Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where N. Loprieno is active.

Publication


Featured researches published by N. Loprieno.


Mutation Research | 1994

Microgel electrophoresis assay (comet test) and SCE analysis in human lymphocytes from 100 normal subjects

Cecilia Betti; Tania Davini; Liliana Giannessi; N. Loprieno; Roberto Barale

Microscopic examination of individual human lymphocytes embedded in agarose, subjected to electrophoresis and stained with a fluorescent DNA-binding dye, provides a novel way of measuring DNA damage as extent of migration of DNA fragments, mainly single-strand breaks. With this relatively simple method, DNA damage arising as a consequence of smoking, age and other factors was examined in peripheral human lymphocytes from 100 healthy individuals living in Pisa (Italy). The extent of DNA migration was found to be significantly increased by smoking. It is noteworthy that the effect of smoking was more significant in men than in women and that DNA migration was similar in the young and in the older people. SCE analysis did not reveal any significant effect of smoking, sex or age in the same population, suggesting a higher responsiveness of the comet test to DNA-damaging agents.


Mutation Research\/genetic Toxicology | 1995

Comparative studies by comet test and SCE analysis in human lymphocytes from 200 healthy subjects

Cecilia Betti; Tania Davini; Liliana Giannessi; N. Loprieno; Roberto Barale

The comet test (single cell gel electrophoresis, SCGE) appears to be a promising tool to estimate DNA damage at the single cell level and it provides information on the presence of damage among individual cells. Previously, we analyzed the degree of DNA damage in peripheral human lymphocytes from 100 healthy subjects living in Pisa (Italy) taking into account age, gender and smoking habit, and we also reported some results aiming at the assessment of the comet test (Betti el al., 1994). In addition, SCE analysis was carried out in order to compare the two endpoints. Because of the interesting results obtained, the present study was extended to 200 individuals, and data analyzed included information concerning number of cigarettes smoked a day, tar/cigarette and job. Data obtained confirmed that the SCGE is more sensitive than SCE in revealing smoking habit effects but comet induction did not seem to be related to the amount of cigarette tar inhaled. Moreover, sampling time was found to play a greater role in the comet assay as compared to SCE. Job position did not significantly influence SCE mean/subject or comet length mean/subject.


Mutation Research\/dnaging | 1991

Micronucleated lymphocytes in people occupationally exposed to potential environmental contaminants: the age effect

Lucia Migliore; M Parrini; Isabella Sbrana; C Biagini; A Battaglia; N. Loprieno

This work is part of a research project on 2 groups of tannery workers (i.e., workers employed in the tanning process and those employed in the finishing department), and 2 control groups consisting of individuals paired with each exposed person according to sex, age and smoking habit. The whole study included the evaluation of micronuclei as well as of chromosomal aberrations and sister-chromatid exchanges in peripheral blood lymphocytes. Data on micronucleus analysis in both controls and exposed persons are shown in this paper. There was no statistically significant difference between MN frequencies in the 2 groups of exposed and controls, nor any positive correlation with smoking habit. The effect of age on basal frequency of micronucleated cells clearly emerges in the present study: both controls and exposed show an increase in MN frequency due to age. This could be correlated with a higher sensitivity to breaks, rearrangements or aneuploidogenic events of circulating lymphocytes in aged people.


Mutation Research | 1976

Mutagenicity of industrial compounds styrene and its possible metabolite styrene oxide

N. Loprieno; Angelo Abbondandolo; Roberto Barale; S Baroncelli; Stefania Bonatti; G Bronzetti; A Cammellini; C Corsi; G Corti; D Frezza; C Leporini; A Mazzaccaro; R Nieri; D Rosellini; Anna Maria Rossi

Styrene and its presumed metabolite, styrene oxide, were tested for their mutagenic effect on a forward mutation system of yeast and of Chinese hamster cells, and on a gene-conversion system of yeast. Experiments with liver microsomal preparations and host-mediated assay with yeast were also carried out. Styrene oxide was mutagenic in all test systems. Styrene was mutagenic only in the host-mediated assay.


Mutation Research | 1987

Evaluation of the genetic and embryotoxic effects of bis(tri-n-butyltin―oxide (TBTO), a broad-spectrum pesticide, in multiple in vivo and in vitro short-term tests

A. Davis; Roberto Barale; Gisèle Brun; R. Forster; T. Günther; H. Hautefeuille; C.A. van der Heijden; A.G.A.C. Knaap; R. Krowke; T. Kuroki; N. Loprieno; C. Malaveille; Hans-Joachim Merker; M. Monaco; P. Mosesso; D. Neubert; H. Norppa; M. Sorsa; E. Vogel; C.E. Voogd; Makoto Umeda; Helmut Bartsch

The genetic and embryotoxic effects of bis(tri-n-butyltin)oxide (TBTO) were evaluated in multiple in vivo and in vitro short-term tests preparatory to its potential wide use as a molluscicide in control of schistosomiasis. When tested in the rec assay in Bacillus subtilis, TBTO was not mutagenic and it did not induce reverse mutations in Klebsiella pneumoniae. Neither in the presence nor in the absecne of rat liver activation system did TBTO produce point mutations in Salmonella typhimurium strains TA1530, TA1535, TA1538, TA97, TA98 or TA100. TBTO was matagenic in strain TA100 in a fluctuation test, but only in the presence of rat liver S9 (Aroclor-induced). TBTO did not induce gene mutations in the yeast Schizosaccharomyces pombe, mitotic gene conversions in the yeast Saccharomyces cerevisiae, nor sister-chromatid exchange in Chinese hamster ovary cells in the presence or absence of rat or mouse liver S9. In the latter cells, structural chromosomal aberrations, endoreduplicated and polyploid cells were induced. TBTO did not induce gene mutations in V79 Chinese hamster cells (to 8-azaguanine-, ouabain- or 6-thioguanine-resistance) in the presence of a rat liver postmitochondrial fraction or in cell (hamster embryo cells and human and mouse epidermal keratinocyte)-mediated assays. In mouse lymphoma cells, TBTO did not induce 6-thioguanine- or BUdR-resistant mutations. As many tumour promoters inhibit metabolic cooperation between V79 Chinese hamster 6-thioguanine-resistant/-sensitive cells, TBTO was tested but showed no such activity. TBTO was examined for the induction of recessive lethal mutations in adult Berlin K male Drosophila melanogaster, either by feeding or by injection. Doses of 0.37 or 0.74 mM did not increase the number of X-linked recessive lethal mutations. An increased number of micronuclei was observed in the polychromatic erythrocytes of male BALB/c mice 48 h after a single oral dose of TBTO (60 mg/kg bw), while a lower dose (30 mg/kg bw) was ineffective. Neither of the two doses had induced micronuclei 30 h after treatment. The reproductive toxicity of TBTO was studied in NMRI mice. In a 10-day toxicity study, the LD50 and LD10 were 74 and 34 mg/kg bw, respectively. An increased frequency of cleft palates was seen in the fetuses of mice (compared with controls, 0.7%) treated orally during pregnancy with 11.7 mg/kg TBTO (7%), 23.4 mg/kg (24%) or 35 mg/kg (48%).(ABSTRACT TRUNCATED AT 400 WORDS)


Mutation Research Letters | 1990

Genotoxicity of two metabolites of benzene: phenol and hydroquinone show strong synergistic effects in vivo

Roberto Barale; A. Marrazzini; Cecilia Betti; V. Vangelisti; N. Loprieno; I. Barrai

Possible interactions between hydroquinone (HQ) and phenol (PHE), 2 known benzene metabolites, in inducing micronuclei in mouse bone marrow cells were investigated. HQ and PHE administered alone gave weak and negative results, respectively, at the doses tested. However, simultaneous administration of both compounds caused a considerable increase in the induction of micronuclei as well as an increase in bone marrow toxicity. Using 3 different statistical methods, it was shown that the observed joint effect was significantly higher than additive interaction, and was close to multiplicative interaction. These findings bring further support to the hypothesis that the toxic and genotoxic effects of benzene are produced by several metabolites acting synergistically.


Mutation Research | 1987

Micronuclei in exfoliated urothelial cells and urine mutagenicity in smokers

D. Reali; F. Di Marino; S. Bahramandpour; A. Carducci; Roberto Barale; N. Loprieno

The use of the micronucleus test on human exfoliated cells has recently been proposed (Stich et al., 1983a) for detecting genotoxic effects produced by mutagens/carcinogens in some human target tissues. So far, increased frequencies of micronucleated cells have been reported only in exfoliated cells of the buccal mucosa from individuals at risk of oral cancer, such as chewers of betel quid, nut and leaf, smokers and alcohol drinkers (Stich et al., 1982a,b, 1983b). As mutagens are present in large quantities in the urine of habital cigarette smokers, their urothelial ceils may represent a possible target for absorbed and excreted mutagens. This is supported by some recent reports on a significant increase in the risk of bladder cancer related to smoking habits (Cartwright et al., 1981; Mommsen and Aagaard, 1983; Vineis et al., 1984). Since an increase in micronucleated exfoliated ceils from the bladder mucosa of therapeutically irradiated patients has also been reported (Stich et al., 1983a), we decided to validate the micronucleus test in urothelial exfoliated cells obtained from urine samples of cigarette smokers. The urinary mutagenicity test (Ames test) was


Mutation Research\/genetic Toxicology | 1976

Evaluation of the genetic effects induced by vinyl chloride monomer (VCM) under mammalian metabolic activation: studies in vitro and in vivo

N. Loprieno; Roberto Barale; S Baroncelli; C Bauer; G Bronzetti; A Cammellini; G Cercignani; C Corsi; G Gervasi; C Leporini; R Nieri; Anna Maria Rossi; G Stretti; G. Turchi

As part of a programme of investigations on the biological effects of the industrial compound vinyl chloride monomer (VCM), the raw material for the production of polyvinyl chloride (PVC), analyses on the genetic effects by this compound have been done by experiments (in vitro) which have taken mammalian metabolism into account. Vinyl chloride in the presence of purified microsomes (sedimented at 105,000 g) obtained from mouse liver was converted into an active metabolite(s) which produced gene mutations in the yeast Schizosaccharomyces pombe (forward mutation) and gene conversions in two loci of a diploid Saccharomyces cerevisiae. Moreover, the compound was active in the host-mediated assay, when mice were treated with an oral dose of 700 mg/kg. The role is discussed of mutagenicity tests for the prediction of both genetic and carcinogenic risks of chemical compounds in industrial use.


Mutation Research\/genetic Toxicology | 1985

Sister-chromatid exchanges in lymphocytes and mutagenicity in urine of nurses handling cytostatic drugs

Roberto Barale; Gabriella Sozzi; Paolo Toniolo; Orietta Borghi; Daniela Reali; N. Loprieno; Giuseppe Della Porta

Sister-chromatid exchanges (SCE) in peripheral blood lymphocytes and mutagenicity of urine (Ames test) were measured in a group of 21 nurses professionally handling antineoplastic drugs and in a group of 21 unexposed controls. No differences in SCE frequencies and in urinary mutagenic activity between exposed and unexposed groups were detected. A clear positive increase in urinary mutagenicity in the TA98 Salmonella strain was observed with increasing number of cigarettes smoked, whereas no evident influence of smoking on SCE was seen. Age, coffee and alcohol consumption did not show any detectable effect in the two tests.


Mutation Research | 1991

Correlations between 15 polyclclic aromatic hydrocarbons (PAH) and the mutagenicity of the total PAH fraction in ambient air particles in La Spezia (Italy)

Roberto Barale; L. Giromini; G. Ghelardini; Chiara Scapoli; N. Loprieno; M. Pala; F. Valerio; I. Barrai

Airborne particulate matter has been monitored 4 times a month for 1 year (1988) in the city of La Spezia (Italy). The polycyclic aromatic hydrocarbon (PAH) fractions were extracted, purified and characterized for the content of 15 individual PAH. In general when concentrations of individual PAH were compared statistical correlation was obtained. Mutagenicity studies were performed by the use of the Ames plate test with the Salmonella strains TA98, TA100, TA98NR and TA98DNP6 with and without metabolic activation (S9 mix). The TA98 strain was by far the most responsive and the S9 mix was absolutely required as expected when PAH are assayed. Besides mutagenicity, toxicity was also considered and it proved to be correlated with mutagenicity in TA98, +S9. The TA98NR and TA98DNP6 strains showed no appreciable differences from the parental strain TA98 indicating the absence of significant amounts of direct-acting nitro derivatives in our PAH samples. Of the 15 PAH considered in this study the amounts of cyclopental[c,d]pyrene (CPP) correlated best with mutagenicity. The role of CPP in contributing to the indirect mutagenicity of urban air PAH samples is discussed.

Collaboration


Dive into the N. Loprieno's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

I. Barrai

University of Ferrara

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge