阿啡类生物碱的体外致裂性。

S Tadaki, T Nozaka, S Yamada, M Ishino, I Morimoto, A Tanaka, J Kunitomo
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引用次数: 13

摘要

用中国仓鼠肺细胞系(CHL)对阿啡碱19种生物碱进行染色体畸变试验,包括阿啡碱加和不加大鼠肝匀浆(S9)混合物。19种生物碱中有18种在存在或不存在S9混合物的情况下诱导染色体畸变。在所检测的生物碱中,亚绿碱、liriodenine和4,5-二氧脱氢crebanine在相对较低的浓度下诱导染色体畸变,分别低至2.5、5和3.13微克/ml。双中心碱、亚绿碱和4,5-二氧脱氢克鲁班碱高频率诱导染色体畸变。12.5微克/毫升阿波啡直接法诱导10%的细胞畸变,100微克/毫升混合S9法诱导12%的细胞畸变。在Ames试验中,对TA100与S9混合最有效的诱变剂Liriodenine和对TA98与S9混合最有效的诱变剂roemerine在有S9混合和没有S9混合的情况下也具有致裂性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clastogenicity of aporphine alkaloids in vitro.

The chromosomal aberration test using a Chinese hamster lung cell line (CHL) was carried out on 19 aporphine alkaloids including apomorphine with and without rat liver homogenates (S9) mix. Eighteen of 19 alkaloids tested induced chromosomal aberration in the presence or absence of S9 mix. Among the alkaloids tested, anolobine, liriodenine and 4,5-dioxodehydrocrebanine induced chromosomal aberrations at relatively low concentrations and as low as 2.5, 5 and 3.13 micrograms/ml, respectively. Dicentrine, anolobine and 4,5-dioxodehydrocrebanine induced chromosomal aberrations with high frequencies. Apomorphine induced 10% aberrant cells at 12.5 micrograms/ml in the direct method and 12% at 100 micrograms/ml with S9 mix in the S9 method. Liriodenine which was the most potent mutagen for TA100 with S9 mix and roemerine which was the most potent for TA98 with S9 mix in Ames test were also clastogenic with and without S9 mix.

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