Lactulose is one of the most frequently utilised agents in the treatme
nt of constipation and hepatic encephalopathy because of its efficacy
and good safety profile. The key to understanding the possible modes o
f action by which lactulose achieves its therapeutic effects in these
disorders lies in certain pharmacological phenomena: (a) lactulose is
a synthetic disaccharide that does not occur naturally; (b) there is n
o disaccharidase on the microvillus membrane of enterocytes in the hum
an small intestine that hydrolyses lactulose; and (c) lactulose is not
absorbed from the small intestine. Thus, the primary site of action i
s the colon in which lactulose is readily fermented by the colonic bac
terial flora with the production of short-chain fatty acids and Variou
s gases. The purpose of this review is to focus on some pertinent basi
c aspects of the clinical pharmacology of lactulose and to discuss the
possible mechanisms by which lactulose benefits patients with constip
ation and hepatic encephalopathy.