Zimmerman Nathan, Marta Aaron, Baker Carly, Korade Zeljka, Mirnics Károly, Shibata Annemarie
Department of Biology, Creighton University, Omaha, NE 68178, USA.
Department of Biomedical Sciences, Creighton University, Omaha, NE 68178, USA.
J Dev Biol. 2025 Jun 27;13(3):22. doi: 10.3390/jdb13030022.
Cholesterol homeostasis is necessary for normal vertebrate development. The disruption of cholesterol homeostasis can cause abnormal body and nervous system development and lead to dysfunctional behavior and increased mortality. Commonly prescribed psychopharmaceuticals can alter cholesterol synthesis and may disrupt early vertebrate development. A high-throughput vertebrate zebrafish model system was used to test the hypothesis that exposure to psychopharmaceutical medications alters cholesterol biosynthesis and disrupts gene transcription, early whole-body and brain development, and nervous system function, resulting in abnormal behavior. Exposure to cariprazine, aripiprazole, trazodone, and AY9944 increased 7-dehydrocholesterol levels compared to vehicle-treated zebrafish. Significant differences in disease-associated gene expression, brain structure, and functional behaviors were observed in psychopharmaceutical and AY9944-treated zebrafish compared to controls. These data reveal that the high-throughput zebrafish model system can discern psychopharmaceutical effects on cholesterol synthesis, gene transcription, and key features of early vertebrate development that influences behavior.
胆固醇稳态对于正常脊椎动物发育至关重要。胆固醇稳态的破坏会导致身体和神经系统发育异常,并导致行为功能失调和死亡率增加。常用的精神药物会改变胆固醇合成,可能会干扰脊椎动物的早期发育。使用高通量脊椎动物斑马鱼模型系统来检验以下假设:暴露于精神药物会改变胆固醇生物合成,破坏基因转录、早期全身和大脑发育以及神经系统功能,从而导致行为异常。与用赋形剂处理的斑马鱼相比,暴露于卡立哌嗪、阿立哌唑、曲唑酮和AY9944会使7-脱氢胆固醇水平升高。与对照组相比,在接受精神药物和AY9944处理的斑马鱼中观察到疾病相关基因表达、脑结构和功能行为的显著差异。这些数据表明,高通量斑马鱼模型系统可以识别精神药物对胆固醇合成、基因转录以及影响行为的早期脊椎动物发育关键特征的影响。