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1.
Lab Anim (NY) ; 37(6): 263-9, 2008 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-18496545

RESUMO

The western mosquitofish (Gambusia affinis affinis) is a useful model for the study of sexual dimorphism and the neural circuits associated with sexual differentiation. This is largely because of its anal fin, which undergoes radical postnatal transformation in males. Understanding the neural mechanisms involved in this process may also help elucidate basic principles of the nervous system. The authors describe the mosquitofish as a model for research and present guidelines for the care and use of this species.


Assuntos
Ciprinodontiformes/anatomia & histologia , Modelos Animais , Vias Neurais/anatomia & histologia , Caracteres Sexuais , Criação de Animais Domésticos/métodos , Animais , Ciprinodontiformes/fisiologia , Feminino , Ciência dos Animais de Laboratório/métodos , Masculino , Neurônios Motores/ultraestrutura , Vias Neurais/fisiologia , Medula Espinal/citologia , Sinapses/ultraestrutura
2.
Mol Cell Neurosci ; 32(1-2): 82-90, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16624571

RESUMO

We traced the cause of a slow-channel syndrome (SCS) in a patient with progressive muscle weakness, repetitive compound muscle action potential and prolonged low amplitude synaptic currents to a V --> F substitution in the M1 domain of the beta subunit (betaV229F) of the muscle acetylcholine receptor (AChR). In vitro expression studies in Xenopus oocytes indicated that the novel mutation betaV229F expressed normal amounts of AChRs and decreased the ACh EC50 by 10-fold compared to wild type. Kinetic analysis indicated that the mutation displayed prolonged mean open duration and repeated openings during activation. Prolonged openings caused by the betaV229F mutation were due to a reduction in the channel closing rate and an increase in the effective channel opening rate. Repeated openings of the channel during activation were caused by a significant reduction in the agonist dissociation constant. In addition, the betaV229F mutation produced an increase in calcium permeability. The kinetic and permeation studies presented in this work are sufficient to explain the consequences of the betaV229F mutation on the miniature endplate currents and thus are direct evidence that the betaV229F mutation is responsible for compromising the safety margin of neuromuscular transmission in the patient.


Assuntos
Acetilcolina/metabolismo , Mutação/genética , Síndromes Miastênicas Congênitas/genética , Junção Neuromuscular/genética , Receptores Nicotínicos/genética , Transmissão Sináptica/genética , Idoso , Substituição de Aminoácidos , Animais , Sinalização do Cálcio/genética , Permeabilidade da Membrana Celular/genética , Potenciais Pós-Sinápticos Excitadores/genética , Feminino , Humanos , Canais Iônicos/genética , Canais Iônicos/metabolismo , Cinética , Masculino , Músculo Esquelético/inervação , Músculo Esquelético/fisiopatologia , Síndromes Miastênicas Congênitas/metabolismo , Síndromes Miastênicas Congênitas/fisiopatologia , Junção Neuromuscular/metabolismo , Junção Neuromuscular/fisiopatologia , Oócitos , Linhagem , Xenopus laevis
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