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磺胺胍对减数分裂染色体畸变的诱导作用。

Induction of meiotic chromosomal aberrations by sulphaguanidine.

作者信息

Murthy D K, Subramanyam S

出版信息

Cytobios. 1985;44(175):41-8.

PMID:4075853
Abstract

Cytological investigations on the effects of sulphaguanidine on meiotic cells have been carried out. Concentrations of 4.165, 6.25 and 8.33 mg of the drug were orally administered to Swiss albino male mice as single and cumulative doses. In the latter the drug was fed consecutively for 5 days at 24 h intervals. Meiotic chromosomal preparations were made after 24 h and at weekly intervals up to the fifth week following drug administration. Structural aberrations like gaps, breaks, fragments and multivalent associations (translocations) were scored for assessing clastogenic activity. Mitoclasic effects were analysed by scoring the polyploids. A high rate of both autosomal and sex chromosomal univalents were recorded in the series treated. A non-clastogenic and a very weak mitoclasic property of the drug is suggestive and is comparable to observations on the effects of sulphadiazine previously reported.

摘要

已对磺胺胍对减数分裂细胞的影响进行了细胞学研究。将4.165、6.25和8.33毫克该药物以单次和累积剂量口服给予瑞士白化雄性小鼠。在累积剂量给药时,该药物以24小时间隔连续喂食5天。在给药后24小时以及直至给药后第五周每周进行减数分裂染色体标本制备。对诸如裂隙、断裂、片段和多价关联(易位)等结构畸变进行评分,以评估致断裂活性。通过对多倍体进行评分来分析有丝分裂破坏作用。在接受治疗的系列中记录到常染色体和性染色体单价体的高发生率。该药物的非致断裂性和非常弱的有丝分裂破坏特性具有提示意义,并且与先前报道的关于磺胺嘧啶作用的观察结果相当。

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