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Characterization of Brain Dysfunction Induced by Bacterial Lipopeptides That Alter Neuronal Activity and Network in Rodent Brains.
Kim, Kwang-Min; Zamaleeva, Alsu I; Lee, Youn Woo; Ahmed, M Rafiuddin; Kim, Eunkyung; Lee, Hye-Ryeon; Pothineni, Venkata Raveendra; Tao, Juan; Rhee, Siyeon; Jayakumar, Mithya; Inayathullah, Mohammed; Sivanesan, Senthilkumar; Red-Horse, Kristy; Palmer, Theo D; Park, Jon; Madison, Daniel V; Lee, Ho-Young; Rajadas, Jayakumar.
Afiliação
  • Kim KM; Biomaterials and Advanced Drug Delivery Laboratory, Stanford University School of Medicine, Palo Alto, California 94304.
  • Zamaleeva AI; Department of Neurosurgery, Stanford University School of Medicine, Stanford, California 94305.
  • Lee YW; Biomaterials and Advanced Drug Delivery Laboratory, Stanford University School of Medicine, Palo Alto, California 94304.
  • Ahmed MR; Department of Nuclear Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
  • Kim E; Biomaterials and Advanced Drug Delivery Laboratory, Stanford University School of Medicine, Palo Alto, California 94304.
  • Lee HR; Department of Nuclear Medicine, Seoul National University, College of Medicine, Seoul, Korea.
  • Pothineni VR; Department of Neurosurgery, Stanford University School of Medicine, Stanford, California 94305.
  • Tao J; Biomaterials and Advanced Drug Delivery Laboratory, Stanford University School of Medicine, Palo Alto, California 94304.
  • Rhee S; Biomaterials and Advanced Drug Delivery Laboratory, Stanford University School of Medicine, Palo Alto, California 94304.
  • Jayakumar M; Department of Biology, and.
  • Inayathullah M; Biomaterials and Advanced Drug Delivery Laboratory, Stanford University School of Medicine, Palo Alto, California 94304.
  • Sivanesan S; Biomaterials and Advanced Drug Delivery Laboratory, Stanford University School of Medicine, Palo Alto, California 94304.
  • Red-Horse K; Biomaterials and Advanced Drug Delivery Laboratory, Stanford University School of Medicine, Palo Alto, California 94304.
  • Palmer TD; Department of Biology, and.
  • Park J; Department of Neurosurgery, Stanford University School of Medicine, Stanford, California 94305.
  • Madison DV; Department of Neurosurgery, Stanford University School of Medicine, Stanford, California 94305.
  • Lee HY; Department of Molecular and Cellular Physiology, Stanford University, Stanford, California 94305.
  • Rajadas J; Department of Nuclear Medicine, Seoul National University Bundang Hospital, Seongnam, Korea, jayraja@stanford.edu md1004@snu.ac.kr.
J Neurosci ; 38(50): 10672-10691, 2018 12 12.
Article em En | MEDLINE | ID: mdl-30381406
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 Pam3CSK4 (PAM), a synthetic bacterial lipopeptide, on synaptic dysfunction of female mice brains and cultured neurons in parallel. Our functional brain imaging using PET with [18F]fluorodeoxyglucose and [18F] 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 in vivo 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 in vitro 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.SIGNIFICANCE STATEMENT 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 in vivo and in vitro experimental models to understand how bacterial lipopeptides impair brain function and network.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Lipopeptídeos / Rede Nervosa / Neurônios Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Neurosci Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Lipopeptídeos / Rede Nervosa / Neurônios Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Neurosci Ano de publicação: 2018 Tipo de documento: Article