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      Dipeptidyl peptidase- IV inhibitor alogliptin improves stress-induced insulin resistance and prothrombotic state in a murine model.

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          Abstract

          Stress evokes lipolytic release of free fatty acid (FFA) and low-grade inflammation in visceral adipose tissue, mediated by increased adipokine secretion, and contributes to glucose metabolism disorder and prothrombotic state. We tested the hypothesis that alogliptin, a dipeptidyl peptidase-4 inhibitor, can ameliorate the biological effects of chronic stress in mice.

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          Author and article information

          Journal
          Psychoneuroendocrinology
          Psychoneuroendocrinology
          Elsevier BV
          1873-3360
          0306-4530
          Nov 2016
          : 73
          Affiliations
          [1 ] Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
          [2 ] Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan; Department of Clinical Laboratory, Nagoya University Hospital, Nagoya, Japan. Electronic address: kyousuke@med.nagoya-u.ac.jp.
          [3 ] Department of Blood Transfusion, Nagoya University Hospital, Nagoya, Japan.
          [4 ] Department of Clinical Laboratory, Nagoya University Hospital, Nagoya, Japan.
          [5 ] Department of Blood Transfusion, Aichi Medical University Hospital, Nagakute, Japan.
          [6 ] Department of Clinical Laboratory, Nagoya University Hospital, Nagoya, Japan; Department of Blood Transfusion, Nagoya University Hospital, Nagoya, Japan.
          [7 ] Department of Pathology, Nagoya University Hospital, Nagoya, Japan.
          Article
          S0306-4530(16)30519-4
          10.1016/j.psyneuen.2016.08.004
          27509090
          a1bc6a09-6c72-46b4-aa99-7574886b237d
          History

          Restraint stress,Reactive oxygen species,DPP-4 Inhibitor,Insulin resistance,Adipose tissue inflammation

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