Modeling the distribution of insulin in pancreas

Maintenance of adequate physical and functional pancreatic β-cell mass is critical for the prevention or delay of diabetes mellitus. It is well established that insulin potently activates mitogenic and anti-apoptotic signaling cascades in cultured β-cells. Loss of β-cell insulin receptors is sufficient to induce type 2 diabetes in mice. However, it remains unclear whether the in vitro effect in human islets and the in vivo effects in mice can be applied to human physiology. The major obstacle to a complete understanding of the effects of insulin's feedback in human pancreas is the absence of technology to measure the concentrations of insulin inside of pancreas. To contextualize recent in vitro data, it is essential to know the local concentration and distribution of insulin in pancreas. To this end, we continue to estimate the local insulin concentration within pancreas. In this paper, we investigate the distribution of insulin concentration along the pancreatic vein through a novel mathematical modeling approach using existing physiological data and islet imaging data, in contrast to our previous work focusing on the insulin level within an islet. Our studies suggest that, in response to an increase in glucose, the insulin concentration along the pancreatic vein increases nearly linearly in the fashion of increasing quicker in tail area but slower in head area depending of the initial distribution.