Methods and compositions using stearoyl-CoA desaturase to identify triglyceride reducing therapeutic agents
The use of screening assays based on the role of human stearoyl-CoA desaturase-1 (“hSCD1”) in human diseases, disorders or conditions relating to serum levels of triglyceride, VLDL, HDL, LDL, total cholesterol, or production of secretions from mucous membranes, monounsaturated fatty acids, wax esters, and the like, is disclosed. Also disclosed are conventions useful in the prevention and/or treatment of such diseases.
1. A method for identifying a stearoyl-CoA desaturase (SCD1)-modulating agent, comprising:
a) contacting a chemical agent and a microsomal membrane fraction having SCD1 activity;
b) detecting a change in said SCD1 activity due to said contacting wherein said SCD1 activity is detected by determining the release of tritiated water from a substrate radiolabeled with tritium at an SCD1 reactive carbon atom; and
wherein said chemical agent does not substantially inhibit delta-5 or delta-6 desaturase
thereby identifying said chemical agent as an SCD1 modulating agent.
2. The method of claim 1 , wherein said microsomal membrane fraction having SCD1 activity comprises an SCD1 polypeptide.
3. The method of claim 1 , wherein said change in activity is an increase in activity.
4. The method of claim 1 , wherein said change in activity is a decrease in activity.
5. A method for identifying an agent that modulates plasma triglyceride levels in a mammal comprising administering to a mammal an agent that has SCD1-modulating activity in the method of claim 1 and detecting a change in plasma triglyceride level in said mammal as a result of said administering thereby identifying a plasma triglyceride modulating agent.
6. The method of claim 5 , wherein said plasma triglyceride modulating activity is a decrease in plasma triglyceride level.
7. The method of claim 5 , wherein said mammal is a human.
8. The method of claim 1 , wherein said radiolabeled substrate is stearoyl-CoA comprising a tritium atom only on C9 and/or C10.
9. The method of claim 1 , wherein said modulating agent is not conjugated to Coenzyme A.
10. The method of claim 5 , wherein said detected change in said SCD1 activity is a decrease in SCD1 activity.
11. The method of claim 5 , wherein said detected change in said SCD1 activity is an increase in SCD1 activity.