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BACKGROUND: Medium-chain triglycerides such as decanoic acid (C10), which is one of the fatty acids that constitute dietary fats, are of substantial interest for their potential therapeutic effects on neuropsychiatric disorders. However, the effects of C10 on attention-deficit/hyperactivity disorder (ADHD) remain to be studied. We explored the effects of C10 on behavioural activity and antioxidant defences in an experimental animal model of ADHD. METHODS: To establish an experimental animal model of ADHD, neonatal rats were subjected to unilateral striatal lesions using 6-hydroxydopamine (6-OHDA). The rats sequentially underwent open-field and Y-maze tests before treatment [postnatal day 25 (PN25)]. After the subcutaneous administration of either vehicle or C10 solution (250 mg/kg) for 14 days, the behavioural tests were repeated on PN39. Next, we examined the effects of C10 on the expression of the constitutive antioxidant enzymes catalase and glutathione peroxidase-1/2 and the phase II transcription factor nuclear factor erythroid 2-related factor 2 in four different regions of the rat brain. RESULTS: Injection of 6-OHDA unilaterally into the striatum resulted in elevated locomotor activity on PN39. The administration of C10 for a period of 14 days did not alter the locomotor hyperactivity. Moreover, the administration of C10 had no significant effects on the expression of proteins related to antioxidant defences in the hippocampus, prefrontal cortex, striatum or cerebellum of both control and lesioned rats. CONCLUSIONS: The lack of significant effects of C10 in our study may depend on the dose and duration of C10 administration. Further exhaustive studies are needed to verify the efficacy and effects of different doses and treatment durations of C10 and to explore the underlying mechanisms.
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Transtorno do Deficit de Atenção com Hiperatividade , Ratos , Animais , Transtorno do Deficit de Atenção com Hiperatividade/tratamento farmacológico , Oxidopamina/farmacologia , Antioxidantes/farmacologia , Modelos Animais de Doenças , Locomoção , Ácidos Decanoicos/uso terapêuticoRESUMO
BACKGROUND: Alzheimer's disease (AD) is a severe neurological illness causes cognitive decline and mortality if not treated early. However, the current therapeutic modalities are inefficient to manage the cognitive dysfunction of AD. Therefore, in the present manuscript, we have enumerated the pharmacological benefit of Poliumoside in the Streptozotocin-induced cognitive dysfunction in Sprague-Dawley (SD) rats. MATERIALS AND METHODS: Initially, the cognitive dysfunction in rats was induced by the intracerebroventricular administration of Streptozotocin, then rats received PMD (5 mg and 10 mg/kg body weight) was given. Various behavioural analysis, such as Morris water maze (MWM), and object recognition tests (ORT), and locomotor analysis was conducted in PMD treated group. Various biochemical analysis was conducted to analyze the effect of PMD on hippocampus oxidative-nitrosative stress and pro-inflammatory cytokines. MTT assay and annexin V/PI staining was performed to analyse the effect of PMD on the cell viability and neuronal toxicity of PC12 cells, respectively. Molecular docking analysis was also conducted with crystal structure of human AChE. RESULTS: PMD treatment improved cognitive capacity in rats in MWM and ORT. Compared to STZ rats, PMD-treated rats had significantly higher locomotor activity and lower AChE activity. PMD also restores dopamine, 5-HT, and NE levels and reduces metabolic their deactivation as evidenced by increased levels of DOPAC, HVA, 5-HIAA. Nitrite, MDA, SOD, CAT, and GSH levels were restored near normal in PMD-treated rats, reducing hippocampus oxidative-nitrosative stress. Pro-inflammatory cytokines were similarly lowered in PMD-treated rats. In in-vitro studies, PMD did not affect PC12 cell survival at the maximal dose of 10 µM. In addition, PMD concentration-dependently prevents H2O2-induced neuronal death in PC12 cells. The in-silico docking analysis showed that the PMD fit snugly into the active site of human AChE by engaging with the anionic domain and the catalytic triad of Trp86, Tyr337, Phe338, and Gly121 residues. CONCLUSIONS: In conclusion, our study demonstrated that PMD have significant impact on AD by inhibiting ACheE and restoring neurotransmitter levels, which enhances Ach levels in rats and improves cognitive impairment in STZ rats.
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PURPOSE: The behavioural activity pattern is a behavioural and biological 24-hour rhythm. Ageing, diseases and memory disorders can change this pattern. Home care staff can utilize knowledge about the behavioural activity pattern of elderly home care clients in many ways. The purpose of this study was to evaluate whether home care staff could identify the behavioural activity pattern of elderly home care clients using activity sensors, namely, actigraphs and motion sensors, could identify the behavioural activity rhythms. MATERIALS AND METHODS: A total of four elderly home care clients and one elderly home rehabilitation client took part in the study. The participants wore actigraphs on their wrist and motion sensors were installed in their apartment. In addition to sensor data, home care staff answered one open-ended question during each home care visit. The data collection period was two weeks. Both quantitative and qualitative methods were used in the analysis. RESULTS: The behavioural activity pattern was easy to identify from the motion sensor data, whereas actigraph data were difficult to interpret. The home care staff members' answers to open-ended questions reinforced the reliability of motion sensor data. CONCLUSIONS: Motion sensors are relatively cheap, unobtrusive and reliable way to identify and detect changes in the behavioural activity patterns of elderly home care clients.Implications for rehabilitationMotion sensors are cheap, user-friendly and highly accepted technology for identifying and monitoring behavioural activity rhythm.Home care staff members can use the data about elderly home care client's behavioural activity rhythm to monitor deviations to the rhythm and detect changes in client's health.The information about behavioural activity rhythm can also be utilized in planning home care visits and interventions.
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Schizophrenia is a neurodevelopmental disorder which is expressed in the form of disturbed behaviour and abnormal mental functions. Patient's non-adherence to the medicine is the main cause of failure of drug therapy and increases incidence of relapses. Thus, for successful management of disease long acting parenteral formulations were developed. Aripiprazole was encapsulated in biocompatible polycaprolactone microsphere by o/w emulsion solvent-evaporation method in order to achieve sustained release of the drug for several weeks after single subcutaneous administration. They were optimised on the basis of various parameters such as physical appearance, particle size (49.4 µm-387.1 µm), encapsulation efficiency (70%-95%), percentage yield (33%-75%) and drug loading (25.9%-47.5%). The surface topography and sphericity of the microspheres was determined by scanning electron microscopy which revealed that the microspheres formed were spherical and non-porous in nature. The in vitro releases from the selected formulations were found to be 87% and 95% respectively after 45 days of dissolution. In vivo efficacy of optimised formulation showed significantly (p < 0.05) amelioration of various positive, negative and cognitive symptoms associated with schizophrenia and oxidative stress markers in ketamine-induced schizophrenia model in rats for 30 days.
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Esquizofrenia , Animais , Aripiprazol , Preparações de Ação Retardada , Ácido Láctico , Microscopia Eletrônica de Varredura , Microesferas , Tamanho da Partícula , Poliésteres , Ratos , Esquizofrenia/tratamento farmacológicoRESUMO
INTRODUCTION: Alzheimer's disease is a type of dementia, and till now there is no suitable drug available for the complete cure of this disease. Now-a-days Probiotics, Lactobacillus strains play a therapeutic role in cognitive disorders through Gut-Brain Axis communication. AIM: The present study was aimed to evaluate the anti-Alzheimer properties of Lactobacillus plantarum MTCC1325 against D-Galactose-induced Alzheimer's disease in albino rats. MATERIALS AND METHODS: Healthy rats (48) of wistar strain were divided into four groups viz., Group-I: control rats received saline, Group-II: rats received intraperitoneal injection of D-Galactose (120 mg/kg body weight) throughout experiment, Group-III: initially animals were subjected to D-Galactose injection for six weeks, then followed by simultaneously received both D-Galactose and L. plantarum MTCC1325 (12×108 CFU/ml; 10 ml/kg body weight) for 60 days and Group-IV: rats which were orally administered only with Lactobacillus plantarum MTCC1325 for 60 days. During the experimentation, both morphometric and behavioural aspects were studied. Later we have examined histopathological changes and estimated cholinergic levels in selected brain regions of all experimental groups of rats including control on selected days. RESULTS: Morphometric, behavioural changes, ACh levels were significantly decreased and pathological hallmarks such as amyloid plaques and tangles were also observed in AD model group. Treatment of AD-group with L. plantarum MTCC1325 for 60 days, not only ameliorated cognition deficits but also restored ACh and the histopathological features to control group. However, no significant effects have been observed in the group treated with L. plantarum alone. CONCLUSION: The study revealed that, L. plantarum MTCC1325 might have anti-Alzheimer properties against D-Galactose induced Alzheimer's disease.
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BACKGROUND: Attractive toxic baits are the prevailing method for managing leaf-cutting ants in the eucalypt forests planted for the production of pulp, paper, timber and charcoal. For successful use in these baits, the insecticidal compounds need to circumvent the typical defences of the eusocial leaf-cutting ants. The challenge is to have an insecticide in the bait that will not directly harm and/or compromise foraging workers, but that will eventually suppress the colony. These underlying mechanisms are poorly known, and here the potential mechanism of fipronil activity in toxic baits for leaf-cutting ants was assessed using colonies of the representative Neotropical Acromyrmex subterraneus subterraneus (Forel, 1893). RESULTS: Although forager activity was not directly impaired by fipronil, the insecticide affected forager nestmate interactions (auto- and allogrooming) and waste removal and, more importantly, greatly affected the minor workers, impairing their activities of fungus garden cultivation and progeny handling. The fast decay of the fungus garden compromised the sustainability of the colonies, ultimately leading to their demise within 8 days. CONCLUSION: The behavioural effects of sublethal insecticide exposure towards minor workers are the main determinants of insecticide activity as ant baits and should be targeted in developing such compounds. © 2016 Society of Chemical Industry.