Cephalic phase insulin secretion is KATP channel independent

J Endocrinol. 2013 May 28;218(1):25-33. doi: 10.1530/JOE-12-0579. Print 2013 Jul.

Abstract

Glucose-induced insulin secretion from pancreatic β-cells critically depends on the activity of ATP-sensitive K⁺ channels (KATP channel). We previously generated mice lacking Kir6.2, the pore subunit of the β-cell KATP channel (Kir6.2(-/-)), that show almost no insulin secretion in response to glucose in vitro. In this study, we compared insulin secretion by voluntary feeding (self-motivated, oral nutrient ingestion) and by forced feeding (intra-gastric nutrient injection via gavage) in wild-type (Kir6.2(+/+) and Kir6.2(-/-) mice. Under ad libitum feeding or during voluntary feeding of standard chow, blood glucose levels and plasma insulin levels were similar in Kir6.2(+/+) and Kir6.2(-/-) mice. By voluntary feeding of carbohydrate alone, insulin secretion was induced significantly in Kir6.2(-/-) mice but was markedly attenuated compared with that in Kir6.2(+/+) mice. On forced feeding of standard chow or carbohydrate alone, the insulin secretory response was markedly impaired or completely absent in Kir6.2(-/-) mice. Pretreatment with a muscarine receptor antagonist, atropine methyl nitrate, which does not cross the blood-brain barrier, almost completely blocked insulin secretion induced by voluntary feeding of standard chow or carbohydrate in Kir6.2(-/-) mice. Substantial glucose-induced insulin secretion was induced in the pancreas perfusion study of Kir6.2(-/-) mice only in the presence of carbamylcholine. These results suggest that a KATP channel-independent mechanism mediated by the vagal nerve plays a critical role in insulin secretion in response to nutrients in vivo.

Keywords: KATP channel; acetylcholine; cephalic phase insulin secretion.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / analysis
  • Cholinergic Agonists / pharmacology
  • Dextrins / administration & dosage
  • Dextrins / metabolism
  • Dietary Carbohydrates / administration & dosage
  • Dietary Carbohydrates / metabolism*
  • Eating*
  • Glucose / administration & dosage
  • Glucose / metabolism
  • In Vitro Techniques
  • Insulin / blood
  • Insulin / metabolism*
  • Insulin Secretion
  • Insulin-Secreting Cells / drug effects
  • Insulin-Secreting Cells / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Muscarinic Antagonists / pharmacology
  • Pancreas / drug effects
  • Pancreas / innervation*
  • Pancreas / metabolism
  • Parasympatholytics / pharmacology
  • Perfusion
  • Postprandial Period
  • Potassium Channels, Inwardly Rectifying / genetics
  • Potassium Channels, Inwardly Rectifying / metabolism*
  • Sympatholytics / pharmacology
  • Vagus Nerve / drug effects
  • Vagus Nerve / metabolism*

Substances

  • Blood Glucose
  • Cholinergic Agonists
  • Dextrins
  • Dietary Carbohydrates
  • Insulin
  • Kir6.2 channel
  • Muscarinic Antagonists
  • Parasympatholytics
  • Potassium Channels, Inwardly Rectifying
  • Sympatholytics
  • Glucose