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Acute, genetic and sub-chronic toxicities of flaxseed derived Maillard reaction products
Chao-Kun Wei1, Zhi-Jing Ni2, Kiran Thakur1
1School of Food and Biological Engineering, Hefei University of Technology, Hefei, 230009, China.
Abstract:
In present study, the acute, genetic, and sub-chronic toxicities of flaxseed derived Maillard reaction products (MRPs) were investigated. Acute toxicity results showed that the 50% lethal dose (LD50) of MRPs in rats was >15.0 g/kg body weight (BW); whereas, the 50% effective dose (ED50) of MRPs was 12.3 g/kg BW. Ames test demonstrated that the back-mutation colonies for MRPs addition of 5,000 μg/dish was positive, which displayed certain mutagenicity. There were no significant differences in micronucleus rate and sperm deformity rate among different dose groups. The sub-chronic toxicity confirmed that less than 0.75 gMRPs/kg BW intake did not affect weight, food intake, mortality, gross pathology, histology, hematology, and serum biochemistry. The obtained results can provide an imperative reference on the safety of a meat flavoring agents.
Insights
Flaxseed-derived Maillard reaction products (MRPs) showed low acute toxicity but potential mutagenicity in Ames tests. Sub-chronic studies indicated safety below 0.75 g/kg body weight, suggesting their use as meat flavoring agents is generally safe.
Area of Science:
- Food Science
- Toxicology
- Chemical Engineering
Background:
- Maillard reaction products (MRPs) are formed during the heating of foods and can contribute to flavor and color.
- Flaxseed is a rich source of nutrients and has been explored for various applications, including food ingredients.
- Understanding the toxicological profile of flaxseed-derived MRPs is crucial for their safe application as food additives.
Purpose of the Study:
- To evaluate the acute, genetic, and sub-chronic toxicity of flaxseed-derived Maillard reaction products (MRPs).
- To determine the safety of MRPs for potential use as meat flavoring agents.
Main Methods:
- Acute toxicity was assessed using LD50 (50% lethal dose) and ED50 (50% effective dose) in rats.
- Genetic toxicity was evaluated using the Ames test for mutagenicity and assessing micronucleus and sperm deformity rates.
- Sub-chronic toxicity was investigated by administering varying doses of MRPs to rats over an extended period, monitoring key health indicators.
Main Results:
- Acute toxicity studies indicated a high LD50 (>15.0 g/kg BW) and an ED50 of 12.3 g/kg BW for MRPs.
- The Ames test showed positive results for mutagenicity at 5,000 μg/dish, indicating a potential genetic risk.
- No significant adverse effects on weight, food intake, mortality, hematology, serum biochemistry, or histology were observed in sub-chronic studies at doses below 0.75 g MRPs/kg BW.
Conclusions:
- Flaxseed-derived MRPs exhibit low acute toxicity but possess some mutagenic potential.
- Sub-chronic exposure to flaxseed-derived MRPs at levels below 0.75 g/kg BW did not induce significant toxicity.
- The findings support the potential use of these MRPs as meat flavoring agents, with a need for careful consideration of their mutagenic properties.
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