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1.
Bratisl Lek Listy ; 119(10): 625-629, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30345769

RESUMO

BACKGROUND: Apelin is an endogenous adipocytokine that plays an important role in the regulation of cardiovascular function. Apelin-36 is a member of apelin family. However cardiac reports related to apelin-36 are very rare. The purpose of this study is to investigate the impact of apelin-36 on hemodynamic variables of the isolated rat hearts. METHODS: Twenty-eight rats were equally divided into four groups: control, apelin-36 at the following concentrations: 1 nM, 10 nM and 100 nM. The isolated hearts were perfused with modified Krebs-Henseleit solution (mK-Hs) by using the Langendorff method. Cardiac parameters, including left ventricular developed pressure (LVDP), maximal rate of pressure development (+dP/dtmax), heart rate (HR) and coronary flow (CF) were measured. Gene expressions relevant to cardiomyocyte contractility were determined by real-time PCR. RESULTS: 10 and 100 nM doses of apelin-36 perfusion led to positive inotropy with an increase of LVDP and +dP/dtmax, which are the indexes of cardiac contractility. Furthermore both doses of apelin-36 increased endothelial nitric oxide synthase (eNOS), sarco/endoplasmic reticulum Ca2+-ATPase (Serca2a) and ß2-Adrenergic receptors (ß2-AR) mRNA. CONCLUSION:  These results showed that apelin-36 had a positive inotropic effect on the isolated rat heart and can induce eNOS, Serca2a and ß2-AR genes activation that enhances contractility of the heart (Tab. 1, Fig. 2, Ref. 23).


Assuntos
Apelina , Frequência Cardíaca , Coração , Contração Miocárdica , Animais , Apelina/fisiologia , Coração/fisiologia , Contração Miocárdica/fisiologia , Miócitos Cardíacos , Perfusão , Ratos
2.
Bratisl Lek Listy ; 118(8): 443-448, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29050480

RESUMO

OBJECTIVE: Our study aimed to investigate the possible modifying effects of leptin and combined use of resveratrol on rat renal I/R injury and their relationship on signal pathways and apoptosis-related mechanisms. BACKGROUND: Renal ischemia-reperfusion (I/R) injury is an important cause of acute renal failure. METHODS: Male Sprague Dawley rats were divided into 5 groups: Control, I/R, I/R+leptin, I/R+resveratrol and I/R+leptin+resveratrol. Leptin (10 µg/kg BW) was administered (i.p.) 30 min prior to I/R. Resveratrol was administered by gavage at 20 mg/kg BW per d for 12 d prior to I/R. The left renal artery was exposed to 1 h of ischemia and 1 h of reperfusion. RESULTS: Resveratrol treatment alone increased TNF-α, TNF-α R1, NF-κB, SIRT-1, STAT1 and STAT3 mRNA levels and decreased caspase 3 protein levels. Leptin treatment alone significantly decreased the caspase 3 protein levels. The combined use of resveratrol and leptin significantly increased STAT3, and caspase 3 mRNA levels, and decreased the caspase 3 protein levels. Apoptosis was significantly decreased especially in the leptin and leptin+resveratrol groups. CONCLUSION: The present study suggest that a combined use of resveratrol and leptin has preventive and regulatory effects on renal I/R injury; the mechanism involves decreasing apoptosis, likely by altering the JAK/STAT pathway and SIRT1 expression (Fig. 8, Ref. 24).


Assuntos
Antioxidantes/farmacologia , Rim/efeitos dos fármacos , Leptina/farmacologia , Traumatismo por Reperfusão/genética , Sirtuína 1/efeitos dos fármacos , Estilbenos/farmacologia , Animais , Apoptose/efeitos dos fármacos , Caspase 3/efeitos dos fármacos , Caspase 3/genética , Caspase 3/metabolismo , Expressão Gênica , Rim/metabolismo , Masculino , NF-kappa B/efeitos dos fármacos , NF-kappa B/genética , RNA Mensageiro/efeitos dos fármacos , RNA Mensageiro/metabolismo , Ratos , Ratos Sprague-Dawley , Receptores do Fator de Necrose Tumoral/efeitos dos fármacos , Receptores do Fator de Necrose Tumoral/genética , Traumatismo por Reperfusão/metabolismo , Resveratrol , Fator de Transcrição STAT1/efeitos dos fármacos , Fator de Transcrição STAT1/genética , Fator de Transcrição STAT3/efeitos dos fármacos , Fator de Transcrição STAT3/genética , Transdução de Sinais , Sirtuína 1/genética , Fator de Necrose Tumoral alfa/efeitos dos fármacos , Fator de Necrose Tumoral alfa/genética
3.
Bratisl Lek Listy ; 118(7): 391-393, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28766347

RESUMO

OBJECTIVE: The aim of this study was to investigate the effects of a novel anti-cancer drug, ceranib-2, which targets the acid ceramidase, in human colon cancer cell line. MATERIALS AND METHODS: The cell lines were treated with 50 µM of ceranib-2. Relative mRNA expression of TNF-alpha, TNF-R1 and ASAH were assessed by quantitative RT-PCR. RESULTS: Ceranib-2 reduced cell viability in a dose-dependent manner and the apoptotic values of cells following treatment with the dose of 50 µM were reduced significantly both at 24 h and 48 h compared to the control cells (p < 0.001). TNF-alpha receptor 1 (TNF-R1) mRNA levels were reduced significantly in the cell lines treated with both 25 µM and 50 µM of ceranib-2 for 24 h compared to the control cells (p < 0.05), whereas the difference between the treatment and the control cell lines diminished at 48 h. The human acid ceramidase gene (ASAH) mRNA levels were significantly higher in the cell lines treated with 50 µM of ceranib-2 for 48 h than in the other cell lines (p < 0.001). CONCLUSION: The study shows that ceranib-2 increased apoptosis by inducing ASAH expression and reduced TNF-R1 expression in human colon cancer cell lines in a dose and time-dependent manner (Fig. 3, Ref. 17).


Assuntos
Antineoplásicos/farmacologia , Neoplasias do Colo/tratamento farmacológico , Quinolonas/farmacologia , Fator de Necrose Tumoral alfa/efeitos dos fármacos , Ceramidase Ácida/efeitos dos fármacos , Apoptose/efeitos dos fármacos , Linhagem Celular , Sobrevivência Celular/efeitos dos fármacos , Humanos
5.
J Hosp Infect ; 62(2): 156-62, 2006 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16307824

RESUMO

This study was conducted to evaluate the impact of central venous catheters impregnated with chlorhexidine and silver sulphadiazine on the incidence of colonization and catheter-related bloodstream infection in critically ill patients. One hundred and thirty-three patients requiring central venous catheterization were chosen at random to receive either an antiseptic-impregnated triple-lumen catheter (N=64) or a standard triple-lumen catheter (N=69). The mean (SD) durations of catheterization for the antiseptic and standard catheters were 11.7 (5.8) days (median 10; range 3-29) and 8.9 (4.6) days (median 8.0; range 3-20), respectively (P=0.006). Fourteen (21.9%) of the antiseptic catheters and 14 (20.3%) of the standard catheters had been colonized at the time of removal (P=0.834). Four cases (6.3%) of catheter-related bloodstream infection were associated with antiseptic catheters and one case (1.4%) was associated with a standard catheter (P=0.195). The catheter colonization rates were 18.7/1000 catheter-days for the antiseptic catheter group and 22.6/1000 catheter-days for the standard catheter group (P=0.640). The catheter-related bloodstream infection rates were 5.3/1000 catheter-days for the antiseptic catheter group and 1.6/1000 catheter-days for the standard catheter group (P=0.452). In conclusion, our results indicate that the use of antiseptic-impregnated central venous catheters has no effect on the incidence of either catheter colonization or catheter-related bloodstream infection in critically ill patients.


Assuntos
Anti-Infecciosos Locais/administração & dosagem , Bacteriemia/epidemiologia , Cateterismo Venoso Central/efeitos adversos , Cateteres de Demora/microbiologia , Unidades de Terapia Intensiva , Anti-Infecciosos Locais/uso terapêutico , Bacteriemia/etiologia , Bacteriemia/prevenção & controle , Infecções Bacterianas/epidemiologia , Infecções Bacterianas/etiologia , Clorexidina/administração & dosagem , Clorexidina/uso terapêutico , Contaminação de Equipamentos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Sulfadiazina de Prata/administração & dosagem , Sulfadiazina de Prata/uso terapêutico , Resultado do Tratamento
6.
Eur J Anaesthesiol ; 19(7): 517-21, 2002 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12113615

RESUMO

BACKGROUND AND OBJECTIVE: The aim was to compare the effects of two different priming doses and priming intervals with the standard intubating dose of rocuronium on the onset time and intubation conditions. METHODS: After induction of anaesthesia, 75 patients were randomly assigned to one of five groups. Patients in Group 1 received a priming dose of rocuronium 0.06 mg kg(-1) followed 2 min later by rocuronium 0.54 mg kg(-1), Group 2 received a priming dose of 0.10 mg kg(-1) followed 2 min later by a rocuronium injection of 0.50 mg kg(-1). Group 3 was given a priming dose of 0.06 mg kg(-1) followed 3 min later by administration 0.54 mg kg(-1), where Group 4 received a priming dose of 0.10 mg kg(-1) followed 3 min later by injection of 0.50 mg kg(-1). Group 5 received a placebo injection followed 3 min later by rocuronium 0.60 mg kg(-1). RESULTS: Priming with a 3 min priming interval shortened the onset time of rocuronium irrespective of the dosage of (P < 0.001). Clinical duration of action was significantly longer after priming in Group 4 than in Group 5. Clinically acceptable intubation conditions were obtained in all patients. CONCLUSIONS: Priming with a 3 min priming interval was effective when rapid tracheal intubation with rocuronium was necessary. However, priming with rocuronium should be used carefully with special attention given to the possibility of hypoxia and aspiration of gastric contents in awake patients.


Assuntos
Androstanóis/administração & dosagem , Intubação Intratraqueal , Fármacos Neuromusculares Despolarizantes/administração & dosagem , Adolescente , Adulto , Idoso , Análise de Variância , Relação Dose-Resposta a Droga , Procedimentos Cirúrgicos Eletivos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Bloqueio Neuromuscular , Rocurônio , Fatores de Tempo
7.
J Int Med Res ; 29(5): 385-8, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-11725824

RESUMO

A randomized, double-blind, placebo-controlled study was carried out to investigate the efficacy of 2 mg versus 5 mg tropisetron in the prevention of post-operative nausea and vomiting. Patients between 22 and 64 years old who were undergoing surgery under general anaesthesia and who had been classified according to the American Society of Anesthesiologists criteria with physical status I or II were included in this trial. Sixty female patients were recruited and divided into three groups (n = 20 in each group). Patients in group 1 received saline solution as control, whereas in groups 2 and 3, 2 mg or 5 mg tropisetron, respectively, was administered intravenously as a single dose during the induction of anaesthesia. The number of patients vomiting within the first 2 h following the operation was significantly less in groups 2 and 3 compared with that in group 1 (one of 20 for each of the groups 2 and 3 versus 12 of 20 in group 1). Three patients required rescue anti-emetic medication in each of the groups 2 and 3. In conclusion, 2 mg tropisetron appears to be equally as efficacious as 5 mg in preventing post-operative nausea and vomiting.


Assuntos
Antieméticos/uso terapêutico , Indóis/uso terapêutico , Náusea/prevenção & controle , Complicações Pós-Operatórias/prevenção & controle , Vômito/prevenção & controle , Adulto , Anestesia Geral/efeitos adversos , Relação Dose-Resposta a Droga , Método Duplo-Cego , Humanos , Pessoa de Meia-Idade , Tropizetrona , Vômito/epidemiologia
8.
J Int Med Res ; 29(5): 437-40, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-11725832

RESUMO

Blind nasoenteric intubation was attempted in a patient with chronic parkinsonism. The tube was inadvertently misplaced and penetrated the left pleural cavity. The next day, the patient developed cardiopulmonary arrest during dietary supplement infusion. This complication ultimately led to the patient's death. We have reviewed the known complications of nasoenteric tube placement and conclude that difficult insertion in patients at risk from tube misplacement should be followed by chest radiography to confirm the correct placement of the tube before nutritional support is started.


Assuntos
Nutrição Enteral/efeitos adversos , Hidrotórax/etiologia , Idoso , Nutrição Enteral/instrumentação , Falha de Equipamento , Evolução Fatal , Parada Cardíaca/etiologia , Humanos , Masculino
9.
J Int Med Res ; 29(6): 541-5, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-11803740

RESUMO

Patients with tracheal stenosis have a high incidence of difficult or failed tracheal intubation. Airway management with the laryngeal mask airway during fibreoptic laryngoscopy was used in two children with acquired subglottic stenosis during spontaneous breathing. The laryngeal mask airway may be superior to tracheal intubation or use of a face mask during anaesthesia management in severe subglottic stenosis. Ventilation may be improved and the use of a laryngeal mask airway can reduce or eliminate some of the problems associated with the other methods of airway management, such as further damage to stenotic tissue and gastric distention.


Assuntos
Glote/patologia , Laringoestenose/terapia , Laringe , Máscaras , Criança , Pré-Escolar , Feminino , Humanos , Laringoestenose/fisiopatologia , Masculino
10.
Eur J Anaesthesiol ; 17(11): 688-91, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11029567

RESUMO

Tracheostomy is necessary in intensive care unit (ICU) patients requiring prolonged mechanical ventilation. As an alternative to the standard surgical method, percutaneous techniques are available. Seventy-two patients were electively selected for percutaneous tracheostomy (PCT) in a nine-bed combined medical-surgical intensive care unit. PCT was performed at bedside with the Portex Percutaneous Tracheostomy Kit that uses the Griggs technique. The procedure time and early complications were recorded. The procedure was successful in all patients. The average duration of placement was 7.4 min. There were no tracheostomy-related deaths. Major bleeding occurred in three patients and required surgical intervention. In one patient, minor bleeding occurred at the stoma site that resolved with applied pressure. Wound infections were treated with local antiseptics in two patients. These findings suggest that PCT is a simple, quick and safe procedure.


Assuntos
Estado Terminal , Traqueostomia/métodos , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Anti-Infecciosos Locais/uso terapêutico , Perda Sanguínea Cirúrgica , Cuidados Críticos , Seguimentos , Humanos , Pessoa de Meia-Idade , Procedimentos Cirúrgicos Minimamente Invasivos , Hemorragia Pós-Operatória/etiologia , Respiração Artificial , Segurança , Infecção da Ferida Cirúrgica/etiologia , Fatores de Tempo , Traqueostomia/efeitos adversos , Resultado do Tratamento
12.
J Emerg Med ; 18(4): 405-8, 2000 May.
Artigo em Inglês | MEDLINE | ID: mdl-10802415

RESUMO

Hemorrhage is a potent stimulus for the release of vasopressin (VP), renin, and adrenocorticotropic hormone (ACTH). The goal of this study was to analyze changes in plasma VP, renin, and ACTH levels during hemorrhagic shock and resuscitation with two different solutions: hypertonic acetate dextran (HAD) and lactated Ringer's (LR) solution. Eight randomized dogs were shocked by removing 37 +/- 9 mL/kg of blood while maintaining the mean arterial pressure (MAP) at 45 +/- 5 mmHg for 1 h. Test solutions were randomized and infused as needed with the hemorrhaged blood to restore the MAP and cardiac index to baseline. Blood samples for hormone analyses were taken in baseline, shock, and resuscitation periods. For each experiment, all hormone levels increased in the postshock period and then returned to baseline values after resuscitation with both solutions. VP and renin levels rapidly returned to baseline values after resuscitation in the LR dogs compared with the HAD dogs (p < 0.05). By contrast, there was no significant difference in ACTH levels between the two solutions. High-volume infusion with LR achieves more rapid restoration than small-volume infusion with HAD for VP and renin levels.


Assuntos
Hormônio Adrenocorticotrópico/sangue , Dextranos/uso terapêutico , Modelos Animais de Doenças , Hidratação/métodos , Soluções Hipertônicas/uso terapêutico , Soluções Isotônicas/uso terapêutico , Substitutos do Plasma/uso terapêutico , Renina/sangue , Ressuscitação/métodos , Choque Hemorrágico/sangue , Choque Hemorrágico/terapia , Vasopressinas/sangue , Animais , Pressão Sanguínea/efeitos dos fármacos , Débito Cardíaco/efeitos dos fármacos , Dextranos/farmacologia , Cães , Avaliação Pré-Clínica de Medicamentos , Monitoramento de Medicamentos , Soluções Hipertônicas/farmacologia , Soluções Isotônicas/farmacologia , Substitutos do Plasma/farmacologia , Distribuição Aleatória , Lactato de Ringer
13.
Intensive Care Med ; 25(9): 1010-2, 1999 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10501761

RESUMO

In this study, the effects of alternate use of imipenem and cefoperazone/sulbactam(CFP/Sul) on antibiotic resistance in the intensive care unit (ICU) were investigated. Between 1 April 1993 and 1 April 1994, the infectious diseases consultant saw patients when required and there was no alternative therapy for antibiotics. For the following 2 years, the same consultant followed up each patient from admission to discharge by daily visits to the ICU and an alternative therapy protocol was initiated. The most common microorganisms were found to be Acinetobacter baumannii and Staphylococcus aureus, followed by Pseudomonas aeruginosa and Klebsiella pneumoniae, respectively, in the two periods. This study demonstrated that sensitivity rates of imipenem, ciprofloxacin and aminoglycosides were improved as a result of this protocol.


Assuntos
Antibacterianos/uso terapêutico , Infecções Bacterianas/tratamento farmacológico , Cuidados Críticos , Infecção Hospitalar/tratamento farmacológico , Encaminhamento e Consulta , Bactérias/efeitos dos fármacos , Bactérias/isolamento & purificação , Infecções Bacterianas/microbiologia , Distribuição de Qui-Quadrado , Protocolos Clínicos , Infecção Hospitalar/microbiologia , Humanos , Testes de Sensibilidade Microbiana/estatística & dados numéricos , Fatores de Tempo
14.
J Int Med Res ; 24(3): 266-70, 1996.
Artigo em Inglês | MEDLINE | ID: mdl-8725987

RESUMO

Post-operative vomiting, especially in ambulatory surgical patients, remains a troublesome problem. This placebo-controlled, randomized, prospective double-blind trial was designed to evaluate the efficacy of two prophylactic anti-emetic regimens on post-operative vomiting in 1-day thyroid surgery. Altogether 60 elective surgical patients were followed for 4 h post-operatively. All patients were American Society of Anesthesiologists physical status of I or II and aged between 22 and 60 years: group 1 was saline control; in groups 2 and 3, metoclopramide (0.2 mg/kg) or tropisetron (5 mg) was administered, respectively, as an intravenous single dose during induction. Patients were pre-medicated. A standardized anaesthetic technique consisting of thiopentone-succinylcholine for induction and fentanyl-nitrous oxide-halothane-pancuronium for maintenance of anaesthesia was used. A 'rescue' anti-emetic was provided in case of continued vomiting or at the patient's request. Anti-emetic inefficacy was defined as request for rescue anti-emetic and/or vomiting episode during the first 4 h post-operation. The number of patients vomiting was 12/20 (60%), 10/20 (50%) and 1/20 (5%) within the first 2 h post-operation in groups 1, 2 and 3, respectively (P > 0.05 for groups 1 and 2; P < 0.01 for groups 2 and 3; P < 0.001 for groups 1 and 3). In group 2, three patients required rescue medication during the first 2 h post-operation, but no significant difference was observed between groups 2 and 3 (P > 0.05). None of the cases in any of the groups needed any rescue medication during post-operative 2-4 h. It is concluded that tropisetron is a highly effective anti-emetic drug in the prophylaxis of post-operative vomiting.


Assuntos
Antieméticos/uso terapêutico , Procedimentos Cirúrgicos Eletivos , Indóis/uso terapêutico , Metoclopramida/uso terapêutico , Complicações Pós-Operatórias/prevenção & controle , Antagonistas da Serotonina/uso terapêutico , Adulto , Método Duplo-Cego , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Placebos , Estudos Prospectivos , Tropizetrona
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