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      Vitisin B, a resveratrol tetramer from Vitis thunbergii var. taiwaniana, ameliorates impaired glucose regulations in nicotinamide/streptozotocin-induced type 2 diabetic mice

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          Abstract

          Background and aim

          In Taiwan, Vitis thunbergii var. taiwaniana (VTT) is used in traditional medicine and as a local tea. VTT rich in resveratrol and resveratrol oligomers have been reported to exhibit anti-obesity and anti-hypertensive activities in animal models; however, no studies have investigated type 2 diabetes mellitus (T2DM) treatments. This study aimed to investigate the anti-T2DM effects of resveratrol tetramers isolated from the VTT in nicotinamide/streptozotocin (STZ)-induced Institute of Cancer Research (ICR) mice.

          Experimental procedure

          The oral glucose tolerance test (OGTT) was used to imitate postprandial blood glucose (BG) regulations in mice by pre-treatment with VTT extracts, resveratrol tetramers of vitisin A, vitisin B, and hopeaphenol 30 min before glucose loads. Vitisin B (50 mg/kg) was administered to treat T2DM-ICR mice once daily for 28 days to investigate its hypoglycemic activity.

          Results and conclusion

          Mice pre-treated with VTT-S-95EE, or vitisin B (100 mg/kg) 30-min before glucose loading showed significant reductions ( P < 0.001) in the area under the curve at 120-min (BG-AUC 0-120) than those without pre-treatment with VTT-S-95 E E or vitisin B. Vitisin B-treated T2DM mice showed hypoglycemic activities via a reduction in plasma dipeptidyl peptidase (DPP)-IV activities to maintain insulin actions and differed significantly than those of untreated T2DM mice ( P < 0.05), and also reduced BG-AUC 0-120 and insulin-AUC 0-120 in the OGTT.

          These in vivo results showed that VTT containing vitisin B would be beneficial for developing nutraceuticals and/or functional foods for glycemic control in patients with T2DM, which should be investigated further.

          Graphical abstract

          Highlights

          • OGTT was used in the healthy ICR mice to imitate postprandial BG regulations by VTT extracts.

          • The nicotinamide/STZ-induced T2DM mice were used to evaluate the impaired glucose regulations.

          • The 28-day treatments of vitisin B improved fasting BG and postprandial BG in OGTT of T2DM mice.

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          Most cited references38

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          Dose translation from animal to human studies revisited.

          As new drugs are developed, it is essential to appropriately translate the drug dosage from one animal species to another. A misunderstanding appears to exist regarding the appropriate method for allometric dose translations, especially when starting new animal or clinical studies. The need for education regarding appropriate translation is evident from the media response regarding some recent studies where authors have shown that resveratrol, a compound found in grapes and red wine, improves the health and life span of mice. Immediately after the online publication of these papers, the scientific community and popular press voiced concerns regarding the relevance of the dose of resveratrol used by the authors. The animal dose should not be extrapolated to a human equivalent dose (HED) by a simple conversion based on body weight, as was reported. For the more appropriate conversion of drug doses from animal studies to human studies, we suggest using the body surface area (BSA) normalization method. BSA correlates well across several mammalian species with several parameters of biology, including oxygen utilization, caloric expenditure, basal metabolism, blood volume, circulating plasma proteins, and renal function. We advocate the use of BSA as a factor when converting a dose for translation from animals to humans, especially for phase I and phase II clinical trials.
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            The biology of incretin hormones.

            Gut peptides, exemplified by glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) are secreted in a nutrient-dependent manner and stimulate glucose-dependent insulin secretion. Both GIP and GLP-1 also promote beta cell proliferation and inhibit apoptosis, leading to expansion of beta cell mass. GLP-1, but not GIP, controls glycemia via additional actions on glucose sensors, inhibition of gastric emptying, food intake and glucagon secretion. Furthermore, GLP-1, unlike GIP, potently stimulates insulin secretion and reduces blood glucose in human subjects with type 2 diabetes. This article summarizes current concepts of incretin action and highlights the potential therapeutic utility of GLP-1 receptor agonists and dipeptidyl peptidase-4 (DPP-4) inhibitors for the treatment of type 2 diabetes.
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              Obesity and insulin resistance.

              B Kahn, J Flier (2000)
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                Author and article information

                Contributors
                Journal
                J Tradit Complement Med
                J Tradit Complement Med
                Journal of Traditional and Complementary Medicine
                Elsevier
                2225-4110
                30 May 2023
                September 2023
                30 May 2023
                : 13
                : 5
                : 479-488
                Affiliations
                [a ]Department of General Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei, 110, Taiwan
                [b ]Division of Gastroenterology, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, 111, Taiwan
                [c ]Graduate Institute of Pharmacognosy, Taipei Medical University, Taipei, 110, Taiwan
                [d ]Ph.D. Program in Clinical Drug Development of Herbal Medicine, College of Pharmacy, Taipei Medical University, Taipei, Taiwan
                [e ]School of Pharmacy, College of Pharmacy, Taipei Medical University, Taipei, 110, Taiwan
                [f ]Department of Biological Science and Technology, National Pingtung University of Science and Technology, Pingtung, 912, Taiwan
                Author notes
                []Corresponding author. wchou@ 123456tmu.edu.tw
                [∗∗ ]Corresponding author. changchii@ 123456mail.npust.edu.tw
                [1]

                These authors contributed equally.

                Article
                S2225-4110(23)00058-5
                10.1016/j.jtcme.2023.05.003
                10491982
                37693102
                0350aaef-74ef-4eac-88aa-a57d59ac80a0
                © 2023 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 1 November 2022
                : 3 May 2023
                : 30 May 2023
                Categories
                Article

                nutraceuticals,resveratrol tetramers of vitisin a,vitisin b,and hopeaphenol,type 2 diabetes mellitus (t2dm),vitis thunbergii var. taiwaniana (vtt)

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