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1 inesterase inhibitors, such as donepezil and galantamine.
2  different modes of action for donepezil and galantamine.
3 ent in patients receiving 16 or 24 mg/day of galantamine.
4  nicotine-evoked responses occurred at 1 muM galantamine.
5 erminant of the therapeutic effectiveness of galantamine.
6 bed dosage ranges, donepezil (1-1000 nM) and galantamine (50-1000 nM) increase action potential-depen
7 ase who were randomly assigned to placebo or galantamine (8, 16, or 24 mg/day) were analyzed.
8 chnique was used to determine the effects of galantamine, a cholinesterase inhibitor and a nicotinic
9                                              Galantamine, a cholinesterase inhibitor used in Alzheime
10 alysis was conducted to assess the impact of galantamine, a cholinesterase inhibitor with nicotinic-r
11                    Here, we demonstrate that galantamine, a reversible and centrally acting AChE inhi
12 and human cerebral cortical slices, 1 microM galantamine, acting as a nicotinic APL, increased gamma-
13                           Likewise, 1 microM galantamine, acting as an APL on presynaptically located
14                             We conclude that galantamine activates the muscle-type ACh receptor by in
15  combination with atropine, a single dose of galantamine administered before or soon after acute expo
16                                        Acute galantamine administration (5.0 mg/kg, i.p.) attenuated
17                                              Galantamine administration also attenuated the reinstate
18 ever, there are no studies examining whether galantamine administration modulates nicotine self-admin
19 ts were designed to determine the effects of galantamine administration on nicotine taking and reinst
20 signed to examine the efficacy and safety of galantamine, an acetylcholinesterase inhibitor that also
21       183 of 207 patients (88%) who received galantamine and 177 of 200 (89%) who received placebo ha
22          Forty-two subjects were assigned to galantamine and 44 were assigned to placebo.
23   The combined cerebral metabolic effects of galantamine and citalopram suggest, consistent with prec
24 ved) by 1.9 (95% CI -0.1 to 3.9) points with galantamine and decreased (worsened) by 3.0 (-5.6 to -0.
25       Ki values of brain AChE inhibition for galantamine and donepezil, respectively, are 7.1 and 2.3
26                The brain-to-plasma ratio for galantamine and donepezil, respectively, ranges from 1.2
27 geted compounds obtained by linking together galantamine and memantine.
28 ad similar effects on receptor activation by galantamine and nicotinic agonists, suggesting that the
29 d previously for the nonselective nAChR PAMs galantamine and physostigmine at the canonical alpha-gam
30 ts performed in the simultaneous presence of galantamine and various nicotinic ligands showed that ch
31 e general features of receptor activation by galantamine are similar to that in the presence of ACh.
32 choline) was not affected by the presence of galantamine at concentrations up to 100 microm.
33                                      Thus, a galantamine-based therapy emerges as an effective and sa
34 r, there is also evidence demonstrating that galantamine can activate the nicotinic ACh receptor or m
35                                              Galantamine can be started and used safely in elderly pa
36 erlie the allocation of attention or whether galantamine changed the mapping from those beliefs to su
37              Studies of direct activation by galantamine demonstrated that this ligand is a low-effic
38  acetylcholinesterase (AChE) in complex with galantamine derivatives.
39                                              Galantamine did not compete for radioligand binding to t
40                                 In addition, galantamine did not reduce the initial rate of binding f
41               These results demonstrate that galantamine does not interfere with the occupation of th
42 patients 2 months after titration to a 24 mg galantamine dose.
43                                              Galantamine doses between 1.5 and 5 mg/kg are appropriat
44 p analyses revealed that the subjects taking galantamine exhibited significant improvements on the WA
45                              The efficacy of galantamine for cognitive impairments was evaluated with
46                                 Clearance of galantamine from the brain is in general faster that don
47       The allosterically potentiating ligand galantamine (Gal) modulates nicotinic cholinergic recept
48             168 of 207 (81%) patients in the galantamine group and 161 of 200 (81%) in the placebo gr
49                   Eight patients (4%) in the galantamine group and 21 patients (11%) in the placebo g
50 eas patients treated with 16 or 24 mg/day of galantamine had no change in total Neuropsychiatric Inve
51 tiation was blocked by mecamylamine, whereas galantamine had no effect on these measures in the absen
52                              The efficacy of galantamine has been shown in patients with mild, modera
53                                              Galantamine has recently been shown to reverse nicotine
54                                    Trials of galantamine, hydrocortisone, IgG, valganciclovir, isopri
55                                              Galantamine improved cognitive function but failed to si
56 onepezil is 40- to 500-fold more potent than galantamine in inhibiting AChE.
57 values for AChE inhibition for donepezil and galantamine in rat, mouse, and rabbit after subcutaneous
58                                              Galantamine is a rather weak acetylcholinesterase (AChE)
59                                              Galantamine is an acetylcholinesterase inhibitor that al
60                                              Galantamine is known to sensitize nAChRs to activation b
61                      Therefore, at 1 microM, galantamine is likely to increase facilitation of synapt
62                                Behaviorally, galantamine led to a greater influence of probabilistic
63 ive impairments in mice, which suggests that galantamine may function to prevent relapse in human smo
64                   Study results suggest that galantamine may have selective benefits for aspects of p
65 maries provide some evidence of benefits for galantamine, modafinil, levodopa, rotigotine, clozapine,
66 me setting were randomly assigned to receive galantamine (n=207), titrated initially to 24 mg/day, or
67                                     Doses of galantamine needed to protect guinea pigs fully against
68 icant between-group differences in favour of galantamine occurred for the SIB domains of memory (p=0.
69  nicotine self-administration, no effects of galantamine on nausea/malaise as measured by pica were n
70                    No significant effects of galantamine on sucrose self-administration or sucrose re
71                     Moreover, the effects of galantamine on sucrose-maintained responding and sucrose
72  inhibitor and nicotinic receptor modulator, galantamine, on the cerebral metabolic response to the s
73                         Three donepezil, two galantamine, one rivastigmine, and two memantine trials,
74                     We administered tacrine, galantamine or memantine to mouse cerebral cortical cult
75                            In SH-SY5Y cells, galantamine potentiated nicotine-evoked increases in int
76 irenz (EFV), acetaminophen, mirtazapine, and galantamine) prescribed for indications unrelated to cho
77  challenge with the cholinesterase inhibitor galantamine (Reminyl).
78                                              Galantamine (Reminyl; Janssen Pharmaceutica, Titusville,
79 lcholinesterase inhibitor and Alzheimer drug galantamine represents the prototypical allosteric ligan
80 king were also examined to determine whether galantamine's effects generalized to other reinforced be
81  of brain AChE inhibition, 3-15 times higher galantamine than donepezil doses are needed.
82                                       Unlike galantamine, the acetylcholinesterase inhibitors rivasti
83                                              Galantamine therapy was associated with reduced emergenc
84  this study, we have examined the ability of galantamine to directly activate the muscle-type nicotin
85 ork was to enhance the transportation of the galantamine to the brain via ascorbic acid grafted PLGA-
86 acebo-controlled trial of methylphenidate or galantamine to treat emotional and cognitive complaints
87                                              Galantamine treatment alone increased metabolism in the
88                          In contrast, during galantamine treatment, citalopram increased metabolism i
89                                    High-dose galantamine was associated with a significant reduction
90 In preventing the lethality of nerve agents, galantamine was far more effective than pyridostigmine,
91    In general, safety analyses revealed that galantamine was well tolerated.
92                                 In addition, galantamine, which is both an inhibitor of AChE and an a
93 m hippocampal slices was also potentiated by galantamine, with an additional component attributable t

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