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Home > Health Conditions > Blood Sugar >
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Cinnamon, a staple ingredient in apple pie, has remained
one of the world’s favorite spices throughout recorded history. The
evergreen cinnamon tree (Cinnamomum verum), considered to be true
cinnamon, is native to Sri Lanka. Chinese cinnamon (Cinnamomum cassia
or Cinnamomum aromaticum), the cinnamon most commonly sold in the
U.S., goes by the name “Cassia.” Usage of cinnamon in Chinese medicine
is said to date back over 4,000 years. Mentioned in the Bible, cinnamon
was imported to Egypt and Europe from the Far East by 500 B.C. In
addition to its value as culinary spice, cinnamon has traditionally been
utilized as a folk medicine for colds and minor digestive complaints.
True cinnamon and cassia are very similar; cassia has a more pungent
flavor. Cassia buds can be found in potpourri and used as a flavoring
agent in sweets and beverages.1
Recent research has revealed that constituents in
cinnamon bark called procyanidin Type-A polymers help maintain the
body’s ability to metabolize glucose in a healthy way.*
Best Cinnamon Extract is Cinnulin PF®, a
patented, water extract of Cinnamon that contains Type-A polymers.
Cinnulin PF® is a registered trademark of Integrity Nutraceuticals
International and is manufactured under US Patent # 6,200,569.
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Use as Part
of Your Diet to Help Maintain a Healthy Blood Sugar Level*
In Vitro and Animal Studies
Research has revealed
that a number of herbs and spices have insulin-like activity.2
In a study published in 2000 by the U.S. Department of Agriculture
(USDA), cinnamon demonstrated the greatest ability to stimulate cellular
glucose metabolism among 49 botanicals tested.3
In a 2001 study,
researchers at the USDA’s Human Nutrition Research Center showed that
bioactive compounds in cinnamon trigger an insulin-like response in fat
cells.4 These compounds stimulated glucose uptake into cells
and increased glycogen (stored glucose) production via activation of the
enzyme, glycogen synthase.
The bioactive compounds in cinnamon appear to
potentiate insulin activity at the level of the cell receptor for
insulin. It has been shown that insulin resistance involves
downregulation of “insulin signaling” characterized by dephosphorylation
of the receptor.5 Enzymes called “protein tyrosine kinases”
(PTPases) are believed to decrease receptor phosphorylation, and
increased PTPase activity has been observed in insulin resistant rats.6
Cinnamon compounds have demonstrated the in vitro ability to
inhibit PTP-1 and increase autophosphorylation of the insulin receptor.7
In a recent animal study, cinnamon (cassia)
extract was administered to rats for three weeks. Following this, the
rats were infused with insulin and glucose to assess their insulin
response. Increased phosphorylation of the insulin receptor was observed
in skeletal muscle of these rats, suggesting that cinnamon has the
ability to potentiate insulin function by normalizing insulin signaling,
leading to improved uptake of glucose into skeletal muscle.8
Until recently, the
precise molecular structure of the bioactive compounds in cinnamon had
not been clearly defined. The USDA has now determined that the bioactive
compounds in cinnamon are water-soluble procyanidin Type-A polymers of
catechin and epicatechin. In a 2004 study, type-A polymers were
isolated from cinnamon and characterized by nuclear magnetic resonance
and mass spectroscopy. Type-A polymers were found to increase in
vitro insulin activity by a factor of 20. Type-A polymers also
exhibited antioxidant activity, as measured by inhibition of free
radical production in platelets. These results suggest that, in addition
to regulating glucose metabolism, cinnamon may help protect cell
membranes by controlling the lipid peroxidation associated with
disruptions in insulin function.9
Human Clinical Trial
The effect of cinnamon
on glucose and blood lipids levels on people with type 2 diabetes was
tested in a recent randomized, placebo-controlled trial. A total of 60
subjects were divided into six groups administered 1, 3, or 6 grams of
cinnamon daily, in 500 mg capsules, or equal numbers of placebo
capsules. The cinnamon or placebo capsules were consumed for two periods
of 20 days each. Serum glucose, triglyceride, cholesterol, LDL
cholesterol and HDL cholesterol were measured after 20 days, 40 days and
again at the end of a 20-day wash-out period, during which neither
cinnamon nor placebo was consumed.
In all three cinnamon
groups, statistically significant reductions in blood glucose levels
occurred, with decreases ranging from 18 to 29 percent. Interestingly,
glucose levels remained significantly lower after the 20-day wash-out
period (60 days from the study start) only in the group that took the
lowest cinnamon dose (1 gram daily). The placebo groups showed no
significant changes.
Decreases in
triglyceride levels ranging from 23 to 30% were observed in all three
cinnamon groups after 40 days. When the study ended at 60 days,
triglyceride levels remained lower than at the study start in the 1 and
3 gram cinnamon groups, but not in the group taking 6 grams daily.
Cholesterol reductions also occurred with the three cinnamon doses, with
decreases ranging from 13 to 25% that were maintained at the study end.
For LDL, the 3 and 6 gram cinnamon groups showed significant reductions
from 10 to 24%, while in the 1 gram cinnamon group, non-significant
reductions occurred after 40 days; LDL levels continued to decrease,
reaching statistical significance at 60 days. With respect to HDL,
significant increases were seen only in the 3 gram cinnamon group after
20 days; non-significant changes occurred in the 1 and 6 gram groups
after 40 days.
The overall results of
this trial demonstrate that cinnamon exerts a beneficial effect on blood
glucose and lipid levels in people with type 2 diabetes, at daily
intakes of 1 gram, and that this low dose is equally efficacious as are
the higher doses of 3 and 6 grams.10
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The various species of
cinnamon are classified as GRAS (generally regarded as safe) herbs.11
The Botanical Safety Handbook lists Cinnamomum cassia a “Class 2b” herb;
not to be used during pregnancy.12 The water-soluble cinnamon
extract is largely free of the lipid-soluble components of cinnamon.9
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Manniche, L. An Ancient Egyptian Herbal. 1989,
Austin,TX: University of Texas Press.
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Khan A, Bryden NA, Polansky MM, Anderson RA. Insulin
potentiating factor and chromium content of selected foods and
spices. Biol Trace Elem Res 1990;24(3):183-8.
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Broadhurst CL, Polansky MM, Anderson R. Insulin-like
biological activity of culinary and medicinal plant aqueous extracts
in vitro. J Agric Food Chem 2000;48(3):849-52.
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Jarvill-Taylor KJ, Anderson RA, Graves DJ. A
hydroxychalcone derived from cinnamon functions as a mimetic for
insulin in 3T3-L1 adipocytes. J Am Coll Nutr 2001;20(4):327-36.
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Nadiv O, Shinitzky M, Manu
H, et al. Elevated protein tyrosine phosphatase activity and
increased membrane viscosity are associated with impaired activation
of the insulin receptor kinase in old rats. Biochem J. 1998;298(Pt
2):443-50.
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Begum N, Sussman KE,
Draznin B. Differential effects of diabetes on adipocyte and liver
phosphotyrosine and phsophoserine phosphatase activities. Diabetes
1991;40(12):1620-9.
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Imparl-Radosevich J, Deas S, Polansky MM, et al.
Regulation of PTP-1 and insulin receptor kinase by fractions from
cinnamon: implications for cinnamon regulation of insulin
signalling. Horm Res 1998;50:177-182.
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Qin B, Nagasaki
M, Ren M, et al. Cinnamon extract
(traditional herb) potentiates in vivo insulin-regulated glucose
utilization via enhanced insulin signaling in rats. Diabetes
Res Clin Pract 2003;62(3):139-48.
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Anderson R, Broadhurst CL, Polansky MM, et al.
Isolation and characterization of polyphenol type-A polymers from
cinnamon with insulin-like biological activity. J Agric Food Chem
2004; 52(1):65-70.
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Khan A, Safdar S, Muzaffar M, et al. Cinnamon
improves glucose and lipids of people with type 2 diabetes. Diabetes
Care 2003;26(12):3215-18.
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Duke, JA. Handbook of Phytochemical Constituents of
GRAS Herbs and Other Economic Plants. 1992. Boca Raton, FL: CRC
Press.
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Botanical Safety Handbook. American Herbal Products
Association. McGuffin M, et al., eds. 1997; Boca Raton, FL: CRC
Press.
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