Curcumin and Turmeric 500 mg, developed by Ray Sahelian, M.D.


Curcumin is one of the major antioxidants found in the spice
turmeric. The roots of the turmeric plant are used as an herb in Asian cooking such as curries. Curcumin
is a major component of Turmeric (Curcuma longa) and extensive
scientific research on curcumin and turmeric has demonstrated their potent antioxidant
properties. Through their antioxidant mechanisms, curcumin and turmeric support
colon health, exert neuroprotective activity and help maintain a healthy
cardiovascular system.
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Potential Benefits of Curcumin
Curcumin
is the major component of
Turmeric
(Curcuma longa L.) and extensive
scientific research on curcumin has demonstrated its potent antioxidant
properties. Through its antioxidant mechanisms, curcumin supports colon
health, exerts neuroprotective activity and helps maintain a healthy
cardiovascular system.
In vitro and animal studies indicate that
curcumin has potential as an antitumor, anti-invasive, and antiangiogenic agent;
as a chemopreventive agent; and as a therapeutic agent in diabetes, Alzheimer
disease, Parkinson disease, cardiovascular disease, pulmonary disease, and
arthritis. Curcumin may play a role in diseases such as Alzheimer's disease,
familial adenomatous polyposis, inflammatory bowel disease, ulcerative colitis,
colon cancer, pancreatic cancer, atherosclerosis, psoriasis, chronic anterior
uveitis and arthritis.
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Alzheimer's Disease
Curcumin has compounds
that may be helpful in Alzheimer's disease. Curcumin
helps prevent the formation of
beta-amyloids which are neural fibrils in the brain that cause Alzheimer's.
Cancer
Curcumin may help fight cancer, including prostate cancer. Researchers have found in the lab that curcumin can
enhance the cancer-fighting power of treatment with TRAIL, a naturally occurring molecule
that helps kill cancer cells. TRAIL stands for tumor necrosis factor-related
apoptosis-inducing ligand. In an experiment with human prostate cancer cells in a
laboratory dish, the combination treatment killed off two to three times more cells than
either treatment alone. Curcumin exerts multiple different suppressive
effects on human breast carcinoma cells in vitro.
In a test tube study, curcumin was found to
have anticancer effects on human Burkitt's lymphoma.
Heart
In a rodent study, curcumin was
found to protect rat myocardium against ischemic insult and the protective
effect could be attributed to its antioxidant properties.
Multiple Sclerosis
Curcumin may block
the progression of multiple sclerosis.
Curcumin safety
Pilot phase I clinical trials show curcumin to be safe even when consumed
at a daily dose of 10 grams a day for 3 months. For more
curcumin turmeric information.
Curcumin for renal
transplant
Beneficial effects of the bioflavonoids
curcumin and quercetin on early
function in cadaveric renal transplantation: a randomized placebo
controlled trial.
Transplantation. 2005 Dec 15;80(11):1556-9. Shoskes D, Lapierre C, et
al. Department of Kidney Transplantation, Cleveland Clinic Florida,
Weston, FL, USA.
The bioflavonoids quercetin and curcumin are renoprotective natural
antioxidants. We wished to examine their effects on early graft function (EF).
43 dialysis dependent cadaveric kidney recipients were enrolled into a
study using Oxy-Q which contains 480 mg of curcumin and 20 mg of quercetin,
started after surgery and taken for 1 month. They were randomized into
three groups: control (placebo), low dose (one capsule, one placebo) and
high dose (two capsules). Bioflavonoid therapy improved early graft
function. Acute rejection and neurotoxicity were lowest in the high dose
group. These bioflavonoids improve early outcomes in cadaveric renal
transplantation, possibly through HO-1 induction.
Curcumin study
Curcumin modulates free radical quenching
in myocardial ischaemia in rats.
Manikandan P. Central Leather Research Institute, Adyar, Chennai 600020, India.
Int J Biochem Cell Biol. 2004 Oct;36(10):1977-90.
This study was designed to investigate the protective effect of curcumin
against isoprenaline induced myocardial ischaemia in rat myocardium. The effect
of single oral dose of curcumin (15mgkg(-1)), administered 30min before and/or
after the onset of ischaemia, was investigated by assessing oxidative stress
related biochemical parameters in rat myocardium. Curcumin pre and
post-treatment (PPT) was shown to decrease the levels of xanthine oxidase,
superoxide anion, lipid peroxides and myeloperoxidase while the levels of
superoxide dismutase, catalase, glutathione peroxidase,
glutathione-S-transferase activities were significantly increased after curcumin PPT. Histopathological and transmission electron microscopical studies
also confirmed the severe myocardial damage occurring as a consequence of
isoprenaline induced ischaemia and they also showed the significant improvement
effected by curcumin PPT. These findings provided evidence that curcumin was
found to protect rat myocardium against ischaemic insult and the protective
effect could be attributed to its antioxidant properties as well as its
inhibitory effects on xanthine dehydrogenase/xanthine oxidase conversion
and resultant superoxide anion production.
Inhibition of colonic aberrant crypt foci by curcumin
in rats is affected by age.
Kwon Y, Malik M, Magnuson BA.
Nutr Cancer. 2004;48(1):37-43.
Curcumin has antioxidative, anti-inflammatory, and chemopreventive activities.
To determine whether aging affects the inhibition of colon carcinogenesis by
curcumin, young (6 wk), mature (12 mo), and old (22 mo) F344 male rats were fed
either AIN-93 containing 0.6% curcumin or AIN-93 control diet. Aberrant crypt
foci (ACF) were induced with two weekly s.c. injections of azoxymethane. After
an additional 3 mo on the diets, the number, multiplicity, and distribution of
ACF were evaluated. Addition of curcumin to the diet reduced the number of ACF
by 49% in young rats and by 55% in old rats. However, interestingly,
no reduction of ACF was found in mature rats fed curcumin. Inhibition of large
ACF was also affected by age, with the greatest reduction of large ACF occurring
in old rats. However, animal age did not significantly alter the effect of
dietary curcumin on reduction of cyclooxygenase-2 mRNA expression in the liver
or reduction of serum total cholesterol levels. These results indicate that age
may play a significant role in the efficacy of chemoprevention of colon cancer
by curcumin.
Curcumin has potent anti-amyloidogenic effects for
Alzheimer's beta-amyloid fibrils in vitro.
Ono K. J Neurosci Res. 2004 Mar
15;75(6):742-50.
Kanazawa University Graduate
School of Medical Science, Kanazawa, Japan.
Inhibition of the accumulation of amyloid beta-peptide (Abeta) and the formation
of beta-amyloid fibrils (fAbeta) from Abeta, as well as the destabilization of
preformed fAbeta in the central nervous system, would be attractive therapeutic
targets for the treatment of Alzheimer's disease (AD). We reported previously
that nordihydroguaiaretic acid (NDGA) and wine-related polyphenols inhibit
fAbeta formation from Abeta(1-40) and Abeta(1-42) and destabilize preformed
fAbeta(1-40) and fAbeta(1-42) dose-dependently in vitro. Using fluorescence
spectroscopic analysis with thioflavin T and electron microscopic studies, we
examined the effects of curcumin and rosmarinic acid (RA) on the
formation, extension, and destabilization of fAbeta(1-40) and fAbeta(1-42) at pH
7.5 at 37 degrees C in vitro. We next compared the anti-amyloidogenic activities
of Curcumin and RA with NDGA. Curcumin and RA dose-dependently inhibited fAbeta formation
from Abeta(1-40) and Abeta(1-42), as well as their extension. In addition, they
dose-dependently destabilized preformed fAbetas. The overall activities of Curcumin,
RA, and NDGA were similar. The effective concentrations (EC(50)) of Curcumin, RA, and NDGA for the formation, extension, and destabilization of fAbetas were in the
order of 0.1-1 microM. Although the mechanism by which Curcumin and RA inhibit fAbeta
formation from Abeta and destabilize preformed fAbeta in vitro remains unclear,
they could be a key molecule for the development of therapeutics for AD.
Curcumin questions
Q. I just purchased several bottles of Curcumin and found a discrepancy that I
would appreciate your assistance in clarifying. The bottle says to take 1 to 3
capsules daily and some sites says to take 1 to 2 a few times a week with
breakfast. Which one should I follow?
A. There is no dosage guideline that is appropriate for everyone.
As a general rule, it is a good idea to start with one capsule and over time
gradually increase to determine the ideal amount that works for you. It is
generally preferable to take 2 or 3 different beneficial herbs in smaller
amounts than to take one herb in a high amount. For more
curcumin information.
Q. Can acai or
Mangosteen one capsule be taken along with one capsule
of curcumin?
A. We don't foresee any problems with the combination of
Acai or mangosteen and curcumin.
Q. I have read that curcumin is basically not
assimilated by the body without the addition of black pepper, in itself not
something desirable in a diet.
A. We have not seen any studies that prove the claim that a
curcumin supplement needs a black pepper extract to be effective.
Q. I wanted to let you know about an interesting
curcumin study.
Effects of curcumin on bladder cancer cells and development of urothelial tumors
in a rat bladder carcinogenesis model - Cancer Lett. 2008 Mar 12 - "Exposure of
human bladder cancer cells to curcumin resulted in the induction of apoptotic
cell death and caused cells to arrest in the G2/M phase. The anti-apoptotic
Bcl-2 and Survivin protein was downregulated by the curcumin treatment together
with enhancement of the Bax and p53 expression. The inhibitory activities of
curcumin were stronger than those of cisplatin and could not be prevented by
catalase pretreatment in T24 cells. Clonal assay indicated large-dose and
short-term curcumin was lethal to bladder cancer cells. Moreover, the in vivo
study revealed curcumin did induce apoptosis in situ, inhibit and slow the
development of bladder cancer. These observations suggest that curcumin could
prove an effective chemopreventive and chemotherapy agent for bladder cancer"
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