Unknown

Dataset Information

0

Voltage-dependent inward currents in smooth muscle cells of skeletal muscle arterioles.


ABSTRACT: Voltage-dependent inward currents responsible for the depolarizing phase of action potentials were characterized in smooth muscle cells of 4th order arterioles in mouse skeletal muscle. Currents through L-type Ca2+ channels were expected to be dominant; however, action potentials were not eliminated in nominally Ca2+-free bathing solution or by addition of L-type Ca2+ channel blocker nifedipine (10 ?M). Instead, Na+ channel blocker tetrodotoxin (TTX, 1 ?M) reduced the maximal velocity of the upstroke at low, but not at normal (2 mM), Ca2+ in the bath. The magnitude of TTX-sensitive currents recorded with 140 mM Na+ was about 20 pA/pF. TTX-sensitive currents decreased five-fold when Ca2+ increased from 2 to 10 mM. The currents reduced three-fold in the presence of 10 mM caffeine, but remained unaltered by 1 mM of isobutylmethylxanthine (IBMX). In addition to L-type Ca2+ currents (15 pA/pF in 20 mM Ca2+), we also found Ca2+ currents that are resistant to 10 ?M nifedipine (5 pA/pF in 20 mM Ca2+). Based on their biophysical properties, these Ca2+ currents are likely to be through voltage-gated T-type Ca2+ channels. Our results suggest that Na+ and at least two types (T- and L-) of Ca2+ voltage-gated channels contribute to depolarization of smooth muscle cells in skeletal muscle arterioles. Voltage-gated Na+ channels appear to be under a tight control by Ca2+ signaling.

SUBMITTER: Ulyanova AV 

PROVIDER: S-EPMC5919073 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

altmetric image

Publications

Voltage-dependent inward currents in smooth muscle cells of skeletal muscle arterioles.

Ulyanova Alexandra V AV   Shirokov Roman E RE  

PloS one 20180425 4


Voltage-dependent inward currents responsible for the depolarizing phase of action potentials were characterized in smooth muscle cells of 4th order arterioles in mouse skeletal muscle. Currents through L-type Ca2+ channels were expected to be dominant; however, action potentials were not eliminated in nominally Ca2+-free bathing solution or by addition of L-type Ca2+ channel blocker nifedipine (10 μM). Instead, Na+ channel blocker tetrodotoxin (TTX, 1 μM) reduced the maximal velocity of the ups  ...[more]

Similar Datasets

| S-EPMC3761174 | biostudies-literature
| S-EPMC2014663 | biostudies-other
| S-EPMC4506201 | biostudies-literature
| S-EPMC6735402 | biostudies-literature
| S-EPMC3086792 | biostudies-literature
| S-EPMC2013798 | biostudies-other
| S-EPMC4144269 | biostudies-literature
| S-EPMC2943204 | biostudies-literature
| S-EPMC7769825 | biostudies-literature
| S-EPMC2761760 | biostudies-literature