Preventive effects of cyclosporin on diabetes in NOD mice. 1986

Y Mori, and M Suko, and H Okudaira, and I Matsuba, and A Tsuruoka, and A Sasaki, and H Yokoyama, and T Tanase, and T Shida, and M Nishimura

Non-obese diabetic mice aged 30 to 60 days were treated orally with Cyclosporin at doses of 25, 15 and 2.5 mg/kg every 2 days until 160 days of age. Diabetes developed in 12 out of 18 oil-treated mice (67%), with partial to complete Langerhans' islet destruction associated with lymphocytic infiltration. The non-obese diabetic mice showed a plasma glucose concentration of 6.62 +/- 0.92 mmol/l (mean +/- SD) at 50 days of age. The plasma glucose level of oil-treated non-obese diabetic mice gradually increased after 130 days of age and reached 14.0 to 19.0 mmol/l at 160 days of age, while Cyclosporin-treated non-obese diabetic mice showed neither clear increase of plasma glucose levels nor development of insulitis. The cumulative incidence of diabetes in Cyclosporin-treated mice was significantly lower than that in oil-treated mice (p less than 0.01). Subsequently, Cyclosporin treatment was started after development of glucose intolerance. Twenty-five mg/kg of Cyclosporin was administered every 2 days for 35 days. Cyclosporin appeared to have little therapeutic effect on diabetes in non-obese diabetic mice.

UI MeSH Term Description Entries
D007004 Hypoglycemic Agents Substances which lower blood glucose levels. Antidiabetic,Antidiabetic Agent,Antidiabetic Drug,Antidiabetics,Antihyperglycemic,Antihyperglycemic Agent,Hypoglycemic,Hypoglycemic Agent,Hypoglycemic Drug,Antidiabetic Agents,Antidiabetic Drugs,Antihyperglycemic Agents,Antihyperglycemics,Hypoglycemic Drugs,Hypoglycemic Effect,Hypoglycemic Effects,Hypoglycemics,Agent, Antidiabetic,Agent, Antihyperglycemic,Agent, Hypoglycemic,Agents, Antidiabetic,Agents, Antihyperglycemic,Agents, Hypoglycemic,Drug, Antidiabetic,Drug, Hypoglycemic,Drugs, Antidiabetic,Drugs, Hypoglycemic,Effect, Hypoglycemic,Effects, Hypoglycemic
D007515 Islets of Langerhans Irregular microscopic structures consisting of cords of endocrine cells that are scattered throughout the PANCREAS among the exocrine acini. Each islet is surrounded by connective tissue fibers and penetrated by a network of capillaries. There are four major cell types. The most abundant beta cells (50-80%) secrete INSULIN. Alpha cells (5-20%) secrete GLUCAGON. PP cells (10-35%) secrete PANCREATIC POLYPEPTIDE. Delta cells (~5%) secrete SOMATOSTATIN. Islands of Langerhans,Islet Cells,Nesidioblasts,Pancreas, Endocrine,Pancreatic Islets,Cell, Islet,Cells, Islet,Endocrine Pancreas,Islet Cell,Islet, Pancreatic,Islets, Pancreatic,Langerhans Islands,Langerhans Islets,Nesidioblast,Pancreatic Islet
D003524 Cyclosporins A group of closely related cyclic undecapeptides from the fungi Trichoderma polysporum and Cylindocarpon lucidum. They have some antineoplastic and antifungal action and significant immunosuppressive effects. Cyclosporins have been proposed as adjuvants in tissue and organ transplantation to suppress graft rejection. Cyclosporines
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
D051379 Mice The common name for the genus Mus. Mice, House,Mus,Mus musculus,Mice, Laboratory,Mouse,Mouse, House,Mouse, Laboratory,Mouse, Swiss,Mus domesticus,Mus musculus domesticus,Swiss Mice,House Mice,House Mouse,Laboratory Mice,Laboratory Mouse,Mice, Swiss,Swiss Mouse,domesticus, Mus musculus

Related Publications

Y Mori, and M Suko, and H Okudaira, and I Matsuba, and A Tsuruoka, and A Sasaki, and H Yokoyama, and T Tanase, and T Shida, and M Nishimura
December 1993, Journal of endocrinological investigation,
Y Mori, and M Suko, and H Okudaira, and I Matsuba, and A Tsuruoka, and A Sasaki, and H Yokoyama, and T Tanase, and T Shida, and M Nishimura
November 2003, Clinical and experimental immunology,
Y Mori, and M Suko, and H Okudaira, and I Matsuba, and A Tsuruoka, and A Sasaki, and H Yokoyama, and T Tanase, and T Shida, and M Nishimura
April 1987, Diabetes,
Y Mori, and M Suko, and H Okudaira, and I Matsuba, and A Tsuruoka, and A Sasaki, and H Yokoyama, and T Tanase, and T Shida, and M Nishimura
August 2013, International immunopharmacology,
Y Mori, and M Suko, and H Okudaira, and I Matsuba, and A Tsuruoka, and A Sasaki, and H Yokoyama, and T Tanase, and T Shida, and M Nishimura
December 2003, Toxicology letters,
Y Mori, and M Suko, and H Okudaira, and I Matsuba, and A Tsuruoka, and A Sasaki, and H Yokoyama, and T Tanase, and T Shida, and M Nishimura
March 2001, DNA and cell biology,
Y Mori, and M Suko, and H Okudaira, and I Matsuba, and A Tsuruoka, and A Sasaki, and H Yokoyama, and T Tanase, and T Shida, and M Nishimura
January 2007, Immunopharmacology and immunotoxicology,
Y Mori, and M Suko, and H Okudaira, and I Matsuba, and A Tsuruoka, and A Sasaki, and H Yokoyama, and T Tanase, and T Shida, and M Nishimura
September 1982, Diabetes,
Y Mori, and M Suko, and H Okudaira, and I Matsuba, and A Tsuruoka, and A Sasaki, and H Yokoyama, and T Tanase, and T Shida, and M Nishimura
July 1993, Diabetes,
Y Mori, and M Suko, and H Okudaira, and I Matsuba, and A Tsuruoka, and A Sasaki, and H Yokoyama, and T Tanase, and T Shida, and M Nishimura
May 1996, Cytokine,
Copied contents to your clipboard!