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在斯普拉格-道利大鼠中进行的[提取物名称]水提取物28天重复口服剂量毒性研究。 (注:原文中“of an aqueous extract of”后面缺少具体提取物名称)

28-day repeated oral dose toxicity study of an aqueous extract of in sprague-dawley rat.

作者信息

Yu Su Hyun, Yu Su-Yeol, Lee Bo-Su, Kim Hyun-Jin, Kim Mi-Ran, Lee Young-Chul

机构信息

Naturetech Co., #450-86, Maebong-Ro, Dongnam-Gu, Cheonan-Si, Chungnam, South Korea.

出版信息

Toxicol Rep. 2020 Apr 25;7:577-582. doi: 10.1016/j.toxrep.2020.04.006. eCollection 2020.

Abstract

This study was performed to demonstrate a No Observed Adverse Effect Level (NOAEL) for an aqueous extract of . According to other studies, using dried material or extract with ethanol or methanol determined a NOAEL dose of 1000 mg/kg or 5000 mg/kg in rats. Therefore, the groups were administered orally at doses of 0, 1000, 2000, and 3000 mg/kg for four weeks. Two-week recovery groups were administered at doses of 0, and 3000 mg/kg. During administration and recovery period, the animals were observed for clinical signs, change of body weight, food consumption, hematology, and clinical chemistry. Rats in each group were periodically sacrificed, and organs were weighed and examined histologically. No difference arose between any of the dosage groups and the control group in clinical signs, histopathological examination, hematology, or clinical chemistry. In conclusion, 3000 mg/kg is a NOAEL dose for extracts in Sprague Dawley rats.

摘要

本研究旨在确定[提取物名称]水提取物的无观察到有害作用水平(NOAEL)。根据其他研究,使用干燥材料或乙醇或甲醇提取物确定大鼠的NOAEL剂量为1000mg/kg或5000mg/kg。因此,各实验组分别以0、1000、2000和3000mg/kg的剂量口服给药四周。两周恢复期组分别以0和3000mg/kg的剂量给药。在给药和恢复期,观察动物的临床症状、体重变化、食物消耗、血液学和临床化学指标。定期处死每组大鼠,称量器官重量并进行组织学检查。在临床症状、组织病理学检查、血液学或临床化学方面,任何剂量组与对照组之间均未出现差异。总之,3000mg/kg是Sprague Dawley大鼠[提取物名称]提取物的NOAEL剂量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69e/7225595/fed27392bc26/ga1.jpg

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