AI Article Synopsis

  • The study explores how bacterial lipoproteins, specifically a synthetic lipopeptide called PamCSK (PAM), affect brain function and synaptic activity, highlighting its impact on female mice and cultured neurons.
  • It finds that PAM-induced brain dysfunction correlates more with disrupted neurotransmitter activity in the limbic system than with decreased overall energy metabolism in neurons.
  • The research shows that PAM causes structural changes in synapses, reducing both synaptic plasticity and the number of functioning synapses, which could complicate diagnosing brain disorders during bacterial infections.

Article Abstract

The immunopathological states of the brain induced by bacterial lipoproteins have been well characterized by using biochemical and histological assays. However, these studies have limitations in determining functional states of damaged brains involving aberrant synaptic activity and network, which makes it difficult to diagnose brain disorders during bacterial infection. To address this, we investigated the effect of PamCSK (PAM), a synthetic bacterial lipopeptide, on synaptic dysfunction of female mice brains and cultured neurons in parallel. Our functional brain imaging using PET with [F]fluorodeoxyglucose and [F] flumazenil revealed that the brain dysfunction induced by PAM is closely aligned to disruption of neurotransmitter-related neuronal activity and functional correlation in the region of the limbic system rather than to decrease of metabolic activity of neurons in the injection area. This finding was verified by tissue experiments that analyzed synaptic and dendritic alterations in the regions where PET imaging showed abnormal neuronal activity and network. Recording of synaptic activity also revealed that PAM reorganized synaptic distribution and decreased synaptic plasticity in hippocampus. Further study using neuron cultures demonstrated that PAM decreased the number of presynapses and the frequency of miniature EPSCs, which suggests PAM disrupts neuronal function by damaging presynapses exclusively. We also showed that PAM caused aggregation of synapses around dendrites, which may have caused no significant change in expression level of synaptic proteins, whereas synaptic number and function were impaired by PAM. Our findings could provide a useful guide for diagnosis and treatment of brain disorders specific to bacterial infection. It is challenging to diagnose brain disorders caused by bacterial infection because neural damage induced by bacterial products involves nonspecific neurological symptoms, which is rarely detected by laboratory tests with low spatiotemporal resolution. To better understand brain pathology, it is essential to detect functional abnormalities of brain over time. To this end, we investigated characteristic patterns of altered neuronal integrity and functional correlation between various regions in mice brains injected with bacterial lipopeptides using PET with a goal to apply new findings to diagnosis of brain disorder specific to bacterial infection. In addition, we analyzed altered synaptic density and function using both and experimental models to understand how bacterial lipopeptides impair brain function and network.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580656PMC
http://dx.doi.org/10.1523/JNEUROSCI.0825-17.2018DOI Listing

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