Abstract
The contraction and desensitization induced by albaconol and the influence of capsazepine,
capsaicin and extracellular Ca2+ were investigated to see whether the actions were mediated via a specific VR receptor
in guinea pig trachea spiral strips in vitro. Both albaconol and capsaicin were contractors of tracheal smooth muscle, but albaconol
was not so potent as capsaicin, with -log (M) EC50 values of 4.23 ± 0.18 (n = 10) and 7.33 ± 0.21 (n = 10) respectively. 2.5 μM capsazepine
competitively antagonized the contractile response to albaconol and capsaicin. Albaconol
increased the contraction induced by a low dose of capsaicin (10-10 to 10-9 M), but non-competitively antagonized the contraction induced by a high dose of capsaicin
(10-8 to 10-3 M). Either albaconol (1 or 100 mM) or capsaicin (3 or 10 μM) was able to desensitize
the isolated guinea pig bronchi to subsequent addition of albaconol. Capsazepine (5.0
μM) significantly prevented the desensitization induced by either albaconol (1 or
100mM) or capsaicin (3 or 10 μM). Extracellular Ca2+ was essential for albaconol to induce excitation, but it did not affect albaconol-
or capsaicin-induced desensitization. In summary, the results from the present study
suggest that albaconol induces contraction and desensitization of guinea pig trachea
in vitro as a partial agonist for VR.
Key words
Albaconol
-
Albatrellus confluens
- Polyporaceae
- capsazepine
- capsaicin
- vanilloid receptor
- guinea pig trachea
- contraction
References
- 1
Szallasi A.
Autoradiographic visualization and pharmacological characterization of vanilloid (capsaicin)
receptors in several species, including man.
Acta Physiol Scand Suppl.
1995;
629
1-68
- 2
Rinder J, Szallasi A, Lundberg J M.
Capsaicin, resiniferatoxin, and lactic acid-evoked vascular effects in the pig nasal
mucosa in vivo with reference to characterization of the vanilloid receptor.
Pharmacol Toxicol.
1996;
78
327-35
- 3
Davis J B, Gray J, Gunthorpe M J, Hatcher J P. et al .
Vanilloid receptor-1 is essential for inflammatory thermal hyperalgesia.
Nature.
2000;
405
183-7
- 4
Ellis J L, Undem B J.
Inhibition by capsazepine of resiniferatoxin and capsaicin-induced contractions of
guinea pig trachea.
J Pharmacol Exp Ther.
1994;
268
85-9
- 5
Yi-Sook J, Tai-Soon C, Chang-Hyun M, Hwa-Sup S.
Capsaicin-induced desensitization is prevented by capsazepine but not by ruthenium
red in guinea pig bronchi.
Eur J Pharmacol.
1998;
362
193-8
- 6
Ding Z H, Dong Z J, Liu J K.
Albaconol, a novel prenylated resorcinol (= benzene-1,3-diol) from basidiomycetes
Albatrellus confluens
.
Helv Chim Acta.
2001;
84
259-62
- 7
Szallasi A, Biro T, Szabo T. et al .
A non-pungent triprenyl phenol of fungal origin, scutigeral, stimulates rat dorsal
root ganglion neurons via interaction at vanilloid receptors.
Br J Pharmacol.
1999;
126
1351-8
- 8
Rouhi A M.
Vanilloids: hot relief for pain.
Chem Eng.
1998;
26
31-4
- 9 Ke J, Zhan P W, Chen W Z. Determinations of isolated trachea tension. In: Xu SY,
Bian RL, Chen X editors
Pharmacological Methodology. The People’s Public Health Publishing House 1994: pp. 983-91
- 10
Dickenson A H, Dray A, Hughes G A, Walpole C SJ.
The selective capsaicin antagonist capsazepine inhibits capsaicin-induced anti-nociception:
electrophysiological studies in rodents.
Br J Pharmacol.
1991;
102
79-83
- 11
Perkins M N, Campbell E A.
Capsazepine reversal of the antinociceptive action of capsaicin in vivo
.
Br J Pharmacol.
1992;
107
329-33
Dr. Ji-Kai Liu
Kunming Institute of Botany
The Chinese Academy of Science
Kunming 650204
P. R. China
Telefon: +86-871-5216327
Fax: +86-871-5150227
eMail: jkl@public.km.yn.cn