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Galactosamine-induced sensitization to the lethal effects of endotoxin.

Open access
Galanos, C, Freudenberg, M A, Reutter, W·1979·Proceedings of the National Academy of Sciences

Abstract

Treatment of rabbits, rats, and mice with D-galactosamine increased their sensitivity to the lethal effects of lipopolysaccharide several thousand fold. The susceptibility of the animals was highest when the lipopolysaccharide was injected together with galactosamine and decreased successively when injection was carried out 1, 2, and 3 hr later. Sensitization was absent when the lipopolysaccharide was administered 1 hr before or 4 hr after galactosamine. The onset of lethality after treatment with galactosamine and lipopolysaccharide occurred faster than with lipopolysaccharide alone; usually all animals died 5-9 hr later. The galactosamine-induced sensitization to lipopolysaccharide could be reversed by uridine which is known to inhibit the early biochemical alterations induced by the amino sugar in the hepatocytes. Although galactosamine is known to exhibit hepatotoxic activity inducing ultimate necrosis of the hepatocytes, the data so far suggests that the sensitization to lipopolysaccharide is related only to the early metabolic effects of the hexosamine.

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Metadata

Authors
Galanos, C., Freudenberg, M. A., & Reutter, W.
Venue
Proceedings of the National Academy of Sciences
Published
1979-11
Volume
76
Issue
11
Pages
5939-5943
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2092289140
Cited by
929
References
0
FWCI
1.26
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Galactosamine-induced sensitization to the lethal effects of endotoxin. https://app.cochat.ai/papers/10.1073/pnas.76.11.5939
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Galanos, C., Freudenberg, M. A., & Reutter, W. (1979). Galactosamine-induced sensitization to the lethal effects of endotoxin. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.76.11.5939

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.