RESUMEN
BACKGROUND: The ECG pattern of right bundle branch block and ST-segment elevation in leads V(1) to V(3) (Brugada syndrome) is associated with high risk of sudden death in patients with a normal heart. Current management and prognosis are based on a single study suggesting a high mortality risk within 3 years for symptomatic and asymptomatic patients alike. As a consequence, aggressive management (implantable cardioverter defibrillator) is recommended for both groups. METHODS AND RESULTS: Sixty patients (45 males aged 40+/-15 years) with the typical ECG pattern were clinically evaluated. Events at follow-up were analyzed for patients with at least one episode of aborted sudden death or syncope of unknown origin before recognition of the syndrome (30 symptomatic patients) and for patients without previous history of events (30 asymptomatic patients). Prevalence of mutations of the cardiac sodium channel was 15%, demonstrating genetic heterogeneity. During a mean follow-up of 33+/-38 months, ventricular fibrillation occurred in 5 (16%) of 30 symptomatic patients and in none of the 30 asymptomatic patients. Programmed electrical stimulation was of limited value in identifying patients at risk (positive predictive value 50%, negative predictive value 46%). Pharmacological challenge with sodium channel blockers was unable to unmask most silent gene carriers (positive predictive value 35%). CONCLUSIONS: At variance with current views, asymptomatic patients are at lower risk for sudden death. Programmed electrical stimulation identifies only a fraction of individuals at risk, and sodium channel blockade fails to unmask most silent gene carriers. This novel evidence mandates a reappraisal of therapeutic management.
Asunto(s)
Bloqueo de Rama/diagnóstico , Bloqueo de Rama/genética , Electrocardiografía , Adulto , Sustitución de Aminoácidos , Bloqueo de Rama/terapia , Estudios de Cohortes , Análisis Mutacional de ADN , Muerte Súbita Cardíaca/etiología , Desfibriladores Implantables , Supervivencia sin Enfermedad , Terapia por Estimulación Eléctrica , Electrocardiografía/efectos de los fármacos , Electrocardiografía Ambulatoria , Femenino , Estudios de Seguimiento , Humanos , Masculino , Canal de Sodio Activado por Voltaje NAV1.5 , Penetrancia , Valor Predictivo de las Pruebas , Reproducibilidad de los Resultados , Medición de Riesgo , Bloqueadores de los Canales de Sodio , Canales de Sodio/genética , Estadísticas no Paramétricas , Síncope/etiología , SíndromeRESUMEN
Because interferon-gamma (IFN gamma) is present in the central nervous system during neurologic diseases associated with inflammation, its effect on endotoxin-induced cytokines was studied. Cerebrospinal fluid (CSF) and serum levels of interleukin (IL)-1beta, IL-6, and tumor necrosis factor-alpha (TNF alpha), their messenger RNA expression in brain areas (hypothalamus, hippocampus, and striatum) and in spleen were evaluated 2 and 8 h after endotoxin [lipopolysaccharide (LPS), 25 microg/rat i.c.v.], IFN gamma (2.5 microg/rat i.c.v.) or after their coadministration in rats. CSF and serum IL-1beta levels were increased by LPS alone and IFN gamma coadministration did not furtherly increase them. IFN gamma potentiated LPS effect on IL-6 and TNF alpha levels in both CSF and serum. LPS and IFN-gamma coadministration did not alter IL-1beta messenger RNA expression induced by LPS in brain areas and in spleen, but it potentiated that of IL-6 and TNF alpha. The present in vivo data show that i.c.v. coadministration of LPS and IFN gamma results in a potentiation of cytokine production (IL-6 and TNF alpha) which may trigger a cascade of events relevant to neurodegenerative processes. This action is independent of IL-1beta because the production of this cytokine is not altered by IFN gamma treatment.
Asunto(s)
Encéfalo/metabolismo , Interferón gamma/farmacología , Interleucina-1/metabolismo , Interleucina-6/metabolismo , Lipopolisacáridos/farmacología , Factor de Necrosis Tumoral alfa/metabolismo , Animales , Encéfalo/efectos de los fármacos , Citocinas/sangre , Citocinas/líquido cefalorraquídeo , Interleucina-1/genética , Interleucina-6/genética , Masculino , ARN Mensajero/metabolismo , Ratas , Ratas Sprague-Dawley , Factor de Necrosis Tumoral alfa/genéticaRESUMEN
OBJECTIVE: To investigate the association between parkin gene mutations and parkinsonism in an Italian family in which three of 12 siblings born to first-degree consanguineous parents had early-onset parkinsonism. BACKGROUND: Several deleting or truncating mutations as well as missense mutations of the parkin gene were associated with early-onset parkinsonism. METHOD: Three brothers were examined clinically at several stages of the disease. Single-strand conformational polymorphism analysis was done on the parkin gene of 32 members of the family. Samples showing mobility shifts were considered for mutation analysis. RESULTS: Direct DNA sequencing revealed a novel homozygous amino acid substitution, Arg42Pro, in all three patients compared with a control DNA sample. The mutation occurred in the ubiquitinlike domain at the N-terminal of the protein. The patients did not display the clinical hallmarks previously seen with parkin mutations and were indistinguishable from patients with sporadic PD. CONCLUSIONS: These findings confirm the recessive character of parkin mutations causing early-onset parkinsonism and the essential role of the ubiquitinlike region, highly conserved among species, and in accordance with the proposed parkin function.
Asunto(s)
Ligasas/genética , Trastornos Parkinsonianos/genética , Ubiquitina-Proteína Ligasas , Ubiquitinas/genética , ADN/análisis , Femenino , Humanos , Italia , Masculino , Persona de Mediana Edad , Mutación/genética , LinajeRESUMEN
To study the role of the sympathetic nervous system in the induction of inflammatory cytokines elicited by central lipopolysaccharide, sympathetic chemical denervation was performed by intraperitoneal injection of 6-hydroxydopamine. Rats received the neurotoxin according to the following schedule: 50 mg/kg on days 1 and 2, 100 mg/kg on days 3, 4 and 7. On day 8, lipopolysaccharide (2.5 microg/6 microl/rat) was injected intracerebroventricularly and rats were killed 2 h later. 6-Hydroxydopamine reduced noradrenaline and dopamine content in the spleen by 88.7% and 88.8% respectively, without affecting striatal contents indicating that the chemical sympathectomy had been effective and selective. In sympathectomized rats, lipopolysaccharide raised interleukin-1beta and interleukin-6 serum levels more than in control rats given the vehicle. Tumour necrosis factor-alpha serum levels in sympathectomized rats were no different from those in vehicle-treated rats. Interleukin-1beta and interleukin-6 messenger RNA expression, measured by northern blot analysis, was clearly detectable in adrenals and spleen of rats given lipopolysaccharide. Sympathectomy increased lipopolysaccharide-induced interleukin-1beta and interleukin-6 messenger RNA in adrenals and spleen. Corticosterone basal levels were raised by central lipopolysaccharide and not further changed by sympathectomy. The present study shows that sympathetic nervous system denervation enhances the synthesis and production of peripheral interleukin-1beta and interleukin-6 in rats given central lipopolysaccharide and suggests a tonic inhibitory control of the sympathetic nervous system on these inflammatory cytokines.
Asunto(s)
Cuerpo Estriado/metabolismo , Interleucina-1/biosíntesis , Interleucina-6/biosíntesis , Lipopolisacáridos/toxicidad , Sistema Nervioso Simpático/fisiología , Animales , Cuerpo Estriado/efectos de los fármacos , Corticosterona/sangre , Dopamina/metabolismo , Escherichia coli , Regulación de la Expresión Génica/efectos de los fármacos , Interleucina-1/sangre , Interleucina-6/sangre , Masculino , Norepinefrina/metabolismo , Oxidopamina , Ratas , Bazo/efectos de los fármacos , Bazo/metabolismo , Simpatectomía Química , Sistema Nervioso Simpático/efectos de los fármacos , Sistema Nervioso Simpático/inmunología , Factor de Necrosis Tumoral alfa/biosíntesisRESUMEN
Previous studies have indicated that peripheral administration of interleukin-6 (IL-6) increases brain concentrations of tryptophan and 5-hydroxyindoleacetic acid (5-HIAA), the major catabolite of serotonin (5-HT). To determine whether these changes were related to increased synaptic release of 5-HT, we studied the responses to peripheral administration of IL-6 by in vivo microdialysis and in vivo amperometry. Intraperitoneal injection of recombinant IL-6 resulted in an elevation of microdialysate concentrations of 5-HT in the rat striatum. Also, amperometric measurements indicated that i.p. IL-6 enhanced the 5-HT-like signal obtained from the striatum following electrical stimulation of the dorsal raphe nucleus. These results indicate that the increases in brain concentrations of 5-HIAA observed in earlier studies indeed reflect increased synaptic release of 5-HT.
Asunto(s)
Cuerpo Estriado/efectos de los fármacos , Cuerpo Estriado/metabolismo , Espacio Extracelular/metabolismo , Interleucina-6/administración & dosificación , Serotonina/metabolismo , Animales , Cromatografía Líquida de Alta Presión , Estimulación Eléctrica , Electrodos Implantados , Inyecciones Intraperitoneales , Masculino , Microdiálisis , Núcleos del Rafe/fisiología , Ratas , Ratas Sprague-Dawley , Proteínas Recombinantes/administración & dosificaciónRESUMEN
Changes in 5-hydroxytryptamine (5-HT) efflux have been studied for the first time using differential pulse amperometry (DPA). In vitro observations show that the oxidation potential of 5-HT at 37 degrees C is 160 mV. The amperometric signal corresponding to 5-HT was measured in the lateral hypothalamus after brief electrical stimulation of the dorsal raphe nucleus (10 s, 25 or 50 Hz, 300 microA) every 5 or 10 min. Pargyline (100 mg/kg ip) and d-norfenfluramine (5 mg/kg ip) increased the signal to 194 and 243%, respectively. Tetrodotoxin (1 microliter, 100 mM), injected in the proximity of the working electrode, caused the signal to disappear. 8-OH-DPAT (250 micrograms/kg sc) reduced it to 64% for about 1 h and this effect was completely prevented by the 5HT1A antagonist WAY 100635 (1 mg/kg sc). L-Tryptophan (100 mg/kg ip) increased the amperometric signal to 136%. No change was detected when the 5-HT precursor was given to rats pretreated with PCPA (150 mg/kg per day p.o. for 3 days). In conclusion, DPA represents a sensitive and selective approach for studying 5-hydroxytryptaminergic function, offering a good temporal and anatomical specificity.
Asunto(s)
Estimulación Eléctrica/métodos , Hipotálamo/metabolismo , Serotonina/metabolismo , Animales , Masculino , RatasRESUMEN
High levels of interleukin 6 (IL-6) have been found in the brain tissue or cerebrospinal fluid (CSF) in several CNS disorders including Alzheimer's disease, AIDS dementia complex, multiple sclerois, stroke, Parkinson's disease, traumatic brain injuries, brain tumors and CNS infections. In these diseases, IL-6 is also found in blood showing that CNS conditions can elicit a peripheral immune response. A direct secretion of IL-6 from brain to blood has been shown to be a major mechanism by which the brain activates peripheral metabolic, endocrine and immune responses. However, this communication is not straightforward and other regulatory mechanisms are likely to be there. Several lines of evidence obtained in the laboratory have shown that the brain significantly modulates IL-6 production in the periphery. Evidence will be given that: (i) central inflammatory stimuli efficiently induce peripheral IL-6; (ii) central opioids are effective modulators of peripheral IL-6, and (iii) the sympathetic nervous system represents an inhibitory pathway to peripheral IL-6.