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The glycaemic outcomes of Cinnamon, a review of the experimental evidence and clinical trials

INTRODUCTION: Cinnamon is currently marketed as a remedy for obesity, glucose intolerance, diabetes mellitus and dyslipidaemia. Integrative medicine is a new concept that combines conventional treatment with evidence-based complementary therapies. AIM: The aim of this review is to critically evaluat...

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Autor principal: Medagama, Arjuna B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4609100/
https://www.ncbi.nlm.nih.gov/pubmed/26475130
http://dx.doi.org/10.1186/s12937-015-0098-9
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author Medagama, Arjuna B.
author_facet Medagama, Arjuna B.
author_sort Medagama, Arjuna B.
collection PubMed
description INTRODUCTION: Cinnamon is currently marketed as a remedy for obesity, glucose intolerance, diabetes mellitus and dyslipidaemia. Integrative medicine is a new concept that combines conventional treatment with evidence-based complementary therapies. AIM: The aim of this review is to critically evaluate the experimental evidence available for cinnamon in improving glycaemic targets in animal models and humans. RESULTS: Insulin receptor auto-phosphorlylation and de-phosphorylation, glucose transporter 4 (GLUT-4 ) receptor synthesis and translocation, modulation of hepatic glucose metabolism through changes in Pyruvate kinase (PK) and Phosphenol Pyruvate Carboxikinase (PEPCK), altering the expression of PPAR (γ) and inhibition of intestinal glucosidases are some of the mechanisms responsible for improving glycaemic control with cinnamon therapy. We reviewed 8 clinical trials that used Cinnamomum cassia in aqueous or powder form in doses ranging from 500 mg to 6 g per day for a duration lasting from 40 days to 4 months as well as 2 clinical trials that used cinnamon on treatment naïve patients with pre-diabetes. An improvement in glycaemic control was seen in patients who received Cinnamon as the sole therapy for diabetes, those with pre-diabetes (IFG or IGT) and in those with high pre-treatment HbA1c. In animal models, cinnamon reduced fasting and postprandial plasma glucose and HbA1c. CONCLUSION: Cinnamon has the potential to be a useful add-on therapy in the discipline of integrative medicine in managing type 2 diabetes. At present the evidence is inconclusive and long-term trials aiming to establish the efficacy and safety of cinnamon is needed. However, high coumarin content of Cinnamomum cassia is a concern, but Cinnamomum zeylanicum with its low coumarin content would be a safer alternate.
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spelling pubmed-46091002015-10-18 The glycaemic outcomes of Cinnamon, a review of the experimental evidence and clinical trials Medagama, Arjuna B. Nutr J Review INTRODUCTION: Cinnamon is currently marketed as a remedy for obesity, glucose intolerance, diabetes mellitus and dyslipidaemia. Integrative medicine is a new concept that combines conventional treatment with evidence-based complementary therapies. AIM: The aim of this review is to critically evaluate the experimental evidence available for cinnamon in improving glycaemic targets in animal models and humans. RESULTS: Insulin receptor auto-phosphorlylation and de-phosphorylation, glucose transporter 4 (GLUT-4 ) receptor synthesis and translocation, modulation of hepatic glucose metabolism through changes in Pyruvate kinase (PK) and Phosphenol Pyruvate Carboxikinase (PEPCK), altering the expression of PPAR (γ) and inhibition of intestinal glucosidases are some of the mechanisms responsible for improving glycaemic control with cinnamon therapy. We reviewed 8 clinical trials that used Cinnamomum cassia in aqueous or powder form in doses ranging from 500 mg to 6 g per day for a duration lasting from 40 days to 4 months as well as 2 clinical trials that used cinnamon on treatment naïve patients with pre-diabetes. An improvement in glycaemic control was seen in patients who received Cinnamon as the sole therapy for diabetes, those with pre-diabetes (IFG or IGT) and in those with high pre-treatment HbA1c. In animal models, cinnamon reduced fasting and postprandial plasma glucose and HbA1c. CONCLUSION: Cinnamon has the potential to be a useful add-on therapy in the discipline of integrative medicine in managing type 2 diabetes. At present the evidence is inconclusive and long-term trials aiming to establish the efficacy and safety of cinnamon is needed. However, high coumarin content of Cinnamomum cassia is a concern, but Cinnamomum zeylanicum with its low coumarin content would be a safer alternate. BioMed Central 2015-10-16 /pmc/articles/PMC4609100/ /pubmed/26475130 http://dx.doi.org/10.1186/s12937-015-0098-9 Text en © Medagama. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Medagama, Arjuna B.
The glycaemic outcomes of Cinnamon, a review of the experimental evidence and clinical trials
title The glycaemic outcomes of Cinnamon, a review of the experimental evidence and clinical trials
title_full The glycaemic outcomes of Cinnamon, a review of the experimental evidence and clinical trials
title_fullStr The glycaemic outcomes of Cinnamon, a review of the experimental evidence and clinical trials
title_full_unstemmed The glycaemic outcomes of Cinnamon, a review of the experimental evidence and clinical trials
title_short The glycaemic outcomes of Cinnamon, a review of the experimental evidence and clinical trials
title_sort glycaemic outcomes of cinnamon, a review of the experimental evidence and clinical trials
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4609100/
https://www.ncbi.nlm.nih.gov/pubmed/26475130
http://dx.doi.org/10.1186/s12937-015-0098-9
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