The development of cross-tolerance to an analgesic effect was observed between two mu-receptor agonists, heroin and fentanyl. Repeated treatments with heroin twice a day for 4 days resulted in a decreased nociceptive effect to fentanyl on day 5. The fentanyl dose-response line shifted to the right, and was considered to be a sign of the development of cross-tolerance. Peripheral treatment with oxytocin did not block the development of heroin-fentanyl cross-tolerance. However, intracerebroventricular administration of oxytocin blocked the development of tolerance, causing a leftward shift in the dose-response curve and supporting the assumption that oxytocin blocks the development of heroin-fentanyl cross-tolerance via CNS mechanisms
<div><p>Functionally selective signaling appears to contribute to the variability in mechanisms that...
Key-press responding of mice was maintained under a fixed-ratio (FR) 30-response schedule of food pr...
Morphine induces antinociception by activating mu opioid receptors (muORs) in spinal and supraspinal...
Oxytocin (OXT), a neurohypophyseal hormone, has a wide range of behavioral effects outside its class...
Our previous studies indicate that oxycodone is a putative kappa-opioid agonist, whereas morphine is...
Tolerance to the antinociceptive effect of mu-opioid receptor (MOPr) agonists, such as morphine and ...
Our previous studies indicate that oxycodone is a putative k-opioid agonist, whereas morphine is a w...
The development of morphine-tolerance after chronic administration, reduces analgesic efficacy and i...
Systemic administration of morphine typically produces greater tolerance than higher efficacy mu-opi...
The irreversible cholinesterase inhibitor diisopropylphosphofluoridate (DFP) causes a naloxone-sensi...
Neuropeptides affect adaptive central nervous system processes related to opiate ethanol and cocaine...
The analgesic effect elicited by intracerebroventricular (icv) administration of either morphine or ...
Development of tolerance and cross-tolerance after acute administration of the μ agonist morphine an...
Fentanyl has been shown to be a potent analgesic with a lower propensity to produce tolerance and ph...
Functionally selective signaling appears to contribute to the variability in mechanisms that underli...
<div><p>Functionally selective signaling appears to contribute to the variability in mechanisms that...
Key-press responding of mice was maintained under a fixed-ratio (FR) 30-response schedule of food pr...
Morphine induces antinociception by activating mu opioid receptors (muORs) in spinal and supraspinal...
Oxytocin (OXT), a neurohypophyseal hormone, has a wide range of behavioral effects outside its class...
Our previous studies indicate that oxycodone is a putative kappa-opioid agonist, whereas morphine is...
Tolerance to the antinociceptive effect of mu-opioid receptor (MOPr) agonists, such as morphine and ...
Our previous studies indicate that oxycodone is a putative k-opioid agonist, whereas morphine is a w...
The development of morphine-tolerance after chronic administration, reduces analgesic efficacy and i...
Systemic administration of morphine typically produces greater tolerance than higher efficacy mu-opi...
The irreversible cholinesterase inhibitor diisopropylphosphofluoridate (DFP) causes a naloxone-sensi...
Neuropeptides affect adaptive central nervous system processes related to opiate ethanol and cocaine...
The analgesic effect elicited by intracerebroventricular (icv) administration of either morphine or ...
Development of tolerance and cross-tolerance after acute administration of the μ agonist morphine an...
Fentanyl has been shown to be a potent analgesic with a lower propensity to produce tolerance and ph...
Functionally selective signaling appears to contribute to the variability in mechanisms that underli...
<div><p>Functionally selective signaling appears to contribute to the variability in mechanisms that...
Key-press responding of mice was maintained under a fixed-ratio (FR) 30-response schedule of food pr...
Morphine induces antinociception by activating mu opioid receptors (muORs) in spinal and supraspinal...