Meliaazedarach. or M. toosendan 川楝Chuān
liàn White cedar, Bead tree, Chinaberry tree Family:
Meliaceae M. toosendan is
much less toxic than M. azedarach.[4]
Melia toosendan should not be confused with the Azadirachta
trees, which are in the same family, but a different genus. All parts of the
plant are bitter and have purgative and anthelmintic properties.[5,6]
苦楝皮Kǔ
liàn pí Dried bark and bark of root-
harvested in Spring or Autumn FLAVOR: Bitter TOXICITY: Slightly
toxic FUNCTIONS GROUP: Antihelminthics
1. Expel Worms. Vermicide.
2. Laxative. Malaria- before the advent of quinine
the bark was used for treatment in India. INDICATIONS
1. Parasitical worm infestation causing abdominal
pain. Round worms. Anthelmintic- used in the United States the dried
berries were soaked in whisky.[5,6]
2. Hernia.
3. Ringworm and weeping lesions.
4. External applications for itching in tinea. PREPARATIONS:Decocted dried bark and bark of root 4-9 g. External
usage 15-30 g.
Decoction 15-30 g.[1]
Or crushed and mixed with boiling water for internal consumption. Decoction can
be used for bathing affected parts.[1]
Dried bark and bark of root 4-9 g.[1] 川楝子Chuān liàn zǐ, Jin lin zi
Dry ripe fruit-
harvested in Winter when the fruits have ripened
FLAVOR: Bitter CHANNELS:
Liver,Heart, Small Intestine, Bladder TOXICITY: Slightly toxic[3] FUNCTIONS- Commonly
used herb for any kind of Hot type abdominal pain GROUP: Regulating
Qi
1. Disperse Liver Qi congestion, relieve pain.
2. Laxative and vermicide- especially for round worms.[3]
Anthelmintic- used in the United States the dried berries were soaked in whisky.[5,6]
3. Alleviates abdominal pain.[3] Clears
moisture.[3] INDICATIONS
1. Stasis of Liver Qi and Liver/Gall bladder excess
Fire: Pain in the chest, ribs and abdomen- better with rib pain than
Chen pi, pain from flatulence, stress
and pain with emotions- ie when feel emotionally better pain goes- intermittent
pain. Anger. Difficulty sleeping, poor appetite. T- body red P- wiry and rapid-
relates to chronic hepatitis. Hot sensations. Nausea.
Relieves abdominal pain.
2. Round worm disease- causing abdominal pain.[3]
Anthelmintic.
3. Hernia or testicle pain with pain from genitals.[3]
4. Blood deficiency causing Wind or toxic Heat in Blood: Head psoriasis/tinea-
Burn the herb until it goes yellow then grind into powder and mix with pig fat
oil and apply to area.[3]
5. Leprosy and scofula (gland swellings)- Used in India.[5,6] CONTRAINDICATIONS: Deficient Spleen and Stomach Cold. Loose stools
and diarrhea.[3] COMBINATIONS - Stagnation of Liver Qi leading to Heat or Blood stasis:Spreads
the Liver Qi, drains Heat, regulate the Qi and alleviates painMelia
fruit & Corydalis- Jin ling zi san. PREPARATIONS:
Decoction 6-12 g.[3] Or crushed and
mixed with boiling water for internal consumption. Decoction can be used for bathing
affected parts.[1] Dried ripe
fruit 4-9 g.[2] HABITAT:
Mostly found growing in wild places, roadsides or cultivated. Rainforest and moist
but sunny places near rivers; central New South Wales to Northern Queensland and
Norejthern Territory. Often planted as an ornamental tree. DESCRIPTION
Deciduous tall tree. Bark; dull-brown young
branches and leaves both emit bitter and unpleasant odor. Leaves; alternate, 2
to 3 times oddly pinnate compound, leaflets ovate or lanceolate, apexes sharp,
bases rounded or obtuse-rounded, margins serrated or almost intact. Blooms; in
summer, purple flowers, terminal, or axillary forming panicle inflorescences.
Drupe; ellipsoid, dull-yellow.
Inner Path can not take any responsibility for any adverse effects from the
use of plants. Always seek advice from a professional before using a plant medicinally.Safety and herb-drug interactions.
The berries of chinaberry trees are round
and start off green when immature but eventually turn yellow as they ripen.
The berries are actually seed pods that contain 3–5 black seeds inside a stone
pit. These berries are the most toxic part of the plant and ripe, yellow berries
might be more harmful than unripe, green berries. The berries have a very bitter
taste, so it’s unusual for an individual to eat a large quantity of them.[1] References
[1] poison.org
Toxicological studies of Melia azedarach L. (flowers and berries)
Zakir-ur-Rahman 1, S Ahmad, S Qureshi, Atiq-ur-Rahman, Y Badar Abstract
Toxicological evaluation of Media azedarach Linn. was carried out in lower laboratory
animals, i.e. rats and mice by oral and intravenous routes. Aqueous and alcoholic
extracts were found to be non-toxic uptil a dose of 1500 mg/kg orally in mice
and rats. When injected aqueous extract intravenously, LD50 was 395, 580 mg/kg
(flowers) and 700, 925 mg/kg (berries) respectively in mice and rats. It was
also observed that alcoholic and aqueous extracts of Melia azedarach have a
mild CNS sedative effect.
Pak J Pharm Sci. 1991 Jul;4(2):153-8. PMID: 16414695
Meliacins, gedunin and derivatives, nimbolins
A and B, melianins A and B, and their decompositions products fraxinellose and
azedainic acid.[1,2]
Protolimonoids: melianon, melianol, melianoldiol and meliantol.[3] Triterpenoids and steriods including 24-methylene-cycloartanone,
cycloeucalenone, cycloeucanol and others.[4]
Miscellaneous substances including vanillic acid and aldeyde, and alkaloid paraisine
(ocaziridine), and an insect repelling substance- meliatin.[5]
Prevents replication of Tacaribe virus in mice, and an anti-neoplastic substance,[6]
also active in mice have been isolated.[7] Vanillic acid, present in the bark is probably the anthelmintic
principle. Alkaloids are present in the bark, leaves ande roots; triterpenes
are present in fruits. Leaves contain polyphenols and traces of saponins.[8]
References
[1] Ekong, D. E. U. and Ibiyemi, S. A. (1971) Chem. Comm. 1177
[2] El Said et al. (1968) Study of certain Nigerian plants used in
Fever. Communications at the Inter- African Symposium. Dakar.
[3] Lavie, D. and Le3vy, E. C. (1969) Tet. Lett. 3525 [4] Kraus, W. and Bokel, M. (1981) Chemische Be4richte 114,
267
[5] Medicinal Plants of Tropical West Africa B. Oliver-Bever. Pub Cambridge
University Press (1986) UK
[6] Andrei, G. M. etal. (1986) Experientia 42 (7), 843
[7] Pat. Appl. 83/234, 294 Japan (1983).
[8] R. Hegnauer, Chemotaxonomie der Pflanzen, Vol. 5, Birkhauser Verlag. Basel,
1969
Research
The Potential Uses of Melia Azedarach L. as Pesticidal and Medicinal Plant, Review
Adnan Y. AL-Rubae Melia azedarach.pdf
EFFECT OF NEEM (Melia azadirachta L.) LEAF AND BISHKATALI (Polygonum hydropiper
L.) ROOT POWDER FOR DECONTAMINATION AND CALCIUM HYDROXIDE FOR DETOXIFICATION OF
AFLATOXIN IN RICE, MAIZE AND WHEAT pdf
Use of toosendanin or melia azedarach extracts for preventing or treating dementia-
Google Patents EP2444091B1 Jin Sung Choi Ildong Pharm Co., Ltd.pdf
Anticancer effects of crude extract from Melia toosendan Sieb. et Zucc
on hepatocellular carcinoma in vitro and in vivo.
Liu XL, Wang H, Zhang L, Wang YL, Wang J, Wang P, He X, He YJ. Abstract
OBJECTIVE:
To investigate the anti-cancer effects of crude extract from Melia toosendan Sieb.
et Zucc and its possible molecular mechanisms in vitro and in vivo.
METHODS:
Transonic alcohol-chloroform extraction method was used to extract toosendanin
from the bark of Melia toosendan Sieb. et Zucc, and the content of toosendanin
in the crude extract was measured by high performance liquid chromatography (HPLC).
Anti-cancer effects of crude extract from Melia toosendan Sieb. et Zucc were investigated
in in vivo and in vitro studies. In the in vitro experiment, human hepatocellular
carcinoma cell lines SMMC-7721 and Hep3B were co-incubated with toosendanin crude
extract of different concentrations, respectively. In the in vivo experiment,
BALB/c mice were subcutaneously inoculated with mouse hepatocellular carcinoma
H22 cells and treated with crude extract.
RESULTS:
HPLC revealed the content of toosendanin was about 15%. Crude extract from Melia
toosendan Sieb. et Zucc inhibited cancer cells growth in a dose- and time-dependent
manner. The 50% inhibitory concentration (IC50, 72 h) was 0.6 mg/L for SMMC-7721
cells and 0.8 mg/L for Hep3B cells. Both high-dose [0.69 mg/(kg d)] and low-dose
[0.138 mg/(kg d)] crude extract could markedly suppress cancer growth, and the
inhibition rate was greater than 50%. Hematoxylin and eosin staining showed necrotic
area in cancers and transmission electron microscopy displayed necrotic and apoptotic
cancer cells with apoptotic bodies. Immunohistochemistry showed that the expression
of Bax and Fas increased and the expression of Bcl-2 reduced.
CONCLUSIONS:
Toosendanin extract has potent anti-cancer effects via suppressing proliferation
and inducing apoptosis of cancer cells in vivo and in vitro. The mechanism of
apoptosis involves in mitochondrial pathway and death receptor pathway.
PMID: 26383159 DOI: 10.1007/s11655-015-2084-7
Chin J Integr Med. 2016 May;22(5):362-9. doi: 10.1007/s11655-015-2084-7. Epub
2015 Sep 17. ncbi.nlm.nih.gov
Limonoids from fruit of Melia toosendan and their cytotoxic activity.
Tada K, Takido M, Kitanaka S. Abstract
Two new limonoids, toosendanal and 12-O-methylvolkensin, were isolated from the
fruits of Melia toosendan Sieb. et Zucc. along with three known limonoids, meliatoxin
B1, trichillin H, and toosendanin. The structures of the new limonoids were established
by spectroscopic methods, with toosendanal having C-1/C-29 and C-19/C-29 acetal
bridges. Both meliatoxin B1 and toosendanin exhibit cytotoxic activity against
KB cells.
PMID: 10389275 Phytochemistry. 1999 Jul;51(6):787-91. ncbi.nlm.nih.gov
Protolimonoids from Melia toosendan.
Sang YS, Zhou CY, Lu AJ, Yin XJ, Min ZD, Tan RX. Abstract
Toosendanone A (1), a new euphane (tirucallane)-type triterpene bearing a five-membered
ring in the side chain and the first cyclopentanyl protolimonoid, was isolated
from the bark of Melia toosendan, along with two new tirucallanes, toosendanic
acids A (2) and B (3). The structure and absolute configuration of compound 1
was elucidated by spectroscopic data interpretation and X-ray diffraction analysis.
Compounds 1-3 were evaluated for cytotoxicity against a small panel of cancer
cell lines.
PMID: 19341288 DOI: 10.1021/np800669c J Nat Prod. 2009 May 22;72(5):917-20. doi:
10.1021/np800669c. ncbi.nlm.nih.gov
Anticancer effects of crude extract from Melia toosendan Sieb. et Zucc
on hepatocellular carcinoma in vitro and in vivo
Xiao-ling Liu (刘小玲)Hong Wang (王 虹)Ling Zhang (张 伶)You-liang Wang (王友良)Jin Wang
(王 进)Peng Wang (王 鹏)Xiao He (贺 潇)Yu-juan He (何於娟)Email author Abstract
Objective
To investigate the anti-cancer effects of crude extract from Melia toosendan Sieb.
et Zucc and its possible molecular mechanisms in vitro and in vivo.
Methods
Transonic alcohol-chloroform extraction method was used to extract toosendanin
from the bark of Melia toosendan Sieb. et Zucc, and the content of toosendanin
in the crude extract was measured by high performance liquid chromatography (HPLC).
Anti-cancer effects of crude extract from Melia toosendan Sieb. et Zucc were investigated
in in vivo and in vitro studies. In the in vitro experiment, human hepatocellular
carcinoma cell lines SMMC-7721 and Hep3B were co-incubated with toosendanin crude
extract of different concentrations, respectively. In the in vivo experiment,
BALB/c mice were subcutaneously inoculated with mouse hepatocellular carcinoma
H22 cells and treated with crude extract.
Results
HPLC revealed the content of toosendanin was about 15%. Crude extract from Melia
toosendan Sieb. et Zucc inhibited cancer cells growth in a dose- and time-dependent
manner. The 50% inhibitory concentration (IC50, 72 h) was 0.6 mg/L for SMMC-7721
cells and 0.8 mg/L for Hep3B cells. Both high-dose [0.69 mg/(kg d)] and low-dose
[0.138 mg/(kg d)] crude extract could markedly suppress cancer growth, and the
inhibition rate was greater than 50%. Hematoxylin and eosin staining showed necrotic
area in cancers and transmission electron microscopy displayed necrotic and apoptotic
cancer cells with apoptotic bodies. Immunohistochemistry showed that the expression
of Bax and Fas increased and the expression of Bcl-2 reduced.
Conclusions
Toosendanin extract has potent anti-cancer effects via suppressing proliferation
and inducing apoptosis of cancer cells in vivo and in vitro. The mechanism of
apoptosis involves in mitochondrial pathway and death receptor pathway.
Chinese Journal of Integrative Medicine May 2016, Volume 22, Issue 5, pp 362–369
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