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A veces tambin se inyectan pptidos de cobre para un aporte ms directo al organismo

Mutations in genes encoding transporters and channels found in the DCT are associated with several diseases in humans including Bartter syndrome, Gitelman syndrome, familial hyperkalemic hypertension, EAST syndrome ( E pilepsy, A taxia, S ensorineural deafness, and salt-wasting renal T ubulopathy), and hereditary hypomagnesemias

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Gabapentin reduces painful bladder hypersensitivity in rats with lipopolysaccharideinduced chronic cystitis

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Diindolylmethane, a naturally occurring compound, induces CYP3A4 and MDR1 gene expression by activating human PXR