Sympathomimetic Effects of Scoparia dulcis L. and Catecholamines Isolated from Plant Extracts

Abstract

Abstract The herb Scoparia dulcis L. is used in Brazilian folk medicine to treat bronchitis, gastric disorders, haemorrhoids, insect bites and skin wounds, and in oriental medicine to treat hypertension. A previous study has shown that extracts of S. dulcis have analgesic and anti-inflammatory properties; in this work the sympathomimetic activity of an ethanolic extract of Scoparia dulcis L. has been investigated in rodent preparations in-vivo and in-vitro. Administration of the extract (0.5-2 mg kg−1, i.v.) to anaesthetized rats produced dose-related hypertension blocked by the α-adrenoceptor antagonist prazosin (1 mg kg−1). Partition of the extract in chloroform-water yielded an aqueous phase 20 times more potent than the extract; this produced hypertension in either reserpine-treated or pithed rats. In untreated and reserpine-treated rats the same fraction (1–3 × 103 μg mL−1) produced concentration-dependent contractions of the vas deferens musculature parallel to those obtained with noradrenaline (10−8-10−4 m). Prazosin (10−7 m) reduced the maximum contractile effect of the aqueous fraction, and shifted the concentration-response curves for noradrenaline to the right. The aqueous fraction (25 and 50 μg mL−1) increased the inotropism of electrically driven left atria of rats, the effect being blocked by propranolol (0.4 μg mL−1). In preparations of guinea-pig tracheal rings the aqueous fraction (1–3 × 103 μg mL−1) relaxed the muscle contraction induced by histamine (10−4 m) in proportion to the concentration. The effect was antagonized competitively by propranolol (1.5 μm). High-performance liquid-chromatographic analysis of the aqueous fraction revealed the presence of both noradrenaline and adrenaline in the plant extract. The results indicated that both catecholamines may account for the hypertensive and inotropic effects obtained after parenteral administration of S. dulcis extracts. This sympathomimetic activity is, however, unrelated to the previously reported analgesic and anti-inflammatory properties of the plant extract, but may explain its effectiveness upon topical application in the healing of mucosal and skin wounds.