Review Article

From Omics to Drug Metabolism and High Content Screen of Natural Product in Zebrafish: A New Model for Discovery of Neuroactive Compound

Table 1

Discrepancies and similarities of the effect of drugs in human and zebrafish.

Area of evaluation in zebrafishTest compoundsProportion of drugs with expected effects (%)Reference

Inhibition of hERG or QTc prolongation Study 1: Amiodarone, bepridil, cisapride, haloperidol, pimozide, procainamide, D,L-sotalol, terfenadine, thioridazineAll compounds, except for procainamide[3]
Study 2: Negative controls: amoxicillin, aspirin
Positive controls: chlorpromazine, cisapride, cromakalim, isoprenaline, moxifloxacin, nicotine, verapamil
7 out of 9 compounds, including negative controls[1]

Visual safety or optomotor response Study 1: 27 compounds, including 19 with positive and 8 with negative effects on inhibition of optomotor responseAbout 70% in overall showed the predicted drug effects.[4]
Study 2: Negative control: aspirin
Positive controls: chloroquine, chlorpromazine, diazepam, nicotine, ouabain, phenytoin, atropine, lithium
7 out of 9 compounds including negative control[1]

Seizure liability25 drugs including 17 positive and 8 negative controls72% in overall[5]

Gut contractionNegative controls: aspirin and moxifloxacin
Positive controls: amoxicillin, chlorpromazine, cisapride, cromakalim, isoprenaline, nicotine, nitrendipine, and verapamil
5 out of 10 compounds including negative controls[1]