The predominant effective dose used in mouse studies is 25 nmol/kg
Fearon, the study's lead author, emphasized the potential of this approach
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For optimal results, pair treatments with a balanced diet and regular exercise
Under conditions of reduced portal insulin-to-glucagon ratio, lipolysis increases in adipose tissue and releases non-esterifed fatty acids which are converted to ketone bodies in the liver through mitochondrial beta oxidation and ketogenesis [25], resulting in a metabolic condition resembling a prolonged fast [26]
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