-
Je něco špatně v tomto záznamu ?
Inhibitor of sarco-endoplasmic reticulum Ca2+-ATPase thapsigargin stimulates production of nitric oxide and secretion of interferon-gamma
E Kmonickova, P Melkusova, J Harmatha, K Vokac, H Farghali, Z Zidek
Jazyk angličtina Země Nizozemsko
Grantová podpora
NR9379
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
ScienceDirect (archiv)
od 1993-01-01 do 2009-12-31
- MeSH
- arginasa MeSH
- buněčné linie MeSH
- Ca2+-ATPasy antagonisté a inhibitory MeSH
- endoplazmatické retikulum enzymologie MeSH
- financování organizované MeSH
- histamin fyziologie MeSH
- indikátory a reagencie MeSH
- inhibitory enzymů farmakologie MeSH
- interferon gama metabolismus MeSH
- krysa rodu rattus MeSH
- lidé MeSH
- lipopolysacharidy chemie MeSH
- makrofágy enzymologie metabolismus účinky léků MeSH
- mitogenem aktivované proteinkinasy p38 metabolismus MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- NF-kappa B metabolismus MeSH
- oxid dusnatý metabolismus MeSH
- potkani inbrední LEW MeSH
- sterilizace MeSH
- techniky in vitro MeSH
- thapsigargin farmakologie MeSH
- viabilita buněk účinky léků MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- lidé MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
Thapsigargin is a sesquiterpene lactone of guaianolide type isolated from the Mediterranean plant Thapsia garganica L. It is widely used experimentally as a potent and selective inhibitor of sarco-endoplasmic reticulum Ca2+-ATPase (SERCA) leading to rapid elevation of intracellular calcium [Ca2+]i. Several previous reports have shown that thapsigargin interferes with production of nitric oxide (NO) by mouse peritoneal macrophages and mouse macrophage cell lines. The present data confirm that thapsigargin is a modest inducer of NO in mouse macrophages, production of NO being slightly enhanced by lipopolysaccharide. However, thapsigargin on its own very potently induces NO in macrophages of rats under conditions in vitro. The highest effect was observed after the concentration of 0.25 microM thapsigargin, producing approximately 30 microM accumulation of nitrites in supernatants of cells cultured for 24 h. The aim of our experiments was to investigate immune mechanisms implicated in activation of high-output NO biosynthesis. It has been found that thapsigargin dose-dependently induces secretion of interferon-gamma (IFN-gamma) in macrophages of both rats and mice, and also in human peripheral blood mononuclear cells. The IFN-gamma production was rather low in macrophages of mice while relatively very high levels of IFN-gamma were found in cultures of rat macrophages and human peripheral blood mononuclear cells. The concentration of IFN-gamma produced by 5 microM thapsigargin within the interval of 24 h exceeded 3 ng/ml in rat macrophages and approached 2 ng/ml in cultures of human peripheral blood mononuclear cells. The effects are mediated by mitogen-activated protein kinases (MAPKs) such as p38 mitogen-activated protein kinase (p38) and extracellular signal-regulated kinases 1/2 (ERK1/2), and by nuclear transcriptional factor NF-kappaB. In summary, the original findings demonstrate immunostimulatory potential of thapsigargin and warrant more detailed preclinical studies.
- 000
- 04302naa 2200577 a 4500
- 001
- bmc11003742
- 003
- CZ-PrNML
- 005
- 20140327110740.0
- 008
- 110302s2008 ne e eng||
- 009
- AR
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Kmoníčková, Eva, $d 1962- $7 jo2002105217
- 245 10
- $a Inhibitor of sarco-endoplasmic reticulum Ca2+-ATPase thapsigargin stimulates production of nitric oxide and secretion of interferon-gamma / $c E Kmonickova, P Melkusova, J Harmatha, K Vokac, H Farghali, Z Zidek
- 314 __
- $a Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Department of Pharmacology, v.v.i., Videnska 1083, 142 20 Prague 4, Czech Republic. kmonickova@biomed.cas.cz
- 520 9_
- $a Thapsigargin is a sesquiterpene lactone of guaianolide type isolated from the Mediterranean plant Thapsia garganica L. It is widely used experimentally as a potent and selective inhibitor of sarco-endoplasmic reticulum Ca2+-ATPase (SERCA) leading to rapid elevation of intracellular calcium [Ca2+]i. Several previous reports have shown that thapsigargin interferes with production of nitric oxide (NO) by mouse peritoneal macrophages and mouse macrophage cell lines. The present data confirm that thapsigargin is a modest inducer of NO in mouse macrophages, production of NO being slightly enhanced by lipopolysaccharide. However, thapsigargin on its own very potently induces NO in macrophages of rats under conditions in vitro. The highest effect was observed after the concentration of 0.25 microM thapsigargin, producing approximately 30 microM accumulation of nitrites in supernatants of cells cultured for 24 h. The aim of our experiments was to investigate immune mechanisms implicated in activation of high-output NO biosynthesis. It has been found that thapsigargin dose-dependently induces secretion of interferon-gamma (IFN-gamma) in macrophages of both rats and mice, and also in human peripheral blood mononuclear cells. The IFN-gamma production was rather low in macrophages of mice while relatively very high levels of IFN-gamma were found in cultures of rat macrophages and human peripheral blood mononuclear cells. The concentration of IFN-gamma produced by 5 microM thapsigargin within the interval of 24 h exceeded 3 ng/ml in rat macrophages and approached 2 ng/ml in cultures of human peripheral blood mononuclear cells. The effects are mediated by mitogen-activated protein kinases (MAPKs) such as p38 mitogen-activated protein kinase (p38) and extracellular signal-regulated kinases 1/2 (ERK1/2), and by nuclear transcriptional factor NF-kappaB. In summary, the original findings demonstrate immunostimulatory potential of thapsigargin and warrant more detailed preclinical studies.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a arginasa $7 D001119
- 650 _2
- $a Ca2+-ATPasy $x antagonisté a inhibitory $7 D000252
- 650 _2
- $a buněčné linie $7 D002460
- 650 _2
- $a viabilita buněk $x účinky léků $7 D002470
- 650 _2
- $a vztah mezi dávkou a účinkem léčiva $7 D004305
- 650 _2
- $a endoplazmatické retikulum $x enzymologie $7 D004721
- 650 _2
- $a inhibitory enzymů $x farmakologie $7 D004791
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a histamin $x fyziologie $7 D006632
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a indikátory a reagencie $7 D007202
- 650 _2
- $a interferon gama $x metabolismus $7 D007371
- 650 _2
- $a lipopolysacharidy $x chemie $7 D008070
- 650 _2
- $a makrofágy $x enzymologie $x metabolismus $x účinky léků $7 D008264
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a myši inbrední C57BL $7 D008810
- 650 _2
- $a NF-kappa B $x metabolismus $7 D016328
- 650 _2
- $a oxid dusnatý $x metabolismus $7 D009569
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani inbrední LEW $7 D011917
- 650 _2
- $a sterilizace $7 D013242
- 650 _2
- $a thapsigargin $x farmakologie $7 D019284
- 650 _2
- $a mitogenem aktivované proteinkinasy p38 $x metabolismus $7 D048051
- 650 _2
- $a financování organizované $7 D005381
- 650 _2
- $a techniky in vitro $7 D066298
- 700 1_
- $a Melkusová, P. $7 _AN046344
- 700 1_
- $a Harmatha, Juraj $7 ola2004217002
- 700 1_
- $a Vokáč, Karel. $7 _AN058874
- 700 1_
- $a Farghali, Hassan, $d 1943- $7 jn20000400659
- 700 1_
- $a Zídek, Zdeněk $7 jk01152582
- 773 0_
- $t European Journal of Pharmacology $w MED00001641 $g Roč. 588, č. 1 (2008), s. 85-92 $x 0014-2999
- 910 __
- $a ABA008 $b x $y 7 $z 0
- 990 __
- $a 20110401095534 $b ABA008
- 991 __
- $a 20140327110814 $b ABA008
- 999 __
- $a ok $b bmc $g 831130 $s 695765
- BAS __
- $a 3
- BMC __
- $a 2008 $b 588 $c 1 $d 85-92 $i 0014-2999 $m European journal of pharmacology $n Eur J Pharmacol $x MED00001641
- GRA __
- $a NR9379 $p MZ0
- LZP __
- $a 2011-3B/vtme