: Characteristics and impact of medial prefrontal cortex and hippocampus disruption

Remembering an experience entails linking what happened, where the event transpired, and when it occurred. Most rodent hippocampal studies involve tests of spatial memory, but fewer investigate temporal and sequential order memory. Here we provide a demonstration of rats learning an aversive sequential order task using a radial arm water maze. Male rats learned a fixed sequence of up to seven spatial locations, with each decision session separated by a temporal delay. Rats relied on visuospatial cues and the number of times they had entered the maze for a given day in order to successfully perform the task. Behavioral patterns during asymptotic performance showed similarities to the serial-position effect, especially with regards to faster first choice latency. Rats at asymptotic performance were implanted with bilateral cannula in medial prefrontal cortex, dorsal, and ventral hippocampus. After re-training, we injected muscimol to temporarily disrupt targeted brain regions. While control rats made prospective errors, rats with mPFC muscimol exhibited more retrospective errors. Rats with hippocampal muscimol no longer exhibited a prospective bias and were at chance levels in their error choices. Taken together, our results suggest disruption of mPFC, but not the hippocampus, produced an error choice bias during an aversive sequential order spatial processing task.

Selection of Norwegian police drone operators: an evaluation of selected cognitive tests from “The Vienna Test System”

ABSTRACT A nationwide sample of 129 police officers participated in a study aimed at validating and presenting practical implications of a selection procedure for applicants to an educational program for Norwegian police drone pilots. The subjects were part of a selection program for a training and qualification course for police drone pilots. The selection program consisted of tests of spatial orientation, logical reasoning, attentional selection, sustained attention, and visual short-term memory, in addition to a performance test in a drone flight simulator. The aim of the study was to evaluate the cognitive tests used in the selection program and their relation to performance during the simulated flight. The results from the untrained applicants revealed low-to-moderate intercorrelations of the cognitive tests. Only spatial orientation, logical reasoning, and attentional selection were correlated to the performance measures of skills and proficiency. Stepwise regression analysis showed that only spatial orientation and attentional selection had unique contributions in explaining the variance in both measures of performance. Implications are discussed on both practical and scientific levels. The positive implications of using untrained respondents, the use of proficiency measures in addition to skills, the building of a clearinghouse for drone selection data, and considering both the job-analyzes and the total test-performance when interpreting the applicant’s test-scores are discussed.

Assessment of depression, anxiety, stress, and cognitive parameters in medical students: A pilot study

Background: As there is an increase in mental health issues among medical students, it is mandatory to assess their mental health status. In our earlier studies, we observed differences in the scores of depression, anxiety, and stress between male and female students. Aims and Objectives: The present study was undertaken to assess depression, anxiety, stress, and cognitive parameters in male and female medical students. Materials and Methods: A total of 100 medical students’ males (n=50) and females (n=50) were part of the study after obtaining voluntary, written informed consent. The required sample size for the study was 97 with a 95% of confidence level, 10% of margin of error, and 50% of the population proportion. This means 97 or more measurements/surveys are needed to have a confidence level of 95% that the real value is within ±10% of the measured/surveyed value. Depression, anxiety, and stress were assessed using the DASS 21 questionnaire. Spatial and verbal memory test was administered to assess the cognitive functions. Results: The depression scores were significantly higher (P<0.0001) in females when compared with males. Anxiety scores were significantly higher in females when compared with males (P<0.0001). Stress scores were significantly higher (P<0.0001) in females when compared with males. Spatial (P<0.0001) and verbal (P=0.0141) memory was significantly higher in females when compared with males. Conclusion: There were significantly higher levels of depression, anxiety, and stress scores in female students when compared with males. Further, spatial and verbal memory was also higher in females. There is a strong need for further detailed studies in this area and for adopting adequate management methods to manage negative psychological emotions in females.

Assessment of psychological parameters and cognitive parameters in peripheral vertigo patients

Background: Assessment of the psychological and cognitive functions will give an indication of the development of vertigo. However, to support this view, there is very less literature available. Aim and Objective: The present study assesses the psychological and cognitive parameters in patients with vertigo. Materials and Methods: Sixty cases of vertigo within the 50 and 70 years and 60 age-matched non-controls were part of the study. A spatial and verbal memory test was administered to assess cognitive functions. DASS 42 was used to assess the psychological parameters. Results: Negative psychological emotions are significantly higher in vertigo patients. Spatial memory was significantly lower in the cases. Verbal memory was significantly lower in the cases. Conclusion: The study results suggest that there were higher levels of depression, anxiety, and stress and significantly lower levels of cognitive functions in the patients with vertigo when compared with healthy controls. The study suggests considering the psychological and cognitive parameters in diagnosing and managing vertigo.

Effects of Personalized Cognitive Training Using Mental Workload Monitoring on Executive Function in Older Adults With Mild Cognitive Impairment.

Although a variety of cognitive training has been performed, its optimally personalized delivery is still unknown. This study established the mental workload classification model using a convolutional neural network based on functional near-infrared spectroscopy-derived data. The dorsolateral prefrontal cortex (DLPFC) while thirty individuals with mild cognitive impairment (MCI) performed spatial working memory testing was found to be a considerable indicator to classify 3 levels of mental workload with an accuracy of over 86%. In the next step, forty subjects with MCI were randomly allocated into the experimental group (EG) that received cognitive training with mental workload-based difficulty adjustment or the control group (CG) that received conventional cognitive training. To compare both groups, the Trail Making Test Part B (TMT-B) and hemodynamic responses in the DLPFC during the TMT-B were measured. After the 16 training sessions, the EG subjects achieved a greater improvement in the TMT-B than the CG subjects (p < 0.05). Also, the EG subject showed a significantly lower DLPFC activity during the TMT-B than the CG subject (p < 0.05). In sum, the EG subjects better performed executive function with lower energy from the DLPFC. These findings imply that the importance of mental workload monitoring to provide personalized cognitive training.

Evaluation of the effects of phenylephrine and prazosin injection into basolateral amygdala on the post-stress experience of memory retrieval in rats

The present study explored the effect of α1-adrenergic receptors in the basolateral amygdala (BLA) on memory formation in the hippocampus under repeated stress. Male rats received injections of the α1-adrenergic receptor agonist (phenylephrine) or antagonist (prazosin) bilaterally into the BLA five min before foot-shock stress, and emotional and spatial memory and in-vivo long-term potentiation (LTP) in the Cornu Ammonis (CA1) region of the hippocampus were examined. Foot-shock stress impaired performance in emotional and spatial memory tests. However, it had no significant effect on any of the LTP parameters in the hippocampus. Intra-BLA phenylephrine injection significantly impaired emotional and spatial memory performance in stressed animals. On the other hand, administration of intra-BLA prazosin significantly reduced emotional and spatial memory in the control (intact) animals. Neither of the two drugs had any significant effects on LTP parameters. Prazosin effectively impaired memory in the control, but not in the stressed rats. Stress appears to have suppressed the effect of prazosin, and it seems to be a significantly stronger stimulus than prazosin. Taken together, these findings provide new insights into the effects of α1-adrenergic receptors in the BLA on memory storage, during the stress experience.

A metabolite attenuates neuroinflammation, synaptic loss and cognitive deficits induced by chronic infection of Toxoplasma gondii.

Neurodegenerative diseases including AD is currently one of intractable problems globally due to the insufficiency of intervention strategies. Long-term infection of Toxoplasma gondii (T. gondii) can induce cognitive impairment in hosts, which is closely implicated in the pathogenesis of neurodegenerative diseases. Aconitate decarboxylase 1 (Acod1) and its produced metabolite itaconate (termed Acod1/itaconate axis), have recently attracted extensive interests due to its anti-inflammatory role in macrophages. However, whether the axis can influence cognitive function remains unknown. A chronic T. gondii-infected mice (C57BL/6J) model was established via administration of cysts by gavage. Novel location (NL), novel object recognition (NOR), Y-maze spatial memory and nest building tests were used to evaluate the behavior performance. Transmission electron microscopy, immunofluorescence, RT-PCR, western-blotting and RNA sequencing were utilized to determine the pathological changes, neuroinflammation and transcription profile in hippocampus tissues post infection, respectively. Moreover, the protective effect of Acod1/itaconate axis in T. gondii-induced cognitive deficits was evaluated. We found that the latent infection of the parasite impaired the cognitive function, which was assessed behaviorally by novel location (NL), novel object recognition (NOR), Y-maze spatial memory and nest building tests. RNA sequencing of hippocampus showed that the infection downregulated the expression of genes related to synaptic plasticity, transmission and cognitive behavior. To our attention, the infection robustly upregulated the expression of genes associated with pro-inflammatory responses, which was characterized by microglia activation and disorder of Acod1/itaconate axis. Interestingly, administration of dimethyl itaconate (DI, an itaconate derivative with cell membrane permeability) could significantly ameliorate the cognitive deficits induced by T. gondii, which was proved by improvement of behavior performance and synaptic ultrastructure impairment, and lower accumulation of pro-inflammatory microglia. Notably, DI administration had a potential therapeutic effect on the cognitive deficits and synaptic impairment induced by the parasitic infection. Overall, these findings provide a novel insight for the pathogenesis of T. gondii-related cognitive deficits in hosts, and also provide a novel clue for the potential therapeutic strategies.

Effectiveness of 8 weeks of vestibular exercises on stress, sleep, and cognitive parameters in hypertensive patients

Background: It was hypothesized that vestibular stimulation causes beneficial effects in hypertensive patients as so as in diabetic individuals. Aims and Objectives: The present study was undertaken to observe the effectiveness of 8 weeks of vestibular exercises on stress, sleep, and cognitive parameters in hypertensive patients. Materials and Methods: A total of eighty male and female stage 1 hypertensive individuals were part of the study after obtaining voluntary, written informed consent. Vestibular exercises comprising three steps with a time period of 45 min per session were administered to the participants of the intervention group. Two sessions per week were administered as mentioned in the literature. Stress levels were assessed by the perceived stress scale. Sleep was assessed by the insomnia severity index. A spatial and verbal memory test was used to assess the spatial and verbal memory scores. Results: There was no significant difference in the demographical parameters of the control and intervention groups. There is no significant difference in stress, sleep scores, and spatial and verbal memory scores among the control and intervention groups. There was a significant decrease in the stress scores and insomnia scores, and a significant improvement in the spatial and verbal memory scores in the intervention group after the intervention when compared with the control group. Conclusion: The present study results suggest that vestibular exercises have a positive impact on reducing stress and improving sleep and cognition in hypertensive individuals. The study highlights the need for further detailed studies in this area to recommend the inclusion of vestibular exercises as adjunctive therapy in the management of hypertension.

Treatment with C5aR1 antagonist attenuates short‐term hippocampal memory decline and prevents DAM signature in Arctic mice.

AbstractBackgroundUpregulation of complement genes in Alzheimer’s disease (AD) mouse models is associated with inflammation and cognitive decline. Genetic ablation of C5aR1 reduces loss of neuronal complexity and cognition in the Arctic mouse model. Inhibition of C5aR1 with PMX205 has shown success in preclinical studies of AD, reducing recruitment of reactive glia and amyloid deposition in the Tg2576 AD model. However, the molecular and cellular mechanisms underlying this neuroprotection are unclear. Thus, we used single cell RNA‐seq to interrogate gene pathways involved in C5aR1‐mediated deficits in the Arctic mouse model.MethodWT and Arctic mice were treated with PMX205 or vehicle via drinking water (20 µg/mL, equivalent to ∼5 mg/kg/day, consistent with previous studies) from 7.5 to 10 months of age. Effects of PMX205 on long‐ and short‐term memory were tested with object location memory (OLM) with a 24hr inter‐trial interval (ITI) and y‐maze spatial reference memory test with a 1hr ITI, respectively. Hippocampi were dissected and immediately prepared for microglial isolation and fixation. The single cell whole transcriptome kit (Parse Biosciences) was used to prepare single cell microglia libraries for RNA‐seq. Libraries were sequenced using NextSeq 2000. Parse Bioscience split‐pipe v0.7.6 was used to demultiplex reads into single‐cells, Scrublets to remove doublets, and Seurat for quality control, normalization, and clustering.ResultPMX205 protected against short‐, but not long‐, term memory deficits. Arctic‐PMX205 mice spent more time in the novel arm (44%) than Arctic‐vehicle mice (30%) in Y‐maze. Microglial single cell RNA‐seq identified 7 microglial clusters. Within these clusters, we probed for genes previously described as homeostatic, DAM1, and DAM2. DAM1 (Tyrobp, Apoe, Trem2) and DAM2 (Cst7, Itgax) genes were enriched in Arctic‐vehicle mice compared to WT mice, and expression was downregulated with PMX205 treatment in Arctic mice, most notably in DAM1 genes.ConclusionPharmacological C5aR1 inhibition confers some protective function even when treatment is initiated months after amyloid pathology onset in this aggressive mouse model of AD, and alters microglial polarization, suppressing detrimental inflammation. These findings complement previous data from genetic ablation of C5aR1, and suggest that C5aR1 may be a viable therapeutic target for individuals with an AD diagnosis.

Different approaches to test orientation of self in space: comparison of a 2D pen-and-paper test and a 3D real-world pointing task

Spatial orientation is based on a complex cortical network with input from multiple sensory systems. It is affected by training, sex and age as well as cultural and psychological factors, resulting in different individual skill levels in healthy subjects. Various neurological disorders can lead to different patterns or specific deficits of spatial orientation and navigation. Accordingly, numerous tests have been proposed to assess these abilities. Here, we compare the results of (1) a validated questionnaire-based self-estimate of orientation/navigation ability (Santa Barbara Sense of Direction Scale, SBSODS) and (2) a validated pen-and-paper two-dimensional perspective test (Perspective Taking Spatial Orientation Test, SOT) with (3) a newly developed test of finger-arm pointing performance in a 3D real-world (3D-RWPT) paradigm using a recently established pointing device. A heterogeneous group of 121 participants (mean age 56.5 ± 17.7 years, 52 females), including 16 healthy volunteers and 105 patients with different vestibular, ocular motor and degenerative brain disorders, was included in this study. A high correlation was found between 2D perspective task and 3D pointing along the horizontal (azimuth) but not along the vertical (polar) plane. Self-estimated navigation ability (SBSODS) could not reliably predict actual performance in either 2D- or 3D-tests. Clinical assessment of spatial orientation and memory should therefore include measurements of actual performance, based on a 2D pen-and-paper test or a 3D pointing task, rather than memory-based questionnaires, since solely relying on the patient’s history of self-estimated navigation ability results in misjudgments. The 3D finger-arm pointing test (3D-RWPT) reveals additional information on vertical (polar) spatial performance which goes undetected in conventional 2D pen-and-paper tests. Diseases or age-specific changes of spatial orientation in the vertical plane should not be clinically neglected. The major aim of this pilot study was to compare the practicability and capability of the three tests but not yet to prove their use for differential diagnosis. The next step will be to establish a suitable clinical bedside test for spatial memory and orientation.

Spread of pathological human Tau from neurons to oligodendrocytes and loss of high-firing pyramidal neurons in aging mice.

Intracellular aggregation of hyperphosphorylated Tau (pTau) in the brain is associated with cognitive and motor impairments, and ultimately neurodegeneration. We investigate how human pTau affects cells and network activity in the hippocampal formation of the THY-Tau22 tauopathy model mice invivo. We find that pTau preferentially accumulates in deep-layer pyramidal neurons, leading to neurodegeneration, and we establish that pTau spreads to oligodendrocytes. During goal-directed virtual navigation in aged transgenic mice, we detect fewer high-firing prosubicular pyramidal cells, but the firing population retains its coupling to theta oscillations. Analysis of network oscillations and firing patterns of pyramidal and GABAergic neurons recorded in head-fixed and freely moving mice suggests preserved neuronal coordination. In spatial memory tests, transgenic mice have reduced short-term familiarity, but spatial working and reference memory are surprisingly normal. We hypothesize that unimpaired subcortical network mechanisms maintain cortical neuronal coordination, counteracting the widespread pTau aggregation, loss of high-firing cells, and neurodegeneration.

Treadmill Exercise Modulates Intestinal Microbes and Suppresses LPS Displacement to Alleviate Neuroinflammation in the Brains of APP/PS1 Mice.

Neuroinflammation occurs throughout the pathogenesis of Alzheimer’s disease (AD). Here, we investigated the effects of treadmill exercise on neuroinflammation in APP/PS1 transgenic AD mice and the potential involvement of microbe–gut–brain axis (MGB) mechanisms based on growing evidence that AD’s pathogenesis is correlated with a deterioration in the function of gut microbiota. APP/PS1 transgenic AD mice were subjected to 12 weeks of treadmill exercise, followed by spatial memory tests. After the behavioral study, the amyloid (Aβ) pathology, gut microbes and metabolites, bacterial lipopolysaccharide (LPS) displacement, and degree of neuroinflammation were analyzed. We found that this strategy of exercise enriched gut microbial diversity and alleviated neuroinflammation in the brain. Notably, exercise led to reductions in pathogenic bacteria such as intestinal Allobaculum, increases in probiotic bacteria such as Akkermansia, increased levels of intestine–brain barrier proteins, and attenuated LPS displacement. These results suggest that prolonged exercise can effectively modulate gut microbes and the intestinal barrier and thereby reduce LPS displacement and ultimately alleviate AD-related neuroinflammation.

Improvements of cognitive functions in mice heavily infected by Angiostrongylus cantonensis after treatment with albendazole, dexamethasone, or co-therapy.

Angiostrongylus cantonensis, the causative agent of human eosinophilic meningitis and eosinophilic meningoencepalitis, has been reported to cause cognitive impairments in the host. To determine whether drug treatment improves the cognitive functions, BALB/c mice infected with 50 third-stage larvae were treated with albendazole, dexamethasone, or co-therapy since day 7 or 14 post-infection for one or two weeks. Abilities of spatial memory and learning of these animals were assessed with the Morris water maze. Our results showed that body weight was significant higher then infected group in the albendazole and combined therapy groups. Significantly lower worm recovery rates were found in mice treated with the same groups. The mice treated with dexamethasone since day 7 for 14 day had significant longer time in the remaining groups were found in forced swimming test. The animals treated with albendazole and combined therapy since day 7 for 14 days was demonstrated to have significantly shorter latencies to the platform in learning memory on day 3 and 4. Mice in these two groups were demonstrated to have significantly higher sores in spatial memory tests. These results indicate that treatment with albendazole or combined therapy may be more efficient in preventing brain damages and depression as well as preserving their capabilities in learning and memory. Therefore, administration of albendazole alone or combined with dexamethasone should have higher efficacies than dexamethasone alone in treatment of BALB/c mice infected with a heavy dose of 50 third-stage larvae of A. cantonensis.

Effectiveness of 12-week Om chanting on reaction time and spatial and verbal memory

Background: Chanting Om was reported to increase the blood supply to brain structures involved in cognitive functions and improve cognition. Aim and Objectives: The present study was undertaken to observe the effectiveness of 12-week Om chanting on reaction time and spatial and verbal memory. Materials and Methods: Apparently, healthy volunteers (n=20; nine men and 11 women) who were right-handed and were consenting to participate in the study were recruited in the study. The age range of the subjects was 25–55 years. The intervention group participants were trained for reciting OM with the help of professional yoga instructor for a week days. After a week, they were instructed to assemble at the meditation hall of the institute at sharp 6:30 am every day and recite Om chanting for 20 min. Spatial and verbal memory was assessed using the standard methods explained in the literature that is spatial and verbal memory test. Auditory and visual reaction time was assessed using RT apparatus. Results: Spatial, verbal memory, and reaction time in control and intervention group participants were compared in this study. There was a significant improvement in the spatial memory scores in the intervention group when compared with control group. There was a significant improvement in the auditory reaction time for high and low pitch sounds and also visual reaction time for red and green light in the intervention group when compared with control group. Conclusion: The study results explain significant improvement in the spatial and verbal memory scores and auditory and visual reaction time after the intervention. The study recommends further detailed studies to support practicing Om chanting for the well-being of general population.

Novel Anti-Neuroinflammatory Properties of a Thiosemicarbazone-Pyridylhydrazone Copper(II) Complex.

Neuroinflammation has a major role in several brain disorders including Alzheimer’s disease (AD), yet at present there are no effective anti-neuroinflammatory therapeutics available. Copper(II) complexes of bis(thiosemicarbazones) (CuII(gtsm) and CuII(atsm)) have broad therapeutic actions in preclinical models of neurodegeneration, with CuII(atsm) demonstrating beneficial outcomes on neuroinflammatory markers in vitro and in vivo. These findings suggest that copper(II) complexes could be harnessed as a new approach to modulate immune function in neurodegenerative diseases. In this study, we examined the anti-neuroinflammatory action of several low-molecular-weight, charge-neutral and lipophilic copper(II) complexes. Our analysis revealed that one compound, a thiosemicarbazone–pyridylhydrazone copper(II) complex (CuL5), delivered copper into cells in vitro and increased the concentration of copper in the brain in vivo. In a primary murine microglia culture, CuL5 was shown to decrease secretion of pro-inflammatory cytokine macrophage chemoattractant protein 1 (MCP-1) and expression of tumor necrosis factor alpha (Tnf), increase expression of metallothionein (Mt1), and modulate expression of Alzheimer’s disease-associated risk genes, Trem2 and Cd33. CuL5 also improved the phagocytic function of microglia in vitro. In 5xFAD model AD mice, treatment with CuL5 led to an improved performance in a spatial working memory test, while, interestingly, increased accumulation of amyloid plaques in treated mice. These findings demonstrate that CuL5 can induce anti-neuroinflammatory effects in vitro and provide selective benefit in vivo. The outcomes provide further support for the development of copper-based compounds to modulate neuroinflammation in brain diseases.