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Biomedical subjects

M Avitabile

Publications and source records attributed to M Avitabile.

At least 19 recordsLinked to original sources
PubMed1995

[A polymorphism study of the DNA extracted from dental tissues].

Often teeth are the only items which can be used for personal identification in forensic medicine. In the present work we describe a method to extract and amplify DNA from dental elements ranging from 2 weeks to 5 year from the avulsion. PCR (polymerase chain reaction) was used to amplify VNTR sequences; the alleles products were electrophoresed, visualized by traditional methods and compared to the amplified products obtained from the matching blood sample. Our results give a new and powerful investigative tool for personal identification in the field of forensic odontostomatology, since such a procedure can be successfully applied both to recent and to ancient teeth.

Apolipoproteins B↗
PubMed1989

[Study of pollen of allergologic significance in the urban atmosphere of Parma in the years 1983-1984].

From 1983 to 1984 pollen air samples from Parma's urban atmosphere were collected weekly by means of a Burkard recording volumetric spore trap. Data regarding a few of the meteorologic variables were also collected at the same time: temperature, insulation, water precipitation, humidity and wind speed. Some of the more allergenic pollens and their concentration/m3 air were determined from the collected samples: Graminea, Urticaceae, Fagaceae, Salicaceae and Betulaceae. Looking at the results from the period of study, it can be seen that Graminea and Urticaceae were the most represented in comparison with the other families. Graminea was most represented in May 1983, in June 1984 and during the first week of September 1984; Urticaceae in September 1983, May 1984 and September 1984. These pollen concentrations were also compared to the meteorologic data.

Italy↗
PubMed1986

DNA-4'-6-diamidine-2-phenylindole interactions: a comparative study employing fluorescence and ultraviolet spectroscopy.

DAPI is a drug that interacts with double-stranded nucleic acids, binding preferentially to A + T base pairs. The interaction is not intercalative, therefore providing a useful model for mimicking the effect of functional molecules in modifying specific sites, namely, A + T segments, of significance in gene expression. Knowledge of the nature of such interaction has been enriched by additional information obtained from comparative analysis of the data acquired by uv spectroscopy and fluorescence. Two classes of binding sites, defined by different apparent affinity constants and numbers of binding sites, are evident. All types of interaction are dependent on the nucleic acid/dye ratio and on the ionic strength of the medium.

Binding Sites↗
PubMed1985

Interaction of papaverine with covalently closed DNA.

Cyclic nucleotides influence viral replication and papaverine, as an inhibitor of phosphodiesterase, also affects the replication of both DNA and RNA viruses through an increase in cAMP levels. Moreover in vitro papaverine affects neither protein synthesis nor several polymerases, while it inhibits DNA synthesis. Static fluorescence studies on the interaction of the drug with ColE1 plasmid covalently closed DNA indicate that the drug binds to the nucleic acid, probably by intercalation. A comparison between the binding characteristics of Papaverine and Actinomycin D is also reported.

Bacteriocin Plasmids↗
PubMed1983

Interaction of diamidino-2-phenylindole (DAPI) with natural and synthetic nucleic acids.

The interaction of DAPI with natural and synthetic polydeoxynucleotides of different base content and sequences was studied with circular dichroism, ultracentrifugation, viscosity and calorimetry. All the polymers show two types of binding. The strength of the interaction and its resistance to ionic strength are related to the content of AT clusters in the chain. On the other hand, sedimentation measurements rule out an intercalation mechanism. A model of DAPI interaction with DNA, similar to that displayed by distamycin and netropsin, is proposed.

Animals↗
PubMed1983

Effect of undernutrition on some enzymes of purine metabolism in different regions of developing rat brain.

The effect of undernutrition on the activity of some enzymes involved in purine metabolism, ie, adenosine aminohydrolase, adenylate aminohydrolase, and inosine phosphorylase in cerebral hemispheres, cerebellum, and brain stem of rats at different days of postnatal development was studied. Adenosine aminohydrolase, adenylate aminohydrolase, and inosine phosphorylase were assayed by radiochemical methods which involve the measurement of the radioactive products formed, ie, inosine, IMP, and hypoxanthine, respectively. The results obtained indicate that undernutrition affects the activity of the enzymes which control the concentration of purine nucleotides to a different degree in the three brain regions examined.

AMP Deaminase↗
PubMed1983

Effect of undernutrition on some enzymes involved in the salvage pathway of purine nucleotides in different regions of developing rat brain.

The effect of undernutrition on the activity of two key enzymes of purine salvage pathway, namely hypoxanthine-guanine phosphoribosyltransferase (HGPRTase) and adenine phosphoribosyltransferase (APRTase), in cerebral hemispheres, cerebellum and brain stem of rats at different days of postnatal development was studied. The activity of HGPRTase and of APRTase is significantly lower in all brain regions of undernourished animals at 5 days after birth; between 10 and 15 days of age there is a recovery of the enzymatic activity which is particularly evident in the cerebellum. Successively both enzymatic activities decrease reaching at 30 days of age values quite similar to those of controls. These results indicate that undernutrition during fetal and postnatal development, impairs and delays the activity of the enzymes of purine salvage pathway.

Adenine Phosphoribosyltransferase↗
PubMed1982

De novo biosynthesis of nucleotides and of nucleic acids in different regions of developing rat brain: effect of undernutrition.

The effect of undernutrition on the de novo biosynthesis of nucleic acids in cerebral hemispheres, cerebellum, and brain stem of rats at different days of postnatal development was studied. The experiments were carried out in vitro by measuring the incorporation of [14C]-formate into the adenine nucleotide of the acid-soluble fraction of RNA and DNA, as well as into the thymine of DNA. The results obtained indicate that undernutrition during fetal and postnatal development impairs the de novo synthesis of the purine nucleotides of RNA and DNA at 5 days of age and delays it thereafter in the various brain regions examined, particularly in the cerebellum.

Adenine↗
PubMed1981

[Intermolecular interactions between fluorescent probes bound to linear DNA].

Intermolecular interactions of fluorescent probes bound to linear DNA. Several fluorescent probes can be widely used in determining the base content, the geometry and the possible conformational transitions of linear and circular DNAs in solution. Data are presented showing that Tb3+ and DAPI bind independently to DNA and can therefore be used to monitor the G+C and A+T content of the nucleic acid respectively.

Amidines↗
PubMed1980

Terbium as a new probe to detect G+C content of DNA.

Tb3+ has been tested as a probe to determine G + C per cent composition of DNA. DAPI, a fluorescent dye specific for A + T bases, has been employed at the same time as a complementary probe. Using calf thymus DNA (G + C = 40%; A + T = 60%), it has been found that the binding of the two dyes is independent, and that one binding site every 12,5 nucleotides exists for Tb3+ and one binding site every 8.3 nucleotides for DAPI. The simultaneous use of Tb3+ and DAPI allows therefore the monitoring of A-T, G-C sequences.

Animals↗
PubMed1980

Polyamine levels in rat placenta during pregnancy.

Polyamine levels in rat placenta during pregnancy have been determined. Spermidine and spermine contents are high at the 15th day of gestation, then decrease gradually until to the term, remaining at levels comparable with those occurring in rapid growth tissues. The high levels of spermidine and spermine at 21th day of pregnancy may be related to RNA and protein turnover which is quite elevated at the end of gestation.

Animals↗
PubMedDate not supplied

Nucleolar and nucleoplasmic RNA polymerase activity in different regions of rat brain during postnatal development.

RNA polymerase activities of whole nuclei, of isolated and purified nucleoli and of the nucleoplasmic fractions obtained from cerebral hemispheres, cerebellum and brain stem of rat at different days of postnatal development have been determined. In the whole nuclei the fraction of RNA polymerase which is sensitive to alpha-amanitin, is strongly affected by salt concentration; at low ionic strength most of the activity is resistant to the drug while at high ionic strength the enzymatic activity shows a greater sensitivity to the drug. In isolated nucleoli RNA synthesis is not inhibited at all by alpha-amanitin. The biosynthesis of RNA, at low ionic strength, is inhibited by low doses of actinomycin D, whereas at high ionic strength it is remarkably inhibited only by higher doses of the drug. The sensitivity of the reaction to alpha-amanitin and actinomycin D provide good evidence that UTP or GTP incorporation into RNA in purified nuclei and nucleoli, is dependent on RNA polymerases acting on DNA template and is not dependent on homopolymer formation. These results show that in the whole brain nuclei at low ionic strength there is a preferential synthesis of rRNA, whereas at high ionic strength the synthesis of heterogenous RNA predominates. In isolated nucleoli the synthesis of RNA is restricted to rRNA.

Aging↗
PubMedDate not supplied

Influence of different counterions on the fluorescent probe-DNA complex.

Studies carried out on both linear and covalently closed DNA have clearly revealed at least two different types of probe-DNA complexes depending on the different experimental procedure adopted, and two main types of binding of the probe have been clearly established and referred to as intercalative and external binding. In order to investigate the influences of the different counterions on the stability of the probe-DNA complex, a set of static fluorimetric measurements were performed in a wide range of concentrations (1 mM to 2 M) of different alkaline-earth chlorides. At low salt concentrations (in the range of millimolar values) no detectable fluorescence intensity changes were evidenced by the use of alkaline salts, but a marked decrease was detected by using alkaline-earth salts. The present work investigates moreover the role played by the different salt, in first place Calcium salts, on the stability of ethidium-DNA complex, by the use of the static fluorimetric titration procedure which is able to discriminate between the two strong and weak binding sites on DNA. Our experimental results have been interpreted in terms of a peculiar Calcium-DNA interaction, involving not only the electrostatic charges of phosphate moiety but also the aromatic rings of the bases, i.e., the intercalation sites on double helix DNA.

Calcium↗
PubMedDate not supplied

[Correlation between serum glutathione reductases and bone densitometry values].

Free radicals, because of their marked chemical activity, have often been found to be involved in many human diseases. Enzymatic antioxidant systems, namely glutathione-reductase, present both in red blood cells and in serum, have been demonstrated to play a key role as free radicals scavengers. The present work has been carried out in order to evaluate the possible role played by free radicals in the demineralization process of the bone matrix. Glutathione-reductase activity, assayed by a slightly modified Horn's method, was related to bone density measurements. All the subjects with reduced densitometric values showed reduced glutathione-reductase levels. Our results seem to support the hypothesis of a strict relationship between low activity of antioxidant systems and demineralization process of the bone, in consequence of enhanced free radical levels.

Aged↗