Literature DB >> 8027929

The disposition of thioperamide, a histamine H3-receptor antagonist, in rats.

E Sakurai1, E Gunji, Y Iizuka, N Hikichi, K Maeyama, T Watanabe.   

Abstract

An HPLC method using an ovomucoid-conjugated column has been developed for measurement of thioperamide, a histamine H3 antagonist, with a minimum quantitation limit of 0.05 micrograms mL-1. The assay was used to study the disposition of thioperamide in rats. After bolus intravenous administration of thioperamide (10 mg kg-1), the plasma concentration decreased monoexponentially with a half-life of 26.9 min. The apparent total body clearance of thioperamide from rat plasma was 74.6 mL min-1 kg-1. Although thioperamide was quickly transferred to various tissues, its concentrations in peripheral tissues were higher than that in the brain. However, the brain regional tissue/plasma ratios of thioperamide increased continuously after its injection.

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Year:  1994        PMID: 8027929     DOI: 10.1111/j.2042-7158.1994.tb03780.x

Source DB:  PubMed          Journal:  J Pharm Pharmacol        ISSN: 0022-3573            Impact factor:   3.765


  4 in total

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3.  Antinociceptive activity of furan-containing congeners of improgan and ranitidine.

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Journal:  Bioorg Med Chem Lett       Date:  2007-08-19       Impact factor: 2.823

4.  Striatal histamine mechanism in the pathogenesis of restless legs syndrome.

Authors:  Yuan-Yang Lai; Kung-Chiao Hsieh; Yu-Hsuan Cheng; Keng-Tee Chew; Darian Nguyen; Lalini Ramanathan; Jerome M Siegel
Journal:  Sleep       Date:  2020-02-13       Impact factor: 6.313

  4 in total

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