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Stem cell therapy in experimental type I diabetes in rats

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dc.contributor.author Nacu, Victoria
dc.contributor.author Trifan, Victoria
dc.contributor.author Bitca, Angela
dc.contributor.author Lisii, Cornel
dc.date.accessioned 2022-02-10T17:32:04Z
dc.date.available 2022-02-10T17:32:04Z
dc.date.issued 2012
dc.identifier.citation NACU, Victoria, TRIFAN, Victoria, BITCA, Angela, LISII, Cornel. Stem cell therapy in experimental type I diabetes in rats. In: MedEspera: the 4th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2012, p. 34. en_US
dc.identifier.uri http://repository.usmf.md/handle/20.500.12710/20089
dc.description.abstract Introduction: Diabetes mellitus is a multisystem disease with biochemical and structural consequences. It is a chronic disease which results from the progressive inability of the pancreas to secrete insulin because of autoimmune destruction of the beta cells. Type 1 diabetes causes an estimated 5%-10% of all diabetes cases or 11-22 million worldwide. Type 1 diabetes usually starts in children aged 4 years or older, with the peak incidence at 11-13 years. The stem cell therapy is a new direction in the treatment of type 1 diabetes mellitus. Matherials and Methods: The experiment was done on 100 rats which weighed 180-220g and were 9-12 months old. The diabetes was induced by intraperitoneal injection of 1 ml of 5% alloxan solution, that causes insulin-dependent diabetes in animals, called alloxanic diabetes, similar to type I diabetes in humans. After 7 days of hyperglycemia, alloxan induced diabetes was considered stable. The pancreatic cells were extracted from the pancreas of donor rats. The pancreases were first cut in small fragments of 1mm3 then washed 2-3 times with HBSS and then digested with 0,5 g/1 collagenase (Sigma Type V 663 U/mg). The pancreatic fragments were incubated for 1 hour in enzyme solution, and then the enzyme was inactivated with Hanks solution. The obtained mass was centrifuged at 1000 rpm and the cells from the upper portion of the supernatant were extracted and then cultivated. The digestion of the pancreatic substance and the extraction of the upper portion of the supernatant were done 3 times. The cells were cultivated in DMEM/F12 (8mM glucose) medium with lg/1 ITS supplement (5mg/l insulin, 5mg/l transferirn, 5mg/l selenium, Sigma), 100 UN/ml penicillin, lOOpg/ml streptomycin, 2g/l BSA, 10 mM nicotinamide and with keratinocid growth factor (KGF). The cells were cultivated 3, 5, 7,9 ,13 days. The umbilical stem cells were obtained from the umbilical cord blood of rat embryos. Results: The animals were treated with pancreatic cells in suspension injected intraperitoneally 1 ml 3 times with an interval of three days between injections and with umbilical stem cells in suspension 9,8 x 106 cells/ml - 1 ml intraperitoneally 3 times with 3 days between injections. The results show that rats treated with umbilical stem cells and pancreatic cells significantly lowered their blood glucose levels and increased their lifespan, as compared with untreated mice. The mice that received pancreatic cells show a blood glucose level slightly lower than in mice treated with umbilical stem cells. en_US
dc.language.iso en en_US
dc.publisher State Medical and Pharmaceutical University Nicolae Testemitanu, Medical Students and Residents Association, Scientific Association of Students and Young Doctors en_US
dc.relation.ispartof MedEspera: The 4th International Medical Congress for Students and Young Doctors, May 17-19, 2012, Chisinau, Republic of Moldova en_US
dc.subject stem cells en_US
dc.subject pancreatic beta cells en_US
dc.subject rats en_US
dc.subject type I diabetes en_US
dc.subject hyperglycemia en_US
dc.subject alloxan en_US
dc.title Stem cell therapy in experimental type I diabetes in rats en_US
dc.type Other en_US


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  • MedEspera 2012
    The 4th International Medical Congress for Students and Young Doctors, May 17-19, 2012

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