-
Je něco špatně v tomto záznamu ?
Modulation of metabolic activity of phagocytes by antihistamines
A. Lojek, M. Cíž, M. Pekarová, G. Ambrožová, O. Vašíček, J. Moravcová, L. Kubala, K. Drábiková, V. Jančinová, T. Perečko, J. Pečivová, T. Mačičková, R. Nosál,
Jazyk angličtina Země Slovensko
Typ dokumentu časopisecké články
NLK
Free Medical Journals
od 2008
PubMed Central
od 2008 do 2019
Europe PubMed Central
od 2008 do 2018
ProQuest Central
od 2008-06-01 do 2021-01-31
Open Access Digital Library
od 2008-01-01
Open Access Digital Library
od 2008-01-01
Open Access Digital Library
od 2009-06-19
Nursing & Allied Health Database (ProQuest)
od 2008-06-01 do 2021-01-31
Health & Medicine (ProQuest)
od 2008-06-01 do 2021-01-31
Public Health Database (ProQuest)
od 2008-06-01 do 2021-01-31
Sciendo
od 2009-06-19
ROAD: Directory of Open Access Scholarly Resources
od 2008
- Publikační typ
- časopisecké články MeSH
The purpose of the study was to investigate the effects of H(1)-antihistamines of the 1(st) generation (antazoline, bromadryl, brompheniramine, dithiaden, cyclizine, chlorcyclizine, chlorpheniramine, clemastine) and the 2(nd) generation (acrivastine, ketotifen, and loratadine) on the respiratory burst of phagocytes. Reactive oxygen species generation in neutrophils isolated from rat blood was measured using luminol-enhanced chemiluminescence. Changes in nitrite formation and iNOS protein expression by RAW 264.7 macrophages were analysed using Griess reaction and Western blotting. The antioxidative properties of drugs in cell-free systems were detected spectrophotometrically, luminometrically, fluorimetrically, and amperometrically. The majority of the H(1)-antihistamines tested (bromadryl, brompheniramine, chlorcyclizine, chlorpheniramine, clemastine, dithiaden, and ketotifen) exhibited a significant inhibitory effect on the chemiluminescence activity of phagocytes. H(1)-antihistamines did not show significant scavenging properties against superoxide anion and hydroxyl radical, thus this could not contribute to the inhibition of chemiluminescence. H(1)-antihistamines had a different ability to modulate nitric oxide production by LPS-stimulated macrophages. Bromadryl, clemastine, and dithiaden were the most effective since they inhibited iNOS expression, which was followed by a significant reduction in nitrite levels. H(1)-antihistamines had no scavenging activity against nitric oxide. It can be concluded that the effects observed in the H(1)-antihistamines tested are not mediated exclusively via H(1)-receptor pathway or by direct antioxidative properties. Based on our results, antihistamines not interfering with the microbicidal mechanisms of leukocytes (antazoline, acrivastine and cyclizine) could be used preferentially in infections. Other antihistamines should be used, under pathological conditions accompanied by the overproduction of reactive oxygen species.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13015897
- 003
- CZ-PrNML
- 005
- 20130424134808.0
- 007
- ta
- 008
- 130424s2011 xo f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.2478/v10102-011-0004-z $2 doi
- 035 __
- $a (PubMed)21577279
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xo
- 100 1_
- $a Lojek, Antonin $u Institute of Biophysics, Academy of Sciences of the Czech Republic, Královopolská 135, 612 65 Brno, Czech Republic.
- 245 10
- $a Modulation of metabolic activity of phagocytes by antihistamines / $c A. Lojek, M. Cíž, M. Pekarová, G. Ambrožová, O. Vašíček, J. Moravcová, L. Kubala, K. Drábiková, V. Jančinová, T. Perečko, J. Pečivová, T. Mačičková, R. Nosál,
- 520 9_
- $a The purpose of the study was to investigate the effects of H(1)-antihistamines of the 1(st) generation (antazoline, bromadryl, brompheniramine, dithiaden, cyclizine, chlorcyclizine, chlorpheniramine, clemastine) and the 2(nd) generation (acrivastine, ketotifen, and loratadine) on the respiratory burst of phagocytes. Reactive oxygen species generation in neutrophils isolated from rat blood was measured using luminol-enhanced chemiluminescence. Changes in nitrite formation and iNOS protein expression by RAW 264.7 macrophages were analysed using Griess reaction and Western blotting. The antioxidative properties of drugs in cell-free systems were detected spectrophotometrically, luminometrically, fluorimetrically, and amperometrically. The majority of the H(1)-antihistamines tested (bromadryl, brompheniramine, chlorcyclizine, chlorpheniramine, clemastine, dithiaden, and ketotifen) exhibited a significant inhibitory effect on the chemiluminescence activity of phagocytes. H(1)-antihistamines did not show significant scavenging properties against superoxide anion and hydroxyl radical, thus this could not contribute to the inhibition of chemiluminescence. H(1)-antihistamines had a different ability to modulate nitric oxide production by LPS-stimulated macrophages. Bromadryl, clemastine, and dithiaden were the most effective since they inhibited iNOS expression, which was followed by a significant reduction in nitrite levels. H(1)-antihistamines had no scavenging activity against nitric oxide. It can be concluded that the effects observed in the H(1)-antihistamines tested are not mediated exclusively via H(1)-receptor pathway or by direct antioxidative properties. Based on our results, antihistamines not interfering with the microbicidal mechanisms of leukocytes (antazoline, acrivastine and cyclizine) could be used preferentially in infections. Other antihistamines should be used, under pathological conditions accompanied by the overproduction of reactive oxygen species.
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Cíž, Milan $u -
- 700 1_
- $a Pekarová, Michaela $u -
- 700 1_
- $a Ambrožová, Gabriela $u - $7 gn_A_00005440
- 700 1_
- $a Vašíček, Ondřej $u -
- 700 1_
- $a Moravcová, Jana $u -
- 700 1_
- $a Kubala, Lukáš $u -
- 700 1_
- $a Drábiková, Katarína $u -
- 700 1_
- $a Jančinová, Viera $u -
- 700 1_
- $a Perečko, Tomáš $u -
- 700 1_
- $a Pečivová, Jana $u -
- 700 1_
- $a Mačičková, Tatiana $u -
- 700 1_
- $a Nosál, Radomír $u -
- 773 0_
- $w MED00174076 $t Interdisciplinary toxicology $x 1337-9569 $g Roč. 4, č. 1 (2011), s. 15-9
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/21577279 $y Pubmed
- 910 __
- $a ABA008 $b B 2642 $c 547 $y a $z 0
- 990 __
- $a 20130424 $b ABA008
- 991 __
- $a 20130424135056 $b ABA008
- 999 __
- $a ind $b bmc $g 979098 $s 814218
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2011 $b 4 $c 1 $d 15-9 $i 1337-9569 $m Interdisciplinary toxicology $n Interdiscip. toxicol. $x MED00174076
- LZP __
- $a Pubmed-20130424