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Other Prescription Weight-Loss Drugs

There are just two weight loss drugs, Xenical and Meridia, that are currently have approval for long-term use in the United States. The FDA is also considering approval of Acomplia.

Any other drugs all are recommended for short-term use. Patients should read the description of the side-effects and risks so they understand what they are.

Acomplia or Rimonabant
Blocks CB1 receptor in Endocannabinoid System, thought to play a critical role in regulation of food intake and physical energy.

Xenical or Orlistat
Active in the intestines and blocks the fat people eat from being absorbed as it's digested.

Meridia or Sibutramine
Decreases appetiite by inhibiting the re-uptake of serotonin, norepinephrine, and brain dopamine.

Ionamin or Phentermine
Activates central nervous system, increasing the heart rate and blood pressure and lessens appetite

Adipex-P or Phentermine
Energizes central nervous system, upping heart rate and blood pressure and decreasing desire for food

Bontril or Phendimetrazine
Boosts central nervous system, drives heart rate and blood pressure and does the reverse for appetite

Didrex or Benzphetamine
Powers central nervous system, increasing the rate of the heart and increases blood pressure while decreasing appetite

Tenuate or diethylpropion
Charges the central nervous system, reving heart rate, ups patient blood pressure and kills the appetite


Diet Drugs, Weight Loss Drugs Beingr Developed

APD356
Arena Pharmaceuticals
serotonin 5-HT2C receptor agonist

Acomplia
Sanofi-Aventis
cannabinoid CB1 receptor antagonist

CP-945598
Pfizer
cannabinoid CB1 receptor antagonist

Peptide YY3-36
Nastech/Merck
satiety

Peptide YY3-36
Amylin Pharmaceuticals
satiety

Simlyn
Amylin Pharmaceuticals
diabetes drug

AMG076
Amgen
MCHR1 receptor antagonist

823093
GlaxoSmithKline
dipeptidyl peptidase (DPP)-IV inhibitor

Vildagliptin (LAF237)
Novartis
dipeptidyl peptidase (DPP)-IV inhibitor

Sitagliptin (MK-0431)
Merck
dipeptidyl peptidase (DPP)-IV inhibitor

Saxagliptin
Bristol-Myers Squibb
dipeptidyl peptidase (DPP)-IV inhibitor

PSN9301
OSI Pharmaceuticals
dipeptidyl peptidase (DPP)-IV inhibitor

CYT009-GhrQb
Cytos Biotechnology
vaccine induces antibodies against ghrelin

Ro27-3225
Roche
melanocortin-4 agonist

AOD9604
Metabolic Pharmaceuticals
peptide that increases fat metabolism

ATL-962
Alizyme/Takeda
inhibitor of gastrointestinal lipases


Serotonin could be a key in regulating body weight

By Lee Bowman
SCRIPPS HOWARD NEWS SERVICE

Tucson, Arizona - 07.20.2006 - The brain chemical serotonin activates some cells that curb appetite and blocks others that normally increase hunger at the same time, according to a new study into the effects of several weight-loss drugs.

Working with mice, researchers from several institutions sought to learn whether serotonin acts on specific brain circuits in the hypothalamus region that are known to regulate the body's energy balance.

Their tracer experiments showed that receptors for serotonin dot specific nerve cells within these circuits. And they found that both serotonin and drugs such as fenfluramine and sibutramine (Meridia), which change levels of serotonin, act on those brain cells to reduce the release of one protein that stimulates appetite and aids the release of another protein that helps curb the desire to eat.
The findings, published today in the journal Neuron, reinforce the role of serotonin in affecting a key molecular pathway that controls weight, in addition to its better-known function as a regulator of sleep, mood and emotions.

Fenfluramine with phentermine, known as fen-phen, helped tens of thousands of people lose weight. But the combination was also linked to heart problems, including defects in the valves of the heart or a form of hypertension, in many patients. It was removed from the market in 1997. The mechanisms of how the drugs caused weight loss never were fully determined.

Researchers led by Dr. Joel Elmquist, then at Harvard Medical School and now at the University of Texas Southwestern Medical Center in Dallas, began studying those molecular pathways that reduce appetite, working with both normal mice and those genetically engineered to be lean or fat.

In 2002, they found that drug-induced serotonin releases activate brain cells to, in turn, release a hormone that reduces appetite.
The team's new study shows how serotonin also simultaneously blocks other neurons from being able to inhibit the activity of the hunger-suppressing system, and concluded that both mechanisms are required to promote weight loss.

"The more we understand about the pathways and the way serotonergic drugs regulate body weight, the more it one day might lead to harnessing the beneficial properties of anti-obesity treatments like fen-phen and minimizing the harmful side effects," said Elmquist, a professor of internal medicine at UT Southwestern.
According to the U.S. Centers for Disease Control and Prevention, about two-thirds of American adults are overweight, as are 16 percent of those from 6 to 19 years old. Being overweight or obese increases the risk of many harmful health conditions, including heart disease, stroke, diabetes and liver disease.
On the Net: Learn more about the findings at www.neuron.org

 

 

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