dc.creatorFraceto L.F.
dc.creatorSpisni A.
dc.creatorSchreier S.
dc.creatorDe Paula E.
dc.date2005
dc.date2015-06-26T14:07:25Z
dc.date2015-11-26T15:41:36Z
dc.date2015-06-26T14:07:25Z
dc.date2015-11-26T15:41:36Z
dc.date.accessioned2018-03-28T22:50:06Z
dc.date.available2018-03-28T22:50:06Z
dc.identifier
dc.identifierBiophysical Chemistry. , v. 115, n. 1, p. 11 - 18, 2005.
dc.identifier3014622
dc.identifier10.1016/j.bpc.2004.12.003
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-17444367311&partnerID=40&md5=15c382f3c1e99ba165b7970f0a1496d8
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/93343
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/93343
dc.identifier2-s2.0-17444367311
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1264655
dc.descriptionWe have collected evidences of a "transient site" for the local anesthetics (LA) lidocaine, etidocaine, bupivacaine and mepivacaine in sonicated egg phosphatidylcholine (EPC) vesicles. The effects of the uncharged anesthetic species at a fixed LA/EPC ratio inside the bilayer were measured by chemical shifts (C.S.) and longitudinal relaxation times (T1) of the lipid hydrogens. Two sort of changes were detected: (I) decrease, indicating specific orientation of the LA aromatic ring (measured as up-field C.S. changes by the short-range ring-current effect) and less rotational freedom (smaller T 1 values) for EPC hydrogens such as the two glycerol-CH2 and the choline-CH2 bound to the PO4- group, probably due to the nearby presence of the LA; (II) increase, indicating the aromatic ring is now perpendicular to the orientation observed before (causing down-field changes in C.S.) and larger T1 values for all the choline and glycerol hydrogens, as a result of LA insertion behind these well-organized bilayer regions. The less hydrophobic, linear and nonlinear (lidocaine and mepivacaine, respectively) aminoamide analogs provide similar effects-described in I; their hydrophobic counterparts (etidocaine and bupivacaine) also produced comparable effects (depicted in II). The preferential positioning and orientation of each LA inside the bilayer is then determined by its hydrophobic and steric properties. We propose that this "transient site" in the lipid milieu exists also in biological membranes, where it can modulates the access of the uncharged LA species to its site(s) of action in the voltage-gated sodium channel. © 2004 Elsevier B.V. All rights reserved.
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dc.languageen
dc.publisher
dc.relationBiophysical Chemistry
dc.rightsfechado
dc.sourceScopus
dc.titleDifferential Effects Of Uncharged Aminoamide Local Anesthetics On Phospholipid Bilayers, As Monitored By 1h-nmr Measurements
dc.typeArtículos de revistas


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