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. 2012 Mar;5(1):21-4.
doi: 10.2478/v10102-012-0004-7.

Acetylcholine and an acetylcholinesterase inhibitor neostigmine can aggravate tularemia progress in BALB/c mice

Affiliations

Acetylcholine and an acetylcholinesterase inhibitor neostigmine can aggravate tularemia progress in BALB/c mice

Miroslav Pohanka et al. Interdiscip Toxicol. 2012 Mar.

Abstract

The present experiment was aimed at assessing the application of neostigmine, an acetylcholinesterase (AChE) pseudo-irreversible inhibitor with poor penetration through the hematoencephalitic barrier, and the neurotransmitter acetylcholine (ACh). The experiment was done to evaluate their ability to modulate an infectious disease: tularemia. Mice infected with Franciselle tularensis and exposed to either ACh or neostigmine had a higher mortality and spleen bacterial burden when compared to infected mice exposed to saline solution only. The activated cholinergic anti-inflammatory pathway suppressed pathways necessary for tularemia resolution. Administration of AChE inhibitors to the individuals suffering from tularemia is contra-indicatory. Drugs based on AChE inhibition should be restricted when tularemia or disease with a similar pathogenesis is suspected.

Keywords: Francisella tularensis; cholinergic anti-inflammatory pathway; cholinergic system; immunomodulation; intracellular pathogen; parasympathicus.

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Figures

Figure 1
Figure 1
mortality after tularemia infection and acetylcholine (ACh) or neostigmine (neo) administration.

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References

    1. Anthony LSD, Burke RD, Nano FE. Growth of Francisella spp. in rodent macrophages. Infect Immun. 1991;59:3291–3296. - PMC - PubMed
    1. Bandouchova H, Sedlackova J, Pohanka M, Novotny L, Hubalek M, Treml F, Vitula F, Pikula J. Tularemia induces different biochemical responses in BALB/c mice and common voles. BMC Infect Dis. 2009a;9:101. - PMC - PubMed
    1. Bandouchova H, Sedlackova J, Hubalek M, Pohanka M, Peckova L, Treml F, Vitula F, Pikula J. Susceptibility of selected murine and microtine species to infection by a wild strain of Francisella tularensis subsp. holarctica. Vet Med (Czech) 2009b;54:64–74.
    1. Bell BL, Mohapatra NP, Gunn JS. Regulation of virulence gene transcripts by the Francisella novicida orphan response regulator PmrA: role of phosphorylation and evidence of MGlA/SspA interaction. Infect Immun. 2010;78:2189–2198. - PMC - PubMed
    1. Bergsbaken T, Cookson BT. Innate immune response during Yersinia infection: critical modulation of cell death mechanisms through phagocyte activation. J Leukoc Biol. 2009;86:1153–1158. - PMC - PubMed

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