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Effect of acyclovir on mammalian embryonic development in culture

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Abstract

1.Acyclovir [9-(2-hydroxyethoxymethyl)guanine] interfered with embryonic development in vitro when assessed with the “whole-embryo” culture technique. The “no-observed-effect level” was at 10 μM acyclovir; 2. Minor impairment of embryonic development (retarded development of ear anlagen) was observed in vitro at 25 μM acyclovir in the culture medium. At high concentrations (100 or 200 μM) development of the ear anlagen was largely inhibited. At concentrations of 50 μM acyclovir or higher, additional disturbances of embryonic differentiation in vitro became obvious, resulting in gross structural abnormalities, especially of the brain (telencephalon); 3. Histological examinations confirmed and extended these observations: at 100 μM acyclovir alterations of the neuroepithelium of the ventricles were pronounced, the telencephalon had developed poorly or was almost completely absent, and necroses were seen in the ear anlagen, the maxillar branch and within the somites; 4. In a limb bud culture (mouse embryos, starting with day 11 of gestation) acyclovir interfered with the differentiation of cartilaginous bone anlagen at concentrations of 200 μM and more in the culture medium. A concentration of 100 μM induced no significant effect. Thus, this organ culture system is less sensitive to the action of acyclovir when compared with whole-embryo culture; 5. Contrary to the results achieved with acyclovir, physiological nucleosides (2′-deoxyguanosine and 2′-deoxyadenosine) did not interfere with embryonic development in vitro even at the highest concentration tested (500 μM).

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Data presented in this paper are part of the doctoral theses of Stephan Klug and Constanze Lewandowski to be presented to the Fachbereich Veterinärmedizin, Freie Universität Berlin

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Klug, S., Lewandowski, C., Blankenburg, G. et al. Effect of acyclovir on mammalian embryonic development in culture. Arch Toxicol 58, 89–96 (1985). https://doi.org/10.1007/BF00348315

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  • DOI: https://doi.org/10.1007/BF00348315

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