Acute Effects of Kawakawa (<i>Piper excelsum</i>) Intake on Postprandial Glycemic and Insulinaemic Response in a Healthy Population.

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dc.contributor.author Ramzan, Farha
dc.contributor.author Jayaprakash, Ramya
dc.contributor.author Pook, Chris
dc.contributor.author Foster, Meika
dc.contributor.author Miles-Chan, Jennifer L
dc.contributor.author Mithen, Richard
dc.coverage.spatial Switzerland
dc.date.accessioned 2022-06-16T23:09:41Z
dc.date.available 2022-06-16T23:09:41Z
dc.date.issued 2022-04-14
dc.identifier.citation (2022). Nutrients, 14(8), 1638-.
dc.identifier.issn 2072-6643
dc.identifier.uri https://hdl.handle.net/2292/59954
dc.description.abstract <h4>Background</h4><i>Piper excelsum</i> (kawakawa) is an endemic shrub of Aotearoa, New Zealand, of cultural and medicinal importance to Māori. Its fruits and leaves are often consumed. These tissues contain several compounds that have been shown to be biologically active and which may underpin its putative health-promoting effects. The current study investigates whether kawakawa tea can modulate postprandial glucose metabolism.<h4>Methods</h4>We report a pilot three-arm randomized crossover study to assess the bioavailability of kawakawa tea (BOKA-T) in six male participants with each arm having an acute intervention of kawakawa tea (4 g/250 mL water; 1 g/250 mL water; water) and a follow-up two-arm randomized crossover study to assess the impact of acute kawakawa tea ingestion on postprandial glucose metabolism in healthy human volunteers (TOAST) (4 g/250 mL water; and water; <i>n</i> = 30 (15 male and 15 female)). Participants consumed 250 mL of kawakawa tea or water control within each study prior to consuming a high-glycemic breakfast. Pre- and postprandial plasma glucose and insulin concentrations were measured, and the Matsuda index was calculated to measure insulin sensitivity.<h4>Results</h4>In the BOKA-T study, lower plasma glucose (<i>p</i> &lt; 0.01) and insulin (<i>p</i> &lt; 0.01) concentrations at 60 min were observed after consumption of a high-dose kawakawa tea in comparison to low-dose or water. In the TOAST study, only plasma insulin (<i>p</i> = 0.01) was lower at 60 min in the high-dose kawakawa group compared to the control group. Both studies showed a trend towards higher insulin sensitivity in the high-dose kawakawa group compared to water only.<h4>Conclusions</h4>Consuming kawakawa tea may modulate postprandial glucose metabolism. Further investigations with a longer-term intervention study are warranted.
dc.format.medium Electronic
dc.language eng
dc.publisher MDPI AG
dc.relation.ispartofseries Nutrients
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher.
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.subject Humans
dc.subject Piper
dc.subject Insulin Resistance
dc.subject Water
dc.subject Insulin
dc.subject Blood Glucose
dc.subject Cross-Over Studies
dc.subject Postprandial Period
dc.subject Tea
dc.subject Female
dc.subject Male
dc.subject Māori traditional medicine
dc.subject insulin sensitivity
dc.subject kawakawa
dc.subject plasma insulin
dc.subject postprandial
dc.subject Clinical Research
dc.subject Nutrition
dc.subject Diabetes
dc.subject Prevention
dc.subject Metabolic and endocrine
dc.subject Science & Technology
dc.subject Life Sciences & Biomedicine
dc.subject Nutrition & Dietetics
dc.subject Maori traditional medicine
dc.subject GREEN TEA EXTRACT
dc.subject MACROPIPER-EXCELSUM
dc.subject GLUCOSE-TOLERANCE
dc.subject SENSITIVITY
dc.subject RESISTANCE
dc.subject MYRISTICIN
dc.subject INGESTION
dc.subject PATHWAYS
dc.subject DAMAGE
dc.subject 0908 Food Sciences
dc.subject 1111 Nutrition and Dietetics
dc.title Acute Effects of Kawakawa (<i>Piper excelsum</i>) Intake on Postprandial Glycemic and Insulinaemic Response in a Healthy Population.
dc.type Journal Article
dc.identifier.doi 10.3390/nu14081638
pubs.issue 8
pubs.begin-page 1638
pubs.volume 14
dc.date.updated 2022-05-24T06:16:05Z
dc.rights.holder Copyright: The author en
dc.identifier.pmid 35458200 (pubmed)
pubs.author-url https://www.ncbi.nlm.nih.gov/pubmed/35458200
pubs.publication-status Published
dc.rights.accessrights http://purl.org/eprint/accessRights/OpenAccess en
pubs.subtype research-article
pubs.subtype Randomized Controlled Trial
pubs.subtype Journal Article
pubs.elements-id 896346
pubs.org-id Liggins Institute
pubs.org-id Science
pubs.org-id Biological Sciences
dc.identifier.eissn 2072-6643
dc.identifier.pii nu14081638
pubs.number ARTN 1638
pubs.record-created-at-source-date 2022-05-24
pubs.online-publication-date 2022-04-14


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