Literature DB >> 2914819

Morphologic changes induced in vitro by 2,5 hexanedione.

W Malorni1, G Formisano, G Donelli.   

Abstract

The effects of 2,5 hexanedione (2,5 HD), a metabolite of n-hexane, were investigated in different in vitro systems. A human mammary carcinoma cell line, a human melanoma cell line, and fetal mouse neuronal cells in primary culture were considered. Light and electron microscopic observations demonstrated clearly that changes in cell proliferation can be detected. Furthermore, morphologic differentiative phenomena characterized by a noticeable increase in cell protrusions and dendriticlike processes can occur. Differences in the features of these processes were also detected between the different cell lines. These data can indicate non-neuronal cells as possible further targets of the toxicant. The possibility could be hypothesized that toxic neuropathies are generalized disorders, being neuronal system exceptionally vulnerable to 2,5 HD. Moreover, results obtained suggest that the sensitivity of in vitro systems could represent a useful tool in studying the mechanisms of action of the neurotoxicant 2,5 HD.

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Year:  1989        PMID: 2914819     DOI: 10.1007/BF02624415

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol        ISSN: 0883-8364


  39 in total

Review 1.  The mechanisms of acrylamide axonopathy.

Authors:  M S Miller; P S Spencer
Journal:  Annu Rev Pharmacol Toxicol       Date:  1985       Impact factor: 13.820

2.  The industrial use of solvents and risk of neurotoxicity.

Authors:  E De Rosa; G B Bartolucci; F Brighenti; G P Gori; M Sigon; D Toffolo
Journal:  Ann Occup Hyg       Date:  1985

3.  Studies on the biochemical basis of distal axonopathies--I. Inhibition of glycolysis by neurotoxic hexacarbon compounds.

Authors:  M I Sabri; C L Moore; P S Spencer
Journal:  J Neurochem       Date:  1979-03       Impact factor: 5.372

4.  The morphogenesis of testicular degeneration induced in rats by orally administered 2,5-hexanedione.

Authors:  R E Chapin; K T Morgan; J S Bus
Journal:  Exp Mol Pathol       Date:  1983-04       Impact factor: 3.362

Review 5.  The enlarging view of hexacarbon neurotoxicity.

Authors:  P S Spencer; H H Schaumburg; M I Sabri; B Veronesi
Journal:  Crit Rev Toxicol       Date:  1980-10       Impact factor: 5.635

6.  The effect of 3,4-dimethyl substitution on the neurotoxicity of 2,5-hexanedione. II. Dimethyl substitution accelerates pyrrole formation and protein crosslinking.

Authors:  D C Anthony; K Boekelheide; C W Anderson; D G Graham
Journal:  Toxicol Appl Pharmacol       Date:  1983-12       Impact factor: 4.219

Review 7.  Pathogenesis of experimental giant neurofilamentous axonopathies: a unified hypothesis based on chemical modification of neurofilaments.

Authors:  L M Sayre; L Autilio-Gambetti; P Gambetti
Journal:  Brain Res       Date:  1985-09       Impact factor: 3.252

8.  Susceptibility of mammary tumor cells to complement-mediated cytolysis after in vitro or in vivo fatty acid manipulation.

Authors:  K L Erickson; I K Thomas
Journal:  J Natl Cancer Inst       Date:  1985-08       Impact factor: 13.506

9.  Alterations of fast axoplasmic transport in experimental methyl n-butyl ketone neuropathy.

Authors:  J R Mendell; Z Sahenk; K Saida; H S Weiss; R Savage; D Couri
Journal:  Brain Res       Date:  1977-09-09       Impact factor: 3.252

10.  Microtubule assembly in cultivated Greene melanoma cells is stimulated by dibutyryl adenosine 3':5'-cyclic monophosphate or cholera toxin.

Authors:  A M DiPasquale; J McGuire; G Moellmann; S J Wasserman
Journal:  J Cell Biol       Date:  1976-12       Impact factor: 10.539

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