001     35073
005     20200402205953.0
024 7 _ |2 pmid
|a pmid:15110934
024 7 _ |2 DOI
|a 10.1016/j.bpc.2003.12.010
024 7 _ |2 WOS
|a WOS:000221368900004
037 _ _ |a PreJuSER-35073
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Biochemistry & Molecular Biology
084 _ _ |2 WoS
|a Biophysics
084 _ _ |2 WoS
|a Chemistry, Physical
100 1 _ |a Uhrikova, D.
|b 0
|0 P:(DE-HGF)0
245 _ _ |a Influence of local anesthetics on the phophatidylcholine model membrane: small-angle synchrotron X-ray diffraction and neutron scattering study
260 _ _ |a Amsterdam [u.a.]
|b Elsevier Science
|c 2004
300 _ _ |a 361 - 373
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Biophysical Chemistry
|x 0301-4622
|0 9184
|v 109
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a The phase preferences of egg yolk phosphatidylcholine (EYPC) have been examined in the presence of tertiary amine anesthetics [2-(propyloxy)phenyl]-2-(1-piperidinyl)ethyl ester of carbamic acid (C3A) and [2-(heptyloxy)phenyl]-2-(1-piperidinyl)ethyl ester of carbamic acid (C7A, heptacaine). Using the synchrotron small-angle X-ray diffraction (SAXD), it is shown that the C3A anesthetic induces the cubic and hexagonal (H(I)) phases at 2 > or = C3A:EYPC > 0.5 and H2O:EYPC < or = 40 molar ratios. In contrast, longer alkyloxy chain homolog C7A has no effect on the bilayer arrangement of EYPC at C7A:EYPC < = 1 molar ratios as observed by SAXD in C7A + EYPC mixtures hydrated at H2O:EYPC < = 40 molar ratios, as well as in sonicated C7A + EYPC mixtures hydrated in excess water as proved by the small-angle neutron scattering (SANS). The bilayer thickness d(L) decreases and the bilayer C7A surface area SC7A increases with the increase of C7A:EYPC molar ratio. It is suggested that the ability of tertiary amine local anesthetics to influence the dL and SC7A values and EYPC polymorphism is caused by their effective molecular shape and by charge. The possibility that anesthetic molecules may exert some of their biological effects by virtue of these properties is discussed.
536 _ _ |a Neurowissenschaften
|c L01
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK255
|x 0
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Amines: chemistry
650 _ 2 |2 MeSH
|a Amines: pharmacology
650 _ 2 |2 MeSH
|a Anesthetics, Local: chemistry
650 _ 2 |2 MeSH
|a Anesthetics, Local: pharmacology
650 _ 2 |2 MeSH
|a Egg Yolk: metabolism
650 _ 2 |2 MeSH
|a Lipid Bilayers: chemistry
650 _ 2 |2 MeSH
|a Membranes: drug effects
650 _ 2 |2 MeSH
|a Models, Biological
650 _ 2 |2 MeSH
|a Neutrons
650 _ 2 |2 MeSH
|a Phosphatidylcholines: chemistry
650 _ 2 |2 MeSH
|a Polymorphism, Genetic
650 _ 2 |2 MeSH
|a Scattering, Radiation
650 _ 2 |2 MeSH
|a Structure-Activity Relationship
650 _ 2 |2 MeSH
|a Synchrotrons
650 _ 2 |2 MeSH
|a X-Ray Diffraction: methods
650 _ 7 |0 0
|2 NLM Chemicals
|a Amines
650 _ 7 |0 0
|2 NLM Chemicals
|a Anesthetics, Local
650 _ 7 |0 0
|2 NLM Chemicals
|a Lipid Bilayers
650 _ 7 |0 0
|2 NLM Chemicals
|a Phosphatidylcholines
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a lipid bilayer
653 2 0 |2 Author
|a local anesthetic
653 2 0 |2 Author
|a [2-(alkyloxy)phenyl]-2-(1-piperidinyl)ethyl esters of carbamic acid
653 2 0 |2 Author
|a phosphatidylcholine
653 2 0 |2 Author
|a X-ray diffraction
653 2 0 |2 Author
|a neutron scattering
700 1 _ |a Rapp, G.
|b 1
|0 P:(DE-HGF)0
700 1 _ |a Yaradaikin, S.
|b 2
|0 P:(DE-HGF)0
700 1 _ |a Gordeliy, I. L.
|b 3
|u FZJ
|0 P:(DE-Juel1)VDB32237
700 1 _ |a Balgavy, P.
|b 4
|0 P:(DE-HGF)0
773 _ _ |a 10.1016/j.bpc.2003.12.010
|g Vol. 109, p. 361 - 373
|p 361 - 373
|q 109<361 - 373
|0 PERI:(DE-600)1496385-1
|t Biophysical chemistry
|v 109
|y 2004
|x 0301-4622
909 C O |o oai:juser.fz-juelich.de:35073
|p VDB
913 1 _ |k L01
|v Neurowissenschaften
|l Funktion und Dysfunktion des Nervensystems
|b Leben
|0 G:(DE-Juel1)FUEK255
|x 0
914 1 _ |y 2004
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |k IBI-2
|l Biologische Strukturforschung
|d 31.12.2006
|g IBI
|0 I:(DE-Juel1)VDB58
|x 0
970 _ _ |a VDB:(DE-Juel1)41673
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
980 _ _ |a I:(DE-Juel1)ISB-2-20090406
980 _ _ |a UNRESTRICTED
980 _ _ |a I:(DE-Juel1)ICS-6-20110106
981 _ _ |a I:(DE-Juel1)IBI-7-20200312
981 _ _ |a I:(DE-Juel1)ISB-2-20090406
981 _ _ |a I:(DE-Juel1)ICS-6-20110106


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