Literature DB >> 3594257

Nervous tissue thiamine metabolism in vivo. III. Influence of ethanol intake on the dynamics of thiamine and its phosphoesters in different brain regions and sciatic nerve of the rat.

G Rindi, V Comincioli, C Reggiani, C Patrini.   

Abstract

The effects of chronic ethanol administration on different steps of the metabolism of thiamine (T), thiamine mono- (TMP) and thiamine pyrophosphate (TPP) in the cerebellum, brainstem, cerebral cortex and sciatic nerve were evaluated in vivo. The radioactivity of T and its phosphoesters was determined in plasma and in the selected nervous structures under steady-state conditions and at fixed time intervals (0.5-192 h) after an i.p. injection of [14C]T (30 micrograms: 1.25 microCi) to rats chronically (35 days) ethanol-treated (daily dose of 4.7 g X kg-1 b.wt. by gastric gavage) and pair-fed controls similarly treated with a sucrose solution isoenergetic with ethanol. All rats were given a nutritionally adequate diet supplying an excess of thiamine, which produced a virtually steady content of thiamine compounds in the tissues. By using a compartmental mathematical model, fractional rate constants, turnover rates and turnover times were calculated. Ethanol caused a reduction of the rate of thiamine compound enzymatic transformations (T phosphorylation to TPP, TPP dephosphorylation to TMP and TMP to T), and a facilitation of the regional uptake of T and TMP, associated to a less relevant influence on their release. Isoenergetic sucrose prevailingly caused an increased rate of thiamine metabolic steps (except phosphorylation in the brainstem and cerebral cortex), with negligible modifications of T and TMP uptake and release. Thus the changes induced by ethanol were virtually opposite to those caused by sucrose.

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Year:  1987        PMID: 3594257     DOI: 10.1016/0006-8993(87)90150-8

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  8 in total

1.  Can megadoses of thiamine prevent ethanol-induced damages of rat hippocampal CA1 pyramidal neurones?

Authors:  S Wenisch; T Steinmetz; B Fortmann; R Leiser; I Bitsch
Journal:  Z Ernahrungswiss       Date:  1996-09

2.  Thiamine pyrophosphate-dependent and thiamine metabolizing enzymes in the deafferented cerebellum and in the intact cerebral cortex of rat.

Authors:  C Patrini; A Nauti; G Rindi
Journal:  Metab Brain Dis       Date:  1998-03       Impact factor: 3.584

Review 3.  Pathogenesis of alcoholic peripheral neuropathy: direct effect of ethanol or nutritional deficit?

Authors:  M L D'Amour; R F Butterworth
Journal:  Metab Brain Dis       Date:  1994-06       Impact factor: 3.584

Review 4.  Alcohol-related peripheral neuropathy: nutritional, toxic, or both?

Authors:  Michelle Mellion; James M Gilchrist; Suzanne de la Monte
Journal:  Muscle Nerve       Date:  2011-03       Impact factor: 3.217

5.  Experimental model of alcohol-related peripheral neuropathy.

Authors:  Michelle L Mellion; Vananh Nguyen; Ming Tong; James Gilchrist; Suzanne De La Monte
Journal:  Muscle Nerve       Date:  2013-06-13       Impact factor: 3.217

6.  Three thiamine analogues differently alter thiamine transport and metabolism in nervous tissue: an in vivo kinetic study using rats.

Authors:  G Rindi; C Patrini; A Nauti; R Bellazzi; P Magni
Journal:  Metab Brain Dis       Date:  2003-12       Impact factor: 3.584

7.  Experimental alcohol-related peripheral neuropathy: role of insulin/IGF resistance.

Authors:  Van Anh Nguyen; Tran Le; Ming Tong; Michelle Mellion; James Gilchrist; Suzanne M de la Monte
Journal:  Nutrients       Date:  2012-08-17       Impact factor: 5.717

8.  Compartmental model identification based on an empirical Bayesian approach: the case of thiamine kinetics in rats.

Authors:  P Magni; R Bellazzi; A Nauti; C Patrini; G Rindi
Journal:  Med Biol Eng Comput       Date:  2001-11       Impact factor: 3.079

  8 in total

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