"Pecos" B-adrenergic and PPAR-G Stimulation Upregulates Lipid Metabolism in Human Subcutaneous Fat
| Status: | Completed |
|---|---|
| Conditions: | Obesity Weight Loss |
| Therapuetic Areas: | Endocrinology |
| Healthy: | No |
| Age Range: | 18 - 50 |
| Updated: | 4/21/2016 |
| Start Date: | January 2003 |
| End Date: | November 2004 |
Synergistic Induction of UCP-1 by Ephedrine/Caffeine and Pioglitazone: A Rationale for Combination Therapy of Obesity
This study compares four treatments to see which one causes the most weight loss, fat loss,
loss of abdominal fat and improvement in blood tests like cholesterol. The four treatments
are: Placebo, Ephedrine plus caffeine, Pioglitazone, Combined pioglitazone and ephedrine
plus caffeine
loss of abdominal fat and improvement in blood tests like cholesterol. The four treatments
are: Placebo, Ephedrine plus caffeine, Pioglitazone, Combined pioglitazone and ephedrine
plus caffeine
The sympathetic nervous system, via the intracellular messenger cAMP and MAPK activation,
and thiazolidinediones via PPARγ control lipid metabolism have been implicated in body
weight regulation. The present study was undertaken to determine whether the simultaneous
activation of these two signaling systems might synergize to exert beneficial effects on the
expression of key genes involved in lipid metabolism and mitochondrial biogenesis in
subcutaneous fat in healthy, non-diabetic subjects. Fifty seven non-diabetic women and men
were randomized into four groups: 1) placebo/placebo (PP); 2) ephedrine plus
caffeine/placebo (ECP); 3) placebo/pioglitazone (PPio); 4) ephedrine plus
caffeine/pioglitazone (ECPio). Adipose tissue samples were obtained after 12 weeks of
treatment to determine gene expression by real time RT-PCR.
and thiazolidinediones via PPARγ control lipid metabolism have been implicated in body
weight regulation. The present study was undertaken to determine whether the simultaneous
activation of these two signaling systems might synergize to exert beneficial effects on the
expression of key genes involved in lipid metabolism and mitochondrial biogenesis in
subcutaneous fat in healthy, non-diabetic subjects. Fifty seven non-diabetic women and men
were randomized into four groups: 1) placebo/placebo (PP); 2) ephedrine plus
caffeine/placebo (ECP); 3) placebo/pioglitazone (PPio); 4) ephedrine plus
caffeine/pioglitazone (ECPio). Adipose tissue samples were obtained after 12 weeks of
treatment to determine gene expression by real time RT-PCR.
Inclusion Criteria:
- generally healthy
- not pregnant or nursing
- using adequate contraception
- between 18 and 50 years of age
- BMI between 30 and 35 kg/m2
Exclusion Criteria:
- significant renal, cardiac, liver, lung or neurological disease
- high blood pressure
- diabetes
- prior use of thiazolidinedione
- prior use of beta-blockers alcohol or drug abuse
- history of thrombophlebitis, vascular or blood clotting disorders
- unwilling or unable to abstain from caffeinated beverages and alcohol prior to
adipose tissue biopsy and metabolic rates measurements
- increased liver function test at baseline
- have metal objects that would interfere with the measurement of the body composition
- use drugs known to affect lipid metabolism, energy metabolism or body weight
- use herbal supplements containing ephedrine and/or caffeine
- take chronic medication, except hormone replacement or contraception
- are a woman unwilling to use effective contraception during the trial
- have heart disease or history of stroke
- have urinary symptoms from enlarged prostate
- have gained and or lost more than 10 pounds in the last 6 month
- have use a monoamine oxidase inhibitor medication in the last month
- have high or low thyroid function that has not been controlled in the normal range
for at least 2 months
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