Suppr超能文献

新型抗肥胖制剂 LI85008F 在动物中的安全性和毒理学评价。

Safety and toxicological evaluation of a novel anti-obesity formulation LI85008F in animals.

机构信息

Laila Impex R&D Centre, Unit-I, Phase-III, Jawahar Autonagar, Vijayawada 520007, India.

出版信息

Toxicol Mech Methods. 2010 Feb;20(2):59-68. doi: 10.3109/15376510903483722.

Abstract

LI85008F is a novel synergistic composition of Moringa oleifera, Murraya koenigi, and Curcuma longa. These herbs are well recognized and widely used in ayurvedic system of medicine for treating a variety of diseases and are also have been used for culinary purposes for thousands of years. LI85008F inhibits preadipocyte differentiation and potentiates lipid breakdown in mature adipocytes. In diet-induced obese rats, LI85008F significantly reduced weight gain and improved serum adiponectin levels. These findings motivated the authors to determine the broad-spectrum safety of LI85008F. Acute oral toxicity, acute dermal toxicity, primary skin irritation, primary eye irritation, and dose-dependent 28-day sub-acute toxicity studies were conducted. The acute oral LD50 of LI85008F was greater than 5000 mg/kg in female SD rats and no changes in body weight or adverse effects were observed following necropsy. Acute dermal LD50 of LI85008F was greater than 2000 mg/kg. LI85008F was classified as non-irritating to skin in a primary dermal irritation study conducted using New Zealand Albino rabbits. LI85008F caused minimal irritation to eyes in a primary eye irritation test conducted on New Zealand Albino rabbits. A dose-dependent 28-day sub-acute toxicity study demonstrated no significant changes in selected organ weights. Evaluations on hematology, clinical chemistry, and histopathology did not show any significant adverse changes. The NOAEL of LI85008F was found to be greater than 2500 mg/kg body weight. These results demonstrate the broad spectrum safety of LI85008F in animal models.

摘要

LI85008F 是辣木叶、九里香和姜黄的一种新型协同组合物。这些草药在印度阿育吠陀医学体系中被广泛用于治疗各种疾病,并且几千年来一直被用于烹饪。LI85008F 抑制前体脂肪细胞分化并增强成熟脂肪细胞中的脂解作用。在饮食诱导肥胖的大鼠中,LI85008F 显著降低体重增加并改善血清脂联素水平。这些发现促使作者确定 LI85008F 的广谱安全性。进行了急性口服毒性、急性皮肤毒性、原发性皮肤刺激、原发性眼睛刺激和剂量依赖性 28 天亚急性毒性研究。LI85008F 的雌性 SD 大鼠急性口服 LD50 大于 5000mg/kg,尸检后未观察到体重变化或不良反应。LI85008F 的急性皮肤 LD50 大于 2000mg/kg。在使用新西兰白化兔进行的原发性皮肤刺激研究中,LI85008F 被归类为无皮肤刺激性。在使用新西兰白化兔进行的原发性眼睛刺激试验中,LI85008F 对眼睛仅有轻微刺激。在一项剂量依赖性 28 天亚急性毒性研究中,未观察到选定器官重量的显著变化。血液学、临床化学和组织病理学评估未显示任何显著的不良反应变化。LI85008F 的 NOAEL 大于 2500mg/kg 体重。这些结果表明 LI85008F 在动物模型中具有广谱安全性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验