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Spontaneous and CRH-Induced Excitability and Calcium Signaling in Mice Corticotrophs Involves Sodium, Calcium, and Cation-Conducting Channels
H. Zemkova, M. Tomić, M. Kucka, G. Aguilera, SS. Stojilkovic,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, Research Support, N.I.H., Intramural, práce podpořená grantem
NLK
Free Medical Journals
od 1997 do Před 1 rokem
Open Access Digital Library
od 1997-01-01
PubMed
26901094
DOI
10.1210/en.2015-1899
Knihovny.cz E-zdroje
- MeSH
- akční potenciály účinky léků MeSH
- AMP cyklický metabolismus MeSH
- dibutyryl cyklický AMP farmakologie MeSH
- hormon uvolňující kortikotropin farmakologie MeSH
- iontové kanály metabolismus MeSH
- kolforsin farmakologie MeSH
- kortikotropní buňky účinky léků metabolismus fyziologie MeSH
- kultivované buňky MeSH
- kyselina arachidonová farmakologie MeSH
- membránové potenciály účinky léků MeSH
- metoda terčíkového zámku MeSH
- myši inbrední C57BL MeSH
- myši transgenní MeSH
- sodík metabolismus MeSH
- vápník metabolismus MeSH
- vápníková signalizace účinky léků MeSH
- vápníkové kanály - typ L metabolismus MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Intramural MeSH
Transgenic mice expressing the tdimer2(12) form of Discosoma red fluorescent protein under control of the proopiomelanocortin gene's regulatory elements are a useful model for studying corticotrophs. Using these mice, we studied the ion channels and mechanisms controlling corticotroph excitability. Corticotrophs were either quiescent or electrically active, with a 22-mV difference in the resting membrane potential (RMP) between the 2 groups. In quiescent cells, CRH depolarized the membrane, leading to initial single spiking and sustained bursting; in active cells, CRH further facilitated or inhibited electrical activity and calcium spiking, depending on the initial activity pattern and CRH concentration. The stimulatory but not inhibitory action of CRH on electrical activity was mimicked by cAMP independently of the presence or absence of arachidonic acid. Removal of bath sodium silenced spiking and hyperpolarized the majority of cells; in contrast, the removal of bath calcium did not affect RMP but reduced CRH-induced depolarization, which abolished bursting electrical activity and decreased the spiking frequency but not the amplitude of single spikes. Corticotrophs with inhibited voltage-gated sodium channels fired calcium-dependent action potentials, whereas cells with inhibited L-type calcium channels fired sodium-dependent spikes; blockade of both channels abolished spiking without affecting the RMP. These results indicate that the background voltage-insensitive sodium conductance influences RMP, the CRH-depolarization current is driven by a cationic conductance, and the interplay between voltage-gated sodium and calcium channels plays a critical role in determining the status and pattern of electrical activity and calcium signaling.
Citace poskytuje Crossref.org
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