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

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AX5-169<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 />

0–500 µM Pb acetate 6 h CHO cells and —<br />

2000 ppm <strong>of</strong> Pb<br />

acetate in drinking<br />

water <strong>for</strong> 5 wks<br />

Taurine<br />

1.1 kg/d<br />

1 mg Pb2+/kg B.wt ,<br />

i.p. Pb acetate<br />

Pb as acetate, 400 mg<br />

Pb2+/mL, drinking<br />

water<br />

0.5 mg/mL<br />

L-methionine<br />

100 µM/kg b.wt. Pb<br />

acetate,<br />

intramuscular, single<br />

100 µg/ Pb acetate,<br />

intra gastric, oral and<br />

intraperitoneal,<br />

treated with or with<br />

out thiamin (25,<br />

50 mg/kg b.wt) and or<br />

Ca EDTA (50 mg/kg<br />

B.wt<br />

5 wks<br />

6th wk<br />

4 wks, treatment<br />

with various<br />

antioxidant in the<br />

5th wk<br />

Fischer 344 rats Controls: 0.43 µg/dL<br />

Pb-exposed:<br />

36.4 µg/dL<br />

Pb + Taurine:<br />

33.8 µg/dL<br />

Antioxidant Taurine reversed the abnormalities associated with lipid<br />

peroxidation parameters such as increased. Malondialdehyde <strong>for</strong>mation<br />

and decreased Glutathione and enhanced CHO cell survival. However,<br />

was not effective in reducing cell and tissue Pb burden in CHO cells and<br />

Pb exposed Fischer rats.<br />

IVRI 2 CQ rats — Pb exposure resulted in increased lipid peroxidation, with tissue specific<br />

changes in liver. Treatment <strong>of</strong> exposed rats with ascorbic acid and αtocopherol<br />

lowered the lipid peroxidation.<br />

10 days Kunming mice<br />

—<br />

4 wks post-Pb<br />

exposure<br />

—<br />

L- methionine has an ameliorative effect on Pb toxicity–Methionine<br />

reduced the decrease in Hb content and depressed body growth caused by<br />

Pb. Treatment with dietary methione along with Pb decreased the MDA<br />

<strong>for</strong>mation as opposed to Pb, moderately reversed the decreased iron<br />

content <strong>of</strong> the organs and decreased organ Pb content.<br />

3 and 24 h Male Albino rats — Pb exposure resulted in significant increases in acid and alkaline<br />

phosphatases, serum GOT and GPT, elevated liver and kidney lipid<br />

peroxidation and decreased antioxidant enzymes at 3 and 24 h after<br />

exposure. Selenium administration prior to Pb exposure produced<br />

pronounced prophylactic effects against Pb exposure by enhancing<br />

endogenous anti oxidant capacity.<br />

3 days CD-1 mice — Two times more whole body Pb was retained by intraperitoneal injection<br />

as compared to intragastric administration. Thiamin treatment increased<br />

the whole body retention <strong>of</strong> both intragastric and intraperitoneal Pb by<br />

about 10%. Calcium EDTA either alone or in combination with thiamin<br />

reduced the whole body retention <strong>of</strong> Pb by about 14% regardless <strong>of</strong> the<br />

route <strong>of</strong> exposure. Regardless <strong>of</strong> the route Ca EDTA in the combined<br />

treatment reduced the relative retention <strong>of</strong> Pb in both in liver and kidney.<br />

These studies indicate the combination treatment with thiamin and Ca<br />

EDTA alters the distribution and retention <strong>of</strong> Pb in a manner which might<br />

have therapeutic application.<br />

Gurer et al. (2001)<br />

Patra et al. (2001)<br />

Xie et al. (2003)<br />

Othman and El<br />

Missiry (1998)<br />

Kim et al. (1992)

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