S M Ferreira, H Zapparoli, C S Mussi, P C Maiorka, A F C Andrade, S L Górniak, A T Gotardo
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引用次数: 0
摘要
l -含羞草胺是一种主要存在于含羞草亚科中的非蛋白氨基酸,在含羞草和含羞草中含量较高。这些植物广泛用于人类和动物营养,以及植物治疗应用。虽然l -氨基糖胺的毒性作用已经在反刍动物中得到了广泛的研究,但它对单胃动物的影响仍未被探索。考虑到这些植物的广泛使用以及对l -氨基模胺对单胃动物毒性的了解有限,本研究旨在通过评估其亚急性毒性来研究其对非啮齿动物单胃动物的毒理学效应。为了实现这一目标,从白头草种子中提取l -氨基糖胺,并以25、40和60 mg/kg的剂量口服给雄性兔,持续28天。虽然没有观察到临床、生化、激素或宏观改变,但组织病理学分析显示肝脏、肾脏、甲状腺和脾脏存在剂量依赖性病变。这些发现表明,家兔可能特别容易受到左旋蜜胺的毒性作用。
Systemic Toxicity of L-Mimosine in Rabbits: A Non-Rodent Model for Safety Assessment.
L-mimosine is a non-protein amino acid primarily found in the Mimosoideae subfamily, with high concentrations in Leucaena leucocephala and Mimosa pudica. These plants are widely used in both human and animal nutrition, as well as in phytotherapeutic applications. While the toxic effects of L-mimosine have been extensively studied in ruminants, its impact on monogastric species remains unexplored. Given the widespread use of these plants and the limited knowledge regarding L-mimosine toxicity in monogastric animals, this study aimed to investigate its toxicological effects in non-rodent monogastric species by assessing its subacute toxicity. To achieve this, L-mimosine was extracted from L. leucocephala seeds and administered orally, incorporated into the feed, at doses of 25, 40, and 60 mg/kg for 28 days in male rabbits. Although no clinical, biochemical, hormonal, or macroscopic alterations were observed, histopathological analyses revealed dose-dependent lesions in the liver, kidneys, thyroid, and spleen. These findings suggest that rabbits may be particularly susceptible to the toxic effects of L-mimosine.
期刊介绍:
Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.