Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 5 de 5
Filter
Add more filters










Database
Publication year range
1.
Toxicon ; 189: 45-47, 2021 Jan 15.
Article in English | MEDLINE | ID: mdl-33212098

ABSTRACT

Holothurians are marine invertebrates also known as sea cucumbers. They are used in fresh or dried forms in various cuisines around the world and have alleged medicinal properties. Consequently, sea cucumbers, notably the orange-footed sea cucumber (Cucumaria frondosa)are increasingly harvested from the environment or farmed via aquaculture. We report three cases of unusual occupational exposure to C. frondosa resulting in cutaneous, respiratory and ocular irritating symptoms. These symptoms occurred as sea cucumbers were cut on half and eviscerated manually, following a machine breakdown in a sea cucumber processing factory. Given the composition of holothurians, these symptoms probably resulted from the aerosolization of various holothurins, saponins secreted by sea cucumbers as mean of defense. Treatment was solely symptomatic and included decontamination of the skin and the eyes, inhaled glucocorticoids, anticholinergic agents and oral glucocorticoids. As the exposure resulted from a machine breakdown, no specific protective equipment was put in place. Employees were advised not to handle manuallythe sea cucumbers in case such a breakdown was to happen again.


Subject(s)
Cucumaria , Holothurin/toxicity , Occupational Exposure , Animals , Humans , Marine Toxins/toxicity
2.
Arch Med Res ; 39(7): 631-8, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18760190

ABSTRACT

BACKGROUND: A recent revelation about increased susceptibility to HIV by use of nonoxynol-9 (N-9) has called for identification of novel molecules with potent sperm-attenuating activity and lower side-effect profile, as suitable alternatives. The present study was designed to investigate spermicidal activity in Bohadschia vitiensis whole-body extracts followed by isolation and characterization of bioactive molecule. METHODS: Bohadschia vitiensis (Semper) was collected from the Southern Andaman coast of India. Freshly collected marine animals were extracted with methanol. A portion of the crude extract was fractionated into four fractions by macerating with hexane, chloroform, and n-butanol successively. All fractions were evaluated for spermicidal activity. Because maximum activity was localized in the n-butanol soluble fraction, it was chromatographed over a silica gel column, and elution with chloroform-methanol-water (35:10:2, v/v) yielded the major compound bivittoside D (400 mg). Bivittoside D [molecular weight (MW) 1426] is a lanostane triterpenoid with six monosaccharide units. The structure of the compound was established on the basis of physicochemical data, acid hydrolysis of saponin, identification of sugar units and aglycon, melting point, and by comparison with data reported in the literature. RESULTS: The aqueous methanol extract of the Bohadschia vitiensis caused 100% mortality of human sperm at 0.01% concentration in vitro, whereas N-9 (reference control) exhibited an equivalent activity at 0.05%. On further fractionation, activity was localized in n-butanol soluble fraction from which the major compound purified was a lanostane triterpenoid called bivittoside D. Bivittoside D was found to be a more potent spermicide (approximately 2.3 times) than N-9 and killed 100% human sperm at the concentration of 350 muM in approximately 20 sec in vitro. Supravital staining and hypoosmotic swelling test revealed sperm membrane permeabilization by bivittoside D as the major mode of spermicidal action. However, bivittoside D was much safer than N-9 towards normal vaginal flora (Lactobacillus) in vitro, although it affected the viability of HeLa cells like other surfactants. CONCLUSION: Bivittoside D from B. vitiensis can adequately replace N-9 in vaginal contraceptives to make them more vaginally safe and ecofriendly.


Subject(s)
Holothurin/analogs & derivatives , Spermatocidal Agents/pharmacology , Spermatozoa/drug effects , Animals , Cell Survival/drug effects , HeLa Cells , Holothurin/chemistry , Holothurin/isolation & purification , Holothurin/pharmacology , Holothurin/toxicity , Humans , Lactobacillus acidophilus/drug effects , Male , Sea Cucumbers , Sperm Motility/drug effects , Spermatocidal Agents/isolation & purification
3.
Toxicon ; 34(4): 475-83, 1996 Apr.
Article in English | MEDLINE | ID: mdl-8735247

ABSTRACT

Hemolysis and K+ loss from mouse erythrocytes, induced by triterpene glycosides and their derivatives from this order of sea cucumbers were studied. Sulfate groups, attached to position 4 of the first xylose residue and to position 6 of the third glucose residue of the branched pentaosides, having 3-O-methyl-groups in terminal monosaccharide moieties increase K+ loss. A sulfate group at C-4 of the first xylose residue increases the hemolytic activity while a sulfate at C-6 of the third monosaccharide unit decreases it. A sulfate group at C-6 of terminal 3-O-methylglucose drastically decreases the hemolytic activity and rate of K+ loss. The presence of a sulfate group at the first xylose residue in glycosides having no 3-O-methyl group at the terminal monosaccharide decreases hemolytic activity and rate of K+ loss. The presence of the 16-ketone group in aglycones having the 7(8)-double bond significantly decreases activity. These results correlate with the previously proposed trends in evolution of sea cucumber glycosides from substances having sulfate groups at C-6 of glucose and 3-O-methylglucose units to substances sulfated at C-4 of the first xylose or having no sulfate groups, and from substances with aglycone 16-ketone to substances having no oxygen functions in this position.


Subject(s)
Erythrocytes/drug effects , Glycosides/toxicity , Marine Toxins/toxicity , Sea Cucumbers/metabolism , Triterpenes/toxicity , 3-O-Methylglucose/metabolism , Animals , Chromatography, Thin Layer , Dose-Response Relationship, Drug , Erythrocytes/cytology , Glycosides/chemistry , Hemolysis/drug effects , Holothurin/chemistry , Holothurin/toxicity , Lethal Dose 50 , Magnetic Resonance Spectroscopy , Marine Toxins/chemistry , Mice , Potassium/metabolism , Structure-Activity Relationship , Sulfates/metabolism , Triterpenes/chemistry
4.
Farmakol Toksikol ; 54(1): 60-1, 1991.
Article in Russian | MEDLINE | ID: mdl-1860504

ABSTRACT

The preclinical study of embryotoxicity of a new immunomodulator cucumariosid was carried out. Cucumariosid at long-term use exerts no effect on the generative function of rats, the general condition of pregnant females and the postnatal development of the offspring, possesses no teratogenic action. The use of the drug in the preimplantation period of pregnancy and the implantation period produces the contraceptive effect.


Subject(s)
Adjuvants, Immunologic/toxicity , Embryo, Mammalian/drug effects , Embryo, Nonmammalian , Holothurin/toxicity , Reproduction/drug effects , Sea Cucumbers , Triterpenes/toxicity , Abnormalities, Drug-Induced/epidemiology , Adjuvants, Immunologic/pharmacology , Animals , Dose-Response Relationship, Drug , Embryo Loss/chemically induced , Female , Glycosides , Holothurin/pharmacology , Male , Pregnancy , Rats , Rats, Inbred Strains , Triterpenes/pharmacology
SELECTION OF CITATIONS
SEARCH DETAIL
...