Calcium channels contribute to albiflorin-mediated antinociceptive effects in mouse model

Neurosci Lett. 2016 Aug 15:628:105-9. doi: 10.1016/j.neulet.2016.03.054. Epub 2016 Mar 31.

Abstract

Albiflorin (AF), one of important bioactive constituents of Paeonia lactiflora Radix, possesses neuro-protective effect. The present study aims to investigate the antinociceptive activities of AF and possible mechanisms. AF suppressed acetic acid-caused writhing, lengthened the latency period of mouse in hot plate test, and reduced the licking and biting response time of the injected mouse paw during phase I and phase II, and it suggested that AF exerted the antinociceptive activity mainly through central nervous system. Nimodipine, a commonly used calcium channels blocker, strongly lengthened AF-enhanced latency period of mouse in hot plate test. Compared with control group, AF reduced the levels of euronal nitric oxide synthase (nNOS), and enhanced the levels of serotonin (5-HT) in serum and/or hypothalamus before and after 30-s thermal stimuli. The reduced activation of calmodulin-dependent protein kinase II and c-Jun N-terminal kinase in hypothalamus was observed in AF-treated mice. Collectively, AF-mediated antinociceptive activities were, at least partially, related to calcium channels.

Keywords: Albiflorin; Antinociception; Calcium channels; Serotonin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics / administration & dosage*
  • Animals
  • Bridged-Ring Compounds / administration & dosage*
  • Calcium Channel Blockers / administration & dosage
  • Calcium Channels / physiology*
  • Female
  • Mice
  • Mice, Inbred BALB C
  • Nimodipine / administration & dosage
  • Nitric Oxide Synthase Type I / blood
  • Nociception / drug effects*
  • Nociception / physiology*
  • Pain Measurement
  • Serotonin / blood

Substances

  • Analgesics
  • Bridged-Ring Compounds
  • Calcium Channel Blockers
  • Calcium Channels
  • Serotonin
  • albiflorin
  • Nimodipine
  • Nitric Oxide Synthase Type I