Remediable Medicinal Plants
used for Dysmenorrhea treatment- A short review
A.K.
Meena1*, Anshul Sinha1, H.C.
Mehta1, M. D. Gupta1, M. M. Rao2 and M. M.
Padhi3
1National Research Institute for Ayurveda -Siddha Human Resource Development, Gwalior-474009
2Ayurveda Central Research Institute, New Delhi
3Central Council for Research in Ayurvedic Sciences, New Delhi-110058,
(India)
ABSTRACT:
The medical term for menstrual cramps is dysmenorrhea. Menstrual cramps are pains that begin in the
lower abdomen and pelvis, i.e. below the waistline. The cramps can be a quite
painful or simply a dull ache. They can be periodic or continual. More than 10000 plant species are used as
traditional medicines in the treatment of dysmenorrhea.
Since the ancient times, plants have been exemplary sources of
medicine. Ayurveda
and other Indian medicinal system literature mention the use of plants in
various human ailments. India has about 45000 plant species and among them
several thousand are claimed to possess medicinal properties. Researchers
conducted in the last few decades on the plants mentioned in ancient literature
or used traditionally for dysmenorrhea. This review
reveals that plants and their extracts used as dysmenorrhea remedy.
KEYWORDS:
Dysmenorrhea, Medicinal plants, Menstruation,
Active constituents.
INTRODUCTION:
Dysmenorrhea is painful menstrual cramps. The pain from menstrual
cramps can range from mild to severe and can involve the lower belly, back, or
thighs. Women may also have headaches, nausea, dizziness or fainting, or
diarrhea or constipation with cramps. There are two types of dysmenorrhea primary and secondary. Primary dysmenorrhea is thought to be caused by excessive levels of
prostaglandins, hormones that make uterus contract during menstruation and
childbirth. Its pain probably results from contractions of uterus that occur
when the blood supply to its lining (endometrium) is
reduced. Secondary dysmenorrhea is menstrual pain
that is generally related to some kind of gynecologic disorder, such as
endometriosis, adenomyosis, uterine fibroids and
infection. Pain from secondary dysmenorrhea usually
begins earlier in the menstrual cycle and last longer than common menstrual
cramps. Most of these disorders can be easily treated with medications or
surgery. Due to secondary dysmenorrhea often start
sooner in the menstrual cycle than those of primary dysmenorrhea
and usually last longer. Secondary dysmenorrhea is
more likely to affect women during adulthood [1-3].
Remediable Medicinal Plants
for Dysmenorrhea:
Some medicinal plants are listed below which are
effective for treatment of dysmenorrhea with minimal
or without side effects.
Trichilia emetica Vahl.
Trichilia emetica fruits
are diuretic and also used against poisoning, hepatitis, ulcer, dysmenorrhoea, asthma, cirrhosis and internal worms
[4]. The plant is used as purgative, antiepileptic, antipyretic, general
tonic and for bronchial inflammation [5]. Trichilia emetica plant contains fats, resin,
tannin, polyphenolic and bitter principle related to calicedrin,[5] limonoids
[6-7]. Trichilia emetica
possess many biological activities like antifungal, bactericidal and antiviral,
antimalarial, insect antifeedant
and growth regulation properties [8-9] and antischistosomiasis
activities [10]. The limonoids are
powerful inhibitors of leukotriene biosynthesis of
human leucocytes [11].
Acorus calamus
Linn. :
Acorus calamus
Linn is commonly known as sweet flag is an aromatic medicinal plant belonging
to the Araceae family, it is wild or cultivated
throughout Himalayas at an altitude ascending up to 6000 ft [12].
Rhizome, roots and leaves contain volatile oil, where asarone
and ß‐asarone are the important constituents, Presence of
small quantities of palmitic, heptylic
and butyric. Main chemical constituents and components are asarone,
alpha pinene, beta asarone,
calamenol, calamene, calamenone, eugenol, methyl eugenol, calamone, azulene, sugars, glucosides and
flavones. Roots contain tricyclic sesquitepene‐ Callaminon, aclamendiol and isocalamendiol [13].
The rhizomes of Acorus calamus
contain aromatic oil and are considered to possess anti‐spasmodic, carminative and anthelmintic, aromatic, expectorant, nauseant,
nervine, sedative, stimulant properties and also used
for the treatment of epilepsy, mental ailments, chronic diarrhea, dysentery, dysmenorrhea bronchial catarrh, intermittent fevers and
glandular and abdominal tumors. Acorus calamus is also employed for kidney and liver troubles,
rheumatism, sinusitis, and eczema [14].
Cannabis indica:
Cannabis indica extracts may represent an
efficacious and safe alternative for treatment of a wide range of conditions in
women including dysmenorrhea, dysuria,
hyperemesis gravidarum, and
menopausal symptoms [15]. Cannabis indica
have great value and it has been found useful in uterine sub involution,
chronic inflammation, irritation, metrorrhagia and
nervous spasmodic. Cannabis indica used in symptomatic treatment of convulsive
disorders, migraine, insomnia and dysmenorrhea [16].
Cannabis sativa:
Cannabis sativa leaves are bitter, astringent,
tonic, aphrodisiac, alterative, intoxicating, stomachic, analgesic and abortifacient. They are used in convulsions, otalgia, abdominal disorders, malaria, dysentery, diarrhea,
skin diseases, hysteria, insomnia, gonorrhea, colic, tetanus and hydrophobia.
Its excessive use causes dyspepsia, cough, impotence, melancholy, dropsy,
restlessness and insanity. The bark is tonic and useful in inflammations,
hemorrhoids and hydrocele. The inflorescence of
female plant is intoxicating, stomachic, soporific, abortifacient
and useful in convulsions. Seeds are carminative, astringent, aphrodisiac,
antiemetic and anti- inflammatory. The resin is smoked to allay hiccough and
bronchitis. It is useful in insomnia, sick headaches, neuralgia, rnigrain, mania, whooping cough, asthma, dysuria and in relieving pain in dysmenorrhoea
and menorrhagia.
Main chemical constituents are Spiro
compounds, viz., cannabispiran,
dehydrocannabi-spiran, and beta- cannabispiranol,
dehydrostilbenes-3-[2-(3-hydroxy-4-methoxyphenyl) ethyll-5-methoxyphenol and canniprene, acylated 0-glucoside
of apigenol,
0-glycosides of vitexin, isovitexin,
orientin , α-bergamotene,
β -caryophyllene, α-humulene,
γ-elemene, α -gurjunene,
β - isabolene, β- caryophyllene-epoxide and α-bisabolol,
cannabinoids, tetrahydro-cannabinol, cannabinol,
α -pinene, myrcene,
limonene, terpinolene, friedelin
epifridelinol, β -sitosterol,
carvone, dihydrocarvone , vitexin, isovitexin, orientin, acyl derivative of apigenol, N-acetyl-glucosamine, N-acetylgalactosamine,
22- 0-glucopyranosylvitexin [17].
Papaver somniferum Linn.
Papaver somniferum have anticonvulsant, analgesic, [18-20] antitissuve,
cardiovascular, synergistic, antinociceptive [21],
anorectic, locomotor, hypotensive,
sedative, antispasmodic [22], hydrolytic [23], antitumour [24], hypoglycaemic,
carcinogenesis protective [25] and antidiarrhoeal
activities. It beneficial in migraine, malaria, dysmenorrhea,
cystitis, menorrhagia and other painful conditions [26-28].
Papaver somniferum contains
about 25 alkaloids among which morphine (10-16%) is the most important base.
The other alkaloids isolated are codeine, narcotine, thebaine, noscapine, narceine, papaverine etc [29].
Fixed oil of Papaver somniferum
contains esters of linoleic, palmitic,
oleic acids [30].
Leucas cephalotes Spreng:
The leaves and
flowers of Leucas cephalotes
are acrid, thermogenic, carminative, digestive, anthelmintic, anti-inflammatory, emmenagogue,
sudorific, antipyretic, expectorant, antibacterial
and depurative. They are useful in colic, dyspepsia, verminosis,
arthralgia, chronic skin eruptions, psoriasis, cough
and catarrh in children, amenorrhoea, dysmenorrhoea, intermittent fevers and ulcers [28].
The whole plant is laxative, diaphoretic, and useful in bronchitis, jaundice,
inflammations, asthma, dyspepsia, paralysis and leukemia [31-33].
Plant is cardiac depressant, hypotensive [34],
antiseptic [35], insectisidal [12],
antiscabies [36] and anticoagulant [37].
Nineteen
compounds were isolated by chromatographic separation of 1-butanolsoluble
fraction of the MeOH extract of Leucas cephalotes [38]. The
structures of known compounds were identified as oleanolic
acid, 7-oxysitisterol [39-40], 7-oxostigmasterol [41], 7
alpha-hydroxy-sitosterol [39],
7 alpha-hydroxystigmasterol [38], stigmasterol [42],
5-hydroxy-7,4,1-dimeathoxy-flavone [43], gonzalitosin
[44], tricin [45] and apigenin 7-0-β-D-(6-O-p-coumaroyl) glucopyranoside
[46-47].
Juniperus communis Linn.
Fruits of Juniperus communis are
carminative, stimulant, styptic, stimulant, emmenagogue,
digestive, diuretic, disinfectant, antiseptic and are useful in chronic bright's disease, dropsy, asthma, cough, respiratory
affections, migraine, rheumatic and painful swellings, nephrotic
dropsy of children, cattarah, gonorrhoea,
pulmonary blennorhoea, arthritis, amenorrhea,
diabetes, infantile tuberculosis, bladder affections, chronic pyelonephritis, dysmenorrhea,
piles and abdominal disorders. The bark is applied in skin infections. The plant is used as appetizer, carminative, anthelmintic, alexipharmic, laxative, useful in diarrhea,
abdominal pains, strangury diseases of the spleen and
abdomen, ascites, tumours,
piles, bronchitis, indigestion, constipation and vaginal discharges [32].
The fruit of Juniperus communis Linn. contains the main
constituents viz. mono-terpenoids, -pinene, myrcene, sabinene, camphene, camphor, cineole, p-cymene [48], cadinenes, bornyl acetate[49], limonene, -pinene, - terpinene,
terpinen-4-ol, -phellandrene; diterpenoids:
caryophyllene, sandaracopinaric
acid, isocupressic acid, isopimaric
acid, imbricatolic acid, 16-epoxy-12- hydroxy-8(17),13(16),14-labdatrien-19-oic acid [50],
flavonoids
luteolin-7-O-D-glucoside,kaempferol-3-O-D-glucoside, quercitrin,
apigenin, luteolin, robustaflavone, apodocar-pusflavone,
hinokiflavone [51], catechins:
(+)- afzelechin, (-)-epiafzelechin,
(+)-catechin, (-)-epicatechin,
(+)-gallocatechin, (-)-epigallocatechin
[52]. The leaf contains essential oils: -pinene
(17%), sabinene (12%), terpinen-4-ol (7.7%), phellandrene (7.3%), widdrene
(6.4%), terpinene (5.9%), - terpinene
(4.3%), -terpinene (3.8%) [53], limonene
(4.2%), terpinen-4-ol (2.7%), myrcene (2.6%), -pinene (2.0%) [54] and also contains biflavonoids: cupressuflavone, amentoflavone, hinokiflavone, isocryptomerin, sciadopitysin[55-56].
Piper cubeba Linn.
The fruits of Piper cubeba
are acrid, bitter, thermogenic, aromatic, stimulant,
carminative, diuretic, expectorant [7], analgesic, dentifrice, antiinflammatory, anthelmintic, deobstruant, vulnerary, appetising,
digestive, stomachic, cardiotonic, rejuvenating, emmenagogue, sedative and antiseptic. It is useful in body ache,
odontalgia, cephalalgia,
halitosis, inflammation, helminthiasis, worm’s
infestation, wounds and ulcers, catarrh, anorexia, dyspepsia, flatulence, haemorrhoids, cardiac debility, cough, asthma, bronchitis
and various respiratory disorders, amenorrhoea and dysmenorrhea, [28]. Fruits contain an essential
oil beneficial as a local remedy in the form of lozengel
of relief throat troubles when taken internally. It exerts a positive
antiseptic effect on urine hence used in genitourinary diseases [17, 26,
57]. Phytochemical screening of Piper
cubeba extracts has detected alkaloids/amides, lignans, neolignans and terpenes, including aschantin, dihydrocubebin, piperine
alkaloid, piperol A, B and C, piperol
A-triacetate, the terpenes α-copaene,
ρ-cymene, germacrene D and limonene(among
others), sesamin and (+)-Zeylinol
[58]. In a more recent review, Usia et al.
reported sixteen known compounds (α-asarone,
(-)-clusin, (-)-dihydroclusin,
ethoxyclusin, (-)-cubebin,
(-)-cubebinin, (-)-cubebininolide,
(-)-dihydrocubebin, α-methylcubebin,
(-)-hinokinin, magnosalin, medioresinol, 2,4,5-trimetoxiphenylacetone,
1-(2,4,5-trimetoxyphenyl)-1,2-propanedione, (-)-thujaplicatin
trimethyl ether, (-)-yatein),
two new lignans ((8R,8’R)-4-hydroxycubebinone and
(8R, 8’R,9’S)-5-methoxyclusin) and two new sesquiterpenes
(5α,8α-2-oxo-1(10),3,7(11)-guaiatrien-12,8-olide and
(1α,2β,5α,8α,10α)-1,10-epoxy-2-hydroxy-3,7(11)-guaiadien-12,8-olide
[59].
Bambusa arundinacea (Retz.)
Willd.
Leaves of Bambusa arundinacea
are antileprotic, anthelmintic,
astringent, emmengogue, beneficial in dysmenorrhoea and haemoptysis [60].
The stem and leaves are useful in diseases of blood and inflammatory
conditions. Seeds are acrid, laxative and beneficial in strangury
and urinary discharges. The juice of the
flowers is used as a drop in the earache and deafness. The plant extract is
used as a remedy in snake and scropion bite [28].
The buds are tonic, its paste is restorative, cooling and stomachic. Leaf, root, shoot and seed of Bambusa arundinacea possess Anti-inflammatory,
Antiulcer, Anti-diabetic, Anti-oxidant [61]. Main chemical constituents of Bambusa arundinacea are silica
90%, silacum, potash, lime, aluminia,
cholin, betain, hydrate of silicic acid, nuclease, urease, proteolytic enzyme, cyanogentic glucoside and an alkaloid. Shoot has active constituents are diferuloyl arabinoxylanhexasaccharide,
diferuloyl oligosaccharide, (5, 5’-di--(diferul-9,
9’-dioyl)-[α-Larabinofuranosyl-(1-3)
-O-β-D-xylopyranosyl-9 (1-4) –D-xylopyranose] (taxiphyllin). Seed contain arginine,
cysteine, histidine, isoleucine, leucine, lysine, methionine, phenylamine, threonine, valine, tyrosine,
niacin, riboflavin, thiamine. Leaves mainly contain Protein, gluteline, contains lysine, methionine,
betain, cholin, proteolytic enzyme, nuclease, urease
[60].
Capparis spinosa Linn.
Fresh fruits of Capparis spinosa used
in sciatica and dropsy. Dry powdered fruit combined with honey is used in
colds, rheumatism, gout, sciatica and backache. In decoction it is said
efficient against gastric pain. Applied on the all body this decoction is said
to be good in epilepsy. Seeds used for treatment of feminine sterility and dysmenorrhea. Crushed seeds used in ulcers, scrofula and
ganglions [61]. Flower
buds are refreshing, stimulant and slightly diuretic. The herb has a hepatoprotective effect it reduced significantly serum transaminases. It has an antitumor activity against human
leukemia in vitro. It has an immunosuppressive effect. Chemical
constituents of Capparis spinosa is Alkaloids ranges 0.91% in the root
bark, 0.86% in the seeds, 0.02% in the leaves and 0.04% in the fruits. Stachydrine was isolated and identified in the plant. Quercetin-3-rutinoside,
quercetin-7-glucorhamnoside,
kaempferol-3-rutinoside, kaempferol-3-rhamnorutinoside and rutin (2.1%). Glucocapparin
volatile oil; sterols and saponins [62]. Capparis spinosa fruit and roots contain spermidine alkaloids [63]
similar to isocodonocarpine [64]. Mainly three alkaloids such as capparispine, capparispine
26-O0-β-D-glucoside and cadabicine
26-O-β-D-glucoside hydrochloride were isolated.
Solanum nigrum Linn.
The plant has been extensively used in traditional medicine in India and
other parts of world to cure liver disorders, chronic skin ailments (psoriasis
and ringworm), inflammatory conditions, painful periods, fevers, diarrhea, eye
diseases, hydrophobia etc [32].
Leaf, root and stalk
used for dysmenorrhea in females [62]. The fruit of Solanum nigrum showed antiulcer, antioxidant and
antitumor, inflammation, tuberculosis, diuretics activities [65-68], plant is also used in the
Oriental systems of medicine for various purposes – as an antitumorigenic,
antioxidant, anti-inflammatory [69]. The Active chemical constituents of
Solanum nigrum are glycoalkaloids
(solanine, solamargine, solanigrine and solasodine),
steroidal glycosides (β-solamargine, solasonine and α, β- solansodamine),
steroidal saponins (diosgenin),
steroidal genin (gitogenin),
tannin and polyphenolic compounds. Mature fruits are
low in alkaloid (solanine) content [70].
Some other important medicinal herbs used in the
treatment of Dysmenorrhea:
Roots of Angelica sinensis,
leaves and stem of Turnera difusa, root
of Chamalerium luteum,
leaves of Petroselinum crispum, Mentha piperita, Trifolium pretense, leaves of Ruta graveolens, Urtica urens Linn.,
Agave americana Linn., Artemisia absinthium Linn., Matricaria chamomilla Linn. Berberis vulgaris Linn., Chenopodium
ambrosioides Linn., Salvia
officinalis Linn. [17,71-74].
ACKNOWLEDGEMENT:
The authors are very grateful to Director
General CCRAS, New Delhi for providing facilities and encouragement for
carrying out this review work.
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Received on 08.10.2012
Modified on 20.10.2012
Accepted on 31.10.2012
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