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Published on: August 19, 2014
Frequency of chromosome aberrations in bone marrow of monkeys and their F1 after aflatoxin B1 injection
Abstract:
A mutagenic effect of aflatoxin B1 (AFB1) in somatic cells of primates is investigated. It is shown that AFB1 elevated the frequency of chromosome aberrations in the bone marrow of two species of monkeys: Macaca mulatta and Papio hamadryas. Beside chromosome aberrations, genome mutations were found in these experimental primates. AFB1-induced chromosome aberrations were constantly revealed during two years of study. Increase in the frequency of chromosome aberrations could be demonstrated in Macaca babies born from females that had received AFB1 at the final stage of pregnancy.
Insights
Aflatoxin B1 (AFB1) causes mutagenic effects in primate somatic cells, increasing chromosome aberrations in monkeys. These genetic mutations were observed long-term and even in offspring of exposed mothers.
Area of Science:
- Toxicology
- Genetics
- Primate research
Background:
- Aflatoxin B1 (AFB1) is a known mycotoxin with potential health risks.
- Investigating AFB1's mutagenic effects in primates is crucial due to their physiological similarities to humans.
Purpose of the Study:
- To investigate the mutagenic effects of aflatoxin B1 (AFB1) in somatic cells of primates.
- To assess the frequency and persistence of AFB1-induced genetic damage in non-human primates.
Main Methods:
- Exposure of Macaca mulatta and Papio hamadryas monkeys to AFB1.
- Analysis of bone marrow cells for chromosome aberrations and genome mutations.
- Long-term monitoring of genetic damage over two years.
- Evaluation of transgenerational effects in offspring of exposed females.
Main Results:
- AFB1 significantly elevated the frequency of chromosome aberrations in the bone marrow of both monkey species.
- Genome mutations were also detected in AFB1-exposed primates.
- AFB1-induced chromosome aberrations persisted consistently over a two-year study period.
- An increased frequency of chromosome aberrations was observed in offspring born to mothers exposed to AFB1 during late pregnancy.
Conclusions:
- Aflatoxin B1 exhibits significant mutagenic activity in primate somatic cells.
- AFB1 exposure can lead to persistent genetic damage and potentially transgenerational effects in primates.
- These findings highlight the genotoxic risk of AFB1 in primate models, relevant to human health concerns.

