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Activation of mu opioid receptors inhibits transient high- and low-threshold Ca2+ currents, but spares a sustained current.
Schroeder, J E; Fischbach, P S; Zheng, D; McCleskey, E W.
Afiliação
  • Schroeder JE; Department of Cell Biology and Physiology, Washington University, St. Louis, Missouri 63110.
Neuron ; 6(1): 13-20, 1991 Jan.
Article em En | MEDLINE | ID: mdl-1846076
Opioids and opiates decrease the duration of action potentials and the amount of neurotransmitter released from sensory neurons. The mu-type opioid receptor, the binding site for morphine, is thought to act exclusively on K+ channels. Here, we show that activation of the mu receptor inhibits Ca2+ channels in rat sensory neurons; the effect is blocked by a mu antagonist and is not mimicked by kappa or delta receptor agonists. Both low-threshold (T-type) and high-threshold Ca2+ currents are partially suppressed. omega-Conotoxin-sensitive and omega-conotoxin-insensitive, high-threshold Ca2+ currents are inhibited. The kinetic effect on high-threshold current is like that caused by diminished rest potential: the transient component is selectively lost, whereas the sustained component is spared.
Assuntos
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Base de dados: MEDLINE Assunto principal: Canais de Cálcio / Receptores Opioides Limite: Animals Idioma: En Ano de publicação: 1991 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Canais de Cálcio / Receptores Opioides Limite: Animals Idioma: En Ano de publicação: 1991 Tipo de documento: Article