Effects of betaine on lipopolysaccharide-induced memory impairment in mice and the involvement of GABA transporter 2

<p>Abstract</p> <p>Background</p> <p>Betaine (glycine betaine or trimethylglycine) plays important roles as an osmolyte and a methyl donor in animals. While betaine is reported to suppress expression of proinflammatory molecules and reduce oxidative stress in aged rat k...

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Main Authors: Miwa Masaya, Tsuboi Mizuki, Noguchi Yumiko, Enokishima Aoi, Nabeshima Toshitaka, Hiramatsu Masayuki
Format: Article
Language:English
Published: BMC 2011-11-01
Series:Journal of Neuroinflammation
Online Access:http://www.jneuroinflammation.com/content/8/1/153
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author Miwa Masaya
Tsuboi Mizuki
Noguchi Yumiko
Enokishima Aoi
Nabeshima Toshitaka
Hiramatsu Masayuki
author_facet Miwa Masaya
Tsuboi Mizuki
Noguchi Yumiko
Enokishima Aoi
Nabeshima Toshitaka
Hiramatsu Masayuki
author_sort Miwa Masaya
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Betaine (glycine betaine or trimethylglycine) plays important roles as an osmolyte and a methyl donor in animals. While betaine is reported to suppress expression of proinflammatory molecules and reduce oxidative stress in aged rat kidney, the effects of betaine on the central nervous system are not well known. In this study, we investigated the effects of betaine on lipopolysaccharide (LPS)-induced memory impairment and on mRNA expression levels of proinflammatory molecules, glial markers, and GABA transporter 2 (GAT2), a betaine/GABA transporter.</p> <p>Methods</p> <p>Mice were continuously treated with betaine for 13 days starting 1 day before they were injected with LPS, or received subacute or acute administration of betaine shortly before or after LPS injection. Then, their memory function was evaluated using Y-maze and novel object recognition tests 7 and 10-12 days after LPS injection (30 μg/mouse, i.c.v.), respectively. In addition, mRNA expression levels in hippocampus were measured by real-time RT-PCR at different time points.</p> <p>Results</p> <p>Repeated administration of betaine (0.163 mmol/kg, s.c.) prevented LPS-induced memory impairment. GAT2 mRNA levels were significantly increased in hippocampus 24 hr after LPS injection, and administration of betaine blocked this increase. However, betaine did not affect LPS-induced increases in levels of mRNA related to inflammatory responses. Both subacute administration (1 hr before, and 1 and 24 hr after LPS injection) and acute administration (1 hr after LPS injection) of betaine also prevented LPS-induced memory impairment in the Y-maze test.</p> <p>Conclusions</p> <p>These data suggest that betaine has protective effects against LPS-induced memory impairment and that prevention of LPS-induced changes in GAT2 mRNA expression is crucial to this ameliorating effect.</p>
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spelling doaj.art-03296b32222147cfa8571b651fb0c2c52022-12-22T02:55:12ZengBMCJournal of Neuroinflammation1742-20942011-11-018115310.1186/1742-2094-8-153Effects of betaine on lipopolysaccharide-induced memory impairment in mice and the involvement of GABA transporter 2Miwa MasayaTsuboi MizukiNoguchi YumikoEnokishima AoiNabeshima ToshitakaHiramatsu Masayuki<p>Abstract</p> <p>Background</p> <p>Betaine (glycine betaine or trimethylglycine) plays important roles as an osmolyte and a methyl donor in animals. While betaine is reported to suppress expression of proinflammatory molecules and reduce oxidative stress in aged rat kidney, the effects of betaine on the central nervous system are not well known. In this study, we investigated the effects of betaine on lipopolysaccharide (LPS)-induced memory impairment and on mRNA expression levels of proinflammatory molecules, glial markers, and GABA transporter 2 (GAT2), a betaine/GABA transporter.</p> <p>Methods</p> <p>Mice were continuously treated with betaine for 13 days starting 1 day before they were injected with LPS, or received subacute or acute administration of betaine shortly before or after LPS injection. Then, their memory function was evaluated using Y-maze and novel object recognition tests 7 and 10-12 days after LPS injection (30 μg/mouse, i.c.v.), respectively. In addition, mRNA expression levels in hippocampus were measured by real-time RT-PCR at different time points.</p> <p>Results</p> <p>Repeated administration of betaine (0.163 mmol/kg, s.c.) prevented LPS-induced memory impairment. GAT2 mRNA levels were significantly increased in hippocampus 24 hr after LPS injection, and administration of betaine blocked this increase. However, betaine did not affect LPS-induced increases in levels of mRNA related to inflammatory responses. Both subacute administration (1 hr before, and 1 and 24 hr after LPS injection) and acute administration (1 hr after LPS injection) of betaine also prevented LPS-induced memory impairment in the Y-maze test.</p> <p>Conclusions</p> <p>These data suggest that betaine has protective effects against LPS-induced memory impairment and that prevention of LPS-induced changes in GAT2 mRNA expression is crucial to this ameliorating effect.</p>http://www.jneuroinflammation.com/content/8/1/153
spellingShingle Miwa Masaya
Tsuboi Mizuki
Noguchi Yumiko
Enokishima Aoi
Nabeshima Toshitaka
Hiramatsu Masayuki
Effects of betaine on lipopolysaccharide-induced memory impairment in mice and the involvement of GABA transporter 2
Journal of Neuroinflammation
title Effects of betaine on lipopolysaccharide-induced memory impairment in mice and the involvement of GABA transporter 2
title_full Effects of betaine on lipopolysaccharide-induced memory impairment in mice and the involvement of GABA transporter 2
title_fullStr Effects of betaine on lipopolysaccharide-induced memory impairment in mice and the involvement of GABA transporter 2
title_full_unstemmed Effects of betaine on lipopolysaccharide-induced memory impairment in mice and the involvement of GABA transporter 2
title_short Effects of betaine on lipopolysaccharide-induced memory impairment in mice and the involvement of GABA transporter 2
title_sort effects of betaine on lipopolysaccharide induced memory impairment in mice and the involvement of gaba transporter 2
url http://www.jneuroinflammation.com/content/8/1/153
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