μ-Opioid Receptor–Mediated Enteric Glial Activation Is Involved in Morphine-Induced Constipation
Among all the side effects, opioid-induced constipation (OIC) has the highest incidence rate
in people who take chronic opioid therapy. Increasing evidence shows that enteric glial cells …
in people who take chronic opioid therapy. Increasing evidence shows that enteric glial cells …
Opioidergic effects on enteric and sensory nerves in the lower GI tract: basic mechanisms and clinical implications
Opioids are one of the most prescribed drug classes for treating acute pain. However,
chronic use is often associated with tolerance as well as debilitating side effects, including …
chronic use is often associated with tolerance as well as debilitating side effects, including …
Design, synthesis, and biological evaluation of 17-cyclopropylmethyl-3, 14β-dihydroxy-4, 5α-epoxy-6β-[(4′-pyridyl) carboxamido] morphinan derivatives as …
Y Yuan, O Elbegdorj, J Chen… - Journal of medicinal …, 2012 - ACS Publications
Peripheral selective μ opioid receptor (MOR) antagonists could alleviate the symptoms of
opioid-induced constipation (OIC) without compromising the analgesic effect of opioids …
opioid-induced constipation (OIC) without compromising the analgesic effect of opioids …
[HTML][HTML] Divergent effect of dezocine, morphine and sufentanil on intestinal motor function in rats
X Bian, R Zhou, Y Yang, P Li, Y Hang… - … journal of medical …, 2015 - ncbi.nlm.nih.gov
Background: Opioid induced bowel dysfunction is the most common side effect of
preoperatively administrated morphine, fentanyl and its derivative. However, the influence of …
preoperatively administrated morphine, fentanyl and its derivative. However, the influence of …
Further investigation of the rapid-onset and short-duration action of the G protein-biased μ-ligand oliceridine
T Mori, Y Takemura, T Arima, Y Iwase, M Narita… - Biochemical and …, 2021 - Elsevier
Abstract TRV130 (oliceridine), a G protein-biased ligand for μ-opioid receptor, has recently
been synthesized. It is considered to have strong antinociceptive effects and only minor …
been synthesized. It is considered to have strong antinociceptive effects and only minor …
6β-N-heterocyclic substituted naltrexamine derivative NAP as a potential lead to develop peripheral mu opioid receptor selective antagonists
Y Yuan, DL Stevens, A Braithwaite, KL Scoggins… - Bioorganic & medicinal …, 2012 - Elsevier
A 6β-N-heterocyclic substituted naltrexamine derivative, NAP, was proposed as a peripheral
mu opioid receptor (MOR) selective antagonist based on the in vitro and in vivo …
mu opioid receptor (MOR) selective antagonist based on the in vitro and in vivo …
New formulation of sustained release naloxone can reverse opioid induced constipation without compromising the desired opioid effects
M Sanders, S Jones, O Löwenstein, JP Jansen… - Pain …, 2015 - academic.oup.com
An international double-blind randomized placebo controlled study evaluated the safety and
efficacy of four doses of a new sustained release naloxone capsule to treat Opioid Induced …
efficacy of four doses of a new sustained release naloxone capsule to treat Opioid Induced …
[PDF][PDF] Low-Efficacy Mu Opioid Agonists as Candidate Analgesics: Effects of Novel C-9 Substituted Phenylmorphans on Pain-Depressed Behavior in Mice
EJ Santos, HI Akbarali, EW Bow… - … of Pharmacology and …, 2024 - researchgate.net
Low efficacy mu opioid receptor (MOR) agonists may serve as novel candidate analgesics
with improved safety relative to high-efficacy opioids. This study used a recently validated …
with improved safety relative to high-efficacy opioids. This study used a recently validated …
Clathrin and GRK2/3 inhibitors block δ-opioid receptor internalization in myenteric neurons and inhibit neuromuscular transmission in the mouse colon
JJ DiCello, P Rajasekhar… - American Journal …, 2019 - journals.physiology.org
Endocytosis is a major mechanism through which cellular signaling by G protein-coupled
receptors (GPCRs) is terminated. However, recent studies demonstrate that GPCRs are …
receptors (GPCRs) is terminated. However, recent studies demonstrate that GPCRs are …