Compositions and methods for inhibiting expression of Nav1.8 gene
View Patent ↗The invention relates to a double-stranded ribonucleic acid (dsRNA) for inhibiting the expression of the Nav1.8 gene (Nav1.8 gene), comprising an antisense strand having a nucleotide sequence which is less that 25 nucleotides in length and which is substantially complementary to at least a part of the Nav1.8 gene. The invention also relates to a pharmaceutical composition comprising the dsRNA together with a pharmaceutically acceptable carrier; methods for treating diseases caused by the expression of the Nav1.8 gene using the pharmaceutical composition; and methods for inhibiting the expression of the Nav1.8 gene gene in a cell.
1. A double-stranded ribonucleic acid (dsRNA) for inhibiting the expression of a human Nav1.8 gene in a cell, wherein said dsRNA comprises a sense strand and an antisense strand, wherein said sense strand and said antisense strand are between 19 and 24 nucleotides in length, and wherein said antisense strand is complementary to at least 19 nucleotides of an mRNA encoding Nav1.8, and wherein said sense strand comprises at least 18 contiguous nucleotides of SEQ ID NO: 59 and wherein said antisense strand comprises at least 18 contiguous nucleotides of SEQ ID NO:60, and wherein said dsRNA, upon contact with a cell expressing said Nav1.8, inhibits expression of said Nav1.8 gene by at least 20%.
2. The dsRNA of claim 1 , wherein said sense strand and said antisense strand each comprise a pair of deoxythymidine residues at their 3′ ends, wherein each pair of deoxythymidine residues comprises a phosphorothioate linkage.
3. The dsRNA of claim 2 , wherein said sense strand consists of SEQ ID NO:59.
4. The dsRNA of claim 2 , wherein said antisense strand consists of SEQ ID NO:60.
5. The dsRNA of claim 2 , wherein said sense strand consists of SEQ ID NO:59 and wherein said antisense strand consists of SEQ ID NO: 60.
6. A cell comprising the dsRNA of any of claims 1 - 5 .
7. A pharmaceutical composition for inhibiting the expression of the Nav1.8 gene in an organism, comprising a dsRNA and a pharmaceutically acceptable carrier, wherein the dsRNA comprises a sense strand and an antisense strand, wherein said sense strand and said antisense strand are between 19 and 24 nucleotides in length, and wherein said antisense strand is complementary to at least 19 nucleotides of an mRNA encoding Nav1.8, and wherein said sense strand comprises at least 18 contiguous nucleotides of SEQ ID NO: 59 and wherein said antisense strand comprises at least 18 contiguous nucleotides of SEQ ID NO:60, and wherein said dsRNA, upon contact with a cell expressing said Nav1.8, inhibits expression of said Nav1.8 gene by at least 20%.
8. A pharmaceutical composition for inhibiting the expression of the Nav1.8 gene in an organism, comprising a dsRNA and a pharmaceutically acceptable carrier, wherein said dsRNA is a dsRNA of any of claims 2 - 5 .
9. The pharmaceutical composition of claim 7 , wherein said composition is formulated for administration selected from the group consisting of intrathecal infusion or injection, or intravenous infusion or injection.
10. A method for inhibiting the expression of the Nav1.8 gene in a cell, the method comprising:
(a) introducing into the cell a double-stranded ribonucleic acid (dsRNA), wherein the dsRNA comprises a sense strand and an antisense strand, wherein said sense strand and said antisense strand are between 19 and 24 nucleotides in length, and wherein said antisense strand is complementary to at least 19 nucleotides of an mRNA encoding Nav1.8, and wherein said sense strand comprises at least 18 contiguous nucleotides of SEQ ID NO: 59 and wherein said antisense strand comprises at least 18 contiguous nucleotides of SEQ ID NO:60, and wherein said dsRNA, upon contact with a cell expressing said Nav1.8, inhibits expression of said Nav1.8 gene by at least 20%; and
(b) maintaining the cell produced in step (a) for a time sufficient to obtain degradation of the mRNA transcript of the Nav1.8 gene, thereby inhibiting expression of the Nav1.8 gene in the cell.
11. The method of claim 10 , wherein said sense strand and said antisense strand each comprise a pair of deoxythymidine residues at their 3′ ends, wherein each pair of deoxythymidine residues comprises a phosphorothioate linkage.