USE OF OXYGENATED CHOLESTEROL SULFATES FOR TREATING INFLAMMATORY CONDITIONS
Aspects of the present disclosure include methods for treating at least one inflammatory condition, such as at least one of dental pulp inflammation, periodontal disease, skin inflammation, psoriasis, ulcerative colitis, osteoarthritis, inflammatory bowel disease (IBD), Crohn's disease, irritable bowel syndrome (IBS), Alzheimer's disease, Parkinson's disease, pancreatitis (acute and/or chronic), hepatitis (viral and/or non-viral), atherosclerosis, myocarditis, idiopathic pulmonary disorder (IPD), chronic obstructive pulmonary disorder (COPD), pneumonia, chronic inflammatory lung disease, bronchitis, asthma, chronic kidney disease (CKD), nephritis, sepsis, ankylosing spondylitis, diverticulitis, and fibromyalgia. In some cases, the at least one inflammatory condition is associated with Epstein-Ban virus infection. In practicing the subject methods, an effective amount of at least one compound selected from 25-hydroxycholesterol-3-sulfate (25HC3S), 25-hydroxycholesterol-disulfate (25HCDS), 27-hydroxycholesterol-3-sulfate (27HC3S), 27-hydroxycholesterol-disulfate (27HCDS), 24-hydroxycholesterol-3-sulfate (24HC3S), 24-hydroxycholesterol-disulfate (24HCDS), and 24,25-epoxycholesterol-3-sulfate, or salt thereof is administered to the subject.
1 . A method of treating at least one inflammatory condition in a subject in need thereof, comprising:
administering to the subject an effective amount of at least one compound selected from 25-hydroxycholesterol-3-sulfate (25HC3S), 25-hydroxycholesterol-disulfate (25HCDS), 27-hydroxycholesterol-3-sulfate (27HC3S), 27-hydroxycholesterol-disulfate (27HCDS), 24-hydroxycholesterol-3-sulfate (24HC3S), 24-hydroxycholesterol-disulfate (24HCDS), and 24,25-epoxycholesterol-3-sulfate, or salt thereof,
wherein the at least one inflammatory condition is optionally associated with Epstein-Barr virus infection.
2 . The method of claim 1 , wherein the at least one inflammatory condition is associated with Epstein-Barr virus infection.
3 . The method of claim 1 , wherein the at least one inflammatory condition comprises at least one of dental pulp inflammation, periodontal disease, skin inflammation, psoriasis, ulcerative colitis, osteoarthritis, inflammatory bowel disease (IBD), Crohn's disease, irritable bowel syndrome (IBS), Alzheimer's disease, Parkinson's disease, pancreatitis (acute and/or chronic), hepatitis (viral and/or non-viral), atherosclerosis, myocarditis, idiopathic pulmonary disorder (IPD), chronic obstructive pulmonary disorder (COPD), pneumonia, chronic inflammatory lung disease, bronchitis, asthma, chronic kidney disease (CKD), nephritis, sepsis, ankylosing spondylitis, diverticulitis, and fibromyalgia.
4 . The method of claim 1 , wherein the at least one inflammatory condition comprises psoriasis associated with Epstein-Barr virus infection.
5 . The method of claim 1 , wherein the method comprises administering to the subject an effective amount of 25-hydroxycholesterol-3-sulfate (25HC3 S) or salt thereof.
6 . The method of claim 1 , wherein the at least one compound is administered in an amount selected from the group consisting of:
(a) an amount ranging from 0.001 mg/kg/day to 100 mg/kg/day;
(b) an amount ranging from 0.1 mg/kg to 100 mg/kg, based on body mass of the subject; and
(c) an amount ranging from 1 mg/kg to 10 mg/kg, based on body mass of the subject.
7 . The method of claim 1 , wherein the administering is performed from once to 3 times per day.
8 . The method of claim 1 , wherein the administering comprises at least one of oral administration, enteric administration, sublingual administration, transdermal administration, intravenous administration, peritoneal administration, parenteral administration, administration by injection, subcutaneous injection, and intramuscular injection.
9 . The method of claim 1 , wherein the administering comprises administering a pharmaceutical composition comprising the at least one compound and a physiologically acceptable excipient, diluent, or carrier.
10 . The method of claim 9 , wherein the pharmaceutical composition is formulated in unit dosage form.
11 . The method of claim 9 , wherein the pharmaceutical composition is in solid form.
12 . The method of claim 9 , wherein the pharmaceutical composition: (a) is in the form of a powder, a tablet, a capsule, or a lozenge; and/or (b) comprises the at least one compound in freeze-dried form together with a bulking agent.
13 . The method of claim 9 , wherein the pharmaceutical composition comprises a carrier that is a liquid.
14 . The method of claim 13 , wherein the at least one compound is solubilized in the liquid or dispersed in the liquid.
15 . The method of claim 13 , wherein: (a) the liquid is aqueous; or (b) the liquid is sterile water for injections or phosphate-buffered saline.
16 . The method of claim 9 , wherein the pharmaceutical composition is in a sealed vial, ampoule, syringe, or bag.