Evaluation of the Adverse Effects of Chronic Exposure to Donepezil (An Acetylcholinesterase Inhibitor) in Adult Zebrafish by Behavioral and Biochemical Assessments

被引:18
|
作者
Audira, Gilbert [1 ,2 ]
Nguyen Thi Ngoc Anh [2 ]
Bui Thi Ngoc Hieu [1 ,2 ]
Malhotra, Nemi [3 ]
Siregar, Petrus [2 ]
Villalobos, Omar [4 ]
Villaflores, Oliver B. [5 ]
Ger, Tzong-Rong [3 ,6 ]
Huang, Jong-Chin [7 ]
Chen, Kelvin H-C [7 ]
Hsiao, Chung-Der [1 ,3 ,6 ]
机构
[1] Chung Yuan Christian Univ, Dept Chem, Chungli 320314, Taiwan
[2] Chung Yuan Christian Univ, Dept Biosci Technol, Chungli 320314, Taiwan
[3] Chung Yuan Christian Univ, Dept Biomed Engn, Chungli 320314, Taiwan
[4] Univ Santo Tomas, Fac Pharm, Dept Pharm, Manila 1008, Philippines
[5] Univ Santo Tomas, Fac Pharm, Dept Biochem, Manila 1008, Philippines
[6] Chung Yuan Christian Univ, Ctr Nanotechnol, Chungli 320314, Taiwan
[7] Natl Pingtung Univ, Dept Appl Chem, Pingtung 900391, Taiwan
关键词
donepezil; acetylcholinesterase inhibitor; dementia; zebrafish; behavior; ALZHEIMERS-DISEASE; OXIDATIVE STRESS; DANIO-RERIO; NEUROTRANSMITTER SYSTEMS; LOCOMOTOR-ACTIVITY; CIRCADIAN-RHYTHMS; CORTISOL-LEVELS; MEMORY; MICE; SAFETY;
D O I
10.3390/biom10091340
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Donepezil (DPZ) is an acetylcholinesterase inhibitor used for the clinical treatment of mild cognitive impairment. However, DPZ has been reported to have adverse effects, including causing abnormal cardiac rhythm, insomnia, vomiting, and muscle cramps. However, the existence of these effects in subjects without Dementia is unknown. In this study, we use zebrafish to conduct a deeper analysis of the potential adverse effects of DPZ on the short-term memory and behaviors of normal zebrafish by performing multiple behavioral and biochemical assays. Adult zebrafish were exposed to 1 ppm and 2.5 ppm of DPZ. From the results, DPZ caused a slight improvement in the short-term memory of zebrafish and induced significant elevation in aggressiveness, while the novel tank and shoaling tests revealed anxiolytic-like behavior to be caused by DPZ. Furthermore, zebrafish circadian locomotor activity displayed a higher reduction of locomotion and abnormal movement orientation in both low- and high-dose groups, compared to the control group. Biomarker assays revealed that these alterations were associated with an elevation of oxytocin and a reduction of cortisol levels in the brain. Moreover, the significant increases in reactive oxygen species (ROS) and malondialdehyde (MDA) levels in muscle tissue suggest DPZ exposure induced muscle tissue oxidative stress and muscle weakness, which may underlie the locomotor activity impairment. In conclusion, we show, for the first time, that chronic waterborne exposure to DPZ can severely induce adverse effects on normal zebrafish in a dose-dependent manner. These unexpected adverse effects on behavioral alteration should be carefully addressed in future studies considering DPZ conducted on zebrafish or other animals.
引用
收藏
页码:1 / 24
页数:25
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