Insulin autoantibodies in non-obese diabetic (NOD) mice and streptozotocin-induced diabetic mice. 1988

T Maruyama, and I Takei, and T Yanagawa, and T Takahashi, and Y Asaba, and K Kataoka, and T Ishii
Department of Internal Medicine, Tokyo Denryoku Hospital, Japan.

Similar to Insulin-dependent diabetes mellitus (IDDM) in man, diabetes in the non-obese diabetic (NOD) mouse and that induced by low-dose of multiple injections of streptozotocin (low-dose SZ) develop in conjunction with the presence of insulitis. We measured insulin autoantibodies (IAA) in NOD and low-dose SZ mice and compared the levels with mice given a single diabetogenic dose of streptozotocin (high-dose SZ) as well as control CD-1 mice. The mean insulin binding in female NOD mice was 3.08 +/- 1.49 (mean + SD)% and that in male NOD mice was 2.86 +/- 3.70%, as compared with 1.10 +/- 0.35% in the control CD-1 mice (p less than 0.01, p less than 0.05). Sera from low-dose SZ and high-dose SZ mice showed 1.07 +/- 0.23% and 0.93 +/- 0.45% of IAA which did not differ from controls. The number of mice with IAA above the mean + 2SD value of CD-1 mice were 8/9 female NOD mice and 9/20 male NOD mice. Insulitis was found in all NOD and low-dose SZ mice but not in any high-dose SZ mice and control CD-1 mice. These results suggest that (a) IAA are markers for islet autoimmunity in the NOD mouse, (b) presence of IAA does not reflect insulitis, and (c) the appearance of IAA may reflect a difference of the immune response genotype.

UI MeSH Term Description Entries
D007328 Insulin A 51-amino acid pancreatic hormone that plays a major role in the regulation of glucose metabolism, directly by suppressing endogenous glucose production (GLYCOGENOLYSIS; GLUCONEOGENESIS) and indirectly by suppressing GLUCAGON secretion and LIPOLYSIS. Native insulin is a globular protein comprised of a zinc-coordinated hexamer. Each insulin monomer containing two chains, A (21 residues) and B (30 residues), linked by two disulfide bonds. Insulin is used as a drug to control insulin-dependent diabetes mellitus (DIABETES MELLITUS, TYPE 1). Iletin,Insulin A Chain,Insulin B Chain,Insulin, Regular,Novolin,Sodium Insulin,Soluble Insulin,Chain, Insulin B,Insulin, Sodium,Insulin, Soluble,Regular Insulin
D007330 Insulin Antibodies Antibodies specific to INSULIN. Antibodies, Insulin
D008297 Male Males
D008815 Mice, Inbred Strains Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations, or by parent x offspring matings carried out with certain restrictions. All animals within an inbred strain trace back to a common ancestor in the twentieth generation. Inbred Mouse Strains,Inbred Strain of Mice,Inbred Strain of Mouse,Inbred Strains of Mice,Mouse, Inbred Strain,Inbred Mouse Strain,Mouse Inbred Strain,Mouse Inbred Strains,Mouse Strain, Inbred,Mouse Strains, Inbred,Strain, Inbred Mouse,Strains, Inbred Mouse
D008820 Mice, Obese Mutant mice exhibiting a marked obesity coupled with overeating, hyperglycemia, hyperinsulinemia, marked insulin resistance, and infertility when in a homozygous state. They may be inbred or hybrid. Hyperglycemic Mice,Obese Mice,Mouse, Hyperglycemic,Mouse, Obese,Hyperglycemic Mouse,Mice, Hyperglycemic,Obese Mouse
D003920 Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE.
D003921 Diabetes Mellitus, Experimental Diabetes mellitus induced experimentally by administration of various diabetogenic agents or by PANCREATECTOMY. Alloxan Diabetes,Streptozocin Diabetes,Streptozotocin Diabetes,Experimental Diabetes Mellitus,Diabete, Streptozocin,Diabetes, Alloxan,Diabetes, Streptozocin,Diabetes, Streptozotocin,Streptozocin Diabete
D005260 Female Females
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001323 Autoantibodies Antibodies that react with self-antigens (AUTOANTIGENS) of the organism that produced them. Autoantibody

Related Publications

T Maruyama, and I Takei, and T Yanagawa, and T Takahashi, and Y Asaba, and K Kataoka, and T Ishii
March 1989, Clinical and experimental immunology,
T Maruyama, and I Takei, and T Yanagawa, and T Takahashi, and Y Asaba, and K Kataoka, and T Ishii
September 1990, Clinical and experimental immunology,
T Maruyama, and I Takei, and T Yanagawa, and T Takahashi, and Y Asaba, and K Kataoka, and T Ishii
October 1987, Clinical and experimental immunology,
T Maruyama, and I Takei, and T Yanagawa, and T Takahashi, and Y Asaba, and K Kataoka, and T Ishii
September 1990, Clinical and experimental immunology,
T Maruyama, and I Takei, and T Yanagawa, and T Takahashi, and Y Asaba, and K Kataoka, and T Ishii
February 2008, Autonomic neuroscience : basic & clinical,
T Maruyama, and I Takei, and T Yanagawa, and T Takahashi, and Y Asaba, and K Kataoka, and T Ishii
July 1997, Diabetes research and clinical practice,
T Maruyama, and I Takei, and T Yanagawa, and T Takahashi, and Y Asaba, and K Kataoka, and T Ishii
January 1988, Journal of immunogenetics,
T Maruyama, and I Takei, and T Yanagawa, and T Takahashi, and Y Asaba, and K Kataoka, and T Ishii
August 1996, The American journal of pathology,
T Maruyama, and I Takei, and T Yanagawa, and T Takahashi, and Y Asaba, and K Kataoka, and T Ishii
January 1993, Diabetes research and clinical practice,
T Maruyama, and I Takei, and T Yanagawa, and T Takahashi, and Y Asaba, and K Kataoka, and T Ishii
June 1982, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme,
Copied contents to your clipboard!