* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Anticonvulsive Effects of Sodium Phenobarbital Experimental purpose
Pharmacognosy wikipedia , lookup
Pharmacokinetics wikipedia , lookup
Polysubstance dependence wikipedia , lookup
Zoopharmacognosy wikipedia , lookup
Drug interaction wikipedia , lookup
Theralizumab wikipedia , lookup
Neuropsychopharmacology wikipedia , lookup
Psychopharmacology wikipedia , lookup
Anticonvulsive Effects of Sodium Phenobarbital Experimental purpose To master the anticonvulsive effects of sodium phenobarbital and the elementary process of chi square test. To be familiar with the experimental condition of screening Anticonvulsants. Sedative and hypnotics are among the most widely prescribed drugs worldwide. Major therapeutic use is to cause sedation or encourage sleep. Anxiety states and sleep disorder are common. Action and use sedative and hypnotics apt to induce tolerance and dependence induce P-450 system adverse effects are common anticonvulsive effects generalized tonic-clonic seizures anesthesia and preanesthetic medication enhance CNS depression graded dose-dependent depression of CNS is a characteristic of sedativehypnotics. at still higher doses---coma and death Mechanism It can activate GABAA receptor, potentiate GABA action on chloride entry into the neuron. The GABAA receptor chloride ion channel complex has a structure assembled from five subunits. Barbiturates Benzodiazepines a increase the open time of Cl- channel b increase the open frequency of Cl- channel Adverse effect drug hangover: tiredness after awakes tolerance: induce P-450 system addiction: abrupt withdrawal may cause tremor, anxiety, weakness, restlessness, nausea and vomiting respiratory depression allergy Poisoning Poisoning: overdoses can cause death, depression of respiration and central cardiovascular depression. Treatment: artificial respiration; purging the stomach of its contents; alkalinization of blood and urine; hemodialysis Experimental animals Mice (of either gender), 18~22g Experimental apparatus Mouse cage injector Experimental drugs 50mg% Dimefline ih 0.4% Sodium Phenobarbital ip 0.9% Sodium Chloride (Normal Saline) ip Experimental indication Tetanic straighten in hind limbs is positive. Experimental procedure Take 48 mice, weigh them. All mice are assigned randomly to experiment group and control group according to the principle that equal weight between groups. Students are divided into twelve groups, every group takes twe mice from experiment group and control group respectively. Mark each mouse, record the marker in the table. Mice in experiment group are administered Phenobarbital intraperitoneal at the dose of 0.5ml/20g. Similarity, mice at the dose 0.5mg/20g. Similarity, mice in control group are administered 0.9% Sodium Chloride intraperitoneal at the dose of 0.5ml/20g. After 30 minutes, each mouse is administered 50mg% Dimefline subcutaneously in the dose of 0.5ml/20g. After administering Dimefline, we observe the responds of mice for 30 minutes. If there is convulsive respond, we need to record it. In the end, all students summary the results. Record the positive and negative number in experiment group and control group in the table. Analyze and handle the results We analyze the results with chi square test to see if there is statistical difference in the percentage of convulsion between experiment group and control group. 1. Calculate χ2 value (1) Calculate χ2 value with basic formula: Table 1. Descriptive chart of results A Experiment group Positive number negtive number Control groupTotal Positive number negtive number total A: observed value T: theory value T A-T (A-T)2/T (2) Calculate χ2 value with quadruple tabular form: Table 2. Descriptive chart of results Experiment group positive number negative number a c ∑ χ2= (ad-bc)2×n/(a+b) (a+c) (c+d) (b+d) Control group b d ∑ 2. Compare the observed value with theory value to assess if there is statistical difference. Question What are the methods of making convulsion model? How to observe drug’s anticonvulsive effect? Why anticonvulsive drug be administered before administering make convulsion drugs in our experiment? Which data does the experiment data belong to? Which method we choose to analyze? How to do it?