Disposition of exogenous tritium-labelled GM1lactone in the rat.

Abstract:

:The disposition of labelled [3H]GM1lactone, the inner ester of ganglioside GM1, was studied in the rat. After i.v. administration [3H]GM1lactone was quickly converted to its corresponding open form most likely by plasma esterases, and then displayed a pharmacokinetic profile identical to [3H]GM1. Following intramuscular administration of [3H]GM1lactone [3H]GM1 levels in plasma and in tissues were higher than those obtained after the administration of an equivalent dose of [3H]GM1. This increased bioavailability means that GM1lactone can be considered as a potential prodrug of GM1.

journal_name

Neurochem Int

authors

Bellato P,Milan F,Facchinetti E,Toffano G

doi

10.1016/0197-0186(92)90050-2

subject

Has Abstract

pub_date

1992-04-01 00:00:00

pages

359-64

issue

3

eissn

0197-0186

issn

1872-9754

journal_volume

20

pub_type

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