One of the top amazon traditional botanicals, it is particularly famous
throughout the western Amazon Basin where it is semi cultivated near
villages, or wildcrafted. Well noted as a liquid extract with
fast-acting general analgesic, anti-inflammatory and muscle relaxing
properties. Often called “Trembling Back” this great tree yields a
powerful bark. Considered a fine, all purpose anti-inflammatory and
anti-rheumatic, it also shows some minor antitumoral and anticancer
properties in trials. One study suggest use for patients with skin
cancer (3), another (5) demonstrated cytotoxicity against lung
carcinonoma. The best known of all jungle remedies for its ability to
relax muscles quickly (46) (10-20).
Suggested Use: Liquids: Use 15-20 drops mixed with water one to
two times daily or as recommended by a practitioner
Cautions: May
increase drowsiness and promote relaxation. Use under care/advice of a
medical practitioner. Not intended for long term therapy.
Contraindications:
Do not use if driving. Do not use in combination with other muscle
relaxing drugs
Ingredients: Full
spectrum bark extracted in distilled water and 40% organic grain
alcohol.
More About Chu Chu Huasi:
1. Genotoxicity of plant extracts.
Vargas VM; Guidobono RR; Henriques JA
Departamento do Meio Ambiente, Secretaria da Saude e Meio Ambiente,
Porto Alegre, RS, Brasil.
Mem Inst Oswaldo Cruz 86 Suppl 2: 67-70 (1991)
2. Chuchuhuasha - a drug used in folk medicine in
the Amazonian and Andean areas. Achemical study of Maytenus laevis.
Gonzalez JG; delle Monache G; delle Monache F; Marini-Bettol GB
J Ethnopharmacol, 5: 1, 1982 Jan, 73-7
3. [First observations on the topical use of
Primin, Plumbagin and Maytenin in patients with skin cancer]
Melo AM; Jardim ML; De Santana CF; Lacet Y; Lobo Filho J; De Lima e
Ivan Leoncio OG
Rev Inst Antibiot (Recife), 14: 1-2, 1974 Dec, 9-16
4. Pharmacologic and toxicologic effects of two
Maytenus species in laboratory animals.
Oliveira MG; Monteiro MG; Macaúúbas C; Barbosa VP; Carlini EA
J Ethnopharmacol, 34: 1, 1991 Aug, 29-41
5. Antitumor agents, 116. Cytotoxic triterpenes
from Maytenus diversifolia.
Nozaki H; Matsuura Y; Hirono S; Kasai R; Chang JJ; Lee KH
J Nat Prod, 53: 4, 1990 Jul-Aug, 1039-41
6. Antiulcerogenic effects of two Maytenus species
in laboratory animals.
Souza-Formigoni ML; Oliveira MG; Monteiro MG; da Silveira-Filho NG;
Braz S; Carlini EA
J Ethnopharmacol, 34: 1, 1991 Aug, 21-7
7. Antiulcerogenic effects of two Maytenus species
in laboratory animals.
Vargas VM; Guidobono RR; Henriques JA
Mem Inst Oswaldo Cruz, 86 Suppl 2:1991, 67-70
8. Cytotoxic aromatic triterpenes from Maytenus
ilicifolia and Maytenus chuchuhuasca.
Shirota O; Morita H; Takeya K; Itokawa H
J Nat Prod, 57: 12, 1994 Dec, 1675-81
9. Macrocarpins A-D, new cytotoxic nor-triterpenes
from Maytenus macrocarpa.
Chavez H, Rodriguez G, Estevez-Braun A, Ravelo AG,
Estevez-Reyes R, Gonzalez AG, Fdez-Puente JL, Garcia-Gravalos D.
Instituto Universitario de Bio-Organica Antonio Gonzalez, Universidad
de La Laguna, Tenerife, Spain.
Bioorg Med Chem Lett. 2000 Apr 17;10(8):759-62.
PMID: 10782680 [PubMed - indexed for MEDLINE]
10. Sesquiterpene polyol esters from the leaves of
maytenus macrocarpa
Chavez H, Callo N, Estevez-Braun A, Ravelo AG, Gonzalez AG.
Instituto Universitario de Bio-Organica “Antonio Gonzalez”,
Universidad de La Laguna, Avenida Astrofisico Fco. Sanchez 2, 38206
Tenerife, Spain.
J Nat Prod. 1999 Nov;62(11):1576-7.
PMID: 10579879 [PubMed - as supplied by publisher]
11. Friedelane triterpenoids from Maytenus
macrocarpa.
Chavez H, Estevez-Braun A, Ravelo AG, Gonzalez AG.
Instituto Universitario de Bio-Organica, Antonio Gonzalez,
Universidad de Laguna, Tenerife, Canary Island, Spain.
J Nat Prod. 1998 Jan;61(1):82-5.
PMID: 9461656 [PubMed - indexed for MEDLINE]
12. New natural sesquiterpenes as modulators of
daunomycin resistance in a multidrug-resistant Leishmania tropica line.
Perez-Victoria JM, Tincusi BM, Jimenez IA, Bazzocchi IL, Gupta MP,
Castanys S, Gamarro F, Ravelo AG.
Instituto de Parasitologia y Biomedicina “Lopez-Neyra”, Consejo
Superior de Investigaciones Cientificas, Ventanilla, 11, 18001 Granada,
Spain.
J Med Chem. 1999 Oct 21;42(21):4388-93.
PMID: 10543882 [PubMed - indexed for MEDLINE]
1. Genotoxicity of plant extracts.
Vargas VM; Guidobono RR; Henriques JA
Departamento do Meio Ambiente, Secretaria da Saude e Meio Ambiente,
Porto Alegre, RS, Brasil.
Mem Inst Oswaldo Cruz 86 Suppl 2: 67-70 (1991)
Aqueous extracts of seven species used in Brazilian popular medicine
(Achyrocline satureoides, Iodina rhombifolia, Desmodium incanum,
Baccharis anomala, Tibouchina asperior, Luehea divaricata, Maytenus
ilicifolia) were screened to the presence of mutagenic activity in the
Ames test (Salmonella/microsome). Positive results were obtained for A.
satureoides, B. anomala and L. divaricata with microsomal activation. As
shown elsewhere (Vargas et al., 1990) the metabolites of A. satureoides
extract also show the capacity to induce prophage and/or SOS response
in microscreen phage induction assay and SOS spot chromotest.
2. Chuchuhuasha - a drug used in folk medicine in
the Amazonian and Andean areas. Achemical study of Maytenus laevis.
Gonzalez JG; delle Monache G; delle Monache F; Marini-Bettol GB
J Ethnopharmacol, 5: 1, 1982 Jan, 73-7
In the high Amazonian basin a plant named chuchuasha, (or chuchuaso)
is used in traditional medicine for several purposes in the form of an
alcoholic extract. This plant, a Maytenus species, most probably
Maytenus laevis, grows in the subandean region of the Amazonian basin
(Peru, Ecuador, Colombia). Antitumor and anti-inflammatory properties
were recently attributed to the extracts of the root bark of the plant.
The composition of the extract of M. laevis from the Putumayo area of
Colombia was studied in order to establish the active principle
responsible for these activities. The presence of phenoldienones
(tingenone, 22-hydroxytingenone), a catechin
(4’-methyl-(-)-epigallocatechin) and proanthocyanidins
(Ouratea-proanthocyanidins A and B) was established. The biological
activities of these compounds confirm the properties of the extracts of
the plant claimed by traditional medicine.
3. [First observations on the topical use of
Primin, Plumbagin and Maytenin in patients with skin cancer]
Melo AM; Jardim ML; De Santana CF; Lacet Y; Lobo Filho J; De Lima e
Ivan Leoncio OG
Rev Inst Antibiot (Recife), 14: 1-2, 1974 Dec, 9-16
Eleven cases of patients bearing basic cellular carcinoma, and one
case of patient bearing Kaposi’s sarcomatosis, all treated with
antibiotics isolated by Goncalves de Lima and Co-workers at the
Instituto de Antibióóticos, are presented by the authors. Primin, an
antibiotic extracted from a vegetal named Miconia sp. (Herb. I.A.-1903)
with a 2-metoxi-6-n-pentil-p benzoquinone structure, presented a strong
antineoplastic action in the cases treated. Plumbagin isolated from
Plumbago scandens in local use, was responsible for a complete healing
of the injuries treated. Maytenin extracted from Maytenus sp.
(Herb.I.A.-1750) showed less activity than the two previous mentioned,
but with a low irritant action and late antineoplastic properties. The
authors are going on these experiments. They believe that these
antibodies, in local use, may advantageously substitute the surgery and
the radiotherapy, meanly in those external ear tumidities and back of
the nose, owing to a hurtful action in cartilage, provoked by
radiotherapy.
4. Pharmacologic and toxicologic effects of two
Maytenus species in laboratory animals.
Oliveira MG; Monteiro MG; Macaúúbas C; Barbosa VP; Carlini EA
J Ethnopharmacol, 34: 1, 1991 Aug, 29-41
Leaves of Maytenus species are used in the popular medicine of Brazil
for their reported antacid and antiulcerogenic activity. The present
work examined the effects of a boiling water extract of equal parts of
M. aquifolium and M. ilicifolia leaves on acute administration in rats
and mice, in an attempt to detect any general depressant, hypnotic,
anticonvulsant and analgesic effects. General depressant and hypnotic
effects were seen only after intraperitoneal administration. After
chronic administration, the overall behavior of animals did not change
and they continued to gain weight at the same rate as controls. Several
biochemical and hematological parameters as well as pathological
examination of different organs did not show any significant alterations
after 3 months of treatment. A search for the potential effects of the
extract on the fertility of female and male rats and on the course of
pregnancy as well as a search for potential teratogenic effects did not
reveal any significant differences from controls. Taken together, the
results indicate that these Maytenus species may be safe for human use
and deserve further investigation.
5. Antitumor agents, 116. Cytotoxic triterpenes
from Maytenus diversifolia.
Nozaki H; Matsuura Y; Hirono S; Kasai R; Chang JJ; Lee KH
J Nat Prod, 53: 4, 1990 Jul-Aug, 1039-41
The known triterpenes 3-oxofriedelan-29-oic acid [1],
3-oxofriedelan-28-oic acid [2], and 28,29-dihydroxyfriedelan-3-one [3]
have been isolated from Maytenus diversifolia. Compounds 1-3
demonstrated cytotoxicity against the A-549 lung carcinoma cells with
ED50 values of 0.21, 1.18, and 0.64 micrograms/ml, respectively.
6. Antiulcerogenic effects of two Maytenus species
in laboratory animals.
Souza-Formigoni ML; Oliveira MG; Monteiro MG; da Silveira-Filho NG;
Braz S; Carlini EA
J Ethnopharmacol, 34: 1, 1991 Aug, 21-7
Leaves of Maytenus species are commonly used in Brazil for the
treatment of gastric ulcers, dyspepsias and other gastric problems. The
present study evaluated the antiulcerogenic potential of a boiling water
extract of equal parts of M. aquifolium and M. ilicifolia leaves
against ulcer lesions induced by indomethacin and cold-restraint stress
in rats. Ranitidine and cimetidine were used as reference drugs. The
oral and intraperitoneal administration of the extract had a potent
antiulcerogenic effect against both types of ulcers. The extract was
shown to cause an increase in volume and pH of gastric juice of the
animals with the pH effects comparable to those of cimetidine. The
results tend to confirm the popular use of the plant.
7. Antiulcerogenic effects of two Maytenus species
in laboratory animals.
Vargas VM; Guidobono RR; Henriques JA
Mem Inst Oswaldo Cruz, 86 Suppl 2:1991, 67-70
Aqueous extracts of seven species used in Brazilian popular medicine
(Achyrocline satureoides, Iodina rhombifolia, Desmodium incanum,
Baccharis anomala, Tibouchina asperior, Luehea divaricata, Maytenus
ilicifolia) were screened to the presence of mutagenic activity in the
Ames test (Salmonella/microsome). Positive results were obtained for A.
satureoides, B. anomala and L. divaricata with microsomal activation. As
shown elsewhere (Vargas et al., 1990) the metabolites of A. satureoides
extract also show the capacity to induce prophage and/or SOS response
in microscreen phage induction assay and SOS spot chromotest.
8. Cytotoxic aromatic triterpenes from Maytenus
ilicifolia and Maytenus chuchuhuasca.
Shirota O; Morita H; Takeya K; Itokawa H
J Nat Prod, 57: 12, 1994 Dec, 1675-81
The isolation and structure elucidation of four cytotoxic aromatic
triterpenes [1-4] along with three known quinoid triterpenes [5-7] from
the South American medicinal plants MaytenusChuchuhuasi
(bark)- Celastracae, Maytenus macrocarpa
9. Macrocarpins A-D, new cytotoxic nor-triterpenes
from Maytenus macrocarpa.
Chavez H, Rodriguez G, Estevez-Braun A, Ravelo AG,
Estevez-Reyes R, Gonzalez AG, Fdez-Puente JL, Garcia-Gravalos D.
Instituto Universitario de Bio-Organica Antonio Gonzalez, Universidad
de La Laguna, Tenerife, Spain.
Bioorg Med Chem Lett. 2000 Apr 17;10(8):759-62.
Macrocarpins A (1), B (2), C (3) and D (4), four new nor-triterpenes,
have been isolated from the roots of Maytenus macrocarpa. The
structures were established by spectroscopic examinations. Natural
compounds 1, 2, 4 and the acetyl derivative 1a are cytotoxic against
four tumoral cell lines with IC50 values ranging between 0.4 and 5.2
microM.
PMID: 10782680 [PubMed - indexed for MEDLINE]
10. Sesquiterpene polyol esters from the leaves of
maytenus macrocarpa
Chavez H, Callo N, Estevez-Braun A, Ravelo AG, Gonzalez AG.
Instituto Universitario de Bio-Organica “Antonio Gonzalez”,
Universidad de La Laguna, Avenida Astrofisico Fco. Sanchez 2, 38206
Tenerife, Spain.
J Nat Prod. 1999 Nov;62(11):1576-7.
The aerial parts of Maytenus macrocarpa yielded three new
beta-dihydroagarofuran sesquiterpene polyol esters. Their structures
were elucidated by spectroscopic analyses including 2D NMR techniques as
6beta,8beta,15-triacetoxy-1alpha,
9alpha-dibenzoyloxy-4beta-hydroxy-beta-dihydroagarofuran (1); 1alpha,
6beta,8beta,
15-tetraacetoxy-9alpha-benzoyloxy-4beta-hydroxy-beta-dihydroagarofura n
(2) and (1S,4S,6R,7R,8R,9R)-1,6,15-triacetoxy-8,
9-dibenzoyloxy-4-hydroxy-beta-dihydroagarofuran (3). Compounds 1 and 2
showed marginal antitumor activity against four cell lines.
PMID: 10579879 [PubMed - as supplied by publisher]
11. Friedelane triterpenoids from Maytenus
macrocarpa.
Chavez H, Estevez-Braun A, Ravelo AG, Gonzalez AG.
Instituto Universitario de Bio-Organica, Antonio Gonzalez,
Universidad de Laguna, Tenerife, Canary Island, Spain.
J Nat Prod. 1998 Jan;61(1):82-5.
A set of friedelane triterpenoids has been isolated from the stem
bark exudates of Maytenus macrocarpa. It includes a new friedelan
triterpene (1), together with the known compounds friedelin,
3-oxo-29-hydroxyfriedelane, 3-oxofriedelan-25-al, and canophyllol. The
structures of these compounds were elucidated by spectroscopic and
chemical evidence. Complete 1H and 13C assignments were achieved by 2D
NMR spectroscopy. The new compound showed weak activity against aldose
reductase. It did not display antitumor activity against P-388 lymphoid
neoplasm, A-549 human lung carcinoma, HT-29 human colon carcinoma, or
MEL-28 human melanoma cell lines.
PMID: 9461656 [PubMed - indexed for MEDLINE]
12. New natural sesquiterpenes as modulators of
daunomycin resistance in a multidrug-resistant Leishmania tropica line.
Perez-Victoria JM, Tincusi BM, Jimenez IA, Bazzocchi IL, Gupta MP,
Castanys S, Gamarro F, Ravelo AG.
Instituto de Parasitologia y Biomedicina “Lopez-Neyra”, Consejo
Superior de Investigaciones Cientificas, Ventanilla, 11, 18001 Granada,
Spain.
J Med Chem. 1999 Oct 21;42(21):4388-93.
The effects produced by nine dihydro-beta-agarofuran sesquiterpenes
isolated from Crossopetalum tonduzii (1-8) and Maytenus macrocarpa (9)
(Celastraceae) on the reversion of the resistant phenotype on a
multidrug-resistant Leishmania line and their binding to recombinant
C-terminal nucleotide-binding domain of Leishmania P-glycoprotein-like
transporter were studied. The structures of the new compounds (1-5) were
elucidated by spectroscopic methods, including (1)H-(13)C heteronuclear
correlation (HMQC), long-range correlation spectra with inversal
detection (HMBC), ROESY experiments, and chemical correlations. The
absolute configuration of one of them (1) was determined by CD studies.
The structure-activity relationship is discussed.
PMID: 10543882 [PubMed - indexed for MEDLINE]
Sekar KV, et al. Mayteine and 6-benzoyl-6-deacetylmayteine from
Maytenus krukovii. Planta Med, 1995 Aug
Lima OG de, et al. [Antimicrobial substances from higher plants.
XXXVI. On the presence of maytenin and pristimerine in the cortical part
of the roots of Maytenus ilicifolia from the South of Brazil] Rev Inst Antibiot (Recife), 1971 Jun
Gessler MC, et al. Screening Tanzanian medicinal plants for
antimalarial activity. Acta Trop, 1994 Feb
Gonzááles AG, et al. Biological study of triterpenequinones from
celastraceae. Farmaco [Sci], 1988 Jun
Wagner H, et al. Spermidine alkaloids and triterpenes from Maytenus
heterophylla and Pleurostylia africana. Chemical constituents of the
Celastraceae--IV. Planta Med, 1977 Sep
Flemming K. [Increase of phagocytosis activity by Maytenus laevis
leaves and Scholler-Tornesch lignine (Porlisan)] Naturwissenschaften,
1965 Jun
Dantanarayana, A. I., V. S. Kumar et al., Phytochemistry 22 (1983)
473.
Smith, C. R. Jr. and R. G. Powell, Alkaloids: Chemical and Biological
Perspectives 2 (1984) 149.
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