Comparative analysis of maple syrup to other natural sweeteners and evaluation of their metabolic responses in healthy rats

•Maple syrup is rich in polyphenolic lignans and in the phytohormone abscisic acid.•Maple syrup produces lower glucose and insulin responses than the dextrose control.•Brown rice and corn syrup induced higher metabolic responses than maple syrup.•Honey caused higher peak responses for insulin, amyli...

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Published inJournal of functional foods Vol. 11; pp. 460 - 471
Main Authors St-Pierre, Philippe, Pilon, Geneviève, Dumais, Valérie, Dion, Christine, Dubois, Marie-Julie, Dubé, Pascal, Desjardins, Yves, Marette, André
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.11.2014
Subjects
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ISSN1756-4646
2214-9414
DOI10.1016/j.jff.2014.10.001

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Abstract •Maple syrup is rich in polyphenolic lignans and in the phytohormone abscisic acid.•Maple syrup produces lower glucose and insulin responses than the dextrose control.•Brown rice and corn syrup induced higher metabolic responses than maple syrup.•Honey caused higher peak responses for insulin, amylin and GIP than maple syrup.•Metabolic effects of agave syrup and molasses were similar to that of maple syrup. Maple syrup is a natural source of carbohydrates but its metabolic impact remains poorly studied. We undertook to systematically compare the chemical composition of maple syrup with that of other natural sweeteners, and assess their metabolic responses in healthy rats. As compared to other sweeteners, maple syrup is particularly rich in polyphenolic lignans and in the phytohormone abscisic acid and its derivatives. Metabolic studies in rats showed that maple syrup produced significantly lower peak and global responses of glucose, insulin, amylin and gastric inhibitory polypeptide (GIP) as compared to brown rice syrup, corn syrup and pure dextrose. The metabolic effects of agave syrup and molasses were similar to that of maple syrup, while honey caused higher peak responses for insulin, amylin and GIP. Both the composition of maple syrup and the metabolic responses to its ingestion in rats indicate that it represents a healthy natural alternative to refined sugar.
AbstractList Maple syrup is a natural source of carbohydrates but its metabolic impact remains poorly studied. We undertook to systematically compare the chemical composition of maple syrup with that of other natural sweeteners, and assess their metabolic responses in healthy rats. As compared to other sweeteners, maple syrup is particularly rich in polyphenolic lignans and in the phytohormone abscisic acid and its derivatives. Metabolic studies in rats showed that maple syrup produced significantly lower peak and global responses of glucose, insulin, amylin and gastric inhibitory polypeptide (GIP) as compared to brown rice syrup, corn syrup and pure dextrose. The metabolic effects of agave syrup and molasses were similar to that of maple syrup, while honey caused higher peak responses for insulin, amylin and GIP. Both the composition of maple syrup and the metabolic responses to its ingestion in rats indicate that it represents a healthy natural alternative to refined sugar.
•Maple syrup is rich in polyphenolic lignans and in the phytohormone abscisic acid.•Maple syrup produces lower glucose and insulin responses than the dextrose control.•Brown rice and corn syrup induced higher metabolic responses than maple syrup.•Honey caused higher peak responses for insulin, amylin and GIP than maple syrup.•Metabolic effects of agave syrup and molasses were similar to that of maple syrup. Maple syrup is a natural source of carbohydrates but its metabolic impact remains poorly studied. We undertook to systematically compare the chemical composition of maple syrup with that of other natural sweeteners, and assess their metabolic responses in healthy rats. As compared to other sweeteners, maple syrup is particularly rich in polyphenolic lignans and in the phytohormone abscisic acid and its derivatives. Metabolic studies in rats showed that maple syrup produced significantly lower peak and global responses of glucose, insulin, amylin and gastric inhibitory polypeptide (GIP) as compared to brown rice syrup, corn syrup and pure dextrose. The metabolic effects of agave syrup and molasses were similar to that of maple syrup, while honey caused higher peak responses for insulin, amylin and GIP. Both the composition of maple syrup and the metabolic responses to its ingestion in rats indicate that it represents a healthy natural alternative to refined sugar.
Author Dubois, Marie-Julie
Pilon, Geneviève
Dion, Christine
Desjardins, Yves
Marette, André
St-Pierre, Philippe
Dumais, Valérie
Dubé, Pascal
Author_xml – sequence: 1
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  surname: St-Pierre
  fullname: St-Pierre, Philippe
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  organization: Québec Heart and Lung Institute, Laval University, Québec, Canada
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  surname: Dubois
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  organization: Québec Heart and Lung Institute, Laval University, Québec, Canada
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  organization: Institute of Nutrition and Functional Foods, Laval University, Québec, Canada
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  givenname: André
  surname: Marette
  fullname: Marette, André
  email: andre.marette@criucpq.ulaval.ca
  organization: Québec Heart and Lung Institute, Laval University, Québec, Canada
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Keywords ABA
ABA-GE
Incretin
GLP-1
Natural sweeteners
GIP
Glycaemia and insulinaemia
CVD
PA
7-OH-ABA
DPA
Maple syrup
trans-ABA
Abscisic acid
Polyphenols
Neo-PA
HbA1c
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Snippet •Maple syrup is rich in polyphenolic lignans and in the phytohormone abscisic acid.•Maple syrup produces lower glucose and insulin responses than the dextrose...
Maple syrup is a natural source of carbohydrates but its metabolic impact remains poorly studied. We undertook to systematically compare the chemical...
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SubjectTerms Abscisic acid
brown rice
chemical composition
corn syrup
gastric inhibitory polypeptide
glucose
Glycaemia and insulinaemia
honey
Incretin
ingestion
insulin
lignans
Maple syrup
metabolic studies
molasses
Natural sweeteners
Polyphenols
rats
refined sugar
sweeteners
Title Comparative analysis of maple syrup to other natural sweeteners and evaluation of their metabolic responses in healthy rats
URI https://dx.doi.org/10.1016/j.jff.2014.10.001
https://www.proquest.com/docview/2000199314
Volume 11
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