Literature DB >> 9051664

Mg2+/Ca(2+)-ATPase activity is not enriched in synaptic vesicles isolated from rat cerebral cortex.

G Rodríguez de Lores Arnaiz1, A Pellegrino de Iraldi.   

Abstract

Neuronal ATPases comprise a wide variety of enzymes which are not uniformly distributed in different membrane preparations. Since purified vesicle fractions have Mg2+/Ca(2+)-ATPase, the purpose of the present study was to know whether such enzyme activities have a preferential concentration in a synaptic vesicle fraction in order to be used as markers for these organelles. Resorting to a procedure developed in this Institute, we fractionated the rat cerebral cortex by differential centrifugation following osmotic shock of a crude mitochondrial fraction and separated a purified synaptic vesicle fraction over discontinuous sucrose gradients. Mg2+/Ca(2+)-ATPase activities and ultrastructural studies of isolated fractions were carried out. It was observed that similar specific activities for Mg2+/Ca(2+)-ATPases were found in all fractions studied which contain synaptic vesicles and/or membranes. Although the present results confirm the presence of Mg2+ and Ca(2+)-ATPase activities in synaptic vesicles preparations, they do not favor the contention that Mg2+/Ca(2+)-ATPase is a good marker for synaptic vesicles.

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Year:  1997        PMID: 9051664     DOI: 10.1023/a:1022490822175

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  14 in total

1.  Enzyme ultracytochemical demonstration of Ca(++)-ATPase in the rat cerebral cortex.

Authors:  V S Zinchuk; V F Tushevsky; A V Bulavka
Journal:  Folia Histochem Cytobiol       Date:  1992       Impact factor: 1.698

2.  SODIUM-POTASSIUM-ACTIVATED ATPASE AND POTASSIUM-ACTIVATED P-NITROPHENYLPHOSPHATASE: A COMPARISON OF THEIR SUBCELLULAR LOCALIZATIONS IN RAT BRAIN.

Authors:  R W ALBERS; E DEROBERTIS
Journal:  Proc Natl Acad Sci U S A       Date:  1965-03       Impact factor: 11.205

3.  Isolation of synaptic vesicles and structural organization of the acetycholine system within brain nerve endings.

Authors:  E DE ROBERTIS; G RODRIGUEZ DE LORES ARNAIZ; L SALGANICOFF; A PELLEGRINO DE IRALDI; L M ZIEHER
Journal:  J Neurochem       Date:  1963-04       Impact factor: 5.372

4.  The determination of inorganic phosphate in the presence of labile phosphate esters.

Authors:  O H LOWRY; J A LOPEZ
Journal:  J Biol Chem       Date:  1946-03       Impact factor: 5.157

5.  Ca++-ATPase in the central nervous system: an EM cytochemical study.

Authors:  M Mata; D J Fink
Journal:  J Histochem Cytochem       Date:  1989-07       Impact factor: 2.479

6.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

7.  Cytochemical localization of high-affinity Ca2(+)-ATPase activity in synaptic terminals.

Authors:  K H Körtje; D Freihöfer; H Rahmann
Journal:  J Histochem Cytochem       Date:  1990-06       Impact factor: 2.479

8.  Ultrastructural and enzymic studies of cholinergic and non-cholinergic synaptic membranes isolated from brain cortex.

Authors:  A Rodríguez de Lores; M Alberici; E De Robertis
Journal:  J Neurochem       Date:  1967-02       Impact factor: 5.372

9.  Age-related alterations by chronic intermittent hypoxia on cerebral synaptosomal ATPase activities.

Authors:  G Benzi; A Gorini; R Arnaboldi; B Ghigini; R F Villa
Journal:  J Neural Transm Suppl       Date:  1994

10.  Characterization of the P-type and V-type ATPases of cholinergic synaptic vesicles and coupling of nucleotide hydrolysis to acetylcholine transport.

Authors:  B W Hicks; S M Parsons
Journal:  J Neurochem       Date:  1992-04       Impact factor: 5.372

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