Human G protein-coupled receptor and modulators thereof for the treatment of cell death-related disorders

Bibliographic Details
Title: Human G protein-coupled receptor and modulators thereof for the treatment of cell death-related disorders
Patent Number: 7,776,558
Publication Date: August 17, 2010
Appl. No: 10/549228
Application Filed: March 15, 2004
Abstract: The present invention relates to methods of identifying whether a candidate compound is a modulator of a G protein-coupled receptor (GPCR). In certain embodiments, the GPCR is human. In certain embodiments, the GPCR is expressed endogenously by neuronal cells or muscle cells. In certain embodiments, the GPCR is neuroprotective or myoprotective. In certain embodiments, the GPCR is a Humanin receptor. The present invention also relates to methods of using a modulator of the GPCR. A preferred modulator is agonist. Agonists of the invention are useful as therapeutic agents for the prevention or treatment of neurodegenerative diseases in general, including Alzheimer's disease, Parkinson's disease, prion-associated disease, stroke and motor-neuron disease in particular, peripheral neuropathy, cerebral amyloid beta-protein angiopathy, and ischemic heart disease, including myocardial infarction and congestive heart failure.
Inventors: Villegas, Sonia (San Diego, CA, US); Kelner, Gregory S. (San Diego, CA, US); Unett, David J. (San Diego, CA, US); Gatlin, Joel (San Diego, CA, US)
Assignees: Arena Pharmaceuticals, Inc. (San Diego, CA, US)
Claim: 1. A method comprising: (a) contacting a candidate compound with a G protein-coupled receptor (GPCR) comprising an amino acid sequence having at least 90% identity to SEQ ID NO:2, wherein said GPCR is present on a cell or isolated membrane thereof; (b) determining the ability of the compound to inhibit or stimulate the GPCR; and (c) determining if said compound modulates neuronal cell death.
Claim: 2. The method of claim 1 , wherein said determining element (c) comprises contacting said compound with a neuron and determining if said compound modulates serum deprivation-induced neuronal cell death, Aβ-induced neuronal cell death or hypoxia/reoxygenation-induced neuronal cell death.
Claim: 3. The method of claim 1 , wherein element (c) comprises administering said compound to a mammal.
Claim: 4. The method of claim 3 , wherein element (c) comprises assaying said mammal for an effect on learning or memory.
Claim: 5. The method of claim 3 , wherein element (c) comprises assaying said compound for a neuroprotective activity.
Claim: 6. The method of claim 3 , wherein said mammal has a neuronal disorder.
Claim: 7. The method of claim 1 , wherein said determining element (b) comprises measuring a second messenger.
Claim: 8. The method of claim 1 , wherein said determining element (b) comprises measuring expression of a reporter.
Claim: 9. The method of claim 1 , wherein said GPCR comprises an amino acid sequence having at least 95% identity to SEQ ID NO:2.
Claim: 10. The method of claim 1 , wherein said GPCR is recombinant.
Claim: 11. The method of claim 1 , wherein said GPCR binds Humanin.
Claim: 12. The method of claim 1 , further comprising admixing said compound with a pharmaceutically acceptable carrier to produce a pharmaceutical composition.
Claim: 13. The method of claim 12 , wherein said method further comprises administering said pharmaceutical composition to a mammal having a neuronal disorder.
Claim: 14. A method comprising: (a) contacting a compound with a G protein-coupled receptor comprising an amino acid sequence having at least 90% identity to SEQ ID NO:2, wherein said G protein-coupled receptor is present on a cell or isolated membrane thereof; (b) determining the ability of the compound to bind to said G protein-coupled receptor; and (c) determining if said compound modulates neuronal cell death.
Claim: 15. A method comprising: (a) contacting a candidate compound with a G protein-coupled receptor (GPCR) comprising an amino acid sequence having at least 90% identical to SEQ ID NO:2, wherein said GPCR is present on a cell or isolated membrane thereof; (b) determining the ability of the compound to inhibit or stimulate the GPCR; and (c) determining if said compound modulates muscle cell death.
Current U.S. Class: 435/721
Patent References Cited: 1514930 March 2005
WO 02/068600 September 2002
WO 03/046205 June 2003
WO 03/080098 October 2003
WO 03/106683 December 2003
WO 2004/008141 January 2004






























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Primary Examiner: Ulm, John D
Attorney, Agent or Firm: Keddie, James S.
Francis, Carol L.
Bozicevic, Field & Francis LLP
Accession Number: edspgr.07776558
Database: USPTO Patent Grants
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Language:English