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淫羊藿苷在大鼠体内的药代动力学、组织分布和代谢研究。

Pharmacokinetics, Tissue Distribution, and Metabolism Study of Icariin in Rat.

机构信息

Guangzhou ImVin Pharmaceutical Co., Ltd., Guangzhou 510663, China.

Guangdong Provincial Hospital of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou 510120, China.

出版信息

Biomed Res Int. 2017;2017:4684962. doi: 10.1155/2017/4684962. Epub 2017 Nov 13.

DOI:10.1155/2017/4684962
PMID:29259982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5702950/
Abstract

Icariin is one of the predominant flavonoids contained in Herba Epimedii (Yin-yang-huo in Chinese), a well-known Chinese medicine for the treatment of cancers and immune system diseases. Although Herba Epimedii has been widely used in China and there are so many and various research reports on the herbal drug and its main flavones, very limited data is available on the tissue distribution and biotransformation of icariin. In the present study, a liquid chromatographic method combined with electrospray ionization tandem mass spectrometry was developed to quantify the concentration of icariin in rat plasma and various tissues collected at different time points after oral administration of the total flavonoid extract of Herba Epimedii at a dose of 0.69 g/kg (corresponding to 42 mg/g icariin). Biological samples were processed by simple protein precipitation. Genistein was chosen as internal standard. The method was successfully applied to plasma pharmacokinetic and tissue distribution studies of icariin in rat. As a result, it was worth noting that the tissue distribution characteristics of icariin exhibited a significant gender difference. Moreover, metabolism of icariin was also investigated. A total of 11 potential metabolites were found in rat feces collected in different time periods after oral and intramuscular administration of icariin. metabolic pathways were involved in hydrolysis, demethylation, oxidation, and conjugation. The preclinical data would be useful for fully understanding disposition of this compound and interpreting the mechanism of its biological response.

摘要

朝藿定 C 是淫羊藿(中药名“淫羊藿”)中主要的黄酮类化合物之一,淫羊藿是一种用于治疗癌症和免疫系统疾病的著名中药。虽然淫羊藿在中国被广泛使用,并且对该草药及其主要类黄酮有很多不同的研究报告,但关于朝藿定 C 的组织分布和生物转化的信息非常有限。在本研究中,建立了一种液相色谱-电喷雾串联质谱联用方法,用于定量测定口服淫羊藿总黄酮提取物(剂量为 0.69g/kg(相当于 42mg/g 朝藿定 C)后不同时间点大鼠血浆和各种组织中朝藿定 C 的浓度。生物样品通过简单的蛋白沉淀进行处理。染料木黄酮被选为内标。该方法成功应用于大鼠朝藿定 C 的药代动力学和组织分布研究。结果值得注意的是,朝藿定 C 的组织分布特征表现出显著的性别差异。此外,还研究了朝藿定 C 的代谢情况。在口服和肌肉注射朝藿定 C 后不同时间点收集的大鼠粪便中发现了 11 种潜在的代谢物。代谢途径涉及水解、去甲基化、氧化和结合。这些临床前数据有助于全面了解该化合物的处置情况,并解释其生物学反应的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/54582226e6f3/BMRI2017-4684962.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/b7692f003733/BMRI2017-4684962.001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/dda8aaadfc2c/BMRI2017-4684962.003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/6bf4ce858427/BMRI2017-4684962.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/97356b42eeaa/BMRI2017-4684962.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/9b4fa7b59e87/BMRI2017-4684962.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/54582226e6f3/BMRI2017-4684962.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/b7692f003733/BMRI2017-4684962.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/6a1bd3a7990e/BMRI2017-4684962.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/dda8aaadfc2c/BMRI2017-4684962.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/6df9bccad263/BMRI2017-4684962.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/6bf4ce858427/BMRI2017-4684962.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/97356b42eeaa/BMRI2017-4684962.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/9b4fa7b59e87/BMRI2017-4684962.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75c/5702950/54582226e6f3/BMRI2017-4684962.008.jpg

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Icariin inhibits TNF-α/IFN-γ induced inflammatory response via inhibition of the substance P and p38-MAPK signaling pathway in human keratinocytes.淫羊藿苷通过抑制人角质形成细胞中P物质和p38丝裂原活化蛋白激酶信号通路来抑制肿瘤坏死因子-α/干扰素-γ诱导的炎症反应。
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