Insulin and the Brain: A Sweet Relationship With Intensive Care

J Intensive Care Med. 2017 Jan;32(1):48-58. doi: 10.1177/0885066615594341. Epub 2015 Jul 12.

Abstract

Background: Insulin receptors (IRs) in the brain have unique molecular features and a characteristic pattern of distribution. Their possible functions extend beyond glucose utilization. In this systematic review, we explore the interactions between insulin and the brain and its implications for anesthesiologists, critical care physicians, and other medical disciplines.

Methods: A literature search of published preclinical and clinical studies between 1978 and 2014 was conducted, yielding 5996 articles. After applying inclusion and exclusion criteria, 92 studies were selected for this systematic review.

Results: The IRs have unique molecular features, pattern of distribution, and mechanism of action. It has effects on neuronal function, metabolism, and neurotransmission. The IRs are involved in neuronal apoptosis and neurodegenerative processes.

Conclusion: In this systematic review, we present a close relationship between insulin and the brain, with discernible effects on memory, learning abilities, and motor functions. The potential therapeutic effects extend from acute brain insults such as traumatic brain injury, brain ischemia, and hemorrhage, to chronic neurodegenerative diseases such as Alzheimer and Parkinson disease. An understanding of the wider effects of insulin conveyed in this review will prompt anaesthesiologists and critical care physicians to consider its therapeutic potential and guide future studies.

Keywords: Insulin receptor; neurodegenerative disease critical care management; neuronal metabolism.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Brain / metabolism*
  • Brain / physiopathology
  • Critical Care*
  • Critical Illness / therapy*
  • Humans
  • Insulin / metabolism*
  • Neurodegenerative Diseases / metabolism
  • Neurodegenerative Diseases / physiopathology*
  • Receptor, Insulin / metabolism*
  • Signal Transduction

Substances

  • Insulin
  • Receptor, Insulin