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Pharmacologic effects of naldemedine, a peripherally acting μ‐opioid receptor antagonist, in in vitro and in vivo models of opioid‐induced constipation
Author(s) -
Kanemasa Toshiyuki,
Koike Katsumi,
Arai Tohko,
Ono Hiroko,
Horita Narumi,
Chiba Hiroki,
Nakamura Atsushi,
Morioka Yasuhide,
Kihara Tsuyoshi,
Hasegawa Minoru
Publication year - 2019
Publication title -
neurogastroenterology and motility
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.489
H-Index - 105
eISSN - 1365-2982
pISSN - 1350-1925
DOI - 10.1111/nmo.13563
Subject(s) - pharmacology , medicine , morphine , opioid , opioid receptor , antagonist , in vivo , receptor antagonist , receptor , biology , microbiology and biotechnology
Background Naldemedine (S‐297995) is a peripherally acting μ‐opioid receptor antagonist developed as a once‐daily oral drug for opioid‐induced constipation (OIC) in adults with chronic noncancer or cancer pain. This study characterized the pharmacological effects of naldemedine in vitro and in vivo. Methods The binding affinity and antagonist activity of naldemedine against recombinant human μ‐, δ‐, and κ‐opioid receptors were assayed in vitro. Pharmacologic effects of naldemedine were investigated using animal models of morphine‐induced inhibition of small and large intestinal transit, castor oil‐induced diarrhea, antinociception, and morphine withdrawal. Key Results Naldemedine showed potent binding affinity and antagonist activities for recombinant human μ‐, δ‐, and κ‐opioid receptors. Naldemedine significantly reduced opioid‐induced inhibition of small intestinal transit (0.03‐10 mg kg −1 ; P < 0.05) and large intestinal transit (0.3‐1 μmol L −1 ; P < 0.05). Naldemedine (0.03‐1 mg kg −1 ) pretreatment significantly reversed the inhibition of castor oil‐induced diarrhea by subcutaneous morphine ( P < 0.01). Naldemedine (1‐30 mg kg −1 ) pretreatment (1 or 2 hours) did not alter the analgesic effects of morphine in a model measuring the latency of a rat to flick its tail following thermal stimulation. However, a significant delayed reduction of the analgesic effect of morphine was seen with higher doses of naldemedine (10‐30 mg kg −1 ). Some centrally mediated and peripherally mediated withdrawal signs in morphine‐dependent rats were seen with naldemedine doses ≥3 and ≥0.3 mg kg −1 , respectively. Conclusions & Inferences Naldemedine displayed potent binding affinity to, and antagonistic activity against, μ‐, δ‐, and κ‐opioid receptors. Naldemedine tempered OIC in vivo without compromising opioid analgesia.