Experimental Pulmonary Tuberculosis in the Absence of Detectable Brain Infection Induces Neuroinflammation and Behavioural Abnormalities in Male BALB/c Mice

Int J Mol Sci. 2020 Dec 13;21(24):9483. doi: 10.3390/ijms21249483.

Abstract

Tuberculosis (TB) is a chronic infectious disease in which prolonged, non-resolutive inflammation of the lung may lead to metabolic and neuroendocrine dysfunction. Previous studies have reported that individuals coursing pulmonary TB experience cognitive or behavioural changes; however, the pathogenic substrate of such manifestations have remained unknown. Here, using a mouse model of progressive pulmonary TB, we report that, even in the absence of brain infection, TB is associated with marked increased synthesis of both inflammatory and anti-inflammatory cytokines in discrete brain areas such as the hypothalamus, the hippocampal formation and cerebellum accompanied by substantial changes in the synthesis of neurotransmitters. Moreover, histopathological findings of neurodegeneration and neuronal death were found as infection progressed with activation of p38, JNK and reduction in the BDNF levels. Finally, we perform behavioural analysis in infected mice throughout the infection, and our data show that the cytokine and neurochemical changes were associated with a marked onset of cognitive impairment as well as depressive- and anxiety-like behaviour. Altogether, our results suggest that besides pulmonary damage, TB is accompanied by an extensive neuroinflammatory and neurodegenerative state which explains some of the behavioural abnormalities found in TB patients.

Keywords: Mycobacterium tuberculosis; behaviour abnormalities; neuroinflammation.

MeSH terms

  • Animals
  • Anxiety / metabolism
  • Anxiety / microbiology
  • Behavioral Symptoms / microbiology
  • Blood-Brain Barrier / cytology
  • Blood-Brain Barrier / metabolism
  • Blood-Brain Barrier / pathology
  • Brain / cytology
  • Brain / enzymology
  • Brain / metabolism*
  • Brain / pathology
  • Brain-Derived Neurotrophic Factor / metabolism
  • Chromatography, High Pressure Liquid
  • Cognitive Dysfunction / metabolism*
  • Cognitive Dysfunction / microbiology
  • Cytokines / metabolism*
  • Depression / metabolism
  • Depression / microbiology
  • Disease Models, Animal
  • Down-Regulation
  • Hippocampus / cytology
  • Hippocampus / immunology
  • Hippocampus / metabolism
  • Hippocampus / pathology
  • Inflammation / metabolism*
  • Janus Kinases / metabolism
  • MAP Kinase Signaling System / genetics
  • Male
  • Mice, Inbred BALB C
  • Mycobacterium tuberculosis / metabolism*
  • Mycobacterium tuberculosis / pathogenicity
  • Neurons / cytology
  • Neurons / pathology*
  • Neurotransmitter Agents / metabolism
  • Tuberculosis, Pulmonary / enzymology
  • Tuberculosis, Pulmonary / metabolism*
  • Tuberculosis, Pulmonary / pathology
  • Tuberculosis, Pulmonary / psychology
  • Up-Regulation
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Bdnf protein, mouse
  • Brain-Derived Neurotrophic Factor
  • Cytokines
  • Neurotransmitter Agents
  • Janus Kinases
  • p38 Mitogen-Activated Protein Kinases