Abstract

Glucosamine is a naturally occurring derivative of glucose and is an essential component of glycoproteins and proteoglycans, important constituents of many eukaryotic proteins. In cells, glucosamine is produced enzymatically by the amidation of glucose 6-phosphate and can then be further modified by acetylation to result in N-acetylglucosamine. Commercially, glucosamine is sold over-the-counter to relieve arthritis. Although there is evidence in favor of the beneficial effects of glucosamine, the mechanism is unknown. Our data demonstrate that glucosamine suppresses the activation of T-lymphoblasts and dendritic cells in vitro as well as allogeneic mixed leukocyte reactivity in a dose-dependent manner. There was no inherent cellular toxicity involved in the inhibition, and the activity was not reproducible with other amine sugars. More importantly, glucosamine administration prolonged allogeneic cardiac allograft survival in vivo. We conclude that, despite its documented effects on insulin sensitivity, glucosamine possesses immunosuppressive activity and could be beneficial as an immunosuppressive agent.

Highlights

  • Glucosamine is a naturally occurring sugar that is synthesized by virtually all cells

  • The results demonstrate that glucosamine inhibited NFAT-dependent transcription stimulated by phorbol 12-myristate 13-acetate (PMA) and ionomycin at similar levels compared with cyclosporin

  • To control for potential nonspecific effects of glucosamine, we examined the effects of other aminated sugars on IL-2 production by Jurkat T-cells in response to PMA and ionomycin

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Summary

Immunosuppressive Effects of Glucosamine*

Despite its documented effects on insulin sensitivity, glucosamine possesses immunosuppressive activity and could be beneficial as an immunosuppressive agent. Glucosamine has been shown to modulate the effects of insulin and glucose on pyruvate kinase [34], glycogen synthase [33, 34], and transforming. A single daily intravenous injection of glucosamine was able to prolong cardiac allograft survival in mice Based on these data, we suggest that glucosamine alone or in its different formulations could be considered as a novel immunosuppressive agent with potential clinical utility

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