Recent progress in the molecular pharmacology of 5-HT receptors and th
e development of selective ligands for various 5-HT receptor subtypes
has advanced our understanding of the role of 5-HT mechanisms in the c
ontrol of food intake and bodyweight. The most intensively investigate
d 5-HT receptor subtypes have been the 5-HT1A receptor, the 5-HT1B rec
eptor and the 5-HT2C receptor, The overall pattern of results to date
suggests that selective 5-HT2C agonists may be novel anorectic drugs a
nd prove useful in the treatment of obesity, However, a number of issu
es remain unresolved, particularly regarding potential side-effects,as
the 5-HT2C receptor agonist mCPP has been reported to induce anxiety
and nausea in humans,actions that would clearly limit its therapeutic
utility, In addition, the possible role of recently cloned 5-HT recept
or subtypes such as 5-ht(5), 5-ht(6) and 5-ht(7) remains unexplored an
d the development of selective ligands for these sites has the potenti
al to lead to new treatments for obesity.