Renal selective inhibition of cytochrome P450 3A5
AssigneeOregon State University
InventorsPatrick L. Iversen, Andrew J. Annalora
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AssigneeOregon State University
InventorsPatrick L. Iversen, Andrew J. Annalora
Estimating the term…
Compositions and methods for treating hypertension in a subject are provided, including administering an antisense oligomer effective to reduce expression of cytochrome P450 3A5 (CYP3A5) enzyme. The antisense oligomer includes phosphorodiamidate morpholino oligonucleotide (PMO), phosphorothioate 2′-O-methyl oligoribonucleotides (PSO), locked nucleic acid nucleotide, locked nucleic acid analog nucleotide, or another modified oligonucleotide backbone or nuclease-resistant backbone. The antisense oligomer is administered transdermally, subcutaneously, or orally, and optionally with a pharmaceutically acceptable carrier. In one embodiment, the antisense oligomer is an oligomer that is antisense to mRNAs that encode CYP3A5, for instance targeted at the AUG start site of the mRNAs that encode CYP3A5 or at a G4 structure within CYP3A5.
A method of treating hypertension in a subject, comprising administering to a subject with elevated systolic blood pressure (SBP), a non-naturally occurring antisense oligomer specifically targeted to cytochrome CYP3A5 mRNA and effective to reduce expression of cytochrome CYP3A5 enzyme.
A method of treating hypertension in a subject, comprising administering to the subject a non-naturally occurring antisense oligomer specifically targeted to cytochrome CYP3A5 mRNA and effective to reduce expression of cytochrome CYP3A5 enzyme, wherein the subject has a systolic blood pressure of greater than 140 mm Hg, a diastolic blood pressure of greater than 90 mm Hg, and a homozygous CYP3A5*1/*1 genotype, thereby treating hypertension in the subject.
Dependencies are inferred from the claim text.