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Glucosamine- Like Supplement Inhibits MS and Type 1 Diabetes
Glucosamine-Like Supplement Inhibits MS and Type 1 Diabetes
Source May 31, 2007 University of California
A glucosamine-like dietary supplement has been found to suppress the damaging autoimmune response seen in
multiple sclerosis and type 1 diabetes mellitus, according to University of California, Irvine health sciences
researchers.
In studies on mice, Dr. Michael Demetriou and colleagues with the UC Irvine Center for Immunology found that
N-acetylglucosamine (GlcNAc), which is similar but more effective than the widely available glucosamine, inhibited
the growth and function of abnormal T-cells that incorrectly direct the immune system to attack specific tissues in
the body, such as brain myelin in MS and insulin-producing cells of the pancreas in diabetes. Study results
appear on the online version of the Journal of Biological Chemistry.
"This finding shows the potential of using a dietary supplement to help treat autoimmune diseases," said
Demetriou, an assistant professor of neurology, and microbiology and molecular genetics. "Most importantly, we
understand how this sugar-based supplement inhibits the cells that attack the body, making metabolic therapy a
rational approach to prevent or treat these debilitating diseases."
The UC Irvine study defines how metabolic therapy with the sugar GlcNAc and other related nutrients modifies
the growth and autoimmune activitiy of T-cells. Virtually all proteins on the surface of cells, including T-cells, are
modified with complex sugars of variable lengths and composition. Recent studies have shown that changes in
these sugars are often associated with T-cell hyperactivity and autoimmune disease.
In mouse models of both MS and type 1 diabetes, Demetriou and colleages found that GlcNAc prevented this
hyperactivity and autoimmune response by increasing sugar modifications to the T-cell proteins. This therapy
normalized T-cell function and prevented development of paralysis in MS and high blood glucose levels in type 1
diabetes.
This study comes on the heels of others showing the potential of GlcNAc in humans. One previous clinical study
reported that 8 of 12 children with treatment-resistant autoimmune inflammatory bowel disease improved
significantly following two years of treatment with GlcNAc. No significant adverse side effects were noted.
"Together, these findings identify metabolic therapy using dietary supplements such as GlcNAc as potential
treatments for autoimmune diseases." Demetriou said. "Excitement for this treatment strategy stems from the
novel mechanism for affecting T-cell function and autoimmunity and the availability and simplicity of its use.
However, additional studies in humans will be required to assess the full potential of this therapeutic approach."
Autoimmune diseases such as MS and type 1 diabetes mellitus result from poorly understood interactions
between inherited genetic risk and environmental exposure. MS results in neurological dysfunction, while
uncontrolled blood glucose in type 1 diabetes can lead to damage of multiple organs.
Ani Grigorian, Sung-Uk Lee, Wenqiang Tian, I-Ju Chen and Guoyan Gao of UC Irvine and Richard Mendelsohn
and James W. Dennis of the Samuel Lunenfeld Research Institute in Toronto participated in the study, which was
funded by the National Institutes of Health, the National Multiple Sclerosis Society, the Juvenile Diabetes
Research Foundation, the Wadsworth Foundation and the Canadian Institutes for Health Research.
About the University of California, Irvine: The University of California, Irvine is a top-ranked university dedicated
to research, scholarship and community service. Founded in 1965, UCI is among the fastest-growing University
of California campuses, with more than 25,000 undergraduate and graduate students and about 1,800 faculty
members. The second-largest employer in dynamic Orange County, UCI contributes an annual economic impact
of $3.7 billion. For more UCI news, visit www.today.uci.edu
Source May 31, 2007 University of California
A glucosamine-like dietary supplement has been found to suppress the damaging autoimmune response seen in
multiple sclerosis and type 1 diabetes mellitus, according to University of California, Irvine health sciences
researchers.
In studies on mice, Dr. Michael Demetriou and colleagues with the UC Irvine Center for Immunology found that
N-acetylglucosamine (GlcNAc), which is similar but more effective than the widely available glucosamine, inhibited
the growth and function of abnormal T-cells that incorrectly direct the immune system to attack specific tissues in
the body, such as brain myelin in MS and insulin-producing cells of the pancreas in diabetes. Study results
appear on the online version of the Journal of Biological Chemistry.
"This finding shows the potential of using a dietary supplement to help treat autoimmune diseases," said
Demetriou, an assistant professor of neurology, and microbiology and molecular genetics. "Most importantly, we
understand how this sugar-based supplement inhibits the cells that attack the body, making metabolic therapy a
rational approach to prevent or treat these debilitating diseases."
The UC Irvine study defines how metabolic therapy with the sugar GlcNAc and other related nutrients modifies
the growth and autoimmune activitiy of T-cells. Virtually all proteins on the surface of cells, including T-cells, are
modified with complex sugars of variable lengths and composition. Recent studies have shown that changes in
these sugars are often associated with T-cell hyperactivity and autoimmune disease.
In mouse models of both MS and type 1 diabetes, Demetriou and colleages found that GlcNAc prevented this
hyperactivity and autoimmune response by increasing sugar modifications to the T-cell proteins. This therapy
normalized T-cell function and prevented development of paralysis in MS and high blood glucose levels in type 1
diabetes.
This study comes on the heels of others showing the potential of GlcNAc in humans. One previous clinical study
reported that 8 of 12 children with treatment-resistant autoimmune inflammatory bowel disease improved
significantly following two years of treatment with GlcNAc. No significant adverse side effects were noted.
"Together, these findings identify metabolic therapy using dietary supplements such as GlcNAc as potential
treatments for autoimmune diseases." Demetriou said. "Excitement for this treatment strategy stems from the
novel mechanism for affecting T-cell function and autoimmunity and the availability and simplicity of its use.
However, additional studies in humans will be required to assess the full potential of this therapeutic approach."
Autoimmune diseases such as MS and type 1 diabetes mellitus result from poorly understood interactions
between inherited genetic risk and environmental exposure. MS results in neurological dysfunction, while
uncontrolled blood glucose in type 1 diabetes can lead to damage of multiple organs.
Ani Grigorian, Sung-Uk Lee, Wenqiang Tian, I-Ju Chen and Guoyan Gao of UC Irvine and Richard Mendelsohn
and James W. Dennis of the Samuel Lunenfeld Research Institute in Toronto participated in the study, which was
funded by the National Institutes of Health, the National Multiple Sclerosis Society, the Juvenile Diabetes
Research Foundation, the Wadsworth Foundation and the Canadian Institutes for Health Research.
About the University of California, Irvine: The University of California, Irvine is a top-ranked university dedicated
to research, scholarship and community service. Founded in 1965, UCI is among the fastest-growing University
of California campuses, with more than 25,000 undergraduate and graduate students and about 1,800 faculty
members. The second-largest employer in dynamic Orange County, UCI contributes an annual economic impact
of $3.7 billion. For more UCI news, visit www.today.uci.edu