Regulation of N-type calcium channels by nociceptin receptors and its possible role in neurological disorders

1Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Activation of nociceptin opioid peptide receptors (NOP, a.k.a. opioid-like receptor-1, ORL-1) by the ligand nociceptin/orphanin FQ, leads to G protein-dependent regulation of Cav2.2 (N-type) voltage-gated calcium channels (VGCCs). This typically causes a reduction in calcium currents, triggering changes in presynaptic calcium levels and thus neurotransmission. Because of the widespread expression patterns of NOP and VGCCs across multiple brain regions, the dorsal horn of the spinal cord, and the dorsal root ganglia, this results in the alteration of numerous neurophysiological features. Here we review the regulation of N-type calcium channels by the NOP-nociceptin system in the context of neurological conditions such as anxiety, addiction, and pain.

Cite

CITATION STYLE

APA

Caminski, E. S., Antunes, F. T. T., Souza, I. A., Dallegrave, E., & Zamponi, G. W. (2022, December 1). Regulation of N-type calcium channels by nociceptin receptors and its possible role in neurological disorders. Molecular Brain. BioMed Central Ltd. https://doi.org/10.1186/s13041-022-00982-z

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free