Chondroitin
Sulfates
G.
Douglas Andersen, DC, DACBSP, CCN
Volume
16, number 10, 5/4/98, page 22
My first article on chondroitin sulfate. It includes a definition, a discussion
about absorption, research supporting it, and my recommendations at the
time. Please note that this was written prior to the studies I reviewed
the following year in my article “Chondroitin Sulfate Research Update
1999.”
Depending on your point of view, chondroitin sulfates (CSs) can be defined
in two ways. Internally, they are one of six glycosaminoglycans (GAGs),
formerly known as mucopolysaccharides. CSs are composed of an amino sugar,
galactosamine (the immediate precursor of which is glucosamine), and a
sugar acid, glucuronic acid. CSs are long chains of repeating disaccharides
that are sulfated. The sulfated GAGs, chondroitin, keratan, and dermatan,
have negative charges, causing them to repel each other and attract water,
which in turn fills space in three dimensions and enable cartilage to
absorb shock. The chains of CS are much longer than the other sulfated
GAGs. This is one of the reasons some scientists feel it is the most important
GAG. The second way CS can be defined is as a dietary supplement in a
new category called chondroprotective nutraceuticals. There has been a
great deal of publicity about the potential of chondroprotective nutraceuticals
to stimulate the body to heal arthritis.
Functions
CS, when taken orally, theoretically stimulates chondrocytes to produce
more glycosaminoglycans and proteoglycans in the connective tissues. When
this occurs in arthritic joints, the symptoms of pain and dysfunction
decrease. Culture studies in the laboratory have shown that when CS was
added to cartilage and chondrocyte cell cultures, production and secretion
of proteoglycans was enhanced.1,2
Absorption
Oral absorption of CS has been a controversial topic within the nutritional
community. Many researchers feel that due to the size of the CS molecule
(which is many times larger than the glucosamine molecule), intact absorption
is impossible. They further feel that the fragments that are absorbed
do not have significant biologic effects. When compared to the glucosamine
molecule, the percentage of CS that is absorbed is considerably less.
Glucosamine, when taken in the sulfate or hydrochloride form, has an absorption
profile of 90-98% in humans.3 In contrast, Murray cites three European
studies, the best of which showed that purified, pharmaceutical grade
CS had only a 13% absorption rate when ingested orally by humans.
Morrison, a cardiovascular researcher in Loma Linda, California, worked
extensively with CS in the treatment of heart disease. In one study, 120
patients were divided into two groups of 60 subjects each. Each group
received traditional allopathic care, but one group also took 1500 mg
a day of CS for 4 (?) years, and then 750 mg for another 18 months. After
six years, four people in the CS group had died, compared to 13 in the
nontreated group. Most impressive was the finding that only six people
in the chondroitin-treated group had acute cardiac incidents over the
six-year period, while 42 patients in the group that did not receive CS
had acute events. Although this was not a direct absorption study, it
was obvious (in this study) that moderate amounts of oral CSs had significant
biological effects in humans. Bucci4 is convinced that, when in their
purified form, CS are absorbed by humans in various chain links. He notes
that the human gut contains specific enzymes (known as chondroitinases)
which are able to digest glycosaminoglycans.
Human Studies
The vast majority of positive studies using CS for patients suffering
from arthritis and connective tissue dysfunction have been done with injectable
forms. Theodosakis et al5 describe a study performed in Europe in the
mid 1980s, when 50 patients were given 800-1200 mg of CS orally or 500
mg of a pain medication for three months. The study compared cartilage
tissue samples at the beginning and the end of the three-month period
and found that the chondroitin group showed marked cartilage regeneration
when the pre- and post-study samples were compared. No such improvement
was found in the pain medication group.6
Recommendations
When comparing the scientific literature on absorption and positive human
trials of CS to glucosamine, glucosamine is far and away superior to CS.
Remember that glucosamine is a precursor to chondroitin, so by taking
glucosamine, the production of CS will be increased. However, the interest
in CS has begun to climb with Luke Bucci's 1995 book, Pain-Free,7
and really took off with Dr. Theodosakis's 1997 book, Arthritis Cure.7
Both authors felt that purified CS could benefit connective tissue when
taken orally in adequate amounts. Hopefully, the publicity garnered from
these books will stimulate more research on CS, both alone and in concert
with glucosamine. For patients with limited funds, the choice between
using CS and glucosamine is a no-brainer. Go for the glucosamine. However,
if funds are available, oral CS is certainly nontoxic to humans and may
be of benefit. Dosing for CSs is approximately 8 mg per pound of body
weight for four to six weeks. If the patient feels no subjective difference,
discontinue. If the patient has benefitted, gradually reduce the dose
to the minimum amount required to control symptoms.
There is one final problem with CS, and that is quality control. There
are very few companies that market a purified product that patients can
purchase over the counter. There is currently ongoing research being conducted
out of the University of Maryland School of Pharmacy analyzing the purity
of many brands of CS and glucosamine. At this time the only health-food
store brand I recommend is from Twin Labs. However, there are brands of
purified CS available from nutrition companies that service healthcare
professionals. Hopefully, these companies will donate product (and look-alike
placebos) to the chiropractic and naturopathic colleges for research purposes,
which will be enthusiastically reported in this column. I also encourage
these companies to submit samples to the University of Maryland for independent
purity certification.
Resources
1. Bollet, A.J. Stimulation of protein chondroitin sulfate synthesis by
normal and osteoarthritic articular cartilage. Arthritis and Rheumatism,
1968, 11:663.
2. Schwartz and Dorfman. Stimulation of chondroitin sulfate proteoglycan
production by chondrocytes in monolayer. 3.Connective Tissue Research,
1975, 3:115.
3. Murray, Michael T. Glucosamine sulfate versus chondroitin sulfate.
American Journal of Natural Medicine, 4(4):7, May 1997.
4. Bucci, L. Nutrition Applied to Injury Rehabilitation in Sports Medicine.
CRC Press. 1995.
5. Theodosakis, Adderly, and Fox. The Arthritis Cure. New York: St. Martin's
Press. 1997.
6. Pipitone. Chondroprotection with chondroitin sulfate. Drugs in Experimental
and Clinical Research, 17(1):3-7. 1991.
7. Bucci, Luke R. Pain-Free. Ft. Worth, Texas: The Summit Group. 1995.
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