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Biochem Biophys Res Commun. 2013 Jul 5;436(3):418-23. doi: 10.1016/j.bbrc.2013.05.117. Epub 2013 Jun 11.

Multiple intravenous infusions of bone marrow mesenchymal stem cells reverse hyperglycemia in experimental type 2 diabetes rats.

Author information

1
Institute of Basic Medicine Science, College of Life Science, Chinese PLA General Hospital, Beijing 100853, China.

Abstract

The worldwide rapid increase in diabetes poses a significant challenge to current therapeutic approaches. Single-dose mesenchymal stem cell (MSC) infusion ameliorates hyperglycemia but fails to restore normoglycemia in diabetic animals. We therefore hypothesized that multiple intravenous MSC infusions may reverse hyperglycemia in type 2 diabetes (T2D) rats. We administered serial allogenous bone-marrow derived MSC infusions (1 × 10(6)cells/infusion) via the tail vein once every 2 weeks to T2D rats, induced by high-fat diet and streptozocin (STZ) administration. Hyperglycemia decreased only transiently after a single infusion in early-phase (1 week) T2D rats, but approximated normal levels after at least three-time infusions. This normal blood level was maintained for at least 9 weeks. Serum concentrations of both insulin and C-peptide were dramatically increased after serial MSC infusions. Oral glucose tolerance tests revealed that glucose metabolism was significantly ameliorated. Immunofluorescence analysis of insulin/glucagon staining revealed the restoration of islet structure and number after multiple MSC treatments. When multiple-MSC treatment was initiated in late-phase (5 week) T2D rats, the results were slightly different. The results of this study suggested that a multiple-MSC infusion strategy offers a viable clinical option for T2D patients.

KEYWORDS:

BM-MSCs; Bone marrow; Hyperglycemia; IPITTs; MSCs; Mesenchymal stem cells; Multiple infusion; OGTTs; STZ; T1D; T2D; Type 2 diabetes; bone-marrow-derived MSC; intraperitoneal insulin tolerance tests; mesenchymal stem cells; oral glucose tolerance tests; streptozocin; type 1 diabetes; type 2 diabetes

PMID:
23770360
DOI:
10.1016/j.bbrc.2013.05.117
[Indexed for MEDLINE]

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