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      Geranylgeraniol Induces PPARγ Expression and Enhances the Biological Effects of a PPARγ Agonist in Adipocyte Lineage Cells

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          Abstract

          Background: The global incidence of diabetes mellitus (DM) has risen precipitously, even in middle- and low-income countries. Peroxisome proliferator-activated receptor γ (PPARγ) plays an important role in the control of cellular glucose metabolism. Activation of PPARγ beneficially results in increased insulin sensitivity. However, the expression of PPARγ is reduced by obesity and several nutritional factors. Here we examined the effect of geranylgeraniol (GGOH), a bioactive compound found naturally in fruits, vegetables, and grains, on the expression and activation of PPARγ. Materials and Methods: C3H10T1/2 mouse embryonic fibroblasts and 3T3-L1 pre-adipocytes were used as in vitro models of adipocyte differentiation and function. Quantitative reverse-transcriptase polymerase chain reaction, western blotting, Oil Red O staining, and luciferase assay were performed to respectively assess mRNA expression, protein levels, lipid droplet formation and transcriptional activity. Results: GGOH increased the expression of PPARγ in adipocyte lineage cells. GGOH also enhanced adipogenesis induced by rosiglitazone, a thiazolidinedione class PPARγ agonist. Conclusion: GGOH induces PPARγ expression and enhances the biological effects of a PPARγ agonist in adipocyte lineage cells.

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          Author and article information

          Journal
          In Vivo
          In Vivo
          In Vivo
          International Institute of Anticancer Research
          0258-851X
          1791-7549
          3 November 2018
          Nov-Dec 2018
          : 32
          : 6
          : 1339-1344
          Affiliations
          [1 ]Division of Molecular Signaling and Biochemistry, Kyushu Dental University, Kitakyushu, Japan
          [3 ]Division of Oral Pathology, Department of Health Promotion, Kyushu Dental University, Kitakyushu, Japan
          [4 ]Division of Dental Anesthesiology, Department of Control of Physical Functions, Kyushu Dental University, Kitakyushu, Japan
          [6 ]Department of Oral Functional Management, School of Oral Health Sciences, Kyushu Dental University, Kitakyushu, Japan
          [2 ]Research Unit, Shriners Hospitals for Children-Canada, Department of Human Genetics, McGill University, Montreal, QC, Canada
          [5 ]Division of Oral and Maxillofacial Surgery, Department of Medicine of Sensory and Motor Organs, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan
          Author notes
          Shoichiro Kokabu, D.D.S, Ph.D., Division of Molecular Signaling and Biochemistry, Department of Health Promotion, Kyushu Dental University, 2-6-1 Kitakyushu, Fukuoka 803-8580, Japan. Tel: +81 932851131, Fax: +81 932856000 r14kokabu@ 123456fa.kyu-dent.ac.jp
          Article
          PMC6365726 PMC6365726 6365726
          10.21873/invivo.11384
          6365726
          30348686
          9f5fcc92-2591-4fc0-a036-a571e887e892
          Copyright 2018, International Institute of Anticancer Research
          History
          : 8 July 2018
          : 6 August 2018
          Categories
          Research Article

          adipogenesis,geranylgeranylation,Diabetes,statin,antidiabetic drug

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