Participation of extracellular calcium in α-hederin-induced contractions of rat isolated stomach strips

J Ethnopharmacol. 2013 Mar 7;146(1):423-6. doi: 10.1016/j.jep.2012.12.023. Epub 2012 Dec 26.

Abstract

Ethnopharmacological relevance: The dry extract of Hedera helix leaves, due to its secretolytic and antispasmodic effects, is commonly used to produce pharmaceuticals applied in case of cough and other respiratory symptoms. The results of some in vitro studies as well as the clinical signs of poisoning caused by Hedera helix suggest however strong contractile effect on smooth muscle. In order to clarify the impact of α-hederin (the main active agent of ivy extract) on smooth muscle, the origin of activated calcium involved in α-hederin-induced contraction of gastric smooth muscle preparations was studied.

Materials and methods: The study was carried out on rat isolated stomach corpus and fundus strips, under isotonic conditions. The effect of α-hederin (100 μM) on smooth muscle preparations was measured before and after the treatment with verapamil during the incubation in modified Krebs-Henseleit solution (M K-HS). Besides, the effect of saponin was measured during the incubation of preparation in Ca2+-free modified Krebs-Henseleit solution or Ca2+-free EGTA-containing modified Krebs-Henseleit solution.

Results: The obtained results revealed that the application of verapamil significantly inhibited the reaction evoked by α-hederin. The incubation of stomach strips in calcium-free modified Krebs-Henseleit solution did not change the force of the observed contraction in comparison to the reaction of the preparations incubated in regular incubation solution (M K-HS). In contrary, the replacement of M K-HS by calcium-free chelator-containing solution inhibited totally the reaction to α-hederin.

Conclusions: The results indicated that α-hederin-induced contraction results from the influx of calcium which is located in intercellular spaces or bound to the outside of the cell membrane. The Ca2+ influx occurs predominantly through voltage-dependent calcium channels of L-type.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / physiology*
  • Calcium Channel Blockers / pharmacology
  • In Vitro Techniques
  • Male
  • Muscle Contraction / drug effects*
  • Muscle Contraction / physiology
  • Muscle, Smooth / drug effects*
  • Muscle, Smooth / physiology
  • Oleanolic Acid / analogs & derivatives*
  • Oleanolic Acid / pharmacology
  • Rats
  • Rats, Wistar
  • Saponins / pharmacology*
  • Stomach / drug effects*
  • Stomach / physiology
  • Verapamil / pharmacology

Substances

  • Calcium Channel Blockers
  • Saponins
  • beta-hederin
  • Oleanolic Acid
  • Verapamil
  • Calcium