Claims
- 1-34. (Canceled)
- 35. A method of measuring the level of lipid peroxidation in a mammal suspected of having an oxidant stress syndrome or disease, wherein said oxidant stress syndrome or disease is selected from the group consisting of Alzheimer's disease, Amyotropic Lateral Sclerosis, Down's syndrome, and Parkinson's disease, said method comprising
a) obtaining a first sample of a tissue or body fluid from said mammal; b) assessing the level of an isoprostane molecular marker for lipid peroxidation present in said first sample, wherein said isoprostane molecular marker is selected from the group consisting of iPF2α-III, iPF2α-VI, and 8,12-iso-iPF2α-VI; and c) comparing the level of said isoprostane molecular marker present in said first sample with the level of said isoprostane molecular marker present in a second sample of a tissue or body fluid obtained from an otherwise identical mammal which is not afflicted with an oxidant stress syndrome or disease, wherein an elevated level of said isoprostane molecular marker in said first sample relative to the level of said isoprostane molecular marker in said second sample, is indicative of an elevated level of lipid peroxidation in said mammal, thereby indicating the presence of an oxidant stress syndrome or disease in said mammal.
- 36. The method of claim 35, further comprising after a) and prior to b) isolating from said first sample said isoprostane molecular marker.
- 37. The method of claim 35, wherein said elevated level of lipid peroxidation comprises an elevated level of a reactive oxygen species (ROS).
- 38. The method of claim 35, wherein said elevated level of lipid peroxidation comprises an elevated level of inflammation.
- 39. The method of claim 38, wherein said elevated level of inflammation comprises elevated cyclooxygenase (COX) activity.
- 40. The method of claim 35, wherein said tissue is brain tissue.
- 41. The method of claim 40, wherein said brain tissue is selected from the group consisting of brain frontal pole tissue and brain temporal pole tissue.
- 42. The method of claim 35, wherein said body fluid is selected from the group consisting of cerebrospinal fluid (CSF), plasma and urine.
- 43. A method of diagnosing an oxidant stress syndrome or disease in a mammal, wherein said oxidant stress syndrome or disease is selected from the group consisting of Alzheimer's disease, Amyotropic Lateral Sclerosis, Down's syndrome, and Parkinson's disease, said method comprising
a) obtaining a first sample of a tissue or body fluid from said mammal; b) assessing the level of said isoprostane molecular marker present in said first sample, wherein said isoprostane molecular marker is selected from the group consisting of iPF2α-III, iPF2α-VI, and 8,12-iso-iPF2-VI; and c) comparing the level of said isoprostane molecular marker present in said first sample with the level of said isoprostane molecular marker present in a second sample of a tissue or body fluid obtained from an otherwise identical mammal which is not afflicted with an oxidant stress syndrome or disease, wherein an elevated level of said isoprostane molecular marker in said first sample relative to the level of said isoprostane molecular marker in said second sample, is indicative of an elevated level of lipid peroxidation in said mammal, thereby indicating the presence of an oxidant stress syndrome or disease in said mammal.
- 44. The method of claim 43, further comprising, after a) and before b) isolating from said first sample said isoprostane molecular marker.
- 45. A method of identifying a compound useful for reducing the level of an isoprostane molecular marker for lipid peroxidation said method comprising
a) measuring the level of an isoprostane molecular marker for lipid peroxidation in either a sample of a tissue or body fluid obtained from a first mammal prior to administering said compound, or, in a sample of a tissue or body fluid obtained from an otherwise identical second mammal which is not to be administered said compound; b) administering said compound to said first mammal; c) thereafter measuring the level of said isoprostane molecular marker in a tissue or body fluid obtained from said first mammal; and d) comparing the level of said isoprostane molecular marker in c) with the level of said isoprostane molecular marker measured in a), wherein when the level of said isoprostane molecular marker measured in c) is reduced relative to the level of said isoprostane molecular marker in a), a compound useful reducing the level of an isoprostane molecular marker for lipid peroxidation in a mammal is identified.
- 46. The method of claim 45, wherein said isoprostane molecular marker of lipid peroxidation is selected from the group consisting iPF2α-III, iPF2α-VI and 8,12-iso-iPF2α-VI.
- 47. The method of claim 45, wherein said tissue is brain tissue selected from the group consisting of brain frontal pole tissue and brain temporal pole tissue.
- 48. The method of claim 45, wherein said body fluid is selected from the group consisting of cerebrospinal fluid (CSF), plasma and urine.
- 49. A kit for diagnosing an oxidant stress syndrome or disease, wherein said oxidant stress syndrome or disease is selected from the group consisting of Alzheimer's disease, Amyotropic Lateral Sclerosis, Down's syndrome, and Parkinson's disease, said kit comprising
a) a sample container for carrying a tissue or body fluid sample from said mammal; b) a solution for use in extraction of an isoprostane molecular marker for lipid peroxidation from said tissue or body fluid sample obtained from said mammal; c) a negative control solution of said isoprostane molecular marker of lipid peroxidation present at a concentration of about the concentration of said isoprostane molecular marker present in a tissue or body fluid sample of a mammal which is not afflicted with an oxidant stress syndrome or disease, wherein said oxidant stress syndrome or disease is selected from the group consisting of Alzheimer's disease, Amyotropic Lateral Sclerosis, Down's syndrome, and Parkinson's disease; d) a positive control solution of said isoprostane molecular marker of lipid peroxidation present at a concentration of about the concentration of said isoprostane molecular marker in a tissue or body fluid sample of a mammal which is afflicted with an oxidant stress syndrome or disease, wherein said oxidant stress syndrome or disease is selected from the group consisting of Alzheimer's disease, Amyotropic Lateral Sclerosis, Down's syndrome, and Parkinson's disease; e) an antibody directed against an isoprostane molecular marker for lipid peroxidation; and f) an instructional material.
- 50. A kit for measuring the level of an isoprostane molecular marker for lipid peroxidation in a tissue or body fluid sample obtained from a mammal, said kit comprising
a) a sample container for carrying a tissue or body fluid sample from said mammal; b) a solution for use in extraction of an isoprostane molecular marker of lipid peroxidation from said tissue or body fluid sample obtained from said mammal; c) a negative control solution of said isoprostane molecular marker of lipid peroxidation present at a concentration of about the concentration of said isoprostane molecular marker present in a tissue or body fluid sample of a mammal which is not afflicted with an oxidant stress syndrome or disease, wherein said oxidant stress syndrome or disease is selected from the group consisting of Alzheimer's disease, Amyotropic Lateral Sclerosis, Down's syndrome, and Parkinson's disease; d) a positive control solution of said isoprostane molecular marker of lipid peroxidation present at a concentration of about the concentration of said isoprostane molecular marker in a tissue or body fluid sample of a mammal which is afflicted with an oxidant stress syndrome or disease, wherein said oxidant stress syndrome or disease is selected from the group consisting of Alzheimer's disease, Amyotropic Lateral Sclerosis, Down's syndrome, and Parkinson's disease; e) an antibody directed against an isoprostane molecular marker for lipid peroxidation; and f) an instructional material.
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is entitled to priority pursuant to 35 U.S.C. §119(e) to U.S. Provisional Patent Application No. 60/110,569, which was filed on Dec. 2, 1998.
STATEMENT REGARDING FEDERALLY SUPPORTED RESEARCH AND DEVELOPMENT
[0002] This invention was supported in part by U.S. Government funds (NIH Grant Nos. HL 5400, AG-09215 and AG-10124), and the U.S. Government may therefore have certain rights in the invention.
Provisional Applications (1)
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Number |
Date |
Country |
|
60110569 |
Dec 1998 |
US |
Continuations (2)
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Number |
Date |
Country |
Parent |
09870762 |
May 2001 |
US |
Child |
10831935 |
Apr 2004 |
US |
Parent |
PCT/US99/28583 |
Dec 1999 |
US |
Child |
09870762 |
May 2001 |
US |