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      GLUT2 proteins and PPARγ transcripts levels are increased in liver of ovariectomized rats: reversal effects of resistance training

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          Abstract

          [Purpose]

          This study investigated the effects of ovariectomy (Ovx) and 12 weeks of resistance training (RT) on gene expression of GLUT2, the main glucose transporter in the liver, and on PPARγ, a transcription factor known to target GLUT2 expression.

          [Methods]

          Forty Holtzman rats were divided into 5 groups: Sham-sedentary (Sed), Sham- RT, Ovx-Sed, Ovx-RT, and Ovx-Sed with hormone replacement (E2). The RT protocol consisted of sessions held every 72 h for 12 weeks, during which the animals performed 4 to 9 vertical climbs (1.1 m) at 2 min intervals with progressively heavier weights (30 g after the fourth climb) tied to the tail. The E2 silastic capsule was inserted into the rats’ backs 48 hours before the first RT session.

          [Results]

          In addition to liver fat, GLUT2 protein levels and PPARγ transcripts were increased ( P < 0.05) in Ovx compared to Sham-Sed animals, suggesting increased hepatic glucose uptake under estrogen deficient conditions. RT and E2 in Ovx rats decreased liver fat accumulation as well as GLUT2 and PPARγ gene expression to the level of Sham- Sed animals.

          [Conclusion]

          The results of this study suggest that liver GLUT2 as well as PPARγ expression in Ovx rats are accompanied by increased fat accumulation and glucose uptake, thus providing a substrate for increased de novo lipogenesis. RT appears to be an appropriate exercise model to circumvent these effects.

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          Most cited references34

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          The ovariectomized rat model of postmenopausal bone loss.

          Dike Kalu (1991)
          An animal model of postmenopausal bone loss can be defined as a living animal in which spontaneous or induced bone loss due to ovarian hormone deficiency can be studied, and in which the characteristics of the bone loss and its sequalae resemble those found in postmenopausal women in one or more respects. Although in comparison to humans, the skeletal mass of rats remains stable for a protracted period during their lifespan, rats can be ovariectomized to make them sex-hormone deficient, and to stimulate the accelerated loss of bone that occurs in women following menopause. Ovariectomy induced bone loss in the rat and postmenopausal bone loss share many similar characteristics. These include: increased rate of bone turnover with resorption exceeding formation; and initial rapid phase of bone loss followed by a much slower phase; greater loss of cancellous than cortical bone; decreased intestinal absorption of calcium; some protection against bone loss by obesity; and similar skeletal response to therapy with estrogen, tamoxifen, bisphosphonates, parathyroid hormone, calcitonin and exercise. These wide-ranging similarities are strong evidence that the ovariectomized rat bone loss model is suitable for studying problems that are relevant to postmenopausal bone loss.
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            Determination of glycogen in small tissue samples.

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              Physiological hypertrophy of the FHL muscle following 8 weeks of progressive resistance exercise in the rat.

              In humans, progressive resistance exercise is recognized for its ability to induce skeletal muscle hypertrophy. In an attempt to develop an animal model which mimics human progressive resistance exercise, Sprague-Dawley rats were trained to climb a 1.1-m vertical (80 degree incline) ladder with weights secured to their tail. The rats were trained once every 3 days for 8 weeks. Each training session consisted of 4-9 (6.02 +/- 0.23) climbs requiring 8-12 dynamic movements per climb. Based on performance, the weight carried during each session was progressively increased. Over the course of 8 weeks, the maximal amount of weight the rats could carry increased 287%, p
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                Author and article information

                Journal
                J Exerc Nutrition Biochem
                J Exerc Nutrition Biochem
                JENB
                Journal of Exercise Nutrition & Biochemistry
                한국운동영양학회
                2233-6834
                2233-6842
                June 2016
                30 June 2016
                : 20
                : 2
                : 51-57
                Affiliations
                [1 ]Department of Physiological Sciences, Federal University of São Carlos, São Carlos, SP Brazil,
                [2 ]Department of Education and Health, Federal University of Sergipe, Lagarto, SE Brazil,
                [3 ]Department of Kinesiology, Université de Montréal, Montréal, QC Canada,
                Author notes
                *Luciane M. Tomaz Department of Physiological Sciences, Federal University of São Carlos, São Carlos, SP, Brazil Email : lumagri@ 123456gmail.com
                Article
                JENB_2016_v20n2_51
                10.20463/jenb.2016.06.20.2.7
                4977907
                27508154
                62ea4550-c42d-42e0-8879-0c7437e24c43
                ©2016 The Korean Society for Exercise Nutrition

                ©2016 Luciane M. Tomaz et al.; Licensee Journal of Exercise Nutrition and Biochemistry. This is an open accessarticle distributed under the terms of the creative commons attribution license ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the orginal work is properly cited.

                History
                : 22 December 2015
                : 30 March 2016
                : 14 April 2016
                Funding
                Funded by: São Paulo Research Foundation
                Award ID: 2011/21607-5
                Funded by: Natural Sciences and Engineering Research Council of Canada
                Award ID: NSERC: 7594
                Categories
                Original Article

                liver fat,pepck,hepatic glycogen,exercise and glucose
                liver fat, pepck, hepatic glycogen, exercise and glucose

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