US2005222123A1PendingUtilityA1
Cholinesterase inhibitors for treating inflammation
Assignee: LONG ISLAND JEWISH RES INSTPriority: Jan 27, 2004Filed: Jan 27, 2005Published: Oct 6, 2005
Est. expiryJan 27, 2024(expired)· nominal 20-yr term from priority
A61P 37/06A61P 29/00A61P 31/00A61P 1/18A61P 1/02A61K 31/439A61K 31/00A61K 31/325A61P 11/06A61K 31/4747A61K 31/407A61K 31/55A61K 31/473A61K 31/50
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Claims
Claims
exact text as granted — not AI-modified1 . A method of treating a subject with a cytokine-mediated inflammatory disorder, comprising:
administering to the subject a pharmaceutically acceptable cholinesterase inhibitor in an amount sufficient to reduce the level of a proinflammatory cytokine, provided that the inhibitor is not galantamine.
2 . The method of claim 1 wherein the inflammatory disorder is asthma, sepsis, peritonitis, pancreatitis, reperfusion injury, endotoxic shock, cachexia, adult respiratory distress syndrome, allograft rejection, cystic fibrosis and graft-versus-host disease.
3 . The method of claim 2 wherein the inflammatory disorder is asthma, peritonitis, pancreatitis, reperfusion injury, endotoxic shock, cachexia, adult respiratory distress syndrome, myocardial ischemia, allograft rejection, cystic fibrosis and graft-versus-host disease.
4 . The method of claim 2 wherein the inflammatory disorder is sepsis.
5 . The method of claim 3 wherein the inflammatory disorder is asthma.
6 . The method of claim 3 wherein the inflammatory disorder is peritonitis.
7 . The method of claim 3 wherein the inflammatory disorder is pancreatitis.
8 . The method of claim 3 wherein the inflammatory disorder is reperfusion injury.
9 . The method of claim 3 wherein the inflammatory disorder is endotoxic shock.
10 . The method of claim 3 wherein the inflammatory disorder is cachexia.
11 . The method of claim 3 wherein the inflammatory disorder is adult respiratory distress syndrome.
12 . The method of claim 3 wherein the inflammatory disorder is myocardial ischemia.
13 . The method of claim 3 wherein the inflammatory disorder is allograft rejection.
14 . The method of claim 3 wherein the inflammatory disorder is cystic fibrosis.
15 . The method of claim 3 wherein the inflammatory disorder is graft-versus-host disease.
16 . The method of claim 2 wherein the cholinesterase inhibitor is tacrine, a tacrine analog, fasciculin, metrifonate, heptyl-physostigmine, norpyridostigmine, norneostigmine, huperzine A or an analogue thereof, physostigmine, heptyl-physostigmine, velnacrine, citicoline, donepizil, 7-methoxytacrine, eptastigmine, icopezil, ipidacrine, zifrosilone, anseculin, suronacrine, linopiridine, rivastigmine, neostigmine, edrophonium, demacarium, ambenonium, arecoline, xanomeline, subcomeline, cevimeline, alvameline, milameline, talsaclidine, or compounds of formulae (XVIII)-(XXI):
17 . The method of claim 2 wherein the cholinesterase inhibitor is tacrine, a tacrine analog, fasciculin, metrifonate, heptyl-physostigmine, norpyridostigmine, norneostigmine, physostigmine, heptyl-physostigmine, velnacrine, citicoline, donepizil, 7-methoxytacrine, eptastigmine, icopezil, ipidacrine, zifrosilone, anseculin, suronacrine, linopiridine, rivastigmine, neostigmine, edrophonium, demacarium, ambenonium, arecoline, xanomeline, subcomeline, cevimeline, alvameline, milameline, talsaclidine, or compounds of formulae (XVIII)-(XXI):
18 . The method of claim 5 wherein the cholinesterase inhibitor is at least 95% pure by weight.
19 . The method of claim 2 wherein the cholinesterase inhibitor is tacrine.
20 . The method of claim 2 wherein the cholinesterase inhibitor is huperzine A.
21 . The method of claim 2 wherein the cholinesterase inhibitor is neostigmine.
22 . The method of claim 2 wherein the cholinesterase inhibitor is physostigmine.
23 . A method of reducing proinflammatory cytokine levels in a subject in need of such reduction, comprising administering to the subject an effective amount of a pharmaceutically acceptable cholinesterase inhibitor, provided that the inhibitor is not galantamine.
24 . A method of treating a subject suffering from a disorder, comprising:
administering to the subject a therapeutically effective amount of pharmaceutically acceptable cholinesterase inhibitor, wherein the disorder is asthma, sepsis, peritonitis, pancreatitis, reperfusion injury, endotoxic shock, cachexia, adult respiratory distress syndrome, allograft rejection, cystic fibrosis or graft-versus-host disease, provided that the inhibitor is not galantamine.Join the waitlist — get patent alerts
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