An Acute, Placebo-Controlled, Single-Blind, Crossover, Dose-Response, Exploratory Study to Assess the Effects of New Zealand Pine Bark Extract (Enzogenol ® ) on Glycaemic Responses in Healthy Participants
An acute, placebo-controlled, single-blind, crossover, dose-response, exploratory study was designed to investigate the hypoglycaemic effects of New Zealand pine bark extract (Enzogenol ). Twenty-five healthy participants categorised into having a monophasic or complex (biphasic or triphasic) glucos...
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description | An acute, placebo-controlled, single-blind, crossover, dose-response, exploratory study was designed to investigate the hypoglycaemic effects of New Zealand pine bark extract (Enzogenol
). Twenty-five healthy participants categorised into having a monophasic or complex (biphasic or triphasic) glucose curve shape at the control visit consumed a placebo and Enzogenol
(50 and 400 mg) on three separate occasions before an oral glucose tolerance test (OGTT). In the monophasic group, 50 and 400 mg of Enzogenol
significantly reduced the mean glucose incremental area under the curve (iAUC) compared to control 241.3 ± 20.2 vs. 335.4 ± 34.0 mmol/L·min,
= 0.034 and 249.3 ± 25.4 vs. 353.6 ± 31.5 mmol/L·min,
= 0.012, respectively. The 400 mg dose further reduced the percentage increment of postprandial glucose (%PG) 31.4% ± 7.9% vs. 47.5% ± 8.6%,
= 0.010, glucose peak 7.9 ± 0.3 vs. 8.9 ± 0.3 mmol/L,
= 0.025 and 2h-OGTT postprandial glucose (2hPG) 6.1 ± 0.3 vs. 6.7 ± 0.3 mmol/L,
= 0.027. Glucose iAUC was not significantly different in the complex group, except for reductions in %PG 28.7% ± 8.2% vs. 43.4% ± 5.9%,
= 0.012 after 50 mg dose and 27.7% ± 5.4% vs. 47.3% ± 7.2%,
= 0.025 after 400 mg dose. The results suggest that Enzogenol
may have hypoglycaemic effects in healthy participants, especially those exhibiting monophasic shapes. |
doi_str_mv | 10.3390/nu12020497 |
format | Article |
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). Twenty-five healthy participants categorised into having a monophasic or complex (biphasic or triphasic) glucose curve shape at the control visit consumed a placebo and Enzogenol
(50 and 400 mg) on three separate occasions before an oral glucose tolerance test (OGTT). In the monophasic group, 50 and 400 mg of Enzogenol
significantly reduced the mean glucose incremental area under the curve (iAUC) compared to control 241.3 ± 20.2 vs. 335.4 ± 34.0 mmol/L·min,
= 0.034 and 249.3 ± 25.4 vs. 353.6 ± 31.5 mmol/L·min,
= 0.012, respectively. The 400 mg dose further reduced the percentage increment of postprandial glucose (%PG) 31.4% ± 7.9% vs. 47.5% ± 8.6%,
= 0.010, glucose peak 7.9 ± 0.3 vs. 8.9 ± 0.3 mmol/L,
= 0.025 and 2h-OGTT postprandial glucose (2hPG) 6.1 ± 0.3 vs. 6.7 ± 0.3 mmol/L,
= 0.027. Glucose iAUC was not significantly different in the complex group, except for reductions in %PG 28.7% ± 8.2% vs. 43.4% ± 5.9%,
= 0.012 after 50 mg dose and 27.7% ± 5.4% vs. 47.3% ± 7.2%,
= 0.025 after 400 mg dose. The results suggest that Enzogenol
may have hypoglycaemic effects in healthy participants, especially those exhibiting monophasic shapes.</description><identifier>ISSN: 2072-6643</identifier><identifier>EISSN: 2072-6643</identifier><identifier>DOI: 10.3390/nu12020497</identifier><identifier>PMID: 32075228</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adolescent ; Adult ; Bark ; Blood Glucose - metabolism ; Carbohydrates ; Cellulose ; Cross-Over Studies ; Diabetes ; Dose-Response Relationship, Drug ; Female ; Flavonoids - administration & dosage ; Flavonoids - pharmacology ; Glucose ; Glucose tolerance ; Glucose Tolerance Test ; Healthy Volunteers ; Humans ; Hypoglycemia ; Hypoglycemic Agents ; Insulin resistance ; Intervention ; Male ; Metabolism ; New Zealand ; Pinus ; Placebos - administration & dosage ; Placebos - pharmacology ; Plant Bark ; Plant extracts ; Plant Extracts - administration & dosage ; Plant Extracts - pharmacology ; Postprandial Period ; Quercetin - administration & dosage ; Quercetin - analogs & derivatives ; Quercetin - pharmacology ; Single-Blind Method ; Studies ; Young Adult</subject><ispartof>Nutrients, 2020-02, Vol.12 (2), p.497</ispartof><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-d7cddd0bcbc36fd4d026fdffa69228ab3d24ebb8dae1d5ebf9233f9020b43a6c3</citedby><cites>FETCH-LOGICAL-c406t-d7cddd0bcbc36fd4d026fdffa69228ab3d24ebb8dae1d5ebf9233f9020b43a6c3</cites><orcidid>0000-0002-5971-4097 ; 0000-0002-9661-4669 ; 0000-0002-4965-975X ; 0000-0001-6326-7501 ; 0000-0002-0222-6324</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7071219/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7071219/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32075228$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lim, Wen Xin Janice</creatorcontrib><creatorcontrib>Chepulis, Lynne</creatorcontrib><creatorcontrib>von Hurst, Pamela</creatorcontrib><creatorcontrib>Gammon, Cheryl S</creatorcontrib><creatorcontrib>Page, Rachel A</creatorcontrib><title>An Acute, Placebo-Controlled, Single-Blind, Crossover, Dose-Response, Exploratory Study to Assess the Effects of New Zealand Pine Bark Extract (Enzogenol ® ) on Glycaemic Responses in Healthy Participants</title><title>Nutrients</title><addtitle>Nutrients</addtitle><description>An acute, placebo-controlled, single-blind, crossover, dose-response, exploratory study was designed to investigate the hypoglycaemic effects of New Zealand pine bark extract (Enzogenol
). Twenty-five healthy participants categorised into having a monophasic or complex (biphasic or triphasic) glucose curve shape at the control visit consumed a placebo and Enzogenol
(50 and 400 mg) on three separate occasions before an oral glucose tolerance test (OGTT). In the monophasic group, 50 and 400 mg of Enzogenol
significantly reduced the mean glucose incremental area under the curve (iAUC) compared to control 241.3 ± 20.2 vs. 335.4 ± 34.0 mmol/L·min,
= 0.034 and 249.3 ± 25.4 vs. 353.6 ± 31.5 mmol/L·min,
= 0.012, respectively. The 400 mg dose further reduced the percentage increment of postprandial glucose (%PG) 31.4% ± 7.9% vs. 47.5% ± 8.6%,
= 0.010, glucose peak 7.9 ± 0.3 vs. 8.9 ± 0.3 mmol/L,
= 0.025 and 2h-OGTT postprandial glucose (2hPG) 6.1 ± 0.3 vs. 6.7 ± 0.3 mmol/L,
= 0.027. Glucose iAUC was not significantly different in the complex group, except for reductions in %PG 28.7% ± 8.2% vs. 43.4% ± 5.9%,
= 0.012 after 50 mg dose and 27.7% ± 5.4% vs. 47.3% ± 7.2%,
= 0.025 after 400 mg dose. The results suggest that Enzogenol
may have hypoglycaemic effects in healthy participants, especially those exhibiting monophasic shapes.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Bark</subject><subject>Blood Glucose - metabolism</subject><subject>Carbohydrates</subject><subject>Cellulose</subject><subject>Cross-Over Studies</subject><subject>Diabetes</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Flavonoids - administration & dosage</subject><subject>Flavonoids - pharmacology</subject><subject>Glucose</subject><subject>Glucose tolerance</subject><subject>Glucose Tolerance Test</subject><subject>Healthy Volunteers</subject><subject>Humans</subject><subject>Hypoglycemia</subject><subject>Hypoglycemic Agents</subject><subject>Insulin resistance</subject><subject>Intervention</subject><subject>Male</subject><subject>Metabolism</subject><subject>New Zealand</subject><subject>Pinus</subject><subject>Placebos - administration & dosage</subject><subject>Placebos - pharmacology</subject><subject>Plant Bark</subject><subject>Plant extracts</subject><subject>Plant Extracts - administration & dosage</subject><subject>Plant Extracts - pharmacology</subject><subject>Postprandial Period</subject><subject>Quercetin - administration & dosage</subject><subject>Quercetin - analogs & derivatives</subject><subject>Quercetin - pharmacology</subject><subject>Single-Blind Method</subject><subject>Studies</subject><subject>Young Adult</subject><issn>2072-6643</issn><issn>2072-6643</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpVkc9u1DAQxiNERavSCw-ARuIC1QYcO5s0F6TtsrRIFawoXLhEjj3edfHaqe0UwkPxENz7TnjVPxRfxtZ8_s3o-7LsWUFeM9aQN3YoKKGkbOpH2R4lNc2rqmSPH9x3s4MQLsj21KSu2JNsl6XmlNKjvex6ZmEmhogTWBousHP53NnonTEoJ3Cu7cpgfmy0Ta-5dyG4K_QTeOcC5p8x9M6G9HfxszfO8-j8COdxkCNEB7MQMASIa4SFUihiAKfgI_6Ab8gNtxKW2iIcc_89AaLnIsLLhf3lVmidgT-_4RU4CydmFBw3WsDdvADawmlixPUIS-6jFrrnNoan2Y7iJuDBbd3Pvr5ffJmf5mefTj7MZ2e5KEkVc1kLKSXpRCdYpWQpCU1FKV41yRTeMUlL7LojybGQU-xUQxlTTbK5KxmvBNvP3t5w-6HboBSYHOOm7b3ecD-2juv2_47V63blrtoUQEGLJgFe3AK8uxwwxPbCDd6mnVvKmimh04puVYc3KrE13qO6n1CQdpt--y_9JH7-cKd76V3W7C8swK9v</recordid><startdate>20200215</startdate><enddate>20200215</enddate><creator>Lim, Wen Xin Janice</creator><creator>Chepulis, Lynne</creator><creator>von Hurst, Pamela</creator><creator>Gammon, Cheryl S</creator><creator>Page, Rachel A</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5971-4097</orcidid><orcidid>https://orcid.org/0000-0002-9661-4669</orcidid><orcidid>https://orcid.org/0000-0002-4965-975X</orcidid><orcidid>https://orcid.org/0000-0001-6326-7501</orcidid><orcidid>https://orcid.org/0000-0002-0222-6324</orcidid></search><sort><creationdate>20200215</creationdate><title>An Acute, Placebo-Controlled, Single-Blind, Crossover, Dose-Response, Exploratory Study to Assess the Effects of New Zealand Pine Bark Extract (Enzogenol ® ) on Glycaemic Responses in Healthy Participants</title><author>Lim, Wen Xin Janice ; 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). Twenty-five healthy participants categorised into having a monophasic or complex (biphasic or triphasic) glucose curve shape at the control visit consumed a placebo and Enzogenol
(50 and 400 mg) on three separate occasions before an oral glucose tolerance test (OGTT). In the monophasic group, 50 and 400 mg of Enzogenol
significantly reduced the mean glucose incremental area under the curve (iAUC) compared to control 241.3 ± 20.2 vs. 335.4 ± 34.0 mmol/L·min,
= 0.034 and 249.3 ± 25.4 vs. 353.6 ± 31.5 mmol/L·min,
= 0.012, respectively. The 400 mg dose further reduced the percentage increment of postprandial glucose (%PG) 31.4% ± 7.9% vs. 47.5% ± 8.6%,
= 0.010, glucose peak 7.9 ± 0.3 vs. 8.9 ± 0.3 mmol/L,
= 0.025 and 2h-OGTT postprandial glucose (2hPG) 6.1 ± 0.3 vs. 6.7 ± 0.3 mmol/L,
= 0.027. Glucose iAUC was not significantly different in the complex group, except for reductions in %PG 28.7% ± 8.2% vs. 43.4% ± 5.9%,
= 0.012 after 50 mg dose and 27.7% ± 5.4% vs. 47.3% ± 7.2%,
= 0.025 after 400 mg dose. The results suggest that Enzogenol
may have hypoglycaemic effects in healthy participants, especially those exhibiting monophasic shapes.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>32075228</pmid><doi>10.3390/nu12020497</doi><orcidid>https://orcid.org/0000-0002-5971-4097</orcidid><orcidid>https://orcid.org/0000-0002-9661-4669</orcidid><orcidid>https://orcid.org/0000-0002-4965-975X</orcidid><orcidid>https://orcid.org/0000-0001-6326-7501</orcidid><orcidid>https://orcid.org/0000-0002-0222-6324</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Bark Blood Glucose - metabolism Carbohydrates Cellulose Cross-Over Studies Diabetes Dose-Response Relationship, Drug Female Flavonoids - administration & dosage Flavonoids - pharmacology Glucose Glucose tolerance Glucose Tolerance Test Healthy Volunteers Humans Hypoglycemia Hypoglycemic Agents Insulin resistance Intervention Male Metabolism New Zealand Pinus Placebos - administration & dosage Placebos - pharmacology Plant Bark Plant extracts Plant Extracts - administration & dosage Plant Extracts - pharmacology Postprandial Period Quercetin - administration & dosage Quercetin - analogs & derivatives Quercetin - pharmacology Single-Blind Method Studies Young Adult |
title | An Acute, Placebo-Controlled, Single-Blind, Crossover, Dose-Response, Exploratory Study to Assess the Effects of New Zealand Pine Bark Extract (Enzogenol ® ) on Glycaemic Responses in Healthy Participants |
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