-
Something wrong with this record ?
Galantamine effect on tularemia pathogenesis in a BALB/c mouse model
M. Pohanka, O. Pavlis, J. Pikula,
Language English Country Iran
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Directory of Open Access Journals
from 1997
Free Medical Journals
from 2003
Freely Accessible Science Journals
from 1997
PubMed Central
from 2010
Europe PubMed Central
from 2010 to 2020
ProQuest Central
from 2009-01-01
Medline Complete (EBSCOhost)
from 2012-01-01
Health & Medicine (ProQuest)
from 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2010
PubMed
23023217
DOI
10.6091/ibj.993.2012
Knihovny.cz E-resources
- MeSH
- Survival Analysis MeSH
- Francisella tularensis drug effects MeSH
- Galantamine pharmacology therapeutic use MeSH
- Interferon-gamma blood MeSH
- Interleukin-6 blood MeSH
- Mice, Inbred BALB C MeSH
- Mice MeSH
- Tularemia blood drug therapy microbiology MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
BACKGROUND: Galantamine is a drug used for the treatment of Alzheimer's disease and some other cognitive disorders. It is an inhibitor of acetylcholinesterase; however, interaction with nicotinic acetylcholine receptors has also been reported. Owing to the significant role of cholinergic anti-inflammatory pathways in neuro-immunomodulation, we decided to examine the effect of galantamine on tularemia-infected BALB/c mice. METHODS: Animals were infected with Francisella tularensis LVS and treated with galantamine (0.1 mg/kg of body weight). Total mortality over the course of tularemia infection was assessed and interleukin 6 (IL-6) and interferon gamma (IFN-gamma) in plasma samples were measured by enzyme-linked immunosorbent assays. Apart from the cytokine assays, biochemical markers such as inorganic phosphate, uric acid, lactate dehydrogenase, gamma glutamyltransferase, creatinine phosphokinase and amylase were assayed. RESULTS: The modulation of immunity by galantamine depended on two opposing processes: up-regulation of IFN-gamma and down-regulation of IL-6. Tularemia infection resulted in significant nephropathy, as hyperphosphataemia and hyperuricaemia occurred in infected animals. In addition, galantamine resulted in the mitigation of nephropathy, and markers of kidney dysfunction were modulated. Alterations in mortality were also found in this study. CONCLUSIONS: Galantamine can significantly influence the immune response via the cholinergic anti-inflammatory pathway. Despite the decrease in IL-6 levels, galantamine treatment enhanced protection against the intracellular pathogen F. tularensis, resulting in the remission of some pathology and reduced mortality.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13031855
- 003
- CZ-PrNML
- 005
- 20200430092047.0
- 007
- ta
- 008
- 131002s2012 ir f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.6091/ibj.993.2012 $2 doi
- 035 __
- $a (PubMed)23023217
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ir
- 100 1_
- $a Pohanka, Miroslav $u University of Defence, Trebesska, Hradec Kralove, Czech Republic. miroslav.pohanka@gmail.com
- 245 10
- $a Galantamine effect on tularemia pathogenesis in a BALB/c mouse model / $c M. Pohanka, O. Pavlis, J. Pikula,
- 520 9_
- $a BACKGROUND: Galantamine is a drug used for the treatment of Alzheimer's disease and some other cognitive disorders. It is an inhibitor of acetylcholinesterase; however, interaction with nicotinic acetylcholine receptors has also been reported. Owing to the significant role of cholinergic anti-inflammatory pathways in neuro-immunomodulation, we decided to examine the effect of galantamine on tularemia-infected BALB/c mice. METHODS: Animals were infected with Francisella tularensis LVS and treated with galantamine (0.1 mg/kg of body weight). Total mortality over the course of tularemia infection was assessed and interleukin 6 (IL-6) and interferon gamma (IFN-gamma) in plasma samples were measured by enzyme-linked immunosorbent assays. Apart from the cytokine assays, biochemical markers such as inorganic phosphate, uric acid, lactate dehydrogenase, gamma glutamyltransferase, creatinine phosphokinase and amylase were assayed. RESULTS: The modulation of immunity by galantamine depended on two opposing processes: up-regulation of IFN-gamma and down-regulation of IL-6. Tularemia infection resulted in significant nephropathy, as hyperphosphataemia and hyperuricaemia occurred in infected animals. In addition, galantamine resulted in the mitigation of nephropathy, and markers of kidney dysfunction were modulated. Alterations in mortality were also found in this study. CONCLUSIONS: Galantamine can significantly influence the immune response via the cholinergic anti-inflammatory pathway. Despite the decrease in IL-6 levels, galantamine treatment enhanced protection against the intracellular pathogen F. tularensis, resulting in the remission of some pathology and reduced mortality.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a Francisella tularensis $x účinky léků $7 D005604
- 650 _2
- $a galantamin $x farmakologie $x terapeutické užití $7 D005702
- 650 _2
- $a interferon gama $x krev $7 D007371
- 650 _2
- $a interleukin-6 $x krev $7 D015850
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a myši inbrední BALB C $7 D008807
- 650 _2
- $a analýza přežití $7 D016019
- 650 _2
- $a tularemie $x krev $x farmakoterapie $x mikrobiologie $7 D014406
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Pavliš, Oto $u - $7 xx0135660
- 700 1_
- $a Pikula, Jiri $u -
- 773 0_
- $w MED00176383 $t Iranian biomedical journal $x 2008-823X $g Roč. 16, č. 3 (2012), s. 156-61
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/23023217 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20131002 $b ABA008
- 991 __
- $a 20200430092041 $b ABA008
- 999 __
- $a ok $b bmc $g 995942 $s 830300
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2012 $b 16 $c 3 $d 156-61 $i 2008-823X $m Iranian biomedical journal $n Iran Biomed J $x MED00176383
- LZP __
- $a Pubmed-20131002