CEYLON CINNAMON

OTHER NAME(S):

Batavia Cassia, Batavia Cinnamon, Canela, Canelero de Ceilán, Cannelier de Ceylan, Cannelle de Ceylan, Cannelle de Saïgon, Cannelle du Sri Lanka, Ceylonzimt, Ceylonzimtbaum, Cinnamomum verum, Cinnamomum zeylanicum, Cinnamon Bark, Corteza de Canela, Dalchini, Écorce de Cannelle, Echter Ceylonzimt, Laurus cinnamomum, Madagascar Cinnamon, Padang-Cassia, Panang Cinnamon, Saigon Cassia, Saigon Cinnamon, Sri Lanka Cinnamon, Thwak, True Cinnamon, Tvak, Xi Lan Rou Gui, Zimtbaum.<br/><br/>

Overview

Overview Information

Ceylon cinnamon comes from a tree called Cinnamomum verum. People use the bark to make medicine.

Ceylon cinnamon is sometimes taken by mouth for stomach upset, diarrhea, and gas. It is also used for diabetes, stimulating appetite, treating infections, and reducing body weight in patients who are overweight or obese. But there is no good scientific research to support any of these or other uses.

In foods, cinnamon is used as a spice and as a flavoring agent in beverages.

In manufacturing, cinnamon oil is used in small amounts in toothpaste, mouthwashes, gargles, lotions, liniments, soaps, detergents, and other pharmaceutical products and cosmetics.

There are lots of different types of cinnamon. Cinnamomum verum (Ceylon cinnamon) and Cinnamomum aromaticum (Cassia cinnamon or Chinese cinnamon) are commonly used. In many cases, the cinnamon spice purchased in food stores contains a combination of these and other types of cinnamon.

How does it work?

The oils found in Ceylon cinnamon are thought to reduce spasms, reduce gas (flatulence), stimulate the appetite, and fight bacteria and fungi. Cinnamon might also decrease blood pressure and blood lipids. Ceylon cinnamon chemicals might work like insulin to lower blood sugar. However, these effects are thought to be fairly weak.

There are also ingredients in Ceylon cinnamon called tannins that might help wounds by acting as an astringent, and also prevent diarrhea.

Uses

Uses & Effectiveness?

Possibly Ineffective for

  • Diabetes. Early research shows that taking Ceylon cinnamon daily does not lower blood sugar in people with well-controlled diabetes. There is weak evidence that it might help people with poorly controlled diabetes. But higher quality research is needed to confirm.
  • Obesity. Taking Ceylon cinnamon every day for 2-3 months does not seem to decrease body weight.

Insufficient Evidence for

  • Yeast infection (candidiasis). Early research shows that taking lozenges containing Ceylon cinnamon for one week might improve yeast infections in the mouth, a condition also known as thrush, in some people with HIV.
  • Mouth sores from dentures. Early research shows that rinsing the mouth with 10 mL of mouthwash containing Ceylon cinnamon leaf oil helps prevent mouth sores in some people with dentures.
  • A hormonal disorder that causes enlarged ovaries with cysts (polycystic ovary syndrome or PCOS). Some early research suggests taking Ceylon cinnamon alone reduces insulin resistance but does not appear to improve fasting blood sugar levels, blood fat levels, weight, or body mass index in women with PCOS. However, some research shows that taking Ceylon cinnamon along with other herbal ingredients for 3 months may lead to regular periods, improve the chances of conception, lower blood pressure, improve quality of life, and decrease symptoms of depression, anxiety, and stress in overweight women with PCOS.
  • Food poisoning (Salmonella infection). Consuming Ceylon cinnamon might help treat a salmonella infection.
  • Appetite stimulation.
  • Common cold.
  • Diabetes.
  • Diarrhea.
  • Gas (flatulence).
  • Hay fever (allergic rhinitis).
  • Infections.
  • Influenza.
  • Irritable bowel syndrome (IBS).
  • Menstrual discomfort.
  • Prediabetes.
  • Premature ejaculation.
  • Spasms.
  • Upset stomach.
  • Worm infestations.
  • Other conditions.
More evidence is needed to rate Ceylon cinnamon for these uses.

Side Effects

Side Effects & Safety

Consuming Ceylon cinnamon in food amounts is LIKELY SAFE. Ceylon cinnamon is POSSIBLY SAFE for most people when taken by mouth in amounts used for medicine for up to 3 months. These amounts are slightly higher than amounts found in food. However, Ceylon cinnamon is POSSIBLY UNSAFE when taken by mouth in large amounts or long term. Also, taking cinnamon oil by mouth is POSSIBLY UNSAFE. The oil can be irritating to the skin and mucous membranes, including the stomach, intestine, and urinary tract. It can cause side effects such as diarrhea, vomiting, dizziness, drowsiness, and others.

Special Precautions & Warnings:

Pregnancy and breast-feeding: Consuming Ceylon cinnamon is LIKELY SAFE when taken in food amounts during pregnancy and breast-feeding. Ceylon cinnamon is LIKELY UNSAFE when taken in amounts greater than those found in foods during pregnancy. Not enough is known about the safety of taking larger amounts during breast-feeding. Stay on the safe side and stick to food amounts.

Diabetes: Ceylon cinnamon might lower blood sugar in people with type 2 diabetes or prediabetes. Watch for signs of low blood sugar (hypoglycemia) and monitor your blood sugar carefully if you have diabetes and use Ceylon cinnamon.

Low blood pressure: Ceylon cinnamon might lower blood pressure. Taking Ceylon cinnamon might cause blood pressure to drop too low in people who already have low blood pressure.

Surgery: Ceylon cinnamon can affect blood pressure and blood sugar levels and might interfere with blood pressure and blood sugar control during and after surgery. Stop taking cinnamon at least 2 weeks before a scheduled surgery.

Interactions

Interactions?

Moderate Interaction

Be cautious with this combination

!

  • Medications for diabetes (Antidiabetes drugs) interacts with CEYLON CINNAMON

    Cinnamon bark might decrease blood sugar. Diabetes medications are also used to lower blood sugar. Taking cinnamon bark along with diabetes medications might cause your blood sugar to go too low. Monitor your blood sugar closely. The dose of your diabetes medication might need to be changed.<br/><br/> Some medications used for diabetes include glimepiride (Amaryl), glyburide (DiaBeta, Glynase PresTab, Micronase), insulin, pioglitazone (Actos), rosiglitazone (Avandia), chlorpropamide (Diabinese), glipizide (Glucotrol), tolbutamide (Orinase), and others.

Dosing

Dosing

The appropriate dose of Ceylon cinnamon depends on several factors such as the user's age, health, and several other conditions. At this time there is not enough scientific information to determine an appropriate range of doses for Ceylon cinnamon. Keep in mind that natural products are not always necessarily safe and dosages can be important. Be sure to follow relevant directions on product labels and consult your pharmacist or physician or other healthcare professional before using.

Previous:
Next: Uses

View References

REFERENCES:

  • Flynn MA, Weaver-Osterholtz D, Sharpe-Timms KL, et al. Dehydroepiandrosterone replacement in aging humans. [Abstract] J Clin Endocrinol Metab 1999;84:1527-33. View abstract.
  • Forrest AD, Drewery J, Fotherby K, Laverty SG. A clinical trial of dehydroepiandrosterone (Diandrone). J Neurol Neurosurg Psychiat 1960;23:52-5. View abstract.
  • Forsblad-d'Elia, H., Carlsten, H., Labrie, F., Konttinen, Y. T., Ohlsson, C. Low serum levels of sex steroids are associated with disease characteristics in primary Sjogren's syndrome; supplementation with dehydroepiandrosterone restores the concentrations. J Clin Endocrinol Metab 2009;94(6):2044-51. View abstract.
  • Foth D, Nawroth F. Effect of soy supplementation on endogenous hormones in postmenopausal women. Gynecol Obstet Invest 2003;55:135-8. View abstract.
  • Freeland-Graves JH, Lin PH. Plasma uptake of manganese as affected by oral loads of manganese, calcium, milk, phosphorus, copper, and zinc. J Am Coll Nutr 1991;10:38-43. View abstract.
  • Frye RF, Kroboth PD, Folan MM, et al. Effect of DHEA on CYP3A-mediated metabolism of triazolam. Clin Pharmacol Ther 2000;67:109 (abstract PI-82).
  • Gebre-Medhin, G., Husebye, E. S., Mallmin, H., Helstrom, L., Berne, C., Karlsson, F. A., Kampe, O. Oral dehydroepiandrosterone (DHEA) replacement therapy in women with Addison's disease. Clin Endocrinol (Oxf) 2000;52(6):775-80. View abstract.
  • Chiesara E, Borghini R, Marabini. Dietary fibre and drug interactions. Eur J Clin Nutr 1995;49:S123-8.
  • Christeff N, Gherbi N, Mammes O, et al. Serum cortisol and DHEA concentrations during HIV infection. Psychoneuroendocrinology 1997;22:S11-8. View abstract.
  • Christiansen, J. J., Andersen, N. H., Sorensen, K. E., Pedersen, E. M., Bennett, P., Andersen, M., Christiansen, J. S., Jorgensen, J. O., Gravholt, C. H. Dehydroepiandrosterone substitution in female adrenal failure: no impact on endothelial function and cardiovascular parameters despite normalization of androgen status. Clin Endocrinol (Oxf) 2007;66(3):426-33. View abstract.
  • Christiansen, J. J., Bruun, J. M., Christiansen, J. S., Jorgensen, J. O., Gravholt, C. H. Long-term DHEA substitution in female adrenocortical failure, body composition, muscle function, and bone metabolism: a randomized trial. Eur J Endocrinol 2011;165(2):293-300. View abstract.
  • Cibula, D., Fanta, M., Vrbikova, J., Stanicka, S., Dvorakova, K., Hill, M., Skrha, J., Zivny, J., Skrenkova, J. The effect of combination therapy with metformin and combined oral contraceptives (COC) versus COC alone on insulin sensitivity, hyperandrogenaemia, SHBG and lipids in PCOS patients. Hum Reprod 2005;20(1):180-4. View abstract.
  • Ciolino H, MacDonald C, Memon O, et al. Dehydroepiandrosterone inhibits the expression of carcinogen-activating enzymes in vivo. Int J Cancer 2003;105:321-5 . View abstract.
  • Cook IJ, Irvine EJ, Campbell D, et al. Effect of dietary fiber on rectosigmoid motility in patients with irritable bowel syndrome: A controlled, crossover study. Gastroenterology 1990;98:66-72. View abstract.
  • Crosbie, D., Black, C., McIntyre, L., Royle, P. L., Thomas, S. Dehydroepiandrosterone for systemic lupus erythematosus. Cochrane Database Syst Rev 2007;(4):CD005114. View abstract.
  • Cui, Y., Choi, I. S., Koh, Y. A., Lin, X. H., Cho, Y. B., Won, Y. H. Effects of combined BCG and DHEA treatment in preventing the development of asthma. Immunol Invest 2008;37(3):191-202. View abstract.
  • Dayal, M., Sammel, M. D., Zhao, J., Hummel, A. C., Vandenbourne, K., Barnhart, K. T. Supplementation with DHEA: effect on muscle size, strength, quality of life, and lipids. J Womens Health (Larchmt) 2005;14(5):391-400. View abstract.
  • Dean CE. Prasterone (DHEA) and mania. Ann Pharmacother 2000;34:1419-22. View abstract.
  • Despotis GJ, Alsoufiev AL, Spitznagel E, et al. DG Response of kaolin ACT to heparin: evaluation with an automated assay and higher heparin doses. Ann Thorac Surg 1996;61:795-9. View abstract.
  • Dhatariya, K. K., Greenlund, L. J., Bigelow, M. L., Thapa, P., Oberg, A. L., Ford, G. C., Schimke, J. M., Nair, K. S. Dehydroepiandrosterone replacement therapy in hypoadrenal women: protein anabolism and skeletal muscle function. Mayo Clin Proc 2008;83(11):1218-25. View abstract.
  • Dorgan, J. F., Reichman, M. E., Judd, J. T., Brown, C., Longcope, C., Schatzkin, A., Forman, M., Campbell, W. S., Franz, C., Kahle, L., Taylor, P. R. Relation of energy, fat, and fiber intakes to plasma concentrations of estrogens and androgens in premenopausal women. Am J Clin Nutr 1996;64(1):25-31. View abstract.
  • Drug Facts and Comparisons. Olin BR, ed. St. Louis, MO: Facts and Comparisons. (updated monthly).
  • Dumas de La Roque, E., Savineau, J. P., Metivier, A. C., Billes, M. A., Kraemer, J. P., Doutreleau, S., Jougon, J., Marthan, R., Moore, N., Fayon, M., Baulieu, E. E., Dromer, C. Dehydroepiandrosterone (DHEA) improves pulmonary hypertension in chronic obstructive pulmonary disease (COPD): a pilot study. Ann Endocrinol (Paris) 2012;73(1):20-2. View abstract.
  • Dyner TS, Lang W, Geaga J, et al. An open-label, dose-escalation trial of oral dehydroepiandrosterone tolerance and pharmacokinetics in patients with HIV disease. J Acquir Immune Defic Syndr 1993;6:459-65. View abstract.
  • Ebeling P, Koivisto VA. Physiological importance of dehydroepiandrosterone. Lancet 1994;343:1479-81. View abstract.
  • Elmer GW, Surawicz CM, McFarland LV. Biotherapeutic Agents, A neglected modality for the treatment and prevention of selected intestinal and vaginal infections. JAMA 1996;275:870-5. View abstract.
  • Elraiyah T, Sonbol MB, Wang Z, et al. Clinical review: The benefits and harms of systemic dehydroepiandrosterone (DHEA) in postmenopausal women with normal adrenal function: a systematic review and meta-analysis. J Clin Endocrinol Metab 2014;99(10):3536-42. View abstract.
  • Fassati, P., Fassati, M., Sonka, J., Lesensky, K. [New approach to the treatment of angina pectoris by dehydroepiandrosterone-sulfate]. Cas Lek Cesk 1971;110(26):606-9. View abstract.
  • Fassati, P., Fassati, M., Sonka, J., Lesensky, K. Dehydroepiandrosterone sulphate--a new approach to some cases of angina pectoris therapy. Agressologie 1970;11(5):445-8. View abstract.
  • FDA News Release: FDA approves Intrarosa for postmenopausal women experiencing pain during sex. FDA Press Announcements, November 17, 2016. Available at: https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm529641.htm.
  • Finckh, A., Berner, I. C., Aubry-Rozier, B., So, A. K. A randomized controlled trial of dehydroepiandrosterone in postmenopausal women with fibromyalgia. J Rheumatol 2005;32(7):1336-40. View abstract.
  • Fischer, L., Mahoney, C., Jeffcoat, A. R., Koch, M. A., Thomas, B. E., Valentine, J. L., Stinchcombe, T., Boan, J., Crowell, J. A., Zeisel, S. H. Clinical characteristics and pharmacokinetics of purified soy isoflavones: multiple-dose administration to men with prostate neoplasia. Nutr Cancer 2004;48(2):160-70. View abstract.
  • Domaracky, M., Rehak, P., Juhas, S., and Koppel, J. Effects of selected plant essential oils on the growth and development of mouse preimplantation embryos in vivo. Physiol Res 2007;56(1):97-104. View abstract.
  • Sambaiah, K. and Srinivasan, K. Effect of cumin, cinnamon, ginger, mustard and tamarind in induced hypercholesterolemic rats. Nahrung 1991;35(1):47-51. View abstract.
  • Admani S, Hill H, Jacob SE. Cinnamon Sugar Scrub Dermatitis: "Natural" Is Not Always Best. Pediatr Dermatol. 2017;34(1):e42-e43. View abstract.
  • Agricultural Research Service. Dr. Duke's Phytochemical and Ethnobotanical Databases. Available at: www.ars-grin.gov/duke/.
  • Alqasoumi S. Anti-secretagogue and antiulcer effects of 'cinnamon' Cinnamomum zeylanicum in rats. J Pharmacog Phytother 2012;4:53-61.
  • Anderson RA, Broadhurst CL, Polansky MM, et al. Isolation and Characterization of Polyphenol Type-A Polymers from Cinnamon with Insulin-like Biological Activity. J Agric Food Chem 2004;52:65-70. View abstract.
  • Arentz S, Smith CA, Abbott J, Fahey P, Cheema BS, Bensoussan A. Combined Lifestyle and Herbal Medicine in Overweight Women with Polycystic Ovary Syndrome (PCOS): A Randomized Controlled Trial. Phytother Res. 2017 Sep;31(9):1330-1340. View abstract.
  • Azimi P, Ghiasvand R Feizi A, Hariri M, Abbasi B. Effects of cinnamon, cardamom, saffron, and ginger consumption on markers of glycemic control, lipid profile, oxidative stress, and inflammation in type 2 diabetes. Rev Diabet Stud. 2014 Fall-Winter;11(3-4):258-66. View abstract.
  • Azimi P, Ghiasvand R, Feizi A, et al. Effect of cinnamon, cardamom, saffron and ginger consumption on blood pressure and a marker of endothelial function in patients with type 2 diabetes mellitus: A randomized controlled clinical trial. Blood Press. 2016;25(3):133-40. View abstract.
  • Blumenthal M, Goldberg A, Brinckmann J, eds. Herbal Medicine Expanded Commission E Monographs. Newton, MA: Integrative Medicine Communications, 2000.
  • Brancheau D, Patel B, Zughaib M. Do cinnamon supplements cause acute hepatitis? Am J Case Rep 2015;16:250-4. View abstract.
  • Choi HK, Jung GW, Moon KH, et al. Clinical study of SS-Cream in patients with lifelong premature ejaculation. Urology 2000;55:257-61. View abstract.
  • Chularisi MU, Picha P, Rienkijkan M, Preechanukool K. The cytotoxic effect of petroleum ether and chloroform extracts from Ceylon cinnamon (Cinnamomum zeylanicum nees) barks on tumor cells in vitro. Int J Crude Drug Res 1984;22:177-80.
  • Concalves JL, Lopes RC, Oliveira DB, et al. In vitro anti-rotavirus activity of some medicinal plants used in Brazil against diarrhea. J Ethnopharmacol 2005;99(3):403-7. View abstract.
  • Corren, J., Lemay, M., Lin, Y., Rozga, L., and Randolph, R. K. Clinical and biochemical effects of a combination botanical product (ClearGuard) for allergy: a pilot randomized double-blind placebo-controlled trial. Nutr.J 2008;7:20. View abstract.
  • Eidi A, Mortazavi P, Bazargam M, Zaringhalam J. Hepatoprotective activity of cinnamon ethanolic extract against CCL 4-induced liver injury in rats. EXCLI J 2012;11:495-507. View abstract.
  • El Az NMTA, Khalil FAM, Shaapan RM. Therapeutic effect of onion (allium cepa) and cinnamon (cinnamomum zeylanicum) oils on cryptosporidiosis in experimentally infected mice. Global Vet 2011;7:179-83.
  • Electronic Code of Federal Regulations. Title 21. Part 182 -- Substances Generally Recognized As Safe. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart=182
  • Farahpour MR, Habibi M. Evaluation of the wound healing activity of an ethanolic extract of Ceylon cinnamon in mice. Vet Med 2012;57:53-7.
  • Hajimonfarednejad M, Nimrouzi M, Heydari M, Zarshenas MM, Raee MJ, Jahromi BN. Insulin resistance improvement by cinnamon powder in polycystic ovary syndrome: a randomized double-blind placebo controlled clinical trial. Phytother Res 2018;32(2):276-83. View abstract.
  • Hassan SA, Barthwal R, Nair MS, Haque SS. Aqueous bark extract of Cinnamomum zeylanicum: a potential therapeutic agent for steptozotocin-induced type 1 diabetes mellitus (T1DM) rats. Top J Pharm Res 2012;11:429-35.
  • Hawrelak, J. A. and Myers, S. P. Effects of two natural medicine formulations on irritable bowel syndrome symptoms: a pilot study. J Altern Complement Med 2010;16(10):1065-1071. View abstract.
  • Isaac-Renton M, Li MK, Parsons LM. Cinnamon spice and everything not nice: many features of intraoral allergy to cinnamic aldehyde. Dermatitis. 2015;26(3):116-21. View abstract.
  • Jain S, Sangma T, Shukla SK, Mediratta PK. Effect of Cinnamomum zeylanicum extract on scopolamine-induced cognitive impairment and oxidative stress in rats. Nutr Neurosci 2015;18(5):210-6. View abstract.
  • Jarvill-Taylor KJ, Anderson RA, Graves DJ. A hydroxychalcone derived from cinnamon functions as a mimetic for insulin in 3T3-L1 adipocytes. J Am Coll Nutr 2001;20:327-36. View abstract.
  • Javed I, Faisal I, Rahman Z, et al. Lipid lowering effect of Cinnamomum zeylanicum in hyperlipidaemic albino rabbits. Pak J Pharm Sci 2012;25(1):141-7. View abstract.
  • Kamath JV, Rana AC, Chowdhury AR. Pro-healing effect of Cinnamomum zeylanicum bark. Phytother Res 2003;17(8):970-2. View abstract.
  • Kanerva L, Estlander T, Jolanki R. Occupational allergic contact dermatitis from spices. Contact Dermatitis 1996;35:157-62. View abstract.
  • Khan A, Safdar M, Ali Khan M, et al. Cinnamon improves glucose and lipids of people with type 2 diabetes. Diabetes Care 2003;26:3215-8. View abstract.
  • Liu Y, Cotillard A, Vatier C, et al. A Dietary Supplement Containing Cinnamon, Chromium and Carnosine Decreases Fasting Plasma Glucose and Increases Lean Mass in Overweight or Obese Pre-Diabetic Subjects: A Randomized, Placebo-Controlled Trial. PLoS One. 201;10(9):e0138646. View abstract.
  • Meades G Jr, Henken RL, Waldrop GL, et al. Constituents of cinnamon inhibit bacterial acetyl CoA carboxylase. Planta Med 2010;76(14):1570-5. View abstract.
  • Mirfeizi M, Mehdizadeh Tourzani Z, Mirfeizi SZ, et al. Controlling type 2 diabetes mellitus with herbal medicines: a triple-blind randomized clinical trial of efficacy and safety. J Diabetes. 2016 Sep;8(5):647-56. View abstract.
  • Nyadjeu P, Dongmo A, Nguelefack TB, Kamanyi A. Antihypertensive and vasorelaxant effects of Cinnamomum zeylanicum stem bark aqueous extracts. J Complement Integr Med 2011;8. View abstract.
  • Oliveira JdA, da Silva IC, Trindade LA, et al. Safety and tolerability of essential oil from Cinnamomum zeylanicum blume leaves with action on oral candidosis and its effect on the physical properties of the acylic resin. Evid Based Complement Alternat Med 2014;2014:325670. View abstract.
  • Onderoglu S, Sozer S, Erbil KM, et al. The evaluation of long-term effcts of cinnamon bark and olive leaf on toxicity induced by streptozotocin administration to rats. J Pharm Pharmacol 1999;51:1305-12. View abstract.
  • Pellagatti Lemonica I, Borro Macedo AMR. Abortive and/or embryofetotoxic effect of Cinnamomum zeylanicum leaf extracts in pregnant rats. Fitoterapia 1994;65(5):431-4.
  • Peterson DW, George RC, Scaramozzino F, et al. Cinnamon extract inhibits tau aggregation associated with Alzheimer's disease in vitro. J Alzheimers Dis 2009;17(3):585-97. View abstract.
  • Pilapil VR. Toxic manifestations of cinnamon oil ingestion in a child. Clin Pediatr (Phila) 1989;28:276.. View abstract.
  • Quale, J. M., Landman, D., Zaman, M. M., Burney, S., and Sathe, S. S. In vitro activity of Cinnamomum zeylanicum against azole resistant and sensitive Candida species and a pilot study of cinnamon for oral candidiasis. Am J Chin Med 1996;24(2):103-109. View abstract.
  • Rana IS, Singh A, Gwal R. In vitro study of antibacterial activity of aromatic and medicinal plants essential oils with special reference to cinnamon oil. Int J Pharm Pharm Sci 2011;3:376-80.
  • Ranasinghe P, Galappaththy P. Health benefits of Ceylon cinnamon (Cinnamomum zeylanicum): a summary of the current evidence. Ceylon Med J 2016;61(1):1-5. View abstract.
  • Ranasinghe P, Jayawardana R, Galappaththy P, et al. Efficacy and safety of 'true' cinnamon (Cinnamomum zeylanicum) as a pharmaceutical agent in diabetes: a systematic review and meta-analysis. Diabet Med 2012;29(12):1480-92. View abstract.
  • Ranasinghe P, Jayawardena R, Galappaththy P, et al. Response to Akilen et al. Efficacy and safety of 'true' cinnamon (Cinnamomum zeylanicum) as a pharmaceutical agent in diabetes: a systematic review and meta-analysis. Diabet Med 2013 Apr;30(4):506-7. View abstract.
  • Ranasinghe P, Jayawardena R, Pigera S, et al. Evaluation of pharmacodynamic properties and safety of Cinnamomum zeylanicum (Ceylon cinnamon) in healthy adults: a phase I clinical trial. BMC Complement Altern Med 2017;17(1):550. View abstract.
  • Ranasinghe P, Pigera S, Premakumara GA, et al. Medicinal properties of 'true' cinnamon (Cinnamomum zeylanicum): a systematic review. BMC Complement Altern Med 2013;13:275. View abstract.
  • Rao HJ, Lakshmi. Anti-diarrhoeal activity of the aqueous extract of the bark of Cinnamomum zeylanicum linn in mice. J Clin Diagn Res 2012;6:117-24.
  • Rosti L, Gastaldi G, Frigiola A. Cinnamon and bacterial enteric infections. Indian J Pediatr 2008;75(5). View abstract.
  • Rosti L, Gastaldi G. Chronic salmonellosis and cinnamon. Pediatrics 2005;116:1057. View abstract.
  • Samarasekera R, Kalhari KS, Weerasinghe IS. Mosquitocidal acitivy of leaf and bark essential oils of Ceylon cinnamomum zeylanicum. J Essent Oil Res 2005;17:301-3.
  • Singh R, Koppikar SJ, Paul P, et al. Comparative analysis of cytotoxic effect of aqueous cinnamon extract from Cinnamomum zeylanicum bark with commercial cinnamaldehyde on various cell lines. Pharm Biol 2009;47:1174-9.
  • Takasao N, Tsuji-Naito K, Ishikura S, et al. Cinnamon extract promotes type I collagen biosynthesis via activation of IGF-I signaling in human dermal fibroblasts. J Agric Food Chem 2012;60(5):1193-200. View abstract.
  • Talaei B, Amouzegar A, Sahranavard S, Hedayati M, Mirmiran P, Azizi F. Effects of cinnamon consumption on glycemic indicators, advanced glycation end products, and antioxidant status in type 2 diabetic patients. Nutrients. 2017 Sep 8;9(9). Pii:E991. View abstract.
  • Tsuji-Naito K. Aldehydic components of cinnamon bark extract suppresses RANKL-induced osteoclastogenesis through NFATc1 downregulation. Bioorg Med Chem 2008;16(20):9176-83. View abstract.
  • Vafa M, Mohammadi F, Shidfar F, Sormaghi MS, Heidari I, Golestan B, Armiri F. Effects of cinnamon consumption on glycemic status, lipid profile and body composition in type 2 diabetic patients. Int J Prev Med. 2012 Aug;3(8):531-6. View abstract.
  • Vandersall A, Katta R. Eyelid dermatitis as a manifestation of systemic contact dermatitis to cinnamon. Dermatitis. 2015 Jul-Aug;26(4):189. View abstract.
  • Verspohl EJ, Bauer K, Neddermann E. Antidiabetic effect of Cinnamomum cassia and Cinnamomum zeylanicum in vivo and in vitro. Phytother Res 2005;19:203-6. View abstract.
  • Wansi SL, Nyadjeu P, Ngamga D, et al. Blood pressure lowering effect of the ethanol extract from the stembark of Cinnamomum zeylanicum (lauraceae) in rats. Pharmacol online 2007;3:166-76.
  • Yang YC, Lee HS, Lee SE, et al. Ovicidal and adulticidal activities of Cinnamomum zeylanicum bark essential oil compounds and related compounds against Pediculus humanus capitis (Anopluar: Pediculicidae). Int J Parasitol 2005;35(14):1595-600. View abstract.

Vitamins Survey

Have you ever purchased CEYLON CINNAMON?

Did you or will you purchase this product in-store or online?

Where did you or where do you plan to purchase this product?

Where did you or where do you plan to purchase this product?

What factors influenced or will influence your purchase? (check all that apply)

Vitamins Survey

Where did you or where do you plan to purchase this product?

Do you buy vitamins online or instore?

What factors are most important to you? (check all that apply)

Thanks for taking our survey!

Recommended For You

Vitamins and Minerals A-Z

More Resources for CEYLON CINNAMON

Search for another Vitamin

CONDITIONS OF USE AND IMPORTANT INFORMATION: This information is meant to supplement, not replace advice from your doctor or healthcare provider and is not meant to cover all possible uses, precautions, interactions or adverse effects. This information may not fit your specific health circumstances. Never delay or disregard seeking professional medical advice from your doctor or other qualified health care provider because of something you have read on WebMD. You should always speak with your doctor or health care professional before you start, stop, or change any prescribed part of your health care plan or treatment and to determine what course of therapy is right for you.

This copyrighted material is provided by Natural Medicines Comprehensive Database Consumer Version. Information from this source is evidence-based and objective, and without commercial influence. For professional medical information on natural medicines, see Natural Medicines Comprehensive Database Professional Version.
© Therapeutic Research Faculty 2018.