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1.
Clinics ; 76: e3131, 2021. graf
Article in English | LILACS | ID: biblio-1350610

ABSTRACT

OBJECTIVES: To investigate the molecular mechanism of edaravone (EDA) in improving the post-traumatic brain injury (TBI) dysfunction in learning and memory. METHODS: In vitro and in vivo TBI models were established using hydrogen peroxide (H2O2) treatment for hippocampal nerve stem cells (NSCs) and surgery for rats, followed by EDA treatment. WST 1 measurement, methylthiazol tetrazolium assay, and flow cytometry were performed to determine the activity, proliferation, and apoptosis of NSCs, and malondialdehyde (MDA), lactic dehydrogenase (LDH), and reactive oxygen species (ROS) detection kits were used to analyze the oxides in NSCs. RESULTS: Following EDA pretreatment, NSCs presented with promising resistance to H2O2-induced oxidative stress, whereas NSCs manifested significant increases in activity and proliferation and a decrease in apoptosis. Meanwhile, for NSCs, EDA pretreatment reduced the levels of MDA, LDH, and ROS, with a significant upregulation of Nrf2/antioxidant response element (ARE) signaling pathway, whereas for EDA-treated TBI rats, a significant reduction was observed in the trauma area and injury to the hippocampus, with improvement in memory and learning performance and upregulation of Nrf2/ARE signaling pathway. CONCLUSIONS: EDA, by regulating the activity of Nrf2/ARE signal pathway, can improve the TBI-induced injury to NSCs and learning and memory dysfunction in rats.


Subject(s)
Animals , Rats , Antioxidant Response Elements , Brain Injuries, Traumatic/physiopathology , Brain Injuries, Traumatic/metabolism , Brain Injuries, Traumatic/drug therapy , Edaravone/pharmacology , Learning/drug effects , Signal Transduction/drug effects , Reactive Oxygen Species/metabolism , Apoptosis/drug effects , Oxidative Stress/drug effects , NF-E2-Related Factor 2/metabolism , Memory/drug effects
2.
Braz. arch. biol. technol ; 63: e20180379, 2020. tab, graf
Article in English | LILACS | ID: biblio-1132267

ABSTRACT

Abstract Hippocampus is a part of the brain that has a major role in spatial learning and memory which can be affected by herbal extracts. Incense resin (Styrax benzoin) has been used by local communities to improve intelligence. However, there is no scientific evidence of the functions of Styrax benzoin for regulating hippocampal function. The aim of this study was intended to analyze and investigate the effect of incense resin on learning, memory, and dendrite complexity of mice. Three months old male Deutch Democratic Yokohama (DDY) mice were injected orally with graded doses of 100, 150, and 200 mg/kg of incense resin aqueous extract daily for 30 days. Spatial learning and memory performance levels were tested with Y-maze alternation, novel object recognition, and Morris water maze. The branches and maximum dendritic span in the dentate gyrus were observed by the Golgi-Cox staining. Overall, our results showed that incense resin extract increased learning and memory ability, and the number of dendrite branching in the dentate gyrus.


Subject(s)
Animals , Male , Mice , Dendritic Cells/drug effects , Plant Extracts/pharmacology , Styrax/chemistry , Spatial Learning/drug effects , Memory/drug effects , Administration, Oral , Maze Learning/drug effects
3.
Rev. méd. Chile ; 147(2): 206-211, Feb. 2019. tab
Article in English | LILACS | ID: biblio-1043153

ABSTRACT

ABSTRACT Background: There is concern about the cognitive consequences of marijuana consumption. Aim: To assess the influence of current and past marijuana use and frequency on verbal learning and memory in a sample of adults aged 21 years old. Material and Methods: Marijuana use was assessed using a clinician administered interview in 654 participants (56% females), who reported frequency of use, age of first use and whether its use led to problems in their lives. The CogState International Shopping List was administered to assess learning and memory. Results: Seventy percent reported ever using marijuana, 46% consuming during the past year and 27% during the past 30 days. The latter scored significantly lower on delayed recall. Current and frequent use were significantly associated with lower accuracy in verbal learning and memory. Conclusions: In this cohort of adults aged 21 years old, marijuana use was prevalent and related to worse verbal memory.


Antecedentes: Existe preocupación acerca de los efectos cognitivos del consumo de marihuana. Objetivo: Estudiar el efecto de consumo de marihuana presente o pasado en la capacidad de aprendizaje verbal y memoria en una muestra de adultos de 21 años. Material y Métodos: El consumo de marihuana fue evaluado mediante una entrevista médica en 654 adultos de 21 años (56% mujeres), quienes informaron acerca de la frecuencia de consumo, edad de comienzo y si el consumo les ha causado problemas en sus vidas. Se les administró el Cogstate International Shopping List para evaluar aprendizaje y memoria. Resultados: El 70% informó haber consumido marihuana alguna vez, 46% la usó durante el último año y el 27% en los últimos 30 días. Estos últimos tuvieron un menor puntaje en memoria tardía. El consumo actual y frecuente se asoció a una menor precisión en la capacidad de aprendizaje verbal y memoria. Conclusiones: En esta cohorte de adultos de 21 años, el consumo de marihuana fue prevalente y relacionado a una menor memoria verbal.


Subject(s)
Humans , Male , Female , Young Adult , Mental Recall/drug effects , Verbal Learning/drug effects , Cannabinoids/pharmacology , Marijuana Use/epidemiology , Memory/drug effects , Time Factors , Chile/epidemiology , Marijuana Abuse/etiology , Marijuana Abuse/epidemiology , Cross-Sectional Studies , Cognition Disorders/complications , Marijuana Use/adverse effects , Neuropsychological Tests
4.
Arq. neuropsiquiatr ; 77(1): 19-24, Jan. 2019. tab
Article in English | LILACS | ID: biblio-983879

ABSTRACT

ABSTRACT Aim: Our aim was to determine whether there is a relationship between vitamin D [25(OH)D] and cognitive functioning in women with low 25(OH)D levels. Methods: Ninety female patients, 25-45 years of age, who attended our outpatient clinic and had 25(OH)D levels < 30 ng/mL, were included. The Montreal Cognitive Assessment (MoCA) scale was used to determine cognitive functioning; the scale is divided into seven subgroups. Patients were divided into three subgroups according to their 25(OH)D levels. After a three-month period of 25(OH) D replacement, the patients underwent a re-evaluation using the MoCA scale. Results: The total MoCA score before treatment was significantly different from the score after treatment (p < 0.05). Language and delayed recall functions were significantly different before and after treatment (p < 0.05). Conclusion: Vitamin D levels were related to cognitive functioning in our study group.


RESUMO Objetivo: Nosso objetivo foi determinar se existe uma relação entre a vitamina D [25(OH)D] e o funcionamento cognitivo em mulheres com baixos níveis de 25(OH)D. Métodos: Noventa pacientes do sexo feminino (25-45 anos de idade) que se apresentaram ao nosso ambulatório e tinham níveis de 25(OH)D <30 ng/mL foram incluídas. A escala de avaliação cognitiva de Montreal (MoCA) foi usada para determinar o funcionamento cognitivo; a escala é dividida em sete subgrupos. As pacientes foram divididas em três subgrupos de acordo com seus níveis de 25(OH)D. Após um período de três meses de reposição de 25(OH)D, as pacientes foram submetidas a uma reavaliação de acordo com a escala MoCA. Resultados: O escore total da MoCA antes do tratamento foi significativamente diferente do escore após o tratamento (p <0,05). As funções de idioma e recordação atrasada foram mais significativamente diferentes entre antes e depois do tratamento (p <0,05). Conclusão: O nível de vitamina D foi relacionado ao funcionamento cognitivo em nosso grupo de estudo.


Subject(s)
Humans , Female , Adult , Middle Aged , Vitamin D/pharmacology , Vitamin D Deficiency/psychology , Cognition/drug effects , Vitamin D/blood , Prospective Studies , Treatment Outcome , Statistics, Nonparametric , Educational Status , Mental Status and Dementia Tests , Memory/drug effects
5.
Braz. J. Pharm. Sci. (Online) ; 55: e18261, 2019. graf
Article in English | LILACS | ID: biblio-1039068

ABSTRACT

Learning and memory play main roles in daily life of human, and memory represents the basis of all trainings and learning. The aim of the current study is to investigate the effects of gallic acid and physical exercise on the levels of passive avoidance memory in rat. In this experimental study, 46 rats weighing 200-300 g were randomLy divided to six groups of eight each: including control group, groups treated with 10 and 20 mg/kg gallic acid, group undergoing physical exercise alone, and groups both undergoing physical exercise and treated with 10 and 20 mg/kg gallic acid. The interventions continued for 10 days. After the intervention, passive avoidance memory was measured by shuttle box, blood samples were taken, and serum and brain antioxidant capacity and malondialdehyde (MDA) levels were measured. Secondary latency in shuttle box significantly increased in groups undergoing treadmill exercise and undergoing treadmill exercise + treating 10 and 20 mg/kg gallic acid. In groups treated with 10 and 20 mg/kg gallic acid alone, secondary latency increased significantly. Results confirmed the effects of gallic acid and physical exercise, either alone or combined, in improving memory.


Subject(s)
Animals , Male , Rats , Exercise/physiology , Gallic Acid/adverse effects , Learning/drug effects , Malondialdehyde/analysis , Memory/drug effects
6.
Braz. J. Psychiatry (São Paulo, 1999, Impr.) ; 40(4): 367-375, Oct.-Dec. 2018. graf
Article in English | LILACS | ID: biblio-959251

ABSTRACT

Objective: To evaluate the effects of Hypericum perforatum (hypericum) on cognitive behavior and neurotrophic factor levels in the brain of male and female rats. Methods: Male and female Wistar rats were treated with hypericum or water during 28 days by gavage. The animals were then subjected to the open-field test, novel object recognition and step-down inhibitory avoidance test. Nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and glial cell-line derived neurotrophic factor (GDNF) levels were evaluated in the hippocampus and frontal cortex. Results: Hypericum impaired the acquisition of short- and long-term aversive memory in male rats, evaluated in the inhibitory avoidance test. Female rats had no immediate memory acquisition and decreased short-term memory acquisition in the inhibitory avoidance test. Hypericum also decreased the recognition index of male rats in the object recognition test. Female rats did not recognize the new object in either the short-term or the long-term memory tasks. Hypericum decreased BDNF in the hippocampus of male and female rats. Hypericum also decreased NGF in the hippocampus of female rats. Conclusions: The long-term administration of hypericum appears to cause significant cognitive impairment in rats, possibly through a reduction in the levels of neurotrophic factors. This effect was more expressive in females than in males.


Subject(s)
Animals , Male , Female , Plant Extracts/pharmacology , Cognition/drug effects , Hypericum , Frontal Lobe/metabolism , Hippocampus/metabolism , Nerve Growth Factors/analysis , Plant Extracts/administration & dosage , Random Allocation , Sex Factors , Treatment Outcome , Rats, Wistar , Models, Animal , Pattern Recognition, Physiological/drug effects , Dose-Response Relationship, Drug , Frontal Lobe/drug effects , Hippocampus/drug effects , Locomotion/drug effects , Memory/drug effects , Nerve Growth Factors/drug effects
7.
Arq. neuropsiquiatr ; 75(4): 204-208, Apr. 2017. tab
Article in English | LILACS | ID: biblio-838898

ABSTRACT

ABSTRACT Objective To compare children with attention-deficit/hyperactivity disorder (ADHD), before and after the use of methylphenidate, and a control group, using tests of working memory, inhibition capacity and mental flexibility. Methods Neuropsychological tests were administrated to 53 boys, 9–12 years old: the WISC-III digit span backward, and arithmetic; Stroop Color; and Trail Making Tests. The case group included 23 boys with ADHD, who were combined type, treatment-naive, and with normal intelligence without comorbidities. The control group (n = 30) were age and gender matched. After three months on methylphenidate, the ADHD children were retested. The control group was also retested after three months. Results Before treatment, ADHD children had lower scores than the control group on the tests (p ≤ 0.001) and after methylphenidate had fewer test errors than before (p ≤ 0.001) Conclusion Methylphenidate treatment improves the working memory, inhibitory control and mental flexibility of ADHD boys.


RESUMO Objetivo Comparar crianças com transtorno de déficit de atenção/hiperatividade (TDAH) com controles, utilizando testes de memória de trabalho, capacidade inibitória e flexibilidade mental, em meninos de 9 a 12 anos. Métodos Testes neuropsicológicos administrados: teste de ordem inversa dos dígitos, teste aritmético (WISC-III), Teste Stroop e Teste de Trilhas. Grupo experimental meninos (n=23), com TDAH combinado, virgens de tratamento, inteligência normal sem comorbidades. Grupo controle (n = 30) com as mesmas características do grupo experimental em termos de idade e sexo. Após três meses com metilfenidato, os grupos TDAH e controle foram novamente testadas. Resultados Antes do tratamento, as crianças com TDAH apresentaram menor pontuação do que o grupo controle nos testes analisados (p≤ 0.001) e o grupo com TDAH apresentou menos erros nos testes após metilfenidato (p ≤ 0.001). Conclusão O tratamento com metilfenidato melhora a memória de trabalho, controle inibitório e flexibilidade mental de meninos com TDAH.


Subject(s)
Humans , Male , Child , Attention Deficit Disorder with Hyperactivity/drug therapy , Central Nervous System Stimulants/administration & dosage , Memory/drug effects , Methylphenidate/administration & dosage , Case-Control Studies , Treatment Outcome , Central Nervous System Stimulants/pharmacology , Methylphenidate/pharmacology , Neuropsychological Tests
8.
Braz. j. med. biol. res ; 50(7): e6037, 2017. graf
Article in English | LILACS | ID: biblio-839319

ABSTRACT

The Quechua term ayahuasca refers to a beverage obtained from decoctions of the liana Banisteriopsis caapi with leaves of Psychotria viridis. The ritualistic use of ayahuasca is becoming a global phenomenon, with some individuals using this beverage throughout life, including in old age. Cognitive impairment is a common manifestation during aging. There are conflicting reports on the ability of some ayahuasca compounds to exert neuroprotective or neurotoxic effects that could improve or impair learning and memory. Animal models provide a relevant and accessible means of investigating the behavioral effects of ayahuasca without the environmental conditions associated with the ritualistic use of the beverage. In this study, we investigated the influence of chronic ayahuasca exposure throughout aging on the spatial reference and habituation memories of mice. Twenty-eight male c57bl/6 mice (6 months old) received ayahuasca or water (1.5 mL/kg, orally) twice a week for 12 months and were tested in the Morris water maze (MWM), open field and elevated plus maze (EPM) tasks before and after treatment. During aging, there was significant impairment in the evocation (but not acquisition) of spatial reference memory and in habituation to the open field. There was also a decrease in locomotor activity in the open field and EPM tests, whereas the anxiety parameters were unaltered. Ayahuasca treatment did not alter any of these parameters associated with aging. These findings indicate that chronic exposure to ayahuasca during aging did not affect memory in mice.


Subject(s)
Animals , Male , Mice , Banisteriopsis/chemistry , Beverages , Locomotion/drug effects , Maze Learning/drug effects , Memory/drug effects , Psychotria/chemistry , Aging/physiology , Anxiety/chemically induced , Mice, Inbred C57BL , Models, Animal , Time Factors
9.
Yonsei Medical Journal ; : 131-138, 2017.
Article in English | WPRIM | ID: wpr-65053

ABSTRACT

PURPOSE: To investigate the effects of hyperbaric oxygen (HBO) pretreatment on cognitive decline and neuronal damage in an Alzheimer’s disease (AD) rat model. MATERIALS AND METHODS: Rats were divided into three groups: normal saline (NS), AD, and HBO+AD. In the AD group, amyloid β peptide (Aβ)₁₋₄₀ was injected into the hippocampal CA1 region of the brain. NS rats received NS injection. In the HBO+AD group, rats received 5 days of daily HBO therapy following Aβ₁₋₄₀ injection. Learning and memory capabilities were examined using the Morris water maze task. Neuronal damage and astrocyte activation were evaluated by hematoxylin-eosin staining and immunohistochemistry, respectively. Dendritic spine density was determined by Golgi-Cox staining. Tumor necrosis factor-α, interleukin-1β, and interleukin-10 production was assessed by enzyme-linked immunosorbent assay. Neuron apoptosis was evaluated by terminal deoxynucleotidyl transferase dUTP nick end labeling. Protein expression was examined by western blotting. RESULTS: Learning and memory dysfunction was ameliorated in the HBO+AD group, as shown by significantly lower swimming distances and escape latency, compared to the AD group. Lower rates of neuronal damage, astrocyte activation, dendritic spine loss, and hippocampal neuron apoptosis were seen in the HBO+AD than in the AD group. A lower rate of hippocampal p38 mitogen-activated protein kinase (MAPK) phosphorylation was observed in the HBO+AD than in the AD group. CONCLUSION: HBO pretreatment improves cognition and reduces hippocampal damage via p38 MAPK in AD rats.


Subject(s)
Animals , Male , Rats , Alzheimer Disease/therapy , Amyloid beta-Peptides/administration & dosage , Apoptosis , Cognition/drug effects , Disease Models, Animal , Enzyme-Linked Immunosorbent Assay , Hippocampus/enzymology , Hyperbaric Oxygenation , In Situ Nick-End Labeling , Interleukin-10/biosynthesis , Interleukin-1beta/biosynthesis , Learning/drug effects , Memory/drug effects , Neurons , Peptide Fragments/administration & dosage , Rats, Sprague-Dawley , Sodium Chloride/administration & dosage , Tumor Necrosis Factor-alpha/biosynthesis , p38 Mitogen-Activated Protein Kinases/metabolism
10.
Arq. neuropsiquiatr ; 74(9): 723-729, Sept. 2016. graf
Article in English | LILACS | ID: lil-796042

ABSTRACT

ABSTRACT The purpose of the present study was to investigate the effect of crocin on brain oxidative damage and memory deficits in a 6-hydroxydopamine (6-OHDA) model of Parkinson’s disease. Male Wistar rats were subjected to unilateral injection of 6-OHDA (16 µg) into the medial forebrain bundle and treated with crocin (30 and 60 mg/kg) for six weeks. The rats were tested for memory performance at six weeks after 6-OHDA infusion, and then were killed for the estimation of biochemical parameters. The increase in thiobarbituric acid reactive substances (TBARS) and nitrite levels in the hippocampus were observed in the 6-OHDA lesioned rats, which was accompanied by memory deficits in a passive avoidance test at the end of week 6. Moreover, treatment with crocin decreased TBARS and nitrite levels in the hippocampus, and improved aversive memory. The present study conclusively demonstrated that crocin acts as an antioxidant and anti-inflammatory agent in the hippocampus of parkinsonian rats and could improve aversive memory through its properties.


RESUMO O objetivo do presente estudo foi investigar o efeito da crocina no dano oxidativo cerebral e nos déficits de memória em um modelo 6-OHDA de doença de Parkinson. Ratos Wistar machos foram submetidos à injeção unilateral de 6-OHDA (16 μg) em MFB e tratados com crocina (30 e 60 mg/kg), durante 6 semanas. Os ratos foram testados quanto ao desempenho da memória 6 semanas após a infusão de 6-OHDA, e, em seguida, foram sacrificados para a estimativa dos parâmetros bioquímicos. O aumento nos níveis de TBARS e de nitrito no hipocampo foram observados em ratos 6-OHDA lesionados, acompanhado por déficits de memória em um teste de esquiva passiva no final da semana 6. Além disso, o tratamento com crocina diminuiu os níveis de nitrito e de TBARS no hipocampo e melhorou a memória aversiva. O presente estudo demonstrou conclusivamente que a crocina age como um antioxidante e um agente anti-inflamatório no hipocampo de ratos parkinsonianos e pode melhorar a memória aversiva através de suas propriedades.


Subject(s)
Animals , Male , Parkinson Disease/drug therapy , Carotenoids/pharmacology , Cerebral Cortex/drug effects , Oxidative Stress/drug effects , Memory Disorders/prevention & control , Antioxidants/pharmacology , Parkinson Disease/physiopathology , Parkinson Disease/metabolism , Sulfhydryl Compounds/analysis , Lipid Peroxidation/drug effects , Random Allocation , Cerebral Cortex/physiopathology , Cerebral Cortex/metabolism , Oxidopamine , Thiobarbituric Acid Reactive Substances/analysis , Rats, Wistar , Disease Models, Animal , Glutathione Peroxidase/analysis , Glutathione Peroxidase/drug effects , Memory/drug effects , Memory/physiology , Memory Disorders/physiopathology , Memory Disorders/metabolism , Nitrites/analysis
11.
Acta cir. bras ; 31(8): 520-526, Aug. 2016. tab, graf
Article in English | LILACS | ID: lil-792414

ABSTRACT

ABSTRACT PURPOSE: To evaluated the long-term effect of scopolamine and sesame oil on spatial memory. METHODS: Memory impairment induced by Intracerebroventricular (ICV) injection of scopolamine hydrochloride (10 μg/ rat). Animals were gavaged for 4 weeks with saline, sesame oil (0.5, 1, or 2 mL/kg/day), or 3 weeks with memantine (30 mg/kg/day) in advance to induction of amnesia. Morris water maze (MWM) test was conducted 6 days after microinjection of scopolamine. Then, blood and brain samples were collected and evaluated for the malondialdehyde (MDA) levels, superoxide dismutase (SOD) and glutathione peroxidase (GPX) activities, and total antioxidant status (TAS) and ferric reducing ability of plasma (FRAP). RESULTS: Scopolamine significantly decreased traveled distance and time spent in target quadrant in probe test. Pretreatment of rats with sesame oil (0.5 mg/kg) mitigated scopolamine-induced behavioral alterations. Measurement of MDA, SOD, and GPX in brain tissue, and FRAP and TAS in blood showed little changes in animals which had received scopolamine or sesame oil. CONCLUSIONS: Intracerebroventricular injection of scopolamine has a residual effect on memory after six days. Sesame oil has an improving effect on spatial memory; however this effect is possibly mediated by mechanisms other than antioxidant effect of sesame oil.


Subject(s)
Animals , Male , Rats , Scopolamine/adverse effects , Sesame Oil/administration & dosage , Amnesia/drug therapy , Adjuvants, Anesthesia/adverse effects , Antioxidants/administration & dosage , Superoxide Dismutase/chemistry , Ferric Compounds/chemistry , Rats, Wistar , Oxidative Stress/drug effects , Maze Learning , Disease Models, Animal , Alzheimer Disease/prevention & control , Glutathione Peroxidase/chemistry , Amnesia/chemically induced , Injections, Intraventricular , Memory/drug effects , Antioxidants/chemistry
12.
Ciênc. cuid. saúde ; 15(1): 101-108, 07/06/2016.
Article in English, Portuguese | LILACS, BDENF | ID: biblio-1120734

ABSTRACT

Pesquisa qualitativa e exploratória -desenvolvida em 2012 e 2013 -em uma unidade de reabilitação para dependentes químicos no Paraná, com objetivo de verificar o impacto do uso de drogas na saúde física e mental do dependente químico. Foram entrevistados vinte dependentes químicos em tratamento. Os dados foram coletados mediante entrevista semiestruturada e tratados com a técnica de análise categorial temática. Os resultados demonstraram impactos na condição física do dependente químico relacionados à intoxicaçãopor drogas, estado de abstinência, alterações de alimentação, sono, higiene e aparência pessoal. Em relação ao impacto das drogas na saúde mental, os resultados apontaram a presença de comorbidades psiquiátricas, como: esquizofrenia e transtorno afetivo bipolar, bem como alterações de pensamento, percepção, memória, cognição e comportamento. Conclui-se que as drogas ocasionam graves impactos na saúde física e mental dos dependentes químicos a partir de consequências nocivas na condição física, no autocuidado, no pensamento, na cognição e no comportamento.


This is a qualitative study of exploratory method, developedin2012 and 2013,in a rehab unity to drug addicts, Paraná, Curitiba, Brazil, its aim is verify the drug use impact in addicts' physical and mental health. Twenty drug addicts in treatment were interviewed.Data collected by through of semi-structured interviews andprocessed using the categorical thematic analysis.The results showed impacts on physical medical condition related to drug poisoning, the state of abstinence, changes on feed, sleep, rest, hygiene and personal appearance.Regarding the impact of substance abuse in mental health, the results indicated the presence of psychiatric comorbidies as schizophrenia and bipolar affective disorder, thought changes, perception, memory and cognition, also behavioral changes. As conclusion, drugs are responsible for huge impacts in addicts' physical and mental health considering the harmful consequences in the physical conditions, self-care, thought, cognition and in the behavior.


Subject(s)
Humans , Male , Adult , Middle Aged , Aged , Pharmaceutical Preparations , Mental Health , Drug Users , Psychiatry , Psychotropic Drugs/adverse effects , Sleep/drug effects , Substance Withdrawal Syndrome/complications , Thinking/drug effects , Behavior/drug effects , Comorbidity , Hygiene , Nursing/statistics & numerical data , Crack Cocaine/adverse effects , Substance-Related Disorders , Cocaine-Related Disorders , Eating/drug effects , Binge Drinking , Hallucinations , Memory/drug effects
13.
Arq. neuropsiquiatr ; 73(9): 784-790, Sept. 2015. ilus
Article in English | LILACS | ID: lil-757393

ABSTRACT

Inflammation and oxidative stress have important roles in memory impairment. The effect of 7-nitroindazole (7NI) on lipopolysaccharide (LPS)-induced memory impairment was investigated. Rats were used, divided into four groups that were treated as follows: (1) control (saline); (2) LPS; (3) 7NI-LPS; and (4) 7NI before passive avoidance (PA). In the LPS group, the latency for entering the dark compartment was shorter than in the controls (p < 0.01 and p < 0.001); while in the 7NI-LPS group, it was longer than in the LPS group (p < 0.01 and p < 0.001). Malondialdehyde (MDA) and nitric oxide (NO) metabolite concentrations in the brain tissues of the LPS group were higher than in the controls (p < 0.001 and p < 0.05); while in the 7NI-LPS group, they were lower than in the LPS group (p < 0.001 and p < 0.05, respectively). The thiol content in the brain of the LPS group was lower than in the controls (p < 0.001); while in the 7NI-LPS group, it was higher than in the LPS group (p < 0.001). It is suggested that brain tissue oxidative damage and NO elevation have a role in the deleterious effects of LPS on memory retention that are preventable using 7NI.


Inflamação e estresse oxidativo tem importante papel no déficit de memória. O efeito do 7-nitroindazol (7NI) no déficit de memória induzido por lipossacarídeos (LPS) foi investigado. Foram utilizados ratos que foram divididos em quatro grupos e tratados da seguinte maneira: (1) controles (solução salina); (2) LPS; (3) 7NI-LPS; e (4) 7NI antes da esquiva passiva (PA). No grupo LPS, a latência para entrar no compartimento escuro foi mais curta que nos controles (p < 0,01 e p < 0,001); enquanto no grupo 7NI-LPS, a latência foi maior que aquela do grupo LPS (p < 0,01 e p < 0,001). Concentrações de malondialdeído (MDA) e metabólitos do ácido nítrico (NO) no tecido cerebral do grupo LPS foram maiores que aquelas dos controles (p < 0,001 e p < 0,05); enquanto no grupo 7NI-LPS, as concentrações foram menores do que no grupo LPS (p < 0,001 e p < 0,05, respectivamente). O conteúdo cerebral de tiol no grupo LPS foi menos do que nos controles (p < 0,001); enquanto no grupo 7NI-LPS, este conteúdo foi maior que no grupo LPS (p < 0,001). Sugere-se que o dano oxidativo cerebral e o aumento de NO tenham um papel nos efeitos deteriorativos dos LPS na memória de retenção, e que isto possa ser prevenido com o uso de 7NI.


Subject(s)
Animals , Male , Rats , Indazoles/pharmacology , Lipopolysaccharides/toxicity , Memory Disorders/prevention & control , Memory/drug effects , Neuroprotective Agents/pharmacology , Brain Chemistry , Memory Disorders/chemically induced , Rats, Wistar
14.
IJPR-Iranian Journal of Pharmaceutical Research. 2015; 14 (2): 547-557
in English | IMEMR | ID: emr-167961

ABSTRACT

Regarding the therapeutic properties of Nigella sativa [NS], the effects of the plant hydro–alcoholic extract on learning, memory and brain tissues oxidative damage were investigated in penthylenetetrazole [PTZ]-induced repeated seizures. There were 4 experimental groups including: 1- control group; received saline, 2- PTZ group; received saline and PTZ [50 mg/Kg, i.p], 3- PTZ-NS 200 and 4- PTZ-NS 400 ; received 200 and 400 mg/Kg of NS extract respectively, before PTZ injection in 5 consecutive days. Seizure scores were lower in PTZ–NS 200 and 400, furthermore the seizure onset latencies were higher in these groups than PTZ group [P<0.05 and P<0.01]. In Morris water maze, the time spent in target quadrant by PTZ group was lower than control group [P<0.05]; while, 400 mg/Kg of the extract increased it [P<0.01]. In the passive avoidance test, delay time to enter the dark by PTZ group was lower than control at 1 and 24 hours after training [P<0.01 - P<0.001]; while, 400 mg/Kg of the extract increased it [P<0.05]. The total thiol concentration in hippocampal and cortical tissues of PTZ group was reduced while, MDA concentration was higher than control [p<0.05 - p<0.001]. Administration of the extract increased the total thiol and decreased the MDA concentrations [p<0.01 - p<0.001]. It is concluded that the hydro-alcoholic extract of NS possess beneficial effects on learning and memory impairments in repeated seizures model which is accompanied by antioxidant effects in the brain


Subject(s)
Animals, Laboratory , Plant Extracts , Memory/drug effects , Brain/drug effects , Oxidative Stress , Seizures , Rats, Wistar , Pentylenetetrazole
15.
Journal of Korean Academy of Nursing ; : 118-128, 2015.
Article in Korean | WPRIM | ID: wpr-69478

ABSTRACT

PURPOSE: Evidence suggests that some patients with breast cancer experience cognitive difficulties following chemotherapy. This longitudinal study was done to examine the prevalence of cognitive impairment and trajectory of cognitive function over time in women with breast cancer, who received adjuvant chemotherapy. METHODS: Participants were 137 patients with breast cancer. They completed neuropsychological tests and the Functional Assessment of Cancer Therapy-Cognitive Function before adjuvant therapy (pretest), toward the end of adjuvant therapy (posttest), and 6 months after the completion of adjuvant therapy (follow-up test). Of the patients, 91 were treated with adjuvant chemotherapy and 46 patients who did not receive chemotherapy made up the comparison group. A reliable-change index and repeated-measure ANOVA were used for statistical analyses. RESULTS: At the posttest point, over 30% of patients showed complex cognitive impairment and reported greater difficulty in subjective cognitive function. At the follow-up test point, 22.0% of patients exhibited complex cognitive impairment and 30.8% of patients complained of subjective cognitive impairment. Repeated-measure ANOVA showed significant decreases after receiving chemotherapy followed by small improvements 6 months after the completion of chemotherapy in cognitive domains of change for attention and concentration, memory, executive function, and subjective cognitive function. CONCLUSION: These results suggest that chemotherapy in patients with breast cancer may be associated with objective and subjective cognitive impairments. Further studies are needed to explore the potential risk factors and predictor of chemotherapy-related cognitive changes. Also nursing interventions for prevention and intervention of cognitive impairments should be developed and tested.


Subject(s)
Adult , Female , Humans , Middle Aged , Analysis of Variance , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Attention/drug effects , Breast Neoplasms/drug therapy , Chemotherapy, Adjuvant , Cognitive Dysfunction/epidemiology , Longitudinal Studies , Memory/drug effects
16.
Braz. j. med. biol. res ; 47(2): 135-143, 2/2014. tab, graf
Article in English | LILACS | ID: lil-699772

ABSTRACT

This study investigated the effects of histamine H1 or H2 receptor antagonists on emotional memory consolidation in mice submitted to the elevated plus maze (EPM). The cerebellar vermis of male mice (Swiss albino) was implanted using a cannula guide. Three days after recovery, behavioral tests were performed in the EPM on 2 consecutive days (T1 and T2). Immediately after exposure to the EPM (T1), animals received a microinjection of saline (SAL) or the H1 antagonist chlorpheniramine (CPA; 0.016, 0.052, or 0.16 nmol/0.1 µL) in Experiment 1, and SAL or the H2 antagonist ranitidine (RA; 0.57, 2.85, or 5.7 nmol/0.1 µL) in Experiment 2. Twenty-four hours later, mice were reexposed to the EPM (T2) under the same experimental conditions but they did not receive any injection. Data were analyzed using one-way ANOVA and the Duncan test. In Experiment 1, mice microinjected with SAL and with CPA entered the open arms less often (%OAE) and spent less time in the open arms (%OAT) in T2, and there was no difference among groups. The results of Experiment 2 demonstrated that the values of %OAE and %OAT in T2 were lower compared to T1 for the groups that were microinjected with SAL and 2.85 nmol/0.1 µL RA. However, when animals were microinjected with 5.7 nmol/0.1 µL RA, they did not show a reduction in %OAE and %OAT. These results demonstrate that CPA did not affect behavior at the doses used in this study, while 5.7 nmol/0.1 µL RA induced impairment of memory consolidation in the EPM.


Subject(s)
Animals , Male , Mice , Cerebellar Vermis/drug effects , Chlorpheniramine/pharmacology , Emotions/drug effects , Histamine H1 Antagonists/pharmacology , /pharmacology , Memory/drug effects , Ranitidine/pharmacology , Microinjections , Memory/physiology
17.
Pejouhandeh: Bimonthly Research Journal. 2014; 19 (2): 78-85
in Persian | IMEMR | ID: emr-148850

ABSTRACT

Alzheimer's disease [AD] is the most familiar disease, which leads to dementia. There are many studies to find the pretreatment and treating drugs in this disease. Many herbs show the protective effect against AD. The protective role of Salvia genus in neurodegenerative disease is well established. In this study, we evaluated the protective role of Salvia hydrangea [S. hydrangea] extract on AD model. Rats were gavaged for 10 days by S. hydrangea. Subsequently, rats were injected by amyloid beta and were tested by shuttle box. The molecular level of Ca[2+]/cAMP response element binding [CREB], caspase-3 antioxidant and acetylcholine esterase activity were evaluated. Our results demonstrated that S. hydrangea could improve memory in AD models rats. S. hydrangea increased antioxidant activity and CREB phosphorylation in pretreated rats. Treating by S. hydrangea decreased neuronal apoptosis in the hippocampus and frontal cortex. Chromatographic analysis showed that S. hydrangea has phenolic compounds such as gentisic acid, chlorogenic acid, caffeic and syringic acid. Our results suggested that S. hydrangea contain a dominant potential in prevention of AD


Subject(s)
Animals, Laboratory , Memory/drug effects , Apoptosis , CREB-Binding Protein , Phosphorylation , Models, Animal , Rats , Alzheimer Disease , Acetylcholinesterase , Antioxidants
18.
Gut and Liver ; : 7-12, 2014.
Article in English | WPRIM | ID: wpr-208928

ABSTRACT

BACKGROUND/AIMS: Flumazenil was administered after the completion of endoscopy under sedation to reduce recovery time and increase patient safety. We evaluated patient satisfaction after endoscopy under sedation according to the timing of a postprocedural flumazenil injection. METHODS: In total, 200 subjects undergoing concurrent colonoscopy and upper endoscopy while sedated with midazolam and meperidine were enrolled in our investigation. We randomly administered 0.3 mg of flumazenil either immediately or 15 minutes after the endoscopic procedure. A postprocedural questionnaire and next day telephone interview were conducted to assess patient satisfaction. RESULTS: Flumazenil injection timing did not affect the time spent in the recovery room when comparing the two groups of patients. However, the subjects in the 15 minutes injection group were more satisfied with undergoing endoscopy under sedation than the patients in the immediate injection group according to the postprocedural survey (p=0.019). However, no difference in overall satisfaction, memory, or willingness to undergo a future endoscopy was observed between the two groups when the telephone survey was conducted on the following day. CONCLUSIONS: This study demonstrated that a delayed flumazenil injection after endoscopic sedation increased patient satisfaction without prolonging recovery time, even though the benefit of the delayed flumazenil injection did not persist into the following day.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Anesthesia Recovery Period , Endoscopy/adverse effects , Flumazenil/administration & dosage , GABA Modulators/administration & dosage , Memory/drug effects , Pain/epidemiology , Patient Satisfaction , Prospective Studies , Time Factors , Treatment Outcome
19.
Indian J Exp Biol ; 2013 Dec; 51(12): 1094-1100
Article in English | IMSEAR | ID: sea-150297

ABSTRACT

Chronic administration of aged garlic extract has been shown to prevent memory impairment in mice. Acute and chronic (21 days) effects of marketed formulation of crude garlic extract (Lasuna) were evaluated on learning and memory in mice using step down latency (SDL) by passive avoidance response and transfer latency (TL) using elevated plus maze. Scopolamine (0.4 mg/kg, ip) was used to induce amnesia in mice and piracetam (200 mg/kg, ip) served as positive control. In the acute study, Lasuna (65 mg/kg, po) partially reversed the scopolamine-induced amnesia but failed to improve learning and memory in untreated animals. Chronic administration of Lasuna (40 mg/kg/day for 21 days) significantly improved learning both in control and scopolamine induced amnesic animals. Influence of Lasuna on central cholinergic activity and its antioxidant properties were also studied by estimating the cortical acetylcholinesterase (AchE) activity and reduced glutathione (GSH) levels respectively. Chronic administration of Lasuna inhibited AchE, while increasing GSH levels. Thus the results indicate that long-term administration of crude garlic extract may improve learning and memory in mice while the underlying mechanism of action may be attributed to the anti-AchE activity and anti-oxidant property of garlic.


Subject(s)
Acetylcholinesterase/metabolism , Amnesia/chemically induced , Amnesia/drug therapy , Amnesia/metabolism , Amnesia/pathology , Animals , Antioxidants/administration & dosage , Antioxidants/chemistry , Avoidance Learning/drug effects , Brain/drug effects , Brain/metabolism , Garlic/chemistry , Glutathione/metabolism , Humans , Learning/drug effects , Maze Learning/drug effects , Memory/drug effects , Mice , Oxidative Stress , Plant Extracts/administration & dosage , Plant Extracts/chemistry , Scopolamine/toxicity
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