Abstract
The coumarin scopoletin was isolated in a pure form from the roots of Brunfelsia hopeana Benth. (Solanaceae). In isolated rat aortic rings, scopoletin (26-520 μM) inhibited to approximately the same extent the contractions induced by a variety of substances, including phenylephrine, potassium chloride, serotonin and PGF2
α. The effect of the coumarin on phenylephrine-induced contractions was not affected by endothelium removal or NO-synthase blockade by L-NAME (100 μM). Scopoletin (78 - 590 μM) antagonized in a concentration-dependent manner (IC50 = 300 ± 20 μM, n = 5), transient contractions in Ca2+-free media induced by noradrenaline, but not those induced by caffeine. Also, scopoletin did not interfere with the refilling of noradrenaline-sensitive intracellular calcium stores. It is suggested that the non-specific spasmolytic action of scopoletin can be attributed, at least in part, to its ability to inhibit the intracellular calcium mobilization from the noradrenaline-sensitive stores.
Key words
Brunfelsia hopeana
- Solanaceae - scopoletin - intracellular calcium - spasmolytic actions - rat aorta
References
-
1
Ojewole J A, Adesina S K.
Cardiovascular and neuromuscular actions of scopoletin from fruit Tetrapleura tetraptera
.
Planta Medica.
1983;
49
99-102
-
2
Ojewole J A, Adesina S K.
Mechanism of the hypotensive effect of scopoletin isolates from the fruit of Tetrapleura tetraptera
.
Planta Medica.
1983;
49
46-50
-
3
Reinecke M G, Minter D E, Jia Q.
Carbon and proton NMR assignments for 6,7-dimethoxycoumarin.
Magnetic Resonance in Chemistry.
1995;
33
757-8
-
4
Altura B M., Altura B T.
Differential effects of substrate on drug-induced contactions of rabbit aorta.
American Journal of Physiology.
1970;
219
1698-705
-
5
Sakata K, Karaki H.
Effects of a novel smooth muscle relaxant, KT-362, on contraction and cytosolic Ca2+ level in the rat aorta.
British Journal of Pharmacology.
1991;
102
174-8
-
6
Nelson M T, Patlak J B, Worley J F, Standen N B.
Calcium channels, potassium channels, and voltage dependence of arterial smooth muscle tone.
American Journal of Physiology (1 Pt 1).
1990;
259
3-18
-
7
Karaki H, Weiss G B.
Calcium release in smooth muscle.
Life Sciences.
1988;
42
111-22
-
8
Gurney A M.
Mechanisms of drug-induced vasodilation.
Journal of Pharmacy and Pharmacology.
1994;
46 (4)
242-51
-
9
Nasa Y, Ichihara K, Yoshida R, Abiko Y.
Positive inotropic and negative chronotropic effects of (-)-cis-diltiazem in rat isolated atria.
British Journal of Pharmacology.
1992;
105 (3)
696-702
-
10
Karaki H, Ozaki H, Hori M, Mitsui-Saito M, Amano K, Harada K, Miyamoto S, Nakazawa H, Won K J, Sato K.
Calcium movements, distribution, and functions in smooth muscle.
Pharmacological Reviews.
1997;
49
157-230
-
11
Clapham D E.
Calcium signaling.
Cell.
1995;
80
259-68
-
12
Bootman M D, Berridge M J.
The elemental principles of calcium signaling.
Cell.
1995;
83
675-8
-
13
Moncada S, Palmer R MJ, Higgs E A.
Nitric oxide: Physiology, pathophysiology and pharmacology.
Pharmacological Reviews.
1991;
43
109-42
-
14
Moncada S, Higgs E A.
The L-arginine-nitric oxide pathway.
New England Journal of Medicine .
1993;
29
2002-12
Prof. Isac Almeida de Medeiros
Laboratório de Tecnologia Farmacêutica
Universidade Federal da Paraíba
Caixa Postal 5009
58051-970 João Pessoa, PB
Brazil
eMail: isacmed@netwaybbs.com.br
Fax: +55-83-216-7511 or 83-216-7366