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Insecticidal activity, mammalian cytotoxicity and mutagenicity of an ethanolic extract from Nerium oleander (Apocynaceae)
Author(s) -
ELSHAZLY M M,
ELZAYAT E M,
HERMERSDÖRFER H
Publication year - 2000
Publication title -
annals of applied biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.677
H-Index - 80
eISSN - 1744-7348
pISSN - 0003-4746
DOI - 10.1111/j.1744-7348.2000.tb00020.x
Subject(s) - apocynaceae , cytotoxicity , biology , bioassay , traditional medicine , hypoxanthine , ames test , glycoside , mutagen , botany , biochemistry , in vitro , medicine , dna , genetics , salmonella , bacteria , enzyme
Summary A bioassay procedures utilising the western‐banded blow fly, Chrysomya albiceps (Diptera‐Calliphoridae) has been used to guide the fractionation of an ethanolic extract from the leaves of Nerium oleander (Apocynaceae). The cardiotonic glycoside, neriifolin: (3‐[(6‐deoxy‐3‐0‐methyl‐α‐L glucopyranosyl) oxy]‐14‐hydroxy‐5 β Card‐20 [22]‐endolide) was crystallised from the insecticidal active fraction of the ethanolic extract. The values of LC 50 of the ethanolic extract, active fraction, isolated crystals and authentic neriifolin were 164 ppm, 57 ppm, 35 ppm and 36 ppm, respectively when incorporated into the blow fly diet. A primary test on the cytotoxicity and mutagenicity of the crude extract against non‐target organisms was achieved by determining the cytotoxicity and mutagenicity on a mammalian cell line using different concentrations of the extract ( in vitro ) through a radioactive thymidine incorporation technique and hypoxanthine phosphoribosyl transferase (HPRT) test, using the Chinese hamster lung fibroblasts (V79‐MZ cell line). Cytotoxicity tests revealed that the LC 50 was approximately 200 ppm, and the mutagenicity was very low compared to the standard active mutagen.