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Role of bone marrow-derived stem cells versus insulin on filiform and fungiform papillae of diabetic albino rats (light,fluorescent and scanning electron microscopic study)
Authors:Rania Osama Mohamed Mohsen  Ahmed M. Halawa  Rabab Hassan
Affiliation:Department of Oral Biology, Faculty of Dentistry, Ain Shams University, Cairo, Egypt
Abstract:BackgroundDiabetes mellitus (DM) is a chronic metabolic disease characterized by high blood glucose levels. DM affects many body’s organs and caused by insulin production deficiency or by the ineffectiveness of the produced insulin. Administration of exogenous insulin is required for management of type I DM; however, it does not cure the disease. Bone marrow-mesenchymal stem cells (BM-MSCs) have been highlighted to offer a novel cell based approach for treatment of diabetes because of their anti-diabetic effect, direct differentiation into a variety of cell types, or release of paracrine factors.AimTo examine the effect of BM-MSCs versus insulin on true filiform and fungiform papillae of diabetic rats.Materials and methodsFifty six male Wistar albino rats weighing 200–250 g were equally divided into: Control group (Gp I): Rats did not receive any drug. Diabetic group (Gp II): Rats received a single intra-peritoneal injection of streptozotocin (40 mg/kg). BM-MSCs treated diabetic group (Gp III): After DM confirmation; rats received a single intravenous injection of BM-MSCs (million units) through tail vein. Insulin treated diabetic group (Gp IV): After DM confirmation; rats received a daily subcutaneous injection of insulin (5IU/kg). After four weeks, half of the tongue specimens were processed and stained by Hematoxyline & Eosin and Anti-proliferating cell nuclear antigen (Anti-PCNA) then examined by light microscope. Fluorescent microscope was used to detect homing of injected labeled BM-MSCs in rats’ filiform and fungiform papillae. While the other half were examined by scanning electron microscope.ResultsTrue filiform and fungiform papillae of Gp II showed significant histological and morphological alterations. In treated groups, Gp III and Gp IV, both papillae showed marked improvements, being more noticeable in Gp IV. There was a significant increase in the number of Anti-PCNA positive cells and a significant decrease in fasting blood glucose level in Gp III and Gp IV in comparison to Gp II.ConclusionsDM had degenerative effects on true filiform and fungiform papillae. Administration of BM-MSCs reduced the deleterious effects of DM on both papillae. Insulin injection caused more obvious improvements in both papillae of diabetic rats than BM-MSCs.
Keywords:Corresponding author at: Department of Oral Biology, Faculty of Dentistry, Ain-Shams University, El-Qobba Bridge, Al Waili, 11566, Cairo, Egypt.  AGEs  advanced glycation end products  PCNA  proliferating cell nuclear antigen  BM-MSCs  bone marrow-mesenchymal stem cells  b.v  blood vessel  c.t  connective tissue  DAB  diaminobenzidine plus chromogen  DM  diabetes mellitus  FBG  fasting blood glucose  FBS  Fetal bovine serum  FM  fluorescent microscope  H&E  hematoxyline & eosin  IRS  insulin receptor substrate  LM  light microscope  L-DMEM  Low-glucose Dulbecco's modified Eagle's medium  PBS  phosphate buffered saline  SEM  scanning electron microscope  STZ  streptozotocin  BM-MSCs  Insulin  Diabetes  True filiform  Fungiform  SEM
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