Cinnamomum
cassia. C aromaticum, C. ligneaChinese
Cinnamon,
Cassia Bark, Bastard Cinnamon, False Cinnamon
Family: Lauraceae
PART USED:Bark The cultivated
trees are kept as coppices, the shoots are not allowed to grow more than 3 m.
The trees are at their best at 10-12 years of age. The bark is cut from
the young shoots when the leaves are red.
The bark is brown, in quilled pieces, sometimes with the remains of the outer
layer present.
TASTE and ODOR: Similar to cinnamon but distinct. ACTIONS
1. Carminative.[1]
2. Spasmolytic.[1] 3. Stomachic.[2] Sstrengthens
gastric secretions.
4. Aromatic.[2]
5. Anti-emetic.[1] Antidiarrheal.[1]
Antimicrobial.[1] Mildly astringent.
6. Tonic.[2]
7. Antipyretic.[2]
8. Diaphoretic.[2]
9. Analgesic.[2]
10. Emmenagogue. Capable of decreasing secretion of milk.
11. Antidiabetic- Modulates insulin sensitivity in Type 2 diabetes. Reduces
inflammatory markers in metabolic syndrome. Stimulates uptake of glucose via
stimulation of GLUT4 protein (primary glucose transporter in muscle, cardiac,
and fat cells).[4] INDICATIONS - useful as a flavoring.
1. Diarrhea.[1]Flatulent
dyspepsia.[1] Nausea.Flatulent
colic.[1]Vomiting. Flatulent
Distension.
2. Common cold.[1] SPECIFIC INDICATIONS: Colic or dyspepsia with flatulent distension
and nausea.[1] COMBINATIONS
- Flatulent dyspepsia, and gastritis, use with Meadowsweet,
Chamomile, and Marshmallow
Root.
- Diarrhea with tormina (griping pains), use with Geranium,
Oak and Catechu.
- Common cold, use with Millefolium,
Peppermint and Sambucus.
COMPARISONS
The bark is thicker, coarser, darker and duller, the flavor more pungent, less
sweet and delicate, and slightly bitter than Cinnamomum zeylanicum= Ceylon Cinnamon. The
stronger flavor is preferred by German and Roman chocolate makers. The volatile
oil is cheaper and more abundant than oil of Ceylon Cinnamon, so Materia
Medicas usually are referring to C. cassia. PREPARATIONS 3X /day
Dried bark 0.5-1g,[1]
or by infusion 1:20.
Tincture (BHP1949) 2-4ml.[1]
PART
USED: Volatile
Oil - Internal or external use is not recomended due to its
concentrated and irritant nature. Mainly used for flavouring medicines,
cosmetics, toothpastes, mouthwashes and foods.
ORIGIN: Distilled from the leaves and twigs. ACTIONS
1. Germicide. Antiseptic.[2]
2. Irritant. Strong local stimulator.
3. Carminative.[2] INDICATIONS
1. Gastro-dynia. Flatulent colic and gastric debility. PREPARATIONS
Oil (BHP1973) Dose 0.05-0.2 ml.[1] PART USED:Unripe Fruit or
Bud
Taste and odor of the bark.
Used as a spice in confectionary and Pot-Pourri. Also in a spiced wine called
Hippocras.[5]ORIGIN: South East Asia and China DESCRIPTION: Evergreen tree. Leaves; flame
colored, oval-oblong body from 15-20 cm long. Fruit; similar to a small olive.
References
[1] British Herbal Pharmacopoeia 1983 Published
by the British Herbal Medicine Association ISBN 0 903032 07 4.
[2] Potter's New Cyclopaedia of Botanical Drugs and Preparations R.C.
Wren Revised by Elizabeth M. Williamson and Fred J Evans. First published in
Great Britain in 1988 and reprinted in 1989 and 1994 by the C. W. Daniel Company
Limited. 1 Church Path, Saffron Walden Essex. Published 1988 Printed and bound
by Biddles, Guildford ISBN 085207 1973.
[3] Australian Medicinal Plants - E.V. Lassak & T. McCarthy. Publisher-
Reed New Holland, Australia 1983. ISBN 1876334703.
[4] healthmasterslive.com
Drug induced nturitional deficiencies and herb drug interaction master class
[5] A Modern Herbal - Mrs M. Grieve Publisher- Penguin- Great Britain. First
published by Jonathan Cape 1931. ISBN 0 14 046-440 9 Images 1. elicriso.it
2.
en.wikipedia.org/wiki by Chaojoker CC BY-SA 3.0
3. en.wikipedia.org
by Itineranttrader Public Domain
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. Constituents.
Cinnamon bark
Volatile oil 1-2%.[1]
Tannins.[1] Starch.
Water soluble polyphenol polymers, which support glucose metabolism Essential oil: The oils value is determined by the amount of cinnamaldehye.
Trans-cinnamaldehyde 75-90%,[1,2,13]
with cinnamylacetate,[5] phenylpropylacetate,
orthocumaric aldehyde and numerous trace constituents including salicylaldehyde
and methyleugenol.[2]Cinnamic acid.[13]
Diterpenes, classified into five different types, including the cinncassiols
A-E and their glucosides.[3,4,5]
Tannins and polyphenols; catechin, epicatechin, procyanidins cinnamonol, cinnamtannins.[6,7]
No hydrolysable tannins, mono- or sesquiterpenes have been isolated.[5,7]
Cinnamaldehyde ia a weak CNS stimulant at low doses and a depressant at high
doses and has spasmolytic activity.[8]
Cinnamaldehyde is hypotensive, hypoglycaemic and increases peripheral blood
flow,[9,10] and it reduces platelet
aggregegability by inhibiting both the cyclooxygenase and lipoxygenase pathways
of arachidonic acid metabolism.[11]
It is however volatile and easily lost from the crude drug and its preparations.[12]
The cinncassiols are thought to be responsible for at least some of the anti-allergic
effects.[3,4] References
[1] British Herbal Pharmacopoeia 1983 Published by the British Herbal Medicine
Association ISBN 0 903032 07 4.
[2] Senayake, U. M. et al (1978) J. Agric. Food Chem. 20, 822
[3] Nohara, T. et al. (1985) Phytochem. 21 (8), 2130
[4] Nohara, T. et al. (1985) Phytochem. 24 (8), 1849
[5] Hikino, H. Edonomic and Medicinal Plant Research, Vol 1. Pub. Academic Press
(1985) UK
[6] Otsuka, H. et al. (1982) Yakugaju Zasshi 102, 162
[7] Morimoto, S. et al. (1982) Abstra. 28th Ann. Meeting Japan Pharm.
Soc. p555.
[8] Pharmacology and Applications of Chinese Materia Medica Vol 1, Ed. H. Chan
and P. But, Pub. World Scientific (1986) Singapore
[9] Harada, M. and Yamazaki, R. (1981) Abstr. 64th Meeting Kanto Branch Japan
Pharmacol. Soc. p27
[10] Harada, M. and Hirayama, Y. (1979) ibid 60th Meeting p34
[11] Yahara, K, et al. (1986) 6th Int. Conf. Prostaglandins and Related
Compounds, Florence, Italy. June 3rd-6th. Pub. Fondzione Giovanni Lorenzini
[12] Potter's New Cyclopaedia of Botanical Drugs and Preparations R.C.
Wren Revised by Elizabeth M. Williamson and Fred J Evans. First published in
Great Britain in 1988 and reprinted in 1989 and 1994 by the C. W. Daniel Company
Limited. 1 Church Path, Saffron Walden Essex. Published 1988 Printed and bound
by Biddles, Guildford ISBN 085207 1973.
[13] Chinese Herbal Medicine Materia Medica - Dan Bensky and Andrew Gamble -
Eastland Press 1986 Seattle Washington ISBN 0-939616-15-7
Research.
Cassia has shown promising results as a radiation protective agent, increasing
survival times and leukocyte and platelet counts in vivo experiments
in China.[1] References
[1] Pharmacology and Applications of Chinese
Materia Medica Vol 1, Ed. H. Chan and P. But, Pub. World Scientific (1986) Singapore
Cinnamon and health.
Gruenwald J, Freder J, Armbruester N. Abstract
Cinnamon has been used as a spice and as traditional herbal medicine for centuries.
The available in vitro and animal in vivo evidence suggests that cinnamon has
anti-inflammatory, antimicrobial, antioxidant, antitumor, cardiovascular, cholesterol-lowering,
and immunomodulatory effects. In vitro studies have demonstrated that cinnamon
may act as an insulin mimetic, to potentiate insulin activity or to stimulate
cellular glucose metabolism. Furthermore, animal studies have demonstrated strong
hypoglycemic properties. However, there are only very few well-controlled clinical
studies, a fact that limits the conclusions that can be made about the potential
health benefits of cinnamon for free-living humans. The use of cinnamon as an
adjunct to the treatment of type 2 diabetes mellitus is the most promising area,
but further research is needed before definitive recommendations can be made.
Crit Rev Food Sci Nutr. 2010 Oct;50(9):822-34. doi: 10.1080/10408390902773052.
ncbi.nlm.nih.gov
Cinnamon use in type 2 diabetes: an updated systematic review and meta-analysis.
Allen RW, Schwartzman E, Baker WL, Coleman CI, Phung OJ. Abstract
PURPOSE:
Cinnamon has been studied in randomized controlled trials (RCTs) for its glycemic-lowering
effects, but studies have been small and show conflicting results. A prior meta-analysis
did not show significant results, but several RCTs have been published since
then. We conducted an updated systematic review and meta-analysis of RCTs evaluating
cinnamon's effect on glycemia and lipid levels. METHODS: MEDLINE, Embase, and Cochrane Central Register of Controlled
Trials (CENTRAL) were searched through February 2012. Included RCTs evaluated
cinnamon compared with control in patients with type 2 diabetes and reported
at least one of the following: glycated hemoglobin (A1c), fasting plasma glucose,
total cholesterol, low-density lipoprotein cholesterol (LDL-C), high-density
lipoprotein cholesterol (HDL-C), or triglycerides. Weighted mean differences
(with 95% confidence intervals) for endpoints were calculated using random-effects
models. RESULTS:
In a meta-analysis of 10 RCTs (n = 543 patients), cinnamon doses of 120 mg/d
to 6 g/d for 4 to 18 weeks reduced levels of fasting plasma glucose (-24.59
mg/dL; 95% CI, -40.52 to -8.67 mg/dL), total cholesterol (-15.60 mg/dL; 95%
CI, -29.76 to -1.44 mg/dL), LDL-C (-9.42 mg/dL; 95% CI, -17.21 to -1.63 mg/dL),
and triglycerides (-29.59 mg/dL; 95% CI, -48.27 to -10.91 mg/dL). Cinnamon also
increased levels of HDL-C (1.66 mg/dL; 95% CI, 1.09 to 2.24 mg/dL). No significant
effect on hemoglobin A1c levels (-0.16%; 95%, CI -0.39% to 0.02%) was seen.
High degrees of heterogeneity were present for all analyses except HDL-C (I(2)
ranging from 66.5% to 94.72%). CONCLUSIONS:
The consumption of cinnamon is associated with a statistically significant decrease
in levels of fasting plasma glucose, total cholesterol, LDL-C, and triglyceride
levels, and an increase in HDL-C levels; however, no significant effect on hemoglobin
A1c was found. The high degree of heterogeneity may limit the ability to apply
these results to patient care, because the preferred dose and duration of therapy
are unclear. Ann Fam Med. 2013 Sep-Oct;11(5):452-9. doi: 10.1370/afm.1517. ncbi.nlm.nih.gov
Antidiabetic effect of Cinnamomum cassia and Cinnamomum zeylanicum in
vivo and in vitro. Verspohl EJ, Bauer K, Neddermann E. Abstract
Rats were given Cinnamomum cassia bark or extracts from Cinnamomum cassia and
zeylanicum to evaluate blood glucose and plasma insulin levels in rats under
various conditions. The cassia extract was superior to the zeylanicum extract.
The cassia extract was slightly more efficacious than the equivalent amount
of Cassia bark. A decrease in blood glucose levels was observed in a glucose
tolerance test (GTT), whereas it was not obvious in rats that were not challenged
by a glucose load. The elevation in plasma insulin was direct since a stimulatory
in vitro effect of insulin release from INS-1 cells (an insulin secreting cell
line) was observed. Thus the cassia extract has a direct antidiabetic potency.
PMID: 15934022 DOI: 10.1002/ptr.1643 Phytother Res. 2005 Mar;19(3):203-6. ncbi.nlm.nih.gov