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12th International Conference on Harmful Algae

12th International Conference on Harmful Algae

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INTERNATIONAL SOCIETY FOR THE STUDY OF HARMFUL ALGAE12 th <str<strong>on</strong>g>Internati<strong>on</strong>al</str<strong>on</strong>g> <str<strong>on</strong>g>C<strong>on</strong>ference</str<strong>on</strong>g> <strong>on</strong> <strong>Harmful</strong> <strong>Algae</strong>, Copenhagen, Denmark, 4-8 September 2006and geographically restricted tooffshore waters between St.Petersburg and Naples. Kareniasp. was further restricted, present<strong>on</strong>ly at higher salinities in the Ft.Myers to Naples area. Thesepatterns of occurrence of thedifferent Karenia species throughoutthe blooms suggest that K. brevisoccupies the broadest ecologicalniche, with other species eitherspatially or temporally restricted.Management implicati<strong>on</strong>s depend<strong>on</strong> impacts, toxins and toxicity ofdifferent strains. The first step isisolati<strong>on</strong> of newly recorded species.O.22-01First evidence for the implicati<strong>on</strong>of nitric oxide in Ciguatera FishPois<strong>on</strong>ingSessi<strong>on</strong>: O.22 - Toxicology 3Presentati<strong>on</strong> time: 14.55 - 15:15S Pauillac, F Vernel-Pauillac, S Kumar-Roine, M-P Sauviat, E Benoit, MChinain, D LaurentInstitut Pasteur de Nouvelle-Caléd<strong>on</strong>ie,NOUMÉA, New Caled<strong>on</strong>iaThe involvement of the nitric oxide(NO) pathway in ciguatera fishpois<strong>on</strong>ing (CFP) has beeninvestigated, in vitro and in vivo, in aciguatoxin (CTX)/mouse model. Theinducti<strong>on</strong> of inducible nitric oxidesynthase (iNOS) synthesis at themRNA level was kineticallymeasured using a real-time PCRprotocol based <strong>on</strong> the LightCycler®technology. CTX-pulsed Neuro-2acells (1 ng/mL) and peripheral bloodm<strong>on</strong><strong>on</strong>uclear cells from CTXinjectedmice (1ng/g), weredem<strong>on</strong>strated to express iNOS in atime-dependent manner. Thisstr<strong>on</strong>gly suggests that NO might beresp<strong>on</strong>sible for certain ciguaterasymptoms (e.g. hypotensi<strong>on</strong>,allergenic effects and Chr<strong>on</strong>icFatigue Syndrome) which could notbe solely explained by the activati<strong>on</strong>of voltage-gated sodium channels.This hypothesis is supported by theobservati<strong>on</strong> that the most currentlyused drugs for the treatment of CFPare free radical scavengers.In c<strong>on</strong>clusi<strong>on</strong>, the implicati<strong>on</strong> of NOin CFP paves the way for newtherapies for both occidental andtraditi<strong>on</strong>al medicines, together withnew CTXs detecti<strong>on</strong> and clinicaldiagnostic tools.O.22-02Implicati<strong>on</strong>s of saxitoxins forpublic health and naturalresources in FloridaSessi<strong>on</strong>: O.22 - Toxicology 3Presentati<strong>on</strong> time: 15:15 – 15.35JH Landsberg 1 , JP Abbott 2 , LJFlewelling 1 , PS Scott 1 , JL Wolny 21 FL Fish & Wildlife C<strong>on</strong>servati<strong>on</strong> Comm.,ST. PETERSBURG, United States ofAmerica2 Florida Institute of Oceanography, ST.PETERSBURG, United States of AmericaIn early 2002, with the <strong>on</strong>set ofpuffer fish pois<strong>on</strong>ing (PFP)originating from the Indian RiverLago<strong>on</strong> (IRL), saxitoxin wasdiscovered in Florida andassociated with Pyrodiniumbahamense for the first time in theUnited States. Saxitoxins areusually associated with potentiallyfatal Paralytic Shellfish Pois<strong>on</strong>ing(PSP), but prior to 2002, there wasno public health risk from PSP inFlorida. Since the detecti<strong>on</strong> ofsaxitoxins in puffer fish, the stateinitiated an intensive statewidem<strong>on</strong>itoring program to determinec<strong>on</strong>centrati<strong>on</strong>s and distributi<strong>on</strong> ofsaxitoxins in biota. Because theyare immune to saxitoxins, puffer fishcan accumulate high toxinc<strong>on</strong>centrati<strong>on</strong>s in the muscle,making them an extreme threat toc<strong>on</strong>sumers. Following FDA acti<strong>on</strong>80

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