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首页> 外文期刊>Reproductive toxicology >Comparative embryotoxicity of different antimalarial peroxides: In vitro study using the rat whole embryo culture model (WEC).
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Comparative embryotoxicity of different antimalarial peroxides: In vitro study using the rat whole embryo culture model (WEC).

机译:不同抗疟疾过氧化物的比较胚胎毒性:使用大鼠全胚培养模型(WEC)进行的体外研究。

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摘要

Three groups of compounds: (i) active peroxides (artemisinin and arterolene), (ii) inactive non-peroxidic derivatives (deoxyartemisinin and carbaOZ277) and (iii) inactive peroxide (OZ381) were tested by WEC system to provide insights into the relationship between chemical structure and embryotoxic potential, and to assess the relationship between embryotoxicity and antimalarial activity. Deoxyartemisinin, OZ381 and carbaOZ277 did not affect rat embryonic development. Artemisinin and arterolane affected primarily nucleated red blood cells (RBCs), inducing anemia and subsequent tissue damage in rat embryos, with NOELs for RBC damage at 0.1 and 0.175mug/mL, respectively. These data support the idea that only active antimalarial peroxides are able to interfere with normal embryonic development. In an attempt to establish whether and to what extent activity as antimalarials and embryotoxicity can be divorced, IC(50)s for activity in Plasmodium falciparum strains and the NOELs for RBCs were compared. From this comparison, arterolane showed a better safety margin than artemisinin.
机译:三组化合物:(i)活性过氧化物(青蒿素和青蒿素),(ii)惰性非过氧化物衍生物(脱氧青蒿素和carbaOZ277)和(iii)惰性过氧化物(OZ381)通过WEC系统进行了测试,以提供对之间化学结构和潜在的胚胎毒性,并评估胚胎毒性和抗疟活性之间的关系。脱氧青蒿素,OZ381和carbaOZ277不影响大鼠胚胎发育。青蒿素和青蒿琥酯主要影响有核的红细胞(RBC),从而引起贫血和随后对大鼠胚胎的组织损害,其中用于RBC损害的NOEL分别为0.1和0.175mug / mL。这些数据支持只有活性抗疟疾过氧化物才能干扰正常胚胎发育的想法。为了确定是否可以将抗疟药活性和胚胎毒性分离到何种程度,将恶性疟原虫菌株的活性IC(50)和RBC的NOELs进行了比较。通过该比较,青蒿烷显示出比青蒿素更好的安全系数。

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