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      Effects of Baccharin Isolated from Brazilian Green Propolis on Adipocyte Differentiation and Hyperglycemia in ob/ob Diabetic Mice

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          Abstract

          Propolis is a honeybee product with various biological activities, including antidiabetic effects. We previously reported that artepillin C, a prenylated cinnamic acid derivative isolated from Brazilian green propolis, acts as a peroxisome proliferator-activated receptor γ (PPARγ) ligand and promotes adipocyte differentiation. In this study, we examined the effect of baccharin, another major component of Brazilian green propolis, on adipocyte differentiation. The treatment of mouse 3T3-L1 preadipocytes with baccharin resulted in increased lipid accumulation, cellular triglyceride levels, glycerol-3-phosphate dehydrogenase activity, and glucose uptake. The mRNA expression levels of PPARγ and its target genes were also increased by baccharin treatment. Furthermore, baccharin enhanced PPARγ-dependent luciferase activity, suggesting that baccharin promotes adipocyte differentiation via PPARγ activation. In diabetic ob/ob mice, intraperitoneal administration of 50 mg/kg baccharin significantly improved blood glucose levels. Our results suggest that baccharin has a hypoglycemic effect on glucose metabolic disorders, such as type 2 diabetes mellitus.

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          Most cited references31

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          Role of Insulin Resistance in Human Disease

          G M Reaven (1988)
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            Obesity and insulin resistance.

            B Kahn, J Flier (2000)
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              Propolis: is there a potential for the development of new drugs?

              Propolis has plenty of biological and pharmacological properties and its mechanisms of action have been widely investigated in the last years, using different experimental models in vitro and in vivo. Researchers have been interested in the investigation of isolated compounds responsible for propolis action; however, there is lack of clinical research on the effects of propolis. Since propolis-containing products have been marketed and humans have used propolis for different purposes, the goal of this review is to discuss the potential of propolis for the development of new drugs, by comparing data from the literature that suggest candidate areas for the establishment of drugs against tumors, infections, allergy, diabetes, ulcers and with immunomodulatory action. The efficacy of propolis in different protocols in vitro and in vivo suggests its therapeutic properties, but before establishing a strategy using this bee product, it is necessary to study: (a) the chemical nature of the propolis sample. (b) Propolis efficacy should be compared to well-established parameters, e.g. positive or negative controls in the experiments. Moreover, possible interactions between propolis and other medicines should be investigated in humans as well. (c) Clinical investigation is needed to evaluate propolis potential in patients or healthy individuals, to understand under which conditions propolis may promote health. Data point out the importance of this research field not only for the readers and researchers in the scientific community waiting for further clarification on the potential of propolis but also for the pharmaceutical industry that looks for new drugs. Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                28 June 2021
                July 2021
                : 22
                : 13
                : 6954
                Affiliations
                [1 ]Research Institute for Biological Functions, Chubu University, Kasugai, Aichi 487-8501, Japan; akio-wa@ 123456jumonji-u.ac.jp (A.W.); jwoo@ 123456isc.chubu.ac.jp (J.-T.W.)
                [2 ]Department of Food Science, Faculty of Human Life, Jumonji University, Niiza, Saitama 352-8510, Japan
                [3 ]School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Avenida do Café, s/n, Ribeirão Preto 14040-903, SP, Brazil; marilia_almeida11@ 123456yahoo.com.br (M.O.d.A.); carolinearruda1501@ 123456gmail.com (C.A.); jkbastos@ 123456fcfrp.usp.br (J.K.B.)
                [4 ]Department of Biological Chemistry, Chubu University, Kasugai, Aichi 487-8501, Japan; deguc3@ 123456gmail.com (Y.D.); hachiya88neko@ 123456gmail.com (R.K.)
                [5 ]Laboratory of Research, Development and Innovation, Apis Flora Indl. Coml. Ltda., Ribeirão Preto 14020-670, SP, Brazil; andresa.berretta@ 123456apisflora.com.br
                Author notes
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-4858-9884
                https://orcid.org/0000-0001-8060-0839
                Article
                ijms-22-06954
                10.3390/ijms22136954
                8267681
                34203569
                51050e60-9b70-41b9-8f06-c20953c80997
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 28 May 2021
                : 22 June 2021
                Categories
                Article

                Molecular biology
                diabetes,propolis,baccharin,pparγ
                Molecular biology
                diabetes, propolis, baccharin, pparγ

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