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      Improvements in HOMA indices and pancreatic endocrinal tissues in type 2-diabetic rats by DPP-4 inhibition and antioxidant potential of an ethanol fruit extract of Withania  coagulans

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          Abstract

          Context

          Withania coagulans (Stocks) Dunal fruits are used in the therapeutics of several ailments due to possessing of potent phytoconstituents which is also used traditionally for curing the diabetes.

          Objective

          The present study was assessing the amelioration potential of the phytochemicals of an ethanol fruit extract of W.  coagulans (Stocks) Dunal in the HOMA (Homeostatic model assessment) indices and pancreatic endocrinal tissues by inhibition of DPP-4 and antioxidants activities.

          Material and methods

          The identification of phytoconstituents of the test extract was performed by LCMS. Further, assessments of in-vitro, in-vivo and in-silico were achieved by following standard methods. In-vivo studies were conducted on type-2 diabetic rats.

          Results

          The chosen extract inhibited DPP-4 activity by 63.2% in an in vitro assay as well as significantly inhibit serum DPP-4 levels. Accordingly, the administration of the ethanol fruit extract resulted in a significant ( P ≤ 0.001) alterations in the lipid profile, antioxidant levels, and HOMA indices. Moreover, pancreatic endocrinal tissues (islet of Langerhans) appeared to have the restoration of normal histoarchitecture as evidenced by increased cellular mass. Molecular docking (Protein-ligands) of identified phytoconstituents with DPP-4 (target enzyme) shown incredibly low binding energy (Kcal/mol) as required for ideal interactions. ADMET analysis of the pharmacokinetics of the identified phytoconstituents indicated an ideal profile as per Lipinski laws.

          Conclusion

          It can be concluded that the phytoconstituents of an ethanol fruit extract of W.  coagulans have the potential to inhibit DPP-4 which result in improved glucose homeostasis and restoration of pancreatic endocrinal tissues in type-2 diabetic rats.

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          Most cited references65

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          The ferric reducing ability of plasma (FRAP) as a measure of "antioxidant power": the FRAP assay.

          A simple, automated test measuring the ferric reducing ability of plasma, the FRAP assay, is presented as a novel method for assessing "antioxidant power." Ferric to ferrous ion reduction at low pH causes a colored ferrous-tripyridyltriazine complex to form. FRAP values are obtained by comparing the absorbance change at 593 nm in test reaction mixtures with those containing ferrous ions in known concentration. Absorbance changes are linear over a wide concentration range with antioxidant mixtures, including plasma, and with solutions containing one antioxidant in purified form. There is no apparent interaction between antioxidants. Measured stoichiometric factors of Trolox, alpha-tocopherol, ascorbic acid, and uric acid are all 2.0; that of bilirubin is 4.0. Activity of albumin is very low. Within- and between-run CVs are <1.0 and <3.0%, respectively, at 100-1000 micromol/liter. FRAP values of fresh plasma of healthy Chinese adults: 612-1634 micromol/liter (mean, 1017; SD, 206; n = 141). The FRAP assay is inexpensive, reagents are simple to prepare, results are highly reproducible, and the procedure is straightforward and speedy. The FRAP assay offers a putative index of antioxidant, or reducing, potential of biological fluids within the technological reach of every laboratory and researcher interested in oxidative stress and its effects.
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            Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man.

            The steady-state basal plasma glucose and insulin concentrations are determined by their interaction in a feedback loop. A computer-solved model has been used to predict the homeostatic concentrations which arise from varying degrees beta-cell deficiency and insulin resistance. Comparison of a patient's fasting values with the model's predictions allows a quantitative assessment of the contributions of insulin resistance and deficient beta-cell function to the fasting hyperglycaemia (homeostasis model assessment, HOMA). The accuracy and precision of the estimate have been determined by comparison with independent measures of insulin resistance and beta-cell function using hyperglycaemic and euglycaemic clamps and an intravenous glucose tolerance test. The estimate of insulin resistance obtained by homeostasis model assessment correlated with estimates obtained by use of the euglycaemic clamp (Rs = 0.88, p less than 0.0001), the fasting insulin concentration (Rs = 0.81, p less than 0.0001), and the hyperglycaemic clamp, (Rs = 0.69, p less than 0.01). There was no correlation with any aspect of insulin-receptor binding. The estimate of deficient beta-cell function obtained by homeostasis model assessment correlated with that derived using the hyperglycaemic clamp (Rs = 0.61, p less than 0.01) and with the estimate from the intravenous glucose tolerance test (Rs = 0.64, p less than 0.05). The low precision of the estimates from the model (coefficients of variation: 31% for insulin resistance and 32% for beta-cell deficit) limits its use, but the correlation of the model's estimates with patient data accords with the hypothesis that basal glucose and insulin interactions are largely determined by a simple feed back loop.
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              Microsomal lipid peroxidation.

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                Author and article information

                Contributors
                hr.zo@jnvu.edu.in
                aalarjani@ksu.edu.sa
                bpsingh@niftem.ac.in
                Journal
                Nutr Metab (Lond)
                Nutr Metab (Lond)
                Nutrition & Metabolism
                BioMed Central (London )
                1743-7075
                21 April 2021
                21 April 2021
                2021
                : 18
                : 43
                Affiliations
                [1 ]GRID grid.444505.4, ISNI 0000 0000 9765 0659, Department of Zoology, , Jai Narain Vyas University, ; Jodhpur, Rajasthan 342001 India
                [2 ]GRID grid.411685.f, ISNI 0000 0004 0498 1133, University School of Biotechnology, , Guru Gobind Singh Indraprastha University, ; Dwarka, Sector 16C, New Delhi, India
                [3 ]GRID grid.411813.e, ISNI 0000 0000 9217 3865, Department of Botany, , Pachhunga University College, ; Aizawl, Mizoram 796001 India
                [4 ]GRID grid.56302.32, ISNI 0000 0004 1773 5396, Plant Production Department, College of Food and Agricultural Sciences, , King Saud University, ; P.O. Box. 2460, Riyadh, 11451 Saudi Arabia
                [5 ]GRID grid.56302.32, ISNI 0000 0004 1773 5396, Botany and Microbiology Department, College of Science, , King Saud University, ; P.O. Box. 2460, Riyadh, 11451 Saudi Arabia
                [6 ]GRID grid.418376.f, ISNI 0000 0004 1800 7673, Mycology and Plant Disease Survey Department, , Plant Pathology Research Institute, ARC, ; Giza, 12511 Egypt
                [7 ]GRID grid.464625.7, ISNI 0000 0004 1775 8475, Department of Agriculture and Environmental Sciences (AES), , National Institute of Food Technology Entrepreneurship and Management (NIFTEM), ; Sonepat, 131028 Haryana India
                Author information
                http://orcid.org/0000-0001-6743-1321
                https://orcid.org/0000-0002-9911-4125
                Article
                547
                10.1186/s12986-021-00547-2
                8059290
                b8a87d58-9af3-480a-b894-3a8eea2a8354
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 31 August 2020
                : 20 January 2021
                Categories
                Research
                Custom metadata
                © The Author(s) 2021

                Nutrition & Dietetics
                homa,β-cells,pancreatic histology,antioxidants,dpp-4,phytochemicals
                Nutrition & Dietetics
                homa, β-cells, pancreatic histology, antioxidants, dpp-4, phytochemicals

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