Anticancer drugs in waters may increase potential threats
on the
future persistence of aquatic organism with their actions on cell
death in targeted cell types of neoplasia, such as cyclophosphamide
(CP). The potential adverse effects of CP may be exacerbated by the
enhanced detection frequency and levels in different waters. Thus,
the mechanisms of CP on the Daphnia magna are elucidated
in this study. Our results found aspartic acid, citric acid, tyrosine,
isoleucine, phenylalanine, phenyl-acetaldehyde, phenyl-acetylglutamine, trans-cinnamate, and methionine as core metabolites identified
in response to CP by LC-MS-based metabolic analysis, implying the
disruption of amino acid, energy, and lipid metabolism pathways. Differentially
expressed genes by transcriptomic analysis were mainly associated
with the nervous system and lipid metabolism. For the behavior and
reproduction performances, CP not only increased the light response
and swimming velocity of D. magna but also delayed
the time to first brood, decreased the number of broods, and increased
the number of neonates per brood. Overall, our findings suggest that
CP alters the behavior and reproduction, the metabolites, and transcriptional
expression associated with the nervous system and metabolism pathways
and provides some evidence on the mechanisms of CP toxicity in D. magna and perhaps other zooplankton.