Inhibition of serotonin expression in gut enteroendocrine cells results in conversion to insulin-positive cells
Disclosed herein are methods involving the targeting of 5HT biosynthesis in gut insulin-negative cells to convert them into insulin-positive cells. Also disclosed are methods for treating a disease or disorder in a mammal, preferably a human, associated with impaired pancreatic endocrine function, by administering a therapeutically effective amount of an enumerated active agent that reduces the expression, biosynthesis, signaling or biological activity of serotonin or increases its degradation, wherein administering comprises delivering the agent to Gut Ins− cells in the mammal. Other embodiments of the method are directed to therapy wherein an agent that significantly reduces FOXO1 expression, biosynthesis, signaling or biological activity or increases its degradation is administered in addition to the agent that reduces serotonin, or alternatively an agent that reduces FOXO1 expression is targeted to serotonin-positive gut enteroendocrine cells.
1. A method comprising administering to a mammal having a disease or disorder associated with impaired pancreatic endocrine function, a therapeutically effective amount of an agent selected from the group consisting of isolated small hairpin RNA (shRNA), small interfering RNA (siRNA), antisense RNA, antisense DNA, chimeric antisense DNA/RNA, and ribozymes that is sufficiently complementary to specifically bind to a gene or mRNA encoding Foxo1 protein thereby reducing the expression, biosynthesis, signaling or biological activity of Foxo1, wherein administering comprises delivering the agent to insulin-negative, serotonin-positive enteroendocrine cells in the gut (Gut-Ins− cells) thereby producing insulin-positive cells that make and secrete biologically active insulin (Gut Ins+ cells) thereby treating the disease or disorder, and wherein the agent is targeted to serotonin-positive enteroendocrine cells.
2. The method of claim 1 , wherein the insulin-positive cells are glucose-responsive cells.
3. The method of claim 1 , wherein the agent is orally administered in an enteric form that releases the therapeutically effective amount in a region of the gut comprising insulin-negative, serotonin-positive enteroendocrine cells or is locally administered directly into or onto the gut region.
4. The method of claim 2 , wherein the gut region is the duodenum, ileum or colon.
5. The method of claim 1 , wherein the disease or disorder is selected from the group consisting of diabetes type 1, diabetes type 2, metabolic syndrome, glucose intolerance, hyperglycemia, decreased insulin sensitivity, increased fasting glucose, increased post-prandial glucose and obesity.
6. The method of claim 1 , wherein the therapeutically effective amount is an amount that produces an effect selected from the group consisting of an increase in glucose tolerance, an increase in serum insulin, an increase insulin sensitivity, a decrease in fasting glucose, a decrease in post-prandial glucose, a decrease in weight gain, a decrease in fat mass, an increase in weight loss and the generation enteroendocrine cells in the gastrointestinal tract that produce and secrete insulin.
7. The method of claim 1 , wherein the agent is administered orally, or parenterally or as a suppository.
8. A method for producing cells in the gut of a mammal that make and secrete biologically active insulin (Gut Ins+ cells), comprising administering to the mammal an agent selected from the group consisting of isolated small hairpin ins RNA (shRNA), small interfering RNA (siRNA), antisense RNA, antisense DNA, chimeric antisense DNA/RNA, and ribozymes that is sufficiently complementary to specifically bind to a gene or mRNA encoding Foxo1 protein thereby reducing the expression, biosynthesis, signaling or biological activity of Foxo1, wherein administering comprises delivering the agent to insulin-negative cells in the gut (Gut-Ins− cells) comprising serotonin-positive, insulin-negative enteroendocrine cells thereby producing gut cells that make and secrete biologically active insulin (Gut Ins+ cells), wherein the agent is targeted to serotonin-positive enteroendocrine cells.
9. The method of claim 8 , wherein the gut+cells are glucose responsive.