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| Latin Name |
English Names |
Sanskrit Names |
Hindi Name |
Areca catechu
Linn.(Arecaceae)
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Arecanut Palm,
Betelnut Palm,
Areca Palm,
Pinang Palm |
Puga, Gubak,
Poogiphalam, Tantusara |
Supari |
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| History |
In Karnataka,
women use the inflorescence to adorn their hair. A perfume is
obtained from the flowers in Malaysia. The nuts are made into
beads and other fancy articles. Galls, called `mocharas', are
a result of the action of certain insects on the palm, and are
used for tanning. In some regions of the Americas, the arecanut
palm is cultivated as an ornamental plant.
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| Habitat |
The tree is
widely distributed in coastal regions, from Maharashtra to Kerala
and Tamil Nadu.It also grows in the Deccan Plateau, Assam, Meghalaya,
West Bengal, and the Andaman and Nicobar Islands. It is also
cultivated in those areas.
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| Morphology
Description (Habit) |
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It is a tree with an annulate stem. The stem is surrounded by a
crown of pinnate leaves. The leaflets are numerous, the petioles
expanded into a broad, tough, sheath-like growth at the lower end;
the inflorescence is a spathe which is compressed and glabrous;
the spadices are much-branched, bearing ebracteate male and female
flowers. The male flowers are small and numerous; the female flowers
are solitary or in groups of two or three and much larger than the
male; bisexual flowers have also been recorded; the fruits are ovoid
or oblong, smooth and orange or scarlet when fully ripe. They are
single-seeded and the endosperm or seed-kernel, popularly called
the "arecanut", is greyish brown and ruminate, with reddish brown
lines.
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| Principal
Constituents |
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The polyphenols of ripe arecanut contain predominantly polymerized
leucocyanidins besides minor amounts of (+)-cetechin, leucopelargonidin
and leucocyanidin. The polyphenols of arecanut are mainly flavonoids,
and their concentration decreases with the maturity of the nut1
Arecanut contains several alkaloids belonging to the pyridine group.
The most important of them physiologically is arecoline. Other alkaloids
present are arecaidine, arecolidine, guvacine, guvacoline, isoguvacine,
norarecaidine and norarecoline2 .
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| Pharmacology |
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The effects of polyphenolics obtained from fresh, unripe areca
nuts were studied on rat uteri under various hormonal influences
and compared with the effects obtained with alkaloidal fractions.
The ethyl acetate fraction of the aqueous extract was a stimulant
of low degree on all uteri but its spasmogenic activity was comparatively
more on uteri treated with progesterone3. The alcoholic
extract of the nuts exerted a distinct oxytocic activity on isolated
rat uterus at a dose of 100mcg4. The aqueous extracts
of the nuts inhibited the growth of Staphylococcus aureus and Trichophyton
rubrum, in vitro, while the alcoholic extract also inhibited the
growth of Escherichia coli, Candida albicans, and C. tropicalis5.
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| Toxicology |
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Four nitroso compounds, N-nitrosoguvacoline, N-nitrosoguvacine,
3-(N-nitrosomethylamino) propionaldehyde and 3-(N-nitrosomethylamino)
propionitrile, have been isolated from the aqueous extract of the
betel nuts. They have been found cytotoxic and genotoxic to human
buccal epithelial cells and also produced pancreatic, lung, nasal
and liver tumours in rats6.
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| Indications |
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The dried nuts are said to sweeten the breath, strengthen the gums,
and produce a stimulant and exhilarant effect on the system. Arecanut
has been reported to be a good source of fluoride, when chewed.
The non-alkaloid fractions of arecanuts are reported to possess
anti-microbial properties.
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| Product
Range |
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Himplasia, Lukol.
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| References |
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Mathew, J Fd Sci Technol, 1971, 8, 140; Govindarajan & Mathew,
Phytochemistry, 1963, 2, 321; Mathew & Govindarajan, ibid, 1964,
3, 657; Mathew et. al., ibid, 1969, 8, 1543.
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Marion in Manske & Holmes, I, 171; Willaman & Schubert, Tech
Bull, U S Dep Agric, No. 1234, 1961, 158; Henry, 8; Chang &
DeVol, Taiwania, 1973, 18, 123.
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Lalithakumari et. al., Ind. J. Pharm., 1964, 26, 268.
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Garg, S.K. and Garg, G.P., Bull. P.G.I. Chandigarh, 1970, 4,
162.
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Lalithakumari, H. et. al., Ind. J. Exptl. Biol., 1965,
3, 66.
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Chem Abstr, 1989, 110, 52690; 1989, 111, 210394; 1991, 115,
225914, 225952.
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