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1 2A and alpha2C, and the 125I-labeled agonist clonidine.
2  normoxic, hypoxic, and hypoxic-treated with clonidine.
3 rawal treatment with either buprenorphine or clonidine.
4 d by the selective alpha2 adrenergic agonist clonidine.
5  dose-dependently by perineural injection of clonidine.
6 intraarterial infusions of phenylephrine and clonidine.
7 agonist phenylephrine and the alpha2-agonist clonidine.
8  increased resistance to M. avium induced by clonidine.
9 sed resistance to M. avium growth induced by clonidine.
10        Pertussis toxin blocked the effect of clonidine.
11  role in the analgesic effect of intrathecal clonidine.
12 mediates the analgesic effect of intrathecal clonidine.
13 thoroughly the neuroprotective properties of clonidine.
14 idine orally; or combined nitroglycerin plus clonidine.
15  was not reduced by peripheral or intra-BSTv clonidine.
16 dies provided data for midazolam and two for clonidine.
17 ll as the adrenergic alpha2 receptor agonist clonidine.
18                                              Clonidine (0.003-0.1 mg/kg, i.p.) dose-dependently atten
19 he intracerebroventricular (ICV) infusion of clonidine (0.03 microgram) caused an increase in NO conc
20 hibited by pretreatment with a fixed dose of clonidine (0.15 mg/kg, s.c.).
21 , patients were randomly assigned to receive clonidine (0.2 mg per day) or placebo just before surger
22 uring iontophoresis of phenylephrine (PE) or clonidine (0.5 mm, seven 0.1 mA pulses followed by one 0
23  interval [CI], -1.70 to -0.57), 4 trials of clonidine (-0.95; 95% CI, -1.44 to -0.47), and 2 trials
24                                         Oral clonidine, 0.1 mg/d, is effective against tamoxifen-indu
25                      Sheep were treated with clonidine (1 mug/kg/hr) or saline-vehicle from 24 to 32
26  cardiac rate, followed by administration of clonidine (1.0 mg/kg).
27       Nanoinjection of the alpha2-AR agonist clonidine (1.2 nmol) into the rostral raphe pallidus are
28 367 and 339, respectively; hazard ratio with clonidine, 1.08; 95% confidence interval [CI], 0.93 to 1
29   Furthermore, the general alpha2-AR agonist clonidine (10 muM) failed to affect sIPSC frequency.
30 onists dexmedetomidine (25 mug/kg, i.v.) and clonidine (100 mug/kg, i.v.) inhibited shivering EMGs, B
31 nylephrine (-11 +/- 4 versus -39 +/- 4%) and clonidine (-12 +/- 4 versus -38 +/- 5%; all P < 0.005) w
32 enylephrine (-3 +/- 3 versus -28 +/- 4%) and clonidine (-15 +/- 4 versus -26 +/- 3%; all P < 0.05).
33 henylephrine (-12 +/- 8 vs. -37 +/- 8 %) and clonidine (-17 +/- 6 vs. -49 +/- 4 %) were significantly
34 lysaccharide, 10.7 [95% CI, 9.9-11.6]; after clonidine, 17.5 [95% CI, 16.7-18.4]).
35 thylphenidate (11.1); antidepressants (3.2); clonidine (2.3); and neuroleptics (0.9).
36  saline, dexmedetomidine (100 mug/kg IV), or clonidine (200 mug/kg IV).
37 tly studied and efficacious medications were clonidine (22 studies; risk ratio: 1.6, numbers needed t
38 older men, but did attenuate the response to clonidine (-22 +/- 3 versus -37 +/- 6%; P < 0.05).
39              Conscious rats received saline, clonidine (30 microg/kg, i.v.), saline plus sodium nitro
40 eatment (72%) relative to those who received clonidine (39%) (P<.05).
41 iglets that were in the Hx+Cl group received clonidine 5 min prior to hypoxia.
42         In vitro stimulation of the NTS with clonidine (50 nmol/L) resulted in an increase in the NO
43 pants choosing naltrexone therapy within the clonidine (8 [22.2%]), tramadol ER (7 [19.4%]), or bupre
44                                              Clonidine, a readily available medication, is useful in
45                                 In contrast, clonidine-activated alpha(2A)AR were switched by voltage
46 , studies were designed to ascertain whether clonidine acts as a free radical scavenger.
47     These results suggest that pre-operative clonidine administration could be a useful supplement to
48  the present study tests the hypothesis that clonidine administration will block increased nuclear Ca
49                                        After clonidine administration, growth hormone rose in PSP sub
50                                              Clonidine alone had no effect, but when administered fol
51 o G protein is more readily achieved for the clonidine/alpha(2)-AR/Goalpha1 complex.
52 release), phenylephrine (alpha1-agonist) and clonidine (alpha2-agonist) were assessed.
53 henylephrine (selective alpha1-agonist), and clonidine (alpha2-agonist) were determined in 10 young (
54 ether the increase in decisiveness driven by clonidine also entails changes in hippocampal search pro
55                                              Clonidine also increased the production of ONOO(-) in M.
56                                              Clonidine also induced lower levels of NE release in the
57                                     Systemic clonidine also prevented the stress-associated increase
58 tions in the LH of two inhibitory compounds, clonidine (an alpha-2 adrenergic agonist) and muscimol (
59 ease), phenylephrine (an alpha1 agonist) and clonidine (an alpha2 agonist) in 10 healthy men during r
60                     This study tests whether clonidine, an alpha(2)-adrenergic receptor agonist, alte
61           These effects were all mimicked by clonidine, an alpha-2 receptor agonist.
62 , including peripheral nerve block or spinal clonidine, an alpha2-adrenergic agonist.
63                      Significance statement: Clonidine, an alpha2-adrenergic receptor agonist, which
64 ns had a higher spontaneous firing rate, and clonidine-an alpha2A-adrenergic agonist-inhibited LC neu
65 w, medium, and high renin, respectively, for clonidine and 83%, 82%, and 83%, respectively, for dilti
66 he effect of noradrenaline was reproduced by clonidine and antagonized by yohimbine, consistent with
67 -dependent adolescents relative to combining clonidine and behavioral interventions.
68  vitro data were generally in agreement that clonidine and bFGF counteracted the effect of NMDA as wo
69 gest that tramadol ER is more effective than clonidine and comparable to buprenorphine in reducing op
70                                              Clonidine and dexmedetomidine have many similar or super
71                                              Clonidine and diltiazem had consistent response rates re
72 in native sympathetic neurons in response to clonidine and guanfacine, two drugs used for treatment o
73  occurred in 329 patients (6.6%) assigned to clonidine and in 295 patients (5.9%) assigned to placebo
74  opioids as adjuncts are being challenged by clonidine and ketamine, which have more benign side effe
75                                              Clonidine and nitroglycerin increased gastric compliance
76 amines and diphenhydramine; second, miosis - clonidine and opioids; third, nystagmus - dextromethorph
77 scending doses of oral naltrexone along with clonidine and other adjunctive medications.
78 ommonly experienced by patients treated with clonidine and other imidazoline-related drugs.
79  is necessary for the hypotensive effects of clonidine and other sympathoinhibitory adrenergic agonis
80                                        Thus, clonidine and oxymetazoline behaved as partial agonists.
81  Gialpha1 increased the relative efficacy of clonidine and oxymetazoline such that the two ligands no
82                           The alpha agonists clonidine and phenylephrine both inhibited the potassium
83 In 16 other healthy subjects, the effects of clonidine and placebo on gastric emptying of solids were
84 y acting alpha2-adrenergic receptor agonist, clonidine), and hypoxia and sympathetic inhibition.Oxyha
85 honium, procaine, phencyclidine, cocaine, or clonidine), and the peptides displayed enhanced selectiv
86 g sedative premedications such as midazolam, clonidine, and dexmedetomidine.
87                          The SSRIs or SNRIs, clonidine, and gabapentin trials provide evidence for ef
88 sed to treat vasovagal syncope (propranolol, clonidine, and paroxetine) in a double-blind crossover s
89 ing exercise and is reversed by propranolol, clonidine, and paroxetine.
90 f ethanol, oxotremorine, nicotine, baclofen, clonidine, and the cannabinoid receptor agonist WIN 55,2
91  Since this treatment completely antagonized clonidine antinociception (40 microg, i.c.v.), supraspin
92 2 channels in mutant mice largely eliminated clonidine antinociception and significantly decreased mo
93                The protective effect of 0.5% clonidine appeared to be greater when topically applied
94  8-day-old rats whether these 2 responses to clonidine are causally related.
95         Alpha-2 adrenoceptor agonists (e.g., clonidine) are effective at preventing many of the behav
96 ties of alpha(2)-adrenoceptor agonists, like clonidine, are very different from betaxolol.
97 a cellular substrate for the clinical use of clonidine as a treatment for hypertension as well as a r
98  likely that the use of epidural ketamine or clonidine as adjuncts to local anaesthetics will grow.
99                                              Clonidine, as compared with placebo, did not reduce the
100                                              Clonidine, as compared with placebo, was associated with
101 .1.1.28) and as inhibitors of the binding of clonidine at the alpha(2)-adrenoceptor.
102 e (PNMT) and as inhibitors of the binding of clonidine at the alpha(2)-adrenoceptor.
103 injection of the alpha2-adrenoceptor agonist clonidine at the site of peripheral nerve injury reduces
104      alpha(2)-adrenoceptor agonists, such as clonidine, attenuate hypoxia-induced damage to brain and
105                                              Clonidine attenuated the increases in c-fos in the mNTS
106                                     Low-dose clonidine attenuates sympathetic outflow and systemic in
107  action, and provide the first evidence that clonidine attenuates the expression of the closely linke
108 he presence and absence of a alpha2-agonist (clonidine), beta-adrenergic receptor antagonist (propran
109 ailed to show displacement of specific [(3)H]clonidine binding to rat brain membranes for either comp
110                   The authors tested whether clonidine blocks stress-induced seeking of heroin and co
111             The fact that both betaxolol and clonidine blunt hypoxia-induced death to retinal ganglio
112                                              Clonidine but not nitroglycerin reduced aggregate and pa
113  with oestrogen, gabapentin, paroxetine, and clonidine, but little or no benefit with other agents; a
114                  Moreover, i.p. injection of clonidine, but not betaxolol, elevated bFGF mRNA levels
115 em to mediate the antinociceptive effects of clonidine, but not that produced by improgan.
116                  Statins, beta-blockers, and clonidine can potentially improve long-term cardiac risk
117              Administration of perioperative clonidine can reduce the risk of perioperative myocardia
118                        This ICV injection of clonidine caused a fall in mean arterial pressure of -22
119 rgic agonists (phenylephrine (PE), alpha(1); clonidine (CL), alpha(2)).
120 deltorphin II (DELT), the alpha(2)AR agonist clonidine (CLON) or their combination to inhibit calcito
121                                              Clonidine (CLON), an alpha-2 agonist, has anxiolytic-lik
122 0.5 mg/kg BW), an alpha2-adrenergic agonist, clonidine (CLON; 0.6 mg/kg BW), or a beta-adrenergic ago
123 microinfusions (1 mul) of the alpha2 agonist clonidine (CLON; 1.32 nmol), and half received the alpha
124                                Perioperative clonidine comes in a patch form that can be used in pati
125 nists such as oxymetazoline, cirazoline, and clonidine, confirming previous evidence that this class
126 ine and synaptic transmission was reduced by clonidine, consistent with an action at presynaptic alph
127 ulation of the release of NO in the brain by clonidine contributes to its central antihypertensive ac
128 thesized that the anxiolytic-like actions of clonidine could be mimicked by stimulation of alpha-2 re
129                                       NE and clonidine decreased calcium currents evoked by depolariz
130                                 The roles of clonidine, dexmedetomidine, ketamine and nalbuphine in t
131                                              Clonidine did not affect basal [(3)H]cAMP levels, but at
132         Although NO production was required, clonidine did not increase the level of NO in M. avium-i
133 s: hydrochlorothiazide, atenolol, captopril, clonidine, diltiazem (sustained release), or prazosin.
134 ous ligand(s) for imidazoline binding sites, clonidine-displacing substance (CDS), has been a major g
135                            Administration of clonidine during hypotensive sepsis reduced renal sympat
136 or antagonists (atropine and scopolamine) on clonidine-elicited nitrite release was more potent than
137 inic antagonists dose-dependently attenuated clonidine-elicited nitrite release.
138                                              Clonidine evoked a decrease in cRCF ( approximately 30%;
139                                              Clonidine evoked both increases and decreases in cRCF be
140 idazoxan (6 nmol) into the rRPa reversed the clonidine-evoked inhibition of BAT SNA and BAT thermogen
141 arinic and nicotinic receptor antagonists on clonidine-evoked nitrite (a stable product of NO) releas
142 e present study, we tested a hypothesis that clonidine-evoked NO release is dependent primarily on mu
143                   Ineffective drugs included clonidine, flunarizine, pizotifen, propranolol, and valp
144 dition, iontophoresis of the alpha-2 agonist clonidine, footshock administration, and LC stimulation
145 s before the clonidine) reduced responses to clonidine for both mean arterial pressure and heart rate
146 nd epidural ones, as well as the addition of clonidine for peripheral neural blockade, have been desc
147  have shown certain benefits from the use of clonidine for regional anesthesia, further investigation
148           Most authors agree that the use of clonidine for regional neural blockade in combination wi
149 itch was notably faster than dissociation of clonidine from alpha(2A)AR, indicating voltage-dependent
150 in quality-of-life scores (0.3 points in the clonidine group compared with -0.2 points in the placebo
151                     During intervention, the clonidine group had a lower number of steps per day (mea
152 prenorphine condition and 5% of those in the clonidine group initiated treatment with naltrexone.
153 se in hot flash frequency was greater in the clonidine group than in the placebo group after 4 weeks
154           Significantly more patients in the clonidine group than in the placebo group had clinically
155 group difference in time to relapse, but the clonidine group took longer to lapse (hazard ratio=0.67,
156  partly decoupled from opioid craving in the clonidine group, supporting the authors' hypothesized me
157                              Propranolol and clonidine had no significant effect on SBP during exerci
158                                  Background- Clonidine has an antihypertensive effect by its action i
159                                              Clonidine has been used for many purposes, including red
160                                              Clonidine has recently been used as a pre-operative medi
161 re therefore undertaken to determine whether clonidine has similar properties.
162                                Perioperative clonidine has some advantages over perioperative beta-bl
163                                              Clonidine hydrochloride capsules (25 microg or 50 microg
164                                         Oral clonidine hydrochloride, 0.1 mg/d, or placebo for 8 week
165                   Administration of low-dose clonidine in patients undergoing noncardiac surgery did
166    The latest articles describing the use of clonidine in regional anesthesia are discussed.
167 dazol-2-yl)-6-quinoxalinamine (UK14,304) and clonidine in spinophilin-null mice.
168          The increased efficacy observed for clonidine in the Goalpha1 transfectants was not due to c
169 se findings, a clinical trial for the use of clonidine in the treatment of persistent vasopressor-ref
170  effect of the alpha(2)-adrenoceptor agonist clonidine in this rat model.
171  BB NHE3 exists in lipid rafts; (ii) EGF and clonidine increase the amount of BB NHE3; (iii) lipid ra
172 mans, the alpha2-adrenergic receptor agonist clonidine increases decisiveness in tasks that require p
173     Prolonged treatment with either DAMGO or clonidine induced a mutual cross-desensitization between
174 pha(2)-adrenergic agonist (alpha(2)-agonist) clonidine induced resistance to M. avium growth in the R
175 uble NHE3 pool, are involved in the EGF- and clonidine-induced acute increase in amount of BB NHE3; (
176                                              Clonidine-induced alpha(2A)AR desensitization, but not r
177 urthermore, the more pronounced morphine and clonidine-induced antinociception in male mice disappear
178         Based on the almost complete loss of clonidine-induced antinociception in the mutant mice, we
179                                This EGF- and clonidine-induced increase of BB NHE3 was associated wit
180 nic, as well as nicotinic, receptors mediate clonidine-induced NO release in the spinal cord.
181 ce has indicated that a key mechanism of the clonidine-induced reversal of the effects of NMDA antago
182          Prenalterol pretreatment suppressed clonidine-induced ultrasound production at both doses.
183  2 mild hyperthermia significantly inhibited clonidine-induced ultrasound production.
184                             Noradrenaline or clonidine inhibited the capsaicin-activated current by a
185 ol5]enkephalin (DAMGO) or the alpha2 agonist clonidine inhibited voltage-gated Ca2+ currents in these
186 ese findings establish a causal link between clonidine inhibition of c-fos expression in brainstem an
187              No evidence could be found that clonidine interacts with sodium or L-type calcium channe
188                                              Clonidine is a partial alpha 2 adrenergic agonist that h
189                                         When clonidine is added to a fentanyl-bupivacaine mixture for
190 lts suggest that the decisiveness seen under clonidine is due to limited exploration of potential opt
191 logues of the alpha2 adrenergic agonist drug clonidine is elaborated.
192                                     Low-dose clonidine is not clinically useful in CFS.
193 ion of alpha(2) adrenergic agonists, such as clonidine, is capable of alleviating neuropathic pain.
194 egy is to combine adjuvants such as opioids, clonidine, ketamine and neostigmine to potentiate the ef
195             Researchers have speculated that clonidine limits the amount of mental search that subjec
196                                 We find that clonidine limits the options searched by rats, suggestin
197             However, the mechanisms by which clonidine makes them more decisive remain unknown.
198                    Yohimbine antagonized the clonidine-mediated adenylyl cyclase inhibition.
199 H enhanced the alpha2-adrenoreceptor agonist clonidine-mediated inhibition (3 microM; NORM, 23 +/- 2%
200 he presence of the NO donor spermine-NO, the clonidine-mediated inhibition of forskolin- and isoprote
201                                              Clonidine, meperidine, tramadol, nefopam, and ketamine w
202 lammatory agents, anticonvulsants, ketamine, clonidine, mexiletine, antidepressants, and anxiolytics
203 cerebroventricularly applied agonists (NMDA, clonidine, muscimol, and baclofen) at several types of r
204                          A 7-day taper using clonidine (n = 36), tramadol ER (n = 36), or buprenorphi
205 angiotensin-converting-enzyme inhibitors, or clonidine (n=15,044), those assigned calcium antagonists
206 prenorphine and randomly assigned to receive clonidine (N=61) or placebo (N=57) for 14 weeks.
207 ase alpha2-adrenergic agonists guanfacine or clonidine (no studies).
208 nts 1 and 2 prevent or dampen the effects of clonidine on cardiac rate.
209 cavenger of ONOO(-), inhibited the effect of clonidine on M. avium growth.
210 the effects of the alpha2-adrenergic agonist clonidine on mean arterial pressure, renal sympathetic n
211  role in the analgesic effect of intrathecal clonidine on neuropathic pain.
212  search processes, we compared the effect of clonidine on spatial representations in hippocampal neur
213 The present study investigated the effect of clonidine on the basal and inducible c-jun and c-fos mRN
214                    Studies of the effects of clonidine on these gastric functions and symptoms in dis
215 aken to determine whether i.p. injections of clonidine or betaxolol affect retinal bFGF mRNA levels.
216 awal (ie, detoxification) from opioids using clonidine or buprenorphine hydrochloride is a widely use
217          Here, we test this hypothesis using clonidine or guanfacine (GFC), another alpha-2 agonist,
218         In contrast, the adrenergic agonists clonidine or norepinephrine, and the K(ATP) channel inhi
219 re randomized 1:1 to treatment with low-dose clonidine or placebo for 9 weeks and monitored for 30 we
220 plications to receive aspirin or placebo and clonidine or placebo.
221 nous nitroglycerin; 0.0125, 0.025, or 0.1 mg clonidine orally; or combined nitroglycerin plus clonidi
222 ipants, surgeons, and sedationists preferred clonidine over the placebo.
223 (AR) transfectants, the alpha(2)-AR agonists clonidine, oxymetazoline, UK-14304, and epinephrine incr
224 tained at the end of the taper compared with clonidine participants (22 [61.1%]); tramadol ER retenti
225 isfaction in the group of patients receiving clonidine plus morphine.
226 ), saline plus sodium nitroprusside (NP), or clonidine plus NP.
227 tment (0.03-0.15 mg/kg, s.c.) and reduced by clonidine posttreatment (0.15 mg/kg, s.c.).
228                                              Clonidine pre-treatment increased and prolonged sedation
229  trial, we characterized the effects of oral clonidine pre-treatment on intravenous diazepam/meperidi
230 s also inhibited in a dose-related manner by clonidine pretreatment (0.03-0.15 mg/kg, s.c.) and reduc
231                                   Perineural clonidine prevented both the increase in leukocyte numbe
232 creased with hypoxia (137 +/- 13%; P =0.02); clonidine prevented the hypoxia induced increase (94 +/-
233                           The data show that clonidine prevents hypoxia-induced increase in CaM KIV a
234              In an intent-to-treat analysis, clonidine produced the longest duration (in consecutive
235 suggest that while most of topically applied clonidine reaches the retina by a systemic route one can
236 rgic (phenylephrine) and alpha 2-adrenergic (clonidine) receptor stimulation were blunted during mode
237 d opioid (morphine) and alpha(2)-adrenergic (clonidine) receptor-induced antinociception in a spinal
238                                Additionally, clonidine reduced the capacity of leukocytes to express
239                                   Similarly, clonidine reduced the frequency of capsaicin-induced mEP
240                       In spinal cord slices, clonidine reduced the frequency of capsaicin-induced min
241                                              Clonidine reduced the number of macrophages and lymphocy
242 cromol; delivered ICV, 30 minutes before the clonidine) reduced responses to clonidine for both mean
243 ne, ketamine, dexmedetomidine, propofol, and clonidine) reduced the risk of delirium (relative risk,
244 nd the alpha(2)-adrenergic receptor agonist, clonidine, reduced the number of Fos-li dopaminergic neu
245 ngs should be reconciled with the absence of clonidine-related GH blunting in the same cohort.
246                                              Clonidine relaxes the stomach and reduces gastric sensat
247 activation of adrenergic alpha2 receptors by clonidine represents a double-hit to pancreatic islets t
248  determine whether the hypotensive action of clonidine resulted from its stimulation of excess NO in
249 of patients' stress to test hypotheses about clonidine's behavioral mechanism of action.
250 ting the authors' hypothesized mechanism for clonidine's benefits.
251                   These results suggest that clonidine's effect on ultrasound production is mediated
252                                              Clonidine significantly increased the numbers of BIS-dep
253                                              Clonidine significantly inhibited GABAergic neurotransmi
254 ising for the treatment of gastroparesis are clonidine, sildenafil, and intrapyloric botulinum toxin.
255 istration of the alpha2 adrenoceptor agonist clonidine simultaneously evokes ultrasound production an
256 e include a belladonna alkaloid preparation, clonidine, soy phyto-oestrogens, vitamin E, gabapentin,
257 P < .001) from stabilization to taper in the clonidine (stabilization mean, 0.64 [SE, .05]; taper mea
258 between 1991 and 1995 across the 3 sites for clonidine, stimulants, and antidepressants, while neurol
259                                 Injection of clonidine suppressed the spatial representation of the u
260 between the taper and post-taper periods for clonidine (taper mean, 13.1; post-taper mean, 3.2; P < .
261               The response to growth hormone-clonidine testing, a neuropharmacological assessment of
262 ogram, while the HMO had nearly 3 times more clonidine than antidepressant use (1.9 vs 0.7).
263 ion and endocytosis of alpha(2A)AR evoked by clonidine than by guanfacine.
264 nsitization of Ca(2+) current suppression by clonidine than guanfacine, which paralleled a more marke
265 dentified a second-line agent, perioperative clonidine, that can be used to reduce the risk of periop
266 r harmane, the alpha(2)-adrenoceptor agonist clonidine, the mu-opioid receptor agonists morphine and
267 ed in anesthesia and pain management include clonidine, tizanidine, and dexmedetomidine.
268 there is little difference in the ability of clonidine to interact with or stabilize alpha(2)-AR-Gial
269                              The addition of clonidine to intravenous regional anesthesia resulted in
270  no difference in onset time.The addition of clonidine to the local anesthetic opioid mixtures seems
271                                              Clonidine treatment prevented the further decline in mea
272 ring amphetamine injections and abolished by clonidine treatment.
273                                 Both EGF and clonidine treatments were associated with a rapid increa
274 a trial was planned to compare midazolam and clonidine, two sedatives widely used within PICUs neithe
275             In another study, the effects of clonidine used for intra-articular administration in com
276 ign to allow separate evaluation of low-dose clonidine versus placebo and low-dose aspirin versus pla
277 son of the dynamics of voltage-dependence of clonidine- vs. norepinephrine-activated receptors uncove
278 owed that co-administration of rapamycin and clonidine was associated with an increased incidence of
279                     The protective effect of clonidine was attenuated when the alpha(2)-adrenoceptor
280              These changes were blunted when clonidine was injected intraperitoneally before or after
281 mplete spinalization (T13) was performed and clonidine was injected to induce rhythmic activities.
282                            No dose effect of clonidine was observed on gastric emptying.
283            Less clear results were seen when clonidine was used for caudal anesthesia in a pediatric
284 pidural analgesia using levobupivacaine with clonidine was used in patients undergoing total hip arth
285                          The higher doses of clonidine were associated with a more cephalad spread of
286                           Patients receiving clonidine were more likely than patients receiving place
287 ly, the electrographic responses to NMDA and clonidine were potentiated, whereas the ECoG effects med
288                        All of the effects of clonidine were prevented by coadministration of an alpha
289                               The effects of clonidine were prevented by the alpha-2A subtype selecti
290 or responses in the leg to phenylephrine and clonidine were similar (or enhanced) postexercise vs. pr
291 esponses in the forearm to phenylephrine and clonidine were similar (or enhanced) postexercise vs. pr
292 for older versus young men, respectively) to clonidine were similar in the 2 groups.
293 ansmission, the effects of noradrenaline and clonidine were tested on the capsaicin-activated current
294 and apraclonidine, acted in a similar way to clonidine when applied topically but because of the numb
295  assessed if the alpha2-autoreceptor agonist clonidine (which decreases norepinephrine release) would
296                                     Low-dose clonidine, which blunts central sympathetic outflow, may
297  blocked the increased resistance induced by clonidine, while a Gs-protein antagonist was without eff
298 cts were identified for midazolam and 16 for clonidine with full texts obtained for 80 and 6 articles
299                        For the comparison of clonidine with placebo, patients were randomly assigned
300  after exposure to forskolin, isoproterenol, clonidine, yohimbine, pertussis toxin, and the NO donor

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