Method Of Treating Or Preventing Pathologic Effects Of Acute Increases In Hyperglycemia And/Or Acute Increases Of Free Fatty Acid Flux

Abstract

One aspect of the present invention relates to a method of treating or preventing pathologic sequelae of acute hyperglycemia and / or increased fatty acid flux in a subject. This method involves administering an ROS inhibitor to the subject. In addition, methods of promoting neovascularization, inhibiting oxidation or excessive release of free fatty acids, and identifying compounds suitable for treatment or prevention of ROS-mediated injury are also disclosed.

Description

[0001]This application claims the benefit of U.S. Provisional Patent Application Ser. No. 60 / 573,947, filed May 24, 2004.FIELD OF THE INVENTION[0002]The present invention relates to a method of treating or preventing pathologic effects of acute increases in hyperglycemia and / or acute increases of fatty acid flux in a subject.BACKGROUND OF THE INVENTION[0003]Cardiovascular Complications Associated with Diabetes are a Major Public Health Problem.[0004]Diabetes mellitus is an epidemic in the United States (Brownlee, “Biochemistry and Molecular Cell Biology of Diabetic Complications,”Nature 414:813-20 (2001); Nishikawa et al., “Normalizing Mitochondrial Superoxide Production Blocks Three Pathways of Hyperglycaemic Damage,”Nature 404:787-90 (2000); Zimmet et al., “Global and Societal Implications of the Diabetes Epidemic,”Nature 414:782-7 (2001)). Currently 15-17 million adults (5% of the adult population) in the U.S. are affected by Type I and Type II diabetes (Harris et al., “Prevalenc...

AI Technical Summary

Benefits of technology

The patent is about a way to help patients with metabolic disorders who have poor blood flow in their limbs and organs. This can reduce the risk of amputation and save lives by preventing damage to the heart and brain. It can also help people with diabetic foot ulcers, which currently have no effective medical treatment.

Problems solved by technology

Moreover, revascularization via coronary angioplasty, coronary artery bypass surgery, or lower extremity revascularization has a significantly lower success rate in diabetic patients even in the presence of a patient bypass conduit, suggesting the existence of a defect at the microcirculatory level (Kip et al., “Coronary Angioplasty in Diabetic Patients.

Given that VEGF production is impaired in diabetes mellitus, it seems likely that various aspects of vasculogenesis, including EPC mobilization, may also be impaired.

The retina is often characterized by excessive angiogenesis, while skin, muscle, and nerves in diabetic patients suffer from a paucity of new vessel formation.

This so-called “diabetic paradox,” by which the diabetic phenotype exhibits both excessive and impaired new blood vessel formation in different tissues, leads to different types of complications.

Intracellular elevations in glucose increase flux of metabolites through glycolysis and the Kreb's cycle, resulting in overproduction of ROS by the mitochondria.

Hyperglycemia-induced reactive oxygen species impair the ability of HIF-1α to mediate appropriate upregulation of VEGF and the chemokine SDF-1 that are required for neovascularization in ischemic settings.

This impairment also affects hypoxia-specific functions of vascular effector cells.

This results in impaired angiogenesis, vasculogenesis, and diminished tissue survival in diabetic states.

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