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1.
Article in Spanish | LILACS, CUMED | ID: biblio-1515286

ABSTRACT

Introducción: La masturbación compulsiva provoca una cascada de sentimientos y emociones que pueden recorrer desde la culpabilidad y el rechazo a la satisfacción hasta el bienestar más placentero y deseado. Objetivo: Exponer una forma de presentación poco frecuente de un adolescente con masturbación compulsiva. Presentación del caso: Adolescente masculino de 14 años de edad, de procedencia rural y antecedentes de salud física. Evaluado en consulta de psiquiatría infanto - juvenil por realizar masturbaciones en sitios públicos, que resultaban cada vez más frecuentes, y al final de esta se producía expulsión de materia fecal. Los estudios clínicos y psicométricos confirmaron el diagnóstico de masturbación compulsiva. Conclusiones: El tratamiento se basó en el modelo cognitivo-conductual y farmacológico con imipramina. Se disminuyó la frecuencia e intensidad, así como la duración de la conducta problema. El caso clínico expuesto resulta de interés por ser poco frecuente la presencia de este trastorno dentro de la población adolescente(AU)


Introduction: Compulsive masturbation provokes a cascade of feelings and emotions that can range from guilt and refusal to satisfaction to the most pleasurable and desired well-being. Aim: To present a rare presentation of an adolescent with compulsive masturbation. Case presentation: 14-year-old male adolescent from a rural area with a history of previous physical health. He was evaluated in a child and adolescent psychiatry clinic for masturbation in public places, which became increasingly frequent and ended with the expulsion of fecal matter. Clinical and psychometric studies confirmed the diagnosis of compulsive masturbation. Conclusions: Treatment was based on the cognitive-behavioral and pharmacological model with imipramine. The frequency and intensity, as well as the duration of the problem behavior was reduced. The clinical case presented was of interest due to the infrequent presence of this disorder in the adolescent population(AU)


Subject(s)
Humans , Male , Adolescent , Pedophilia , Referral and Consultation , Imipramine/therapeutic use , Masturbation/diagnosis , Psychometrics/methods
2.
J. Health Biol. Sci. (Online) ; 10(1): 1-12, 01/jan./2022. tab, ilus
Article in English | LILACS | ID: biblio-1378476

ABSTRACT

Objective: Analyze lysosomotropic agents and their action on COVID-19 targets using the molecular docking technique. Methods: Molecular docking analyses of these lysosomotropic agents were performed, namely of fluoxetine, imipramine, chloroquine, verapamil, tamoxifen, amitriptyline, and chlorpromazine against important targets for the pathogenesis of SARS-CoV-2. Results: The results revealed that the inhibitors bind to distinct regions of Mpro COVID-19, with variations in RMSD values from 1.325 to 1.962 Å and binding free energy of -5.2 to -4.3 kcal/mol. Furthermore, the analysis of the second target showed that all inhibitors bonded at the same site as the enzyme, and the interaction resulted in an RMSD variation of 0.735 to 1.562 Å and binding free energy ranging from -6.0 to -8.7 kcal/mol. Conclusion: Therefore, this study allows proposing the use of these lysosomotropic compounds. However, these computer simulations are just an initial step toward conceiving new projects for the development of antiviral molecules.


Objetivo: aAnalisar agentes lisossomotrópicos e sua ação em alvos de COVID-19 usando a técnica de docking molecular. Métodos: Foram realizadas análises de docagem molecular destes agentes lisossomotrópicos, nomeadamente de fluoxetina, imipramina, cloroquina, verapamil, tamoxifeno, amitriptilina e clorpromazina contra alvos importantes para a patogenia do SARS-CoV-2. Resultados: Os resultados revelaram que os inibidores se ligam a regiões distintas do Mpro COVID-19, com variações nos valores de RMSD de 1.325 a 1.962 Å e energia livre de ligação de -5,2 a -4,3 kcal/mol. Além disso, a análise do segundo alvo mostrou que todos os inibidores se ligaram no mesmo sítio da enzima, e a interação resultante em uma variação de RMSD de 0,735 a 1.562 Å e energia livre de ligação variando de -6,0 a -8,7 kcal/mol. Conclusão: Portanto, este estudo permite propor o uso desses compostos lisossomotrópicos. No entanto, essas simulações em computador são apenas um passo inicial para a concepção de novos projetos para o desenvolvimento de moléculas antivirais.


Subject(s)
SARS-CoV-2 , COVID-19 , Antiviral Agents , Chloroquine , Mass Screening , Fluoxetine , Amitriptyline , Imipramine
4.
Porto Alegre; Universidade Federal do Rio Grande do Sul. Telessaúde; 2017.
Non-conventional in Portuguese | LILACS | ID: biblio-995604

ABSTRACT

A ansiedade pode ser vista como sintoma psiquiátrico e/ou como reação emocional não patológica associada a diversos contextos de vida. Ela representa um sinal de alarme a determinado estímulo percebido pelo indivíduo como perigoso. Em geral, é composta por uma combinação variável de sintomas físicos, pensamentos catastróficos e alterações de comportamento. A ansiedade pode ser compreendida como mecanismo evolutivo, isto é, uma ferramenta que nos ajuda a detectar o perigo e adotar as medidas necessárias para lidar com ele. No entanto, esse recurso adaptativo muitas vezes encontra-se desregulado, causando sofrimento e prejuízo ao desempenho social e/ou profissional. A ansiedade se torna um transtorno psiquiátrico quando representa emoção desconfortável e inconveniente, surgindo na ausência de um estímulo externo claro ou com magnitude suficiente para justificá-la, e apresenta intensidade, persistência e frequência desproporcionais. Estudos epidemiológicos indicam os transtornos de ansiedade como os mais prevalentes dentre os transtornos psiquiátricos. Na grande maioria dos casos, não há como estabelecer uma causa específica aos transtornos aqui tratados. A interação entre fatores genéticos e ambientais resume a etiologia atualmente proposta e aceita. Esta guia apresenta informação que orienta a conduta para casos de ansiedade no contexto da Atenção Primária à Saúde, incluindo: Diagnóstico, Diagramas diagnósticos, Condições de saúde associadas aos sintomas, Fármacos associados aos sintomas, Abordagem psicoeducativa/psicossocial, Tratamento conforme diagnóstico, Medicamentos e dose, Quando encaminhar.


Subject(s)
Humans , Anxiety/diagnosis , Anxiety/therapy , Primary Health Care , Citalopram/therapeutic use , Cognitive Behavioral Therapy , Paroxetine/therapeutic use , Sertraline/therapeutic use , Venlafaxine Hydrochloride/therapeutic use , Duloxetine Hydrochloride/therapeutic use , Imipramine/therapeutic use
5.
Psychiatry Investigation ; : 74-80, 2017.
Article in English | WPRIM | ID: wpr-71427

ABSTRACT

OBJECTIVE: The aims of the present study were to explore the behavioural effects and to understand the possible mode of action of Bacopa monnieri extract (BME) on chronic unpredictable stress (CUS) induced depressive model and the biochemical alterations such as brain derived neurotrophic factor (BDNF), Akt, cyclic-AMP response element binding (CREB) protein level in the hippocampus of rats. METHODS: We examined the effects of chronic administration of BME on CUS exposed rats for 28 days. Behavioural changes were assessed by sucrose consumption and open field test to assess the effect of BME on CUS-induced depression. The mechanisms underlying antidepressant like action of BME was further evaluated by measuring levels of BDNF, Akt, and CREB in the hippocampus of rat brain and compared with the standard tricyclic antidepressant drug imipramine (20 mg/kg body weight). RESULTS: Exposure to CUS for 28 days produced depression-like behavior in rats, as indicated by significant decreases in sucrose consumption, locomotor activity including decreased BDNF, Akt and CREB levels in the hippocampus. Daily administration of BME at a dose of (80 mg/kg body weight) significantly reverses the behavioral alteration and restored the normal level of BDNF, total and phospho-Akt, total and phospho CREB in the hippocampus of CUS induced rats as compared to vehicle treated control rats. CONCLUSION: These findings suggest that BME ameliorates CUS induced behavioural depression in rats and that can be used as a potent therapeutic agent in treating depressive like behavior.


Subject(s)
Animals , Rats , Bacopa , Brain , Brain-Derived Neurotrophic Factor , Depression , Hippocampus , Imipramine , Motor Activity , Response Elements , Sucrose
6.
Journal of the Korean Medical Association ; : 796-799, 2017.
Article in Korean | WPRIM | ID: wpr-16251

ABSTRACT

Nocturnal enuresis is a common problem of children during sleeping at preschool or school age. It may affect negatively the psychosocial development of children. Children with enuresis may have lower self-esteem and lower quality of life. There are three main factors of the pathophysiology of enuresis: high nocturnal urine production, nocturnal low bladder capacity or increased detrusor muscle activity, and arousal disorder. As pharmacological therapy for nocturnal enuresis, several medications including desmopressin, anticholinergics, imipramine have been used for a long time. As first-line therapy, desmopressin combined with anticholinergics has good response in primary monosymptomatic nocturnal enuresis. Because imipramine has serious and lethal cardiotoxic effect with overdosage, imipramine should be prescribed after EKG to rule out the conduction problem of heart.


Subject(s)
Child , Humans , Arousal , Cholinergic Antagonists , Deamino Arginine Vasopressin , Electrocardiography , Enuresis , Heart , Imipramine , Nocturnal Enuresis , Quality of Life , Urinary Bladder
7.
Bogotá; IETS; mayo 2016. tab, graf, ilus.
Monography in Spanish | LILACS, BRISA | ID: biblio-846680

ABSTRACT

Problema de investigación: Describir los costos y la efectividad de escitalopram comparado con paroxetina, sertralina, fluoxetina, imipramina y fluvoxamina como terapia de mantenimiento en adultos con diagnóstico de trastorno de pánico en Colombia. Tipo de evaluación económica: Análisis de costo-efectividad. Población objetivo: Adultos colombianos con diagnóstico de trastorno de pánico. Intervención y comparadores: Intervención: escitalopram, Comparadores: paroxetina, sertralina, fluoxetina, imipramina y fluvoxamina. Horizonte temporal: 32 semanas. Perspectiva: SGSSS de Colombia. Tasa de descuento: No aplica. Estructura del modelo: Se estructuró un árbol de decisión, teniendo en cuenta modelos publicados en la literatura. Fuentes de datos de efectividad y seguridad: Reporte de efectividad y seguridad elaborado en diciembre de 2014 en el IETS, Ensayo s clínicos a leatorizados. Desenlaces y valoración: Ausencia de crisis de pánico, Semanas libres de crisis de pánico. Costos incluidos: Costo de los medicamentos, Costo de procedimientos, Costo de los eventos adversos. Fuentes de datos de costos: SISMED, Manual tarifario ISS 2001. Resultados del caso base: Para el caso base, escitalopram, fluvoxamina y fluoxetina e imipramina fueron tecnologías dominadas por sertralina y paroxetina. El costo adicional por crisis de pánico evitada en tratamiento con paroxetina comparado con trasertralina se estimó en $4.814.953. Análisis de sensibilidad: Los análisis de sensibilidad y el diagrama de tornado muestran a la probabilidad de lograr ausencia de crisis de pánico y la probabilidad de recaída, como a las variables con mayor impacto sobre las estimaciones de la razón de costo-efectividad. Conclusiones y discusión: De acuerdo con los hallazgos aquí presentados, paroxetina, ofrece mayor razón de costo-efectividad, respecto a sus comparadores. No obstante, es \r\nnecesario tener en cuenta que cualquiera de las alternativas aquí estudiadas, puede ser costo-efectiva, debido a que las pequeñas variaciones en la probabilidad de ausencia de crisis de pánico pueden cambiar el resultado. La principal limitación de este estudio es la ausencia de información roveniente de estudios de investigación clínica, que muestre el desempeño comparativo entre las tecnologías, así como el seguimiento de los participantes en los estudios, en escenarios de más largo plazo que los existentes al momento de elaborar este documento.(AU)


Subject(s)
Humans , Adult , Preventive Maintenance , Panic Disorder/therapy , Health Evaluation/economics , Citalopram/therapeutic use , Fluoxetine/therapeutic use , Fluvoxamine/therapeutic use , Cost-Benefit Analysis/economics , Paroxetine/therapeutic use , Sertraline/therapeutic use , Biomedical Technology , Imipramine/therapeutic use
8.
Acta Physiologica Sinica ; (6): 12-18, 2016.
Article in Chinese | WPRIM | ID: wpr-331688

ABSTRACT

The aim of the present study was to investigate the effects of ketamine, imipramine, and ketamine plus imipramine on chronic depression-like behaviors of Wistar Kyoto (WKY) rats and underlying mechanism. Six-week-old Wistar rats were used as normal control. WKY rats, depression model animal, were injected intraperitoneally with ketamine (1 week, replaced with saline in 2(nd) week), imipramine (2 weeks), or ketamine in combination with imipramine. The depression-like behaviors were assessed by sucrose preference and forced swimming tests. Protein expressions of β form of calcium/calmodulin-dependent protein kinase type II (βCaMKII) and membrane fraction of glutamate receptor 1 (GluR1) were measured in corresponding brain tissue with Western blot. The results showed that, compared with Wistar rats, WKY rats exhibited decreased sucrose preference and extended immobility time. Ketamine alone did not affect depression-like behaviors of WKY, whereas imipramine or its combination with ketamine could significantly decrease the immobility time. Compared with Wistar rats, WKY rats showed up-regulated levels of βCaMKII and membrane GluR1 protein expressions in habenula, and down-regulated level of membrane GluR1 protein expressions in the prefrontal cortex. Imipramine or its combination with ketamine could reverse these changes of protein expressions in WKY rats. There was no difference in reversing effect between imipramine and its combination with ketamine. Ketamine alone did not affect the βCaMKII and membrane GluR1 protein expressions in the habenula, but increased membrane GluR1 protein expression in the prefrontal cortex of WKY rats. These results suggest 2-week imipramine treatment significantly improves depressive behavior in WKY rats; however, the addition of ketamine in the first week fails to enhance the effect of imipramine. The underlying mechanisms of imipramine's anti-depressive effect may be associated with the down-regulation of βCaMKII and membrane GluR1 in the habenula, as well as the up-regulation of membrane GluR1 in the prefrontal cortex.


Subject(s)
Animals , Male , Rats , Brain , Depression , Depressive Disorder , Disease Models, Animal , Down-Regulation , Imipramine , Ketamine , Rats, Inbred WKY , Swimming , Up-Regulation
9.
Evid. actual. práct. ambul ; 19(3): 71-75, 2016. ilus, graf, tab
Article in Spanish | LILACS | ID: biblio-1150657

ABSTRACT

El emblemático ensayo clínico 329, financiado por Smith Kline Beecham (actualmente GlaxoSmith-Kline) y publicado en2001, permitió posicionar a la paroxetina como un tratamiento efectivo y seguro para la depresión mayor en adolescentes. En la presente editorial el autor describe los sucesos ocurridos luego de su publicación, partiendo de los cuestionamientos iniciales respecto de su eficacia, hasta llegar a los resultados de su reciente reanálisis (llevando adelante por la iniciativa internacional RIAT), el cual concluyo que dicho fármaco no solo no provee un beneficio adicional al placebo para la condición y población utilizada, sino que además se asocia a efectos adversos sustanciales que no habían sido reportados en el informe original. Se exploran además las repercusiones de este suceso en la comunidad científica y se hace un señalamiento de la necesidad de permitir el acceso a las bases de datos originales que sustentan los resultados y conclusiones de las investigaciones publicadas, como mecanismo de transparencia superador a la revisión por pares. (AU)


The emblematic 329 study, funded by Smith Kline Beecham (now GlaxoSmith-Kline) and published in 2001, allowed to position paroxetine as an effective and safe treatment for major depression in adolescents. In this editorial, the author describes the events after its publication, from the initial concerns about its effectiveness, to the results of its recent reanalysis (accounted by the international RIAT initiative), which concluded that the drug not only does not provide an additional benefit than placebo, but is also associated with significant adverse effects that were not reported in the original report. It also explores the repercussions generated in the scientific community by this event, pointing out the need to allow access to original databases that support the findings and conclusions of published research, as an overcoming mechanism for transparency to the traditional peerreview. Agustín Ciapponi Study's 329 hiddens face and scientifics evidence manipulation. (AU)


Subject(s)
Humans , Male , Female , Adolescent , Clinical Trials as Topic/ethics , Paroxetine/adverse effects , Peer Review/ethics , Suicide/statistics & numerical data , Analysis of Variance , Clinical Trials as Topic/instrumentation , Clinical Trials as Topic/methods , Databases as Topic/trends , Depression/drug therapy , Research Financing , Off-Label Use/ethics , Suicidal Ideation , Imipramine/administration & dosage
11.
MedicalExpress (São Paulo, Online) ; 2(3)May-June 2015. tab, graf
Article in English | LILACS | ID: lil-776651

ABSTRACT

OBJECTIVE: The present study aims to analyze the effect of pharmacological treatment for panic disorder on temperament and character dimensions and to compare the effect of imipramine and fluoxetine on this outcome. METHOD: Temperament and character dimensions were evaluated in panic disorder patients before and after six months of pharmacological treatment with imipramine and fluoxetine, using the Temperament and Character Inventory-Revised. Patients were randomized between groups and both (patient and investigators) were blinded to the intervention drug. Furthermore, 34 non-panic controls answered the revised Temperament and Character Inventory through an Internet survey. RESULTS: Panic disorder patients showed higher scores for Harm Avoidance and lower scores for Persistence, Self-Directedness, and Cooperativeness than controls at baseline, but only the low Persistence value remained different from controls after treatment. Responder patients presented significant reduction in Harm Avoidance scores and a significant increase in Self-Directedness scores, whereas non-responders showed a significant increase of Harm Avoidance levels. Fluoxetine and Imipramine showed similar effects on the revised Temperament and Character Inventory dimensions. CONCLUSION: High Harm Avoidance and low Self-Directedness, Persistence, and Cooperativeness are associated with panic disorder. Treatment of acute panic disorder symptoms lead to the reduction of Harm Avoidance and to an increase in Self-Directedness scores. However, there was no difference between treatment with fluoxetine and imipramine for the effect on the revised Temperament and Character Inventory dimensions.


OBJETIVO: O presente estudo tem como objetivo analisar o efeito do tratamento farmacológico do transtorno do pânico nas dimensões de temperamento e caráter, comparando os efeitos das medicações imipramina e fluoxetina neste desfecho. METODOLOGIA: As dimensões de temperamento e caráter foram avaliadas em pacientes com transtorno do pânico antes e depois de seis meses de tratamento com imipramina ou fluoxetina, utilizando-se o "Temperament and Character Inventory- Revised" (TCI-R). O estudo foi randomizado e duplo-cego. Além disso, 34 controles sem transtorno do pânico responderam ao TCI-R via internet. RESULTADOS: Pacientes com transtorno do pânico apresentaram maior pontuação para "Harm Avoidance" e menor pontuação para "Persistence", "Self-Directedness" e "Cooperativeness" que os controles antes do tratamento, mas apenas "Persistence" manteve a diferença após o tratamento. Pacientes respondedores apresentaram redução significativa da pontuação para "Harm Avoidance" e aumento significativo para "Self-Directedness" após o tratamento, enquanto os não-respondedores mostraram aumento significativo na pontuação para "Harm Avoidance". A fluoxetina e a imipramina apresentaram efeitos semelhantes nas dimensões do TCI-R. CONCLUSÃO: Alta pontuação para "Harm Avoidance" e baixa para "Persistence", "Self-Directness" e "Cooperativeness" estão associados ao transtorno do pânico. O tratamento sintomático do transtorno do pânico leva a redução da pontuação para "Harm Avoidance" e aumento de pontuação para "Self-Directedness". No entanto, não há diferença entre os efeitos da imipramina e da fluoxetina nestas dimensões do TCI-R.


Subject(s)
Humans , Temperament , Character , Fluoxetine/therapeutic use , Panic Disorder/drug therapy , Imipramine/therapeutic use
12.
Rev. chil. urol ; 80(2): 32-36, 2015. tab, graf
Article in Spanish | LILACS | ID: lil-786485

ABSTRACT

El síndrome de dolor vesical (SDV) es un cuadro que forma parte del dolor pelviano crónico (DPC), donde el origen del dolor esta en mecanismos de neuromodulación. En este sentido, los antidepresivos tricíclicos (ATC), especialmente amitriptilina, son la terapia de primera línea. Sin embargo, los efectos adversos dificultan la adherencia a la terapia. Imipramina, otro ATC, presenta menores efectos adversos, aunque su eficacia no ha sido evaluada en SDV. Objetivo: Evaluar la eficacia de imipramina en el tratamiento de SDV en un estudio piloto. Metodología: Veinte pacientes con diagnóstico de SDV, fueron tratadas con imipramina 25 mg cada 8 horas vía oral durante 30 días. Se evaluó intensidad de dolor según EVA antes y al término del tratamiento. Además se evaluó sintomatología urinaria utilizando el cuestionario PUF. Resultados: Diecinueve pacientes completaron el tratamiento. Una paciente abandonó el tratamiento por síntomas gastrointestinales. Ocho de 19 pacientes mostraron una mejoría total del dolor al término del tratamiento. Tres pacientes más lograron una respuesta completa con 3 meses de tratamiento con imipramina. La intensidad del dolor según EVA y la puntuación en el cuestionario PUF mejoraron significativamente al término del tratamiento. Efectos secundarios a imipramina fueron referidos por 4 de 19 pacientes, y fueron menores. Conclusión: Imipramina mostró ser una terapia efectiva en el manejo de SDV, con efectos adversos menores. Se requieren estudios comparativos con mayor número de pacientes para considerar su utilidad clínica en el manejo del SDV...


Bladder pain syndrome (BPS) is a symptom which is part of chronic pelvic pain (CPP), where the origin of the pain is in the neuromodulation mechanisms. In this context, tricyclic antidepressants (TCAs), especially amitriptyline, are a first line therapy. However, adverse effects make continuing with the therapy difficult. Imipramine, another TCA, has lesser adverse effects, although its effectiveness has not been evaluated in BPS. Objective: Evaluate the effectiveness of imipramine in the treatment of BPS in a pilot study. Methodology: Twenty patients with a diagnosis of BPS were treated taking 25 mg of imipramine orally every 8 hours, for 30 days. The intensity of the pain following PIS was evaluated before and after the treatment. In addition, the urinary symptomatology was evaluated using the PUF questionnaire. Results: Nineteen patients completed the treatment. One patient abandoned the treatment due to gastrointestinal symptoms. Eight of the 19 patients had completely recovered at the end of the treatment. Three other patients achieved a complete recovery after 3 months of treatment with imipramine. The intensity of the pain following the PIS, and the score on the PUF questionnaire, significantly improved by the end of the treatment. Secondary effects to imipramine were referred by 4 of the 19 patients, and these were minor. Conclusion: Imipramine was shown to be an effective therapy for dealing with BPS, with minor adverse effects. Comparative studies are required with a higher number of patients to consider its clinical use in the handling of BPS...


Subject(s)
Humans , Female , Adult , Middle Aged , Antidepressive Agents, Tricyclic/therapeutic use , Pelvic Pain/drug therapy , Urinary Bladder Diseases/drug therapy , Imipramine/therapeutic use , Cystitis, Interstitial , Pain Measurement , Pelvic Pain/etiology , Urinary Bladder Diseases/complications , Prospective Studies , Pilot Projects
13.
Yeungnam University Journal of Medicine ; : 85-89, 2015.
Article in English | WPRIM | ID: wpr-89915

ABSTRACT

BACKGROUND: We examined the usefulness of urine osmolality, as a predictive factor in the treatment of monosymptomatic nocturnal enuresis (NE) with combination therapy of imipramine and desmopressin. METHODS: From May 2014 to April 2015, 59 monosymptomatic NE patients participated in this study. Early morning urine osmolality was measured at 1 week and 1 day before combination therapy of imipramine and desmopressin, and at 1 week and 2 weeks after therapy. The response to combination therapy was evaluated at 3 months after treatment. The mean period of combination therapy was 6.4+/-4.2 weeks. Therapeutic response was classified as complete (0-1 wet night/week), partial (over 50% reduction of night) and non-responders (less than 50% reduction of night). RESULTS: The cumulative rate of the complete and partial responders was 76.3%. Among the 3 groups, the statistically lowest value of pre-treatment urine osmolality was observed in the complete responder group (p<0.001). Urine osmolality increased in all groups after treatment, however, statistically the greatest difference between pre and post-treatment urine osmolality was observed in the complete responder group (p=0.024). No serious side effects were observed. CONCLUSION: Early morning urine osmolality and change of urine osmolality between pre and post-treatment have predictive values in the response to combined imipramine and desmopressin for treatment of monosymptomatic NE.


Subject(s)
Humans , Deamino Arginine Vasopressin , Enuresis , Imipramine , Nocturnal Enuresis , Osmolar Concentration
14.
Experimental Neurobiology ; : 156-168, 2015.
Article in English | WPRIM | ID: wpr-30210

ABSTRACT

Antidepressants are clinically used for patients with major depression. Antidepressant treatments in certain groups of patients are effective for relieving depression as well as anxiety disorder. However, it is not clearly known whether the use of current antidepressants in healthy persons is beneficial for upcoming depression- and anxiety-inducing life events. To address this question, normal mice were intraperitoneally administered with imipramine or fluoxetine for more than 2 weeks, and behaviors related to anxiety and depression were evaluated. Mice treated with imipramine or fluoxetine for more than 14 days exhibited significantly decreased immobility time in the forced swim test and tail suspension test, but these mice exhibited enhanced anxiety in several behavioral tests. Furthermore, chronic antidepressant treatments followed by sub-threshold level of stress in normal mice profoundly aggravated antidepressant-induced anxiety-like behaviors without further affecting depression-related behaviors. Chronic antidepressant treatments followed by sub-threshold level of stress produced swollen vesicles and ulcerations on the lips as well as a watery and inflammatory nose. Mice given chronic antidepressant treatments displayed intestinal abnormalities evidenced by a highly enlarged and inflamed small intestine full of defecation materials. These results suggest that chronic antidepressant treatment in normal mice provokes anxiety-like behaviors and impairs their stress-coping ability.


Subject(s)
Animals , Humans , Mice , Antidepressive Agents , Anxiety Disorders , Anxiety , Defecation , Depression , Fluoxetine , Hindlimb Suspension , Imipramine , Intestine, Small , Lip , Nose , Ulcer
15.
Bogotá; IETS; dic. 2014. 68 p. ilus.
Monography in Spanish | LILACS, BRISA | ID: biblio-847182

ABSTRACT

Introducción: La prevalencia de Trastorno de Pánico en la población general es del 2,7%; en Colombia tiene mayor incidencia en mujeres. El TP puede ir acompañado de depresión, consumo de sustancias adictivas como el alcohol, drogas, incrementando el riesgo de suicidio. El escitalopram y la risperidona, ha demostrado tener una respuesta adecuada en el control de los síntomas. Objetivo: Examinar los beneficios y riesgos del uso del escitalopram y la risperidona en el Trastorno de Pánico, como uno de los criterios para informar la toma de decisiones relacionada con la posible inclusión de tecnologías en el Plan Obligatorio de Salud, en el marco de su actualización integral para el año 2015. Metodología: A partir de la pregunta PICO se establecieron los criterios de elegibilidad para la realización de la búsqueda de la evidencia científica (a ensayos clínicos, revisiones sistemáticas de estudios observacionales y estudios de cohortes analíticas), se realizó la tamización y selección de la evidencia evaluando su calidad y posteriormente se realizó la extracción de datos y la síntesis de la evidencia. Resultados: El escitalopram es considerado medicamento de primera línea para el tratamiento de esta entidad mostrando mayor efectividad y seguridad que otros medicamentos. La risperidona a dosis no convencionales es efectiva en el control de síntomas y no presenta diferencia en la presencia de efectos adversos comparados con otros medicamentos utilizados para el tratamiento de esta entidad; no es considerado tratamiento de primera línea. Conclusiones: La interpretación de los resultados deben ser evaluados con precaución teniendo en cuenta las limitaciones de la evidencia científica y metodológica de los estudios incluidos. El escitalopram o la risperidona mostraron ser eficaces y seguros en el manejo del Trastorno de Pánico comparado con otros medicamentos que se emplean para el tratamiento de este mismo trastorno. (AU)


Subject(s)
Humans , Citalopram/administration & dosage , Panic Disorder/drug therapy , Psychotherapy/methods , Technology Assessment, Biomedical , Fluoxetine/administration & dosage , Reproducibility of Results , Treatment Outcome , Fluvoxamine/administration & dosage , Paroxetine/administration & dosage , Colombia , Risperidone/administration & dosage , Sertraline/administration & dosage , Imipramine/administration & dosage
16.
Einstein (Säo Paulo) ; 12(3): 310-313, Jul-Sep/2014.
Article in English | LILACS | ID: lil-723917

ABSTRACT

Objective To evaluate the use of a therapeutic regimen to treat attention deficit hyperactivity disorder patients. Methods A total of 140 patients initially underwent physical, neurological and laboratory evaluation. Thereafter, treatment was initiated with a compounding product consisting of a tricyclic antidepressant and an anxiolytic. Results The response was positive in 71.43% of patients in controlling hyperactivity and improving dispersion and attention deficit. Conclusion The therapeutic regimen utilized proved to be an effective therapeutic alternative, especially for patients who do not adapt to psychostimulant drugs. .


Objetivo Avaliar a aplicação de um esquema terapêutico para o tratamento do transtorno do déficit de atenção e hiperatividade. Métodos Os 140 pacientes foram submetidos inicialmente à avaliação clínico-neurológica e laboratorial. Posteriormente, foi iniciado um tratamento com medicamento formulado composto por um antidepressivo tricíclico e um ansiolítico. Resultados A resposta foi positiva em 71,43% dos pacientes no controle da hiperatividade e na melhoria do quadro de dispersão e desatenção. Conclusão O esquema terapêutico aplicado se mostrou uma alternativa terapêutica eficaz, especialmente para os pacientes que não se adaptam aos medicamentos psicoestimulantes. .


Subject(s)
Child , Humans , Anti-Anxiety Agents/therapeutic use , Antidepressive Agents, Tricyclic/therapeutic use , Attention Deficit Disorder with Hyperactivity/drug therapy , Chlordiazepoxide/therapeutic use , Imipramine/therapeutic use , Drug Therapy, Combination/methods , Retrospective Studies , Treatment Outcome
18.
The Korean Journal of Physiology and Pharmacology ; : 365-369, 2014.
Article in English | WPRIM | ID: wpr-728455

ABSTRACT

Cedrus deodara (Pinaceae) has been used traditionally in Ayurveda for the treatment of central nervous system disorders. 3,4-bis(3,4-dimethoxyphenyl)furan-2,5-dione (BDFD) was isolated from heart wood of Cedrus deodara and was shown to have antiepileptic and anxiolytic activity. Thus, the present study was aimed to explore its anti-depressant effect and to correlate the effect with serotonin and nor adrenaline levels of brain. Albino mice were used as experimental animal. Animals were divided in to three groups; vehicle control, imipramine (30 mg/kg i.p.), BDFD (100 mg/kg i.p.). Tail suspension test (TST) and forced swim test (FST) was performed to evaluate antidepressant effect of BDFD. BDFD (100 mg/kg, i.p.) showed a significant decrease in immobility time when subjected to FST whereas immobility time was not significantly altered in TST. BDFD treatment increased serotonin and noradrenaline levels in the brain which is indicative of BDFD having possible atypical antidepressant action.


Subject(s)
Animals , Mice , Brain , Cedrus , Central Nervous System Diseases , Epinephrine , Heart , Hindlimb Suspension , Imipramine , Norepinephrine , Rodentia , Serotonin , Wood
19.
Rev. cuba. pediatr ; 85(2): 213-220, abr.-jun. 2013.
Article in Spanish | LILACS | ID: lil-678133

ABSTRACT

Introducción: la enuresis, que se define como la emisión involuntaria de orina después de la edad en que el control vesical debía haberse alcanzado, alrededor de los 5 años, es un trastorno conocido desde épocas remotas, que ha merecido la atención de numerosos investigadores, y sobre el cual se plantean aún en la actualidad criterios muy disímiles en relación con su etiología. Objetivo: identificar la efectividad de la imipramina en la enuresis nocturna. Métodos: se investigan 150 niños de ambos sexos procedentes del área de salud del Policlínico Docente Plaza de la Revolución que presentaban enuresis nocturna, previamente estudiados, sin encontrar lesión orgánica. Se les impuso tratamiento con imipramina durante un año. Se analizan en estos pacientes variables como la edad y el sexo, se estudió la escolaridad, la clasificación de la enuresis, la frecuencia de las micciones y el umbral de sueño recogido de forma muy subjetiva. Resultados: se obtuvo que el grupo mayor de niños osciló entre los 6 a 8 años de edad, con predominio del sexo femenino en todos los grupos de edades. La escolaridad fue normal en 145 niños, que representa la inmensa mayoría de la muestra. Predominó ampliamente la enuresis primaria, que se manifestó en 148 pacientes, y fueron más frecuentes las micciones diarias y más de una vez por semana en el grupo de 6 a 8 años de edad. Casi todos los pacientes (132) permanecían dormidos después de orinarse. El tratamiento con imipramina se realizó con dosis crecientes de acuerdo con la edad, hasta una dosis máxima de 75 mg, y resultó eficaz en el 48,6 por ciento de los pacientes, en los cuales desapareció totalmente la sintomatología, y en un 28 por ciento se produjo mejoría en la presentación del síntoma. Conclusiones: la imipramina fue eficaz en la mayoría de los pacientes, pues desapareció totalmente la sintomatología


Introduction: enuresis, which is said to be the involuntary discharge of urine after the age at which the urinary control should has been achieved, that is, around 5 years-old, is a well-known disorder since ancient times. It has deserved the attention of numerous researchers but there are still very different criteria about its etiology at the present time. Objective: to identify the effectiveness of imipramine to treat night enuresis. Methods: one hundred and fifty children of both sexes with no previous lesions and night enuresis, who were attended at Plaza de la Revolucion teaching polyclinics, were studied. They were treated with imipramine for a year. Several variables such as age, sex, schooling, classification of enuresis, frequency of urination and sleep threshold, the latter being determined in a very subjective way, were all analyzed. Results: the elder group of children aged 6 to 8 years, with females predominating in all the age groups. Schooling was normal in 145 children who accounted for the vast majority of the sample. Primary enuresis extensively prevailed and the most frequent forms were daily involuntary urination and once a week in the 6-8 years-old group. Almost all the patients (132) remained asleep after urination. The imipramine-based treatment was given at growing doses, according to the age, up to maximum dose of 75 mg, and proved to be effective in 48.6 percent of patients, whose symptoms completely disappeared and in 28 percent of them who experienced some improvement in the presentation of symptoms. Conclusions: imipramine was effective in most of patients since the symptoms disappeared completely


Subject(s)
Humans , Male , Female , Child , Nocturnal Enuresis/drug therapy , Imipramine/therapeutic use
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