Insulin modulation of glucagon secretion: The role of insulin and other factors in the regulation of glucagon secretion

التفاصيل البيبلوغرافية
العنوان: Insulin modulation of glucagon secretion: The role of insulin and other factors in the regulation of glucagon secretion
المؤلفون: Rohit N. Kulkarni, Dan Kawamori
المصدر: Islets. 1:276-279
بيانات النشر: Informa UK Limited, 2009.
سنة النشر: 2009
مصطلحات موضوعية: Male, endocrine system, medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, medicine.medical_treatment, Hypoglycemia, Glucagon, Streptozocin, Diabetes Mellitus, Experimental, Mice, Endocrinology, Diabetes mellitus, Internal medicine, medicine, Animals, Hypoglycemic Agents, Insulin, Glucose homeostasis, Mice, Knockout, biology, Chemistry, digestive, oral, and skin physiology, Glucagon secretion, medicine.disease, Receptor, Insulin, Insulin receptor, Glucagon-Secreting Cells, biology.protein, hormones, hormone substitutes, and hormone antagonists, Hyperglucagonemia
الوصف: Glucagon plays a critical counter-regulatory role to insulin to maintain optimal glucose homeostasis. Glucagon secretion from pancreatic α-cells is regulated by glycemia, neural input, and secretion from neighboring β-cells. Recently, we provided direct genetic evidence of a critical role for insulin signaling in the regulation of glucagon secretion in vivo. Pancreatic α-cell targeted disruption of insulin receptor expression in mice resulted in glucose intolerance, hyperglycemia and hyperglucagonemia coupled with an abnormal glucagon response to hypoglycemia. Furthermore, streptozotocin treated mice exhibited paradoxically increased plasma glucagon suggesting a dominant role for insulin in the regulation of glucagon secretion compared with glucose. In fact, normalization of hyperglycemia by phrolidzin treatment decreased plasma glucagon levels suggesting a stimulatory effect of glucose on glucagon secretion and also revealed the significance of insulin in hyperglycemic states. Together these studies provide novel insights into intra-islet regulatory pathways in the modulation of glucagon secretion and provide potential opportunities to develop therapeutic approaches for the correction of α-cell dysfunction in diabetes.
تدمد: 1938-2022
1938-2014
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aec5116fcd26c00e8802e6c079c46faTest
https://doi.org/10.4161/isl.1.3.9967Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....5aec5116fcd26c00e8802e6c079c46fa
قاعدة البيانات: OpenAIRE