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Air Quality Criteria for Lead Volume II of II - (NEPIS)(EPA) - US ...

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AX5-167<br />

Table AX5-10.4 (cont’d). <strong>Lead</strong>, Oxidative Stress, and Chelation Therapy<br />

Concentration and<br />

Compound Duration Species Blood <strong>Lead</strong> Effects Reference<br />

550 ppm Pb acetate,<br />

oral DMSA treatment.<br />

Pb acetate Dose to<br />

achieve blood Pb<br />

levels <strong>of</strong> 35–<br />

40 µg/dL.<br />

Biweekly dose<br />

adjustments, oral<br />

followed by treatment<br />

with chelator.<br />

5 mg Pb kg−1, i.p Pb<br />

acetate followed by<br />

chelators <strong>for</strong> various<br />

time points.<br />

50 mg/kg Pb as Pb<br />

nitrate, i.p, two<br />

injections, 16h apart<br />

50% Ethanol, 0.5 mL,<br />

two injections, 16 h<br />

apart<br />

0.1% Pb acetate in<br />

drinking water with<br />

and without Sodium<br />

Molybdate, i.p<br />

(A) Pb <strong>for</strong> 35 +<br />

21 days<br />

(B) Pb 35 days and<br />

Pb and DMSA<br />

<strong>for</strong> 21 days<br />

(C) Pb 35 days and<br />

DMSA <strong>for</strong><br />

21 days<br />

(D) Acedified Di H2O<br />

<strong>for</strong> 35 days and<br />

Di water <strong>for</strong><br />

21 days<br />

1 yr, chelator <strong>for</strong><br />

two successive<br />

19 day period<br />

following Pb<br />

exposure.<br />

6–7 Wk old male<br />

Sprague-Dawley<br />

rats<br />

Infant rhesus<br />

monkeys<br />

Analyses at Day 5 Suckling Wistar<br />

rats<br />

Pb-exposed:<br />

50 µg/dL<br />

Pb 35 days: Ranged<br />

from 5–20 µg/dL +<br />

DMSA from 0–<br />

240 µg/kg/d<br />

Pb-exposed:<br />

35–40 µg/dL<br />

DMSA reversed the hematological effects <strong>of</strong> Pb, decreased the blood,<br />

brain , bone, kidney and liver concentration and produced marked Pb<br />

diuresis, even when challenged with ongoing Pb exposure.<br />

Specific emphasis on the beneficial effects <strong>of</strong> succimer treatment to<br />

cessation <strong>of</strong> Pb exposure. These data demonstrated that succimer<br />

efficiently reduces blood Pb levels which does not persist beyond the<br />

completion <strong>of</strong> treatment. They also demonstrate the relative benefit <strong>of</strong><br />

eliminating Pb exposures , which serves to underscore the importance <strong>of</strong><br />

primary prevention <strong>of</strong> Pb exposure. Neither DMSA treatment nor the<br />

cessation <strong>of</strong> Pb exposure were beneficial in reducing skeletal Pb levels.<br />

— Meso—DMSA is the treatment <strong>of</strong> choice <strong>for</strong> acute Pb poisoning in infants<br />

compared to EDTA and Rac-DMSA.<br />

24 h Male Albino rats — S-Adenosyl methionine confers protection against alterations in several<br />

parameters (ALAD, GSH, MDA) indicative <strong>of</strong> lipid peroxidation in blood,<br />

liver and brain in Pb and acute Pb and ethanol exposed animals as well as<br />

the organ concentration <strong>of</strong> Pb.<br />

4 wks Male Albino rats Pb-exposed:<br />

39 µg/dL<br />

Pb + chelators:<br />

4.6–13.1 µg/dL<br />

Sodium molybdate significantly protected the uptake <strong>of</strong> Pb in blood, liver<br />

and kidney. The treatment with molybdate also restored the Pb induced<br />

inhibited activity <strong>of</strong> blood δ-aminolevulinic acid dehydratase and the<br />

elevation <strong>of</strong> blood Zn protoporphyrin , hepatic lipid peroxidation and<br />

serum ceruloplasmin.<br />

Pappas et al. (1995)<br />

Smith et al. (2000)<br />

Kostial et al. (1999)<br />

Flora and Seth<br />

(1999)<br />

Flora et al. (1993)

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