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Loren Pickart estimated that toxic effects would begin at approximately 22,500 mg, which represents a 300-fold margin above effective therapeutic doses

These trigger systemic immune activation that manifests in the skin

The increase of intravascular mechanical stress and turbulence promotes the activation of uPA in endothelial cells and other cells

antioxidant and anti-inflammatory gene expression modulation

Emerging research suggests that DSIP may have analgesic properties, making it a potential option for pain management

Membrane-permeable C-terminal dopamine transporter peptides attenuate amphetamine-evoked dopamine release*,