Experimental studies have shown that otilonium bromide (OB) inhibits both b
aseline and chemically or physically stimulated gastrointestinal motility,
The spasmolytic activity of OB in the gastrointestinal tract occurs at dose
s that do not affect gastric secretion or produce typical atropine-like sid
e-effects. The mechanism of action is composite: interference with calcium
ion movement from intra- and extracellular sites; blockade of calcium chann
els; and binding to muscarinic receptors and tachykinin neurokinin-2 recept
ors, Pharmacokinetic studies have shown that OB accumulates in the lower in
testine and has poor systemic absorption, Clinical studies have confirmed O
B as a potent spasmolytic drug with a good tolerability profile. Studies in
patients with irritable bowel syndrome demonstrated OB to be superior to p
lacebo and reference drugs in parameters such as pain, abdominal distension
and motility. The composite and local mechanism of OB action reduces hyper
motility and modulates visceral sensation: factors thought to be responsibl
e for pain improvement recorded in clinical trials, The compound is markete
d worldwide and no serious adverse events have been reported as yet, confir
ming its excellent tolerability.