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Biomedical subjects

P Mandel

Publications and source records attributed to P Mandel.

At least 163 records · Page 9Linked to original sources

Positive cooperativity in high affinity binding sites for gamma-hydroxybutyric acid in rat brain.

High affinity binding sites for gamma-hydroxybutyrate have recently been shown to exist on crude membranes of rat brain. These sites exhibit a dissociation constant of 95 nM and a capacity of 557 fentomoles per mg protein. However, after more extensive washing of the crude membrane fraction and performing binding experiments at a lower concentration of radioactive GHB (below 20 nM), the existence of another binding site for GHB with a higher affinity than previously described was discovered. The data concerning this binding site are in favour of positive cooperative binding characteristics. This binding site may play a role in the mediation of the multiple physiological and pharmacological effects of GHB in the rat CNS and its presence provides additional evidence in favour of a neuromodulator or neurotransmitter role of GHB.

Animals↗

Effects of n-di-propylacetate on aggressive behavior and brain GABA level in isolated mice.

n-di-Propylacetate (nDPA, valproate) a GABA-T inhibitor, injected IP at the dose of 300 mg/kg antagonized agonistic behavior of isolated DBA/2 mice in a time-dependent fashion in parallel to an increase of GABA levels in olfactory bulb, striatum, posterior colliculus and septum. After 75 min, aggressive responses were higher than those after 15 to 45 min and significantly lower in comparison with those of saline injected mice. After 120 min aggressive behavior was not different from that of control mice. The concentration of GABA in the striatum and olfactory bulb returned to control value 75 and 120 min after drug administration, respectively. After 120 min GABA levels in posterior colliculus and septum were lower than those after 15 to 75 min, although significantly higher in comparison with those of saline injected mice. The results are discussed in terms of the possible involvement of olfactory bulb and striatum in GABA-mediated control of isolation-induced aggressive behavior in mice.

Aggression↗

Comparative investigations of glutaminase development in cerebral cortex of chick embryo and in primary cultures of neurons and glial cells.

Glutaminase activity was determined in pure cultures of neurons, glial cells and in mixed cultures obtained from chick embryo brain. The development of this enzyme was observed periodically over time and compared to its evolution in corresponding cerebral hemispheres during embryonic and postnatal development. The specific activity of brain glutaminase increased between the twelfth and sixteenth day of embryogenesis. A similar increase was observed in cultures of neuroblasts during the corresponding period of time, although the activity in culture was about one-third lower than in vivo. In contrast to neurons, there was no significant increase of glutaminase activity in glial cells before the fifteenth day of culture. The enzyme level in glial cells between the thirteenth and fifteenth days of culture was approximately 25% of that in 7- and 8-day-old neurons. The different development of glutaminase activity in neurons and glial cells was demonstrated in both pure and mixed cultures. The results support the hypothesis that there is a glutamine shunt from glial cells to neurons.

Animals↗

Antinociceptive action of sodium valproate in the mouse.

The antinociceptive action of sodium valproate (VPA) was examined using male NMRI mice. Using the hot-plate assay at 60 degrees C, orally-administered VPA (50-400 mg/kg) produced antinociceptive effects; the ED50 was about 160 mg/kg. Oral doses of VPA (6.3-400 mg/kg) decreased the writhing response elicited by intraperitoneally-injected acetic acid. The antinociceptive effect of VPA, as determined with the writhing test, exhibited complex characteristics, the most pronounced effect occurring at doses of 12.5-50 mg/kg. The antinociceptive effect of VPA in the writhing test was not antagonized by bicuculline or by naloxone. VPA, like other agents which enhance central GABA-ergic mechanisms, might possess analgesic activity.

Acetates↗

Presence of somatostatin, enkephalins, and substance P-like peptides in cultured neurons from embryonic chick cerebral hemispheres.

The presence of peptides in pure cultures of neurons from 8-day-old chick embryo cerebral hemispheres has been investigated by means of specific radioimmunoassays and chromatographic purification. Somatostatin, Met-enkephalin, Leu-enkephalin, and substance P immunoreactive substances have been detected in 8-day-old cultures grown in serum-free culture medium. The peptides were present in the cellular extracts, as well as in the culture medium extracts. beta-Endorphin, thyroliberin, luteinizing hormone-releasing hormone, and ACTH could not be detected. The largest amount was accounted by somatostatin (48 +/- 2 ng/mg protein). Some 60% of the somatostatin-immunoreactive material was found in the culture medium. Met-enkephalin, Leu-enkephalin, and substance P were present at lower concentrations: 1.61 +/- 0.27, 0.24 +/- 0.02, and 0.14 +/- 0.005 ng/mg protein, respectively. The identities of somatostatin- and enkephalin-immunoreactive materials were confirmed by high pressure liquid chromatography. The findings suggest that cultured neurons that express dopaminergic and GABAergic properties contain peptides similar, if not identical, to somatostatin, Met-enkephalin, Leu-enkephalin, and substance P.

Animals↗

Depolarization-evoked release of gamma-hydroxybutyrate from rat brain slices.

The release of gamma-hydroxybutyrate from preloaded rat brain striatal slices was investigated. K+-induced depolarization caused an efflux of gamma-hydroxybutyrate of about 50 fmol min-1 mg-1 (wet weight), but in a Ca2+-free medium containing Mg2+, the evoked release was reduced by 50-60%. The release was higher when 100 microM veratridine was used as a depolarizing agent. The efflux of gamma-hydroxybutyrate is related to veratridine and K+ concentration, and is strongly inhibited by 10 microM tetrodotoxin. The Ca2+ channel blocker verapamil induces a large decrease in the efflux of gamma-hydroxybutyrate after both K+- and veratridine-induced depolarization. These results are in favour of a possible transmitter function for gamma-hydroxybutyrate in rat striatum.

Animals↗

Bovine brain S100 proteins: separation and characterization of a new S100 protein species.

Three S100 protein species (S100a, S100b, S100a') have been purified from bovine brain using a modification of standard preparative methods. A higher yield for each protein was obtained at the last separation step. Characterization by urea/sodium dodecyl sulfate/polyacrylamide gel electrophoresis, UV absorption spectra, and fluorescence parameters provided evidence of a new tryptophan-containing S100 protein called S100a', which exhibits, as S100a and S100b, the properties of a Ca2+ binding protein.

Animals↗

Some electron microscopic aspects of poly(ADPR) polymerase-DNA interactions and of auto-poly(ADP-ribosyl)ation reaction.

Interaction of calf thymus poly(ADP-ribose(ADPR] polymerase with a copurified DNA fraction (sDNA) was investigated. Electron microscopic studies of sDNA which appeared to be a powerful poly(ADPR) polymerase activator have shown that the purified poly(ADPR) polymerase-DNA complexes possess a "nucleosome like structure", with DNA wrapping around the enzyme molecule. Examination of the DNA linked poly(ADPR) polymerase preparations revealed the presence of Y-structures in sDNA. The enrichment in the sDNA fraction of the Y shape DNA suggests the existence of replication fork structures in the poly(ADPR) polymerase linked DNA and or in the vicinity of the enzyme. With increasing auto-poly(ADP-ribosyl)ation the enzyme molecule becomes much denser, increases in size and detaches from the DNA. When poly(ADPR) formed was purified and examined by electron microscopy, branched polymers of different sizes were observed. The formation of these polymers may explain the size gained by poly ADP-ribosylated enzyme molecules. When the interaction of poly(ADPR) polymerase with the plasmid pBR 322 was tested, a slight contamination of our enzyme preparation with topoisomerase I was detected. The contaminant topoisomerase I activity, however, was completely abolished by ADP-ribosylation. Further experiments with purified calf thymus topoisomerase I confirmed that this enzyme loses its activity following ADP-ribosylation with poly(ADPR) polymerase. These results may suggest that ADP-ribosylation of topoisomerase I can be one of the regulatory mechanisms of its activity. Furthermore, these results confirm that a topoisomerase I contaminant does not interfere with the ADP-ribosylation experiments of purified poly(ADPR) polymerase preparation.

Adenosine Diphosphate Ribose↗

Nucleosomal poly(ADP-ribose) polymerase: properties and relaxation of the chromatin structure.

The properties of poly(ADP-ribose) polymerase associated to nucleosomes and nuclei were analyzed by measuring enzymatic activity, isolating poly(ADP-ribosylated) histones and by electron microscopy. The enzyme was found to be most active in tri- and tetranucleosomes. The presence of NaC1 (0 to 200 mM) in the incubation medium showed a very small inhibitory effect on the enzymatic activity of isolated nucleosomes; however, the enzyme activity of incubated nuclei showed a gradual reduction with increasing salt concentrations leading to an almost complete inhibition at 200 mM NaC1. In parallel, the histones H1 extracted from isolated nucleosomes incubated at 200 mM NaC1 were hyper(ADP-ribosylated), whereas the histones H1 extracted from nuclei chromatin showed no highly modified forms at 200 mM NaC1. The effect of ethidium bromide (EB) was also analyzed and was found to stimulate enzyme activity in tetranucleosomes and octanucleosomes but not in dinucleosomes and nucleosomes of 20 repeat units. Electron microscopic analysis of poly(ADP-ribosylated) nucleosomes does not show the presence of aggregates at low ionic strength. However at higher ionic strengths the presence of localized relaxed domains of chromatin is evidenced in condensed nucleosomes.

Cell Nucleus↗

[Existence of UDP galactose: galactosyltransferase activity at the external surface of cultured neurons].

The existence of UDP-galactose:galactosyltransferase activities at the external surface of cultured neurons from chick embryo hemispheres, was demonstrated. [14C]-galactose was transferred upon cellular substrates present on the neuronal surface and upon exogenous substrates (ovomucoïd) bound to Sepharose beads. The activity of ectogalactosyltransferase was not due to a leakage of intracellular enzymes into the incubation medium nor to an intracellular enzymatic activity utilizing [14C]-galactose obtained from the hydrolysis of UDP-[14C]-galactose. Kinetics of these ectogalactosyltransferases were analysed. The results support the hypothesis of a communication and/or interaction among the nerve cell surfaces via glycoconjugates or their biosynthetic enzymes.

Animals↗

[Calcium-dependent liberation of gamma-hydroxybutyrate after depolarization of rat brain slices].

The release of gamma-hydroxybutyrate from preloaded Rat brain striatal slices was investigated. Potassium induced depolarisation caused an efflux of gamma-hydroxybutyrate in the incubation medium. This release is significantly decreased by a calcium free medium, containing magnesium salt and EGTA. Taking into account our previous results concerning synthesis, uptake and binding of gamma-hydroxybutyrate, this calcium-dependent release strongly suggest a possible role of gamma-hydroxybutyrate in neurotransmission in the C.N.S.

Animals↗

[Turnover of gamma-aminobutyric acid (GABA) in neurons and glial cells of the chick embryo in culture].

The turnover rates of gamma-aminobutyric acid (GABA) in cultured neurons and glial cells of Chicken embryo were measured by using a gas chromatography/mass spectrometric method. The method followed involved monitoring of the time course of changes in the enrichment of deuterium in GABA following incubation with pentadeuterated glutamate in the medium. The GABA turnover rate in neurons was found to be nearly eight fold greater than in glial cells.

Animals↗