| Literature DB >> 28234328 |
José M Alvarez-Suarez1,2, Massimiliano Gasparrini3, Tamara Y Forbes-Hernández4,5, Luca Mazzoni6, Francesca Giampieri7.
Abstract
Honey has been used as a food and medical product since the earliest times. It has been used in many cultures for its medicinal properties, as a remedy for burns, cataracts, ulcers and wound healing, because it exerts a soothing effect when initially applied to open wounds. Depending on its origin, honey can be classified in different categories among which, monofloral honey seems to be the most promising and interesting as a natural remedy. Manuka honey, a monofloral honey derived from the manuka tree (Leptospermum scoparium), has greatly attracted the attention of researchers for its biological properties, especially its antimicrobial and antioxidant capacities. Our manuscript reviews the chemical composition and the variety of beneficial nutritional and health effects of manuka honey. Firstly, the chemical composition of manuka honey is described, with special attention given to its polyphenolic composition and other bioactive compounds, such as glyoxal and methylglyoxal. Then, the effect of manuka honey in wound treatment is described, as well as its antioxidant activity and other important biological effects.Entities:
Keywords: antimicrobial activity; manuka honey; polyphenolic composition; wound treatments
Year: 2014 PMID: 28234328 PMCID: PMC5302252 DOI: 10.3390/foods3030420
Source DB: PubMed Journal: Foods ISSN: 2304-8158
Most common compounds identified in manuka honey.
| Phenolic Acid and Flavonoids | Ref. | Other Compounds | Ref. |
|---|---|---|---|
| Caffeic acid | [ | Phenyllactic acid | [ |
| Isoferulic acid | [ | 4-Methoxyphenolactic acid | [ |
| [ | Kojic acid | [ | |
| Gallic acid | [ | 5-Hydroxymethylfurfural | [ |
| 4-Hydrobenzoic acid | [ | 2-Methoxybenzoic acid | [ |
| Syringin acid | [ | Phenylacetic acid | [ |
| Quercetin | [ | Methyl syringate | [ |
| Luteolin | [ | Dehydrovomifoliol | [ |
| 8-Methoxykaempferol | [ | Leptosin | [ |
| Pinocembrin | [ | Glyoxal | [ |
| Isorhamnetin | [ | Methylglyoxal | [ |
| Kaempferol | [ | 3-Deoxyglucosulose | [ |
| Chrysin | [ | - | - |
| Galangin | [ | - | - |
| Pinobanksin | [ | - | - |
Figure 1Chemical structures of methyl syringate and leptosin.
Figure 2(A) Chemical structures of the methylglyoxal (MGO). (B) Homology model of defensin-1 from Apis mellifera. The model of the mature protein (residues 44–94) was obtained using the experimentally-resolved structure of lucifensin from Lucilia sericata (PDB ID: 2LLD) as a template. Alignment and modeling was performed using the Swiss Model server [41]; the figure has been obtained through PyMOL Molecular Graphics System, Version 1.5.0.4, Schrödinger, LLC (Portland, OR, USA).
List of microorganisms that have been found to be sensitive to manuka honeys [49].
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| Coagulase negative staphylococci |
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| Coagulase-negative |
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