INT5660
From wiki-pain
|
|
|
|
|
Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
In contrast, administration of the nonselective opioid receptor alkylating antagonist beta-chlornaltexamine (beta-CNA) over a similar range of doses was found to be nonselective for either delta radioligand, and produced greater inhibition of Oprm1 relative to Oprd1 binding, consistent with the nonselective pharmacological activity of this antagonist. | |||||||||||||||
| |||||||||||||||
|
The influence of replacing the phenolic hydroxyl by the methoxy group on opioid receptor binding, analgesic and antitussive action was investigated in the corresponding couples morphine-codeine, hydromorphone-hydrocodone and O-desmethyltramadol (L 235)-tramadol. | |||||||||||||||
| |||||||||||||||
|
Reversal by naloxone of the morphine-induced depression of the cutaneo-adrenal nerve reflexes indicates that the opioid receptor is associated with these effects of morphine. | |||||||||||||||
| |||||||||||||||
|
These differences for the effects of butorphanol from those of morphine and pentazocine seemed to result from the antagonist-agonist property of butorphanol and from a different manner of interaction with the opioid receptor. | |||||||||||||||
| |||||||||||||||
|
Repeated restraint stress reduces opioid receptor binding in different rat CNS structures. | |||||||||||||||
| |||||||||||||||
|
Other derivatives were synthesized as a control using a tripeptide which does not bind to the opioid receptor. | |||||||||||||||
| |||||||||||||||
|
Perineural block produced by meperidine was attributed to local anesthetic-like effect, rather than to drug interaction with opioid receptor.
| |||||||||||||||
| |||||||||||||||
|
Enhanced binding of morphine and nalorphine to opioid delta receptor by glucuronate and sulfate conjugations at the 6-position. | |||||||||||||||
| |||||||||||||||
|
Heterogeneity of opioid receptor binding in brain slices. | |||||||||||||||
| |||||||||||||||
|
These results suggest that eptazocine interacts with opioid receptor, and is classified as one of the opiate agonist-antagonist analgesics. | |||||||||||||||
| |||||||||||||||
|
Prenatal exposure to morphine differentially alters gonadal hormone regulation of delta-opioid receptor binding in male and female rats. | |||||||||||||||
| |||||||||||||||
|
These compounds were tested for opioid receptor binding in rat brain synaptosomal plasma membranes and for biological activity on the guinea pig ileum. | |||||||||||||||
| |||||||||||||||
|
The effect of zinc (Zn2+) and several other trace elements was studied on the binding of the opioid receptor agonists [3H] DAGO [( ([Tyr-D-Ala-Gly-Methyl-Phe-Glyol]-enkephalin)a, [3H] DSTLE ([Tyr-D-Ser-Gly-Phe-Leu-Thr]-enkephalin) and [3H] EKC (ethylketocyclazocine), which are specific for the mu, delta and kappa opioid receptors, respectively, in the cerebral cortex of the rat. | |||||||||||||||
| |||||||||||||||
|
Magnesium and manganese were stimulatory to opioid receptor binding, whereas cobalt and nickel had dual (stimulatory and inhibitory) effects. | |||||||||||||||
| |||||||||||||||
|
The present study was designed to examine the effects of interfering with opioid-receptor interaction during re-epithelialization of the cornea in the rat using both systemic injections and topical applications of the potent opioid antagonist naltrexone (NTX). | |||||||||||||||
| |||||||||||||||
|
Measurement of changes in opioid receptor binding in vivo during trigeminal neuralgic pain using [11C] diprenorphine and positron emission tomography. | |||||||||||||||
| |||||||||||||||
|
Central poststroke pain and reduced opioid receptor binding within pain processing circuitries: a [11C]diprenorphine PET study. | |||||||||||||||
| |||||||||||||||
|
These behavioral responses in stress are accompanied by changes in the contents of opioid peptides, the mRNAs encoding their precursors and opioid receptor binding in the brain. | |||||||||||||||
| |||||||||||||||
|
Mixed kappa agonists and mu agonists/antagonists as potential pharmacotherapeutics for cocaine abuse: synthesis and opioid receptor binding affinity of N-substituted derivatives of morphinan. | |||||||||||||||
| |||||||||||||||
|
The possibility of different modes of interaction with a single opioid receptor population also is discussed. | |||||||||||||||
| |||||||||||||||
|
General Comments
This test has worked.