Second-Generation Antipsychotics and Dysregulation of Glucose Metabolism: Beyond Weight Gain.
Diana GrajalesVitor FerreiraÁngela M ValverdePublished in: Cells (2019)
Second-generation antipsychotics (SGAs) are the cornerstone of treatment for schizophrenia because of their high clinical efficacy. However, SGA treatment is associated with severe metabolic alterations and body weight gain, which can increase the risk of type 2 diabetes and cardiovascular disease, and greatly accelerate mortality. Several underlying mechanisms have been proposed for antipsychotic-induced weight gain (AIWG), but some studies suggest that metabolic changes in insulin-sensitive tissues can be triggered before the onset of AIWG. In this review, we give an outlook on current research about the metabolic disturbances provoked by SGAs, with a particular focus on whole-body glucose homeostasis disturbances induced independently of AIWG, lipid dysregulation or adipose tissue disturbances. Specifically, we discuss the mechanistic insights gleamed from cellular and preclinical animal studies that have reported on the impact of SGAs on insulin signaling, endogenous glucose production, glucose uptake and insulin secretion in the liver, skeletal muscle and the endocrine pancreas. Finally, we discuss some of the genetic and epigenetic changes that might explain the different susceptibilities of SGA-treated patients to the metabolic side-effects of antipsychotics.
Keyphrases
- early onset
- weight gain
- body mass index
- birth weight
- cardiovascular disease
- type diabetes
- skeletal muscle
- adipose tissue
- weight loss
- gene expression
- high glucose
- newly diagnosed
- insulin resistance
- diabetic rats
- bipolar disorder
- end stage renal disease
- ejection fraction
- dna methylation
- drug induced
- high fat diet
- metabolic syndrome
- stem cells
- combination therapy
- case control
- blood pressure
- endothelial cells
- risk factors
- gestational age
- bone marrow
- cardiovascular risk factors