The effect of combination therapy with cyclosporine A and hydrocortisone on glucose metabolism in diabetic rats following pancreatic islet transplantation
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
8789318
Knihovny.cz E-zdroje
- MeSH
- antiflogistika farmakologie MeSH
- cyklosporin krev farmakologie MeSH
- experimentální diabetes mellitus metabolismus chirurgie MeSH
- glukosa metabolismus MeSH
- glukózový toleranční test MeSH
- hydrokortison farmakologie MeSH
- imunosupresiva farmakologie MeSH
- inzulin metabolismus MeSH
- játra krevní zásobení cytologie MeSH
- kombinovaná farmakoterapie MeSH
- kreatinin krev MeSH
- krevní glukóza MeSH
- krysa rodu Rattus MeSH
- ledviny cytologie MeSH
- metabolismus lipidů MeSH
- modely nemocí na zvířatech MeSH
- omezení příjmu potravy MeSH
- potkani Wistar MeSH
- radioizotopy uhlíku MeSH
- sekrece inzulinu MeSH
- transplantace Langerhansových ostrůvků * MeSH
- vena portae cytologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antiflogistika MeSH
- cyklosporin MeSH
- glukosa MeSH
- hydrokortison MeSH
- imunosupresiva MeSH
- inzulin MeSH
- kreatinin MeSH
- krevní glukóza MeSH
- radioizotopy uhlíku MeSH
Glucose tolerance, insulin secretion and in vitro insulin action were examined in streptozotocin-induced diabetic rats following pancreatic islet allotransplantation treated with combination of oral cyclosporine A (10 mg/kg) and hydrocortisone (1.5 mg/kg) intramuscularly. 1400 pure islets from multiple donors were implanted either into the portal vein (n = 10) or under the renal capsule (n = 11). Ten sham-operated non-diabetic animals receiving the same immunosuppressive therapy, 8 healthy animals without any treatment and 10 diabetic animals without immunosuppression following islet transplantation were used as controls. In all transplanted animals blood glucose was normalized by day 3 after transplantation with lower levels in those transplanted intraportally (p < 0.05). Non-immunosuppressed animals rejected the graft after 6.5 +/- 1.2 days after transplantation, immunosuppressed animals in both groups remained normoglycaemic till the end of the experiment on day 28. Oral glucose tolerance tests and insulin levels on days 10 and 28 improved dramatically. No differences in glucose and insulin levels between intraportal and subcapsular groups were found. Post-load glucose levels in immunosuppressed non-transplanted animals were higher on day 28 than before treatment and were also higher than in the healthy non-treated group (p < 0.05). In vitro insulin action determined by the incorporation of labelled glucose into adipose tissue was impaired only in animals in which islets were transplanted into the liver (p < 0.05 vs other groups). In conclusion, therapy with cyclosporine A and hydrocortisone prevents allogeneic islet rejection in rats during a short-term experiment. Although glucose tolerance is not completely normalized following transplantation, slight impairment is also demonstrable in healthy animals on the same drug therapy.