Type 2 Diabetes and Alzheimer's Disease: The Emerging Role of Cellular Lipotoxicity.
Nicola MarranoGiuseppina BiondiAnna BorrelliMartina RellaTommaso ZambettaLudovico Di GioiaMariangela CaporussoGiancarlo LogroscinoFrancesco GiorginoFrancesco GiorginoAnnalisa NatalicchioPublished in: Biomolecules (2023)
Type 2 diabetes (T2D) and Alzheimer's diseases (AD) represent major health issues that have reached alarming levels in the last decades. Although growing evidence demonstrates that AD is a significant comorbidity of T2D, and there is a ~1.4-2-fold increase in the risk of developing AD among T2D patients, the involvement of possible common triggers in the pathogenesis of these two diseases remains largely unknown. Of note, recent mechanistic insights suggest that lipotoxicity could represent the missing ring in the pathogenetic mechanisms linking T2D to AD. Indeed, obesity, which represents the main cause of lipotoxicity, has been recognized as a major risk factor for both pathological conditions. Lipotoxicity can lead to inflammation, insulin resistance, oxidative stress, ceramide and amyloid accumulation, endoplasmic reticulum stress, ferroptosis, and autophagy, which are shared biological events in the pathogenesis of T2D and AD. In the current review, we try to provide a critical and comprehensive view of the common molecular pathways activated by lipotoxicity in T2D and AD, attempting to summarize how these mechanisms can drive future research and open the way to new therapeutic perspectives.
Keyphrases
- type diabetes
- endoplasmic reticulum stress
- insulin resistance
- oxidative stress
- induced apoptosis
- metabolic syndrome
- cell death
- glycemic control
- newly diagnosed
- healthcare
- end stage renal disease
- skeletal muscle
- ejection fraction
- minimally invasive
- mental health
- high fat diet induced
- polycystic ovary syndrome
- signaling pathway
- weight loss
- ischemia reperfusion injury
- current status
- climate change
- diabetic rats
- weight gain
- heat stress
- human health
- heat shock protein