holothurin has been researched along with Hemolysis* in 3 studies
3 other study(ies) available for holothurin and Hemolysis
Article | Year |
---|---|
Hemolytic activities of triterpene glycosides from the holothurian order Dendrochirotida: some trends in the evolution of this group of toxins.
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. Topics: 3-O-Methylglucose; Animals; Chromatography, Thin Layer; Dose-Response Relationship, Drug; Erythrocytes; Glycosides; Hemolysis; Holothurin; Lethal Dose 50; Magnetic Resonance Spectroscopy; Marine Toxins; Mice; Potassium; Sea Cucumbers; Structure-Activity Relationship; Sulfates; Triterpenes | 1996 |
Positive inotropic action of saponins on isolated atrial and papillary muscles from the guinea-pig.
The effects of several saponins of animal and plant origin on the contractile activity of atrial and papillary muscles of the guinea-pig were tested. In a concentration of 1 X 10(-5)M, holothurin-A (HL-A), holothurin-B, echinoside-A, echinoside-B and sakuraso-saponin (Saku) exhibited positive inotropic and chronotropic actions whereas desacyl-jego-saponin and ginsenoside-Rd did not. Saponins having a positive inotropic action caused haemolysis of rabbit erythrocytes whereas those without inotropic action did not cause haemolysis. The positive inotropic action of saponins was not affected by practolol, chlorpheniramine, cimetidine and indomethacin. Verapamil (10(-6)M) inhibited the inotropic actions due to HL-A and isoprenaline (10(-8)M) to the same extent but had a small effect on those due to ouabain (10(-7)M). In high K+ (30 mM K+) medium where the action potential and the contraction were depressed, HL-A, Saku and isoprenaline restored the action potential and the contraction of the 'slow response' type whereas ouabain failed to do so. In normal medium HL-A and Saku reduced the resting membrane potential by 15-20 mV. These results suggest that modification of the Ca channel is involved in the positive inotropic action of saponins. Topics: Animals; Erythrocytes; Female; Guinea Pigs; Hemolysis; Holothurin; In Vitro Techniques; Isoproterenol; Male; Membrane Potentials; Myocardial Contraction; Ouabain; Papillary Muscles; Rabbits; Saponins; Stimulation, Chemical | 1986 |
HEMOLYSIS BY HOLOTHURIN A, DIGITONIN, AND QUILLAIA SAPONIN: ESTIMATES OF THE REQUIRED CELLULAR LYSIN UPTAKES AND FREE LYSIN CONCENTRATIONS.
Topics: Cell Death; Chemical Phenomena; Chemistry; Digitalis Glycosides; Digitonin; Erythrocytes; Glycosides; Hemolysis; Holothurin; Mucoproteins; Quillaja; Research; Saponins | 1964 |