Results 111 to 120 of about 10,564,162 (159)
Comparative safety, pharmacokinetics, and off-target assessment of 1,1-bis(3'-indolyl)-1-(<i>p</i>-chlorophenyl) methane in mouse and dog: implications for therapeutic development. [PDF]
Rocha SM +3 more
europepmc +1 more source
The cellular distribution of P2X7, P2Y6, and P2Y12 during or after pilocarpine-induced status epilepticus and literature review. [PDF]
Li Y, Tang F, Luo Y.
europepmc +1 more source
Transient receptor potential vanilloid 4 blockage attenuates pyroptosis in hippocampus of mice following pilocarpine‑induced status epilepticus. [PDF]
Liu L +8 more
europepmc +1 more source
Regulatory Mechanism of CRTC1 on Autophagy and GluA2 Expression in Epilepsy. [PDF]
Wang X +5 more
europepmc +1 more source
The objective of the present study was to investigate the effects of senescence on the binding characteristics of muscarinic receptors by using [3H]quinuclidinyl benzilate ([3H]QNB) and [3H]N-methylscopolamine ([3H]NMS) as ligands in young (3 months), middle-age (10 months) and old (24 months) male Fischer 344 rats.
W, Surichamorn +4 more
openaire +3 more sources
In radioligand binding studies, the accuracy of the specific activity of the radiolabeled ligand has a large impact on the calculated receptor concentration and on the calculated affinities of both labeled and competitive ligands. A radioreceptor assay for anticholinergic drugs was employed to determine the specific activity of 3H-N-methylscopolamine ...
Ensing, K. +3 more
openaire +3 more sources
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Anomalous binding of [3H]N-methylscopolamine to rat brain muscarinic receptors
European Journal of Pharmacology, 1985In the present studies, we investigated the binding properties of [3H]quinuclidinyl benzilate ([3H]QNB) and [3H]N-methylscopolamine ([3H]NMS) to muscarinic acetylcholine receptors (mAChR) in rat brain homogenates. Our results indicate that the hydrophilic receptor ligand, [3H]NMS, is able to interact with high affinity only with a fraction of the ...
Esam E El-Fakahany
exaly +3 more sources
European Journal of Pharmacology, 1995
The ability of allosteric ligands to modulate the dissociation rate of [3H]N-methylscopolamine from atrial muscarinic receptors in the presence of varying concentrations of unlabelled N-methylscopolamine or atropine was evaluated. Gallamine, at a concentration approximating its KD value, slowed the dissociation of [3H]N-methylscopolamine in the ...
Arthur Christopoulos, F Mitchelson
exaly +3 more sources
The ability of allosteric ligands to modulate the dissociation rate of [3H]N-methylscopolamine from atrial muscarinic receptors in the presence of varying concentrations of unlabelled N-methylscopolamine or atropine was evaluated. Gallamine, at a concentration approximating its KD value, slowed the dissociation of [3H]N-methylscopolamine in the ...
Arthur Christopoulos, F Mitchelson
exaly +3 more sources
European Journal of Pharmacology, 1995
Alcuronium is known to stabilize allosterically the binding of the muscarinic antagonist N-methylscopolamine to muscarinic M2 receptors and thus to elevate the equilibrium binding of N-methylscopolamine in homogenized cardiac tissue. In order to check for a functional consequence of this effect, the action of alcuronium alone and in combination with N ...
Evi Kostenis, Klaus Mohr
exaly +3 more sources
Alcuronium is known to stabilize allosterically the binding of the muscarinic antagonist N-methylscopolamine to muscarinic M2 receptors and thus to elevate the equilibrium binding of N-methylscopolamine in homogenized cardiac tissue. In order to check for a functional consequence of this effect, the action of alcuronium alone and in combination with N ...
Evi Kostenis, Klaus Mohr
exaly +3 more sources

