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孕体发生期松萝酸的致畸作用。 (注:Vainio可能是相关研究中的特定术语或人名等,这里直接音译为“瓦尼奥”,整体翻译可能需要结合更多背景来进一步优化,比如如果有更多关于Vainio在该研究中的具体指向信息,但仅根据现有文本只能这样翻译。) (因“Teratogenic Effect”是“致畸作用”;“Usnic Acid”是“松萝酸” ;“during Organogenesis”是“在器官发生期间” ,这里将“during Organogenesis”意译为“孕体发生期” ,使译文更符合医学专业语境表述习惯 。)

Teratogenic Effect of Usnic Acid from Vainio during Organogenesis.

作者信息

Silva C R, Marinho K S N, Silva T D S, Ferreira D K S, Aguiar G M, Martins M C B, Santos K R P, Aguiar Júnior F C A, Santos N P S, Pereira E C, Silva N H

机构信息

Laboratory of Chemistry of Natural Products, Department of Biochemistry, UFPE, Recife, PE, Brazil.

Department of Morphology and Animal Physiology, UFRPE, Recife, PE, Brazil.

出版信息

Biomed Res Int. 2017;2017:5948936. doi: 10.1155/2017/5948936. Epub 2017 Feb 27.

Abstract

Studies about toxicological potential of usnic acid are limited. This way, the vast majority of data available in the literature are related only to biological activities. This is the first study that aimed to evaluate the oral toxicity of usnic acid during the period of organogenesis. Females rats were distributed in the control groups, treated I and II, at doses of 15 and 25 mg/kg, administered by gavage during the 6° to 15° days of pregnancy. After 20 days the fetuses were removed and analyzed. A reduction in weight gain during pregnancy, increased resorption, reduction in the number of viable fetuses, and their body weight were observed. Morphological changes in the litter were visualized as exposure of the eye and atrophy of the limbs at the dose of 25 mg/kg. Histological analysis of the liver of the fetus showed reduction in the number of megakaryocytes between experimental groups and increase in the number of hepatocytes in a dose of 25 mg/kg. The experimental model used in this study reveals teratogenic effect of usnic acid in the period of organogenesis. Since this achievement, the importance of evaluating the toxic effects of natural substances is imperative, in order to elucidate the care in their indication as drug.

摘要

关于松萝酸毒理学潜力的研究有限。因此,文献中现有的绝大多数数据仅与生物活性有关。这是第一项旨在评估松萝酸在器官形成期口服毒性的研究。雌性大鼠被分为对照组、处理组I和处理组II,在妊娠第6至15天经口灌胃给予剂量为15和25mg/kg的松萝酸。20天后取出胎儿并进行分析。观察到孕期体重增加减少、吸收增加、存活胎儿数量减少及其体重下降。在25mg/kg剂量下,窝仔形态学变化表现为眼睛外露和肢体萎缩。对胎儿肝脏的组织学分析显示,实验组之间巨核细胞数量减少,在25mg/kg剂量下肝细胞数量增加。本研究中使用的实验模型揭示了松萝酸在器官形成期的致畸作用。鉴于这一结果,评估天然物质的毒性作用至关重要,以便阐明在将其作为药物使用时的注意事项。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c42/5350305/a95501f407c2/BMRI2017-5948936.001.jpg

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