RÉSUMÉ
Chronic use of omeprazole has been linked to central effects alongside with the global concern of increasing appearance of neuropsychiatric disorders. This study aimed to identifying behavioral, inflammatory, and oxidative stress alterations after long-term administration of omeprazole. C57BL/6 mice were divided in groups: OME and Sham, each received either solutions of omeprazole or vehicle, administered for 28 days by gavage. Results observed in the omeprazole-treated mice: Decrease in the crossing parameter in the open field, no change in the motor performance assessed by rotarod, an immobility time reduction in the forced swimming test, improved percentage of correct alternances in the Ymaze and an exploration time of the novel object reduction in the novel object recognition. Furthermore, a reduced weight gain and hippocampal weight were observed. There was an increase in the cytokine IL1-ß levels in both prefrontal cortex (PFC) and serum, whereas TNF-α increased only in the PFC. Nitrite levels increased in the hippocampus (HP) and PFC, while malondialdehyde (MDA) and glutathione (GSH) levels decreased. These findings suggest that omeprazole improves depressive-like behavior and working memory, likely through the increase in nitrite and reduction in MDA levels in PFC and HP, whereas, the impairment of the recognition memory is more likely to be related to the reduced hippocampal weight. The diminished weight gain might be associated with the IL-1ß increased levels in the peripheral blood. Altogether, omeprazole showed to have the potential to impact at central level and inflammatory and oxidative parameters might exert a role between it.
Sujet(s)
Comportement animal , Hippocampe , Souris de lignée C57BL , Oméprazole , Stress oxydatif , Animaux , Stress oxydatif/effets des médicaments et des substances chimiques , Oméprazole/pharmacologie , Oméprazole/administration et posologie , Mâle , Comportement animal/effets des médicaments et des substances chimiques , Hippocampe/effets des médicaments et des substances chimiques , Hippocampe/métabolisme , Cortex préfrontal/effets des médicaments et des substances chimiques , Cortex préfrontal/métabolisme , Souris , Glutathion/métabolisme , Malonaldéhyde/métabolisme , Interleukine-1 bêta/sang , Interleukine-1 bêta/métabolisme , Inflammation/traitement médicamenteux , Inflammation/métabolisme , Facteur de nécrose tumorale alpha/sang , Facteur de nécrose tumorale alpha/métabolisme , Dépression/traitement médicamenteux , Dépression/métabolisme , Inhibiteurs de la pompe à protons/pharmacologie , Inhibiteurs de la pompe à protons/administration et posologie , Nitrites/sangRÉSUMÉ
The use of inhibitors of gastric acid secretion (IGAS), especially proton pump inhibitors (PPI), has been associated with increased cardiovascular risk. While the mechanisms involved are not known, there is evidence supporting increased oxidative stress, a major activator of matrix metalloproteinases (MMP), as an important player in such effect. However, there is no study showing whether other IGAS such as histamine H2-receptor blockers (H2RB) cause similar effects. This study aimed at examining whether treatment with the H2RB ranitidine promotes oxidative stress resulting in vascular MMP activation and corresponding functional and structural alterations in the vasculature, as compared with those found with the PPI omeprazole. Male Wistar rats were treated (4 weeks) with vehicle (2% tween 20), omeprazole (10 mg/Kg/day; i.p.) or ranitidine (100 mg/Kg/day; gavage). Then the aorta was collected to perform functional, biochemical, and morphometric analysis. Both ranitidine and omeprazole increased gastric pH and oxidative stress assessed in situ with the fluorescent dye dihydroethidium (DHE) and with lucigenin chemiluminescence assay. Both IGAS augmented vascular activated MMP-2. These findings were associated with aortic remodeling (increased media/lumen ratio and number of cells/µm2). Both IGAS also impaired the endothelium-dependent relaxation induced by acetylcholine (isolated aortic ring preparation). This study provides evidence that the H2RB ranitidine induces vascular dysfunction, redox alterations, and remodeling similar to those found with the PPI omeprazole. These findings strongly suggest that IGAS increase oxidative stress and matrix metalloproteinase-2 activity leading to vascular remodeling, which helps to explain the increased cardiovascular risk associated with the use of those drugs.
Sujet(s)
Acide gastrique , Matrix metalloproteinase 2 , Oméprazole , Stress oxydatif , Ranitidine , Rat Wistar , Remodelage vasculaire , Animaux , Stress oxydatif/effets des médicaments et des substances chimiques , Mâle , Rats , Matrix metalloproteinase 2/métabolisme , Oméprazole/pharmacologie , Ranitidine/pharmacologie , Acide gastrique/métabolisme , Remodelage vasculaire/effets des médicaments et des substances chimiques , Inhibiteurs de la pompe à protons/pharmacologie , Inhibiteurs de la pompe à protons/effets indésirables , Antihistaminiques des récepteurs H2/pharmacologieRÉSUMÉ
INTRODUCCIÓN. La necrosis esofágica aguda es un síndrome raro que se caracteriza endoscópicamente por una apariencia negra circunferencial irregular o difusa de la mucosa esofágica intratorácica, la afectación es generalmente del esófago distal y la transición abrupta de mucosa normal en la unión gastroesofágica, con extensión proximal variable. CASOS. Se presentan dos casos con diferentes comorbiliades, presentación de signos y síntomas, antecedentes y tratamiento, teniendo en común el diagnóstico a través de endoscopía digestiva alta. RESULTADOS. Caso clínico 1: tratamiento clínico basado en hidratación, suspensión de vía oral, omeprazol intravenoso y sucralfato; mala evolución clínica caracterizada por: disfagia, intolerancia oral y recurrencia del sangrado digestivo alto, se realiza colocación de gastrostomía endoscópica. Caso clínico 2: esófago con mucosa con fibrina y parches de necrosis extensa, se realiza compensación tanto de foco infeccioso pulmonar como hidratación y nutrición, en estudios complementarios se observa masa colónica, con estudio histopatológico confirmatorio de adenocarcinoma de colon en estado avanzado. DISCUSIÓN. La esofagitis necrotizante aguda es una entidad inusual, de baja prevalencia e incidencia, asociada con estados de hipoperfusión sistémica y múltiples comorbilidades que favorezcan un sustrato isquémico. Al revisar los reportes de casos que hay en la literatura médica, los casos que reportamos se correlaciona con las características clínicas, epidemiológicas, endoscópicas y factores de riesgo causales de la enfermedad. La presentación clínica más frecuente es el sangrado digestivo alto, que se debe correlacionar con el hallazgo endoscópico clásico. Nuestro primer caso reportado termina con la colocación de una gastrostomía para poder alimentarse. CONCLUSIÓN. El pronóstico de la necrosis esofágica aguda es malo y se requiere un alto índice de sospecha clínica y conocimiento de esta infrecuente patología para un diagnóstico temprano y un manejo oportuno. Se requiere una evaluación por endoscopia digestiva alta. Es una causa de sangrado gastrointestinal que conlleva tasas altas de mortalidad, principalmente en adultos mayores frágiles. El reconocimiento temprano y la reanimación agresiva son los principios fundamentales para un mejor resultado de la enfermedad.
INTRODUCTION. Acute esophageal necrosis is a rare syndrome that is characterized endoscopically by an irregular or diffuse circumferential black appearance of the intrathoracic esophageal mucosa, the involvement is generally of the distal esophagus and the abrupt transition of normal mucosa at the gastroesophageal junction, with variable proximal extension. CASES. Two cases are presented with different comorbidities, presentation of signs and symptoms, history and treatment, having in common the diagnosis through upper gastrointestinal endoscopy. RESULTS. Clinical case 1: clinical treatment based on hydration, oral suspension, intravenous omeprazole and sucralfate; poor clinical evolution characterized by: dysphagia, oral intolerance and recurrence of upper digestive bleeding, endoscopic gastrostomy placement was performed. Clinical case 2: esophagus with mucosa with fibrin and patches of extensive necrosis, compensation of both the pulmonary infectious focus and hydration and nutrition is performed, in complementary studies a colonic mass is observed, with a confirmatory histopathological study of colon adenocarcinoma in an advanced state. DISCUSSION. Acute necrotizing esophagitis is an unusual entity, with low prevalence and incidence, associated with states of systemic hypoperfusion and multiple comorbidities that favor an ischemic substrate. When reviewing the case reports in the medical literature, the cases we report correlate with the clinical, epidemiological, endoscopic characteristics and causal risk factors of the disease. The most common clinical presentation is upper gastrointestinal bleeding, which must be correlated with the classic endoscopic finding. Our first reported case ends with the placement of a gastrostomy to be able to feed. CONCLUSION. The prognosis of acute esophageal necrosis is poor and a high index of clinical suspicion and knowledge of this rare pathology is required for early diagnosis and timely management. Evaluation by upper gastrointestinal endoscopy is required. It is a cause of gastrointestinal bleeding that carries high mortality rates, mainly in frail older adults. Early recognition and aggressive resuscitation are the fundamental principles for a better outcome of the disease.
Sujet(s)
Humains , Mâle , Femelle , Adulte d'âge moyen , Sujet âgé , Gastrostomie , Endoscopie digestive , Maladies de l'oesophage , Gastroentérologie , Hémorragie gastro-intestinale/traitement médicamenteux , Nécrose , Anatomopathologie , Oméprazole , Sucralfate , Troubles de la déglutition , Mortalité , Endoscopie gastrointestinale , Équateur , Muqueuse oesophagienneRÉSUMÉ
Resumen Objetivo: Este estudio tiene como objetivo principal determinar la respuesta al esquema de tratamiento de primera línea con triple terapia estándar (amoxicilina, claritromicina, omeprazol), para erradicación de Helicobacter pylori en una determinada población, para determinar si este esquema propuesto en guías internacionales es aún una opción adecuada para pacientes en una determinada región de Costa Rica. Métodos: Se realizó una búsqueda en el servicio de gastroenterología del Hospital San Francisco de Asís, Grecia, Alajuela, Costa Rica; de todos los pacientes con infección por Helicobacter pylori y que recibieron tratamiento de primera línea con triple terapia (amoxicilina, claritromicina y omeprazol) por 14 días, en el periodo comprendido entre febrero 2017 a febrero 2019, incluyendo para el análisis solamente en los que se contaba con una prueba confirmatoria posterior a tratamiento, ya fuera por antígeno fecal de H. pylori o biopsia convencional. Resultados: Se identificaron un total de 369 casos. El diagnóstico se realizó con biopsia en el 96,4% de los pacientes. La respuesta al tratamiento de primera línea se alcanzó en un 90.5% corroborada por antígeno fecal en el 92.1% de los casos. Conclusiones: Este estudio muestra que la terapia triple con amoxicilina, claritromicina e Inhibidor de bomba de protones por 14 días mantiene un adecuado nivel de eficacia. Sin embargo, hay que tomar en cuenta que estos datos son únicamente de un área de atracción determinada y puede que no reflejen la realidad de todo el país.
Abstract Aim: The main objective of this study is to determine the response to the firstline treatment regimen with triple standard therapy (amoxicillin, clarithromycin, omeprazole), to eradicate Helicobacter pylori in a certain population. The goal is to determine if the proposed regimen in international guidelines services is still a suitable option for patients in a certain region of Costa Rica. Methods: The study took place in San Francisco de Asís Hospital, Grecia, Alajuela, Costa Rica. All patients with a Helicobacter pylori infection that were given first- line treatment with triple therapy (amoxicillin, clarithromycin and omeprazole) for its eradication for 14 days, in the period between February of 2017 and February of 2019, were included in the study. Results: A total of 369 cases were identified. The diagnosis was made with biopsy in 96.4% of patients. Response to first-line treatment was achieved in 90.5% corroborated by fecal antigen in 92.1% of all cases. Conclusions: This study shows that triple therapy with amoxicillin, clarithromycin and omeprazole for 14 days maintains an adequate level of efficacy. However, it must be considered that these results are from a specific area and may not reflect the reality of the entire country.
Sujet(s)
Humains , Mâle , Femelle , Oméprazole/usage thérapeutique , Helicobacter pylori/effets des médicaments et des substances chimiques , Infections à Helicobacter/épidémiologie , Clarithromycine/usage thérapeutique , Amoxicilline/usage thérapeutique , Costa Rica , Résistance bactérienne aux médicamentsRÉSUMÉ
Conditions experienced in early life have long-lasting effects on offspring health. Despite this, little is known about how maternal exposure to drugs during pregnancy affects offspring teeth morphogenesis. In humans, omeprazole is a common drug used to mitigate Gastroesophageal Reflux Disease. Importantly, omeprazole is a non-specific proton-pump inhibitor, which may inhibit the proton pumps expressed in the developing tooth germ. To date, however, the effects of intrauterine life exposure to omeprazole on offspring tooth development remain unknown. In this study, we addressed this gap in a murine model. Pregnant female Swiss mice were exposed to daily doses of 40 mg/kg of omeprazole from the 5th to the 17th day of pregnancy and the effects of such exposure on offspring odontogenesis parameters such as morphological abnormalities, disruptions in the ameloblast and odontoblast layers and the presence of dentin matrix were measured. Omeprazole exposure significantly increased the prevalence (control: 21.6%; treatment: 60%; p = 0.001) and the risk (posterior mean and 95% credible interval; control: 0.230 [0.129; 0.347]; treatment: 0.593 [0.449; 0.730]) of offspring teeth morphological abnormalities, although there were no statistically significant effects of omeprazole exposure on other parameters of tooth development. These findings suggest that there are potential side-effects to offspring oral health of omeprazole use during pregnancy.
Sujet(s)
Reflux gastro-oesophagien , Oméprazole , Humains , Grossesse , Femelle , Animaux , Souris , Oméprazole/effets indésirables , Modèles animaux de maladie humaine , Inhibiteurs de la pompe à protons/effets indésirables , OdontogenèseRÉSUMÉ
Objetivo: Pesquisa desenvolvida para indentificar as indicações do omeprazol e estratégias para promoção do seu uso racional na Atenção Primária de uma região do município de São Paulo. Método: Trata-se de estudo transversal por meio de inquérito realizado com médicos e farmacêuticos. Resultados: Os 157 médicos participantes referiram prescrever omeprazol para doença de refluxo gastroesofágico (73,3%), úlcera gástrica decorrente de infecção por Helicobacter pylori (65,1%), síndrome dispéptica (62,3%), esofagite erosiva (46,6%), úlcera gástrica e duodenal (43,2%), úlcera gástrica secundária a anti-inflamatórios não esteroides (20,5%), condições específicas (16,4%) e outras indicações (15,8%). Os 45 farmacêuticos participantes referiram realizar orientação farmacêutica (100%), consulta farmacêutica (97,8%), reunião de equipe (73,3%), grupos educativos (68,9%), atendimento domiciliar (66,7%), educação permanente (53,3%) e abordagem voltada ao omeprazol (48,9%). Conclusão: A maioria dos médicos referiu prescrever omeprazol para as indicações fundamentadas por evidências científicas. A maioria dos farmacêuticos referiu desenvolver serviços clínicos para o uso racional de medicamentos e, parte deles, também para ações voltadas ao omeprazol. Um baixo percentual de farmacêuticos referiu realizar atividades educativas.
Sujet(s)
Oméprazole , Inhibiteurs de la pompe à protons , Pratique pharmaceutique fondée sur des preuvesRÉSUMÉ
Tecnologia: Esomeprazol e lansoprazol. Indicação: Tratamento de doença do refluxo gastroesofágico em adultos. Pergunta: Esomeprazol e lansoprazol são mais eficazes e toleráveis que o omeprazol já incorporado ao SUS para o tratamento de Doença do Refluxo Gastroesofágico (DRGE) em adultos? Métodos: Uma revisão rápida de evidências, uma revisão de revisões sistemáticas, com levantamento bibliográfico realizado na base de dados PUBMED, utilizando estratégia estruturada de busca. A qualidade metodológica das revisões sistemáticas foi avaliada com AMSTAR-2 (Assessing the Methodological Quality of Systematic Reviews). Resultados: Foram selecionadas três revisões sistemáticas com meta-análise, que atendiam aos critérios de inclusão. Conclusão: O esomeprazol era mais eficaz para cicatrização da lesão nos casos de esofagite erosiva, prevenção da mucosa do esôfago, maior controle de ácido no tratamento de curto prazo (4 e 8 semanas) de esomeprazol 40mg e tratamento de longo prazo (6 meses) de esomeprazol 20mg. A taxa de resposta no alívio dos sintomas, o esomeprazol 20mg e 40mg apresentou ser mais eficaz, especialmente, na azia e dor epigástrica. Quanto ao perfil de segurança, não houve diferença significativa entre as taxas de eventos adversos, todos medicamentos eram parecidos entre si
Technology: Esomeprazole and Lansoprazole. Indication: Treatment of gastroesophageal reflux disease in adults. Question: Are Esomeprazole and Lansoprazole more effective and tolerable than omeprazole already incorporated into SUS for the treatment of Gastroesophageal Reflux Disease (GERD) in adults? Methods: A rapid review of evidence, an overview of systematic reviews, with bibliographic survey carried out in the PUBMED database, using a structured search strategy. The methodological quality of systematic reviews was assessed using AMSTAR-2 (Assessing the Methodological Quality of Systematic Reviews). Results: Three systematic reviews with meta-analysis were selected, which met the inclusion criteria. Conclusion: Esomeprazole was more effective in achieving wound healing in cases of erosive esophagitis, prevention of esophageal mucosa, greater acid control in short-term treatment (4 and 8 weeks) of esomeprazole 40mg and long-term treatment (6 months) of esomeprazole 20mg. the response rate in symptom relief, esomeprazole 20mg and 40mg proved to be more effective, especially in heartburn and epigastric pain. As for the safety profile, there was no significant difference between the rates of adverse events, all drugs were similar to each other
Sujet(s)
Humains , Mâle , Femelle , Adulte , Adulte d'âge moyen , Sujet âgé , Sujet âgé de 80 ans ou plus , Jeune adulte , Oméprazole/usage thérapeutique , Reflux gastro-oesophagien/traitement médicamenteux , Ésoméprazole/usage thérapeutique , Lansoprazole/usage thérapeutique , Oesophagite/traitement médicamenteux , Recherche comparative sur l'efficacitéRÉSUMÉ
Heartburn occurs in 75% of patients with digestive discomfort of any origin and is one of the main symptoms of gastroesophageal reflux disease. Treatment focuses on lifestyle modification and symptomatology management with various drugs; when heartburn is moderate to severe, a proton pump inhibitor is more suitable. Omeprazole (OMZ) combined with sodium bicarbonate (BC) has demonstrated significant and sustained suppression of acid secretion. The objective was to compare the effect of sequential OMZ/BC therapy compared to OMZ monotherapy for the improvement of heartburn in Mexican individuals. The study was a double-blind, randomized, controlled, multicenter clinical study including 277 subjects with moderate to severe heartburn. Patients received 7 days of OMZ/BC and 7 days of OMZ (OMZ/BC7) or 14 days of OMZ (OMZ14). The primary endpoint was defined as the change in the number of days a week that the patient has heartburn, it was evaluated at 14 days. Both treatments reduced time (days) with heartburn by less than 4 days (OMZ14 3.9 vs. 4.2 days OMZ/BC7), as well as duration, number of events and intensity of heartburn. The treatments improved the quality of life, and the control of the symptoms. The proportion of adverse events was lower with OMZ/BC. The non-inferiority of OMZ/BC7 with respect to OMZ14 was verified.
La pirosis se presenta en el 75% de los pacientes con molestias digestivas de cualquier origen y es uno de los principales síntomas de la enfermedad por reflujo gastroesofágico. El tratamiento se enfoca en la modificación del estilo de vida y el manejo de la sintomatología con diversos fármacos; cuando la pirosis es moderada a severa, un inhibidor de la bomba de protones es más adecuado. El omeprazol (OMZ) combinado con bicarbonato de sodio (BC) ha demostrado supresión significativa y sostenida de la secreción ácida. El objetivo fue comparar el efecto de la terapia secuencial de OMZ/BC en comparación con el tratamiento continuo de OMZ para la mejoría de la pirosis en individuos mexicanos. Estudio clínico multicéntrico, doble ciego, controlado, aleatorizado que incluyó 277 sujetos con pirosis moderada a severa. Los pacientes recibieron 7 días de OMZ/BC y 7 días de OMZ (OMZ/BC7) o 14 días de OMZ (OMZ14). La variable primaria fue definida como el cambio del número de días a la semana que el paciente presenta pirosis, se evaluó a los 14 días. Ambos tratamientos redujeron los días con pirosis en menos 4 días (OMZ14 3,9 vs. 4,2 días OMZ/BC7), así como la duración, el número de eventos e intensidad de la pirosis. Los tratamientos mejoraron los indicadores de calidad de vida, y el control del padecimiento. La proporción de eventos adversos fue menor con OMZ/BC. Se comprobó la no-inferioridad de OMZ/BC7 respecto OMZ14.
Sujet(s)
Humains , Mâle , Femelle , Adulte , Adulte d'âge moyen , Oméprazole/usage thérapeutique , Hydrogénocarbonate de sodium/usage thérapeutique , Pyrosis/traitement médicamenteux , Oméprazole/administration et posologie , Oméprazole/effets indésirables , Méthode en double aveugle , Études prospectives , Résultat thérapeutique , Hydrogénocarbonate de sodium/administration et posologie , Hydrogénocarbonate de sodium/effets indésirables , Association de médicamentsRÉSUMÉ
Introducción: Los medicamentos antiulcerosos son utilizados frecuentemente en pacientes hospitalizados, sin embargo, a menudo este uso no está indicado. Objetivo: Describir la frecuencia de prescripción e indicación de medicamentos para prevenir el sangrado gastrointestinal en pacientes hospitalizados. Materiales y métodos: Estudio de corte trasversal, descriptivo, prospectivo del servicio de Medicina Interna de la Sociedad de Cirugía de Bogotá- Hospital de San José de Bogotá, Colombia. Se excluyeron pacientes con diagnóstico de sangrado gastrointestinal o antecedente de alergia a los medicamentos antiulcerosos. Se recolectaron datos demográficos, así como fármacos prescritos. Se determinó si la indicación del fármaco era adecuada y se identificó el tipo de error de prescripción. Resultados: Se incluyeron 179 pacientes, 102 (57%) mujeres. Promedio de edad de 61,3 años (±20,2). El principal diagnóstico de ingreso fue enfermedad infecciosa 76 (42,4%). Del total de pacientes, 165 (92,17%) recibieron medicamento para prevención del sangrado gastrointestinal. La indicación fue adecuada en 75 pacientes (41,89%). El error más frecuente fue el uso en pacientes de bajo riesgo de sangrado, 101 (97,1%). Conclusión: Un alto porcentaje de los pacientes recibió medicación para la prevención del sangrado gastrointestinal. En aproximadamente la mitad de estos no estaba indicada.
Introduction: Anti-ulcer medications are frequently used in hospitalized patients, yet their use is not usually indicated. Objective: To describe the frequency of prescription and indication of medications to prevent gastrointestinal bleeding in hospitalized patients. Materials and methods: A cross-sectional, descriptive, prospective study was carried out in the Internal Medicine service of the Surgery Society of Bogota-San Jose Hospital of Bogota (Colombia). Excluded patients were those with either a gastrointestinal bleeding diagnosis or a history of allergy to anti-ulcer medications. Demographic data and information regarding prescribed medications were collected. It was determined whether the medicine indication was adequate and the type of prescription error was identified. Results: 179 patients were included in the study, 57% (102) of which were women. The average age was 61.3 (±20.2) years old. Infectious disease was the main admission diagnosis (76; 42.4%). A 92.17% (165) of the total number of patients received medications to prevent gastrointestinal bleeding. This indication was adequate for 75 (41.89%) patients. The most frequent error was their use in bleeding low-risk patients (101; 97.1%). Conclusion: A high percentage of patients received medication to prevent gastrointestinal bleeding. However, in about half of these patients it was not indicated.
Sujet(s)
Humains , Préparations pharmaceutiques , Santé publique , Maladie , Ranitidine , Oméprazole , Directives , Prévention des Maladies , Hémorragie gastro-intestinaleRÉSUMÉ
A dirofilariose é uma enfermidade antropozoonótica que acomete, frequentemente, cães em regiões litorâneas, locais que favorecem a multiplicação de vetores transmissores de Dirofilariaspp. O objetivo deste trabalho foi relatar a possível ocorrência do primeiro caso autóctone de dirofilariose em cão doméstico, no município de Cambé, Paraná, distante cerca de 500 km do litoral. O paciente, um Lhasa Apso de 9 meses de idade e 4,8 Kg, foi atendido em clínica particular com histórico de apatia, hiporexia, êmese ecansaço intenso após exercício. O diagnóstico de dirofilariose foi confirmado a partir do Teste SNAP 4Dx Plus. O animal foi tratado com Doxiciclina 50 mg/kg/SID durante 30 dias, Moxidectina injetável e omeprazol 10 mg/kg uma vez ao dia, durante 30 dias. No retorno, um mês após o início do tratamento, o canino apresentou melhoras nas condições gerais e remissão de todos os sinais clínicos antes apresentados, evidenciando sucesso no protocolo farmacológico adotado. A ocorrência dessa doença em região não endêmica é preocupante, pois revela expansão da área de ocorrência, acompanhada, possivelmente, do número de insetos transmissores, responsáveis, também, pela disseminação de arboviroses, como a dengue. Assim, medidas de controle contra esses vetores e pesquisas a respeito da ocorrência de dirofilariose em áreas não endêmicas fazem-se necessárias.(AU)
Heartworm is a zoonotic disease that often affects dogs in coastal regions, places with favorable temperature conditions and humidity for Dirofilariaspp.' vectors replication. The aim of this study was to report the possible occurrence of the first autochthonous case of heartworm disease in a domestic dog, in the municipality of Cambé, Paraná, about 500 km from the coast. The patient, a 9-month-old Lhasa Apso weighing 4.8 Kg, was attended at a private clinic with a medical history of apathy, hyporexia, emesis and intense tiredness after exercise. The diagnosis of heartworm was confirmed by the SNAP 4Dx Plus Test. The animal was treated with Doxycycline 50 mg/kg/once a day for 30 days, injectable Moxidectin every six months and omeprazole 10 mg/kg once a day for 30 days. On return, 30 days after the start of treatment, the canine showed improvement in general conditions and remission of all clinical signs previously presented, evidencing success in the pharmacological protocol adopted. The occurrence of this disease in a non-endemic region is worrying and revels an expansion of the occurrence area, possibly accompanied by the number of transmitting insects, which are also responsible for the arboviruses spread, such as dengue. Therefore, control measures against this vectors and research on the occurrence of heartworm disease in non-endemic areas are necessary.(AU)
La dirofilariosis es una enfermedad antropozoótica que afecta, frecuentemente, a perros en regiones costeras, lugares que favorecen la multiplicación de vectores transmisores de Dirofilaria spp. El objetivo de este trabajo fue informar la posible ocurrencia del primer caso autóctono de dirofilariosis en perro doméstico, en la ciudad de Cambé, Paraná, distante cerca de 500 km del litoral. El paciente, un Lhasa Apso de 9 meses y 4,8 kg de peso, fue atendido en una clínica privada con una historia de apatía, hiporexia, emesis y cansancio intenso después del ejercicio. El diagnóstico de dirofilariosis se confirmó con la prueba SNAP 4Dx Plus. El animal fue tratado con Doxiciclina 50 mg/kg/SID durante 30 días, Moxidectina inyectable y omeprazol 10 mg/kg una vez al día durante 30 días. A su regreso, un mes después del inicio del tratamiento, el canino presentó una mejoría en su estado general y la remisión de todos los signos clínicos que presentaba anteriormente, lo que demuestra el éxito del protocolo farmacológico adoptado. La aparición de esta enfermedad en una región no endémica es preocupante, ya que revela una expansión del área de ocurrencia, posiblemente acompañada de un aumento del número de insectos que transmiten la enfermedad, que también son responsables de la diseminación de arbovirosis, como el dengue. Por ello, es necesario adoptar medidas de control contra estos vectores e investigar la aparición de la dirofilariosis en zonas no endémicas.(AU)
Sujet(s)
Animaux , Dirofilaria/pathogénicité , Dirofilariose/diagnostic , Dirofilariose/transmission , Oméprazole/administration et posologie , Brésil , Doxycycline/administration et posologie , Chiens/parasitologie , Anthelminthiques/administration et posologieRÉSUMÉ
The present study aims to compare the effectiveness of surgical and medical therapy in reducing the risk of cancer in Barrett's esophagus in a long-term evaluation. A prospective cohort was designed that compared Barrett's esophagus patients submitted to medical treatment with omeprazole or laparoscopic Nissen fundoplication. The groups were compared using propensity score matching paired by Barrett's esophagus length. A total of 398 patients met inclusion criteria. There were 207 patients in the omeprazole group (Group A) and 191 in the total fundoplication group (Group B). After applying the propensity score matching paired by Barrett's esophagus length, the groups were 180 (Group A) and 190 (Group B). Median follow-up was 80 months. Group B was significantly superior for controlling GERD symptoms. Group B was more efficient than Group A in promoting Barrett's esophagus regression or blocking its progression. Group B was more efficient than Group A in preventing the development of dysplasia and cancer. Logistic regression was performed for the outcomes of adenocarcinoma and dysplasia. Age and body mass index were used as covariates in the logistic regression models. Even after regression analysis, Group B was still superior to Group A to prevent esophageal adenocarcinoma or dysplasia transformation (odds ratio [OR]: 0.51; 95% confidence interval [CI]: 0.27-0.97, for adenocarcinoma or any dysplasia; and OR: 0.26; 95% CI: 0.08-0.81, for adenocarcinoma or high-grade dysplasia). Surgical treatment is superior to medical management, allowing for better symptom control, less need for reflux medication use, higher regression rate of the columnar epithelium and intestinal metaplasia, and lower risk for progression to dysplasia and cancer.
Sujet(s)
Adénocarcinome , Oesophage de Barrett , Tumeurs de l'oesophage , Laparoscopie , Humains , Oesophage de Barrett/complications , Oesophage de Barrett/traitement médicamenteux , Oesophage de Barrett/chirurgie , Gastroplicature , Études prospectives , Tumeurs de l'oesophage/étiologie , Tumeurs de l'oesophage/prévention et contrôle , Tumeurs de l'oesophage/diagnostic , Adénocarcinome/étiologie , Adénocarcinome/prévention et contrôle , Adénocarcinome/chirurgie , OméprazoleRÉSUMÉ
OBJECTIVES: To evaluate the differences concerning cognitive performance, oxidative stress and vitamin B12 levels in omeprazole users under treatment for longer than six months. METHODS: A case-control study was developed with 44 omeprazole users (OU; 81.8 % female, 66 ± 8.7 years old) and 35 nonusers (NOU; 88.6 % female, 62 ± 8.7 years old). The cognitive ability was assessed through tests approaching attention, memory and executive functions. The vitamin B12 was dosage using a chemiluminescent immunoassay and oxidative stress analysis, based on the evaluation of malondialdehyde, enzymatic activity of extracellular superoxide dismutase, glutathione peroxidase, catalase and the ferric reducing antioxidant power in plasma. KEY FINDINGS: A significant increase of the ferric reducing antioxidant power [omeprazole users (OU) group = 1690 µM ± 441 and nonusers (NOU) group = 1308 ± 616; P value=0.002] and a decrease on glutathione peroxidase levels [OU group = 0.534 (0.27-10.63) and NOU group = 71.86 (14.36-173.1); P value=0.006] were found on omeprazole users group, as well as differences on cognitive performance, with impairments on executive functions, automatic and attentional processing. CONCLUSIONS: Long-term use of omeprazole is suggested to induce an oxidative stress condition, which causes neurotoxicity and cognitive decline.
Sujet(s)
Antioxydants , Oméprazole , Sujet âgé , Antioxydants/analyse , Études cas-témoins , Cognition , Femelle , Glutathione peroxidase , Humains , Mâle , Adulte d'âge moyen , Oméprazole/effets indésirables , Stress oxydatif , Superoxide dismutase/métabolisme , Vitamine B12RÉSUMÉ
Introducción: Los inhibidores de la bomba de protones son fármacos usados en múltiples gastropatías. El omeprazol pertenece a este grupo de medicamentos y es aprobado y catalogado como indispensable por la Organización Mundial de la Salud. Esto ha causado que su uso se vuelva constante y hasta cierto punto equívoco. Pese a ser medicamentos seguros muestran efectos secundarios, dentro de los cuales uno ocasional es el trastorno hidroelectrolítico. Objetivo: Presentar un caso clínico en el cual se constató la presencia de efectos secundarios tras el uso de un fármaco de uso constante por la comunidad médica: el omeprazol. Caso clínico: Se presenta a continuación el caso clínico de un paciente masculino con antecedente de hipertensión arterial y gastropatía crónica que muestra uso por 8 años consecutivos de inhibidores de la bomba de protones, al cual se le diagnostica hipomagnesemia e hipocalcemia. Se obtuvieron resultados de laboratorio normales tras administración de suplementos orales y uso de ranitidina con supresión de terapéutica con omeprazol. Conclusiones: Un control constante de los fármacos que usan los pacientes crónicos es fundamental en atención primaria de salud. El uso de inhibidores de la bomba de protones se ha convertido en rutinario y es necesario corroborar siempre la dosis y el tiempo de uso de los fármacos además de la relación con otros medicamentos que use el paciente(AU)
Introduction: Proton-pump inhibitors are drugs used in multiple gastropathies. Omeprazole belongs to this group of medicines; it is approved and classified as essential by the World Health Organization. This has permitted for its use to become constant and, to some extent, misleading. Despite being safe drugs, they show side effects, among which an occasional one is fluid and electrolyte disorders. Objective: To present a clinical case in which the occurrence of side effects was verified after the administration of a drug constantly used by the medical community. Clinical case: The following is a clinical case of a male patient with a history of arterial hypertension and chronic gastropathy, characterized by the usage of proton-pump inhibitors for eight consecutive years, diagnosed with hypomagnesemia and hypocalcemia. Normal laboratory results were obtained after oral supplementation and usage of ranitidine with suppression of omeprazole therapy. Conclusions: Constant control of the drugs used by chronic patients is essential in primary health care. The usage of proton-pump inhibitors has become a routine. It is always necessary to check the dose and time for using the drugs as well as the relationship with other drugs used by the patient(AU)
Sujet(s)
Humains , Mâle , Soins de santé primaires , Ranitidine/usage thérapeutique , Maladies de l'estomac/épidémiologie , Oméprazole/usage thérapeutique , Inhibiteurs de la pompe à protons , Hypocalcémie/diagnosticRÉSUMÉ
Giardiasis represents a latent problem in public health due to the exceptionally pathogenic strategies of the parasite Giardia lamblia for evading the human immune system. Strains resistant to first-line drugs are also a challenge. Therefore, new antigiardial therapies are urgently needed. Here, we tested giardial arginine deiminase (GlADI) as a target against giardiasis. GlADI belongs to an essential pathway in Giardia for the synthesis of ATP, which is absent in humans. In silico docking with six thiol-reactive compounds was performed; four of which are approved drugs for humans. Recombinant GlADI was used in enzyme inhibition assays, and computational in silico predictions and spectroscopic studies were applied to follow the enzyme's structural disturbance and identify possible effective drugs. Inhibition by modification of cysteines was corroborated using Ellman's method. The efficacy of these drugs on parasite viability was assayed on Giardia trophozoites, along with the inhibition of the endogenous GlADI. The most potent drug against GlADI was assayed on Giardia encystment. The tested drugs inhibited the recombinant GlADI by modifying its cysteines and, potentially, by altering its 3D structure. Only rabeprazole and omeprazole decreased trophozoite survival by inhibiting endogenous GlADI, while rabeprazole also decreased the Giardia encystment rate. These findings demonstrate the potential of GlADI as a target against giardiasis.
Sujet(s)
Giardia lamblia/effets des médicaments et des substances chimiques , Giardiase/traitement médicamenteux , Hydrolases/métabolisme , Animaux , Antiprotozoaires/pharmacologie , Simulation numérique , Cystéine/composition chimique , Évaluation préclinique de médicament/méthodes , Repositionnement des médicaments/méthodes , Giardia lamblia/pathogénicité , Giardiase/immunologie , Aurothiomalate de sodium/pharmacologie , Humains , Hydrolases/effets des médicaments et des substances chimiques , Hydrolases/ultrastructure , Oméprazole/pharmacologie , Inhibiteurs de la pompe à protons/pharmacologie , Rabéprazole , Thiamine/analogues et dérivés , Thiamine/pharmacologie , Trophozoïtes/effets des médicaments et des substances chimiquesRÉSUMÉ
ETHNOPHARMACOLOGICAL RELEVANCE: Peptic ulcer is an inflammatory disease that therapeutic options are mainly focused in antisecretory drugs. Sedum dendroideum Moc & Sessé ex DC (Crassulaceae) is employed in folk medicine for the treatment of gastric ulcers. Recently, our group demonstrated that Sedum dendroideum infusion (SDI) is rich in polyphenols (flavonol glycosides, myricetin, quercetin and kaempferol) and promoted gastroprotection against acute ulcer models, without changes gastric acid secretion. AIM OF THE STUDY: Here, we follow the investigation of the healing effects of SDI (ED50 = 191 mg/kg) in the chronic gastric ulcer model induced by 80% acetic acid in rats, elucidating underlying mechanisms. MATERIAL AND METHODS: Rats were orally treated with vehicle (water, 1 mL/kg), SDI (191 mg/kg), omeprazole (40 mg/kg) or sucralfate (100 mg/kg) twice daily for 5 days after ulcer induction. Following treatments, toxicological effects, macroscopic ulcer appearance, microscopic histological (HE, mucin PAS-staining) and immunohistochemical (PCNA and HSP70) analysis, inflammatory (MPO and NAG activity, cytokine levels measurements) and antioxidant (SOD and CAT) parameters were investigated in gastric ulcer tissues. RESULTS: Oral treatment with SDI accelerated gastric ulcer healing, maintained mucin content and promoted epithelial cell proliferation. SDI also reduced neutrophil and mononuclear leukocyte infiltration, TNF-α and IL-1ß levels and the oxidative stress, restoring SOD and CAT activities in the ulcer tissue. CONCLUSIONS: The gastric healing effect of SDI was mediated through endogenous protective events as well as due to the anti-inflammatory and antioxidant actions. Our observations support and reinforce the traditional utilize of Sedum dendroideum as a natural nontoxic therapeutic alternative for the treatment of gastric ulcers.
Sujet(s)
Antiulcéreux/pharmacologie , Sedum/composition chimique , Ulcère gastrique/prévention et contrôle , Animaux , Anti-inflammatoires/isolement et purification , Anti-inflammatoires/pharmacologie , Antiulcéreux/isolement et purification , Antioxydants/isolement et purification , Antioxydants/pharmacologie , Modèles animaux de maladie humaine , Femelle , Oméprazole/pharmacologie , Stress oxydatif/effets des médicaments et des substances chimiques , Extraits de plantes/pharmacologie , Polyphénols/isolement et purification , Polyphénols/pharmacologie , Rats , Rat Wistar , Sucralfate/pharmacologieRÉSUMÉ
La ulceración esofágica por ingestión de doxiciclina es una de las causas más frecuentes de lesión esofágica. Ha sido subdiagnosticada y escasamente reconocida en dermatología. El dolor retroesternal, la odinofagia de aparición brusca y el antecedente de ingesta de doxiciclina u otros fármacos son características que facilitan su diagnóstico. Puede presentar complicaciones serias, como hemorragias, estenosis y mediastinitis.
Esophageal ulceration due to ingestion of doxycycline is one of the most frequent causes of esophageal injury. It has been underdiagnosed and scarcely recognized in dermatology. Retrosternal pain, sudden odynophagia and a history of doxycycline or other drugs intake are some of the characteristics that lead to diagnosis. It may cause severe complications such as bleeding, stenosis and mediastinitis.
Sujet(s)
Humains , Femelle , Adulte , Jeune adulte , Ulcère/induit chimiquement , Doxycycline/effets indésirables , Maladies de l'oesophage/induit chimiquement , Antibactériens/effets indésirables , Ulcère/diagnostic , Ulcère/traitement médicamenteux , Oméprazole/administration et posologie , Maladies de l'oesophage/diagnostic , Maladies de l'oesophage/traitement médicamenteux , Endoscopie par capsule , Antiulcéreux/administration et posologieRÉSUMÉ
Proton pump inhibitors (PPI) are commonly used drugs that may increase the cardiovascular risk by mechanisms not entirely known. We examined whether the PPI omeprazole promotes vascular oxidative stress mediated by xanthine oxidoreductase (XOR) leading to activation of matrix metalloproteinases (MMPs) and vascular remodeling. We studied Wistar rats treated with omeprazole (or vehicle) combined with the XOR inhibitor allopurinol (or vehicle) for four weeks. Systolic blood pressure (SBP) measured by tail-cuff plethysmography was not affected by treatments. Omeprazole treatment increased the aortic cross-sectional area and media/lumen ratio by 25% (P < 0.05). Omeprazole treatment decreased gastric pH and induced vascular remodeling accompanied by impaired endothelium-dependent aortic responses (assessed with isolated aortic ring preparation) to acetylcholine (P < 0.05). Omeprazole increased vascular active MMP-2 expression and activity assessed by gel zymography and in situ zymography, respectively (P < 0.05). Moreover, omeprazole enhanced vascular oxidative stress assessed in situ with the fluorescent dye DHE and with the lucigenin chemiluminescence assay (both P < 0.05). All these biochemical changes caused by omeprazole were associated with increased vascular XOR activity (but not XOR expression assessed by Western blot) and treatment with allopurinol fully prevented them (all P < 0.05). Importantly, treatment with allopurinol prevented the vascular dysfunction and remodeling caused by omeprazole. Our results suggest that the long-term use of omeprazole induces vascular dysfunction and remodeling by promoting XOR-derived reactive oxygen species formation and MMP activation. These findings provide evidence of a new mechanism that may underlie the unfavorable cardiovascular outcomes observed with PPI therapy. Clinical studies are warranted to validate our findings.