TRPA1 and TRPV4 inhibitors and methods of using the same for organ-specific inflammation and itch
Provided are methods of treating and/or preventing dermatological disorders. Provided are methods of reducing skin inflammation, reducing pain, and/or reducing itch in a subject in need thereof. The methods may include administering to the subject an effective amount of a TRPA1 and/or TRPV4 inhibitor. Further provided are compositions including a TRPA1 and/or TRPV4 inhibitor compound in combination with a carrier, vehicle, or diluent that is suitable for topical application.
1. A method of reducing periostin release from keratinocytes in a subject in need thereof, the method comprising administering to the subject an effective amount of a TRPV4 and TRPA1 inhibitor, wherein the TRPV4 and TRPA1 inhibitor is according to Formula I:
wherein A, B, and C are independently selected from aromatic, heteroaromatic, cycloalkenyl, and heterocycloalkenyl groups;
D is C 1 -C 3 alkylene;
E is a bond, or C 1 -C 2 alkylene; and
R is selected from hydrogen, hydroxyl, amino, alkyl, alkenyl, heteroalkyl, aromatic ring, or heteroaromatic ring, and
wherein periostin release from keratinocytes in the subject is inhibited upon administration of the TRPV4 and TRPA1 inhibitor.
2. The method of claim 1 , wherein the inhibitor does not inhibit TRPV1, TRPV2, or TRPV3.
3. The method of claim 1 , wherein the TRPV4 and TRPA1 inhibitor is selected from the following:
or any combination thereof.
4. The method of claim 1 , wherein B is phenyl.
5. The method of claim 1 , wherein C is phenyl.
6. The method of claim 1 , wherein B is phenyl and C is phenyl.
7. The method of claim 1 , wherein A is selected from phenyl and pyridine.
8. The method of claim 1 , wherein R is selected from hydrogen, hydroxyl, amino, alkyl, and alkenyl.
9. The method of claim 1 , wherein R is selected from hydrogen and alkyl.
10. The method of claim 1 , wherein D is C 1 alkylene.
11. The method of claim 1 , wherein E is C 1 alkylene.
12. The method of claim 1 , wherein E is C 2 alkylene.
13. The method of claim 1 , wherein administration of the TRPV4 and TRPA1 inhibitor to the subject thereby treats a fibrotic skin disease in the subject, and wherein the fibrotic skin disease comprises at least one disorder or condition selected from scleroderma, scar formation, keloid formation, atopic dermatitis, and skin fibrosis.
14. The method of claim 1 , wherein administration of the TRPV4 and TRPA1 inhibitor to the subject thereby treats a fibrotic skin disease in the subject, and wherein the fibrotic skin disease comprises at least one disorder or condition selected from keloid formation, chemical or actinic injury, a pathologic response to skin irradiation (“radio-derm”), psoriasis, chronic atopic dermatitis, chronic UV-dermatitis, scleroderma, conditions characterized by a chronic maladaptive injury response to an ongoing noxious insult to the skin, and scar formation.
15. A method of reducing periostin release from keratinocytes in a subject in need thereof, the method comprising administering to the subject an effective amount of a TRPV4 and TRPA1 inhibitor, wherein the TRPV4 and TRPA1 inhibitor is according to the below:
and
wherein periostin release from keratinocytes in the subject is inhibited upon administration of the TRPV4 and TRPA1 inhibitor.
16. The method of claim 15 , wherein the inhibitor does not inhibit TRPV1, TRPV2, or TRPV3.