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Grape Seed
(skin) extract is an extract from the seed (skin)s of grapes. The seed (skin) s left
over from the production of wine or juice are
harvested, ground and extracted. They have a high content of compounds
known as OPCs (oligomeric
proanthocyanidins). Since
French researcher, Dr. Jack Masquelier isolated OPCs from peanut skin in
1947, OPCs is found in many plants and has been declared to be a potent
antioxidant of non-toxic, non-mutagenic, non-carcinogenic, and free of
side effects according to a review of numerous researches.
Function:
The antioxidant
capacity of Grape Seed (skin) Extract comes from proanthocyanidins (oligomeric
proanthocyanidins) (OPCs). With an antioxidant power 20 times stronger
than Vitamin C and 50 times stronger than Vitamin E [20], OPCs is known as a powerful antioxidant to neutralize free radicals,
which play a major role in degenerative diseases, cardiovascular diseases,
impaired vision, sun damage and premature aging.
1.
Cardiovascular Diseases
Researches have
assured that OPCs helps
strengthen capillaries, arteries and veins, which endows it several
important clinical applications. OPCs appear to stabilize the walls of
blood vessels, reduce inflammation, and generally support tissues
containing collagen and elastin. [14]
1).
Atherosclerosis:
It has been
proved that the oxidation of LDL plays an important role in
atherosclerosis. By its excellent antioxidant activity, OPCs eliminates
damages that free radicals, as well as collagenase and elastinase do to
the arteries, thus prevents or reverses atherosclerosis. Animal evidence
suggested that OPCs could slow or reverse atherosclerosis. [29,32]
2).
Venous Insufficiency (Varicose Veins)
Varicose Veins
refers to the situation when blood pools in the legs, causing pain,
heaviness, swelling, fatigue, and unsightly visible veins. By
strengthening capillary and reduce capillary osmosis, OPCs can relieve the
pain and swelling of venous insufficiency. [8,9,10] For the
same reason, OPCs is recommended as a treatment for hemorrhoids as well.
There is also some evidence that OPCs can be useful for the swelling that
often follows injuries or surgery. [11,12,13] OPCs appear to
speed the disappearance of swelling, by strengthening damaged blood and
lymph vessels that are leaking fluid.
A
double-blind placebo-controlled study of 92 subjects found that OPCs,
taken at a dose of 100 mg 3 times daily,
significantly improved major symptoms, including heaviness, swelling, and
leg discomfort. [21] Over a period of 1 m
onth, 75% of the participants treated with OPCs improved substantially.
Another placebo-controlled study that enrolled 364
individuals with varicose veins also found that treatment with OPCs
produced results superior to those of placebo. [22]
3).
Retinopathy/Vision Improvement
The capacity of
OPCs in strengthening capillary and reduce capillary osmosis is effective
for patients suffering from stroke
and retinopathy. OPCs has been proved to improve retinopathy caused by
diabetics, atherosclerosis, inflammation and
aging. It has also been reported that OPCs can speed vision recovery after
strong light, and improve vision acuity of those
who suffer from eye fatigue because of long-time computer using.
A 6-week,
controlled (but not blinded) study evaluated the ability of grape seed
(skin) OPCs to improve night vision in normal subjects. [27,28]
In this trial of 100 healthy volunteers, those who received 200 mg per day
of OPCs showed improvements in night vision and glare recovery as compared
to untreated subjects.
2.
Aging/Alzheimer Disease
Because OPCs
can easily pass the Blood-Brain Barrier, it can effectively inhibit the
damage that free radicals do to the brain organism, so that Alzheimer
Disease is prevented and reversed.
3.
Skin Care
Because of its
antioxidant activity, OPCs is thought to prevent the skin from excessive
ultraviolet radiation and free radicals. Considerable evidences indicate
that OPCs protects and strengthens collagen and elastin of the skin, so
that wrinkle is prevented and elasticity of the skin is kept. [14,19]
OPCs in cream form are a popular treatment for aging skin, on the
theory that by repairing elastin and collagen they will return skin to a
more youthful appearance.
4.Anti-cancer,
Anti-inflammation and Anti- allergic Activity
Since free
radicals play a vital role in tumor formation, OPCs is reasonably used for
its anti-cancer activity. Also for its inhibition of inflammatory factors
such as PG, 5-HT and Leukotriene, as well as selective binding to
connective tissue of the joints to relieve pain and swelling, OPCs is
helpful for kinds of arthritis. The anti-allergic activity of OPCs is
thought to be the result of anti-histamine. Compared with other
anti-allergic drugs, OPCs has the same efficacy and does not have the same
side effects such as drowsiness.
Dosage:
For use as
a general antioxidant much as you might use vitamin E or vitamin C, 50 mg
of OPCs daily are sufficient. A higher dosage of 150 to 300 mg daily is
generally used for treating specific diseases such as varicose veins.
Safety:
OPCs have been
extensively tested for safety and are generally considered to be
essentially nontoxic. [33]
Side effects are rare, but when they do occur they are limited to
occasional allergic reactions and mild digestive distress. However,
maximum safe dosages for young children, pregnant or nursing women, or
those with severe liver or kidney disease have not been established.
OPCs may
have some anticoagulant properties when taken in high doses, and should be
used only under medical supervision by individuals on blood-thinner drugs.
When taking Coumadin (warfarin), heparin, Trental (pentoxifylline), or
aspirin, high doses of OPCs might cause a risk of excessive bleeding.
Chemistry:
This
Product is composed of procyanidolic oligomers (OPCs). Structural formulas
are followed:

(C30H26O12)nnn=2~4
(C44H32O12)n
n=2~4
References:
1.
Schwitters B, et al. OPC in practice. Bioflavanols and their applications.
Rome, Italy: Alfa Omega, 1993.
2. Masquelier J, et al. Stabilization of collagen by procyanidolic
oligomers. Acta Ther 7: 101105, 1981.
3. Masquelier J. Procyanidolic oligomers. J Parums Cosm Arom 95: 8997,
1990.
4. Tixier JM, et al. Evidence by in vivo and in vitro studies that binding
of pycnogenols to elastin affects its rate of degradation by elastases.
Biochem Pharmacol 33: 39333939, 1984.
5. Facino RM, et al. Free radical scavenging action and anti-enzyme
activities of procyanidines from Vitis vinifera. A mechanism for their
capillary protective action. Arzneimittelforschung 44: 592601, 1994.
6. Kuttan R, et al. Collagen treated with catechin becomes resistant to
the action of mammalian collagenase. Experientia 37: 221223, 1981.
7. Masquelier J, et al. Stabilization of collagen by procyanidolic
oligomers. Acta Ther 7: 101105, 1981.
8. Thebaut JF, et
al. Study of endotelon in functional manifestations of peripheral venous
insufficiency. Gazette Medicale 92: 12, 1985.
9. Henriet JP. Exemplary study for a phlebotropic substance, the EIVE
study. On file with Primary Services International, Southport,
Connecticut.
10. Delacroix P, et al. Double-blind study of endotelon in chronic venous
insufficiency. La Revue de Medecine 2728, 31, 17931802, 1981.
11. Pecking A, et al. Oligomeric proanthocyanidins (endotelon) in the
treatment of post therapeutic lymphedema in the upper limbs. Association
de Lymphologie de Lange Francaise, Hopital Saint-Louis, 75010, Paris,
France 69-73, 1989.
12. Baruch J. Effect of endotelon in post-surgical edemas. Ann Chir Plast
Esthet 29(4): 393395, 1984.
13. Parienti JJ, et al. Post traumatic edemas in sports: a controlled test
of endotelon. Gaz Med France 90: 231236, 1983.
14. Facino RM, et al. Free radical scavenging action and anti-enzyme
activities of procyanidines from vitis vinifera. A mechanism for their
capillary protective action. Arzneimittelforschung 44: 592601, 1994.
15. Kuttan R, et al. Collagen treated with catechin becomes resistant to
the action of mammalian collagenase. Experientia 37: 221223, 1981.
16. Masquelier J. Procyanidolic oligomers. J Parums Cosm Arom 95: 8997,
1990.
17. Masquelier J, et al. Stabilization of collagen by procyanidolic
oligomers. Acta Therap 7: 101105, 1981.
18. Schwitters B, et al. OPC in practice. Bioflavanols and their
applications. Alfa Omega.Rome, Italy, 1993.
19. Tixier JM, et al. Evidence by in vivo and in vitro studies that
binding of pycnogenols to elastin affects its rate of degradation by
elastases. Biochem Pharmacol 33: 39333939, 1984.
20. Bagchi D, Garg A, Krohn RL, et al. Oxygen free radical scavenging
abilities of vitamins C and E, and a grape seed skin) proanthocyanidin
extract in vitro. Res Commun Mol Pathol Pharmacol 95: 179189, 1997.
21. Thebaut JF, et al. Study of endotelon in functional manifestations of
peripheral venous insufficiency. Gazette Medicale 92: 12, 1985.
22. Henriet, JP. Exemplary study for a phleboteropic substance, the EIVE
study. On file with Primary Services International, Southport, CT.
23. Delacroix P, et al. Double-blind study of Endotelon in chronic venous
insufficiency. English abstract only. La Revue de Medecine 2728, 31:
17931802.
24. Pecking A, et al. Oligomeric proanthocyanidins (Endotelons) in the
treatment of post-therapeutic lymphedema in the upper limbs. English
abstract only. Association de Lymphologie de Lange Frangaise, Htpital
Saint-Louis, 75010, Paris, France 6973, 1989.
25. Baruch J. Effect of Endotelon in post-surgical edemas. English
abstract only. Ann Chir Plast Esthet 29 (4): 393395, 1984.
26. Parienti JJ, et al. Post-traumatic edemas in sports: A controlled test
of Endotelon. English abstract only. Gaz Med France 90 (3): 231236.
27. Corbe C, et al. Light vision and chorioretinal circulation. Study of
the effect of procyanidolic oligomers (Endotelon). J Fr Ophtalmol 11:
453460, 1988.
28. Boissin JP, et al. Chorioretinal circulation and dazzling: Use of
procyanidol oligomers. Bull Soc Ophtamol Fr 88: 173174, 177179, 1988.
29. Schwitters B, et al. OPC in practice. Bioflavanols and their
applications. Rome, Italy: Alfa Omega, 1993.
30. Wegrowski J, et al. The effect of procyanidolic oligomers on the
composition of normal and hypercholesterolemic rabbit aortas. Biochem
Pharmacol 33: 34913497, 1984.
31. Uchida S, et al. Condensed tannins scavenge active free radicals. Med
Sci Res 15: 831832, 1987.
32. Gendre P. Effet protecteur des oligomeres procyandiloques sur le
lathyrisme experimental chez le rat. Ann Pharm Fr 43(1): 6171, 1985.
33. Schulz V, et al. Rational phytotherapy. New York: Springer Verlag,
1998: 283.
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