
IndraLab
Statements
Calcium_channels activates CACNA1A. 21 / 21
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sparser
"Somatic heterozygous mutations in the genes KCNJ5 coding for the potassium channel GIRK4, ATP1A1 coding for the α1 subunit of the Na + /K + -ATPase, ATP2B3 coding for the plasma membrane Ca 2+ -ATPase, type 3 PMCA3, and CACNA1D encoding the Cav1.3 voltage dependent calcium channel were identified in approximately 50% of APA. xref - xref These mutations are responsible for chronic zona glomerulosa cell membrane depolarization ( KCNJ5 and ATP1A1 mutations) leading to opening of voltage-dependent calcium channels, for impaired intracellular calcium recycling ( ATP2B3 mutations), or voltage-dependent calcium channel activation and opening at lower voltages ( CACNA1D mutations). xref – xref All these genetic abnormalities converge towards an increase in intracellular calcium concentration and activation of calcium signaling, which plays a central role in the regulation of aldosterone production, in particular by increasing the expression of CYP11B2 encoding aldosterone synthase."
sparser
"While these putative functional NMDA receptors are generally assumed to be at axonal locations, the existence of presynaptic, axonal NMDA receptors has been challenged by the discovery that somatodendritic NMDA receptor activation can affect axonal Ca 2+ levels through voltage-dependent calcium channel activation, at least in cerebellar stellate cells (Christie and Jahr, xref )."
sparser
"The authors show that BDNF release from
cultured cortical cells is dependent on both AMPAR and voltage-dependent calcium channel
activation and that BDNF dose-dependently increases extracellular signal-regulated
kinase 1/2 phosphorylation via a tropomyosin receptor kinase B–dependent
mechanism."
sparser
"Another GWAS (n=2323) observed trending associations (ie, p<0.05, but not genome-wide significance) between CACNA1C variants and both increased sleep latency (p<0.0001) and poorer sleep quality (p<0.0001). xref Another study found no significant association between variants and sleep latency (n=2034); xref however, a candidate gene study observed associations between CACNA1C variants and poor sleep quality (p<0.017). xref Furthermore, the rare, homozygous recessive genotype (three of 932 individuals) for this CACNA1C variant was associated with reduced sleep latency (p<0.005) and higher reports of depressive symptoms (p<0.001). xref CACNA1C encodes an L-type voltage-dependent calcium channel activated by the wake-promoting neuropeptide orexin, and has been implicated in depression, bipolar disorder, schizophrenia, and one small (n=602) candidate gene study of narcolepsy ( xref , xref )."
sparser
"Under these conditions, X-Rhod-5F and Fluo4-FF could detect calcium changes (signal twice that of noise) in the dendrite due to voltage dependent calcium channel activation after single action potentials while with the same criterion GCaMP required 5 action potentials, camgaroo-2, 33, and inverse pericam over 20."
sparser
"KCNJ5 and ATP1A1 mutations are responsible for chronic zona glomerulosa cell membrane depolarization leading to opening of voltage-dependent calcium channels, while ATP2B3 mutations affect intracellular calcium recycling and CACNA1D mutations lead to voltage-dependent calcium channel activation and opening at lower voltages ( xref , xref , xref , xref )."
sparser
"In addition to a potential direct contribution to calcium influx, Trpc channels are thought to promote calcium entry by providing a depolarizing stimulus (sodium and calcium currents) for voltage-dependent calcium channel activation and subsequent smooth muscle cell contraction [ xref , xref ]."
sparser
"It has been hypothesized that L-type voltage-dependent calcium channel activation or locally generated, spatially restricted dendritic spikes in proximal dendrites could contribute to postsynaptic depolarization and calcium entry, which shifts the balance to LTP rather than LTD in this region (Golding et al., xref ; Parvez et al., xref )."