The function of this incretin mimetic is to inhibit the action of DPPIV, thus improving the glycaemic control by prolonging the action of glucagon-like peptide-1 (GLP1) and gastric inhibitory polypeptide (GIP). Moreover, the MK0431 can still stimulate the recovery and the maintenance of pancreatic cells.12, 13, 14, 16, 17, 18 and 19 The salivary gland may be considered similar
to pancreas in some aspects.20 Accordingly, there is evidence indicating Icotinib molecular weight a relationship between insulin production and the salivary tissues. Although the salivary glands are typically exocrine, He et al. demonstrated endocrine secretions related to these tissues. Sánchez García et al., observed that insulin levels found in saliva were similar to plasma levels under normal conditions and suggested that the insulin might be a product of the salivary glands.21 and 22 Thus, knowing this relationship between salivary glands and pancreas, the therapy with MK0431 can lead as yet to the recovery of salivary tissues, similar to the observed in pancreatic cells. However, doubts still exist regarding the efficacy of this treatment in recovery of tissues damaged
by type 1 diabetes. Therefore, this study evaluated the treatment with MK0431 in salivary glands of spontaneously diabetic mice, focusing mainly on the possible therapeutic and hypoglycaemic effects of this dipeptide peptidase IV inhibitor in the recovery of these salivary tissues. Twenty 15-week-old female NOD mice, weighing on average 25 g, were divided into two groups: 10 diabetic Nintedanib in vitro NOD mice (group I) and 10 also
diabetic Isotretinoin NOD mice (group II). The animals were obtained from the Animal House of State University of Campinas (CEMIB-UNICAMP) and were kept under standard conditions of housing, feeding and treatment at the Sector of Laboratory Animal Experimentation (SEA), Department of Morphology and Basic Pathology, Faculty of Medicine of Jundiaí, Brazil. Blood glucose (mg/dL) was measured weekly in all animals with a blood glucose meter (Accu-Chek Performa, Roche, Switzerland). After characterization of the diabetic condition, animals of both groups presented glucose levels higher than 300 mg/dL.23 Then, the animals of group II received MK0431 mixed in pelleted diet (11 g/kg) similar to Lamont and Drucker24 for a period of 4 weeks.17 In order to simulate the experimental conditions of treated group, animals of the group I were manipulated in the same way and received pelleted diet and water ad libitum, however, without hypoglycaemic agents. After treatment, the animals were anaesthetised (imp.) with a mixture of ketamine hydrochloride (130 mg/kg, Francotar, Virbac, Brazil) and xylazine hydrochloride (6.8 mg/kg, 2% Virbaxyl, Virbac, Brazil) and salivary gland samples were collected for analyses by transmitted and polarized light microscopy.