Literature DB >> 3386776

Biotin transport and metabolism in the central nervous system.

R Spector1, D M Mock.   

Abstract

The mechanisms by which biotin enters and leaves brain, choroid plexus and cerebrospinal fluid (CSF) were investigated by injecting [3H]biotin either intravenously or intraventricularly into adult rabbits. [3H] biotin, either alone or together with unlabeled biotin was infused at a constant rate into conscious rabbits. At 180 minutes, [3H]biotin had entered CSF, choroid plexus, and brain. In brain, CSF, and plasma, greater than 90% of the nonvolatile 3H was associated with [3H]biotin. The addition of 400 mumol/kg unlabeled biotin to the infusion syringe decreased the penetration of [3H]biotin into brain and CSF by approximately 70 percent. Two hours after an intraventricular injection, [3H]biotin was cleared from the CSF more rapidly than mannitol and minimal metabolism of the [3H]biotin had occurred in brain. However, 18 hours after an intraventricular injection, approximately 35% of the [3H]biotin remaining in brain had been covalently incorporated into proteins, presumably into carboxylase apoenzymes. These results show that biotin enters CSF and brain by saturable transport systems that do not depend on metabolism of the biotin. However, [3H]biotin is very slowly incorporated covalently into proteins in brain in vivo.

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Year:  1988        PMID: 3386776     DOI: 10.1007/bf00971535

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  16 in total

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Journal:  J Neurochem       Date:  1979-10       Impact factor: 5.372

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Authors:  R Spector
Journal:  Am J Physiol       Date:  1986-02

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Authors:  D M Mock; D B DuBois
Journal:  Anal Biochem       Date:  1986-03       Impact factor: 3.365

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Journal:  J Nutr       Date:  1972-11       Impact factor: 4.798

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Authors:  H N Bhagavan; D B Coursin
Journal:  J Neurochem       Date:  1970-02       Impact factor: 5.372

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Authors:  R Spector
Journal:  J Neurochem       Date:  1980-11       Impact factor: 5.372

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Authors:  R Spector; C Sivesind; D Kinzenbaw
Journal:  J Neurochem       Date:  1986-09       Impact factor: 5.372

9.  Neurologic symptoms of biotinidase deficiency: possible explanation.

Authors:  S F Suchy; J S McVoy; B Wolf
Journal:  Neurology       Date:  1985-10       Impact factor: 9.910

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Authors:  J E Sander; S Packman; J J Townsend
Journal:  Neurology       Date:  1982-08       Impact factor: 9.910

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  9 in total

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Authors:  Paul Hoerbelt; Julia W Nalwalk; James G Phillips; Mark P Wentland; Zhixing Shan; Lindsay B Hough
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4.  Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD).

Authors:  Shanti Balasubramaniam; B Lewis; D M Mock; H M Said; M Tarailo-Graovac; A Mattman; C D van Karnebeek; D R Thorburn; R J Rodenburg; J Christodoulou
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5.  Na(+)-dependent biotin transport into brush-border membrane vesicles from human kidney cortex.

Authors:  B Baur; E R Baumgartner
Journal:  Pflugers Arch       Date:  1993-02       Impact factor: 3.657

6.  Management of a patient with holocarboxylase synthetase deficiency.

Authors:  Johan L K Van Hove; Sagi Josefsberg; Cynthia Freehauf; Janet A Thomas; Le Phuc Thuy; Bruce A Barshop; Michael Woontner; Donald M Mock; Pei-Wen Chiang; Elaine Spector; Iván Meneses-Morales; Rafael Cervantes-Roldán; Alfonso León-Del-Río
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8.  Analysis of biotinylated generation 4 poly(amidoamine) (PAMAM) dendrimer distribution in the rat brain and toxicity in a cellular model of the blood-brain barrier.

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9.  The Effect of Biotinylated PAMAM G3 Dendrimers Conjugated with COX-2 Inhibitor (celecoxib) and PPARγ Agonist (Fmoc-L-Leucine) on Human Normal Fibroblasts, Immortalized Keratinocytes and Glioma Cells in Vitro.

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