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Effects of KDT501 on Metabolic Parameters in Insulin-Resistant Prediabetic Humans
CONTEXT: KDT501 is an isohumulone drug that has demonstrated beneficial effects on metabolic parameters in mice. OBJECTIVE: This study was intended to examine potential improvements in metabolism in humans. DESIGN AND SETTING: Changes in carbohydrate and lipid metabolism, along with inflammatory mar...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Endocrine Society
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686568/ https://www.ncbi.nlm.nih.gov/pubmed/29264518 http://dx.doi.org/10.1210/js.2017-00202 |
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author | Kern, Philip A. Finlin, Brian S. Ross, Dorothy Boyechko, Tania Zhu, Beibei Grayson, Neile Sims, Robert Bland, Jeffrey S. |
author_facet | Kern, Philip A. Finlin, Brian S. Ross, Dorothy Boyechko, Tania Zhu, Beibei Grayson, Neile Sims, Robert Bland, Jeffrey S. |
author_sort | Kern, Philip A. |
collection | PubMed |
description | CONTEXT: KDT501 is an isohumulone drug that has demonstrated beneficial effects on metabolic parameters in mice. OBJECTIVE: This study was intended to examine potential improvements in metabolism in humans. DESIGN AND SETTING: Changes in carbohydrate and lipid metabolism, along with inflammatory markers, were evaluated in prediabetic humans in a clinical research center. PARTICIPANTS: Nine obese patients participated. All had prediabetes or normal glucose tolerance plus three features of metabolic syndrome. INTERVENTION: All participants were treated with escalating doses of KDT501 to a maximum dose of 1000 mg every 12 hours for a total of 28 days. OUTCOME MEASURES: Changes in carbohydrate metabolism were measured with oral glucose tolerance, homeostatic model of insulin resistance, and euglycemic clamp; changes in plasma lipids and response to a lipid tolerance test; and changes in plasma inflammatory markers. RESULTS: The drug was well tolerated. After KDT501 treatment, plasma triglycerides were reduced at 4 hours during a lipid tolerance test. Furthermore, plasma adiponectin and high-molecular-weight adiponectin increased significantly, and plasma tumor necrosis factor-α decreased significantly. There were no significant changes in oral glucose tolerance test results or insulin sensitivity measures. CONCLUSIONS: Despite the small sample size and the short duration of therapy, KDT501 administration reduced measures of systemic inflammation and improved postmeal plasma triglyceride levels, which may be beneficial in participants with insulin resistance or metabolic syndrome. |
format | Online Article Text |
id | pubmed-5686568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Endocrine Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56865682017-12-20 Effects of KDT501 on Metabolic Parameters in Insulin-Resistant Prediabetic Humans Kern, Philip A. Finlin, Brian S. Ross, Dorothy Boyechko, Tania Zhu, Beibei Grayson, Neile Sims, Robert Bland, Jeffrey S. J Endocr Soc Clinical Research Articles CONTEXT: KDT501 is an isohumulone drug that has demonstrated beneficial effects on metabolic parameters in mice. OBJECTIVE: This study was intended to examine potential improvements in metabolism in humans. DESIGN AND SETTING: Changes in carbohydrate and lipid metabolism, along with inflammatory markers, were evaluated in prediabetic humans in a clinical research center. PARTICIPANTS: Nine obese patients participated. All had prediabetes or normal glucose tolerance plus three features of metabolic syndrome. INTERVENTION: All participants were treated with escalating doses of KDT501 to a maximum dose of 1000 mg every 12 hours for a total of 28 days. OUTCOME MEASURES: Changes in carbohydrate metabolism were measured with oral glucose tolerance, homeostatic model of insulin resistance, and euglycemic clamp; changes in plasma lipids and response to a lipid tolerance test; and changes in plasma inflammatory markers. RESULTS: The drug was well tolerated. After KDT501 treatment, plasma triglycerides were reduced at 4 hours during a lipid tolerance test. Furthermore, plasma adiponectin and high-molecular-weight adiponectin increased significantly, and plasma tumor necrosis factor-α decreased significantly. There were no significant changes in oral glucose tolerance test results or insulin sensitivity measures. CONCLUSIONS: Despite the small sample size and the short duration of therapy, KDT501 administration reduced measures of systemic inflammation and improved postmeal plasma triglyceride levels, which may be beneficial in participants with insulin resistance or metabolic syndrome. Endocrine Society 2017-04-21 /pmc/articles/PMC5686568/ /pubmed/29264518 http://dx.doi.org/10.1210/js.2017-00202 Text en Copyright © 2017 Endocrine Society https://creativecommons.org/licenses/by-nc-nd/4.0/ This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Clinical Research Articles Kern, Philip A. Finlin, Brian S. Ross, Dorothy Boyechko, Tania Zhu, Beibei Grayson, Neile Sims, Robert Bland, Jeffrey S. Effects of KDT501 on Metabolic Parameters in Insulin-Resistant Prediabetic Humans |
title | Effects of KDT501 on Metabolic Parameters in Insulin-Resistant Prediabetic Humans |
title_full | Effects of KDT501 on Metabolic Parameters in Insulin-Resistant Prediabetic Humans |
title_fullStr | Effects of KDT501 on Metabolic Parameters in Insulin-Resistant Prediabetic Humans |
title_full_unstemmed | Effects of KDT501 on Metabolic Parameters in Insulin-Resistant Prediabetic Humans |
title_short | Effects of KDT501 on Metabolic Parameters in Insulin-Resistant Prediabetic Humans |
title_sort | effects of kdt501 on metabolic parameters in insulin-resistant prediabetic humans |
topic | Clinical Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686568/ https://www.ncbi.nlm.nih.gov/pubmed/29264518 http://dx.doi.org/10.1210/js.2017-00202 |
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