کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2547564 1124062 2009 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The cytotoxicity to leukemia cells and antiviral effects of Isatis indigotica extracts on pseudorabies virus
موضوعات مرتبط
علوم پزشکی و سلامت داروسازی، سم شناسی و علوم دارویی داروشناسی
پیش نمایش صفحه اول مقاله
The cytotoxicity to leukemia cells and antiviral effects of Isatis indigotica extracts on pseudorabies virus
چکیده انگلیسی

Aim of the studyIsatis indigotica (I. indigotica), Cruciferae, has been used in Chinese medicine for anti-leukemia and anti-severe acute respiratory syndrome (SARS). The aim of this study was to evaluate the cytotoxicity of Isatis indigotica extracts on human leukemia cell line (HL-60) and the antiviral activity on swine pseudorabies virus (PrV) in in vitro assays.Materials and methodsExtracts and derived fractions of Isatisindigotica were prepared from root (R) and leaf (L) using methanol (M), ethyl acetate (E) and distilled water (D). The cytotoxic effect of extracts on swine peripheral blood mononuclear cells (PBMCs) and HL-60 was assessed by MTT method. The cytopathic effect (CPE) reduction, plaque reduction and inhibition assays on viral replication, and virucidal activity were further conducted to investigate the anti-PrV activity.ResultsIndirubin, one of the biological active compounds of Isatis indigotica, had the most significant cytotoxicity on HL-60 cells and inhibitory effect on PrV replication. Extracts from roots and leaves of Isatis indigotica also presented CPE inhibition either before or after infection of PrV on porcine kidney (PK-15) cells. Leaf extracts had better virucidal activity than roots, and ethyl acetate extracts exhibited the highest efficacy among extracts tested.ConclusionIsatis indigotica posses a valuable virucidal effect in disease control of pseudorabies virus infection in swine.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Ethnopharmacology - Volume 123, Issue 1, 4 May 2009, Pages 61–67
نویسندگان
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