Objective: To study the effect of L-type of Calcium channel blocker nimodipine and T-type of calcium channel blocker funarizine on locomotor activity in mice without pretreatment by any other drug. Materials and method: The study was carried out following permission from the Institutional animal ethics committee. Healthy Swiss albino mice of either sex were selected by the strict inclusion and exclusion criteria and the grouping is done. Group A is control treated with normal saline, Group B and C received two titrated doses of nimodipine while Group D and E received two titrated doses of flunarizine. The animals were then observed for motor control on inclined plane and the Statistical analysis was done by using unpairedt test. Results:...
Background: Skeletal muscle relaxants are a heterogeneous group of drugs. As a group, they are struc...
The laser scanning confocal microscope and fluorescence spectrophotometer were used to investigate t...
The antinociceptive action of four Ca2+ channel blockers, nifedipine, nimodipine, verapamil and dilt...
Background: Changes in the intracellular concentration of Ca2+ control a number of cellular and phys...
The relationship between opioid actions and L-type Ca2+ channel blockers has been well documented. H...
SUMMARY — Tardive dyskinesia (TI>), a serious complications of neuroleptic chronic use, has no ef...
Tardive dyskinesia (TD), a serious complications of neuroleptic chronic use, has no effective therap...
OBJECTIVE: The goal of this study was to investigate the potential protective effects of nimodipine ...
The present study was undertaken to investigate the effect of diltiazem, a L-type calcium channel bl...
Purpose: The study aimed to assess the depressant or antidepressant effects of several Nonsteroidal ...
<p>(A) The T-type calcium channel blockers NNC 55–0396 and mibefradil inhibit inflammatory mechanica...
The anticonvulsant effect of the dihydropyridine calcium channel blocker, nimodipine (NMD) was evalu...
The anticonvulsant effect of the dihydropyridine calcium channel blocker, nimodipine (NMD) was evalu...
Background and purpose: Spinal cord injuries are often followed by profound motor and sensory defici...
OBJECTIVE: To evaluate the acute adverse effects with respect to exploratory and spontaneous locomot...
Background: Skeletal muscle relaxants are a heterogeneous group of drugs. As a group, they are struc...
The laser scanning confocal microscope and fluorescence spectrophotometer were used to investigate t...
The antinociceptive action of four Ca2+ channel blockers, nifedipine, nimodipine, verapamil and dilt...
Background: Changes in the intracellular concentration of Ca2+ control a number of cellular and phys...
The relationship between opioid actions and L-type Ca2+ channel blockers has been well documented. H...
SUMMARY — Tardive dyskinesia (TI>), a serious complications of neuroleptic chronic use, has no ef...
Tardive dyskinesia (TD), a serious complications of neuroleptic chronic use, has no effective therap...
OBJECTIVE: The goal of this study was to investigate the potential protective effects of nimodipine ...
The present study was undertaken to investigate the effect of diltiazem, a L-type calcium channel bl...
Purpose: The study aimed to assess the depressant or antidepressant effects of several Nonsteroidal ...
<p>(A) The T-type calcium channel blockers NNC 55–0396 and mibefradil inhibit inflammatory mechanica...
The anticonvulsant effect of the dihydropyridine calcium channel blocker, nimodipine (NMD) was evalu...
The anticonvulsant effect of the dihydropyridine calcium channel blocker, nimodipine (NMD) was evalu...
Background and purpose: Spinal cord injuries are often followed by profound motor and sensory defici...
OBJECTIVE: To evaluate the acute adverse effects with respect to exploratory and spontaneous locomot...
Background: Skeletal muscle relaxants are a heterogeneous group of drugs. As a group, they are struc...
The laser scanning confocal microscope and fluorescence spectrophotometer were used to investigate t...
The antinociceptive action of four Ca2+ channel blockers, nifedipine, nimodipine, verapamil and dilt...