کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2040129 | 1073099 | 2016 | 9 صفحه PDF | دانلود رایگان |
• Autonomic innervation of pancreatic islets develops during mid-gestation in mice
• Leptin is required for normal parasympathetic innervation of pancreatic β cells
• Acute leptin injections in embryos cause lifelong disturbances in glucose homeostasis
• Leptin acts directly on the hindbrain to modulate cholinergic axon growth
SummaryThe autonomic nervous system plays a critical role in glucose metabolism through both its sympathetic and parasympathetic branches, but the mechanisms that underlie the development of the autonomic innervation of the pancreas remain poorly understood. Here, we report that cholinergic innervation of pancreatic islets develops during mid-gestation under the influence of leptin. Leptin-deficient mice display a greater cholinergic innervation of pancreatic islets beginning in embryonic life, and this increase persists into adulthood. Remarkably, a single intracerebroventricular injection of leptin in embryos caused a permanent reduction in parasympathetic innervation of pancreatic β cells and long-term impairments in glucose homeostasis. These developmental effects of leptin involve a direct inhibitory effect on the outgrowth of preganglionic axons from the hindbrain. These studies reveal an unanticipated regulatory role of leptin on the parasympathetic nervous system during embryonic development and may have important implications for our understanding of the early mechanisms that contribute to diabetes.
Graphical AbstractFigure optionsDownload as PowerPoint slide
Journal: - Volume 15, Issue 1, 5 April 2016, Pages 36–44