Loperamide effects on hepatobiliary function, intestinal transit and analgesia in mice.

Abstract:

:Loperamide effects on hepatobiliary function, analgesia and gut transit were studied in mice. Varying doses of the antidiarrheal drug, loperamide, were administered to mice by intracerebroventricular, intravenous, subcutaneous and intragastric routes. Gut motility was determined by intestinal transit of India ink, analgesia by warm water tail flick latency, and hepatobiliary function by retention of the anionic dye, sulfobromophthalein in plasma and liver. When given by all routes at modest doses, loperamide slowed intestinal transit. Analgesia, a centrally mediated opiate effect, was only detected after intracerebroventricular or subcutaneous loperamide at high, near-toxic doses. Elevations of plasma and liver sulfobromophthalein were noted at routes and doses which slowed gut transit, well below those needed for analgesia. Intragastric loperamide at one fortieth its LD50 caused marked elevation of sulfobromophthalein levels and gut slowing, but no analgesia. Sulfobromophthalein elevation and gut slowing by intragastric loperamide were not affected by spinal cord transection but were reversed by naltrexone, an opiate antagonist. Non-toxic doses of loperamide slow gut transit and modify hepatobiliary function in mice by opiate actions at peripheral sites.

journal_name

Life Sci

journal_title

Life sciences

authors

Hurwitz A,Sztern MI,Looney GA,Ben-Zvi Z

doi

10.1016/0024-3205(94)00609-1

subject

Has Abstract

pub_date

1994-01-01 00:00:00

pages

1687-98

issue

22

eissn

0024-3205

issn

1879-0631

pii

0024-3205(94)00609-1

journal_volume

54

pub_type

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