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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Holzer, P.
Treatment of opioid-induced gut dysfunction.
Expert Opin Investig Drugs. 2007; 16(2): 181-194. Doi: 10.1517/13543784.16.2.181
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Führende Autor*innen der Med Uni Graz
Holzer Peter
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Abstract:
Opioid analgesics are the mainstay in the treatment of moderate-to-severe pain, yet their use is frequently associated with adverse effects, the most common and debilitating being constipation. Opioid-induced motor stasis results from blockade of gastrointestinal peristalsis and fluid secretion, and reflects the action of the endogenous opioid system in the gut. Methylnaltrexone and alvimopan are new investigational drugs that selectively target peripheral mu-opioid receptors because they are poorly absorbed in the intestine and do not enter the brain. Clinical studies have proved the concept that these drugs prevent opioid-induced bowel dysfunction without interfering with analgesia. As reviewed in this article, opioid receptor antagonists with a peripherally restricted site of action also hold therapeutic promise in postoperative ileus and chronic constipation due to the fact that they have been found to stimulate intestinal transit.
Find related publications in this database (using NLM MeSH Indexing)
Analgesics, Opioid - adverse effects
Animals - adverse effects
Drugs, Investigational - pharmacology
Gastrointestinal Diseases - chemically induced
Gastrointestinal Motility - drug effects
Humans - drug effects
Narcotic Antagonists - pharmacology
Receptors, Opioid, mu - antagonists and inhibitors

Find related publications in this database (Keywords)
alvimopan
constipation
enteric nervous system
intestinal peristalsis
naloxone
N-methylnaltrexone
opioid peptides
opioid-induced bowel dysfunction
peripherally restricted opioid receptor antagonists
prokinetic effects
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