| Literature DB >> 26085001 |
Yuki Kojima1, Asuka Higashikawa, Maki Kimura, Masaki Sato, Hiroyuki Mochizuki, Kazuhiro Ogura, Toshiyuki Sase, Akinori Shinya, Kunio Kobune, Tadashi Furuya, Toru Sato, Yoshiyuki Shibukawa, Masakazu Tazaki.
Abstract
Odontoblasts play an important role in the transduction of the sensory signals underlying dentinal pain. Transmembrane voltage-independent Ca(2+) influx in odontoblasts has been well described. Voltage-dependent Ca(2+) influx has also been reported, but its biophysical properties remain unclear. The aim of the present study was to investigate the desensitizing effect of voltage-dependent Ca(2+) influx in rat odontoblasts by measuring depolarization-induced intracellular free Ca(2+) concentrations ([Ca(2+) ]i ). Odontoblasts on dental pulp slices from newborn rats were acutely isolated and [Ca(2+) ]i measured by using fura-2 fluorescence. Repeated application of extracellular high-K(+) solution (50 mM), which induces membrane depolarization-elicited repeated and transient increases in [Ca(2+) ]i in the presence of extracellular Ca(2+). Increases in depolarization-induced [Ca(2+) ]i showed no significant desensitizing effect (p >0.05; Friedman test). These results suggest that odontoblasts express a voltage-dependent Ca(2+) influx pathway with no desensitizing properties.Entities:
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Year: 2015 PMID: 26085001 DOI: 10.2209/tdcpublication.56.131
Source DB: PubMed Journal: Bull Tokyo Dent Coll ISSN: 0040-8891