Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Toxicity sodium vanadate

Vanadium is an element, and as such, is not metabolized. However, in the body, there is an interconversion of two oxidation states of vanadium, the tetravalent form, vanadyl (V+4), and the pentavalent form, vanadate (V+5). Vanadium can reversibly bind to transferrin protein in the blood and then be taken up into erythrocytes. These two factors may affect the biphasic clearance of vanadium that occurs in the blood. Vanadate is considered more toxic than vanadyl, because vanadate is reactive with a number of enzymes and is a potent inhibitor of the Na+K+-ATPase of plasma membranes (Harris et al. 1984 Patterson et al. 1986). There is a slower uptake of vanadyl into erythrocytes compared to the vanadate form. Five minutes after an intravenous administration of radiolabeled vanadate or vandadyl in dogs, 30% of the vanadate dose and 12% of the vanadyl dose is found in erythrocytes (Harris et al. 1984). It is suggested that this difference in uptake is due to the time required for the vanadyl form to be oxidized to vanadate. When V+4 or V+5 is administered intravenously, a balance is reached in which vanadium moves in and out of the cells at a rate that is comparable to the rate of vanadium removal from the blood (Harris et al. 1984). Initially, vanadyl leaves the blood more rapidly than vandate, possibly due to the slower uptake of vanadyl into cells (Harris et al. 1984). Five hours after administration, blood clearance is essentially identical for the two forms. A decrease in glutathione, NADPH, and NADH occurs within an hour after intraperitoneal injection of sodium vanadate in mice (Bruech et al. 1984). It is believed that vanadate requires these cytochrome P-450 components for oxidation to the vanadyl form. A consequence of this action is the diversion of electrons from the monooxygenase system resulting in the inhibition of drug dealkylation (Bruech et al. 1984). [Pg.34]

Toxicology ACGIH TLV/TWA 0.05 mg(V205)/m LD50 (oral, rat) 140 mg/kg extremely toxic poison by ing. toxic by inh., skin contact corrosive irritant to eyes, skin, mucous membranes causes burns TSCA listed Precaution DOT Corrosive explosive reaction with sodium violent reaction with rubidium ( 60 C), potassium reacts violently with water exposure to moisture in air produces HCI and vanadic acid... [Pg.4659]


See other pages where Toxicity sodium vanadate is mentioned: [Pg.380]    [Pg.160]    [Pg.1171]    [Pg.1417]    [Pg.37]    [Pg.2808]    [Pg.98]    [Pg.1000]    [Pg.64]   
See also in sourсe #XX -- [ Pg.1171 ]




SEARCH



Sodium vanadate

Vanadates

© 2024 chempedia.info