28-day repeated dose response study of diglycolic acid: Renal and hepatic effects
Autor: | Zachary Keltner, Nicholas Olejnik, Martine Ferguson, Sanah Vohra, Miriam E. Mossoba, T.N. Black, Cynthia B. Stine, Eric Evans, Jessica Sprando, Robert L. Sprando, Howard Toomer |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Pathology medicine.medical_specialty Diglycolic acid Physiology Spleen Kidney Toxicology Rats Sprague-Dawley 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Blood serum Toxicity Tests medicine Dose group Animals 030212 general & internal medicine Dose-Response Relationship Drug business.industry Stomach Animal Structures General Medicine Dose Response Study Glycolates Rats 030104 developmental biology medicine.anatomical_structure Liver chemistry Toxicity Female Bone marrow business Food Science |
Zdroj: | Food and Chemical Toxicology. 106:558-567 |
ISSN: | 0278-6915 |
DOI: | 10.1016/j.fct.2017.03.047 |
Popis: | The acute oral toxicity of diglycolic acid (DGA) was evaluated. Groups of female rats (n = 8 rats/group) received 28 consecutive daily single doses of 0.3, 1.0, 3.0, 10.0, 30.0, 100.0 or 300.0 mg DGA/kg body weight by gastric intubation. One group of animals served as vehicle control. Tissues and blood serum were collected at necropsy on day 29. Select organs were weighed and fixed in formalin for histopathological analysis. Animals from the 300 mg/kg bw dose group were removed from the study after 5 consecutive days of treatment as a consequence of adverse treatment related effects. The animals in the remaining treatment groups survived the exposure period. No adverse clinical signs were observed throughout the exposure period in the surviving animals. No significant differences from controls were observed for feed and fluid consumption or body weight gain in the surviving animals. Lesions were observed in the kidneys, liver, stomach, intestine, thymus, spleen and bone marrow in rats from the 300 mg/kg dose group and signs of renal tubular regeneration were observed only in the 100 mg/kg dose group. These results suggest that high levels of pure DGA would need to be consumed before renal and other forms of organ toxicity are observed. |
Databáze: | OpenAIRE |
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