- 【Updated on May 12, 2025】 Integration of CiNii Dissertations and CiNii Books into CiNii Research
- Trial version of CiNii Research Knowledge Graph Search feature is available on CiNii Labs
- 【Updated on June 30, 2025】Suspension and deletion of data provided by Nikkei BP
- Regarding the recording of “Research Data” and “Evidence Data”
Safety Evaluation of<i>Artocarpus altilis</i>as Pharmaceutical Agent in Wistar Rats
-
- Sudha Sairam
- Department of Studies in Food Science and Nutrition, University of Mysore, Mysore 570006, India
-
- Asna Urooj
- Department of Studies in Food Science and Nutrition, University of Mysore, Mysore 570006, India
Search this article
Description
<jats:p>This study was designed to elucidate the acute toxicity of<jats:italic>Artocarpus altilis</jats:italic>leaf and bark extracts. In acute toxicity study, no mortality or any toxic reaction was recorded in any group after 14 days of administering the extracts (2000 mg Kg<jats:sup>−1</jats:sup>BW). The extracts (ALA, ABA, ALM, and ABM) did not cause any behavioural or physical changes in experimental rats. There was no significant (<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M1"><mml:mrow><mml:mi>P</mml:mi><mml:mo>≤</mml:mo><mml:mn>0.05</mml:mn></mml:mrow></mml:math>) difference in the biochemical parameters analysed between the groups. Slight elevation in activities of AST and ALT in extract treated groups was observed, but this did not exert any deleterious effect on the normal metabolism which was supported by the histopathology of liver. Histopathological studies showed no remarkable changes after 14 days of oral administration of ALA, ABA, ALM, and ABM extracts. The study contributes to establishing the nontoxic quality parameters of<jats:italic>Artocarpus altilis</jats:italic>leaf and bark parts and the results suggest the safety of the extracts in therapeutic uses.</jats:p>
Journal
-
- Journal of Toxicology
-
Journal of Toxicology 2014 1-8, 2014
Wiley
- Tweet
Details 詳細情報について
-
- CRID
- 1362825894261621760
-
- ISSN
- 16878205
- 16878191
-
- Data Source
-
- Crossref