ENHANCED MEDICAL TREATMENTS RESULTING FROM CHEMICAL IDENTIFICATION OF CALCIUM INFLUX FACTOR, IDENTITY WITH THE FACTOR ACTIVATING PHOSPHOLIPOLYSIS AND PRECIPITATING SUDDEN DEATH DURING MYOCARDIAL INFARCTION, AND DETERMINATION OF SIMILAR ACTIVATING MECHANISMS IN MULTIPLE CELL TYPES THROUGH DISINHIBITION OF CALCIUM-INDEPENDENT PHOSPHOLIPASE A2beta

a technology of calcium influx factor and chemical identification, applied in the field of biomarker screening, can solve the problems of serious life-threatening, poorly understood biochemical mechanisms underlying metabolic syndrome and its end-organ sequelae, and inability to detect the presence of a single molecule in the body,

Inactive Publication Date: 2007-11-15
WASHINGTON UNIV IN SAINT LOUIS
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  • Abstract
  • Description
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Problems solved by technology

Despite the enormous proportions of this public health problem, the biochemical mechanisms underlying the metabolic syndrome and its end-organ sequelae are poorly understood.
However, when glucose builds up in the blood instead of going into cells (e.g., insulin resistance), it can cause serious life threatening problems which results in type 2 diabetes.
In this condition the body does not

Method used

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  • ENHANCED MEDICAL TREATMENTS RESULTING FROM CHEMICAL IDENTIFICATION OF CALCIUM INFLUX FACTOR, IDENTITY WITH THE FACTOR ACTIVATING PHOSPHOLIPOLYSIS AND PRECIPITATING SUDDEN DEATH DURING MYOCARDIAL INFARCTION, AND DETERMINATION OF SIMILAR ACTIVATING MECHANISMS IN MULTIPLE CELL TYPES THROUGH DISINHIBITION OF CALCIUM-INDEPENDENT PHOSPHOLIPASE A2beta
  • ENHANCED MEDICAL TREATMENTS RESULTING FROM CHEMICAL IDENTIFICATION OF CALCIUM INFLUX FACTOR, IDENTITY WITH THE FACTOR ACTIVATING PHOSPHOLIPOLYSIS AND PRECIPITATING SUDDEN DEATH DURING MYOCARDIAL INFARCTION, AND DETERMINATION OF SIMILAR ACTIVATING MECHANISMS IN MULTIPLE CELL TYPES THROUGH DISINHIBITION OF CALCIUM-INDEPENDENT PHOSPHOLIPASE A2beta
  • ENHANCED MEDICAL TREATMENTS RESULTING FROM CHEMICAL IDENTIFICATION OF CALCIUM INFLUX FACTOR, IDENTITY WITH THE FACTOR ACTIVATING PHOSPHOLIPOLYSIS AND PRECIPITATING SUDDEN DEATH DURING MYOCARDIAL INFARCTION, AND DETERMINATION OF SIMILAR ACTIVATING MECHANISMS IN MULTIPLE CELL TYPES THROUGH DISINHIBITION OF CALCIUM-INDEPENDENT PHOSPHOLIPASE A2beta

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[0080] Materials—[1-14C]-palmitoyl-CoA and [1-14C]-oleoyl-CoA, and 1-palmitoyl-2-[1-14C]-oleoyl-sn-glycero-3-phosphocholine were obtained from Perkin-Elmer. [1-14C]-Arachidonoyl-CoA, [1-14C]-myristoyl-CoA, [1-14C]-stearoyl-CoA, and [methyl-14C] human albumin were obtained from American Radiolabeled Chemicals. 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) and 1,2-dioleoyl-sn-glycero-3-[phospho-L-serine] (DOPS) were purchased from Avanti Polar Lipids. 2-decanoyl-1-(O-(11-(4,4-difluoro-5,7-dimethyl-4-bora-3α,4α-diaza-s-indacene-3-propionyl)amino)undecyl)-sn-glycero3phosphocholine (BODIPY-PC) was purchased from Invitogen. High purity bovine calmodulin was obtained from Calbiochem. Most other materials were obtained from either Sigma or Fisher Scientific. BEL was purchased from Cayman Chemical and separated into individual enantiomers as described previously (62).

[0081] Expression and Affinity Purification of iPLA2β(His)6 from Sf9 Cells—Following infection of 3×100 ml cultures...

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Abstract

A method for treating a mammal comprises administering at least one of a gene, enzyme and pharmaceutical which modulates the concentration of iPLA2β through transcriptional and/or translational regulation or effectively modulate the inhibition of iPLA2β through calmodulin or derivatives thereof.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS [0001] This application claims the priority of U.S. Provisional Patent Application Ser. No. 60 / 723,685 filed Oct. 5, 2005, which is hereby incorporated by referenced in its entirety.STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH AND DEVELOPMENT [0002] This invention was made under contracts NIH 5P01HL57278 and NIH 5R01HL41250. The government has certain rights in the invention.BACKGROUND OF THE INVENTION [0003] This invention relates generally to biomarker screening and more particularly to identifying new targets for pharmacological inhibition. [0004] This invention also relates generally to analytical (assays) methods for identifying compounds useful for promoting health in living mammalian systems. In particular this invention relates to assays and analytical tools for monitoring health in living mammals. [0005] The function of complex living biological organisms relies on the meticulous control of cellular activity, including close regul...

Claims

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Application Information

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IPC IPC(8): A61K38/43A61K31/7052A61P3/04A61P9/12A61P9/00A61K38/16
CPCA61K31/7052A61P3/04A61P9/00A61P9/12
Inventor GROSS, RICHARD W.JENKINS, CHRISTOPHER
Owner WASHINGTON UNIV IN SAINT LOUIS
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