首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >A comparative study on the tissue distributions of rhubarb anthraquinones in normal and CCl4-injured rats orally administered rhubarb extract.
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A comparative study on the tissue distributions of rhubarb anthraquinones in normal and CCl4-injured rats orally administered rhubarb extract.

机译:口服大黄提取物对正常和CCl4损伤大鼠大黄蒽醌组织分布的比较研究。

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摘要

AIM OF THE STUDY: The present study comparatively investigated the tissue distributions of rhubarb anthraquinone derivatives (AQs) to examine whether they undergo different uptakes in normal or CCl(4)-induced liver-damaged rats, to explore possible reasons for the different toxicities of AQs in pathological model rats and normal rats at the tissue distribution level. MATERIALS AND METHODS: The total rhubarb extract (14.49 g kg(-1) of body weight per day based on the quantity of crude material) was administrated orally to normal and model rats for 12 weeks. The concentrations of free AQs in tissues were quantitated by liquid chromatography-tandem mass spectrometry (LC-MS). After drug withdrawal for 4 weeks, tissue distributions were again determined. RESULTS: The five free AQs-aloe-emodin, rhein, emodin, chrysophanol and physcion--were detected in the liver, kidney and spleen, while only rhein, aloe-emodin and emodin reached the quantitative limit. The tissue distributions of rhein (p < 0.001), aloe-emodin (p < 0.001) and emodin (p < 0.05) in normal rats were higher than those in model rats with rhein>aloe-emodin>emodin in kidney and spleen tissues and aloe-emodin > rhein > emodin in liver tissues. Free AQs were not detected in the tissues after drug withdrawal for 4 weeks. CONCLUSIONS: These results suggest that the tissue toxicity of AQs in normal animals is higher than that in pathological model animals with little accumulative toxicity of rhubarb. The results are concordant with the traditional Chinese theory of You Gu Wu Yun recorded first in Su Wen, a classical Chinese medical treatise.
机译:研究目的:本研究比较了大黄蒽醌衍生物(AQs)的组织分布,以检查大黄蒽醌衍生物在正常或CCl(4)诱导的肝损伤大鼠中是否摄取不同,以探讨其不同毒性的可能原因。在组织分布水平上,病理模型大鼠和正常大鼠的AQs。材料与方法:将大黄提取物(按粗物质的量计算,每天14.49 g kg(-1)体重)口服给予正常和模型大鼠12周。通过液相色谱-串联质谱法(LC-MS)对组织中游离AQ的浓度进行定量。停药4周后,再次确定组织分布。结果:在肝脏,肾脏和脾脏中检出了5种游离的AQs-芦荟大黄素,大黄素,大黄素,大黄酚和physcion,而仅大黄酸,芦荟大黄素和大黄素达到了定量极限。大黄素(p <0.001),芦荟大黄素(p <0.001)和大黄素(p <0.05)在正常大鼠中的组织分布高于大黄素>芦荟大黄素>大黄素的模型大鼠在肾脏和脾脏组织中的分布。肝组织中的芦荟大黄素>大黄酸>大黄素。停药4周后未在组织中检测到游离AQ。结论:这些结果表明,正常动物的AQs的组织毒性高于大黄累积毒性很小的病理模型动物。结果与中国古典医学论文《苏问》中最早记载的中国传统的“幽谷无韵”理论相吻合。

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