Coupling Between GABA(A)-R Ligand-Binding Activity and Membrane Organization in beta-Cyclodextrin-Treated Synaptosomal Membranes from Bovine Brain Cortex: New Insights from EPR Experiments


Autoria(s): Turina, Anahi V.; Schreier, Shirley; Perillo, Maria A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

24/10/2013

24/10/2013

02/08/2013

Resumo

Correlations between GABA(A) receptor (GABA(A)-R) activity and molecular organization of synaptosomal membranes (SM) were studied along the protocol for cholesterol (Cho) extraction with beta-cyclodextrin (beta-CD). The mere pre-incubation (PI) at 37A degrees C accompanying the beta-CD treatment was an underlying source of perturbations increasing [H-3]-FNZ maximal binding (70%) and K (d) (38%), plus a stiffening of SMs' hydrocarbon core region. The latter was inferred from an increased compressibility modulus (K) of SM-derived Langmuir films, a blue-shifted DPH fluorescence emission spectrum and the hysteresis in DPH fluorescence anisotropy (A (DPH)) in SMs submitted to a heating-cooling cycle (4-37-4A degrees C) with A (DPH,heating) < A (DPH,cooling). Compared with PI samples, the beta-CD treatment reduced B (max) by 5% which correlated with a 45%-decrement in the relative Cho content of SM, a decrease in K and in the order parameter in the EPR spectrum of a lipid spin probe labeled at C5 (5-SASL), and significantly increased A (TMA-DPH). PI, but not beta-CD treatment, could affect the binding affinity. EPR spectra of 5-SASL complexes with beta-CD-, SM-partitioned, and free in solution showed that, contrary to what is usually assumed, beta-CD is not completely eliminated from the system through centrifugation washings. It was concluded that beta-CD treatment involves effects of at least three different types of events affecting membrane organization: (a) effect of PI on membrane annealing, (b) effect of residual beta-CD on SM organization, and (c) Cho depletion. Consequently, molecular stiffness increases within the membrane core and decreases near the polar head groups, leading to a net increase in GABA(A)-R density, relative to untreated samples.

CONICET

CONICET

SECyT-Universidad Nacional de Cordoba

SECyTUniversidad Nacional de Cordoba

MincytPcia.Cordoba

Mincyt-Pcia.Cordoba

ANPCyT from Argentina

ANPCyT from Argentina

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo, Brasil

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo, Brasil

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico, Brasil

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico, Brasil

Identificador

CELL BIOCHEMISTRY AND BIOPHYSICS, TOTOWA, v. 63, n. 1, supl. 4, Part 1-2, pp. 17-33, MAY, 2012

1085-9195

http://www.producao.usp.br/handle/BDPI/35805

10.1007/s12013-012-9338-1

http://dx.doi.org/10.1007/s12013-012-9338-1

Idioma(s)

eng

Publicador

HUMANA PRESS INC

TOTOWA

Relação

CELL BIOCHEMISTRY AND BIOPHYSICS

Direitos

closedAccess

Copyright HUMANA PRESS INC

Palavras-Chave #CYCLODEXTRIN #GABA(A) RECEPTOR #EPR #FLUORESCENCE ANISOTROPY #LANGMUIR FILMS #CHOLESTEROL CONTENT #RECEPTOR FUNCTION #WATER-INTERFACE #SPIN-LABEL #HIPPOCAMPAL MEMBRANES #ERYTHROCYTE-MEMBRANES #PARTITION-COEFFICIENT #PHOSPHOLIPID-BILAYERS #GAMMA-CYCLODEXTRINS #AIR-WATER #BIOCHEMISTRY & MOLECULAR BIOLOGY #BIOPHYSICS #CELL BIOLOGY
Tipo

article

original article

publishedVersion