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In addition, oral administration of CB in a diabetic mouse model has been proved to increase glucose tolerance and insulin sensitivity [101]
The dual agonist mechanism allows for simultaneous regulation of glucose metabolism and fat oxidation, leading to enhanced metabolic outcomes compared to single-target therapies2
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In fact, increased NOX activity and intracellular production of ROS were observed in subjects with psoriasis in conjunction with decreased TAC and increased TBARS [21]
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