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British Journal of Pharmacology
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January 1999, Volume 126, Issue 1, Pages 301 - 311 |
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| Original Article |
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Modulation of acute and chronic inflammatory processes by cacospongionolide B, a novel inhibitor of human synovial phospholipase A2
Pablo García Pastor1, Salvatore De Rosa2, Alfonso De Giulio2, Miguel Payá1 & M. José Alcaraz1,3 1Departamento de Farmacología, Universidad de Valencia, Facultad de Farmacia, Avda. Vicent Andrés Estellés s/n, 46100 Burjassot, Valencia, Spain 2Istituto per la Chimica di Molecole di Interesse Biologico CNR, via Toiano 6, 80072 Arco Felice, Napoli, Italy3Author for correspondence |
| Keywords |
| Inflammation;
phospholipase A2;
rat and mouse air pouch;
adjuvant arthritis;
manoalide;
cacospongionolide B |
| Abstract |
1 Cacospongionolide B is a novel marine metabolite isolated from the sponge Fasciospongia cavernosa. In in vitro studies, this compound inhibited phospholipase A2 (PLA2), showing selectivity for secretory PLA2 (sPLA2) versus cytosolic PLA2 (cPLA2), and its potency on the human synovial enzyme (group II) was similar to that of manoalide. 2 This activity was confirmed in vivo in the 8 h zymosan-injected rat air pouch, on the secretory enzyme accumulating in the pouch exudate. Cacospongionolide B, that is bioavailable when is given orally, reduced the elevated levels of sPLA2 present in paw homogenates of rats with adjuvant arthritis. 3 This marine metabolite showed topical anti-inflammatory activity on the mouse ear oedema induced by 12-O-tetradecanoylphorbol acetate (TPA) and decreased carrageenin paw oedema in mice after oral administration of 5, 10 or 20 mg kg-1. 4 In the mouse air pouch injected with zymosan, cacospongionolide B administered into the pouch, induced a dose-dependent reduction in the levels of eicosanoids and tumour necrosis factor 5 The inflammatory response of adjuvant arthritis was reduced by cacospongionolide B, which did not significantly affect eicosanoid levels in serum, paw or stomach homogenates and did not induce toxic effects. 6 Cacospongionolide B is a new inhibitor of sPLA2 in vitro and in vivo, with anti-inflammatory properties in acute and chronic inflammation. This marine metabolite was active after oral administration and able to modify TNF |
Received 3 July 1998; Revised 10 October 1998; Accepted 16 October 1998