Further studies on the mechanism of vasodepressor response in cats after intravenous administration of venom from the snake Dendroaspis jamesoni (Jameson's mamba).
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Biomedical subjects
Publications and source records attributed to R K Raina.
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Several agents with specific action on biologically active substances in brain were investigated for their influence on morphine analgesia. It was observed that imipramine, chlorpheniramine, and haloperidol antagonized morphine analgesia. The probable mechanism of action has been discussed.
Pharmacokinetics of a sustained release (SR) and conventional formulations of theophylline plus hydroxyethyltheophylline was compared with tablet aminophylline. Time concentration curve of serum theophylline with the three formulations after single and multiple dosage schedules revealed significantly retarded absorption with the SR preparation. SR tablet was also seen to produce uniform steady state levels with fluctuation of serum concentrations within the therapeutic range for a duration of over 12 hours. In comparison, aminophylline and conventional theophylline hydroxyethyltheophylline tablets produced sharp swings in steady state levels with trough levels dipping to subtherapeutic concentrations within 4-6 hours. SR formulation, therefore, is likely provide consistent serum levels and better therapeutic control in comparison to the other two conventional tablets.
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