Literature DB >> 7771652

Ethanol's effect on tissue polyamines and ornithine decarboxylase activity: a concise review.

I A Shibley1, M D Gavigan, S N Pennington.   

Abstract

An extraordinarily diverse literature describes the cellular/tissue systems in which the molecular effects of both acute and chronic alcohol exposure seem to be mediated by changes in polyamine levels and/or ornithine decarboxylase (ODC) activity. The single unifying factor that links most of these studies is that they all, in some way, involve tissues that are undergoing relatively rapid cell division. Non-dividing cells expressing the NMDA receptor are a notable exception in that ethanol and the polyamines seem to act via discrete regions of that receptor. Under most cellular conditions, ODC activity is a reflection of the relative tissue polyamine content, and an increase in ODC activity and polyamine content seems to be one of the early events in the progression of quiescent cells toward cell division. Thus, it is not surprising that ethanol, which has been widely reported to delay cell division, should be found to interact with the ODC/polyamine pathway. Perhaps the most unique aspect of these studies is the fact that, with rare exception, both acute and chronic ethanol exposure have been found to slow growth and to lower tissue polyamine (putrescine) content. Furthermore, in most studies, the ethanol-induced suppression of cell division could be overcome by the administration of exogenous putrescine. These data suggest that the ethanol-induced suppression of cell division resulted from the loss of putrescine. In addition, because the cells were able to respond to the exogenous putrescine, the studies suggest that the signaling pathway remained intact beyond the polyamine synthesis step.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1995        PMID: 7771652     DOI: 10.1111/j.1530-0277.1995.tb01494.x

Source DB:  PubMed          Journal:  Alcohol Clin Exp Res        ISSN: 0145-6008            Impact factor:   3.455


  6 in total

1.  Metabolic biomarkers of prenatal alcohol exposure in human embryonic stem cell-derived neural lineages.

Authors:  Jessica A Palmer; Ashley M Poenitzsch; Susan M Smith; Kevin R Conard; Paul R West; Gabriela G Cezar
Journal:  Alcohol Clin Exp Res       Date:  2012-02-10       Impact factor: 3.455

2.  Agmatine reduces balance deficits in a rat model of third trimester binge-like ethanol exposure.

Authors:  B Lewis; K A Wellmann; S Barron
Journal:  Pharmacol Biochem Behav       Date:  2007-07-25       Impact factor: 3.533

3.  Difluoromethylornithine (DFMO) reduces deficits in isolation-induced ultrasonic vocalizations and balance following neonatal ethanol exposure in rats.

Authors:  Maribel A Rubin; Kristen A Wellmann; Ben Lewis; Ben J Overgaauw; John M Littleton; Susan Barron
Journal:  Pharmacol Biochem Behav       Date:  2008-10-25       Impact factor: 3.533

4.  Agmatine reduces ultrasonic vocalization deficits in female rat pups exposed neonatally to ethanol.

Authors:  Kristen Wellmann; Ben Lewis; Susan Barron
Journal:  Neurotoxicol Teratol       Date:  2009-11-27       Impact factor: 3.763

5.  A screen of zebrafish mutants identifies ethanol-sensitive genetic loci.

Authors:  Mary E Swartz; Michael B Wells; Melissa Griffin; Neil McCarthy; Charles B Lovely; Patrick McGurk; Jenna Rozacky; Johann K Eberhart
Journal:  Alcohol Clin Exp Res       Date:  2013-10-24       Impact factor: 3.455

Review 6.  Transglutaminase 2 has opposing roles in the regulation of cellular functions as well as cell growth and death.

Authors:  H Tatsukawa; Y Furutani; K Hitomi; S Kojima
Journal:  Cell Death Dis       Date:  2016-06-02       Impact factor: 8.469

  6 in total

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