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Published on: August 8, 2020
A review of reproductive toxicity of microcystins
Liang Chen1, Jun Chen2, Xuezhen Zhang3
1Donghu Experimental Station of Lake Ecosystems, State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Abstract:
Animal studies provide strong evidence of positive associations between microcystins (MCs) exposure and reproductive toxicity, representing a threat to human reproductive health and the biodiversity of wild life. This paper reviews current knowledge of the reproductive toxicity of MCs, with regard to mammals, fishes, amphibians, and birds, mostly in males. Toxicity of MCs is primarily governed by the inhibition of protein phosphatases 1 and 2A (PP1 and PP2A) and disturbance of cellular phosphorylation balance. MCs exposure is related to excessive production of reactive oxygen species (ROS) and oxidative stress, leading to cytoskeleton disruption, mitochondria dysfunction, endoplasmic reticulum (ER) stress, and DNA damage. MCs induce cell apoptosis mediated by the mitochondrial and ROS and ER pathways. Through PP1/2A inhibition and oxidative stress, MCs lead to differential expression/activity of transcriptional factors and proteins involved in the pathways of cellular differentiation, proliferation, and tumor promotion. MC-induced DNA damage is also involved in carcinogenicity. Apart from a direct effect on testes and ovaries, MCs indirectly affect sex hormones by damaging the hypothalamic-pituitary-gonad (HPG) axis and liver. Parental exposure to MCs may result in hepatotoxicity and neurotoxicity of offspring. We also summarize the current research gaps which should be addressed by further studies.
Insights
Microcystins (MCs) exposure causes reproductive toxicity in animals by inhibiting protein phosphatases and increasing oxidative stress. This review details MCs
Area of Science:
- Environmental toxicology
- Reproductive toxicology
- Biochemistry
Background:
- Microcystins (MCs) are cyanotoxins linked to reproductive toxicity in wildlife and potential human health risks.
- Understanding MCs' mechanisms of toxicity is crucial for assessing ecological and human health impacts.
Purpose of the Study:
- To review current knowledge on the reproductive toxicity of microcystins across various animal species.
- To elucidate the molecular mechanisms underlying MCs-induced reproductive damage.
- To identify research gaps in MCs reproductive toxicity.
Main Methods:
- Literature review of animal studies on microcystin exposure and reproductive outcomes.
- Analysis of toxicological pathways including protein phosphatase inhibition, oxidative stress, and apoptosis.
- Examination of effects on reproductive organs, sex hormones, and offspring health.
Main Results:
- MCs primarily exert toxicity by inhibiting protein phosphatases 1 and 2A (PP1 and PP2A), leading to cellular dysfunction.
- Exposure to MCs induces oxidative stress, DNA damage, apoptosis, and disrupts cellular signaling pathways.
- MCs impact male and female reproductive systems directly and indirectly via the hypothalamic-pituitary-gonad (HPG) axis and liver, with potential transgenerational effects.
Conclusions:
- Microcystins pose a significant threat to reproductive health in diverse animal species through multiple toxicological mechanisms.
- Further research is needed to fully understand the long-term reproductive consequences and transgenerational effects of MCs exposure.
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