18
views
0
recommends
+1 Recommend
2 collections
    0
    shares

          The flagship journal of the Society for Endocrinology. Learn more

      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Leptin pharmacokinetics in male mice

      research-article

      Read this article at

      ScienceOpenPublisherPMC
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Pharmacokinetics of leptin in mammals has not been studied in detail and only one study has examined more than one time point in non-mutant mice and this was in a female mice. This is the first study to describe leptin distribution over a detailed time course in normal male mice. A physiologic dose (12 ng) of radiolabelled leptin was injected into adult male mice via the lateral tail vein and tissues were dissected out and measured for radioactivity over a time course of up to two hours. Major targets were the digestive tract, kidneys, skin and lungs. The brain was not a major target, and 0.15% of the total dose was recovered from the brain 5 min after administration. Major differences appear to exist in the distribution of leptin between the male and female mice, indicating a high degree of sexual dimorphism. Although the half-lives were similar between male and female mice, almost twice the proportion of leptin was recovered from the digestive tract of male mice in comparison to that reported previously for females. This would seem to indicate a major difference in leptin distribution and possibly function between males and females.

          Related collections

          Most cited references51

          • Record: found
          • Abstract: found
          • Article: not found

          Abnormal splicing of the leptin receptor in diabetic mice.

          Mutations in the mouse diabetes (db) gene result in obesity and diabetes in a syndrome resembling morbid human obesity. Previous data suggest that the db gene encodes the receptor for the obese (ob) gene product, leptin. A leptin receptor was recently cloned from choroid plexus and shown to map to the same 6-cM interval on mouse chromosome 4 as db. This receptor maps to the same 300-kilobase interval as db, and has at least six alternatively spliced forms. One of these splice variants is expressed at a high level in the hypothalamus, and is abnormally spliced in C57BL/Ks db/db mice. The mutant protein is missing the cytoplasmic region, and is likely to be defective in signal transduction. This suggests that the weight-reducing effects of leptin may be mediated by signal transduction through a leptin receptor in the hypothalamus.
            • Record: found
            • Abstract: not found
            • Article: not found

            Obese, a new mutation in the house mouse.

              • Record: found
              • Abstract: found
              • Article: not found

              Diabetes, a new mutation in the mouse.

              Diabetes (db), which occurred in an inbred strain of mouse, is inherited as a unit autosomal recessive and is characterized by a metabolic disturbance resembling diabetes mellitus in man. Abnormal deposition of fat at 3 to 4 weeks of age is followed shortly by hyperglycemia, polyuria, and glycosuria. Accompanying morphological changes in the islets of Langerhans suggest neogenesis to compensate for insulin depletion.

                Author and article information

                Journal
                Endocr Connect
                Endocr Connect
                EC
                Endocrine Connections
                Bioscientifica Ltd (Bristol )
                2049-3614
                January 2017
                20 December 2016
                : 6
                : 1
                : 20-26
                Affiliations
                [1 ]Centre for Bioactive Discovery in Health and Ageing University of New England, Armidale, New South Wales, Australia
                [2 ]NSW Department of Primary Industries Armidale, New South Wales, Australia
                Author notes
                Correspondence should be addressed to R A Hart; Email: rhart7@ 123456une.edu.au
                Article
                EC160089
                10.1530/EC-16-0089
                5302164
                27998953
                16977435-30b7-4d3a-8c1f-c348016c1450
                © 2017 The authors

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 14 December 2016
                : 19 December 2016
                Categories
                Research

                leptin,pharmacokinetics,gastrointestinal tract,dimorphism,mice

                Comments

                Comment on this article

                Related Documents Log