FGF21-dependent signaling downstream FGF receptors (FGFr) are extremely complicated
signaling downstream FGF receptors are tissue specific
FGF21 is activated and released in different conditions such as energy stress, ER stress, mitochondrial dysfunction, and cold-stress
FGF19 subfamily appears to require additional cofactors to stably bind the FGFRs in the target tissue such as:
aging-suppressor gene Klotho and Beta-Klotho with FGF21-Klotho complex binding multiple FGFRs, including FGFR1c, -2c, -3c, and -4
is a starvation-induced protein that is elevated after 7 days of fasting and regulates the utilization of fuel to adapt metabolism in the late phase of the absence of nutrients
mediates the adaptive starvation response to induce ketogenesis, gluconeogenesis, lipolysis, and lipid β-oxidation
stimulates the oxidation of fatty acids, the production of ketone bodies, and the inhibition of lipogenesis
administrating FGF21 prevents diet-induced obesity and insulin resistance in mice and humans
there is a paradoxically positive correlation with elevated serum FGF21 levels and metabolic disorders like obesity, diabetes, mitochondrial diseases, and aging (all these conditions have muscle loss as a common factor)
pathophysiological roles:
promotion of muscle atrophy, bone loss and reduced bone mineral density
acts as a stress-induced myokine, which is released during starvation, ER stress, and mitochondrial dysfunction
roles in alcohol intoxication:
alcohol is one of the most potent inducers of FGF21 hepatic production in both mice and humans
increases the urge in mice to drink water while intoxicated
may actively suppress the desire for alcohol
in 2023, researchers were able to quickly sober up drunk FGF21-null mice by boosting their levels of FGF21 and that this sobering effect comes from how it activates a specific part of the brain that controls alertness, known as the noradrenergic nervous system