In vivo effects of antiviral protein kinase C modulators on zebrafish development and survival.

ISRN Toxicology Pub Date : 2011-12-20 Print Date: 2011-01-01 DOI:10.5402/2011/248280
Richard V Davis, Lisa N McKernan, Jennifer Rhodes, Joseph Kulkosky
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引用次数: 5

Abstract

Clinical interventions using protein kinase C (PKC) modulators have been proposed for eradication of HIV-1-infected cellular reservoirs which persist in patients despite prolonged antiretroviral therapy. The effects of some of these agents have not been assessed in a developing vertebrate model. This study examines the developmental and toxicological effects of these compounds on zebrafish embryos and larvae. Treatment of zebrafish through the first week of development with various PKC pathway modulators did not elicit gross physical defects or elevated incidences of death at lower doses. Higher concentrations resulted in rapid death for both later-stage embryos and larvae. Each compound had a threshold dose for lethality. The defined nonlethal doses may be useful toward assessing the effects of modulating PKC activity on zebrafish development. They may further provide some guidance for the potential dosing of PKC modulators in clinical trials toward the goal of HIV-1 reservoir eradication.

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抗病毒蛋白激酶C调节剂对斑马鱼发育和存活的体内影响。
使用蛋白激酶C (PKC)调节剂的临床干预已被提出用于根除hiv -1感染的细胞储存库,尽管长期抗逆转录病毒治疗仍存在于患者体内。其中一些药物的作用尚未在发育中的脊椎动物模型中进行评估。本研究考察了这些化合物对斑马鱼胚胎和幼虫的发育和毒理学影响。在斑马鱼发育的第一周,用各种PKC通路调节剂治疗斑马鱼,在低剂量下不会引起严重的身体缺陷或死亡率升高。较高的浓度导致后期胚胎和幼虫的快速死亡。每种化合物都有致死的阈值剂量。定义的非致死剂量可能有助于评估调节PKC活性对斑马鱼发育的影响。它们可能进一步为临床试验中PKC调节剂的潜在剂量提供一些指导,以实现根除HIV-1储存库的目标。
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