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Title: Effects of morphine and naloxone on feline colonic transit. Author: Krevsky B, Libster B, Maurer AH, Chase BJ, Fisher RS. Journal: Life Sci; 1989; 44(13):873-9. PubMed ID: 2927248. Abstract: The effects of endogenous and exogenous opioid substances on feline colonic transit were evaluated using colonic transit scintigraphy. Naloxone (0.3 mg/kg, i.m.) accelerated emptying of the cecum and ascending colon, and filling of the transverse colon. Endogenous opioid peptides thus appear to play a significant role in the regulation of colonic transit. At a moderate dose of morphine (0.1 mg/kg, i.m.), cecum and ascending colon transit was accelerated, while at a larger dose (1.0 mg/kg, i.m.) morphine had no effect. Since naloxone, a relatively nonspecific opioid antagonist, and morphine, a principally mu opioid receptor agonist, both accelerate proximal colonic transit, a decelerating role for at least one of the other opioid receptors is inferred.[Abstract] [Full Text] [Related] [New Search]