*Biocell Collagen
II® (extracted from chicken sternal cartilage)
(Biocell collagen II does not contain hormones, steroids, antibiotics,
or pesticides.)
What is Collagen and It’s Importance
in Joint Health?
Collagen is a protein that makes up about 25% of the protein found in
the human body.1, 2, 3, 4 There are 14 different types
of collagen and collagen II is the most predominant.2, 3, 4
It’s important to the structural integrity of connective tissue located
throughout the body especially bone, cartilage, tendons, and ligaments.
If collagen production declines or if it should become defective, this
would result in weakened connective tissue contributing to weakened
bone, cartilage, tendons, and ligaments, all important structural components
critical to healthy joint function. An example of how important collagen
II is to the health of the joint, we find that collagen makes up about
50% to 60% of the dry weight of articular cartilage with collagen II
consisting of about 90% to 98% of the total tissue collagen.5,
6 Maintaining the health and production of collagen II will
result in stronger and more resilient connective tissue. In turn, the
bone, cartilage, tendons, and ligaments will be healthy and resilient
as well.
Free Radicals Contribute to Joint
Damage
One factor that contributes to the destruction of the joint is free
radical damage. Whenever oxygen rich synovial fluid goes back into the
cartilage cells the oxygen component generates free radicals.7
Unless these free radicals are neutralized, they will attack and degrade
the cartilage and the lining of the joint - the synovial membrane which
produces the lubricating fluid. Also, hyaluronan, found in the synovial
fluid, important to its lubricating effectiveness, is degraded.7
This attack on hyaluronan and the synovial membrane will reduce the
ability of the synovial fluid to lubricate the joint causing painful
inflammation, swelling, and further deterioration.
When the cartilage matrix becomes defective,
more chondrocytes are produced in an effort to restore normal structural
integrity.8 The result is an overproduction of collagen
II and mucopolysaccaharides causing the influx of too much water resulting
in the washing away of these important structural components.8,
9 With less collagen II and mucopolysaccaharides the once dense
cartilage matrix loses its ability to hold water. The cartilage begins
to dry, making it easy to damage, and if not corrected will wear away
very quickly. Also, the chondrocytes may begin to produce higher than
normal levels of collagen dissolving enzymes.9 The
destruction of collagen II will result in the destruction of the cartilage
since collagen II is the primary collagen and backbone of cartilage
which acts as a glue to hold the mucopolysaccaharides throughout the
cartilage matrix. These same collagen destroying enzymes destroy the
mucopolysaccaharides as well.9 Eventually when the
cartilage is completely destroyed and all cushioning is gone, the bones
themselves will begin to wear and show signs of damage causing further
pain and disability.9
Chondrocytes also become destructive when pieces of cartilage are eaten
by synoviocytes (synovial fluid cells within the joint fluid) which
causes these cells to release cytokines that produce inflammation due
to immune cell accumulation at the site of the joint. The chondrocytes
are then reprogrammed by the cytokines causing them to destroy cartilage
cells and left unchecked would eventually destroy the joint.10
Collagen II Re-programs Defective
Chondrocytes, Protects Against Free Radicals,
and Provides the Richest Source of Proteoglycans
Collagen II contains a natural occurring proteoglycan called cartilage
matrix glycoprotein (CMGP) which is able to reprogram the chondrocytes
restoring their normal functions.11 CMGP also acts
as a powerful antioxidant protecting the cartilage from free radicals
when new oxygen rich synovial fluid comes back into the cartilage. CMPG
does this by carrying copper into the chondrocytes where it is needed
to maintain healthy levels of SOD (Super Oxide Dismutase), a powerful
free radical scavenger. SOD protects the joints from the deadly effects
of not only oxygen, but also free radicals which in turn reduces the
inflammation and pain associated with arthritis.11
Also, collagen type ll contains components that are powerful cartilage
digesting enzyme inhibitors that will protect the cartilage.12
Chicken Collagen II, the richest source of naturally occurring proteoglycans
such as glucosamine sulfate, is able to provide the necessary components
essential to restoring the normal collagen and mucopolysaccharide functions
of holding water and producing a normal, dense and resilient cartilage
matrix.13
Collagen II Prevents
New Blood Vessel Formation
In a normal healthy joint there is no blood. Nourishment is accomplished
by diffusion through distant capillary beds and waste removal through
cartilage cells and synovial fluid. If blood vessels form within the
joint capsule or blood leaks in due to an injury, too much oxygen and
other free radicals in the blood would overwhelm the environment causing
massive free radical damage and washing away of collagen and mucopolysaccaharides.
Chicken collagen II contains what are called angiangiogenic substances.
In other words these substances prevent the growth of new blood vessels
preventing the exposure of the delicate joint environment to the hostile
effects of excessive exposure of oxygen and free radicals in the blood.14
Double-Blind Studies Prove Chicken
Collagen II Effective for Rheumatoid Arthritis
Scientific studies have shown when collagen type ll from chicken sternal
cartilage was given to rheumatoid arthritis patients there was a significant
improvement from joint swelling, tenderness, and pain. In one double-blind
study, four patients had a complete resolution of the disease. Scientists
believe these results are produced because of the GALT mechanism, an
abbreviation for "gut activated lymphoid tissue". This GALT
system allows us to eat protein such as beef and chicken, or any foreign
protein, by suppressing the immune response. When the foreign protein
enters the body by the digestive tract, the immune system is programmed
not to attack it. This allows us to eat without becoming violently allergic
to the beef or chicken the second time we eat it. Since the rheumatoid
arthritic patient's own immune system is attacking its own collagen
type ll, scientists have discovered that by orally administering type
ll collagen, the immune system recognizes its own type ll collagen and
ceases to attack it.15
Double-Blind Studies Prove Chicken
Collagen II Effective for Juvenile Rheumatoid Arthritis
1. Title: A pilot trial of oral
type II collagen in the treatment
of juvenile rheumatoid arthritis.
Author
Barnett ML; Combitchi D; Trentham DE
Title: A pilot trial of
oral type II collagen in the treatment of
juvenile rheumatoid arthritis.
Abstract: OBJECTIVE: To evaluate the efficacy of oral
chicken type II collagen (CCII) in the treatment of juvenile rheumatoid
arthritis (JRA). METHODS: Ten patients with active JRA
were treated with CCII for 12 weeks. Efficacy parameters, which included
swollen and tender joint count and score, grip strength, 50-foot walking
time, duration of morning stiffness, and patient and physician global
scores of disease severity, were assessed monthly.
RESULTS: All patients
completed the full course of therapy. Eight patients had reductions
in both swollen and tender joint counts after 3 months of CCII. The
mean changes from baseline in swollen and tender joint counts for the
8 responders at the end of the study were -61% and -54%, respectively.
Mean values for other efficacy parameters also showed improvement from
baseline. There were no adverse events that were considered to be treatment
related. CONCLUSION: Oral CCII
may be a safe and effective therapy for JRA, and its use in this disease
warrants further investigation.16
Excerpts from the Harvard Medical
School article
published in the prestigious journal ScienceSeptember 24, 1993
"Effects of Oral Administration of Type II Collagen on Rheumatoid
Arthritis"
Author Trentham DE; Dynesius-Trentham RA; Orav EJ; Combitchi D; Lorenzo
C; Sewell KL; Hafler DA; Weiner HL
Department of Medicine, Beth Israel Hospital, Boston, MA.
ABSTRACT:
(actual text, emphasis added)"Rheumatoid arthritis
is an inflammatory synovial disease thought to involve T cells reacting
to an antigen within the joint. Type II collagen
is a major protein in articular cartilage
and is a potential autoantigen in this disease. Oral tolerization to
autoantigens suppresses animal models of T cell-mediated autoimmune
disease, including two models of rheumatoid arthritis.
In this randomized, double-blind trial involving 60 patients with severe
active rheumatoid arthritis, a decrease in
the number of swollen joints and tender joints occurred in subjects
fed chicken type II collagen for 3 months,
but not in those that received a placebo. Four patients in the collagen
group had complete remission of the disease. No side effects were evident.
These data demonstrate clinical efficacy of an oral tolerization approach
for rheumatoid arthritis."
SELECTED QUOTE MATERIAL FROM THE
ARTICLE TEXT:
| • |
Although the pathogenetic
mechanisms underlying the disease are unknown, rheumatoid arthritis
is associated with human lymphocyte antigen (HLA)-DR4 and considered
to be an autoimmune [self-attacking-self] disorder in which activated
T cells participate. |
| • |
Current treatments are inadequate
in that they only partially control established rheumatoid arthritis.
They also have side effects that limit use early in the disease
process and interfere with prolonged administration. |
| • |
Experimental findings [from two animal
studies] provided the rationale for a pilot [Phase One trial], open-label
dose-escalation and safety study in 10 [human] patients with recalcitrant
rheumatoid arthritis. Subjects were taken off their immunosuppressive
and disease-modifying drugs consisting of methotrexate, 6-mercaptopurine,
azathioprine, or auranofin and fed 0.1 mg of solubilized type II
collagen daily for 1 month and then switched to 0.5 mg for the next
2 months. |
| • |
Six of the 10 patients experienced
a substantial clinical response, defined by a greater than 50% improvement
in both swollen and tender joint counts with two additional disease
measures improving by greater than 50% in morning stiffness, 15-m
walk time, grip strength. These improvements lasted for at least
2 months after the treatment period. Complete disease remission
lasting for 26 months occurred in one of the ten subjects; included
discontinuation of nonsteroidal anti-inflamatory drugs (NSAID). |
| • |
Based on the results of this Phase
One study, a double-blind, placebo-controlled, Phase Two trial with
60 patients was undertaken to determine whether clinical efficacy
could be demonstrated. |
| • |
Among the collagen patients the decline
in the number of swollen joints, tender joints, and joint-swelling
and tenderness indices were all significant in comparison to the
placebo patients. |
| • |
Four of the collagen patients (14%),
as compared with none in the placebo group, had complete resolution
of disease. At the beginning of the study these patients had severe,
active rheumatoid arthritis. |
| • |
While collagen patients were off immunosuppressive
drugs, stability or improvement occurred, whereas patients in the
placebo group tended to deteriorate. |
| • |
This controlled trial provides evidence
that oral administration of type II collagen is both safe and can
improve the daily physical challenges of rheumatoid arthritis. |
| • |
Oral type II collagen is a
preferable treatment because it appears to improve the health of
the arthritic joint as evidenced by the joint functionality for
several months after intake was canceled. |
| • |
Oral type II collagen is not toxic
like drugs. |
THE HARVARD STUDY
September 24,1993
Harvard Medical School took 29 volunteers who were scheduled for joint
replacement surgery in VA Hospital and gave them a tablespoon of chicken
cartilage in their orange juice for 90 days. They did this in order
to dispel a "rumor" that Collagen and Glucosamine Sulphate
(animal cartilage) were being used by some doctors to treat and cure
arthritis on humans. The results were not what they expected. Within
10 days, there was a marked decrease in the swelling of the patient's
joints. Within 60 days, most of the patients could open up a new pickle
jar. Within 90 days, 28 out of the 29 were "clinically cured".
Patented Biocell™ Chicken Collagen Type II
The form of chicken sternal cartilage type ll used in Flex Naturally™
is from Biocell™ Technology. Biocell developed a special patented
process that delicately extracts the bioactive chicken sternal collagen
type ll which preserves the joint-saving, arthritis fighting, soluble
proteoglycans. This special process also allows for greater absorption
of the joint protecting proteoglycans, like glucosamine sulfate, to
pass through the intestinal wall into the blood stream and through the
synovial membrane into the cartilage matrix.
Chicken Collagen II Absorbed Better Than Cartilage
When researchers compared the absorption rate of cartilage to collagen
type II, they discovered that cartilage had an 8% absorption rate while
the components of collagen type II had a 70 to 90% absorption rate.17
Chicken Collagen II is Superior to Shark Cartilage
Chicken Sternal Cartilage has been proven to contain the highest level
of anti-inflammatory proteoglycans (also called mucopolysaccaharides)
and healing potential over any other form of cartilage, including bovine
and shark.
Please note what Dr. Duarte says in his book, The Collagen Type II Cure,
pages 4 & 5,
”Please understand that cartilage is difficult to absorb, requiring
12 (750 milligram) capsules daily to get a response. Also, shark cartilage
is high in calcium and can be constipating. Soluble collagen
type II is more absorbable, requiring less volume to be consumed
in order to get an equivalent response. Collagen type II does not have
a lot of minerals, it is not constipating, and ounce for ounce
contains more of those joint saving, pain killing proteoglycans.
This makes collagen type II not only more therapeutically effective
but also more cost effective. Also, it has no offensive odor. Recently,
Biocell Technology, a California based company, has made an incredible
technological breakthrough in delicately extracting bioactive chicken
sternal collagen type II. Biocell holds a patent pending on this extraordinary
process that preserves the joint-saving, arthritis fighting, soluble
proteoglycans.” 17
(NOTE: Biocell now has three U.S. patents)
In summary;
Biocell™ Chicken Collagen Type II is a chondro-protective agent
which can:
| • |
prevent enzymes from destroying
healthy cartilage cells; |
| • |
reduce inflammation by
reprogramming destructive chondrocytes and cytokines; |
| • |
promote healthy cartilage cell and
proteoglycan (glucosamine and chondroitin sulfate) production; |
| • |
enhance the production of hyaluronic
acid, responsible for creating a thick effective, lubricating, synovial
fluid for the joint itself; |
| • |
protect the cartilage from oxidative
damage; |
| • |
help control pain and inflammation,
|
| • |
prevent the formation of blood vessels
(antiangiogiogenesis) within cartilage |
Biocell™ chicken collagen
type ll is a powerful inhibitor of any type of degeneration of the joint
at the cellular level of the cartilage itself.
| References:
|
| 1 |
Gerard J. Tortora, Sandra
Reynolds Garbowski, Principles of Anatomy and Physiology (1996):105 |
| 2 |
Miller E. J: The structure
of fibril-forming collagens. Ann NY Academy of Science 460:1-13,
1985 |
| 3 |
Structure and Function of Collagen
Types. Edited by Mayne R. Burgeson RE. New York, Academic Press,
1987 |
| 4 |
van der Rest M, Garrone R: Collagen
family of proteins. FASEB J 5:2814-2823, 1991 |
| 5 |
Buckwalter J, Hunziker E. Rosenberg
L. et al: Articular Cartilage: composition and structure, Injury
and Repair of the Musculoskeletal Soft Tissues. Edited by Woo SLY,
Buckwater JA, (1987, Savannah, GA), Chicago, American Academy of
Orthopaedic Surgeons, 1991, pp 405-425 |
| 6 |
Mankin HS, Brandt KD: Biochemistry
and metabolism of cartilage in osteoarthritis, Osteoarthritis Diagnosis
and Management. Edited by Moskowitz RW, Howell DS, Goldberg VM,
et al. Philadelphia, WB Saunders, 1992, pp 109-15 |
| 7 |
Alex Duarte, O.D., Ph.D., The Chicken
Sternal Collagen Type II Cure (1997):38 |
| 8 |
Alex Duarte, O.D., Ph.D., The Chicken
Sternal Collagen Type II Cure (1997):23 |
| 9 |
Alex Duarte, O.D., Ph.D., The Chicken
Sternal Collagen Type II Cure (1997):23, 24 |
| 10 |
Alex Duarte, O.D., Ph.D., The Chicken
Sternal Collagen Type II Cure (1997):38 |
| 11 |
Alex Duarte, O.D., Ph.D., The Chicken
Sternal Collagen Type II Cure (1997):38, 39 |
| 12 |
Alex Duarte, O.D., Ph.D., The Chicken
Sternal Collagen Type II Cure (1997):37 |
| 13 |
Alex Duarte, O.D., Ph.D., The Chicken
Sternal Collagen Type II Cure (1997):26, 33 |
| 14 |
Alex Duarte, O.D., Ph.D., The Chicken
Sternal Collagen Type II Cure (1997):3, 37 |
| 15 |
Alex Duarte, O.D., Ph.D., The Chicken
Sternal Collagen Type II Cure (1997):45-48 |
| 16 |
Alex Duarte, O.D., Ph.D., T he Chicken
Sternal Collagen Type II Cure (1997):55, 56 |
| 17 |
Alex Duarte, O.D., Ph.D., The Chicken
Sternal Collagen Type II Cure (1997):5-7 |
| 18 |
Alex Duarte, O.D., Ph.D., The Chicken
Sternal Collagen Type II Cure (1997): |
* These statements have not been
evaluated by the Food and Drug Administration.
This product is not intended to diagnose, treat, cure, or prevent
any disease.
Disclaimer
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