ciguatoxins and Hypothermia

ciguatoxins has been researched along with Hypothermia* in 3 studies

Other Studies

3 other study(ies) available for ciguatoxins and Hypothermia

ArticleYear
Solid-phase extraction clean-up of ciguatoxin-contaminated coral fish extracts for use in the mouse bioassay.
    Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 2009, Volume: 26, Issue:2

    Florisil solid-phase extraction (SPE) cartridges were used for purifying ciguatoxin (CTX)-contaminated coral fish extracts, with the aim of removing extracted lipid but retaining optimal level of CTXs in the purified fractions. The CTX-containing fraction (target fraction) in fish ether extract was isolated and purified by eluting through a commercially available Florisil cartridge with hexane-acetone-methanol solvent mixtures of increasing polarity (hexane-acetone (4:1, v/v) < acetone-methanol (7:3, v/v) < 100% methanol). Application of Florisil SPE using acetone-methanol (7:3, v/v) condition facilitated the separation of 4.2 +/- 0.4 mg (mean +/- standard error of the mean (SEM)) of purified target fraction from 20 mg ether extract with good retention of CTXs. The mouse bioassay was used to demonstrate that the average CTX recovery of the target fraction from CTX-spiked samples was 75.8% +/- 3.3%, which was significantly increased by 96.7% +/- 15% when compared with CTX recovery from ether extracts (44.8% +/- 5.2%) without performing SPE purification. Over 70% of non-target lipids were removed in which no CTX toxicity was found. Moreover, the target fractions of both CTX-spiked and naturally CTX-contaminated samples gave more prominent toxic responses of hypothermia and/or induced more rapid death of the mice. The use of acetone-methanol (7:3, v/v) condition in the elution could significantly improve overall recovery of CTXs, while minimizing the possible interferences of lipid matrix from co-extractants on mice.

    Topics: Animals; Biological Assay; China; Ciguatera Poisoning; Ciguatoxins; Fishes; Food Contamination; Humans; Hypothermia; Lethal Dose 50; Marine Toxins; Mice; Poisons; Solid Phase Extraction; Tissue Extracts

2009
Ciguatera and mannitol: in vivo and in vitro assessment in mice.
    Toxicon : official journal of the International Society on Toxinology, 1993, Volume: 31, Issue:8

    Mannitol (1 g/kg i.v.) is currently the treatment of choice for acute ciguatera, but confirmation of this treatment's apparent efficacy awaits further experimental or controlled clinical evidence. In mice, mannitol (1 g/kg i.v.) administered before or after i.p. ciguatoxin did not influence the signs of intoxication or the time to death. The effects of oral ciguatoxin differed from those following i.p. ciguatoxin, but again i.v. mannitol provided no detectable benefit. Development of hypothermia was rapid in mice receiving i.p. or oral ciguatoxin and was unaffected by i.v. mannitol. A sublethal i.p. dose of ciguatoxin initially retarded (day 0-4) but then accelerated (day 4-12) the growth of mice. Mannitol (i.v.) had no influence on these effects of ciguatoxin on the growth of mice. Ciguatoxin inhibited responses of isolated diaphragms to nerve stimulation (ED50 = 9 x 10(-11) M), while directly stimulated diaphragms were inhibited by five-fold higher concentrations. Mannitol (50 mM) added to the organ bath did not influence the ciguatoxin-induced inhibition of diaphragm responses to nerve stimulation in vitro. Responses of isolated diaphragm to nerve stimulation were normal in preparations removed from ciguatoxin-treated mice displaying pronounced dyspnoea (gasping). However, responses to nerve stimulation were reduced in preparations removed from mice immediately following death from ciguatoxin. Mannitol (i.v.) partially protected the phrenic nerve-diaphragm from this effect of ciguatoxin in vivo. We conclude that the lethal effects of ciguatoxin in mice probably stem from a central action, and suggest that species differences may account for the absence of any marked beneficial effect of i.v. mannitol in the mouse model for ciguatera in humans.

    Topics: Animals; Body Weight; Ciguatera Poisoning; Ciguatoxins; Diaphragm; Disease Models, Animal; Female; Hypothermia; Lethal Dose 50; Male; Mannitol; Mice; Muscle Contraction; Phrenic Nerve

1993
[Biological assay of ciguatoxin in the chicken: analysis of the symptoms induced and toxicity of extracts of ciguatoxic chickens of the island of Saint Barthelemy].
    Bulletin de la Societe de pathologie exotique et de ses filiales, 1986, Volume: 79, Issue:1

    Ciguatera poisoning was studied in the chicken where it gave rise to internal hypersalivation, acute motor ataxia, low rectal temperature and arrested growth. LD50 figures indicated that the chicken is two to five time at least more sensitive to ciguatoxin than the mouse. So the chick is very convenient for laboratory studies in ciguatera research.

    Topics: Animals; Ataxia; Chickens; Ciguatoxins; Growth Disorders; Hypothermia; Marine Toxins; Mice; Sialorrhea; West Indies

1986