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Despite the intense efforts by scientists, most drugs that are required to treat human diseases still
remain undiscovered. Marine organisms are a remarkable source of secondary metabolites that
are biologically active molecules with potential therapeutic usage. Marine sponges are ranked on
top of the hierarchy of marine organisms with bioactive secondary metabolites. Marine
environments were systematically investigated over the last 50 years and at present research is
ongoing for systematic identification and drug discovery from marine organisms in general, and
more specifically from marine sponges. The present study investigated the immunomodulatory
activity of a few selected Sri Lankan marine sponges, with a comprehensive
immunopharmacological study on Haliclona (Soestellci) sp, identified presumably as a novel
marine sponge species from Sri Lankan marine waters.
The vast marine sponge diversity of Sri Lanka led to the taxonomic identification of some
selected sponge species, using spicule and skeleton morphology using light and scanning
electron microscopy (SEM). A total of 11 sponge species of Class Demospongiae were identified
and classified. This is the first report on the use of SEM for sponge identification in spongology
in Sri Lanka.
Immunomodulatroy activity of 4 Sri Lankan marine sponges were reported, including that of
Haliclona (Soestellci)sp. Crude sponge extracts of Dyctionells conglomerate , Fasciospongia
ondacitjeana, Slylissa carteri affirmed immunomodulatory activity with respect to non
functional and functional immunological measures. Nevertheless. Haliclona (Soestella) sp was
selected for the comprehensive immunopharmacological and toxicological study, due to its
abundance. A number of in vitro, ex vivo and in vivo tests were performed to investigate the
immunomodulatory effects of the Haliclona (Sostella) sp. sponge crude extract (HSCE).
Antioxidant activity of the HSCE was tested using a few radicals in vitro and in vivo nitric oxide
(NO) radical scavenging assay. Further, zoo chemical analysis of the HSCE resulted in the
presence of alkaloids saponins and amino acids, followed by bioassay guided fractionation to
isolate the bioactive compounds.
Immunomodulatory activity of the HSCE revealed immunosuppressive, immunostimulant and
acute anti-inflammatory properties. Immunosupression was evident in the following tested
parameters:m vivo WBC, WBC DC, platelet, bone marrow cell and splenocyte counts, ex vivo
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immune cell proliferation and cytokine production. Nonetheless, the HSCE showed
immunoslimulalion with respect to in vitro phagocytic capacity of peritoneal macrophages. The
HSCE showed potent anti inflammatory activity against acute phase oedema as revealed by the
Carrageenan induced paw oedema and suppression of pro inflammatory cytokine production.
Both anti radical activity on quenching DPPH radicals and in vivo NO scavenging activity of the
HSCE established its antioxidant properties,
demonstrated that it was devoid of general toxicity, and hepato and renotoxic effects.
Conversely, the HSCE was moderately haematotoxic and stressogenic. Nevertheless, the HSCE
showed marked cytotoxic effect by inhibition of proliferation of the human larynx carcinoma cell
line, Hep2, at a IC 50 value of 19.63 pg/tnL, manifesting notable anticancer activity. The
chloroform fraction of the HSCE also showed anti proliferative activity of Hep2 at IC50 value of
29.52 pg/mL. Therefore, this fraction of the HSCE warrants LC-MS and NMR analyses for
chemical characterization and structure elucidation of this anti cancer compound.
Toxicological evaluation of the HSCE
In conclusion, Haliclona (Sosle/la) sp., presumably a novel Sri Lankan marine sponge species,
demonstrated immunosuppressant, immunostimulant, acute anti-inflammatory, antioxidant and
anti-cancer properties with associated moderate haematotoxic and stressogenic effects. This
prototype, comprehensive study on immunopharmacological and toxicological activity of a
marine sponge species forms the baseline for future pharmacognosy studies on Sri Lankan
marine organisms . |
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