Investigating Simvastatin as a Treatment for Polycystic Ovary Syndrome

Hattman, Emma (2014) Investigating Simvastatin as a Treatment for Polycystic Ovary Syndrome. [Abstract]

Full text not available from this repository. (Request a copy)

Abstract

Polycystic Ovary syndrome is a disorder associated with numerous clinical, endocrine and metabolic complications, such as menstrual dysfunction, hyperandrogenism and insulin resistance. The relationship between hyperandrogenism and insulin resistance is a highly studied aspect of PCOS, and, a current target for treatment. High levels of testosterone interfere with the insulin receptor and its substrates to compromise a cell’s ability to translocate GLUT4 to the cell membrane to allow for the entry of glucose. To investigate the potential of the emerging drug simvastatin, cultured C2C-12 myoblast cells were treated with the drug for 24 hours followed by insulin stimulation for 2 hours. Phosphorylation ratios of IRS-1(Ser612) to total IRS-1 along with GLUT4 translocation were measured to detect how the drug interacts with the insulin pathway. There was no significant difference between treatment with and without simvastatin regarding the relative level of IRS-1(Ser612) phosphorylation. Flow cytometry results measuring the translocation of GLUT4 to the plasma membrane indicate that treatment with simvastatin increased GLUT4 translocation by 7.5%, but without experimental repeats there is no way to know if these results represent a significant difference. Overall these results show that treatment with simvastatin for 24hr does not change insulin signaling or GLUT-4 translocation in a mouse muscle cell line.

Item Type: Abstract
Created by Student or Faculty: Student
Uncontrolled Keywords: Polycystic Ovary Syndrome, Simvastatin, Insulin Receptor Substrate 1 (IRS-1), GLUT4
Subjects: Undergrad Research Symposium > Biology
Undergrad Research Symposium
Depositing User: Emmaline Hattman
Date Deposited: 16 Apr 2014 15:27
Last Modified: 17 Apr 2014 09:02
URI: http://fortworks.fortlewis.edu/id/eprint/506


© FortWorks - powered by EPrints 3 - sponsored and maintained by the John F. Reed Library at Fort Lewis College