Anti-Inflammatory and Antinociceptive Activity of Coumarins from Seseli gummiferum subsp. corymbosum (Apiaceae)

Author:

Tosun Alev1,Akkol Esra Küpeli2,Yeşilada Erdem3

Affiliation:

1. Department of Pharmacognosy, Faculty of Pharmacy, Ankara University, Tandogan 06100, Ankara, Turkey

2. Department of Pharmacognosy, Faculty of Pharmacy, Gazi University, Etiler 06330, Ankara, Turkey

3. Faculty of Pharmacy, Yeditepe University, Kadıköy 34755, Istanbul, Turkey

Abstract

1 n-Hexane and ethyl acetate extracts as well as coumarin derivatives obtained from the n-hexane extract of the aerial parts of Seseli gummiferum Pall. ex Sm. subsp. corymbosum (Boiss. & Heldr.) P.H. Davis (Apiaceae) were evaluated in vivo for their anti-inflammatory and antinociceptive activities. The n-hexane and ethyl acetate extracts of the species were shown to possess significant inhibitory activity against the carrageenan-induced hind paw edema and p-benzoquinone-induced writhing models in mice. Among the isolated coumarin derivatives; (−)-(3’S,4’S)-3’-acetoxy-4’-isovaleryloxy-3’,4’-dihydroseselin (), (−)-(3’S,4’S)-3’- acetoxy-4’-angeloyloxy-3’,4’-dihydroseselin (2), (+)-(3’S,4’S)-3’-hydroxy-4’-angeloyloxy-3’,4’- dihydroseselin (D-laserpitin) (3), (−)-(3’S,4’S)-3’-angeloyloxy-4’-hydroxy-3’,4’-dihydroseselin (4), and osthole (5), only the 3’-acetoxy derivatives 1 and 2 were found to possess potent antinociceptive and anti-infl ammatory activities, per os, without inducing any apparent acute toxicity as well as gastric damage, while all other compounds and extracts were found to be ineffective in the TPA-induced mouse ear edema model assay.

Publisher

Walter de Gruyter GmbH

Subject

General Biochemistry, Genetics and Molecular Biology

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