Sallam HS, Oliveira HM, Gan HT, Herndon DN, Chen JDZ. Ghrelin improves burn-induced delayed gastrointestinal transit in rats. Am J Physiol Regul Integr Comp Physiol 292: R253-R257, 2007. First published September 7, 2006; doi:10.1152/ajpregu.00100.2006.-Delayed gastrointestinal transit is common in patients with severe burn. Ghrelin is a potent prokinetic peptide. We aimed at testing the effect of ghrelin on burn-induced delayed gastrointestinal transit in rats. Gastric emptying (GE), intestinal transit (IT), and colonic transit (CT) studies were performed in male Sprague-Dawley rats. Rats were randomized into two main groups as follows: sham injury and ghrelin-treated burn injury with doses of 0, 2, 5, and 10 nmol/rat ip 6 h after burn. Sham/burn injury was induced under anesthesia. Rats received a phenol red meal 20 min following ghrelin injection. Based on the most effective ghrelin dose, 1 mg/kg sc atropine was given 30 min before the ghrelin in one group of rats for each study. The rats in each group were killed 30 -90 min later; their stomachs, intestines, and colons were harvested immediately, and the amount of phenol red recovered was measured. Percentage of gastric emptying (GE%) and geometric center for IT and CT were calculated. We found 1) severe cutaneous burn injury significantly delayed GE, IT, and CT compared with sham injury (P Ͻ 0.05); 2) ghrelin normalized both GE and IT, but not the CT; 3) the most effective dose of ghrelin was 2 nmol/rat; and 4) atropine blocked the prokinetic effects of ghrelin on GE% and IT. In conclusion, ghrelin normalizes burn-induced delayed GE and IT but has no effect on CT in rats. The prokinetic effects of ghrelin are exerted via the cholinergic pathway. Ghrelin may have a therapeutic potential for burn patients with delayed upper gastrointestinal transit.ghrelin; burn; gastric emptying; intestinal transit; colon transit SEVERE BURN IS A STRESSFUL condition challenging all body homeostatic mechanisms. In patients with severe cutaneous burns, impairment of the gastrointestinal functions is not uncommon. The body response to the stress caused by burn injury involves the triggering of the sympathetic nervous system (35) with an increase in catecholamine release (10), constriction of the mesenteric blood flow to the gut (17), and the release of various inflammatory mediators, including cyclooxygenase-2 (COX-2) and induced nitric oxide synthase (iNOS) enzyme pathways (16). Burn-induced gastroparesis is common in patients with severe large burns and is responsible for the delayed oral fluid resuscitation, an important goal in burn shock treatment (25). Enteral resuscitation within the 1st h after burn can enhance gut mucosal integrity and blood supply, thus reducing bacterial and endotoxin translocation and eventually the risk for sepsis in burn patients (6,25).Ghrelin is a 28-amino-acid peptide, synthesized mainly by the gastric oxyntic A-like cells in the fundic mucosa and was found to stimulate the growth hormone secretagogue receptor, resulting in the release of the g...