Method for treating inflammation by administering a compound which binds LDL-receptor-related protein (LRP) ligand binding domain
The present invention relates to the field of therapeutic methods, compositions and uses thereof, that affect, directly or indirectly, the behavior of LRP receptors. These compositions and methods result in the treatment of inflammatory, immunological and metabolic conditions. More particularly, the methods and compositions of the invention are directed to the identification of small molecules, drugs and/or pharmacological agents that affect the Wnt pathway by affecting normal complex formation among various signaling receptors, the LRP5 and LRP6 receptor, and related ligands.
1. A method for treating inflammation in a subject, comprising the administration of a therapeutically effective amount of a compound to said subject, wherein said compound binds to an LDL-receptor-related protein (LRP) ligand binding domain, wherein the LRP is LRP-5 or LRP-6 and the ligand is selected from Dickkopf protein (Dkk) or sclerostm, and wherein said compound is a cyclic molecule or a heterocyclic organic molecule.
2. The method of claim 1 , wherein said inflammation is caused by an autoimmune disease or a chronic inflammatory disease.
3. The method of claim 2 , Wherein said inflammation is caused by Acute disseminated encephalomyelitis, Addison's disease, Ankylosing spondylitis, Antiphospholipid antibody syndrome, Aplastic anemia, Autoimmune hepatitis, Autoimmune Oophoritis, Coeliac disease, Crohn's disease, Diabetes mellitus, Gestational pemphigoid, Goodpasture's syndrome, Grave's disease, Guilian-Barre syndrome, Hashimoto's disease, Idiopathic thrombocytopenic purpura, Lupus erythematosus, Multiple sclerosis, Myasthenia gravis, Opsoclonus myoclonus syndrome, Optic neuritis, Ord's thyroiditis, Pemphigus, Pernicious anemia, Polyarthritis, Primary biliary cirrhosis, Rheumatoid arthritis, Reiter's syndrome, Sjogren's syndrome, Takayasu's arteritis, Warm autoimmune hemolytic anemia, or Wegener's granulomatosis.
4. The method of claim 2 , wherein said inflammation is caused by Tuberculosis, Chronic cholecystitis, Bronehiectasis, ulcerative colitis, silicosis or another pneumoconiosis disease.
5. The method of claim 1 , wherein said inflammation is caused by Crohn's disease or periodontitis.
6. The method of claim 1 , wherein said compound is:
7. A method of treating inflammation caused by Crohn's disease in a subject comprising administration of a therapeutically effective amount of a compound to the subject selected from
wherein said compound binds to an LDL-receptor-related protein (LRP) ligand binding domain, wherein the LRP is LRP-5 or LRP-6 and the ligand is selected from Dkk or sclerostin.