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Results The disruption of D2R-DAT stimulates locomotor activity As aforementioned, we developed an interfering peptide (TAT-DAT NT ) to disrupt the interaction between DAT and D2R, which can increase locomotor activity in mice [25]

Most of the biologically active T 3 in the circulation and inside cells is generated by the removal of one iodine atom from T 4 in a reaction catalyzed by selenium-dependent iodothyronine deiodinase enzymes

Copper ions enhance the potency of this tripeptide, making GHK-Cu more bioactive than Pal-GHK [11]

These properties have drawn the attention of clinicians and scientists worldwide, leading to the development of therapeutic peptides [16]