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(Reprinted from) LE Magazine February 2004
Turmeric is perhaps most familiar as the star ingredient in powdered curry mixes. Curcumin, a group of polyphenolic plant pigments, is responsible for turmerics characteristic canary yellow color. Curry is the signature seasoning and fragrant dish of the Indian subcontinent. Indias relationship with turmeric, and thus curcumin, goes back thousands of years. Both ginger and turmeric have been cultivated in India and southeast Asia for millennia. India produces and consumes most of the worlds turmeric. A cousin of ginger, turmeric was revered by the ancient Romans and Greeks, who valued its medicinal properties. Indeed, its English name derives from its Latin moniker, which roughly translates as earth-merit. Turmeric powder also is a popular remedy for stomach complaints throughout Asia. In Hawaii, it is reportedly used to treat swimmers ear (infection) and sinus infections. Perhaps one of its most important applications is as an anti-inflammatory for the treatment of arthritis; it has been used as such in China and India for thousands of years. Modern Science Meets Ancient Faith As if that were not enough, this hard-working spice shows promise as a potential treatment for multiple sclerosis,38 and may ameliorate the damaging effects of long-term diabetes.39 It is even being investigated as a topical treatment to speed diabetic wound healing.37 Some researchers also have noted an exciting link between turmeric consumption and a dramatically decreased incidence of Alzheimers disease, an effect that may well be related to curcumins ability to block signaling pathways that lead to inflammation.40,41 Turmeric Patent Granted Several years ago, two expatriate Indians associated with the
University of Mississippi Medical Center filed for a US patent
on turmeric. The patent was granted in 1995, but after an outcry
from an Indian agriculture group, it was promptly revoked.50 Protesters
challenged the patents validity on the grounds that turmeric
is a previously available product that has been used medicinally
in Asia for centuries. Since novelty is a condition
of patent protection, it was determined that turmeric is not subject
to such protection. The patent was revoked. Much discussion lately has focused on the use of cyclooxygenase-2 (COX-2) inhibitorssuch as the prescription medications Celebrex® and Vioxx®. This new approach arose from the observation that people who routinely take anti-inflammatory non-steroidal drugs (NSAIDs) are statistically less likely to develop disease than those who do not. Unfortunately, NSAIDs are poorly tolerated by some and can even cause bleeding in the gastrointestinal tract. Naturally occurring COX-2 inhibitors such as curcumin and certain phytosterols have been proven to be effective as chemopreventive agents against colon carcinogenesis with minimal gastrointestinal toxicity.18 Additionally, other studies using cells grown in the laboratory in vitro have demonstrated curcumins ability to prompt apoptosis, or programmed cell death, among leukemia, B lymphoma, and other cells. Curcumin has been used as a topical application to successfully induce apoptosis both in vitro and in animal models. One researcher understated the matter, noting, curcumin should be considered for further development as [a] preventive agent.43 Earlier this year, researchers at the University of Texas M.D. Anderson Cancer Center noted that curcumin has been found to be safe for human consumption, even in doses ranging as high as 10 grams per day.10 But other researchers have observed that more is not necessarily better. A recently published study out of India found that among rats fed a diet causing high blood sugar, those given low doses of curcumin did not develop experimentally induced cataracts as often as control subjects. But rats receiving high doses of curcumin actually developed cataracts somewhat faster, possibly due to increased oxidative stress.32 The difference in dosing was extreme, but these findings underscore the importance of further inquiry into the uses of curcumin in humans for a variety of diseases and under a variety of conditions. Contrary to the many remarkably encouraging reports on curcumins benefits, at least one study reported that curcumin
interfered with, rather than potentiated, the effects of
chemotherapy.19 Another study found no significant therapeutic
effect against prostate cancer,20 a finding that stands in stark
contrast to numerous other studies that have noted significant
activity by curcumin.12,13 This lack of consensus
has led some experts to caution against taking curcumin during
chemotherapy, except under an oncologists supervision. Researchers in Egypt noted that curcumin protected rats from oxidative stress injury following experimentally induced stroke.46 Stroke is a common result of thrombosis and/or atherosclerosis, which leads to clogging of the arteries that supply the brain with vital oxygen and nutrients. It is believed that such injury, known as ischemia/reperfusion (I/R) insult, is responsible for many of the deficits seen in stroke victims. Researchers concluded that curcumin protected the rats from I/R damage. They noted that when curcumin was administered at the highest levels, injury-related oxidants, believed to be responsible for the majority of I/R damage, were significantly reduced.46 Among the Reactive Oxygen Species (ROS) whose levels or activities were reduced by curcumin were xanthine oxidase, superoxide anion, malondialdehyde, glutathionine peroxidase, superoxide dismutase, and lactate dehydrogenase. As most readers of Life Extension already know, scientists attribute many of the undesirable effects of aging to the rogue activities of damaging free radicals, and antioxidants are crucial for their control. As noted previously, curcumin is a powerful antioxidant and many of its beneficial effects may be directly related to its ability to scavenge and neutralize these ROS. Positive Effects on Cholesterol Still more intriguing than its ability to limit peroxidation is the finding that curcumin raises HDL (good) cholesterol levels, even as it reduces LDL levels. In a small study of human volunteers, researchers reported a highly significant 29% increase in HDL among subjects who consumed one-half gram (500 mg) of curcumin per day for seven days. Subjects also experienced a decrease in total serum cholesterol of more than 11%, and a decrease in serum lipid peroxides of 33%.48 Further human studies are needed, but these preliminary findings are promising. As one research team noted: Administration of a nutritional dose of C. longa extracts [curcumin] may contribute to the prevention of effects caused by a diet high in fat and cholesterol in blood and liver during the development of atherosclerosis.27 Although scientific investigation into the therapeutic properties
of curcumin is ongoing, it seems clear that this plant pigment
from a humble tuber has powerful healing potential. The data are
occasionally conflicting, but it seems likely that adding curcumin
to ones diet makes exceptionally good sense. Curcumin appears
to inhibit cardiovascular disease, and
quell inflammation, and may even offer protection against Alzheimers
disease. Because it has been consumed safely by millions of people
literally for millennia, the choice to supplement ones diet
regularly with curcumin would seem to be a no-brainer. One word
of caution, however: curcumin is poorly absorbed by the gut. Its
absorption and bioavailability are significantly enhanced by the
addition of an agent such as piperine, a natural alkaloid derived
from black pepper.49 2. Navis I, Sriganth P, Premalatha B. Dietary curcumin with cisplatin administration modu- lates tumor marker indices in experimental fibrosarcoma. Pharmacological Research. 1999 Mar;39(3):175-79. 3. Ichiki K, Mitani N, Doki Y, Hara H, Misaki T, Saiki I. Regulation of activator protein-1 activity in the mediastinal lymph node metas- tasis of lung cancer. Clin Exp Metastasis. 2000;18(7):539-45. 4. Bharti AC, Donato N, Singh S, Aggarwal BB. Curcumin (diferuloylmethane) down-regu- lates the constitutive activation of nuclear fac- tor-kappa B and IkappaBalpha kinase in human multiple myeloma cells, leading to suppression of proliferation and induction of apoptosis. Blood. 2003 Feb;101(3):1053-62. 5. Lin JK, Chen YC, Huang YT, Lin-Shiau SY. Suppression of protein kinase C and nuclear oncogene expression as possible molecular mechanisms of cancer chemoprevention by apigenin and curcumin. J Cell Biochem Suppl. 1997;28-29:39-48. 6. Cheng AL, Hsu Ch, Lin JK, et al. Phase I clini- cal trial of curcumin, a chemopreventive agent, in patients with high-risk or pre-malig- nant lesions. Anticancer Res. Jul-Aug 2001;21(4B):2895-2900. 7. Miyoshi N, Nakamura Y, Ueda Y, et al. Dietary ginger constituents, galanals A and B, are potent apoptosis inducers in Human T lymphoma Jurkat cells. Cancer Lett. 2003 Sep 25;199(2):113-9. 8. Chan WH, Wu CC, Yu JS. Curcumin inhibits UV-induced oxidative stress and apoptotic biochemical changes in human epidermoid carcinoma A431 cells. J Cell Biochem. Oct 2003;90(2):327-38. 9. Menon LG, Kuttan R, Kuttan G. Antimeta- static activity of curcumin and catechin. Cancer Lett 1999 Jul 1;141(1-2):159-65. 10. Aggarwal BB, Kumar A, Bharti AC. Anticancer potential of curcumin: preclinical and clinical studies. Anticancer Res. Jan-Feb 2003;23(1A):363-98. 11. Ikezaki S, Nishikawa A, Furukawa F, et al. Chemopreventive effects of curcumin on glandular stomach carcinogenesis induced by N-methyl-N-nitro-N-nitrosoguanidine and sodium chloride in rats. Anticancer Res. 2001 Sep-Oct;21(5):3407-11. 12. Dorai T, Cao YC, Dorai B, Buttyan R, Katz AE. Therapeutic potential of curcumin in human prostate cancer. III. Curcumin inhibits proliferation, induces apoptosis, and inhibits angiogenesis of LNCaP prostate can- cer cells in vivo. Prostate. 2001 Jun 1;47(4):293-303. 13. Nakamura K, Yasunaga Y, Segawa T, et al. Curcumin down-regulates AR gene expres- sion and activation in prostate cancer cell lines. Int J Oncol. 2002 Oct;21(4):825-30. 14. Hour TC, Chen J, Huang CY, Guan JY, Lu SH, Pu YS. Curcumin enhances cytotoxicity of chemotherapeutic agents in prostate can- cer cells by inducing p21(WAF1/CIP1) and C/EBPbeta expressions and suppressing NF- kappaB activation. Prostate. 2002 May 15;51(3):211-8. 15. Gururaj AE, Belakavadi M, Venkatesh DA, Marme D, Salimath BP. Molecular mecha- nisms of anti-angiogenic effect of curcumin. Biochem Biophys Res Commun. 2002 Oct 4;297(4):934-42. 16. Cheng PY, Wang M, Morgan ET. Rapid transcriptional suppression of rat Cyto- chrome P450 genes by endotoxin treatment and its inhibition by curcumin. J Pharmacol Exp Ther. 2003 Oct 13 [Epub ahead of print]. 17. Ray SN, Chattopadhyay N, Mitra A, Siddiqi M, Chatterjee A. Curcumin exhibits anti- metastatic properties by modulating inte- grin receptors, collagenase activity, and expression of Nm23 and E-cadherin. J Environ Pathol Toxicol Oncol. 2003;22(1):49-58. 18. Reddy BS, Rao CV. Novel approaches for colon cancer prevention by cyclooxygenase-2 inhibitors. J Environ Pathol Toxicol Oncol 2002;21(2):155-64. 19. Somasundaram S, Edmund NA, Moore DT, Small GW, Shi YY, Orlowski RZ. Dietary curcumin inhibits chemotherapy-induced apoptosis in models of human breast cancer. Cancer Res. 2002 Jul 1;62(13):3868-75. 20. Imaida K, Tamano S, Kato K, et al. 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