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Abstract Wilsons disease (WD) is an inherited disorder that is characterized by abnormal copper metabolism, and treatment of this condition in the clinic focuses on promoting copper ion excretion

The human equivalent of approximately 35 micrograms represents a very safe dosage with profound behavioral effects, potentially through stress hormone and cytokine modulation

Albumin acts as a circulating depot, slowly releasing active peptide and extending the half-life from ~7 minutes (native GHRH) to 5.88.1 days

Hepatocyte growth factor promotes lymphatic vessel formation and function

doi: 10.1523/JNEUROSCI.0578-19.2019

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