This application is focussed on bombesin receptors in frog and in rat. Four mammalian bombesin receptors have been identified; one binds gastrin-releasing peptide (GRP) with highest affinity, another binds neuromedin B (NMB) with highest affinity, the third is an orphan receptor which binds the known bombesin-like peptides with low affinity, and the fourth has recently been isolated by the applicant. In addition, there is evidence that at least one additional form, and possibly several additional forms, of the bombesin receptor exists; these additional forms are highly related to the recently identified fourth receptor form. The studies proposed in this application will further characterize the forms of the bombesin receptors in both frog and rat. cDNA clones will be expressed in cell lines and in Xenopus oocytes and the properties of the receptors determined. Existing peptides will be tested as agonists and antagonists for the various receptor forms. Finally, these agonists and antagonists will be injected into rats and the effects of several behaviors will be examined, with a focus on body temperature and grooming. These studies will provide a better understanding of the physiological function of the various bombesin receptors.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
7R01NS035580-04
Application #
6096044
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Program Officer
Kitt, Cheryl A
Project Start
1996-09-01
Project End
2001-07-31
Budget Start
1999-08-01
Budget End
2001-07-31
Support Year
4
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Oregon Health and Science University
Department
Type
Other Domestic Higher Education
DUNS #
009584210
City
Portland
State
OR
Country
United States
Zip Code
97239
Katsuno, T; Pradhan, T K; Ryan, R R et al. (1999) Pharmacology and cell biology of the bombesin receptor subtype 4 (BB4-R). Biochemistry 38:7307-20
Leng, N; Gu, G; Simerly, R B et al. (1999) Molecular cloning and characterization of two putative G protein-coupled receptors which are highly expressed in the central nervous system. Brain Res Mol Brain Res 69:73-83