Alzheimer’s Disease and Diabetes: Insulin Signaling as the Bridge Linking Two Pathologies

• Published in: Molecular neurobiology 2020-04, Vol.57 (4), p.1966-1977
• Main Authors: Shieh, Jonathan Chang-Cheng, Huang, Pai-Tsang, Lin, Yung-Feng
• Format: Article
• Language: English
• Subjects: Advanced glycosylation end products; Alzheimer Disease - metabolism; Alzheimer Disease - pathology; Alzheimer's disease; Amyloid precursor protein; Animals; Biomedical and Life Sciences; Biomedicine; Cell Biology; Central nervous system; Dementia disorders; Diabetes; Diabetes mellitus; Diabetes Mellitus - metabolism; Diabetes Mellitus - pathology; Geriatrics; Glycosylation; Hap1 protein; Humans; Huntingtin; Hyperglycemia; Insulin; Insulin - metabolism; Insulin Resistance; Kinesin; Life span; Nerve Degeneration - pathology; Nervous system; Neurobiology; Neurodegeneration; Neurodegenerative diseases; Neurology; Neurosciences; Proteins; Risk factors; Signal Transduction; Sirtuins; Tau protein
• ISSN: 0893-7648; 1559-1182
• DOI: 10.1007/s12035-019-01858-5

Alzheimer’s (or Alzheimer) disease (AD) is the most prevalent subset of dementia, affecting elderly populations worldwide. The cumulative costs of the AD care are rapidly accelerating as the average lifespan increases. Onset and risk factors for AD and AD-like dementias have been largely unknown until recently. Studies show that chronic type II diabetes mellitus (DM) is closely associated with neurodegeneration, especially AD. Type II DM is characterized by the cells’ inability to take up insulin, as well as chronic hyperglycemia. In the central nervous system, insulin has crucial regulatory roles, while chronic hyperglycemia leads to formation and accumulation of advanced glycation end products (AGEs). AGEs are the major contributor to insulin resistance in diabetic cells, due to their regulatory role on sirtuin expression. Insulin activity in the central nervous system is known to interact with key proteins affected in neurodegenerative conditions, such as amyloid-β precursor protein (AβPP or APP), huntingtin-associated protein-1 (HAP1), Abelson helper integration site-1 (AHI1 or Jouberin), kinesin, and tau. Sirtuins have been theorized to be the mechanism for insulin resistance, and have been found to be affected in neurodegenerative conditions as well. There are hints that all these neuronal proteins may be closely related, although the mechanisms remain unclear. This review will gather existing research on these proteins and highlight the link between neurodegenerative conditions and diabetes mellitus.