FROM:
Alternative Medicine Review 1998 (Apr); 3 (2): 140–143 ~ FULL TEXT
Description:
Quercetin is widely
distributed in the plant kingdom and is the most abundant of the flavonoid
molecules. It is found in many often-consumed foods, including apple, onion,
tea, berries, and brassica vegetables, as well as many seeds, nuts, flowers,
barks, and leaves. It is also found in medicinal botanicals, including
Ginkgo biloba, Hypericum perforatum (St. John's Wort), Sambucus canadensis
(Elder), and many others. It is often a major component of the medicinal
activity of the plant, and has been shown in experimental studies to have
numerous effects on the body.
All flavonoids have the same basic
chemical structure, a three-ringed molecule with hydroxyl (OH) groups attached
(see Figure). A multitude of other substitutions can occur, giving rise
to the many types of flavonoids. Flavonoids often occur in foods as a glycoside,
meaning they have a sugar molecule (rhamnose, glucose, galactose, etc.)
attached to the center (C) ring. Quercetin is the aglycone (meaning minus
the sugar molecule) of a number of other flavonoids, including rutin, quercetrin,
isoquercetin, and hyperoside. These molecules have the same structure as
quercetin except they have a specific sugar molecule in place of one of
quercetin's hydroxyl groups on the C ring, which dramatically changes the
activity of the molecule. Activity comparison studies have identified other
flavonoids as often having similar effects as quercetin; but quercetin
usually has the greatest activity.
Quercetin appears to have many beneficial
effects on human health, including cardiovascular protection, anti-cancer
activity, anti-ulcer effects, anti-allergy activity, cataract prevention,
antiviral activity, and anti-inflammatory effects.
Mechanisms of Action:
Flavonoids,
as a rule, are antioxidants, and a number of quercetin's effects appear
to be due to its antioxidant activity. Quercetin scavenges oxygen radicals, [1, 2] inhibits xanthine oxidase, [3] and inhibits
lipid peroxidation in vitro. [4] As another
indicator of its antioxidant effects, quercetin inhibits oxidation of LDL
cholesterol in vitro, probably by inhibiting LDL oxidation itself, by protecting
vitamin E in LDL from being oxidized or by regenerating oxidized vitamin
E. [5] By itself, and paired with ascorbic
acid, quercetin reduced the incidence of oxidative damage to neurovasculature
structures in skin, and inhibited damage to neurons caused by experimental
glutathione depletion. [6]
Quercetin's anti-inflammatory activity
appears to be due to its antioxidant and inhibitory effects on inflammation-producing
enzymes (cyclooxygenase, lipoxygenase) and the subsequent inhibition of
inflammatory mediators, including leukotrienes and prostaglandins. [7, 8]
Inhibition of histamine release by mast cells and basophils [9, 10]
also contributes to quercetin's anti-inflammatory activity.
Aldose reductase, the enzyme which catalyzes the conversion of glucose to sorbitol, is especially important in the eye, and plays a part in the formation of diabetic cataracts. Quercetin is a strong inhibitor of human lens aldose reductase. [11]
Quercetin exerts antiviral activity
against reverse transcriptase of HIV and other retroviruses, and was shown
to reduce the infectivity and cellular replication of Herpes simplex virus
type 1, polio-virus type 1, parainfluenza virus type 3, and respiratory
syncytial virus (RSV). [12]
Early studies on quercetin reported
that administration to rats caused an increased incidence of urinary bladder
tumors. Subsequent studies on rats, mice, and hamsters were unable to confirm
the potential carcinogenicity of this molecule. [13, 14]
In fact, much of the recent research on quercetin has shown it to be an
anticarcinogen to numerous cancer cell types, including breast, [15–17]
leukemia, [18, 19] colon, [20]
ovary, [21, 22] squamous cell, [23]
endometrial, [21] gastric, [24]
and non-small-cell lung. [25]
Clinical Indications:
Allergies: Quercetin's mast-cell-stabilizing effects make it an obvious choice for
use in preventing histamine release in allergy cases, similar to the synthetic
flavonoid analogue cromolyn sodium. Absorption of the pure aglycone quercetin
is poor (see below); however, much of quercetin's anti-allergy effects
may be due to anti-inflammatory and anti-histaminic effects in the gut.
Cardiovascular Disease Prevention: Quercetin's cardiovascular effects center on its antioxidant and anti-inflammatory
activity, and its ability to inhibit platelet aggregation ex vivo.[26]The
Zutphen Elderly Study investigated dietary flavonoid intake and risk of
coronary heart disease. The risk of heart disease mortality decreased significantly
as flavonoid intake increased. Individuals in the upper 25 percent of flavonoid
intake had a relative risk of 0.42 compared to the lowest 25 percent in
this 5-year follow-up study of men ages 65–84. Interestingly, the flavonoid-containing
foods most commonly eaten in this study contain a high amount of quercetin
(tea, onions, apples). [27] In a cohort of
the same study, dietary flavonoids (mainly quercetin) were inversely associated
with stroke incidence. [28]
Inflammation: Quercetin is indicated
in any inflammatory condition, as it inhibits the formation of the inflammatory
mediators prostaglandins and leukotrienes, as well as histamine release.
This may be especially helpful in asthma, as leukotriene B4 is a potent
bronchial constrictor. Quercetin's inhibition of xanthine oxidase decreases
the formation of uric acid, and thus it may be of value in the treatment
of gout.
Anti-ulcer/Gastroprotective effects: Animal studies have shown quercetin to be protective of gastric ulceration
caused by ethanol, probably by inhibiting lipid peroxidation of gastric
cells [29, 30] and/or by inhibition of gastric
acid secretion.[31] An interesting aspect
of quercetin's anti-ulcer effect is that it has been shown to inhibit growth
of Helicobacter pylori in a dose-dependent manner in vitro. [31]
Cancer: As mentioned above, quercetin
has been investigated in a number of animal models and human cancer cell
lines, and has been found to have antiproliferative effects. It may also
increase the effectiveness of chemotherapeutic agents.[21, 22]
More clinically-oriented research needs to be done in this area to discover
effective dosage ranges and protocols.
Diabetic Complications: Quercetin's
aldose reductase-inhibiting properties make it a useful addition to diabetic
nutritional supplementation, to prevent cataract and neurovascular complications.
Viral Infections: Quercetin may
be useful in viral infections; however, none of the research so far is
clinically-based. Even so, concentration on ingesting quercetin-rich foods
or supplementation with the pure substance may be helpful during viral
illnesses.
Pharmacokinetics: Few human quercetin
absorption studies exist. It appears that only a small percentage of quercetin
is absorbed after an oral dose, possibly only two percent, according to
one study. [32] A recent study of absorption
in "healthy" ileostomy patients revealed an absorption of 24
percent of the pure aglycone and 52 percent of quercetin glycosides from
onions. [33] However, no intestinal permeability
values were obtained in this group, and thus the results might not be reliable.
Quercetin undergoes bacterial metabolism in the intestinal tract, and is
converted into phenolic acids. Absorbed quercetin is transported to the
liver bound to albumin, where some may be converted via methylation, hydroxylation,
or conjugation. [34]
Dosage An oral dose of 400-500 mg
three times per day is typically used in clinical practice. Since solubility
is an issue in quercetin absorption, [34]
a new, water-soluble quercetin molecule, quercetin chalcone, might be used
in smaller doses, typically 250 mg three times per day.