Planta Med 2002; 68(7): 601-604
DOI: 10.1055/s-2002-32897
Original Paper
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

Effects of a Labdane Diterpene Isolated from Brickellia paniculata on Intracellular Ca2+ Deposit of Guinea-Pig Ileal Longitudinal Muscle

Mariana Meckes1 , Rubén Román-Ramos2 , Salud Pérez3 , Fernando Calzada1 , Héctor Ponce-Monter4
  • 1U.I.M Farmacología de Productos Naturales. Hospital de Pediatría, CMN Siglo XXI, IMSS. Col. Doctores, México DF
  • 2Laboratorio de Farmacología. Universidad Autónoma Metropolitana, Iztapalapa, México DF
  • 3Laboratorio de Química. Universidad Autónoma Metropolitana, Xochimilco, México DF
  • 4U.I.M Farmacología. Hospital de Especialidades, CMN Siglo XXI, IMSS, Col. Doctores, México DF
Further Information

Publication History

Received: October 19, 2001

Accepted: February 3, 2002

Publication Date:
22 July 2002 (online)

Preview

Introduction

Brickellia paniculata (Asteraceae) is a medicinal plant commonly used in Southeastern Mexico to treat colics, abdominal pains and watery diarrhoea [1], [2]. In a previous study, from the methanolic extract were isolated a flavonoid (xanthomicrol) and a labdane diterpene, this latter compound was structurally characterized as 3α-angeloyloxy-2α-hydroxy-13,14Z-dehydrocativic acid (AAHDD) [3]. The structures have already been reported and their identity was confirmed by comparison with published physical and spectroscopic data [4], [5], [6]. Both compounds relaxed the segments of isolated guinea-pig ileum stimulated with high K+ and the effect was correlated with an interference of Ca2+ mobilization in the cell. Furthermore, a competitive calcium-antagonistic activity was described for AAHDD, although the precise mechanism underlying this effect was not demonstrated. It is well documented that in the guinea pig ileum, K+ depolarization induces the opening of the voltage-dependent calcium channels increasing the influx of Ca2+ into the cell; as a response to the rise of free Ca2+ in the cytosol, the muscle contracts. Calcium entry is the primary but not the sole mechanism of increasing [Ca2+]i, since the release of the cation from intracellular deposits can also occur. Phasic response to K+ has been attributed to a rise in cytosolic free Ca2+ which is released from intracellular stores. On the other hand, the tonic component has been associated with the opening of the voltage-dependent calcium channels causing Ca2+ influx to increase [7], [8], [9].

As has been observed, the compound AAHDD inhibited with the same potency the K+ evoked phasic and tonic components of the contractile response. This work was undertaken to gain further information about a possible blocking action of AAHDD at intracellular Ca2+ stores.[]

References

Mariana Meckes

Unidad de Investigación Médica en Farmacología de Productos Naturales


Hospital de Pediatría, Centro Médico Nacional Siglo XXI, IMSS

Av. Cuauhtémoc, 330, Col Doctores cp. 06725, México D.F

Fax: +57-61-0952

Email: meck7707@prodigy.net.mx