Claims
- 1. A method for identifying an agent that inhibits an FATP1 activity comprising:
a) optionally inducing insulin resistance in a non-human mammal or providing an insulin resistant non-human mammal; b) administering an agent to the mammal; c) determining a biological activity level of the mammal; and d) comparing the biological activity of the mammal administered the agent with the biological activity of a mammal not administered agent, wherein the biological activity measured is selected from the group consisting of glucose uptake, glucose clearance, muscle triglyceride accumulation, fatty acid transport, and FATP1 mediated acyl-CoA synthetase activity; and whereby if the biological activity of the mammal that had been administered the agent is altered from the biological activity of the mammal that not been administered the agent, then the agent inhibits FATP1.
- 2. The method of claim 1 wherein the test agent is administered prior to, after, or substantially simultaneously with inducing insulin resistance.
- 3. The method of claim 1 wherein insulin resistance is induced by a high fat diet or by lipid infusion.
- 4. The method of claim 1 wherein insulin is administered to the mammal prior to, after, or substantially simultaneously with the agent.
- 5. A method for identifying an agent that inhibits an FATP1 activity comprising:
a) optionally inducing insulin resistance in a non-human mammal comprising a wild-type FATP1 gene and a non-human mammal comprising a disrupted FATP1 gene, or providing an insulin-resistant non-human mammal comprising a wild-type FATP1 gene and a non-human mammal comprising a disrupted FATP1 gene; b. administering an agent to the mammal comprising a wild-type FATP1 gene; c. administering an agent to the mammal comprising a disrupted FATP1 gene; d. determining a biological activity level of the mammals; and e. comparing the biological activity of the mammal whose genome comprises a wild-type FATP1 gene and the mammal whose genome comprises a disrupted FATP1 gene, wherein the biological activity measured is selected from the group consisting of glucose uptake, glucose clearance, muscle triglyceride accumulation, fatty acid transport, and FATP1 mediated acyl-CoA synthetase activity; and whereby if the biological activity of the mammal whose genome comprises a wild-type FATP1 gene is similar to the biological activity of the mammal whose genome comprises a disrupted FATP1 gene, then the agent inhibits FATP1.
- 6. The method of claim 5 wherein the mammal in which the genome comprises a disruption of the FATP1 gene is a homozygous disruption or a heterozygous disruption.
- 7. The method of claim 5 wherein the test agent is administered prior to, after, or substantially simultaneously with inducing insulin resistance.
- 8. The method of claim 5 wherein insulin resistance is induced by a high fat diet or by lipid infusion.
- 9. The method of claim 5 wherein insulin is administered to the mammal prior to, after, or substantially simultaneously with the agent.
- 10. A method for identifying a candidate agent useful for the treatment of an FATP1-mediated metabolic disorder comprising:
a) contacting a test agent with a composition comprising mammalian FATP1; b) measuring the activity of FATP1 the presence of the test agent; c) comparing the level of FATP1 activity in the presence of the test agent to the level of FATP1 activity in the absence of the test agent; and d) identifying the agent as a candidate agent useful for the treatment of an FATP1 mediated metabolic disorder where the level of the FATP1 activity is altered in the presence of the test agent; wherein the FATP1 activity measured is selected from the group consisting of acyl-CoA synthetase enzyme activity, fatty acid transport, and glucose uptake; and wherein the FATP1-mediated disorder is selected from the group consisting of insulin resistance, non-insulin dependent diabetes mellitus, and cellular triglyceride accumulation.
- 11. The method of claim 10 wherein the composition comprising mammalian FATP1 is selected from the group consisting of: purified FATP1 polypeptide, membrane preparations comprising FATP1, and cells comprising FATP1.
- 12. The method of claim 10 wherein the activity of FATP1 is measured using an assay selected from the group consisting of: an in vitro acyl-CoA synthetase enzyme assay, a cell-based fatty acid transport assay, a tissue-based fatty acid transport assay, or an in vivo assay.
- 13. The method of claim 12 wherein the acyl-CoA synthetase activity of FATP1 is determined by measuring the production of a product selected from the group consisting of phosphate, fatty acyl-CoA and AMP.
- 14. The method of claim 12 wherein the acyl-CoA synthetase activity of FATP1 is determined by measuring consumption of a substrate selected from the group consisting of coenzyme A, ATP, and fatty acid.
- 15. The method of claim 10, further comprising:
e) administering the identified candidate agent to a mammal having insulin resistance; f) determining a level of FATP1-mediated biological activity of the mammal; g) comparing the biological activity of the mammal administered the agent with the biological activity of a mammal not administered agent, and h) identifying the agent as an agent useful for the treatment of an FATP1-mediated metabolic disorders when the biological activity of the mammal administered agent is altered from the biological activity of the mammal not administered agent; wherein the biological activity measured is selected from the group consisting of glucose uptake, glucose clearance, triglyceride accumulation, fatty acid transport, and FATP1 mediated acyl-CoA synthetase activity; and wherein the FATP1-mediated disorder is selected from the group consisting of insulin resistance, non-insulin dependent diabetes mellitus, and muscle triglyceride accumulation.
- 16. The method of claim 15, wherein the test agent is administered prior to, after, or substantially simultaneously with inducing insulin resistance.
- 17. The method of claim 15 wherein insulin resistance is induced by a high fat diet or by lipid infusion.
- 18. The method of claim 15 wherein insulin is administered to the mammal prior to, after, or substantially simultaneously with the agent..
- 19. A method of modulating an FATP1 mediated disorder in an individual comprising administering to the individual an effective amount of an agent that inhibits FATP1 activity.
- 20. The method of claim 19 wherein modulation an FATP1-mediated disorder comprises any one of reducing insulin resistance; increasing insulin stimulated whole body glucose uptake; decreasing blood glucose; reducing muscle triglyceride accumulation; or treating non-insulin dependent diabetes mellitus in an individual.
- 21. A non-human mammal with a genome comprising a disruption of a FATP1 gene such that the mammal lacks or has reduced levels of functional FATP1 protein, and wherein the mammal exhibits an altered insulin/glucose homeostasis and responsiveness to glucose stimulation compared to a wild-type or non-transgenic mammal.
- 22. A method of producing the non-human mammal of claim 21 comprising:
a) introducing a targeting vector that disrupts the FATP1 gene in an embryonic stem cell, thereby producing a transgenic embryonic stem cell that comprises a disrupted FATP1 gene; b) selecting a transgenic embryonic stem cell that comprises the disrupted FATP1 gene; c) introducing the selected transgenic embryonic stem cell into a blastocyst, thereby forming a chimeric blastocyst; and d) introducing the chimeric blastocyst into the uterus of a pseudopregnant mammal; whereby the pseudopregnant mammal gives birth to a transgenic mammal with a genome comprising a disruption of a FATP1 gene such that the mammal lacks or has reduced levels of functional FATP1 protein, and wherein the mammal exhibits an altered insulin/glucose homeostasis and responsiveness to glucose stimulation compared to a wild-type or non-transgenic mammal.
RELATED APPLICATION
[0001] This application claims the benefit of U.S. Provisional Application No. 60/341,163 filed Dec. 13, 2001.
[0002] The entire teachings of the above application are incorporated herein by reference.
GOVERNMENT SUPPORT
[0003] The invention was supported, in whole or in part, by Grant Number R01 DK 40936 from the National Institutes of Health. The Government has certain rights in the invention.
Provisional Applications (1)
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Number |
Date |
Country |
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60341163 |
Dec 2001 |
US |