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QUERCETIN
Description
Quercetin (kwer’-suh-tin) may be the reason the saying "an
apple a day keeps the doctor away" got started. Like so many
other nutrients used by
PDI against Peyronie’s disease (PD),
quercetin in particular appears to help a host of disorders,
from asthma to heart disease. Quercetin belongs to a group of
plant pigments called flavonoids that are largely responsible
for the colors of many fruits, flowers, and vegetables.
However, quercetin is a special type of flavonoid that is a
building block for all other members of the flavonoid family.
It is primarily found in apples, onions, dark berries, citrus
fruits, parsley, olive oil and black tea.
Because it is a flavonoid, quercetin acts as an antioxidant
combating the destructive free radical molecules that play a
part in many diseases – by now you know this can apply
especially well to PD. Free radical particles occur naturally
during thousands of biochemical processes constantly taking
place in the body. When left to wander about in the body, free radicals can
damage cell membranes, damage genetic material, and possibly
contribute to the aging process, as well as development of
many conditions including heart disease and cancer.
Antioxidants such as quercetin neutralize free radicals and
may reduce or even help prevent some of the damage they cause. Flavonoids, especially quercetin, offer many other
health-promoting benefits. They act as antihistamines (useful
in reducing allergy symptoms) and help reduce inflammation
associated with various forms of arthritis. Among people with
high dietary intakes of quercetin and other major flavonoids,
studies show lower rates of stomach, lung, pancreatic, and
breast cancers. Quercetin inhibits the buildup of a type of
blood sugar that could otherwise lead to cataract formation in
the lens of the eye.
Of note, quercetin seems to work better when used with
bromelain, a digestive enzyme found in pineapples. This is the
reason our recommended quercetin product contains a good
dose of bromelain. All on its own, bromelain is a
particularly effective treatment for PD because it is an
enzyme that attacks abnormal fibrous tissue in the body --
such as the Peyronie's scar.
Quercetin General
Health Benefits
- Reduce cancer risk(1-13)
The quercetin content of apples is high. Lung cancer was 58%
lower among people who ate the most apples compared to those
who ate the least. Quercetin and other flavonoids have also
been shown to help reduce the risk of several cancers.
- Prevent heart attack(14-18)
One cause of heart disease is overgrowth of smooth muscle
cells in artery walls, a key component in the development of
atherosclerosis. As it does with cancer cells, there is
evidence that quercetin works in a similar way to stop the
overgrowth of cells that harm the heart. A 2002 study in the
journal "Surgery" reported that in laboratory tests, quercetin
arrested the development of vascular smooth muscle cells by
locking them in a "no-growth" state. The Rotterdam Study,
published in the 2002 American Journal of Clinical
Nutrition, examined the tea-drinking habits and dietary
flavonoid intakes of nearly 5,000 adults in Holland.
Apparently due to black tea's high flavonoid concentration,
daily consumption of the brew reduced the risk of heart
attack overall for tea drinkers.
- Stave off cataracts(8,19-21)
A lifetime of unprotected sun exposure can damage the eyes
as well as the skin. Ultraviolet (UV) rays, particularly the
burning UVB rays, damage proteins in the lens of the eye,
causing them to clump together in a whitish cloud. Cigarette
smoking and a deficiency in antioxidant vitamins are other
major causes of cataracts. Research indicates that quercetin
blocks an enzyme that leads to accumulation of sorbitol, a
type of sugar that contributes to cataract formation.
- Control asthma(22-26)
Quercetin may be useful in relieving asthma (and possibly
hay fever and sinusitis) as a result of its ability to
reduce inflammation in the airways, and prevent the release
of histamine.
- Maintain health when suffering from Crohn's disease(27-30)
Quercetin, a natural anti-inflammatory, may be helpful in
countering the hallmark of Crohn's disease: chronic
inflammation of the gastrointestinal tract. Crohn's chief
signs are abdominal pain, fever, diarrhea, and weight loss.
The small intestine is primarily affected, and the patient
develops real problems in absorbing important nutrients.
- Helps fibromyalgia(8,
24, 25, 31, 32) Similar to the case reports for arthritis,
people with fibromyalgia who switched from a typical Western
diet to a vegan diet high in flavonoids such as quercetin
experienced improvement in their symptoms.
- Protects Prostate health(8,
25, 33-36) Some studies suggest quercetin reduces pain and
other symptoms in chronic prostatitis (inflammation of the
prostate). Preliminary studies indicate quercetin may
inhibit the growth of prostate cancer cells in test tubes.
How this will translate to prevention or treatment of
prostate cancer is unknown.
Cautions
Don't take quercetin if you use the calcium channel blocker
felodipine, for high blood pressure. In test tubes studies,
quercetin inhibited enzymes that break down felodipine; in
theory this could increase blood levels of the drug and lead
to unwanted side effects.
Quercetin and
Chemotherapy
Test tube and animal studies suggest that quercetin may
enhance the effects of doxorubicin and cisplatin, two
chemotherapy medications used to treat cancer. More research
is needed to determine if quercetin has any application to
people being treated with either of these agents. In addition,
use of antioxidants at the same time as chemotherapy is
somewhat controversial. Therefore, more research is needed
before conclusions about safety and effectiveness can be
drawn.
Possible Side
Effects
There are no known side effects associated with quercetin in
supplement form. No long-term adverse effects from the use of
quercetin are noted in the medical literature.
However, it is always best to use any supplement only in
cooperation and knowledge of your healthcare provider.
Science
Flavonoids are important for human health. Of the flavonoids,
quercetin (3,3',4',5-7-pentahydroxyflavone) has shown the
greatest biochemical activity among the flavonoids studied in
experimental models. For this reason quercetin has been the
subject of hundreds of scientific reports in the past two
decades; it has been extensively studied by researchers around
the world, starting with the discovery of both vitamin C and
flavonoids by Albert Szent-Gyorgyi who received the Nobel
Price in 1937 for research in this area. Like vitamins,
flavonoid compounds are not produced in the body and must be
supplied through the diet or by supplements. Due to its
antioxidant effect, quercetin can inhibit inflammatory
processes mediated by leukotrienes, the inflammatory mediators
a thousand times more powerful than histamines, and lysosomal
enzymes that support localized inflammation. In addition, it
stabilizes mast cell membranes and prevents the release of
histamine and other inflammatory agents.
Many flavonoids inhibit tumor formation, with quercetin
consistently demonstrating significant anti-tumor activity
against a wide range of cancers: squamous cell carcinoma;
leukemia; and cancers of the breast, ovaries, colon, rectum,
and brain.
Safety of
Quercetin
Quercetin appears to be extremely safe to use. Carcinogenic
and teratogenic studies in rats and rabbits have shown that it
is without apparent side effects even when consumed in very
large quantities (2,000 mg. per Kg. of body weight) for long
periods of time (up to 2 years).
Unlike the citrus flavonoids, quercetin has no interaction
with any drug. It can be used even during pregnancy.
PD Connection
After reading all the good things that quercetin does for so
many different health conditions, we might expect it to have a
very good report in relation to PD – and it does, but as
usual this relationship must be indirectly applied from
studies of cellular activity in other areas.
Quercetin functions like other flavonoids in enhancing the
collagen structural network. The theory behind using
nutritional components of scar tissue to treat excessive scar
tissue, which research seems to support, is that in a
deficiency of a flavonoid the structural integrity of the
collagen (scar) network is weakened. This structural
problem is expressed as an excessive development of the
fibrous network, resulting in a greater than usual scar. Some
would think that a scar or excess fibrous tissue would result
from an excess of nutrients, or flavonoids, but actually the
opposite happens. In a state of nutritional deficiency, as
with a flavonoid like quercetin, there is such a weak and
disorganized production of the collagen support structure that
the body keeps on producing more and more tissue material
since it is of poor quality. Only when there are sufficient
flavonoid, and therefore good quality tissue structure, is
there a reduced need for structural material and therefore a
smaller scar results. It works like this: If you had to
build a house of lumber, but only had cracked, split and
knotty wood to build with, you would have to use more of it –
really lay it on – to make sure that the house would have some
degree of strength. If it you were working with good wood, you
could afford to use less of it. The same thing apparently
happens in the body under this theory: Deficient quercetin
levels result in weak collagen and fibrous tissue elements, more of
it is needed for tissue repair, resulting in a larger but
weaker scar.
A 2003 study in Singapore investigated the role of quercetin
in relation to excess scar development as a result of
over proliferation of fibroblasts, overproduction of collagen,
and contraction of scar material that characterize pathologic
scars. The conclusion drawn from this work was, “(f)rom this
in-vitro study, quercetin seemed to have good potent effects
to inhibit proliferation and contraction of excessive
scar-derived fibroblasts”.(38)
Another paper from the same group in Singapore reports after
doing additional study that “the described activities of
quercetin on the IGF system and collagen expression may
provide a novel approach for the use of quercetin in treatment
and/or prevention of hypertrophic (excess) scar…”(39)
Northwestern University Medical School, at their Plastic and
Reconstructive Surgery Unit, reported on research they
performed on excess scar formation on rabbit ear tissue. They
concluded, “…a significant improvement in dermal collagen
organization was noted on comparing Mederma-treated scars with
untreated control scars…The active product in Mederma, allium
cepa, has as its derivative quercetin, a bioflavonoid noted
for its antiproliferative effects on both normal and malignant
cells, and its antihistamine release effects. These properties
could theoretically prove beneficial in reversing the
inflammatory and proliferative responses noted in hypertrophic
scars. Despite the authors' inability to demonstrate a
reduction in scar hypertrophy, the improvement in collagen
organization noted in the Mederma-treated scars suggests it
may have an effect on the pathophysiology of hypertrophic scar
formation.”(40)
From the Netherlands comes a rating of the protective effect
of 12 different naturally occurring oxidants on fibroblasts.
Vitamin E was found to have the greatest protective ability of
the 12 investigated, and quercetin had the next greatest
protective ability.(41)
Two reports from Europe, one from England the other from
Italy, state that quercetin displays antioxidant ability
against free radical attack of fibroblasts.(42, 43)
Lastly three sources reported favorably on the ability of
quercetin to inhibit or block growth of fibroblast cells via
different biochemical processes.(44-46)
Quercetin has been heavily studied for the last 30 years
because it seems to do good things for a broad assortment of
problems. It is a widely used and popular nutritional product
for this reason. It would stand to reason, just like vitamin
E, vitamin C, and copper, because quercetin is involved in a
wide variety of human biochemical activities it has the
potential to influence a wide variety of health problems. The
long list of problems for which quercetin has been given
strong endorsement by medical research is impressive. It is
reasonable to think that something as widely distributed in
nature as quercetin, and broadly fundamental to health, might
also be useful in reducing the excess scar of PD.
Quercetin is strongly supported by diverse research as being
beneficial in scar tissue reduction; it has more good science
and research than most therapies that can be used for PD.
However, all this information must still be connected back to
PD, since the two have not been researched together. But it
should be noted that few nutrients have been given so much
study for its effect on fibroblast activity and antioxidant
activity, both of which are critically important to PD.
Abundant and strong correlation to scar tissue activity
supports the use of quercetin as part of any PD treatment
plan.
Quercetin Product
Recommendation
PDI uses Quercetin-Bromelain Complex made by Douglas Labs/Amni.
It is our opinion it is the best value for the money, and it
comes from a large and well established 50-year old nutrition
company.
PDI has found no other formula that comes close to
this quercetin formula. It has a very high dose of quercetin
at 333 mg per capsule, coupled with 100 mg of bromelain, 200
mg of vitamin C and magnesium ascorbate to assist assimilation
of the nutrients.
Recommended
Quercetin Therapy
Quercetin is best taken when paired with bromelain, a natural
anti-inflammatory derived from pineapples. Bromelain has
anti-inflammatory and anti-allergy activity of its own, but is
of even greater importance because it also increases the
absorption of quercetin through the digestive membrane.
As a suggestion, taking two to four of these tablets, twice
daily between meals might be a good way to get a therapeutic
dose. After improvement has stabilized, taking one to two,
twice daily between meals might be a good maintenance dose.
For ideas and suggestions to put it all together, click
Create a PD Treatment Plan.
Order Quercetin
Why Buy from
PDI?
1. Service
PDI offers email support and
assistance for the products and services we provide. We
provide experience and interest in helping you with PD.
PDI
is here to help you with questions about the
products we sell. This is an extremely valuable service
the others cannot possibly match.
2. Quality and Quantity Repairing the Peyronie’s
scar is such an important mission. It is critical you
use a high quality and quantity of nutrients. We have
done the hard part selecting good companies and
products. Buy with confidence.
3. Value
PDI has a competitive pricing structure
of which we are proud. We doubt you can find better
products that deliver the quality and quantity for the
prices we have set.
4. Convenience The longer you take to start
treating PD, the longer and more difficult treatment
becomes, and the likelihood of success deteriorates.
Everything you need is here, right now, in one place. |
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1. Gross M,
Pfeiffer M, Martini M, Campbell D, Slavin J, Potter J. The
quantitation of metabolites of quercetin flavonols in human
urine. Cancer Epidemiol Biomarkers Prevent. 1996;5(9):711-720.
2. Hofmann J, Fiebig HH, Winterhalter BR, Berger DP, Grunicke
H. Enhancement of the antiproliferative activity of
cis-diamminedichloroplatinum (II) by quercetin. Int J Cancer.
1990;45(3):536-539.
3. Trcihopoulou A, Katsouyanni K, Stuver S, Tzala L,
Cnardellis C, Rimm E, Trichopoulos D. Consumption of olive oil
and specific food groups in relation to breast cancer risk in
Greece. J National Cancer Inst. 1995;87(2):110-116.
4. Scambia G, Ranelletti FO, Benedetti Panici P, et al.
Quercetin potentiates the effect of adriamycin in a
multi-drug-resistant MCF-7 human breast-cancer cell line:
P-glycoprotein as a possible target. Cancer Chemother
Pharmacol. 1994;34:459-464.
5. Young JF, Nielsen SE, Haraldsdottir J, et al. Effect of
fruit juice intake on urinary quercetin excretion and
biomarkers of antioxidative status. Am J Clin Nutr. 1999;
69(1):87-94.
6. Hollman PC, Van Trijp JM, Mengelers MJ, De Vries JH, Katan,
MB. Bioavailability of the dietary antioxidant flavonol
quercetin in man. Cancer Lett. 1997;114(1-2):139-140.
7. Ferry DR, Smith A, Malkhandi J, et al. Phase I clinical
trial of the flavonoid quercetin pharmacokinetics and evidence
for in vivo tyrosine kinase inhibition. Clin Cancer Res.
1996;2(4):659-668.
8. Werbach MR. Nutritional Influences on Illness. 2nd ed.
Tarzana, Calif: Third Line Press; 1993:179, 259, 267, 389.
9. Lamson DW, Brignall MS. Antioxidants and cancer III:
quercetin. Alt Med Rev. 2000;5(3):196-208.
10. Owen RW, Giacosa A, Hull WE, Haubner R, Spiegelhalder B,
Bartsch H. The antioxidant/anticancer potential of phenolic
compounds isolated from olive oil. Eur J Cancer.
2000a;36(10):1235-1247.
11. Owen RW, Mier W, Giacosa A, Hull WE, Spiegelhalder B,
Bartsch H. Identification of lignans as major components in
the phenolic fraction of olive oil. Clin Chem.
2000b;46(7):976-988.
12. Piantelli M, Maggiano N, Ricci R, et al. Tamoxifen and
quercetin interact with type II estrogen binding sites and
inhibit the growth of human melanoma cells. J Invest Dermatol.
1995;105(2):248-53.
13. Rodgers EH, Grant MH. The effect of the flavonoids,
quercetin, myricetin, and epicatechin on the growth and enzyme
activities of MCF7 human breast cancer cells. Chem Bio
Interactions. 1998;116(3):213-228
14. Hayek T, Fuhrman B, Vaya J, Rosenblat M, Belinky P,
Coleman R et al. Reduced progression of atherosclerosis in
apolipoprotein E-deficient mice following consumption of red
wine, or its polyphenols quercetin or catechin, is associated
with reduced susceptibility of LDL to oxidation and
aggregation. Arterioscler Thromb Vasc Biol.
1997;17(11):2744-2752.
15. Van Golde PH, Sloots LM, Vermeulen WP, et al. The role of
alcohol in the anti low density lipoprotein oxidation activity
of red wine. Atherosclerosis. 1999;147(2):365-370.
16. Constant J. Alcohol, ischemic heart disease, and the
French paradox. Clin Card. 1997;20(5):420-424.
17. Knekt P, Jarvinen R, Reunanen A, Maatela J. Flavonoid
intake and coronary mortality in Finland: a cohort study. BMJ
(Clinical Research Ed.). 1996;312(7029):478-481.
18. Kurowska EM, Spence JD, Jordan J, Wetmore S, Freeman DJ,
Piche LA, Serratore P. HDL-cholesterol-raising effect of
orange juice in subjects with hypercholesterolemia. Am J Clin
Nutr. 2000;72(5):1095-1100.
19. Anderson J, McLauchlan WR, Williamson G. Querctein
inhibits hydrogen peroxide-induced oxidation of the rat lens.
Free Radic Biol Med. 1999;26(5-6):639-645.
20. Cai J, Nelson KC, Wu M, Sternberg P Jr, Jones DP.
Oxidative damage and protection of the RPE. Prog Retin Eye
Res. 2000;19(2):205-221.
21. Head KA. Natural therapies for ocular disorders. Part 1:
diseases of the retina. Alt Med Rev. Oct. 1999;(4):5:342-359.
22. Duthie SJ, Collins AR, Duthie GG, Dobson VL. Quercetin and
myricetin protect against hydrogen peroxide-induced DNA damage
(strand breaks and oxidised pyrimidines) in human lymphocytes.
Mutat Res. 1997;393(3):223-231.
23. Otsuka H, Inaba M, Fuikikura T, Kunitomo M. Histochemical
and functional characteristics of metachromatic cells in the
nasal epithelium in allergic rhinitis: studies of nasal
scrapings and their dispersed cells. J Allergy Clin Immunol.
1995;96(4):528-536.
24. Shils ME, Olson JA, Shike M, Ross AC. Modern Nutrition in
Health and Disease. 9th ed. Baltimore, Md: Williams & Wilkins;
1999:1274-1277.
25. White L, Mavor S. Kids, Herbs, Health. Loveland, Colo:
Interweave Press; 1998:22, 84.
26. Young JF, Nielsen SE, Haraldsdottir J, et al. Effect of
fruit juice intake on urinary quercetin excretion and
biomarkers of antioxidative status. Am J Clin Nutr. 1999;
69(1):87-94.
27. Lee E, Choi EJ, Cheong H, Kim YR, Ryu SY, Kim KM.
Anti-allergic actions of the leaves of Castanea crenata and
isolation of an active component responsible for the
inhibition of mast cell degranulation. Arch Pharm Res.
1999;22(3):320-323.
28. Longanga OA, Vercruysse A, Foriers A. Contribution to the
ethnobotanical, phytochemical and pharmacological studies of
traditionally used medicinal plants in the treatment of
dysentery and diarrhoea in Lomela area, Democratic Republic of
Congo (DRC). J Ethnopharmacol. 2000;71(3):411-423.
29. Ottshudi AL, Foriers A, Vercruysse A, Van Zeebroeck A,
Lauwers S. In vitro antimicorbial activity of six medicinal
plants traditionally used for the treatment of dysentery and
diarrhoea in Democratic Republic of Congo (DRC). Phytomedicine.
2000;7(2):167-172.
30. Thornhill SM, Kelly AM. Natural treatment of perennial
allergic rhinitis. Alt Med Rev. 2000;5(5):448-454.
31. Guardia T, Rotelli AE, Juarez AO, Pelzer LE.
Anti-inflammatory properties of plant flavonoids. Effects of
rutin, quercetin, and hesperidin on adjuvant arthritis in rat.
Farmaco. 2001;56(9):683-687.
32. Hanninen, Kaartinen K, Rauma AL, Nenonen M, Torronen R,
Hakkinen AS, Adlercreutz H, Laakso J. Antioxidants in vegan
diet and rheumatic disorders. Toxicology. 2000;155(1-3):45-53.
33. Shoskes DA, Zeitlin SI, Shahed A, Rajfer J. Quercetin in
men with category III chronic prostatitis: a preliminary
prospective, double-blind, placebo-controlled trial. Urology.
1999;54(6):960-963.
34.Shoskes D. Use of bioflavonoid quercetin in patients with
long-standing chronic prostatitis J Am Neutraceut Assoc
1999;2:18-21.
35.Nickel, et al. For the International Prostatitis
Collaborative Network, research guidelines for chronic
prostatitis: consensus report from the First National
Institutes of Health International Prostatitis Collaborative
Network. Urology 1999;54:229-33.
36. Xing N, Chen Y, Mitchell SH, Young CY. Quercetin inhibits
the expression and function of the androgen receptor in LNCaP
prostate cancer cells. Carcinogenesis. 2001;22(3):409-414.
37. Chan MM, Mattiacci JA, Hwang HS, Shah A, Fong D. Synergy
between ethanol and grape polyphenols, quercetin, and
resveratrol, in the inhibition of the inducible nitric oxide
synthase pathway. Bio Pharm. 2000;60(10):1539-1548.
38. Phan TT, Sun L, Bay BH, Chan SY, Lee ST.Dietary compounds
inhibit proliferation and contraction of keloid and
hypertrophic scar-derived fibroblasts in vitro: therapeutic
implication for excessive scarring. J Trauma. 2003
Jun;54(6):1212-24 Department of Plastic Surgery, Singapore
General Hospital, National University of Singapore.
39. Phan TT, See P, Tran E, Nguyen TT, Chan SY, Lee ST, Huynh
H. Suppression of insulin-like growth factor signaling pathway
and collagen expression in keloid-derived fibroblasts by
quercetin: its therapeutic potential use in the treatment
and/or prevention of keloids. Br J Dermatol. 2003
Mar;148(3):544-52.Department of Plastic Surgery, Singapore
General Hospital, Singapore.
40. Saulis AS, Mogford JH, Mustoe TA. Effect of Mederma on
hypertrophic scarring in the rabbit ear model. Plast Reconstr
Surg. 2002 Jul;110(1):177-83; discussion 184-6 Division of
Plastic and Reconstructive Surgery, Northwestern University
Medical School, Galter Pavilion, 675 N Saint Claire, Chicago,
IL 60611, USA.
41. Drummen GP, Makkinje M, Verkleij AJ, Op den Kamp JA, Post
JA. Attenuation of lipid peroxidation by antioxidants in rat-1
fibroblasts: comparison of the lipid peroxidation reporter
molecules cis-parinaric acid and C11-BODIPY(581/591) in a
biological setting. Biochim Biophys Acta. 2004 Mar
22;1636(2-3):136-50 Department of Biochemistry of Lipids,
Institute and Graduate School of Biomembranes, Utrecht
University, Padualaan 8, 3584CH Utrecht, The Netherlands.
42. Hu HL, Forsey RJ, Blades TJ, Barratt ME, Parmar P, Powell
JR. Antioxidants may contribute in the fight against ageing:
an in vitro model. Mech Ageing Dev. 2000 Dec
20;121(1-3):217-30 Molecular Physiology, Unilever Research
Laboratory Colworth, Sharnbrook, Bedford MK44 1LQ, UK.
43. Skaper SD, Fabris M, Ferrari V, Dalle Carbonare M, Leon A.
Quercetin protects cutaneous tissue-associated cell types
including sensory neurons from oxidative stress induced by
glutathione depletion: cooperative effects of ascorbic acid.
Free Radic Biol Med. 1997;22(4):669-78.Researchlife S.c.p.A.,
Castelfranco Veneto, Italy.
44. Posypanova GA, Severin SE, Kondratyev AD.Effect of protein
kinase modulators on the induction of morphological
differentiation of pheochromocytoma PC12 cells by nerve and
fibroblast growth factors. Biotechnol Appl Biochem. 1990
Feb;12(1):20-7. Research Center of Molecular Diagnostics, USSR
Ministry of Health, Moscow.
45. Vladutiu GD, Middleton E Jr.Effects of flavonoids on
enzyme secretion and endocytosis in normal and mucolipidosis
II fibroblasts. Life Sci. 1986 Aug 25;39(8):717-26.
46. Pawlikowska-Pawlega B, Gawron A.Effect of quercetin on the
growth of mouse fibroblast cells in vitro. Pol J Pharmacol.
1995 Nov-Dec;47(6):531-5.
Department of Comparative Anatomy and Anthropology, Maria
Curie-Sklodwska University, Lublin, Poland.
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