Effect of Pioglitazone on Mitochondrial Function in Muscle and Adipose Tissue in Humans
| Status: | Recruiting |
|---|---|
| Conditions: | Diabetes |
| Therapuetic Areas: | Endocrinology |
| Healthy: | No |
| Age Range: | 18 - 65 |
| Updated: | 4/2/2016 |
| Start Date: | May 2008 |
| Contact: | Christian Meyer, MD |
| Email: | Christian.Meyer@asu.edu |
| Phone: | (480) 965-2473 |
Mitochondrial dysfunction in skeletal muscle results in decreased muscle fatty acid
oxidation, leading to conversion of fatty acids into triglycerides and its accumulation
inside the muscle tissue. Moreover, in adipose tissue mitochondrial dysfunction results in
decreased fatty acid oxidation and triglyceride synthesis, leading to increased circulating
fatty acid concentrations, which in turn also leads to lipid accumulation inside muscle
tissue. Lipid accumulation inside muscle tissue interferes with the insulin signaling
pathway and causes insulin resistance. Mitochondrial dysfunction in both tissues has
therefore been proposed to play an important role in insulin resistance in humans.
Pioglitazone, a thiazolidinedione, is an FDA approved medication for the treatment of type 2
diabetes. It improves muscle insulin sensitivity at least in part by lowering intramuscular
lipid concentrations but the mechanism by which this occurs is unclear. In the present
study, we shall therefore test the hypothesis that pioglitazone improves mitochondrial
function in muscle and adipose tissue in humans who are insulin resistant.
oxidation, leading to conversion of fatty acids into triglycerides and its accumulation
inside the muscle tissue. Moreover, in adipose tissue mitochondrial dysfunction results in
decreased fatty acid oxidation and triglyceride synthesis, leading to increased circulating
fatty acid concentrations, which in turn also leads to lipid accumulation inside muscle
tissue. Lipid accumulation inside muscle tissue interferes with the insulin signaling
pathway and causes insulin resistance. Mitochondrial dysfunction in both tissues has
therefore been proposed to play an important role in insulin resistance in humans.
Pioglitazone, a thiazolidinedione, is an FDA approved medication for the treatment of type 2
diabetes. It improves muscle insulin sensitivity at least in part by lowering intramuscular
lipid concentrations but the mechanism by which this occurs is unclear. In the present
study, we shall therefore test the hypothesis that pioglitazone improves mitochondrial
function in muscle and adipose tissue in humans who are insulin resistant.
Inclusion Criteria:
1. Subjects must be able to communicate meaningfully with the investigator and must be
legally competent to provide written informed consent.
2. Subjects may be of either sex with age as described in each protocol. Female subjects
must be non-lactating and will be eligible only if they have a negative pregnancy
test throughout the study period.
3. Subjects must range in age from 18-65.
4. Subjects must have the following laboratory values:
- 2-hour OGTT plasma glucose 140-250 mg/dl
- Hematocrit ≥ 35 vol%
- Serum creatinine ≤ 1.6 mg/dl
- AST (SGOT) < 2.5 times upper limit of normal
- ALT (SGPT) < 2.5 times upper limit of normal
- PT, PTT within the normal range
Exclusion Criteria:
1. Subjects must not be receiving any medications with known effects on glucose
tolerance unless the subject has been on stable dose of such agents for the past
three months before entry into the study. Subjects taking systemic glucocorticoids
will be excluded. Subjects may be taking a stable dose of estrogens or other hormonal
replacement therapy, if the subject has been on these agents for the prior three
months.
2. History of clinically significant heart disease, including ischemic heart disease
(New York Heart Classification greater than grade II; more than non-specific ST-T
wave changes on the EKG) and congestive heart failure
3. History of peripheral vascular disease (history of claudication)
4. History of pulmonary disease (dyspnea on exertion of one flight or less; abnormal
breath sounds on auscultation).
5. History of peripheral edema
6. Uncontrolled hypertension with systolic BP>160 mmHg, diastolic BP>100 mmHg
7. Resting heart rate >100 beats/min
8. Autonomic neuropathy
9. Heavy alcohol consumption (> 2 drinks/day)
We found this trial at
1
site
Click here to add this to my saved trials
