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Encyclopedia > Anorexigenic

Anorectics, anorexigenics or appetite suppressants, are substances which reduce the desire to eat ("anorectic", from the Greek an- = "not" and oreg- = "extend, reach").


Used on a short term basis clinically to treat obesity, some appetite suppressants are also available over the counter. Drugs of this class are frequently stimulants of the phenethylamine family, related to amphetamine (speed). Indeed, amphetamine itself was sold commercially as an appetite suppressant until it was outlawed in most parts of the world in the late 1950s due to increasing exploitation of its stimulant properties ("abuse"). Many amphetamines produce side effects including addiction, tachycardia and hypertension, making prolonged unsupervised use dangerous.


Epidemics of fatal pulmonary hypertension and heart valve damage associated with anorectic agents have led to the withdrawal of products from the market. This was the case with aminorex in the 1960s, and again in the 1990s with fenfluramine (see: Fen-phen). Likewise, association of the related appetite suppressant phenylpropanolamine with hemorrhagic stroke led the FDA to request its withdrawal from the market in the United States in 2000, and similar concerns regarding ephedrine resulted in an FDA ban on its inclusion in dietary supplements, in 2004.


In spite of these precedents, numerous related compounds are still marketed today as appetite suppressants. These include phentermine (Fastin®, Adipex®, Ionamin® and others), diethylpropion (Tenuate®), phendimetrazine (Prelu-2®), benzphetamine (Didrex®) and others. Sibutramine (Medaria®, Reductil®) is a recent addition, which is used with orlistat by doctors to control obesity. The new cannabinoid receptor antagonist Rimonabant (Acomplia®) will be available in 2006.


References

  • Abenhaim L, Moride Y, Brenot F, Rich S, Benichou J, Kurz X, Higenbottam T, Oakley C, Wouters E, Aubier M, Simonneau G, Begaud B. Appetite_Suppressant Drugs and the Risk of Primary Pulmonary Hypertension. N Engl J Med 1996;335:609. Fulltext (http://content.nejm.org/cgi/content/full/335/9/609). Medline abstract (http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list-uids=8692238) (PMID 8692238).
  • Fishman AP. Aminorex to Fen/Phen: An Epidemic Foretold. Circulation 1999;99:156. Fulltext (http://circ.ahajournals.org/cgi/content/full/99/1/156). Medline abstract (http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list-uids=9884392) (PMID 9884392).

External links

  • Questions and Answers about appetite suppressant medication treatment from the Medical College of Wisconsin (http://healthlink.mcw.edu/article/933126929.html)



  Results from FactBites:
 
Interacting Appetite-Regulating Pathways in the Hypothalamic Regulation of Body Weight -- Kalra et al. 20 (1): 68 -- ... (9549 words)
MSH, an anorexigenic peptide derived from the POMC precursor
PVN in response to administration of orexigenic (103, 104) and anorexigenic
the influence of anorexigenic messengers on the release and
Postgraduate Medicine: Future directions in weight control (3055 words)
These neurotransmitters are either anorexigenic (appetite inhibiting) and catabolic or orexigenic (appetite stimulating) and anabolic (6) (table 1).
While anorexigenic substances now hold our attention for their potential to treat the obese patient, their function was probably less important 100,000 years ago when they evolved.
Neuropeptide Y: NPY is produced and released in specific nuclei of the hypothalamus, where it binds to specific receptors and stimulates a marked increase in food intake.
  More results at FactBites »


 
 

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