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1 adpoles to pentylenetetrazole (PTZ), a known convulsant.
2 -CCM is a GABAA receptor inverse agonist and convulsant.
3  during the age when CRF is most potent as a convulsant.
4  are anaesthetics but a few unexpectedly are convulsants.
5 lity and reduce seizure threshold to further convulsants.
6  currents and decreased binding of the caged-convulsant [(35)S]TBPS to GABA(A) receptors.
7 x and allosterically modulate the binding of convulsant ([35S]t-butylbicyclophosphorothionate, [35S]T
8                                          The convulsant 4-aminopyridine (4AP) facilitates the synchro
9                                          The convulsant 4-aminopyridine was used to induce interictal
10 re administered subconvulsant (25 mg/kg) and convulsant (60 mg/kg) doses of PTZ during a week, and br
11                  It is unknown whether these convulsants act as negative allosteric modulators by bin
12 tory sites are not enantioselective, and the convulsant action of S-mTFD-MPPB results from its neglig
13 ll pharmacological profile suggests that the convulsant actions of PS are mediated predominantly via
14 the low affinity site, but without potential convulsant activity, inherent to agents which block GABA
15 say and also inhibited delta agonist-induced convulsant activity.
16 etermine the functional consequences of anti-convulsant administration directed against seizure activ
17 nula was placed in the lateral ventricle for convulsant agent administration (20 microg of NMDA), whi
18 tylenetetrazol (PTZ), which is a widely used convulsant agent, on rat brain.
19  study was to examine the effect of the anti-convulsant agent, riluzole, on high-affinity glutamate u
20 izure phenotype of DKO mice at high doses of convulsant agents and advanced stages of seizures.
21 nyl) barbituric acid (S-mTFD-MPPB) acts as a convulsant and GABAAR inhibitor.
22 arbiturates have been discovered that act as convulsants and inhibitors of gamma-aminobutyric acid ty
23 es (e.g. endosulfan and fipronil) are potent convulsants and insecticides that block the GABA-gated c
24 , including trycyclic anti-depressants, anti-convulsants, and opiates.
25 tigated the effect of carbamazepine, an anti-convulsant, as it is known to have membrane stabilising
26 (S-mTFD-MPPB), a photoreactive analog of the convulsant barbiturate S-MPPB, inhibits alpha1beta3gamma
27                In mice the S-enantiomer is a convulsant, but the R-enantiomer is an anticonvulsant.
28 electroencephalographic seizures produced by convulsant compounds, and these effects were associated
29  DM-CocE administered to rats 10 min after a convulsant dose of cocaine alters the normal metabolism
30 er maze before and after administration of a convulsant dose of pilocarpine at P34.
31 nsity of the seizure response to intravenous convulsant doses of cocaine and lidocaine individually (
32  Bicuculline injected intracortically in non-convulsant doses produced a stereotypy indistinguishable
33 lts from the present study suggest that anti-convulsant drug administration directed against subclini
34                                         Anti-convulsant drug administration or recurrent seizures can
35 ctional recovery than seizures alone or anti-convulsant drug treatment after seizure activity has occ
36                                 Certain anti-convulsant drugs, as well as convulsive seizures impede
37 es reported in immature zebrafish exposed to convulsant drugs.
38 suggest that alpha4betadelta GABARs are anti-convulsant during adolescence.
39 er, MK-906, along with P, prevented this pro-convulsant effect of P withdrawal, suggesting that the G
40 ic acid in the brain contributes to the anti-convulsant effect of the medium chain triglyceride ketog
41 BA in the hippocampus, and result in an anti-convulsant effect with this peptide.
42 These data are consistent with T having anti-convulsant effects and that 5alpha-reduced metabolites m
43 this report, we test the hypothesis that pro-convulsant effects are produced by withdrawal from the G
44 ich are likely to contribute to the additive convulsant effects noted when these drugs are abused in
45 +)-deficient mice were more sensitive to the convulsant effects of a peripheral injection of NMDA (10
46                    However, tolerance to the convulsant effects of CRF develops rapidly.
47 lly regulated CRF1 receptor in mediating the convulsant effects of CRF in the developing brain.
48 und that +/T mice were more sensitive to the convulsant effects of nicotine compared with their wild-
49 nt of epilepsy, as well as the pro- and anti-convulsant effects of the newer anesthetic agents.
50 ent which may be functionally related to the convulsant effects of this excitotoxin.
51 rimarily upon a differential response to the convulsant effects of various drugs.
52 on of food intake, reward behaviour and anti-convulsant effects.
53 s cognition in animals without anxiogenic or convulsant effects.
54 ced in otherwise normal rats by the volatile convulsant flurothyl decrease the accuracy of locating a
55 ssy fiber sprouting is neither pro- nor anti-convulsant; however, there are caveats.
56 eptors expressed in Xenopus oocytes and were convulsant in mice after parenteral administration.
57 )-251D and aPTX (+)-267A proved to be potent convulsants in mice, with (+)-267A being approximately 5
58  However, they reduce thresholds to chemical convulsants in vivo and electrical stimulation in vitro,
59 reover, intervention after birth reduces the convulsant-induced seizure threshold to a level similar
60 ensitivity of naive mice to several chemical convulsant-induced seizures was also correlated with EtO
61 riform cortex" ("area tempestas") from which convulsants initiate temporal lobe seizures, and blockad
62 se in sensitivity to seizures induced by the convulsant kainic acid.
63 The application of drugs targeting different convulsant mechanisms (4-Aminopyridine, Pentylenetetrazo
64 anesthetics, non-anesthetics, and anesthetic/convulsants on tubulin dynamics.
65 ippocampal-dependent memory task-without the convulsant or proconvulsant activity associated with non
66 r to measuring seizure susceptibility to the convulsant pentylenetetrazol (PTZ), given via timed tail
67  a subthreshold dose (40 mg/kg) of the chemo-convulsant pentylenetetrazol and events recorded over 1
68 e showed an elevated seizure response to the convulsant pentylenetetrazol compared with sham mice, as
69 tin levels and delayed the onset of chemical convulsant pentylenetetrazole-induced generalized convul
70 bupivacaine (IC50 = 68 microM), and the anti-convulsant phenytoin ( approximately 50% inhibition at 2
71                   The central nervous system convulsant picrotoxin (PTX) inhibits GABA(A) and glutama
72 d bilobalide) have structures similar to the convulsant picrotoxin, a GABA(A) receptor antagonist, so
73 f many pharmacological agents, including the convulsant picrotoxin.
74 mg/kg failed to induce seizures or alter the convulsant potencies of pentylenetetrazol and NMDA.
75  of PS (50 nmol) significantly increased the convulsant potencies of systemically administered pentyl
76                  This study investigated the convulsant potency of cocaine and lidocaine alone and in
77                      It does not exhibit the convulsant, proconvulsant, or anxiogenic activity associ
78 azole-induced seizures, consistent with anti-convulsant properties and possible anxiolytic activity.
79 A receptors substantially contributed to the convulsant properties of acetylene analog 9.
80 campus, and that this action may confer anti-convulsant properties on agonists acting at the BB(2) re
81 alone, further suggesting that SNC80 has pro-convulsant properties.
82 SR mice than in WSP mice, suggesting an anti-convulsant role for receptor activation.
83                   The in vivo actions of the convulsant S-enantiomer are accounted for by its interac
84                                          The convulsant S-enantiomer binds solely at an inhibitory si
85 ognitive disorders because of anxiogenic and convulsant side effects.
86  the GABAAR transmembrane domain or to known convulsant sites in the ion channel or extracellular dom
87     To apply the same strategy to locate the convulsant sites requires the creation and mechanistic c
88 toxication) or seizure activity (produced by convulsants) slowed diffusion by >10-fold and created de
89                         One hour before each convulsant, Sprague Dawley rats received either saline (
90 activation of glutamate receptors, and other convulsant stimuli, the specific molecular steps require
91  mutant (Dbh -/-) mouse using four different convulsant stimuli: 2,2,2-trifluroethyl ether (flurothyl
92                          It is the target of convulsants such as picrotoxin and is mutated in some fo
93 ce exhibiting greater sensitivity in various convulsant tests compared to C57 mice.
94       4-Aminopyridine (4-AP) is a well known convulsant that enhances the release of both excitatory
95  long-term enhanced susceptibility to limbic convulsants that lasted to adulthood.
96                       However, after the pro-convulsant, the test mice (n = 9) had increased numbers
97  kinase, which may be the basis for new anti-convulsant therapies.
98 ures nor increased seizure susceptibility to convulsant were observed when Lgi1 was deleted in parval
99              In mice, S-mTFD-MPPB acted as a convulsant, whereas R-mTFD-MPPB acted as an anticonvulsa
100  are anaesthetics but unexpectedly a few are convulsants whose mechanism of action is poorly understo
101                                          Pro-convulsant withdrawal properties have been reported for

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