Curcuma: Turmeric by Jill Hoppe, Clinical Herbalist Medical Herbalism 11(4):1,3-5 Curcuma longa (turmeric) is a perennial herb of the Zingiberaceae (ginger) family that has been revered as a food and medicine for thousands of years. Having a long history of use for its anti-inflammatory effects, turmeric is an herb of major importance in the East and has been used extensively in the Indian (both Ayurveda and Unani Tibb) and Chinese systems of medicine. Turmeric is cultivated in many parts of the world, but India produces most of the world’s supply. Curcuma longa is the most popular species of turmeric grown in India. Turmeric is widely used as a condiment in Indian curries and prepared mustard and its powerful antioxidant actions assist in preserving the freshness of food by preventing oxidation. The part used in commerce is the cured (boiled, cleaned, sun dried and polished) rhizome. Indian Materia Medica Part Used: Tubers and rhizomes Preparations: Powder, paste, ointment, oil, lotion, inhalant, confection Actions: Aromatic, stimulant, tonic, carminative, anthelmintic Uses: Internally used as an antiparasitic. Used for jaundice and other liver afflictions. Root used for intermittent fevers. 1000-1300 mg. twice daily for flatulence, dyspepsia and weak state of the stomach. Internally and externally for skin diseases due to blood impurity. A paste applied hot to sprains, bruises, wounds and inflammatory troubles of the joints. Juice of the fresh rhizome applied to wounds, bruises and leech-bites. A thin paste applied to facilitate the scabbing process in chickenpox. A decoction (1 ounce of the bruised root to 20 ounces of water) applied as a lotion to relieve burning in catarrhal and purulent opthalmia conjunctivitis and other eye inflammations. A piece of cloth soaked in the decoction, and placed over the afflicted eye, relieves the symptoms. Sprinkled
on
ulcers to stimulate them to healthy action.
Mixed with ghee to relieve cough. A paste, alone or in combination with the pulp of neem leaves, used in ringworm, obstinate itching, eczema and parasitic skin diseases. An ointment of turmeric, hemp leaves, onions and warm mustard or linseed oil for painful and protruding hemorrhoids, and for eczema and other itchy conditions. A thick coating of mustard oil, dusted with turmeric, is applied for shingles. Sprinkled over burning charcoal for scorpion stings, with the smoke applied to the affected part for a few minutes. With alum powder in proportion of 1 part turmeric to 20 parts alum, blown into the ear for inflammation of the ear with discharge. Internally for urinary tract diseases. A good digestive compound powder: equal parts turmeric, long pepper, ginger, cardamom, with ˝ part black pepper. (Nadkarni) Chinese Medicine In Chinese Medicine, turmeric is considered an herb that invigorates the Blood. This class of herbs may be used to treat pain, abscesses and ulcers, and abdominal masses. In Chinese Medicine, the rhizome and tuber are distinguished as decribed in the box on page three.. Clinical Trials Most
research has taken place in India and has
focused upon turmeric’s
active
curcuminoids (the most well known being
curcumin) and volatile oil. The
curcuminoids are an important class of
antioxidant and
anti-inflammatory
constituents and are responsible for turmeric’s
vibrant yellow color.
Turmeric
has been investigated for its anti-inflammatory,
antibacterial,
antiparasitic,
choleretic, antiviral, antiplatelet, analgesic,
antioxidant,
anticancer,
antihepatotoxic and antitumor effects. Most
investigations have been in
vitro and vivo. Some of the human clinical
trials have studied its
ability
to influence the secretion of bile (Ammon),
gallbladder contraction
(Rasyid),
effects against inflammation (Satoskar),
anti-rheumatic activity
(Deodhar)
ability to reduce cholesterol and lipid
peroxides (Soni), and
cancer-protective
effects in chronic smokers (Polasa). Turmeric is
useful for treating
pain
and inflammation for people coming off
non-steroidal anti-inflammatory
drugs (NSAIDs), particularly in combination with
other anti-
inflammatories
such as Ananas sativas (bromelain, a
proteolytic enzyme from
the
stem of the pineapple) and bioflavonoids such as
quercetin (high in
onions,
evening primrose leaf). See Case Study. In human
clinical trials the
constituent
curcumin has been shown as effective as NSAIDs,
without the side
effects.
In one double-blind study, 45 patients aged
15-68 received either 400
mg.
curcumin, placebo, or 100 mg. of the NSAID
phenylbutazone three times
daily
for six days following inguinal hernia and/or
hydrocele (accumulation
of
fluid in scrotum or spermatic cord) surgery.
Patients receiving the
drug
or curcumin produced a significantly greater
anti-inflammatory response
than placebo, and only curcumin reduced
spermatic cord edema and cord
tenderness
significantly (Satoskar). In another
double-blind study, patients were
administered 1,200 mg. curcumin or 300 mg.
phenylbutazone daily.
Improvements
in the duration of morning stiffness, walking
time, and joint swelling
were comparable in both groups (Deodhar).
Although the mechanism of
action
is not fully understood, turmeric’s
anti-inflammatory actions are
thought
due to its ability as an antioxidant to quench
free radicals, hindering
tissue degeneration and its ability to inhibit
the arachidonic acid
(AA)
cascade. The AA cascade is a pathway in fatty
acid metabolism that
builds
the pro-inflammatory series 2 prostaglandins
(PGE2s). Curcumin has been
shown to be a dual inhibitor of AA metabolism
since it inhibits both
the
enzymes lipogenase and cycloxygenase (Ammon,
Safayhi). The activity of
lipogenase is required to transform AA to
leukotrienes (triggers for
the
inflammatory process). Vitamin E,
eicosapentaenoic acid (EPA), onion,
garlic
and Boswellia serata (boswellin) have
also been shown to
inhibit
lipogenase. Cyclooxygenase is required to
transform arachidonic acid to
the series 2 prostaglandins and series 2
thromboxanes. Curcumin was
shown
to inhibit the activity of cyclooxygenase-2
(COX-2) in several
gastrointestinal
cell lines (Zhang). Two isoforms of
cyclooxygenase are cyclooxygenase-1
(COX-1) and cyclooxygenase-2 (COX-2). COX-1 is
involved in metabolic
activities
such as maintaining stomach lining integrity,
regulating blood flow
within
the kidneys and balancing platelet function and
is produced widely
throughout
the body. COX-2 is produced in response to
tissue injury and plays a
role
in inflammation, infections, and cellular
proliferation (Feldman). Most
NSAIDs inhibit both COX-1 and COX-2 and studies
have proposed COX-1
inhibition
is the reason that long-term NSAID use leads to
gastric ulcerations and
perforations in 10 – 20% of patients using these
drugs (Lichtenstein).
The new NSAID celebrex (celecoxib) appears to
inhibit COX-2
selectively,
with less inhibition of COX-1. A recent
meta-analysis showed that
celebrex
caused ulcers at only about one-third to
one-half the rate of other
NSAIDs
(Silverstein). The lower rate is about the same
as the rate of ulcers
in
the general population not taking NSAID
according to an editorial in
the
Journal of the American Medical Association
(Lichtenstein). Curcumin
has
also been compared to an NSAID for ulcerogenic
potential in an animal
study,
where it had about one-third the ulcerogenic
index score compared to
phenylbutazone
(Srimal). In another animal trial, curcumin
protected against ulcer
formation
induced by phenylbutazone (Bhatia).
General Dosage Ground turmeric rhizome: 1 teaspoon blended in water or juice up to four times daily (approximately 10 grams) Standardized turmeric extract containing 400 – 600 mg curcumin three times daily (typically standardized to 95% curcuminoids) Tincture: 1 – 1˝ teaspoon three times daily (dried rhizome 1:5, 50% alcohol) Side Effects According
to
the German Commission E, turmeric is
contraindicated in persons with
obstruction of bile passages. This is most
likely due to turmeric’s
cholagogue
activity. The Botanical Safety Handbook
states that use of
turmeric
should be avoided with bile duct obstruction or
gallstones, and should
not be administered to people who suffer from
stomach ulcers or
hyperacidity.
It is also contraindicated in pregnancy. High
doses should not be given
to patients taking antiplatelet or anticoagulant
drugs. Used in the recommended amounts, turmeric is generally considered safe. It has been used in large quantities as a condiment with no adverse reactions. Table 1 Curcuma: Rhizoma Curcumae (Jiang Huang) Properties: Acrid, bitter, warm Channels Entered: The Spleen, Stomach, Liver meridians Clinical Uses Invigorates the Blood and promotes menstruation. Used for chest or abdominal pain, amenorrhea, or dysmenorrhea due to Congealed Blood generated by Deficiency Cold. Used for pain and swelling from trauma. Moves Qi and alleviates pain. Used for epigastric and abdominal pain due to Stagnant Qi. Expels Wind and moves Blood. Used for damp painful obstruction with Congealed Blood, especially in the shoulders. Stimulates bile secretion and increases detoxifying abilities of the liver. Used for general pain, arthritis in the shoulders. Stimulates the uterus, causing it to contract for five to seven hours. Tuber Curcumae (Yu-Jin) Properties: Bitter, pungent flavor, cool Channels entered: The Heart, Lung, and Liver meridians Clinical Uses Invigorates the Blood and breaks up Congealed Blood. Used topically and internally for pain related to traumatic injury and to hasten the healing of chronic sores. Used
for chest, abdominal, flank, or menstrual pain
from constrained Liver
Qi.
Used for constrained Liver Qi patterns with heat
signs. Clears the Heart and cools the Blood. Used when hot phlegm obstructs the Heart orifices with symptoms such as anxiety, agitation, seizures, or mental derangement. Facilitates gallbladder function by promoting the secretion of bile from the liver. Used for jaundice. Stimulates gastric secretion, thereby increasing appetite. Contraindications for rhizome and tuber When either Stagnant Qi or Congealed Blood are not present Cases of Deficient Yin from loss of blood Pregnancy Dosage for rhizome and tuber 3 – 9 g (Bensky and Gamble; Hsu) References Ammon HPT, Wahl MA. Pharmacology of Curcuma longa. Planta Medica 1991;57:1-6 Ammon HP, Safayhi H, Mack T, Sabieraj J. Mechanism of anti-inflammatory actions of curcumine and boswellic acids. Journal of Ethnopharmacology. 1993;38(2-3):113-119 Bensky D, Gamble A, with Kaptchuk T. Chinese Herbal Medicine Materia Medica. Seattle, Washington: Eastland Press, Inc., 1986 Bhatia A, Singh GB, Khanna, NM, Indian Journal of Experimental Biology. 1964;2: 158-160 Blumenthal M. Herbal Medicine Expanded Commission E Monographs. Boston, Massachusetts: Integrative Medicine Communications, 2000 Buhner SH. Herb for Hepatitis C and the Liver. Pownal Vermont: Storey Books, 2000 Deodhar SD, Sethi R, Srimal RC. Preliminary study of antirheumatic activity of curcumin (diferuloyl methane). Indian Journal of Medical Research 1980; 71:632-634 Feldman M, McMahon A. Do Cyclooxygenase-2 Inhibitors Provide Benefits Similar to Those of Traditional Nonsteroidal AntiInflammatory Drugs, with Less Gastrointestinal toxicity? Annals of Internal Medicine. 2000;132(2):134-143 Gerard, J. The Herbal or General History of Plants. New York, New York: Dover Publications, Inc., 1975 (reprinted from the 1633 original) Hsu
HY, Chen Y, Shen S, Hsu C, Chen C, Change H. Oriental
Materia Medica.
New Canaan, Connecticut: Keats Publishing, 1986
Lichtenstein D, Wolfe M. COX-2 Selective NSAIDs. New and Improved? JAMA. 2000;284(10) McCaleb R, Leigh E, Morien K. The Encyclopedia of Popular Herbs. Rocklin, California: Prima Publishing, 2000 Mills S., Bone K. Principles and Practice of Phytotherapy. London, England: Churchill Livingstone, 2000 Nadkarni’s KM. Indian Materia Medica. Mumbai, India: Popular Prakashan Private Limited, 1999 Pizzorno J. Total Wellness. Rocklin, California: Prima Publishing, 1998 Polasa K, Raghuram TC, Krishna TP, Krishnaswamy K. Effect of turmeric on urinary mutagens in smokers. Mutagenesis 1992;2:107-109 Ramirez-Bosc A, Soler A, Gutierrez MAC, et al. Antioxidant Curcuma extracts decrease the blood lipid peroxide levels of human subjects. Age 1995; 18:167-16 Rasyid A, Lelo A. The effect of curcumin and placebo on human gall-bladder function: an ultrasound study. Ailment Pharmacological Therapy 1999; 13(2): 245-249 Satoskar RR, Shah SJ, Shenoy SG. Evaluation of anti-inflammatory property of curcumin (diferuloyl methane) in patients with postoperative inflammation. International Journal of Clinical Pharmacology, Therapy and Toxicology 1986; 24(12):651-654 Silverstein FE, Faich G, Golsdstein JL, Simon LS, et al. Gastrointestinal Toxicity With Celecoxib vs Nonsteroidal Anti-inflammatory Drugs for Osteoarthritis and Rheumatoid Arthritis: The CLASS Study: A Randomized Controlled Trial. JAMA 2000; 284(10):1247-1255 Soni KB, Kuttan R. Effect of oral curcumin administration on serum peroxides and cholesterol levels in human volunteers. Indian Journal of Physiology and Pharmacology 1992;36(4):273-275 Srimal RC, Dhawan BN. Journal Pharm Pharmacology 1973; 25(6)447-452 Cited in: Mills S., Bone, K, Werbach M, Murray M. Botanical Influences on Illness A Sourcebook of Clinical Research. Tarzana, California: Third Line Press, Inc., 2000 Zjang
F, Altorki N, Mestre J, Subbaramaiah K,
Dannenberg A. Curcumin inhibits
cyclooxygenase-2 transcription in bile acid and
phorbol ester-treated
human
gastrointestinal epithelial cells. Carcinogenesis.
1999;20(3):445-451
Copyright 2001 Paul Bergner |
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