Premium
Dependence liability of two antidiarrheals, nufenoxole and loperamide
Author(s) -
Korey Andrew,
Zilm D H,
Sellers E M
Publication year - 1980
Publication title -
clinical pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.941
H-Index - 188
eISSN - 1532-6535
pISSN - 0009-9236
DOI - 10.1038/clpt.1980.93
Subject(s) - loperamide , (+) naloxone , anesthesia , medicine , clinical pharmacology , nortriptyline , pharmacology , opioid , amitriptyline , diarrhea , receptor
We compared the dependence liabilities of therapeutic doses of nufenoxole and loperamide. Ten subjects received 10 mg nufenoxole every 12 hr for 10 days, and 9 others received 4 mg loperamide every 12 hr for 10 days. On the eighth day of drug a sensitive single‐blind intravenous naloxone challenge was used to assess dependence liability. After 0.2, 0.4, and 0.6 mg naloxone, pupillary constriction (0.618 to 0.540 cm, p < 0.005) was measured in subjects receiving nufenoxole, whereas slight dilation (0.596 to 0.622 cm, p < 0.05) was observed in those receiving loperamide. Trapezius electromyograin activity decreased by 30% for nufenoxole and 12% for loperamide. There were slight decreases in core and skin temperatures (0.06° to 0.12°) in both groups, partly attributable to experimental conditions. Changes in physiologic measurements after naloxone were similar in both groups and not of sufficient importance to suggest physical dependence liability for either loperamide or nufenoxole at the doses used. Clinical Pharmacology and Therapeutics (1980) 27, 659–664; doi: 10.1038/clpt.1980.93