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1 nistration of mu opioids fails to produce an analgesic effect.
2 sary for associative tolerance to morphine's analgesic effect.
3 eous administration of RTX had a generalized analgesic effect.
4 s in the CNS to produce a centrally mediated analgesic effect.
5 idenced by induction of a centrally mediated analgesic effect.
6 ive opioid receptor agonist with very potent analgesic effect.
7 stricted sodium channel may have a selective analgesic effect.
8 9L and morphine resulted in a dose-dependent analgesic effect.
9 ave been shown to possess antinociceptive or analgesic effects.
10  to a favourable pharmacokinetic profile and analgesic effects.
11 rs (CBRs) have been implicated in the opioid analgesic effects.
12  ability of the opioid antagonist to produce analgesic effects.
13 ctive muscarinic agonists display pronounced analgesic effects.
14 ioside in mice rapidly attenuates morphine's analgesic effects.
15 nergic receptors (alpha(2)ARs) leads to mild analgesic effects.
16 mical pathways in exerting their supraspinal analgesic effects.
17 ists has been shown to result in synergistic analgesic effects.
18 the ACC in vivo produces both anxiolytic and analgesic effects.
19  and to exhibit CB1-mediated hypothermic and analgesic effects.
20                   Each pathway would produce analgesic effects.
21 ENK for opioid receptor binding affinity and analgesic effects.
22 accounted for 25% of the variance in placebo analgesic effects.
23 report and loperamide produced a significant analgesic effect (2-fold increase in response times) whe
24                         KOR agonists exhibit analgesic effects, although the adverse effects produced
25 ine causes addiction, tolerance to its acute analgesic effects, and profound physical dependence by s
26 how different frequencies of SCS produce the analgesic effect are unclear.
27                                        These analgesic effects are many times greater than unmodified
28 onizing mu opioid-induced analgesia or a net analgesic effect by reducing the hyperalgesia during opi
29           Morphine mediates its euphoric and analgesic effects by acting on the mu-opioid receptor (M
30      Morphine exerts its acute rewarding and analgesic effects by activation of inhibitory guanine nu
31 s alfentanil bolus has a clinically relevant analgesic effect compared with placebo in patients under
32 ncture point was sufficient to eliminate the analgesic effect, dismissing the systemic action of caff
33  require arrestin recruitment, whereas their analgesic effects do not.
34 eption, altruistic behavior had an intrinsic analgesic effect for the recipient.
35 d with an enhanced sensitivity to the opioid analgesic effect (IL-1beta, P = 0.0218; TNF-alpha, P = 0
36 he resolvin precursor 17-HDHA shows a strong analgesic effect in animal models of osteoarthritis and
37 onsubtype-selective alpha2AR agonist, had no analgesic effect in D79N mice, whereas the analgesic pot
38 oxylase (QHGAD67) release GABA to produce an analgesic effect in rodent models of pain.
39 inhibitors may be used to enhance the opioid analgesic effect in the treatment of chronic neuropathic
40  this technique we demonstrate a significant analgesic effect in transgenic mouse models of SCD and c
41 h synaptically and behaviorally in producing analgesic effects in a PLA(2)-dependent fashion, support
42                        Moreover, 4a produced analgesic effects in a rodent model of acute inflammator
43  G9a in diminished MOR expression and opioid analgesic effects in animal models of neuropathic pain.
44 nomolar IC50), and has been shown to produce analgesic effects in animals.
45 ls, HUP-A treatment demonstrates significant analgesic effects in both regimens.
46                          Consistent with its analgesic effects in humans, sanshool treatment in mice
47 al models; however, they exhibit only modest analgesic effects in humans.
48 -dependent anxiolytic, antiinflammatory, and analgesic effects in mice by increasing endocannabinoid
49 ecrosis factor (anti-TNF) therapy, which has analgesic effects in models of inflammation as well as i
50 at P and 3 alpha-Diol at moderate doses have analgesic effects in part via membrane actions within th
51 denosine kinase inhibition produces powerful analgesic effects in rodent models of experimental neuro
52 de deactivation in vivo and exerted profound analgesic effects in rodent models of nociceptive and in
53 mu opioid receptor, the most responsible for analgesic effects in the central nervous system.
54 NK gene transfer into the OT did not produce analgesic effects in the tail-flick test.
55 c agonists can produce both hyperalgesic and analgesic effects in vivo.
56 ogical profile ASIC channels to exert strong analgesic effects in vivo.
57 ctive muscarinic agonists resulted in robust analgesic effects, indicating that muscarinic analgesia
58                                          The analgesic effects induced by combination of alcohol and
59                      The cannabinoid-induced analgesic effect is absent in mice lacking the alpha3 Gl
60                                         This analgesic effect is attributed to activation of peripher
61 rodent dorsal root ganglion (DRG) show their analgesic effect is mediated by inhibition of N-type (Ca
62      In Experiment 2, we tested whether this analgesic effect is mediated by the brainstem nucleus ra
63                               This ingestion analgesic effect is reversed when the hedonic valence of
64 in states, and have shown that NR2B-mediated analgesic effects might be supra- rather than intra-spin
65 e found to be expressed, to show an enhanced analgesic effect, no opioid-induced tolerance, and to pr
66 effects of acupuncture may contribute to the analgesic effect observed in genuine acupuncture analges
67    In light of our previous finding that the analgesic effect of acupuncture is mediated by adenosine
68 adenosine A1 receptor agonist replicated the analgesic effect of acupuncture.
69                             Tolerance to the analgesic effect of an opioid is a pharmacological pheno
70 on of TGF-beta1, but not IL-10, reversed the analgesic effect of BMSCs.
71                The findings suggest that the analgesic effect of BreEStim is not likely attributed to
72    The underlying mechanisms involved in the analgesic effect of BreEStim were considered to result f
73                                          The analgesic effect of clinically used exogenous opioids, s
74  did not alter the tail-flick latency or the analgesic effect of deltorphin II.
75                                 Finally, the analgesic effect of donepezil was markedly reduced by a
76  which was associated with a decrease in the analgesic effect of endogenous inhibitory G-protein-coup
77  spinal GIRK channels selectively blunts the analgesic effect of high but not lower doses of intrathe
78 spinal GIRK channels selectively blunted the analgesic effect of high but not lower doses of the mu-o
79 onist icilin in vitro and to investigate the analgesic effect of icilin in a neuropathic pain model i
80  cord likely plays a predominant role in the analgesic effect of intrathecal clonidine on neuropathic
81 carinic receptors play a greater role in the analgesic effect of intrathecal clonidine.
82 t that spinal nitric oxide (NO) mediates the analgesic effect of intrathecal clonidine.
83 letion of the Mrgpr cluster also blocked the analgesic effect of intrathecally applied bovine adrenal
84     Finally, we show that TRPM8 mediates the analgesic effect of moderate cooling after administratio
85 se studies tested whether IS potentiates the analgesic effect of MOR microinjected in the DRN, as pre
86  for treating bone cancer pain and improving analgesic effect of morphine clinically.
87 t as inhibiting JNK in reducing the enhanced analgesic effect of morphine in beta-arr2-/- mice to +/+
88 e, we examine the effect of tolerance to the analgesic effect of morphine on ischemic tolerance in mi
89 fferent JNK inhibitors reversed the enhanced analgesic effect of morphine, a known phenotype of beta-
90 arkable potentiation and prolongation of the analgesic effect of morphine, suggesting that muOR desen
91  during the pain challenge and the resulting analgesic effect of mu-opioid receptor activation was mo
92            These results demonstrate a novel analgesic effect of non-informative vision of the body.
93 termine the receptor subtype involved in the analgesic effect of NT69L and morphine.
94  constipation (OIC) without compromising the analgesic effect of opioids.
95 al of emotional experiences also mediate the analgesic effect of perceived control over pain.
96 praisal view of control and suggest that the analgesic effect of perceived control relies on activati
97    Behavioral results confirmed the expected analgesic effect of seeing the body, while fMRI results
98                             Importantly, the analgesic effect of several antidepressant drugs, includ
99 ical studies that have demonstrated that the analgesic effect of spinally administered lipid-soluble
100 which spinal mu opioid receptors mediate the analgesic effect of systemic mu opioids.
101                             In contrast, the analgesic effect of the agonist (trans)-3,4-dichloro-N-m
102  disinhibition, supporting the view that the analgesic effect of the GluN2B antagonist on neuropathic
103 binoid signaling is also responsible for the analgesic effects of acetaminophen against inflammatory
104  amount of caffeine can reversibly block the analgesic effects of acupuncture, and controlling caffei
105 nates cells expressing this receptor and the analgesic effects of alpha2-AR agonists.
106                             Tolerance to the analgesic effects of an opioid occurs after its chronic
107                                          The analgesic effects of BMAs are modest, and they should no
108  noradrenergic cell groups contribute to the analgesic effects of both NMDA receptor antagonists and
109                The mechanisms underlying the analgesic effects of botulinum toxin serotype A (BoNT-A)
110 of TRPV1 and block of TRPA1 may underlie the analgesic effects of camphor.
111 effects of morphine is also required for the analgesic effects of cannabinoids.
112 l insight into the topical mechanisms of the analgesic effects of capsaicin and the strategies to imp
113  plays a modulatory role in the mediation of analgesic effects of certain compounds, for example tric
114                                 Finally, the analgesic effects of combining Cereport and loperamide w
115 tonic pain in animals and for evaluating the analgesic effects of drugs.
116 eys is the source of the ACh involved in the analgesic effects of epidural neostigmine and could be m
117 del, but it is a potential mechanism for the analgesic effects of icilin in other pain models.
118 pheral opioid receptors and tolerance to the analgesic effects of intraarticular morphine.
119 tify the neural circuitry that underlies the analgesic effects of left DLPFC rTMS, and to examine how
120 the cellular sites for the spinally mediated analgesic effects of MOR activation and the potential an
121 iors, correlative neurochemical changes, and analgesic effects of morphine and cannabinoids in transg
122 e, but also reduced their sensitivity to the analgesic effects of morphine and led to faster developm
123 esting either a decreased sensitivity to the analgesic effects of morphine and/or basal hyperalgesia.
124 hine and the development of tolerance to the analgesic effects of morphine remained unaltered by the
125  has been hypothesized that tolerance to the analgesic effects of morphine results from the developme
126 xaggerated responses to cocaine, reduces the analgesic effects of morphine, and abolishes the effects
127               How hnRNP K contributes to the analgesic effects of morphine, however, is largely unkno
128 lammatory response that directly opposes the analgesic effects of morphine.
129 cated in the development of tolerance to the analgesic effects of morphine.
130 and, in some cases, reverse tolerance to the analgesic effects of morphine.
131  analgesia, they are unlikely to mediate the analgesic effects of morphine.
132 ts in the mu opioid receptor gene change the analgesic effects of morphine.
133 binds with beta-arrestin 2 and modulates the analgesic effects of morphine.
134 how that the mu opioid receptor mediates the analgesic effects of morphine; they further suggest that
135 1bf/f/p mice exhibited significantly reduced analgesic effects of mu and delta opioid receptor agonis
136  agonists, and provide insights into the non-analgesic effects of mu opioids.
137 ents may contribute to the anesthetic and/or analgesic effects of N(2)O.
138 oid analgesia, is proposed to facilitate the analgesic effects of nonserotonergic RM terminals in the
139         Recent data have demonstrated potent analgesic effects of one factor (glial cell line-derived
140                                  Many of the analgesic effects of opiate drugs and of endogenous opio
141        Mu opioid receptors (MOR) mediate the analgesic effects of opioid drugs such as morphine.
142                             Tolerance to the analgesic effects of opioids is a major problem in chron
143 te opioid-induced somnolence, to augment the analgesic effects of opioids, to treat depression, and t
144 e (including drug craving), reinforcing, and analgesic effects of oxycodone in human volunteers diagn
145  opioid use disorders and it may enhance the analgesic effects of oxycodone.
146 study compared the magnitude and duration of analgesic effects of smoked marijuana and dronabinol und
147 ion is not simply the sum of the independent analgesic effects of spinal kappa and delta opioid syste
148              It has been postulated that the analgesic effects of TCAs are determined by their abilit
149 endent contributions of GIRK channels to the analgesic effects of the -opioid receptor-selective agon
150 ation, providing a neurobiological basis for analgesic effects of the CB2 receptor in this model of O
151 dered by the development of tolerance to the analgesic effects of the drug.
152 are insensitive to the ataxic, sedative, and analgesic effects of the novel hypnotic drug, gaboxadol.
153  mutant receptor could be used to elicit the analgesic effects of the opioids without the accompanyin
154 nvolved in mediating the neuromodulatory and analgesic effects of the peptide.
155                                          The analgesic effects of these compounds involve long-term d
156                                    While the analgesic effects of these drugs are mediated by mu-opio
157 V1 antagonists in various types of pain, the analgesic effects of two TRPV1 antagonists with similar
158                        The findings that the analgesic effects of various antidepressant drugs are di
159                         We evaluate here the analgesic effect on rats of epidurally administered RTX,
160            Vision of the body produced clear analgesic effects on both subjective ratings of pain and
161  neurotensin receptors (NTS1 and NTS2) exert analgesic effects on different types of nociceptive moda
162 ateral prefrontal cortex (DLPFC) can produce analgesic effects on postoperative and laboratory-induce
163 ICa(V) in DRG neurons is unlikely to mediate analgesic effects or contribute directly to the pathogen
164 rols as to their capacity to predict placebo analgesic effects, placebo-induced activation of mu-opio
165            Although most opiates exert their analgesic effects primarily via mu opioid receptors, a n
166 atecholamine neurons may mediate part of the analgesic effect produced by systemic administration of
167 ly-Phe-Leu-Ser(beta-D-Glc)-CONH(2), produces analgesic effects similar to morphine, even when adminis
168 atively small study, but the dose-responsive analgesic effects suggest that NP2 may be effective in r
169 ne applied to skin-harvest sites produced an analgesic effect that reduced narcotic requirements comp
170 limbs, but corpus callosotomy eliminated the analgesic effect that was ipsilateral, but not contralat
171          However, in addition to the desired analgesic effects, this TRPV1 antagonist significantly i
172             mu-Opioid agonists mediate their analgesic effect through GPCRs that are generated via al
173                                          The analgesic effect was assessed by prolongation of the paw
174                            Importantly, this analgesic effect was maintained even in animals with lat
175  prefrontal cortex (L-DLPFC) tDCS induced an analgesic effect, which was explained by reduced perfusi
176 uce better biological profiles (e.g., higher analgesic effect with significantly less adverse side ef
177 assay in mice, the pyridomorphinans produced analgesic effects with varying potencies and efficacies
178  been implicated in the formation of placebo analgesic effects, with initial reports dating back thre

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