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Development of a zebrafish model for toxicity evaluation of adulterated Apis mellifera honey
被引:0
|作者:
Fakhlaei R.
[1
,2
]
Selamat J.
[3
]
Abdull Razis A.F.
[3
,4
]
Sukor R.
[2
,3
]
Ahmad S.
[5
]
Khatib A.
[6
]
Zou X.
[1
]
机构:
[1] School of Food and Biological Engineering, Jiangsu University, 301 Xuefu Rd, Zhenjiang, 212013, Jiangsu
[2] Food Safety and Food Integrity (FOSFI), Institute of Tropical Agriculture and Food Security, Universiti Putra Malaysia, Selangor, Serdang
[3] Department of Food Science, Faculty of Food Science and Technology, Universiti Putra Malaysia, Selangor, Serdang
[4] Natural Medicines and Products Research Laboratory, Universiti Putra Malaysia, Selangor, Serdang
[5] Department of Biochemistry, Faculty of Biotechnology & Biomolecular Sciences, Universiti Putra Malaysia, Selangor, Serdang
[6] Department of Pharmaceutical Chemistry, Kulliyyah of Pharmacy, International Islamic University Malaysia, Pahang, Kuantan
来源:
关键词:
Apis mellifera honey;
Danio rerio;
Embryotoxicity assay;
Honey adulteration;
Honey quality;
Toxicity evaluation;
D O I:
10.1016/j.chemosphere.2024.141736
中图分类号:
学科分类号:
摘要:
Since ancient times, honey has been used for medical purposes and the treatment of various disorders. As a high-quality food product, the honey industry is prone to fraud and adulteration. Moreover, limited experimental studies have investigated the impact of adulterated honey consumption using zebrafish as the animal model. The aims of this study were: (1) to calculate the lethal concentration (LC50) of acid-adulterated Apis mellifera honey on embryos, (2) to investigate the effect of pure and acid-adulterated A. mellifera honey on hatching rate (%) and heart rate of zebrafish (embryos and larvae), (3) to elucidate toxicology of selected adulterated honey based on lethal dose (LD50) using adult zebrafish and (4) to screen the metabolites profile of adulterated honey from blood serum of adult zebrafish. The result indicated the LC50 of 31.10 ± 1.63 (mg/ml) for pure A. mellifera honey, while acetic acid demonstrates the lowest LC50 (4.98 ± 0.06 mg/ml) among acid adulterants with the highest mortality rate at 96 hpf. The treatment of zebrafish embryos with adulterated A. mellifera honey significantly (p ≤ 0.05) increased the hatching rate (%) and decreased the heartbeat rate. Acute, prolong-acute, and sub-acute toxicology tests on adult zebrafish were conducted at a concentration of 7% w/w of acid adulterants. Furthermore, the blood serum metabolite profile of adulterated-honey-treated zebrafish was screened by LC-MS/MS analysis and three endogenous metabolites have been revealed: (1) Xanthotoxol or 8-Hydroxypsoralen, (2) 16-Oxoandrostenediol, and (3) 3,5-Dicaffeoyl-4-succinoylquinic acid. These results prove that employed honey adulterants cause mortality that contributes to higher toxicity. Moreover, this study introduces the zebrafish toxicity test as a new promising standard technique for the potential toxicity assessment of acid-adulterated honey in this study and hazardous food adulterants for future studies. © 2024
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