| Literature DB >> 1846076 |
J E Schroeder1, P S Fischbach, D Zheng, E W McCleskey.
Abstract
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.Entities:
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Year: 1991 PMID: 1846076 DOI: 10.1016/0896-6273(91)90117-i
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173