The ultimate goal of this project is to establish the laboratory opossum, Monodelphis domestica, as a unique model for determining the effects of diet and genotype on lipoprotein phenotypes and development of atherosclerosis. In conjunction with Project 5 and 6 Project 4 will help identify specific genes that control dietary responsiveness and ascertain their mechanisms of action. We will study a total of 350 opossums derived from different genetic stocks; high responders to saturated fat and cholesterol diet, low responders to the same diet, and two other previously uncharacterized genetic stocks. All animals will be bled while feeding the basal maintenance diet and 8, 16 and 24 weeks after feeding one of five diets differing in amounts and types of fat and in cholesterol levels. The first specific aim is to determine lipoprotein phenotypes in plasma samples taken from each animal while consuming the basal diet, and periodically during 24 weeks while consuming one of the challenge diets. Lipoprotein phenotypes will be total cholesterol determined using nondenaturing gradient gel electrophoresis. The results will enable us to determine whether, for some stocks but not others, significant changes in lipoprotein phenotypes are attributable to increases in either of two types of fat (polyunsaturated and saturated) or in cholesterol. The second specific aim is to measure extent and severity of atherosclerotic lesions in all animals and to determine their relationship with time-weighted or aggregate lipoprotein phenotypes. Animals will necropsied after the last (24 week) blood sampling in order to quantify atherosclerotic lesions. The results will enable us to determine whether aspects of lipoprotein phenotypes (including cholesterol levels and particle sizes for the two major types of lipoprotein, very low density plus low density lipoprotein and high density lipoprotein) are associated with extent and severity of lesions. Previous results indicating genetic control of responder phenotype and of high density lipoprotein levels suggest the exciting potential of the opossum model in determining genetic and environmental factors relevant to cardiovascular disease.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Research Program Projects (P01)
Project #
5P01RR009919-02
Application #
3745099
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Southwest Foundation for Biomedical Research
Department
Type
DUNS #
City
San Antonio
State
TX
Country
United States
Zip Code
78245
Kammerer, Candace M; Rainwater, David L; Gouin, Nicolas et al. (2010) Localization of genes for V+LDL plasma cholesterol levels on two diets in the opossum Monodelphis domestica. J Lipid Res 51:2929-39
Samollow, Paul B; Kammerer, Candace M; Mahaney, Susan M et al. (2004) First-generation linkage map of the gray, short-tailed opossum, Monodelphis domestica, reveals genome-wide reduction in female recombination rates. Genetics 166:307-29
Wang, Z; Atencio, J; Robinson, E S et al. (2001) Ultraviolet B-induced melanoma in Monodelphis domestica occurs in the absence of alterations in the structure or expression of the p53 gene. Melanoma Res 11:239-45
Chan, J; Robinson, E S; Atencio, J et al. (2001) Characterization of the CDKN2A and ARF genes in UV-induced melanocytic hyperplasias and melanomas of an opossum (Monodelphis domestica). Mol Carcinog 31:16-26
Robinson, E S; Hill Jr, R H; Kripke, M L et al. (2000) The Monodelphis melanoma model: initial report on large ultraviolet A exposures of suckling young. Photochem Photobiol 71:743-6
Stone, W H; Brunn, D A; Foster, E B et al. (1998) Absence of a significant mixed lymphocyte reaction in a marsupial (Monodelphis domestica). Lab Anim Sci 48:184-9
Robinson, E S; Dooley, T P; Williams, K L (1998) UV-induced melanoma cell lines and their potential for proteome analysis: a review. J Exp Zool 282:48-53
Rainwater, D L (1998) Electrophoretic separation of LDL and HDL subclasses. Methods Mol Biol 110:137-51
Robinson, E S; Hubbard, G B; Colon, G et al. (1998) Low-dose ultraviolet exposure early in development can lead to widespread melanoma in the opossum model. Int J Exp Pathol 79:235-44
Sokolova, O V; van Oorschot, R A; VandeBerg, J L (1997) Aldolase C polymorphism in the laboratory opossum, Monodelphis domestica. Anim Genet 28:358-9

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