RESUMEN
Paralytic shellfish poisoning results from consumption of seafood naturally contaminated by saxitoxin and its congeners, the paralytic shellfish toxins (PSTs). The levels of such toxins are regulated internationally, and maximum permitted concentrations in seafood have been established in many countries. A mouse bioassay is an approved method for estimating the levels of PSTs in seafood, but this is now being superseded in many countries by instrumental methods of analysis. Such analyses provide data on the levels of many PSTs in seafood, but for risk assessment, knowledge of the relative toxicities of the congeners is required. These are expressed as "Toxicity Equivalence Factors" (TEFs). At present, TEFs are largely based on relative specific activities following intraperitoneal injection in a mouse bioassay rather than on acute toxicity determinations. A more relevant parameter for comparison would be median lethal doses via oral administration, since this is the route through which humans are exposed to PSTs. In the present study, the median lethal doses of gonyautoxin 5, gonyautoxin 6, decarbamoyl neosaxitoxin and of equilibrium mixtures of decarbamoyl gonyautoxins 2&3, C1&2 and C3&4 by oral administration to mice have been determined and compared with toxicities via intraperitoneal injection. The results indicate that the TEFs of several of these substances require revision in order to more accurately reflect the risk these toxins present to human health.
Asunto(s)
Saxitoxina/análogos & derivados , Administración Oral , Animales , Femenino , Inyecciones Intraperitoneales , Dosificación Letal Mediana , Ratones , Nivel sin Efectos Adversos Observados , Saxitoxina/administración & dosificación , Saxitoxina/toxicidadRESUMEN
Hypochlorous acid formed by activated neutrophils reacts with amines to produce chloramines. Chloramines vary in stability, reactivity, and cell permeability. We have examined whether chloramine exchange occurs between physiologically important amines or amino acids and if this affects interactions of chloramines with cells. We have demonstrated transchlorination reactions between histamine, glycine, and taurine chloramines by measuring chloramine decay rates with mixtures as well as by mass spectrometry. Kinetic analysis suggested the formation of an intermediate complex with a high Km. Apparent second-order rate constants, determined for concentrations Asunto(s)
Cloraminas/química
, Cloro/química
, Glicina/química
, Histamina/química
, Taurina/química
, Células Cultivadas
, Células Endoteliales/química
, Células Endoteliales/citología
, Gliceraldehído-3-Fosfato Deshidrogenasas/química
, Humanos
, Ácido Hipocloroso/química
, Células Jurkat
RESUMEN
Hypochlorous acid formed by activated neutrophils reacts with amines to produce chloramines. Chloramines vary in stability, reactivity, and cell permeability. We have examined whether chloramine exchange occurs between physiologically important amines or amino acids and if this affects interactions of chloramines with cells. We have demonstrated transchlorination reactions between histamine, glycine, and taurine chloramines by measuring chloramine decay rates with mixtures as well as by mass spectrometry. Kinetic analysis suggested the formation of an intermediate complex with a high K(m). Apparent second-order rate constants, determined for concentrations Asunto(s)
Cloraminas/química
, Cloro/química
, Glicina/química
, Histamina/química
, Taurina/química
, Células Cultivadas
, Células Endoteliales/química
, Células Endoteliales/citología
, Gliceraldehído-3-Fosfato Deshidrogenasas/química
, Humanos
, Ácido Hipocloroso/química
, Células Jurkat
RESUMEN
The crude extract of a New Zealand marine bryozoan Cribricellina cribraria was examined and resulted in the isolation of the previously described, 6-hydroxyharman (1) and the new beta-carboline metabolite, 8-hydroxyharman (2).