Literature DB >> 2612780

Release and metabolism of dopamine in a clonal line of pheochromocytoma (PC12) cells exposed to fenthion.

S M Tuler1, A A Hazen, J M Bowen.   

Abstract

The effects of an organophosphate (OP) pesticide, fenthion (FEN), on the release and metabolism of dopamine were evaluated in a clonal line of rat pheochromocytoma (PC12) cells. HPLC was used to determine media concentrations of DA and the DA metabolites norepinephrine (NE), 3,4-dihydroxyphenylacetic acid (DOPAC), and homovanillic acid (HVA). The FEN formulation solvent did not significantly affect DA metabolism. In the first study, cultures were treated with 10(-5) or 10(-6) M FEN or 10(-5) M neostigmine, a non-OP acetylcholinesterase inhibitor. Concentrations of both catecholamines were elevated in cultures treated with 10(-5) M FEN by 2.8-fold for DA and 3.5-fold for NE. Neostigmine effects were of smaller magnitude and DA was decreased after 24 hr. Cultures were also treated with depolarizing levels of K+, but the effect of FEN was not altered, suggesting that FEN does not act by increasing DA release. In the second study, the effect of 10(-6) M FEN was evaluated in cultures treated with the DA uptake inhibitor benztropine, the monoamine oxidase (MAO) inhibitor pargyline, or the catechol-O-methyltransferase (COMT) inhibitor tropolone. Inhibitor effects were consistent with their known mechanisms of action. In all cultures treated with FEN, the ratio HVA/DOPAC was decreased after 3 and 6 hr of exposure. A decrease in HVA/DOPAC was also observed in cultures treated with neostigmine and tropolone. In combination with pargyline, FEN decreased DA in contrast to its usual effect of increasing DA. Neither the stimulation of DA release nor the inhibition of DA uptake affected the observed action of FEN in PC12 cultures.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1989        PMID: 2612780     DOI: 10.1016/0272-0590(89)90284-4

Source DB:  PubMed          Journal:  Fundam Appl Toxicol        ISSN: 0272-0590


  21 in total

1.  Organophosphate exposure during a critical developmental stage reprograms adenylyl cyclase signaling in PC12 cells.

Authors:  Abayomi A Adigun; Ian T Ryde; Frederic J Seidler; Theodore A Slotkin
Journal:  Brain Res       Date:  2010-03-16       Impact factor: 3.252

2.  Diverse neurotoxicants converge on gene expression for neuropeptides and their receptors in an in vitro model of neurodifferentiation: effects of chlorpyrifos, diazinon, dieldrin and divalent nickel in PC12 cells.

Authors:  Theodore A Slotkin; Frederic J Seidler
Journal:  Brain Res       Date:  2010-08-01       Impact factor: 3.252

3.  Disparate developmental neurotoxicants converge on the cyclic AMP signaling cascade, revealed by transcriptional profiles in vitro and in vivo.

Authors:  Abayomi A Adigun; Frederic J Seidler; Theodore A Slotkin
Journal:  Brain Res       Date:  2009-12-21       Impact factor: 3.252

4.  Transcriptional profiles reveal similarities and differences in the effects of developmental neurotoxicants on differentiation into neurotransmitter phenotypes in PC12 cells.

Authors:  Theodore Slotkin; Frederic Seidler
Journal:  Brain Res Bull       Date:  2008-09-22       Impact factor: 4.077

5.  Benzo[a]pyrene impairs neurodifferentiation in PC12 cells.

Authors:  Theodore A Slotkin; Frederic J Seidler
Journal:  Brain Res Bull       Date:  2009-06-17       Impact factor: 4.077

6.  The sea urchin embryo, an invertebrate model for mammalian developmental neurotoxicity, reveals multiple neurotransmitter mechanisms for effects of chlorpyrifos: therapeutic interventions and a comparison with the monoamine depleter, reserpine.

Authors:  Gennady A Buznikov; Lyudmila A Nikitina; Ljubisa M Rakić; Ivan Milosević; Vladimir V Bezuglov; Jean M Lauder; Theodore A Slotkin
Journal:  Brain Res Bull       Date:  2007-07-06       Impact factor: 4.077

7.  Unrelated developmental neurotoxicants elicit similar transcriptional profiles for effects on neurotrophic factors and their receptors in an in vitro model.

Authors:  Theodore A Slotkin; Frederic J Seidler; Fabio Fumagalli
Journal:  Neurotoxicol Teratol       Date:  2008-12-13       Impact factor: 3.763

8.  Developmental neurotoxicants target neurodifferentiation into the serotonin phenotype: Chlorpyrifos, diazinon, dieldrin and divalent nickel.

Authors:  Theodore A Slotkin; Frederic J Seidler
Journal:  Toxicol Appl Pharmacol       Date:  2008-09-16       Impact factor: 4.219

9.  Oxidative and excitatory mechanisms of developmental neurotoxicity: transcriptional profiles for chlorpyrifos, diazinon, dieldrin, and divalent nickel in PC12 cells.

Authors:  Theodore A Slotkin; Frederic J Seidler
Journal:  Environ Health Perspect       Date:  2008-12-05       Impact factor: 9.031

10.  Ultraviolet photolysis of chlorpyrifos: developmental neurotoxicity modeled in PC12 cells.

Authors:  Theodore A Slotkin; Frederic J Seidler; Changlong Wu; Emiko A MacKillop; Karl G Linden
Journal:  Environ Health Perspect       Date:  2008-09-09       Impact factor: 9.031

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