-
Je něco špatně v tomto záznamu ?
Linoleic acid-induced ultra-weak photon emission from Chlamydomonas reinhardtii as a tool for monitoring of lipid peroxidation in the cell membranes
A. Prasad, P. Pospíšil,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2006
Free Medical Journals
od 2006
Public Library of Science (PLoS)
od 2006
PubMed Central
od 2006
Europe PubMed Central
od 2006
ProQuest Central
od 2006-12-01
Open Access Digital Library
od 2006-01-01
Open Access Digital Library
od 2006-01-01
Open Access Digital Library
od 2006-10-01
Medline Complete (EBSCOhost)
od 2008-01-01
Nursing & Allied Health Database (ProQuest)
od 2006-12-01
Health & Medicine (ProQuest)
od 2006-12-01
Public Health Database (ProQuest)
od 2006-12-01
ROAD: Directory of Open Access Scholarly Resources
od 2006
- MeSH
- buněčná membrána účinky léků metabolismus MeSH
- Chlamydomonas reinhardtii cytologie účinky léků metabolismus MeSH
- fotony MeSH
- histidin farmakologie MeSH
- hydroxylový radikál metabolismus MeSH
- inhibitory lipoxygenas farmakologie MeSH
- kyselina linolová farmakologie MeSH
- kyslík metabolismus MeSH
- lipoxygenasa metabolismus MeSH
- malondialdehyd metabolismus MeSH
- mannitol farmakologie MeSH
- peroxidace lipidů účinky léků MeSH
- thiobarbituráty metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Reactive oxygen species formed as a response to various abiotic and biotic stresses cause an oxidative damage of cellular component such are lipids, proteins and nucleic acids. Lipid peroxidation is considered as one of the major processes responsible for the oxidative damage of the polyunsaturated fatty acid in the cell membranes. Various methods such as a loss of polyunsaturated fatty acids, amount of the primary and the secondary products are used to monitor the level of lipid peroxidation. To investigate the use of ultra-weak photon emission as a non-invasive tool for monitoring of lipid peroxidation, the involvement of lipid peroxidation in ultra-weak photon emission was studied in the unicellular green alga Chlamydomonas reinhardtii. Lipid peroxidation initiated by addition of exogenous linoleic acid to the cells was monitored by ultra-weak photon emission measured with the employment of highly sensitive charged couple device camera and photomultiplier tube. It was found that the addition of linoleic acid to the cells significantly increased the ultra-weak photon emission that correlates with the accumulation of lipid peroxidation product as measured using thiobarbituric acid assay. Scavenging of hydroxyl radical by mannitol, inhibition of intrinsic lipoxygenase by catechol and removal of molecular oxygen considerably suppressed ultra-weak photon emission measured after the addition of linoleic acid. The photon emission dominated at the red region of the spectrum with emission maximum at 680 nm. These observations reveal that the oxidation of linoleic acid by hydroxyl radical and intrinsic lipoxygenase results in the ultra-weak photon emission. Electronically excited species such as excited triplet carbonyls are the likely candidates for the primary excited species formed during the lipid peroxidation, whereas chlorophylls are the final emitters of photons. We propose here that the ultra-weak photon emission can be used as a non-invasive tool for the detection of lipid peroxidation in the cell membranes.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12028144
- 003
- CZ-PrNML
- 005
- 20121207113220.0
- 007
- ta
- 008
- 120817e20110725xxu f 000 0#eng||
- 009
- AR
- 024 7_
- $a 10.1371/journal.pone.0022345 $2 doi
- 035 __
- $a (PubMed)21799835
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Prasad, Ankush $u Department of Biophysics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Olomouc, Czech Republic.
- 245 10
- $a Linoleic acid-induced ultra-weak photon emission from Chlamydomonas reinhardtii as a tool for monitoring of lipid peroxidation in the cell membranes / $c A. Prasad, P. Pospíšil,
- 520 9_
- $a Reactive oxygen species formed as a response to various abiotic and biotic stresses cause an oxidative damage of cellular component such are lipids, proteins and nucleic acids. Lipid peroxidation is considered as one of the major processes responsible for the oxidative damage of the polyunsaturated fatty acid in the cell membranes. Various methods such as a loss of polyunsaturated fatty acids, amount of the primary and the secondary products are used to monitor the level of lipid peroxidation. To investigate the use of ultra-weak photon emission as a non-invasive tool for monitoring of lipid peroxidation, the involvement of lipid peroxidation in ultra-weak photon emission was studied in the unicellular green alga Chlamydomonas reinhardtii. Lipid peroxidation initiated by addition of exogenous linoleic acid to the cells was monitored by ultra-weak photon emission measured with the employment of highly sensitive charged couple device camera and photomultiplier tube. It was found that the addition of linoleic acid to the cells significantly increased the ultra-weak photon emission that correlates with the accumulation of lipid peroxidation product as measured using thiobarbituric acid assay. Scavenging of hydroxyl radical by mannitol, inhibition of intrinsic lipoxygenase by catechol and removal of molecular oxygen considerably suppressed ultra-weak photon emission measured after the addition of linoleic acid. The photon emission dominated at the red region of the spectrum with emission maximum at 680 nm. These observations reveal that the oxidation of linoleic acid by hydroxyl radical and intrinsic lipoxygenase results in the ultra-weak photon emission. Electronically excited species such as excited triplet carbonyls are the likely candidates for the primary excited species formed during the lipid peroxidation, whereas chlorophylls are the final emitters of photons. We propose here that the ultra-weak photon emission can be used as a non-invasive tool for the detection of lipid peroxidation in the cell membranes.
- 650 _2
- $a buněčná membrána $x účinky léků $x metabolismus $7 D002462
- 650 _2
- $a Chlamydomonas reinhardtii $x cytologie $x účinky léků $x metabolismus $7 D016825
- 650 _2
- $a histidin $x farmakologie $7 D006639
- 650 _2
- $a hydroxylový radikál $x metabolismus $7 D017665
- 650 _2
- $a kyselina linolová $x farmakologie $7 D019787
- 650 _2
- $a peroxidace lipidů $x účinky léků $7 D015227
- 650 _2
- $a lipoxygenasa $x metabolismus $7 D008084
- 650 _2
- $a inhibitory lipoxygenas $x farmakologie $7 D016859
- 650 _2
- $a malondialdehyd $x metabolismus $7 D008315
- 650 _2
- $a mannitol $x farmakologie $7 D008353
- 650 _2
- $a kyslík $x metabolismus $7 D010100
- 650 _2
- $a fotony $7 D017785
- 650 _2
- $a thiobarbituráty $x metabolismus $7 D013858
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Pospíšil, Pavel
- 773 0_
- $w MED00180950 $t PLoS ONE $x 1932-6203 $g Roč. 6, č. 7 (20110725), s. e22345
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/21799835 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y m
- 990 __
- $a 20120817 $b ABA008
- 991 __
- $a 20121207113255 $b ABA008
- 999 __
- $a ok $b bmc $g 950186 $s 785490
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2011 $b 6 $c 7 $d e22345 $e 20110725 $i 1932-6203 $m PLoS One $n PLoS One $x MED00180950
- LZP __
- $a Pubmed-20120817/11/04