Davis Richard V, McKernan Lisa N, Rhodes Jennifer, Kulkosky Joseph
Department of Biology, Chestnut Hill College, Philadelphia, PA 19118, USA.
ISRN Toxicol. 2011 Dec 20;2011:248280. doi: 10.5402/2011/248280. Print 2011.
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.
尽管进行了长期抗逆转录病毒治疗,但患者体内仍存在持续存在的HIV-1感染细胞储存库,为此有人提出使用蛋白激酶C(PKC)调节剂进行临床干预以根除这些储存库。其中一些药物的效果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体的发育及毒理学影响。在发育的第一周用各种PKC途径调节剂处理斑马鱼,在较低剂量下未引发明显的身体缺陷或死亡率升高。较高浓度导致后期胚胎和幼体迅速死亡。每种化合物都有一个致死阈值剂量。确定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。它们还可能为临床试验中PKC调节剂的潜在给药剂量提供一些指导,以实现根除HIV-1储存库的目标。