Existing pharmacotherapeutic options for the treatment of patients with irr
itable bowel syndrome (IBS) are limited in treating the multiple symptoms a
ssociated with the disorder. There is much interest in the use of serotonin
agents as new therapeutics. Acting primarily through 5-MT, and 5-MT, recep
tors, serotonin elicits changes in motor function and possibly visceral sen
sation. Two serotonin agents were developed specifically for IBS: tegaserod
, a 5-HT4 receptor partial agonist, and alosetron, a 5-HT3 receptor antagon
ist (which is no longer available). Phase III clinical trial data show that
during a 12-week treatment period with tegaserod, IBS patients with abdomi
nal pain and discomfort, bloating, and constipation experienced significant
global relief tie, improvement in overall wellbeing, abdominal pain, and b
owel habit) compared with placebo. Improvement in bowel movement frequency
and consistency was achieved and pain was relieved by 1 week. During 12 wee
ks of treatment, alosetron was shown to elicit significant relief of abdomi
nal pain and discomfort compared with placebo or mebeverine in female IBS p
atients with diarrhea, Alosetron slowed colonic transit and treatment effic
acy was apparent after a week of treatment. Another 5-MT, receptor agonist,
prucalopride, which is being developed for chronic constipation, accelerat
es colonic transit and increases stool frequency. Therefore, this agent may
be of benefit in]BS patients with constipation.