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采用体外RAW 264.7细胞培养、抗氧化测定以及生物活性化合物粉防己碱的分离,对轮环藤进行生物测定导向的分级分离。

Bioassay guided fractionation of Cyclea peltata using in vitro RAW 264.7 cell culture, antioxidant assays and isolation of bioactive compound tetrandrine.

作者信息

Shine V J, Anuja G I, Suja S R, Raj Gopan, Latha P G

机构信息

Ethnomedicine and Ethnopharmacology Division, Jawaharlal Nehru Tropical Botanic Garden and Research Institute, Palode, Thiruvananthapuram, 695562, India.

Ethnomedicine and Ethnopharmacology Division, Jawaharlal Nehru Tropical Botanic Garden and Research Institute, Palode, Thiruvananthapuram, 695562, India.

出版信息

J Ayurveda Integr Med. 2020 Jul-Sep;11(3):281-286. doi: 10.1016/j.jaim.2018.05.009. Epub 2018 Oct 23.

DOI:10.1016/j.jaim.2018.05.009
PMID:30366785
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7527820/
Abstract

BACKGROUND

Cyclea peltata is one of the herbs mentioned in ancient scriptures of Ayurveda and is used in different types of Ayurvedic gritham preparations. Moreover, in traditional/tribal medicine C. peltata is used as digestive, anti-inflammatory, diuretic and to treat jaundice, digestive disorders, etc. OBJECTIVE: Activity guided fractionation of C. peltata and in correlation with the levels of bioactive compound tetrandrine.

MATERIALS AND METHODS

Preliminary phytochemical screening, estimation of total alkaloid content, preparation of different extracts of C. peltata (crude extract CP, hexane extract HCP, chloroform extract CCP, methanol extract MCP, alkaloid fraction ACP). In vitro anti-inflammatory studies using RAW 264.7 cells and in vitro antioxidant assays of the different extracts of C. peltata. HPTLC estimation of tetrandrine (TET) was carried out using solvent system toluene: ethyl acetate: diethylamine (7.2: 2: 0.8) and isolation of TET from ACP.

RESULTS

Preliminary phytochemical studies of C. peltata showed the presence of alkaloid content in all extracts. Whereas, saponins, steroids and terpenoids were detected in CP and CCP. ACP and TET showed significant in vitro anti-inflammatory and antioxidant activity when compared to other extracts. ACP and TET (100 μg/ml) treatment significantly inhibited the mRNA expression of iNOS, COX-2, TNF-α in LPS treated RAW 264.7 cells. HPTLC estimation of bioactive compound tetrandrine was highest in ACP-228.4 μg/mg followed by CP-29.62 μg/mg, CCP-23.46 μg/mg, MCP-18.82 μg/mg and HCP-1.25 μg/mg. TET has been isolated from ACP.

CONCLUSION

The results of the present in vitro assays revealed that the alkaloid fraction (ACP) is the most active fraction when compared to other extracts and has a positive correlation with the levels of bioactive compound tetrandrine.

摘要

背景

轮环藤是阿育吠陀古代经文中提到的草药之一,用于不同类型的阿育吠陀糊剂制剂。此外,在传统/部落医学中,轮环藤被用作消化剂、抗炎剂、利尿剂,并用于治疗黄疸、消化系统疾病等。目的:对轮环藤进行活性导向分离,并与生物活性化合物粉防己碱的含量相关联。

材料与方法

初步植物化学筛选、总生物碱含量测定、制备轮环藤的不同提取物(粗提物CP、己烷提取物HCP、氯仿提取物CCP、甲醇提取物MCP、生物碱部分ACP)。使用RAW 264.7细胞进行体外抗炎研究以及轮环藤不同提取物的体外抗氧化测定。使用甲苯:乙酸乙酯:二乙胺(7.2:2:0.8)的溶剂系统进行粉防己碱(TET)的高效薄层层析测定,并从ACP中分离TET。

结果

轮环藤的初步植物化学研究表明所有提取物中均存在生物碱成分。而在CP和CCP中检测到了皂苷、甾体和萜类化合物。与其他提取物相比,ACP和TET显示出显著的体外抗炎和抗氧化活性。ACP和TET(100μg/ml)处理显著抑制了LPS处理的RAW 264.7细胞中iNOS、COX-2、TNF-α的mRNA表达。生物活性化合物粉防己碱的高效薄层层析测定结果在ACP中最高,为228.4μg/mg,其次是CP为29.62μg/mg、CCP为23.46μg/mg、MCP为18.82μg/mg以及HCP为1.25μg/mg。已从ACP中分离出TET。

结论

目前体外试验的结果表明,与其他提取物相比,生物碱部分(ACP)是最具活性的部分,并且与生物活性化合物粉防己碱的含量呈正相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/7527820/0035ae83d6f5/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/7527820/ef6c4195d4dc/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/7527820/d07c542dc551/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/7527820/851028a1124f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/7527820/adc8f973b340/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/7527820/0035ae83d6f5/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/7527820/ef6c4195d4dc/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/7527820/d07c542dc551/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/7527820/851028a1124f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/7527820/adc8f973b340/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/7527820/0035ae83d6f5/gr5.jpg

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