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1.
Article in Spanish | LILACS | ID: biblio-1428415

ABSTRACT

El manejo farmacológico del episodio depresivo en contexto del trastorno bipolar constituye un desafío para el clínico tanto en psiquiatría adultos como infantoadolescente. El presente trabajo tiene por objetivo actualizar y sintetizar la evidencia disponible respecto al manejo farmacológico para la depresión bipolar en población pediátrica. Metodología: Se realizó una búsqueda de las publicaciones de los últimos 5 años en bases de datos. Resultados: La evidencia muestra como primera línea el uso de antipsicóticos de segunda generación por sobre los estabilizadores del ánimo en este grupo etario; demostrando lurasidona y lanzapina/fluoxetina eficacia similares. Lurasidona es una opción con mejor perfil de seguridad por asociarse a menos efectos adversos y mejor adherencia. El uso de antidepresivos debe considerarse dentro de los pasos iniciales del manejo, asociado a un antipsicótico de segunda generación. Conclusiones: Se destaca la importancia de la sospecha, evaluación y diagnóstico adecuado para guiar la decisión de manejo integral. A pesar de los riesgos y consideraciones existentes, es importante considerar el uso en primera línea de antipsicóticos de segunda generación y de antidepresivos en el manejo de un cuadro depresivo en contexto de la enfermedad bipolar. La escasez de estudios en el tratamiento farmacológico de la depresión bipolar en general y especialmente en población pediátrica limita la generalización y extrapolación de los resultados a la realidad local.


The pharmacological management of the depressive episode in the context of bipolar disorder constitutes a challenge for the clinician both in adult and child-adolescent population. The objective of this paper is to update and synthesize the available evidence regarding the pharmacological management of bipolar depression in the pediatric population. Methodology: A search of the publications of the last 5 years in databases was carried out. Results: The evidence shows the use of second generation antipsychotics over mood stabilizers as the first line in this age group; demonstrating similar efficacy. Results: The evidence shows the use of second generation antipsychotics over mood stabilizers as the first line in this age group; demonstrating similar efficacy lurasidone and lanzapine/fluoxetine. Lurasidone is an option with a better safety profile as it is associated with fewer adverse effects and better adherence. The use of antidepressants should be considered within the initial steps of management, associated with a second generation antipsychotic. Conclusions: The importance of suspicion, evaluation and adequate diagnosis to guide the decision of comprehensive management is highlighted. Despite the existing risks and considerations, it is important to consider the first-line use of second-generation antipsychotics and antidepressants in the management of a depressive episode in the context of bipolar illness. The scarcity of studies on the pharmacological treatment of bipolar depression in general and especially in the pediatric population limits the generalization and extrapolation of the results to the local reality.


Subject(s)
Humans , Child , Adolescent , Bipolar Disorder/drug therapy , Antidepressive Agents, Second-Generation/therapeutic use , Depression/drug therapy , Antipsychotic Agents/therapeutic use , Lurasidone Hydrochloride/therapeutic use , Olanzapine/therapeutic use
2.
Braz. J. Psychiatry (São Paulo, 1999, Impr.) ; 42(2): 128-135, Mar.-Apr. 2020. tab
Article in English | LILACS | ID: biblio-1089246

ABSTRACT

Objective: We investigated whether single nucleotide polymorphisms (SNPs) associated with neuroplasticity and activity of monoamine neurotransmitters, such as the brain-derived neurotrophic factor (BDNF, rs6265), the serotonin transporter (SLC6A4, rs25531), the tryptophan hydroxylase 1 (TPH1, rs1800532), the 5-hydroxytryptamine receptor 2A (HTR2A, rs6311, rs6313, rs7997012), and the catechol-O-methyltransferase (COMT, rs4680) genes, are associated with efficacy of transcranial direct current stimulation (tDCS) in major depression. Methods: Data from the Escitalopram vs. Electrical Current Therapy for Treating Depression Clinical Study (ELECT-TDCS) were used. Participants were antidepressant-free at baseline and presented with an acute, moderate-to-severe unipolar depressive episode. They were randomized to receive escitalopram/tDCS-sham (n=75), tDCS/placebo-pill (n=75), or placebo-pill/sham-tDCS (n=45). General linear models assessed the interaction between treatment group and allele-wise carriers. Additional analyses were performed for each group and each genotype separately. Results: Pairwise group comparisons (tDCS vs. placebo, tDCS vs. escitalopram, and escitalopram vs. placebo) did not identify alleles associated with depression improvement. In addition, exploratory analyses also did not identify any SNP unequivocally associated with improvement of depression in any treatment group. Conclusion: Larger, combined datasets are necessary to identify candidate genes for tDCS response.


Subject(s)
Humans , Male , Female , Adolescent , Adult , Young Adult , Citalopram/therapeutic use , Antidepressive Agents, Second-Generation/therapeutic use , Depressive Disorder, Major/genetics , Depressive Disorder, Major/therapy , Transcranial Direct Current Stimulation , Catechol O-Methyltransferase/genetics , Double-Blind Method , Treatment Outcome , Combined Modality Therapy , Brain-Derived Neurotrophic Factor/genetics , Polymorphism, Single Nucleotide , Receptor, Serotonin, 5-HT2A/genetics , Serotonin Plasma Membrane Transport Proteins/genetics , Mixed Function Oxygenases/genetics , Middle Aged , Antidepressive Agents/therapeutic use
4.
Rev. méd. Chile ; 146(5): 665-669, mayo 2018. graf
Article in Spanish | LILACS | ID: biblio-961444

ABSTRACT

Upgaze or sustained elevation of the eyes, is an alteration of ocular motility initially described in hypoxic coma. We report a 65-year-old woman admitted with hypotension and alteration of sensorium due to the ingestion of 9.5 g of Bupropion. She presented two seizures of short duration, without epileptic activity on the EEG. She had a persistent asynchronous myoclonus in extremities, tachycardia and prolonged Q-t. She suffered a cardiac arrest caused by asystole, which recovered quickly in five minutes. At that moment, upgaze appeared, associated with a persistent ocular opening, which persisted for days, but finally disappeared, without remission of coma. A magnetic resonance imaging done at the eighth day, showed hyperintensity of the oval center and corpus callosum which disappeared in a new imaging study done 30 days later, where images of hypoxia in the basal nuclei and cortex appeared. The patient died forty seven days after admission. Up-gaze is an ominous oculomotor alteration linked to an important but incomplete damage in the cerebral cortex, a condition that perverts some sequences of the ocular opening, reversing the Bell phenomenon and producing eyelid retraction.


Subject(s)
Humans , Female , Aged , Ocular Motility Disorders/chemically induced , Hypoxia, Brain/chemically induced , Bupropion/adverse effects , Coma/chemically induced , Antidepressive Agents, Second-Generation/adverse effects , Drug Overdose/complications , Personality Disorders/drug therapy , Suicide , Magnetic Resonance Imaging , Fatal Outcome
5.
Rev. medica electron ; 40(2): 420-432, mar.-abr. 2018. ilus
Article in Spanish | LILACS, CUMED | ID: biblio-902309

ABSTRACT

RESUMEN Las reacciones adversas a los medicamentos, son una reacción nociva o no intencionada. Ocurre con las dosis habituales empleadas en el ser humano para la profilaxis, diagnóstico o tratamiento de enfermedades y también para modificar las funciones fisiológicas. Con esta revisión se pretendió proporcionar una actualización de las reacciones de los fármacos antidepresivos. Se tuvo en cuenta cuestiones importantes, tales como: la selección, forma de uso, duración de la terapia y consideraciones relacionadas con situaciones patológicas particulares (AU).


ABSTRACT Adverse reactions to drugs are a noxious and non-intended reaction. It occurs with the doses usually used for prophylaxis, diagnosis and disease treatment in the human being, and also for modifying the physiologic functions. The aim of this review was giving an update of the reactions to anti-depressant drugs. Important questions were taken into account like drug choose, form of use, therapy lasting and considerations related to particular pathologic situations (AU).


Subject(s)
Humans , Depression/epidemiology , Drug-Related Side Effects and Adverse Reactions/epidemiology , Antidepressive Agents/adverse effects , Antidepressive Agents/therapeutic use , Bibliography of Medicine , Antidepressive Agents, Second-Generation/adverse effects , Antidepressive Agents, Tricyclic/therapeutic use , Antidepressive Agents, Tricyclic/pharmacology
6.
Braz. j. med. biol. res ; 51(7): e7212, 2018. tab, graf
Article in English | LILACS | ID: biblio-889122

ABSTRACT

Aberrant expression of microRNAs (miRNAs) has been shown to be involved in early observations of depression. The aim of this study was to determine if serum levels of miRNA-451a, miRNA-34a-5p, and miRNA-221-3p can serve as indicators of disease progression or therapeutic efficacy in depression. We collected data from 84 depressed patients and 78 control volunteers recruited from the medical staff at the West China Hospital. Depression severity was rated using the 24-item Hamilton Depression Scale (HAMD). Serum miRNA-451a, miRNA-34a-5p, and miRNA-221-3p levels were determined in samples from the depressed patients before and 8 weeks after antidepressant treatment as well as in samples from controls. Compared with the controls, the patients had lower miRNA-451a levels, higher miRNA-34a-5p and miRNA-221-3p levels, and increased HAMD scores whether they underwent antidepressant treatment or not. Eight weeks after antidepressant treatment, the patients exhibited increased miRNA-451a levels, decreased miRNA-34a-5p and miRNA-221-3p levels, and reduced HAMD scores. The serum level of miRNA-451a was negatively correlated with HAMD scores of the patients, while the serum levels of miRNA-34a-5p and miRNA-221-3p were positively correlated with HAMD scores whether the patients underwent antidepressant treatment or not. Paroxetine was markedly effective in 50 patients who also displayed an increased level of miRNA-451a but reduced levels of miRNA-34a-5p and miRNA-221-3p. In contrast, paroxetine was moderately effective or ineffective in 34 patients. In conclusion, depressed patients had lower serum miRNA-451a but higher serum miRNA-34a-5p and miRNA-221-3p, and these miRNAs are potential predictors of the efficacy of antidepressants.


Subject(s)
Humans , Male , Female , Adult , Paroxetine/therapeutic use , Antidepressive Agents, Second-Generation/therapeutic use , MicroRNAs/blood , Depression/blood , Suicidal Ideation , Psychiatric Status Rating Scales , Biomarkers/blood , Case-Control Studies , Treatment Outcome , Gene Expression Profiling , Depression/drug therapy , Educational Status , Real-Time Polymerase Chain Reaction
7.
Arch. argent. pediatr ; 115(6): 424-427, dic. 2017.
Article in English, Spanish | LILACS, BINACIS | ID: biblio-887406

ABSTRACT

El síndrome de abstinencia neonatal (SAN) debido a la exposición prenatal al citalopram se desarrolla durante los primeros días de vida, incluso con una exposición al fármaco en dosis bajas. El tratamiento de apoyo es la primera opción, aunque puede usarse el fenobarbital en el tratamiento de este síndrome. No debe interrumpirse la lactancia. Debe hacerse un seguimiento de estos recién nacidos para establecer el desenlace del SAN y las consecuencias en el desarrollo neurológico. En este artículo presentamos el caso de un recién nacido con SAN debido a exposición al citalopram en una dosis más baja que lo informado previamente en la bibliografía durante los últimos seis meses del embarazo. Se utilizó el fenobarbital debido al fracaso del tratamiento no farmacológico.


Neonatal abstinence syndrome (NAS) due to prenatally exposure to citalopram can develop during the first days of life even with low dose of drug exposure. Supportive management is the first choice but phenobarbital can be used in treatment of this syndrome. Breastfeeding should not be interrupted. These neonates should be followed both for NAS and neurodevelopmental outcome. In this article, we reported a newborn with NAS due to citalopram exposure with a lower dose than previously reported in the literature, during the last six months of pregnancy. Phenobarbital was used because of non-pharmacological treatment failure.


Subject(s)
Humans , Male , Pregnancy , Infant, Newborn , Neonatal Abstinence Syndrome/etiology , Citalopram/adverse effects , Antidepressive Agents, Second-Generation/adverse effects , Phenobarbital/therapeutic use , Pregnancy Complications/psychology , Pregnancy Complications/drug therapy , Prenatal Exposure Delayed Effects , Neonatal Abstinence Syndrome/drug therapy , Depressive Disorder, Major/drug therapy , Anticonvulsants/therapeutic use
8.
An. acad. bras. ciênc ; 89(1): 273-283, Jan,-Mar. 2017. tab, graf
Article in English | LILACS | ID: biblio-886645

ABSTRACT

ABSTRACT Tryptophan is the only precursor of serotonin and mediates serotonergic activity in the brain. Previous studies have shown that the administration of tryptophan or tryptophan depletion significantly alters cognition, mood and anxiety. Nevertheless, the neurobiological alterations that follow these changes have not yet been fully investigated. The aim of this study was to verify the effects of a tryptophan-enriched diet on immunoreactivity to Fos-protein in the rat brain. Sixteen male Wistar rats were distributed into two groups that either received standard chow diet or a tryptophan-enriched diet for a period of thirty days. On the morning of the 31st day, animals were euthanized and subsequently analyzed for Fos-immunoreactivity (Fos-ir) in the dorsal and median raphe nuclei and in regions that receive serotonin innervation from these two brain areas. Treatment with a tryptophan-enriched diet increased Fos-ir in the prefrontal cortex, nucleus accumbens, paraventricular hypothalamus, arcuate and ventromedial hypothalamus, dorsolateral and dorsomedial periaqueductal grey and dorsal and median raphe nucleus. These observations suggest that the physiological and behavioral alterations that follow the administration of tryptophan are associated with the activation of brain regions that regulate cognition and mood/anxiety-related responses.


Subject(s)
Animals , Male , Anxiety/drug therapy , Brain/drug effects , Proto-Oncogene Proteins c-fos/drug effects , Cognition/drug effects , Antidepressive Agents, Second-Generation/administration & dosage , Affect/drug effects , Anxiety/metabolism , Time Factors , Tryptophan/administration & dosage , Brain/metabolism , Immunohistochemistry , Serotonin/metabolism , Reproducibility of Results , Treatment Outcome , Proto-Oncogene Proteins c-fos/metabolism , Rats, Wistar , Dietary Supplements , Diet Therapy/methods
9.
Braz. J. Psychiatry (São Paulo, 1999, Impr.) ; 39(1): 12-20, Jan.-Mar. 2017. tab, graf
Article in English | LILACS | ID: biblio-844167

ABSTRACT

Objective: To identify neurocognitive and sociodemographic variables that could be associated with clinical response to three modalities of treatment for depression, as well as variables that predicted superior response to one treatment over the others. Method: The present study derives from a research project in which depressed patients (n=272) received one of three treatments – long-term psychodynamic psychotherapy (n=90), fluoxetine therapy (n=91), or a combination thereof (n=91) – over a 24-month period. Results: Sociodemographic variables were not found to be predictive. Six predictive neurocognitive variables were identified: three prognostic variables related to working memory and abstract reasoning; one prescriptive variable related to working memory; and two variables found to be moderators. Conclusions: The results of this study indicate subgroups of patients who might benefit from specific therapeutic strategies and subgroups that seem to respond well to long-term psychodynamic psychotherapy and combined therapy. The moderators found suggest that abstract reasoning and processing speed may influence the magnitude and/or direction of clinical improvement.


Subject(s)
Humans , Male , Female , Adult , Cognitive Behavioral Therapy , Fluoxetine/administration & dosage , Antidepressive Agents, Second-Generation/administration & dosage , Depression/therapy , Prognosis , Treatment Outcome , Combined Modality Therapy/methods
11.
Rev. bras. anestesiol ; 66(6): 651-653, Nov.-Dec. 2016.
Article in English | LILACS | ID: biblio-829712

ABSTRACT

Abstract The mechanism of the antidepressant effect of bupropion is not fully understood. Besides, using it in the treatment of depression, it is found to be effective in reducing withdrawal symptoms due to smoking cessation. A 28-year-old female patient with a history of depression was admitted to emergency department an hour after ingestion of bupropion, quetiapine, and levothyroxine in high doses to commit suicide. While accepting her into the Intensive Care Unit, she was awake, alert, disoriented and agitated. After 2 h, the patient had a generalized tonic-clonic seizure. The necessary treatment was given and 9 h later with hemodynamic improvement, the patients’ mental status improved. Bupropion may cause unusual behaviors such as delusions, paranoia, hallucinations, or confusion. The risk of seizure is strongly dose-dependent. We want to emphasize the importance of early gastric lavage and administration of activated charcoal.


Resumo O mecanismo do efeito antidepressivo de bupropiona ainda não está bem esclarecido. Contudo, seu uso no tratamento de depressão revelou ser eficaz para reduzir os sintomas de abstinência relacionados à cessação do tabagismo. Uma paciente do sexo feminino, 28 anos, com história de depressão, deu entrada no setor de emergência uma hora após a ingestão de bupropiona, quetiapina e levotiroxina em doses elevadas para cometer suicídio. Ao ser internada em unidade de terapia intensiva, estava acordada, alerta, desorientada e agitada. Após duas horas, apresentou uma crise tônico-clônica generalizada. O tratamento necessário foi administrado e nove horas mais tarde, com a estabilização hemodinâmica, o estado mental da paciente melhorou. Bupropiona pode causar comportamentos incomuns, incluindo delírios, paranoia, alucinações ou confusão mental. O risco de convulsão é altamente dependente da dose. Queremos enfatizar a importância da lavagem gástrica precoce e da administração de carvão ativado.


Subject(s)
Humans , Female , Adult , Seizures/chemically induced , Bupropion/poisoning , Antidepressive Agents, Second-Generation/poisoning , Suicide, Attempted , Thyroxine/poisoning , Antipsychotic Agents/poisoning , Epilepsy, Tonic-Clonic/chemically induced , Quetiapine Fumarate/poisoning
13.
Einstein (Säo Paulo) ; 13(3): 430-434, July-Sep. 2015.
Article in English | LILACS | ID: lil-761939

ABSTRACT

Sleep disorders are common in patients with Alzheimer dementia and affect the quality of life of patients and of their caregivers. Despite the rising number of studies in the area, almost all of them are about non-pharmacological treatment. Our objective was to review the literature concerning pharmacological and non-pharmacological approaches to treat sleep disorders of elderly patients with Alzheimer dementia in the ambulatory setting. The treatments revised consisted of sleep hygiene and/or use of intense light coupled or not with use of melatonin, cholinesterase inhibitors, antipsychotics, hypnotics or antidepressants. In addition to the non-pharmacological measures, there is evidence that the use of trazodone may aid the treatment of sleep disorders of older individuals with Alzheimer dementia. More studies are necessary to examine the non-pharmacological and pharmacological treatments revised herein.


Os transtornos do sono são comuns nos pacientes com doença de Alzheimer e interferem na qualidade de vida do paciente e de seu cuidador. Apesar da alta prevalência desses transtornos, existe pouca evidência em relação ao seu tratamento. Nosso objetivo foi revisar a literatura em relação ao tratamento não farmacológico e farmacológico dos transtornos do sono nos idosos com doença de Alzheimer em comunidade. Os tratamentos incluídos consistiram na higiene do sono e/ou no uso da luz intensa, combinados ou não com o uso da melatonina, nos inibidores de acetilcolinesterases, antipsicóticos, hipnóticos ou antidepressivos. Para além das medidas não farmacológicas, há evidência de que o uso da trazodona é efetivo no tratamento dos transtornos do sono de pacientes com doença de Alzheimer. Mais estudos sobre as estratégias farmacológicas e não farmacológicas aqui revisadas ou outras são desejáveis.


Subject(s)
Humans , Alzheimer Disease/complications , Sleep Wake Disorders/therapy , Antidepressive Agents, Second-Generation/therapeutic use , Outpatients , Phototherapy/methods , Sleep Wake Disorders/drug therapy , Sleep Wake Disorders/etiology , Trazodone/therapeutic use
14.
São Paulo med. j ; 133(3): 252-263, May-Jun/2015. tab, graf
Article in English | LILACS | ID: lil-752121

ABSTRACT

CONTEXT AND OBJECTIVE: Major depressive disorder (MDD) is a common psychiatric condition, mostly treated with antidepressant drugs, which are limited due to refractoriness and adverse effects. We describe the study rationale and design of ELECT-TDCS (Escitalopram versus Electric Current Therapy for Treating Depression Clinical Study), which is investigating a non-pharmacological treatment known as transcranial direct current stimulation (tDCS). DESIGN AND SETTING: Phase-III, randomized, non-inferiority, triple-arm, placebo-controlled study, ongoing in São Paulo, Brazil. METHODS: ELECT-TDCS compares the efficacy of active tDCS/placebo pill, sham tDCS/escitalopram 20 mg/day and sham tDCS/placebo pill, for ten weeks, randomizing 240 patients in a 3:3:2 ratio, respectively. Our primary aim is to show that tDCS is not inferior to escitalopram with a non-inferiority margin of at least 50% of the escitalopram effect, in relation to placebo. As secondary aims, we investigate several biomarkers such as genetic polymorphisms, neurotrophin serum markers, motor cortical excitability, heart rate variability and neuroimaging. RESULTS: Proving that tDCS is similarly effective to antidepressants would have a tremendous impact on clinical psychiatry, since tDCS is virtually devoid of adverse effects. Its ease of use, portability and low price are further compelling characteristics for its use in primary and secondary healthcare. Multimodal investigation of biomarkers will also contribute towards understanding the antidepressant mechanisms of action of tDCS. CONCLUSION: Our results have the potential to introduce a novel technique to the therapeutic arsenal of treatments for depression. .


CONTEXTO E OBJETIVO: O transtorno depressivo maior (TDM) é uma condição psiquiátrica comum, tratada com medicamentos antidepressivos, os quais são limitados devido à refratariedade e efeitos adversos. Descrevemos o racional e o desenho do Estudo Clínico Escitalopram versus Eletroterapia no Tratamento da Depressão (ELECT-TDCS), que investiga um tratamento não farmacológico, conhecido como estimulação transcraniana por corrente contínua (ETCC). DESENHO E LOCAL: Ensaio de fase III, randomizado, de não inferioridade, de três braços, placebo-controlado, em execução em São Paulo, Brasil. MÉTODOS: O estudo compara a eficácia da ETCC ativa/pílula placebo, ETCC simulada/escitalopram 20 mg/dia e ETCC simulada/pílula placebo durante 10 semanas, randomizando 240 pacientes em uma proporção 3:3:2, respectivamente. O objetivo principal é demostrar que a ETCC não é inferior ao escitalopram com uma margem de não inferioridade de pelo menos 50% do efeito de escitalopram em relação ao placebo. Como objetivos secundários, investigamos biomarcadores como polimorfismos genéticos, marcadores séricos, excitabilidade cortical motora, variabilidade da frequência cardíaca e neuroimagem. RESULTADOS: Provar que ETCC é igualmente eficaz a antidepressivos teria um tremendo impacto na psiquiatria clínica, uma vez que a ETCC é praticamente isenta de efeitos adversos. Sua facilidade de uso, portabilidade e preço baixo são outras características atraentes para uso na atenção primária e secundária de saúde. A investigação multimodal de biomarcadores também contribuirá para a compreensão dos mecanismos de ação antidepressivos da ETCC. CONCLUSÃO: Os nossos resultados podem introduzir uma nova técnica no arsenal terapêutico do tratamento da depressão. .


Subject(s)
Adolescent , Adult , Aged , Female , Humans , Male , Middle Aged , Young Adult , Antidepressive Agents, Second-Generation/therapeutic use , Citalopram/therapeutic use , Depressive Disorder, Major/therapy , Transcranial Direct Current Stimulation/methods , Analysis of Variance , Combined Modality Therapy , Placebo Effect , Psychiatric Status Rating Scales , Reproducibility of Results , Time Factors , Treatment Outcome
15.
Rev. saúde pública ; 49: 1-4, 27/02/2015.
Article in English | LILACS | ID: lil-742294

ABSTRACT

This review aimed to discuss the importance of the comprehensive treatment of depression among older adults in Brazil. The abuse of selective serotonin reuptake inhibitors, including fluoxetine hydrochloride, as antidepressants has been considered a serious public health problem, particularly among older adults. Despite the consensus on the need for a comprehensive treatment of depression in this population, Brazil is still unprepared. The interface between pharmacotherapy and psychotherapy is limited due to the lack of healthcare services, specialized professionals, and effective healthcare planning. Fluoxetine has been used among older adults as an all-purpose drug for the treatment of depressive disorders because of psychosocial adversities, lack of social support, and limited access to adequate healthcare services for the treatment of this disorder. Preparing health professionals is a sine qua non for the reversal of the age pyramid, but this is not happening yet.


Esse comentário tem como objetivo discutir a importância da multidisciplinariedade do tratamento da depressão do idoso no Brasil. O abuso de prescrições de antidepressivos inibidores seletivos da receptação de serotonina, como o cloridrato de fluoxetina, já tem sido apontado como grave problema de saúde pública, especialmente entre idosos. Embora seja consenso a necessidade de multidisciplinariedade no tratamento da depressão nessa população, o Brasil ainda encontra-se despreparado. A interface entre farmacoterapia e psicoterapia encontra-se prejudicada por falta de serviços, de profissionais especializados e de planejamento assistencial efetivo. A fluoxetina tornou-se uma “muleta” para a cura de males causados pelas adversidades psicossociais, falta de suporte social e de acesso a serviços de saúde adequados para o tratamento desse transtorno em idosos. É condição sine qua non haver preparo para a inversão das pirâmides etárias, o que parece não acontecer atualmente.


Subject(s)
Aged , Humans , Antidepressive Agents, Second-Generation/adverse effects , Depressive Disorder/psychology , Depressive Disorder/therapy , Fluoxetine/adverse effects , Brazil , Combined Modality Therapy , Comprehensive Health Care , Cost of Illness , Fluoxetine/economics , Psychotherapy
16.
J. bras. pneumol ; 40(3): 313-318, May-Jun/2014. graf
Article in English | LILACS | ID: lil-714682

ABSTRACT

Venlafaxine is a serotonin-norepinephrine reuptake inhibitor used as an antidepressant. Interindividual variability and herb-drug interactions can lead to drug-induced toxicity. We report the case of a 35-year-old female patient diagnosed with synchronous pneumonitis and acute cardiomyopathy attributed to venlafaxine. The patient sought medical attention due to dyspnea and dry cough that started three months after initiating treatment with venlafaxine for depression. The patient was concomitantly taking Centella asiatica and Fucus vesiculosus as phytotherapeutic agents. Chest CT angiography and chest X-ray revealed parenchymal lung disease (diffuse micronodules and focal ground-glass opacities) and simultaneous dilated cardiomyopathy. Ecocardiography revealed a left ventricular ejection fraction (LVEF) of 21%. A thorough investigation was carried out, including BAL, imaging studies, autoimmune testing, right heart catheterization, and myocardial biopsy. After excluding other etiologies and applying the Naranjo Adverse Drug Reaction Probability Scale, a diagnosis of synchronous pneumonitis/cardiomyopathy associated with venlafaxine was assumed. The herbal supplements taken by the patient have a known potential to inhibit cytochrome P450 enzyme complex, which is responsible for the metabolization of venlafaxine. After venlafaxine discontinuation, there was rapid improvement, with regression of the radiological abnormalities and normalization of the LVEF. This was an important case of drug-induced cardiopulmonary toxicity. The circumstantial intake of inhibitors of the CYP2D6 isoenzyme and the presence of a CYP2D6 slow metabolism phenotype might have resulted in the toxic accumulation of venlafaxine and the subsequent clinical manifestations. Here, we also discuss why macrophage-dominant phospholipidosis was the most likely mechanism of toxicity in this case.


A venlafaxina é um inibidor de recaptação de serotonina e noradrenalina utilizado como antidepressivo. A variabilidade individual ou interações entre fitoterápicos e fármacos podem causar toxicidade induzida por drogas. Relatamos o caso de uma paciente de 35 anos diagnosticada com pneumonite intersticial e miocardiopatia dilatada atribuídas à venlafaxina. A paciente procurou atendimento médico devido a dispneia e tosse seca, que começaram três meses após iniciar tratamento com venlafaxina para depressão. Concomitantemente tomava suplementos fitoterápicos contendo Centella asiatica e Fucus vesiculosus. A radiografia e a CT de tórax revelaram doença pulmonar parenquimatosa (micronódulos difusos e opacidades em vidro fosco) e, simultaneamente, foi diagnosticada uma miocardiopatia por ecocardiograma, que revelou uma fração de ejeção ventricular esquerda (FEVE) de 21%. Uma investigação ampla foi realizada, incluindo LBA, estudos de imagem, detecção de doenças autoimunes, cateterismo cardíaco direito e biópsia miocárdica. Após a exclusão de outras etiologias e a aplicação da Escala de Probabilidade de Reações Adversas a Medicamentos de Naranjo, foi assumido o diagnóstico de pneumonite/miocardiopatia síncronas associadas à venlafaxina. Já foi demonstrado que os suplementos fitoterápicos utilizados pela paciente podem inibir a isoenzima do complexo enzimático citocromo P450, responsável pelo metabolismo da venlafaxina. Após a descontinuação da venlafaxina, verificou-se uma rápida melhora clínica com regressão das alterações radiológicas e normalização da FEVE. Este é um importante caso de toxicidade cardiopulmonar induzida por droga. A administração circunstancial de inibidores da isoenzima CYP2D6 e a presença de um fenótipo de metabolização lenta de CYP2D6 podem ter resultado na acumulação tóxica da venlafaxina e na manifestação clínica subsequente. Aqui, é discutida a hipótese de a fosfolipidose macrofágica ser o mecanismo de toxicidade.


Subject(s)
Adult , Female , Humans , Antidepressive Agents, Second-Generation/adverse effects , Cardiomyopathies/chemically induced , Cyclohexanols/adverse effects , Lung Diseases, Interstitial/chemically induced , Cardiomyopathies/diagnosis , Depressive Disorder/drug therapy , Lung Diseases, Interstitial/diagnosis
17.
Braz. j. med. biol. res ; 47(3): 237-244, 03/2014. tab, graf
Article in English | LILACS | ID: lil-704626

ABSTRACT

Studies have indicated that early-life or early-onset depression is associated with a 2- to 4-fold increased risk of developing Alzheimers disease (AD). In AD, aggregation of an abnormally phosphorylated form of the tau protein may be a key pathological event. Tau is known to play a major role in promoting microtubule assembly and stabilization, and in maintaining the normal morphology of neurons. Several studies have reported that stress may induce tau phosphorylation. The main aim of the present study was to investigate possible alterations in the tau protein in the hippocampus and frontal cortex of 32 male Sprague-Dawley rats exposed to chronic unpredictable mild stress (CUMS) and then re-exposed to CUMS to mimic depression and the recurrence of depression, respectively, in humans. We evaluated the effects of CUMS, fluoxetine, and CUMS re-exposure on tau and phospho-tau. Our results showed that a single exposure to CUMS caused a significant reduction in sucrose preference, indicating a state of anhedonia. The change in behavior was accompanied by specific alterations in phospho-tau protein levels, but fluoxetine treatment reversed the CUMS-induced impairments. Moreover, changes in sucrose preference and phospho-tau were more pronounced in rats re-exposed to CUMS than in those subjected to a single exposure. Our results suggest that changes in tau phosphorylation may contribute to the link between depression and AD.


Subject(s)
Animals , Male , Depression/metabolism , Frontal Lobe/metabolism , Hippocampus/metabolism , Stress, Psychological/metabolism , tau Proteins/metabolism , Analysis of Variance , Anhedonia , Alzheimer Disease/complications , Antidepressive Agents, Second-Generation/therapeutic use , Depression/complications , Depression/drug therapy , Fluoxetine/therapeutic use , Food Preferences/psychology , Phosphorylation , Rats, Sprague-Dawley , Stress, Psychological/complications , Stress, Psychological/drug therapy
18.
Chinese Medical Sciences Journal ; (4): 43-47, 2014.
Article in English | WPRIM | ID: wpr-242902

ABSTRACT

This paper summarized the Chinese literatures in the previous 5 years about the pre-clinical animal researches on the application of electro-acupuncture (EA) treatment for depression, searched in China National Knowledge Infrastructure (CNKI). The efficiency of EA treatment for depression and the mechanism of it were discussed, to shed light on new ideas and new fronts for the further research on depression in clinical or pre-clinical fields.


Subject(s)
Animals , Animal Experimentation , Antidepressive Agents, Second-Generation , Therapeutic Uses , Behavior, Animal , Physiology , Combined Modality Therapy , Depression , Drug Therapy , Metabolism , Psychology , Therapeutics , Disease Models, Animal , Electroacupuncture , Methods , Fluoxetine , Therapeutic Uses , Medicine, Chinese Traditional , Stress, Psychological , Drug Therapy , Metabolism , Psychology , Therapeutics
19.
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 838-844, 2014.
Article in English | WPRIM | ID: wpr-331135

ABSTRACT

In recent years, more attention has been paid to the role of the glutamate transporter 1 (GLT-1, EAAT2) in major depressive disorder (MDD). However, experimental data on brain GLT-1 levels are, to some extent, inconsistent in human postmortem and animal studies. These discrepancies imply that the role of GLT-1 in the pathophysiology of MDD and the action of antidepressants remain obscure. This work was designed to study the impact of chronic unpredictable stress (CUS) for 2 sessions per day for 35 days and four weeks of fluoxetine (FLX) on depressive-like behaviors in rats, as well as the concomitant expression of the GLT-1 protein in the hippocampus. Behavioral changes were assessed by the sucrose preference and open field tests. GLT-1 levels were detected by immunohistchemistry and Western blot analysis. Our study demonstrated that the animals exposed to CUS showed depressive-like behaviors and exhibited a significant decrease in GLT-1 expression in the hippocampus. Chronic FLX treatment reversed the behavioral deficits and the CUS-induced decrease in GLT-1 levels. Taken together, our results support the reduction of GLT-1 in human postmortem studies in MDD and suggest that GLT-1 may be involved in the antidepressant activity of FLX. Our studies further support the notion that GLT-1 is an attractive candidate molecule associated with the fundamental processes of MDD and may be a potential, and novel pharmacological target for the treatment of MDD.


Subject(s)
Animals , Humans , Male , Rats , Antidepressive Agents, Second-Generation , Pharmacology , Behavior, Animal , Brain , Metabolism , Pathology , Chronic Disease , Depressive Disorder, Major , Drug Therapy , Metabolism , Pathology , Excitatory Amino Acid Transporter 2 , Metabolism , Fluoxetine , Pharmacology , Rats, Sprague-Dawley , Stress, Psychological , Drug Therapy , Metabolism , Pathology
20.
Psicofarmacologia (B. Aires) ; 13(82): 21-27, oct. 2013. tab
Article in Spanish | LILACS | ID: lil-726100

ABSTRACT

Introducción: A pesar de que la obesidad es un evento adverso frecuente en el tratamiento con antipsicóticos atípico, no ha sido suficientemente elucidado el grado de su contribución independiente al riesgo de enfermedad coronaria en estos pacientes. Objetivo: Determinar si la obesidad inducida por antipsicóticos de segunda generación o atípicos es un factor de riesgo independiente para el aumento de incidencia de enfermedad arterial coronaria y eventos cardíacos. Método: Se utilizó un modelo similar al usado en el estudio de Framingham basado en estimar los siguientes parámetros: edad, género, presión arterial, consumo de cigarrillo y niveles de lipoproteínas de colesterol de alta densidad, con el objetivo de determinar el riesgo prospectivo de padecer enfermedad arterial coronaria en aquellos pacientes tratados con antipsicóticos atípicos que cursaban un cuadro de obesidad (N=33; edad media 38.1, 54 % hombres) comparados con aquellos con peso normal (N=33; edad media 39.9 años, 47.0 % hombres). Se excluyeron aquellos pacientes con síndrome metabólico, medicados con drogas antihipertensivas, hipoglucemiantes o estatinas. Resultados: El riesgo de enfermedad arterial coronaria fue mayor para la muestra de pacientes obesos comparado con la muestra de pacientes con peso normal (5.3±2.7 vs. 2.1±0.62, RR=2.17 IC 95%=1.94-2.39; p=0.017), incluyendo un aumento de 12 unidades de IMC (p<0.0001) y 16 cm de circunferencia de cintura mayor (p<0.0001) en la población con obesidad inducida por antipsicóticos atípicos. El riesgo fue mayor para hombres (5.9±2.9 vs. 2.8±0.4, RR=2.98, IC 95%=1.97-3.16; p=0.0034) comparados con las mujeres (3.1±1.2 vs. 1.2±0.5; RR=1.78, IC 95 %=1.58-1.94; p=0.011). Limitaciones: la validez predictiva para el riesgo de enfermedad coronaria en pacientes psiquiátricos basada en el sistema de clasificación de Framingham requiere una confirmación prospectiva...


Obesity is an adverse effect frequently observed during second generation antipsychotics treatment. In spite of that, its independent contribution to coronary artery disease in patients treated with this class of drugs remains unsolved. Objective: assess whether antipsychotics induced obesity is an independent risk factor contributing to an increase in cardiac events and coronary artery disease. Methods: a similar model to that used in Framingham Study was used based on an estimate of following parameters: age, gender, blood pressure, cigarette use, high density cholesterol lipoproteins levels with the goal of estimate prospective risk of suffering coronary artery disease between those patients treated with second generation antipsychotics which also had obesity (N=33; average age 38.1 years, 54% men) compared with those on normal weight (N=33; average age 39.9 years, 47.0% men). Excluded were those patients with metablic Syndrome treated with antihypertensive drugs, hypoglycemic drugs and statins. Results: risk of coronary artery diseases was higher for obese patients compared with normal wight ones (5.3 ±2.7 vs. 2.1±0.62, RR=2.17 IC 95%=1.94 - 2.39; p=0.017), including an increase of 12 units in BMI (p<0.0001) and 16 cm in abdominal waist (p<0.0001) in antipsychotic drugs induced obesity sample...


Subject(s)
Humans , Male , Antidepressive Agents, Second-Generation/adverse effects , Antidepressive Agents, Second-Generation/therapeutic use , Coronary Disease/pathology , Obesity , Risk Factors , Metabolic Syndrome/pathology
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