Literature DB >> 15269290

Ca2+ channels as integrators of G protein-mediated signaling in neurons.

Jesse Strock1, María A Diversé-Pierluissi.   

Abstract

The observations from Dunlap and Fischbach that transmitter-mediated shortening of the duration of action potentials could be caused by a decrease in calcium conductance led to numerous studies of the mechanisms of modulation of voltage-dependent calcium channels. Calcium channels are well known targets for inhibition by receptor-G protein pathways, and multiple forms of inhibition have been described. Inhibition of Ca(2+) channels can be mediated by G protein betagamma-subunits or by kinases, such as protein kinase C and tyrosine kinases. In the last few years, it has been shown that integration of G protein signaling can take place at the level of the calcium channel by regulation of the interaction of the channel pore-forming subunit with different cellular proteins.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15269290     DOI: 10.1124/mol.104.002261

Source DB:  PubMed          Journal:  Mol Pharmacol        ISSN: 0026-895X            Impact factor:   4.436


  18 in total

Review 1.  The ß subunit of voltage-gated Ca2+ channels.

Authors:  Zafir Buraei; Jian Yang
Journal:  Physiol Rev       Date:  2010-10       Impact factor: 37.312

2.  Src family kinases mediate the inhibition of substance P release in the rat spinal cord by μ-opioid receptors and GABA(B) receptors, but not α2 adrenergic receptors.

Authors:  Guohua Zhang; Wenling Chen; Juan Carlos G Marvizón
Journal:  Eur J Neurosci       Date:  2010-08-19       Impact factor: 3.386

3.  Alternative splicing controls G protein-dependent inhibition of N-type calcium channels in nociceptors.

Authors:  Jesica Raingo; Andrew J Castiglioni; Diane Lipscombe
Journal:  Nat Neurosci       Date:  2007-02-11       Impact factor: 24.884

Review 4.  Neuronal calcium channels: splicing for optimal performance.

Authors:  Annette C Gray; Jesica Raingo; Diane Lipscombe
Journal:  Cell Calcium       Date:  2007-05-18       Impact factor: 6.817

Review 5.  In search of analgesia: emerging roles of GPCRs in pain.

Authors:  Laura S Stone; Derek C Molliver
Journal:  Mol Interv       Date:  2009-10

6.  Mechanisms of μ-opioid receptor inhibition of NMDA receptor-induced substance P release in the rat spinal cord.

Authors:  Wenling Chen; Helena S Ennes; James A McRoberts; Juan Carlos Marvizón
Journal:  Neuropharmacology       Date:  2017-10-16       Impact factor: 5.250

Review 7.  Norepinephrine: a neuromodulator that boosts the function of multiple cell types to optimize CNS performance.

Authors:  John O'Donnell; Douglas Zeppenfeld; Evan McConnell; Salvador Pena; Maiken Nedergaard
Journal:  Neurochem Res       Date:  2012-06-21       Impact factor: 3.996

8.  L-histidine sensing by calcium sensing receptor inhibits voltage-dependent calcium channel activity and insulin secretion in β-cells.

Authors:  Jai Parkash; Kamlesh Asotra
Journal:  Life Sci       Date:  2011-01-08       Impact factor: 5.037

9.  μ-Opioid receptor inhibition of substance P release from primary afferents disappears in neuropathic pain but not inflammatory pain.

Authors:  W Chen; J A McRoberts; J C G Marvizón
Journal:  Neuroscience       Date:  2014-02-26       Impact factor: 3.590

10.  Cannabinoid CB1 receptor facilitation of substance P release in the rat spinal cord, measured as neurokinin 1 receptor internalization.

Authors:  Guohua Zhang; Wenling Chen; Lijun Lao; Juan Carlos G Marvizón
Journal:  Eur J Neurosci       Date:  2010-01-13       Impact factor: 3.386

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.