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Gut Microbiota as a Potential Player in Mn-Induced Neurotoxicity
Alexey A Tinkov1,2, Airton C Martins3, Daiana Silva Avila4
1Laboratory of Ecobiomonitoring and Quality Control, Yaroslavl State University, 150003 Yaroslavl, Russia.
Abstract:
Manganese (Mn) is an essential metal, which at high exposures causes neurotoxic effects and neurodegeneration. The neurotoxic effects of Mn are mediated by neuroinflammation, oxidative and endoplasmic reticulum stress, mitochondrial dysfunction, and other mechanisms. Recent findings have demonstrated the potential impact of Mn overexposure on gut microbiota dysbiosis, which is known to contribute to neurodegeneration via secretion of neuroactive and proinflammatory metabolites. Therefore, in this review, we discuss the existing data on the impact of Mn exposure on gut microbiota biodiversity, bacterial metabolite production, and gut wall permeability regulating systemic levels. Recent data have demonstrated that Mn exposure may affect gut microbiota biodiversity by altering the abundance of Shiegella, Ruminococcus, Dorea, Fusicatenibacter, Roseburia, Parabacteroides, Bacteroidetes, Firmicutes, Ruminococcaceae, Streptococcaceae, and other bacterial phyla. A Mn-induced increase in Bacteroidetes abundance and a reduced Firmicutes/Bacteroidetes ratio may increase lipopolysaccharide levels. Moreover, in addition to increased systemic lipopolysaccharide (LPS) levels, Mn is capable of potentiating LPS neurotoxicity. Due to the high metabolic activity of intestinal microflora, Mn-induced perturbations in gut microbiota result in a significant alteration in the gut metabolome that has the potential to at least partially mediate the biological effects of Mn overexposure. At the same time, a recent study demonstrated that healthy microbiome transplantation alleviates Mn-induced neurotoxicity, which is indicative of the significant role of gut microflora in the cascade of Mn-mediated neurotoxicity. High doses of Mn may cause enterocyte toxicity and affect gut wall integrity through disruption of tight junctions. The resulting increase in gut wall permeability further promotes increased translocation of LPS and neuroactive bacterial metabolites to the systemic blood flow, ultimately gaining access to the brain and leading to neuroinflammation and neurotransmitter imbalance. Therefore, the existing data lead us to hypothesize that gut microbiota should be considered as a potential target of Mn toxicity, although more detailed studies are required to characterize the interplay between Mn exposure and the gut, as well as its role in the pathogenesis of neurodegeneration and other diseases.
Insights
Manganese overexposure can harm the gut microbiome, increasing neuroinflammation and neurodegeneration risk. Targeting gut bacteria may offer new strategies for manganese toxicity and related neurological diseases.
Area of Science:
- Neuroscience
- Toxicology
- Microbiology
Background:
- Manganese (Mn) is essential but toxic at high levels, causing neurodegeneration via inflammation and stress.
- Gut microbiota dysbiosis is increasingly linked to neurodegeneration through metabolite production.
Purpose of the Study:
- To review the impact of manganese exposure on gut microbiota biodiversity, metabolite production, and gut barrier function.
- To explore the role of the gut microbiome in manganese-induced neurotoxicity.
Main Methods:
- Literature review of studies investigating manganese exposure and gut microbiota.
- Analysis of data on changes in bacterial phyla, metabolite levels, and gut permeability.
- Examination of the effects of microbiome transplantation on manganese neurotoxicity.
Main Results:
- Manganese exposure alters gut microbiota composition, increasing harmful bacteria like Bacteroidetes and reducing beneficial ones.
- Increased gut permeability and lipopolysaccharide (LPS) translocation contribute to neuroinflammation.
- Healthy microbiome transplantation mitigated manganese-induced neurotoxicity, highlighting the gut's role.
Conclusions:
- Manganese toxicity significantly impacts gut microbiota and barrier function, contributing to neuroinflammation and neurodegeneration.
- The gut microbiome is a potential therapeutic target for managing manganese toxicity.
- Further research is needed to fully elucidate the Mn-gut-brain axis in neurodegenerative diseases.
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