Investigation of the anti-inflammatory and analgesic effects from an extract of Aplysina caissara, a marine sponge

Fundamental and Clinical Pharmacology

Volumn 22, Issue 5, 2008, Pages 549-556

  Azevedo, Luciana Gutterres ^a   Peraza, Gianni Goulart ^a   Lerner, Clea ^b   Soares, Andrea ^c   Murcia, Nícolas ^a   Muccillo Baisch, Ana Luiza ^a  

^a FEDERAL UNIVERSITY OF RIO GRANDE   (Brazil)

^b Fundacao Zoobotanica Do Rio   (Brazil)

^c Gota d'Água ^*  (Brazil)

Author keywords

Anti inflammatory; Antinociceptive; Aplysina caissara; Marine sponge; Natural products

Indexed keywords

APLYSINA CAISSARA EXTRACT; NATURAL PRODUCT; UNCLASSIFIED DRUG;

ANALGESIC ACTIVITY; ANIMAL EXPERIMENT; ANIMAL MODEL; ANTIINFLAMMATORY ACTIVITY; ANTINOCICEPTION; APLYSINA CAISSARA; ARTICLE; COELENTERATE; CONTROLLED STUDY; DOSE RESPONSE; DRUG EFFECT; DRUG MECHANISM; DRUG SCREENING; EXPERIMENTAL MODEL; HOT PLATE TEST; LATENT PERIOD; LD 50; MALE; MORTALITY; MOUSE; NONHUMAN; PAW EDEMA; PRIORITY JOURNAL; WRITHING TEST;

ANALGESICS; ANIMALS; ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL; DOSE-RESPONSE RELATIONSHIP, DRUG; INFLAMMATION MEDIATORS; MALE; MICE; PAIN; PAIN MEASUREMENT; PORIFERA;

EID: 52449083320     PISSN: 07673981     EISSN: 14728206     Source Type: Journal    
DOI: 10.1111/j.1472-8206.2008.00624.x     Document Type: Article

References (40)

1. Belarbi E.H., Gomez A.C., Chisti Y., Camacho F.G., Grima E.M. Producing drugs from marine sponges. Biotechnol. Adv. (2003) 21 585 598.
2. Randazzo A., Bifulco G., Giannini C. et al. Halipeptins A and B: two novel potent anti-inflammatory cyclic depsipeptides from the Vanuatu marine sponge Haliclona species. J. Am. Chem. Soc. (2001) 123 10870 10876.
3. McCarthy P.J., Pitts T.P., Gunawardana G.P., Kelly-Borges M., Pomponi S.A. Antifungal activity of meridine, a natural product from the marine sponge Corticium sp. J. Nat. Prod. (1992) 55 1664 1668.
4. Kim D.K., Lee M.Y., Lee H.S. Polyacetylenes from a marine sponge Petrosia sp. inhibit DNA replication at the level of initiation. Cancer Lett. 2002) 185 95 101.
5. Mayer A.M.S. Marine pharmacology in 1998: antitumor and cytotoxic compounds. Pharmacologist (1999) 41 159 164.
6. Mayer A.M.S., Hamann M.T. Marine pharmacology in 2000: marine compounds with antibacterial, anticoagulant, antifungical, anti-inflamatory, antimalarial, antiplatelet, antituberculosis, and antiviral activities; affecting the cardiovascular, immune, and nervous systems and other miscellaneous mechanisms of action. Mar. Biotechnol. (2004) 6 37 52.
7. Garcia-Pastor P., Randazzo A., Gomez-Paloma L., Alcaraz M.J., Paya M. Effects of petrosaspongiolide M, a novel phospholipase A2 inhibitor, on acute and chronic inflammation. J. Pharmacol. Exp. Ther. (1999) 289 166 172.
8. Saeki B.M., Granato A.C., Berlinck R.G.S. et al. Two unprecedented dibromotyrosine-derived alkaloids from the Brazilian endemic marine sponge Aplysina caissara. J. Nat. Prod. (2002) 65 796 799.
9. Lira T.O., Berlinck R.S., Nascimento G.G.F., Hadju E. Further dibromotyrosin-derived metabolites from the marine sponge Aplysina caissara. J. Braz. Chem. Soc. (2006) 7 1233 1240.
10. Pinheiro U.S., Hadju E. Shallow-water Aplysina nardoa (Aplysinidae, Verongida, Dermospogiae) from the São Sebastião Channel and its environs (Tropical southwestern Atlantic), with the description of a new species and a literature review of other Brazilian records of the genus. Rev. Bras. Zool. (2001) 18 (Suppl. 1) 143 160.
11. Berlinck R.G.S., Hadju E., Rocha R.M. et al. Reviews - challenges and rewards of research in marine products chemistry in Brasil. J. Nat. Prod. (2004) 67 510 522.
12. Colégio Brasileiro de Experimentação Animal 1991). Os princípios éticos da experimentação animal. Colégio Brasileiro de Experimentação Animal, São Paulo, SP.
13. Zimmermann M. Ethical guidelines for investigations of experimental pain in conscious animals. Pain (1983) 16 109 110.
14. Miller L.L.C., Tainer T.L. Estimation of the DL50 and its error by means of logarithmic-probits graph paper. Proc. Soc. Exp. Biol. Med. (1944) 57 261 264.
15. Koster R., Anderson M., de Beer E.J. Acetic acid for analgesic screening. Fed. Proc. (1959) 18 412 416.
16. Hunskaar S., Hole K. The formalin test in mice: dissociation between inflammatory and non-inflammatory pain. Pain 1987) 30 103 114.
17. Eddy N.B., Leimbach D. Synthetic analgesics. II. Dithienylbutenyl and dithienylbutenylamines. J. Pharmacol. Exp. Ther. (1953) 107 385 393.
18. Süleyman H., Yildirim D., Aslan A., Göçer F., Gepdiremen A., Güvenalp Z. An investigation of the antiinflamatory effects of an extract from Cladonia rangiformis HOFFM. Biol. Pharm. Bull. (2002) 25 10 13.
19. Collier H.O.J., Dinnen L.C., Johnson C.A., Schneider C. The abdominal constriction response and its suppression by analgesic drugs in mice. Br. J. Pharmacol. Chemother. (1968) 32 295 310.
20. Choi J.-H., Jung B.-H., Kang O.-H. et al. The anti-inflammatory and anti-nociceptive effects of ethyl acetate fraction of Cynanchi Paniculati radix. Biol. Pharm. Bull. (2006) 29 971.
21. Thomazzi S.M., Ribeiro R.A., Campos D.I., Cunha F.Q., Gerreira S.H. Tumor necrosis factor, interleukin-1 and interleukin-8 mediate the nociceptive activity of the supernatant of LPS-stimulated macrophages. Mediators Inflamm. (1997) 6 192 200.
22. Ribeiro R.A., Vale M.L., Thomazzi S.M. et al. Involvement of resident macrophages and mast cells in the writhing nociceptive response induced by zymosan and acetic acid in mice. Eur. J. Pharmacol. (2000) 387 111 118.
23. Parker A.G., Peraza G.G., Sena J. et al. Antinociceptive effects of the aqueous extract of Brugmansia suaveolens flowers in mice. Biol. Res. Nurs. (2007) 8 234 239.
24. Tjolsen A., Berge O.G., Hunskaar S., Rosland J.H., Hole K. The formalin test: an evaluation of the method. Pain (1992) 51 5 17.
25. Shibata M., Ohkubo T., Takahashi H., Inoki R. Modified formalin test: characteristic biphasic pain response. Pain (1989) 38 347 352.
26. Le Bars D., Gozariu M., Caden S.W. Animal models of nociception. Pharmacol. Rev. (2001) 53 597 602.
27. Correa C.R., Calixto J.B. Evidence for participation of B1 and B2 kinin receptors in formalin-induced nociceptive response in the mouse. Br. J. Pharmacol. (1993) 110 193 198.
28. Chapman V., Dickenson A.H. The spinal and peripheral roles of bradykinin and prostaglandins in nociceptive processing in the rat. Eur. J. Pharmacol. (1992) 219 427 433.
29. Dray A., Perkins M. Bradykinin and inflammatory pain. Trends Neurosci. (1993) 16 99 104.
30. Iwamoto I., Ueki I.F., Borson D.B., Nadel J.A. Neutral endopeptidase modulates tachykinin-induced increase in vascular permeability in guinea pig skin. Int. Arch. Allergy Appl. Immunol. (1989) 88 288 293.
31. Rupniak N.M., Boyce S., Williams A.R. et al. Antinociceptive activity of NK1 receptor antagonists: non-specific effects of racemic RP67580. Br. J. Pharmacol. (1993) 110 1607 1613.
32. De Silva E.D., Scheuer P.J. Manoalide, na antibiotic sesterpenoid from the marine sponge Luffariella variabilis. Tetrahedron Lett. (1980) 21 1611 1614.
33. Mayer A.M.S., Jacobs R.S. Manoalide: an anti-inflammatory and analgesic marine natural product. Mem. Calif. Acad. Sci. (1988) 13 133.
34. 2 sharing unusual chemical features. Life Sci. (2000) 67 3007 3014.
35. D'Acquisto F., Lanzotti V., Carnuccio R. Cyclolinteinone, a sesterterpene from sponge Cacospongia linteiformis, prevents inducible nitric oxide synthase and inducible cyclo-oxygenase protein expression by blocking nuclear factor-kappaB activation in J774 macrophages. Biochem. J. (2000) 346 793 798.
36. Lee W.L., Gilchrist B.M. Carotenoid patterns in twenty-nine species of sponges in the order Poecilosclerida (Porifera: Demospongiae): a possible tool for chemosystematic. Mar. Biol. (1985) 86 21 35.
37. Kelecom A., Kannengiesser G.J. Chemical constituents of Verongia Sponges I-A comparison between Brazilian and Mediterranean species. An. Acad. Bras. Ciênc. (1979) 51 633 637.
38. Ciminiello P., Constantino V., Fattorusso E., Magno S., Mangoni A., Pansini M. Chemistry of Verongida sponges II. Constituents of the Caribeean Sponges Aplysina fistularis forma fulva. J. Nat. Prod. (1994) 57 705 712.
39. Ohgami K., Shiratori K., Kotake S. et al. Effects of Astaxanthin on lipopolysaccharide-induced inflammation in vivo. Invest. Ophtalmol. Vis. Sci. (2003) 44 2694 2701.
40. Azevedo L.G., Muccillo-Baisch A.L., Filgueira D.M.V.B. et al. Comparative cytotoxic and anti-tuberculosis activity of Aplysina caissara marine sponge crude extracts. Comp. Biochem. Physiol. C. Toxicol. Pharmacol. (2008) 147 36 42.