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TOXICOLOGICAL PROFILE FOR BARIUM AND COMPOUNDS ...

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51<br />

2. HEALTH EFFECTS<br />

Singh 1970; Diengott et al. 1964; McNally 1925; Ogen et al. 1967; Talwar and<br />

Sharma 1979), a single intermediate-duration experimental study (Wones et al.<br />

1990), and several human epidemiological studies or statistical studies<br />

examining mortality and morbidity rates in communities having exposure to<br />

barium through drinking water supplies (Brenniman and Levy 1985; Brenniman et<br />

al. 1979a, 1979b, 1981; Elwood et al. 1974; Schroeder and Kraemer 1974).<br />

Dermal studies are limited to one case report of an exposed individual<br />

(Stewart and Hummel 1984).<br />

The majority of studies conducted on animals have been oral exposure<br />

studies (Figure 2-2). These oral studies have focused on examining mortality<br />

or various systemic effects following acute (Borzelleca et al. 1988; Boyd and<br />

Abel 1966; Tardiff et al. 1980), intermediate (McCauley et al. 1985; Perry et<br />

al. 1983, 1985, 1989; Tarasenko et al. 1977; Tardiff et al. 1980), and chronic<br />

exposure (Kopp et al. 1985; McCauley et al. 1985; Perry et al. 1983, 1985,<br />

1989; Schroeder and Mitchener 1975a, 1975b). Available inhalation studies<br />

with experimental animals (Hicks et al. 1986; Tarasenko et al. 1977) can only<br />

suggest information on the health effects of barium because these studies have<br />

a number of limitations and deficiencies. Dermal studies with experimental<br />

animals are limited to one skin irritation study (Tarasenko et al. 1977) and<br />

one study evaluating the tumor-promoting activity of barium (Van Duuren et al.<br />

1968).<br />

2.9.2 Data Needs<br />

Acute-Duration Exposure. The majority of experimental studies involving<br />

acute.exposure to barium chloride have focused on oral exposure of rats<br />

(Borzelleca et al. 1988; Tardiff et al. 1980). These studies have determined<br />

acute oral LD 50<br />

values, as well as evaluated systemic effects. Systemic<br />

effects were evaluated primarily by monitoring body weights, selected organ<br />

weights, and various hematological and blood chemistry parameters, and by<br />

performing gross and microscopic examinations of selected organs and tissues.<br />

These studies have provided evidence that barium chloride is lethal by oral<br />

ingestion (LD 50<br />

s range from 132 to 277 mg/kg). The study by Borzelleca et al.<br />

(1988) has also provided evidence that acute oral barium exposure is<br />

associated with reduced blood urea nitrogen, inflammation of the intestines,<br />

accumulation of fluid in the trachea, decreased liver/brain weight ratio,<br />

darkened liver, increased kidney/body weight ratio, decreased body weight,<br />

decreased ovary weight, and decreased ovaries/brain weight ratio. This study<br />

has also provided information as to the barium levels inducing these effects<br />

in experimental animals. In the only available acute inhalation study,<br />

limited evidence was provided suggesting that barium exposure is potentially<br />

associated in rats with increased blood pressure and bronchoconstriction<br />

(Hicks et al. 1986). However, this inhalation study was limited in that no<br />

controls were used, Limited acute testing of experimental animals also has<br />

provided suggestive evidence that barium carbonate is both a dermal and ocular<br />

irritant (Tarasenko et al. 1977). Given the available data from acute

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