Abstract
BACKGROUND: Islet transplantation for diabetes therapy has remained a challenge. None of the currently used transplantation sites have provided satisfactory results as islets seem to require a specific tissue for survival and growth. Since the submandibular gland (SMG) shares physiological and anatomical similarities with the pancreas, we attempted to use this tissue as the transplantation site. METHODS: In Experiment 1, a group of 10 female Syrian Golden hamsters' (SGH) received isolated and purified homologous islets transplanted into their right SMG. In Experiment 2, 15 female SGH received islet transplant into their left SMG as above, except that the recipient hamsters were made diabetic by streptozotocin (STZ) before islet transplantation. In Experiment 3, isolated and purified human islets were transplanted into the SMG of 10 female hamsters. RESULTS: In 8 out of 10 hamsters in Experiment 1 the islets survived and showed the same morphological structure and endocrine cell content, as intrapancreatic islets and presented signs of rapid growth and distribution. Also, as in Experiment 1, well-established islets were present in Experiment 2. Ten of the 15 hamsters pretreated with STZ had blood glucose values between 96 and 125 mg/dl, whereas three hamsters remained hyperglycemic (glucose levels between 194 and 417 mg/dl). Remarkably, the islets in the pancreas of 10 STZ-treated hamsters with functioning SMG islets remained atrophic even after 12 weeks. In two hamsters transplanted islets showed degeneration and remained diabetic until their pancreatic islets regenerated. In Experiment 3, transplanted human islets were completely destroyed. CONCLUSIONS: SMG appears to be the most suitable site for islet transplantation for the treatment of diabetes.