Japanese Herbal Medicine TJ-48 Prevents Autoimmune Diabetes in NOD Mice

DOI Web Site PubMed 被引用文献2件
  • Tetsuya Ikemoto
    Baylor Research Institute Fort-Worth Campus, 1400 Eight Avenue, Fort Worth, TX 76104, USA
  • Koji Sugimoto
    Baylor Research Institute Fort-Worth Campus, 1400 Eight Avenue, Fort Worth, TX 76104, USA
  • Morihito Takita
    Baylor Research Institute Fort-Worth Campus, 1400 Eight Avenue, Fort Worth, TX 76104, USA
  • Masayuki Shimoda
    Division of Cardiology, Department of Internal Medicine, Baylor University Medical Center, Baylor Heart and Vascular Institute, Dallas, TX 75246, USA
  • Hirofumi Noguchi
    Baylor Research Institute Fort-Worth Campus, 1400 Eight Avenue, Fort Worth, TX 76104, USA
  • Bashoo Naziruddin
    Baylor Regional Transplantation Institute, 3500 Gaston Avenue, Roberts 4F, Dallas, TX 75246, USA
  • Marlon F Levy
    Baylor Regional Transplantation Institute, 3500 Gaston Avenue, Roberts 4F, Dallas, TX 75246, USA
  • Mitsuo Shimada
    Department of Digestive and Transplant Surgery, The University of Tokushima, 3-18-15, Kuramoto, Tokushima, 770-8503, Japan
  • Shinichi Matsumoto
    Baylor Research Institute Fort-Worth Campus, 1400 Eight Avenue, Fort Worth, TX 76104, USA

説明

<jats:p>Type 1 diabetes mellitus (T1DM) is mainly caused by CD8<jats:sup>+</jats:sup>cytotoxic T cell infiltration into islets. Recently, the role of regulatory T cells (Tregs) in the prevention of the onset of T1DM was reported. We reported that TJ-48, a common Japanese herbal medicine, decreased Treg population in cancer patients, thus we investigated whether TJ-48 had an influence on T1DM onset using NOD mice. In the TJ-48 group, TJ-48 (2.0g/kg/day) was administered in the drinking water for NOD mice from three weeks of age to 20 weeks of age. Their body weight and fast blood glucose (FBG) were measured every week. Histology (Hematoxylin-Eosin staining) was investigated every month. Lymphocyte profiles were investigated every month with FACS. The results were compared to the age-matched NOD mice control group. FBG of the control group mice showed diabetic status of 66.7% at 18 weeks of age. On the other hand, the TJ-48 group mice showed diabetic status of 16.7% at 18 weeks of age (p = 1.905E-06). There were no significant differences in general conditions or body weight between the two groups. Lymphocyte infiltrations into islets were dramatically suppressed in the TJ-48 group. The effect of TJ-48 on decreasing Tregs was less apparent in the NOD mice model. TJ-48 inhibited lymphocyte infiltrations into islets, which led to preventing the onset of T1DM in NOD mice.</jats:p>

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