Involvement of small-conductance Ca2+-activated K+ (SKCa2) channels in spontaneous Ca2+ oscillations in rat pinealocytes

Biochem Biophys Res Commun. 2022 Jul 30:615:157-162. doi: 10.1016/j.bbrc.2022.05.052. Epub 2022 May 21.

Abstract

Melatonin secretion from the pineal glands regulates circadian rhythms in mammals. Melatonin production is decreased by an increase in cytosolic Ca2+ concentration following the activation of nicotinic acetylcholine receptors in parasympathetic systems. We previously reported that pineal Ca2+ oscillations were regulated by voltage-dependent Ca2+ channels and large-conductance Ca2+-activated K+ (BKCa) channels, which inhibited melatonin production. In the present study, the contribution of small- and intermediate-conductance Ca2+-activated K+ (SKCa and IKCa) channels to the regulation of spontaneous Ca2+ oscillations was examined in rat pinealocytes. The amplitude and frequency of spontaneous Ca2+ oscillations were increased by a SKCa channel blocker (100 nM apamin), but not by an IKCa channel blocker (1 μM TRAM-34). On the other hand, they were decreased by a SKCa channel opener (100 μM DCEBIO), but not by an IKCa channel opener (1 μM DCEBIO). Expression analyses using quantitative real-time PCR, immunocytochemical staining, and Western blotting revealed that the SKCa2 channel subtype was abundantly expressed in rat pinealocytes. Moreover, the enhanced amplitude of Ca2+ oscillations in the presence of apamin was further increased by a BKCa channel blocker (1 μM paxilline). These results suggest that the activity of SKCa2 channels regulates cytosolic Ca2+ signaling and melatonin production during parasympathetic activation in pineal glands.

Keywords: Apamin; Calcium oscillation; Calcium-activated potassium channel; DCEBIO; Pineal gland; SK(Ca)2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apamin / pharmacology
  • Calcium / metabolism
  • Large-Conductance Calcium-Activated Potassium Channels / metabolism
  • Melatonin* / metabolism
  • Pineal Gland* / metabolism
  • Potassium Channels, Calcium-Activated* / metabolism
  • Pyrazoles / pharmacology
  • Rats
  • Small-Conductance Calcium-Activated Potassium Channels / metabolism

Substances

  • Large-Conductance Calcium-Activated Potassium Channels
  • Potassium Channels, Calcium-Activated
  • Pyrazoles
  • Small-Conductance Calcium-Activated Potassium Channels
  • Apamin
  • Melatonin
  • Calcium