کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5853172 1130856 2011 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Acute and 90-day subchronic toxicity studies of Silk peptide E5K6, in Sprague-Dawley rats
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم کشاورزی و بیولوژیک دانش تغذیه
پیش نمایش صفحه اول مقاله
Acute and 90-day subchronic toxicity studies of Silk peptide E5K6, in Sprague-Dawley rats
چکیده انگلیسی

Acute and 90-day subchronic oral toxicity studies of Silk peptide E5K6 were performed in Sprague-Dawley rats. In the acute toxicity study, Silk peptide E5K6 was administered orally to male and female rats at a single dose of 2000 and 5000 mg/kg. Mortality, clinical signs and body weight changes were monitored for 14 days. There were no treatment-related changes in these parameters. Therefore, the Approximate Lethal Dose (ALD) of Silk peptide E5K6 in male and female rats is higher than 5000 mg/kg. In the subchronic toxicity study, Silk peptide E5K6 was administered orally to male and female rats for 90 days at a single dose of 500, 1000, and 2000 mg/kg. There were no toxicologically significant changes in clinical signs, body weight, food and water consumptions, ophthalmoscopic examination, urinalysis, hematological and serum biochemical examinations, necropsy findings, organ weights and histopathological examination of all of the animals treated with Silk peptide E5K6. These results suggest that the oral No Observed Adverse-Effect Level (NOAEL) of Silk peptide E5K6 is greater than 2000 mg/kg/day in both sexes and the target organs were not established.

► We performed acute and 90-day subchronic oral toxicity studies of Silk peptide E5K6. ► Acute oral ALD of E5K6 was considered to be higher than 5000 mg/kg in rats. ► Subchronic oral NOAEL of E5K6 was considered to be higher than 2000 mg/kg in rats. ► The target organ was not identified in subchronic toxicity study.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Food and Chemical Toxicology - Volume 49, Issue 9, September 2011, Pages 2408-2414
نویسندگان
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