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AMMONIUM SULFATE CAS N°: 7783-20-2

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OECD SIDS<br />

<strong>AMMONIUM</strong> <strong>SULFATE</strong><br />

5. TOXICITY ID: <strong>7783</strong>-<strong>20</strong>-2<br />

DATE: 18.04.<strong>20</strong>06<br />

results.<br />

Harlan Sprague Dawley (Indianapolis, Ind.). were acclimated<br />

for 1 week at 21 °C, 50% humidity, and a 12:12 h light/dark<br />

cycle. The mean initial body weight was 23.0 +/- 1.7g. Mice<br />

were housed in groups of five, and maintained on commercial<br />

rodent chow (Harlan Teklad 22/5 rodent diet, Harlan Teklad,<br />

Madison, Wis.).<br />

EXPOSURE TO TEST SUBSTANCE: Mice were administered aluminum<br />

ammonium sulfate in deionized drinking water ad lib at<br />

levels of 0, 5, 25, and 125 ppm as aluminum for 1 month.<br />

Controls received deionized water. An additional group was<br />

administered 0.611 g/L of ammonium sulfate to provide an<br />

ammonium ion concentration of 250 ppm. The results of this<br />

additional group were compared with those of the control to<br />

determine whether ammonium or sulfate ions affected the<br />

EXAMINATIONS: The weights of mice were recorded weekly and<br />

water<br />

consumption measured daily. Animals were observed daily for<br />

general behavior such as appearance, activity, grooming, and<br />

locomotion. On the last day of treatment, brains were<br />

isolated and the cerebrum was dissected from brain. A<br />

representative sample of whole cerebrum was employed to<br />

extract RNA. RNA was quantified by spectrophotometric<br />

absorbance at 260 nm. In PCR amplified samples, the<br />

following cytokines were determined: TNF-alpha, IL-1beta,<br />

and IFN-gamma. beta-actin from cDNA was also amplified and<br />

served as internal standard. Splenic macrophages and<br />

lymphocytes were collected according to the method<br />

previously described by Sharma, 1996. Liver, kidney and spleen<br />

were weighed.<br />

STATISTICAL EVALUATION:<br />

The log-transformed data of control and treatment groups<br />

were compared by one-way analysis of variance (ANOVA)<br />

followed by Fisher`s post-hoc least significant difference<br />

(PLSD) test using the Statview software (Abacus Concept,<br />

Berkeley, Calif.). For statistical analyses different<br />

treatment groups were compared to the group given deionized<br />

water.<br />

YEAR of STUDY CONDUCT: not reported.<br />

Reliability: (2) valid with restrictions<br />

limited documentation, no guideline study, no histopathology,<br />

only three organ weights determined, only one dose tested<br />

10-APR-<strong>20</strong>06 (135)<br />

Type:<br />

Sub-acute<br />

Species: rabbit Sex: female<br />

Strain:<br />

no data<br />

Route of administration: oral unspecified<br />

Exposure period:<br />

5-16 months<br />

Frequency of treatment: on alternate days<br />

Post exposure period: no<br />

Method:<br />

GLP:<br />

Test substance:<br />

other: see Test Condition<br />

no<br />

other TS: ammonium sulfate, not further specified<br />

Result: At necropsy, mean body weights were between 4,100 and 4,800<br />

grams. Parathyroid weights were between 15 and 33 mg (mean<br />

value 27.5 mg). Parathyroids of control animals (n=50)<br />

178<br />

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