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Evaluation of CNS Stimulants
1.
Presented by :
Mr. Nirav S. Vachhani M.Pharm Pharmacology (Sem-II) Guided by: Dr. Rina H. Gokani (Associate professor) S. J. Thakkar pharmacy college, Rajkot.
2.
What is CNS
? • CNS is made of BRAIN and SPINAL CORD. • The brain is divided into three parts – Forebrain, Midbrain, and Hindbrain. • Spinal cord begins from the brain stems and extends till the lowest end of backbone • Both the brain and spinal cord contain fluid filled spaces or cavities. The fluid in these spaces is called cerebrospinal fluid (CSF), and contains nutrients, hormones, white blood cells to maintain the CNS. • Brain and Spinal cord mainly responsible for information processing, imagination, memory and communication. © SJTPC, Rajkot. 2
3.
© SJTPC, Rajkot.
3
4.
Central Neurotransmitters :
• Amino Acids • Glutamate • GABA • Glycine • Acetylcholine • Monoamines • Dopamine • Norepinephrine • 5-Hydroxytriptamine • Peptides • Nitric oxide • Endocannabinoids © SJTPC, Rajkot. 4
5.
What are CNS
stimulants ? • Central Nervous System Stimulants may be used to reduce tiredness and increase alertness, competitiveness and aggression. • CNS stimulants may be defined as “Drug substance that most specifically afford an enhancement in excitability either very much within the different portions of the brain or the spinal cord which may lead to convulsion.” • CNS stimulants may be classified as below: 1. Analeptics (convulsant) • Doxapram (respiratory stimulant) • Nikethamide (respiratory stimulant) • Strychnine • Picrotoxin • Bicuculline © SJTPC, Rajkot. 5
6.
2. Psychomotor stimulants
• Amphetamine & Methamphetamine • Methylphenidate • Cocaine • Phentemine • Fenfluramine 3. General cellular stimulants • Methylxanthines derivatives • Caffeine (Caffee) • Theophylline (Tea) • Theobromine (Chocolate) 4. Clinical antidepressants • MAO inhibitors • Catecholamine reuptake inhibitors 5. Psychotomimetic (Hallucinogenic) © SJTPC, Rajkot. 6
7.
EVALUATION METHODS :
1. Screening of analeptics by PHOTOACTOMETER 2. Strychnine induced convulsion 3. Sand displacement method 4. Runway test 5. Ptosis test 6. Duration of anaesthesia 7. Jiggle cage method 8. Treadwheel method 9. Rotarod method 10. Barbiturate induced sleeping time © SJTPC, Rajkot. 7
8.
1. Screening of
analeptics by PHOTOACTOMETER • Purpose : CNS stimulants like Amphetamine increase the locomotor activity in animal. • Procedure : Mice weighing 20-25 gm are divided in in to 3 groups, each contain 4 animals. Control : Saline Standard : Amphetamine (1 mg/kg I.P.) Test : Drug to be evaluated Mice from each group, separately placed in photoactometer for 10 min duration at the intervals of 30 min till the maximum effect of drug is observed. • Evaluation : No. of “ cut off ” is compared between groups. © SJTPC, Rajkot. 8
9.
Digital Photoactometer
© SJTPC, Rajkot. 9
10.
2. Strychnine induced
convulsion • Purpose : Drugs like strychnine produce convulsion and hyperreflexia by inhibiting glycin in CNS. • Procedure : Groups of 10 mice of either sex with a weight between 18 and 22 gm mice are injected with 2 mg/kg strychnine nitrate i.p. in std group and in test group test drug is given after few minutes convulsions are observed • Evaluation : Time required to produce convulsion is compared. • Modifications : Some other drugs produce same effects like Picotoxin Pentylenetetrazole Bucuculine © SJTPC, Rajkot. 10
11.
3. Sand displacement
method : • Purpose : Drug like Caffeine stimulate the motoractivity in animal by inhibiting the adenosine transmission in the brain. • Procedure : A cage with sand is calibrated for amount of sand displaced per unit time. Mice weighing 20-25 gm are divided in 3 groups Control : saline Standard : caffeine (20 mg/kg orally) Test : drug to be evaluated After 1 hour the animal is placed in cage for 15 min • Evaluation : Volume of sand displaced in each group is compared. © SJTPC, Rajkot. 11
12.
4. Runway test
: • Purpose : To study the spontaneous activity of CNS stimulants • Process : Wistar rats of either sex weighing 250-300 gm are grouped Trained to run in a RUNWAY apparatus for 3 days to achieve constant time and speed to pass runway Control : Saline Standard : Methamphetamine (2 mg/kg I.P.) Test : Drug to be evaluated After 30 min of administration of drug test is performed • Evaluation : Running time from door opening to pressing the goal lever was recorded using a microcomputer. © SJTPC, Rajkot. 12
13.
Runway Apparatus: • The
runway apparatus, made using a 5 mm acrylic board, consisted of a start box (26.5-cm wide, 26-cm long, and 30-cm high), • A controlled start door (26.5- cm wide, and 30-cm high) that opened by dropping down a runway (18-cm wide, 180-cm long, and 30-cm high), • Priming box (30x30x30 cm). • A retractable lever (the goal lever) was set at the end of the runway 7 cm above the floor. • Stimulation was provided from constant current stimulators in the form of 0.2 ms pulses of 60 Hz alternating current. The stimulation current was individually adjusted for each rat. © SJTPC, Rajkot. 13
14.
5. Ptosis test
: • Purpose : Reserpine decreases central sympathetic outflow and leads to ptosis in eye. • Procedure:Albino mice of either sex weighing 18-24 gm are grouped Reserpine is given in all group (4 mg/kg I.P.) After 2 hr 45 min Control : saline Standard : Amphetamine (1 mg/kg I.P.) Test : drug to be evaluated After 15 min ptotic rating is made • Evaluation : 4 for complete ptosis 3 for ¾ ptosis 2 for ½ ptosis © SJTPC, Rajkot. 14 1 for ¼ ptosis
15.
6. Duration of
anesthesia : • Purpose : Analeptics produces diminution in duration of anesthesia & also produces respiration stimulation • Procedure : SD rats weighing 250-350 gm are grouped and Given Pentobarbital sodium (50 mg/kg I.P.) After 20 min Control : Saline Standard : Methamphetamine (2 mg/kg I.P.) Test : Drug to be evaluated After this, animal are placed on its back and recovery from LRR is checked when animal had righted itself 3 times in 1 min • Evaluation : Recovery time from LRR is compared • Modifications :Guinea pig, Rabbit, Mice, Monkey, Cat © SJTPC, Rajkot. 15
16.
7. Jiggle cage
method : • Purpose : Test is used to evaluate the effect of drug on motor activity of animal. • Procedure : Wistar rats of either sex weighing 250-300 gm are grouped Control : Saline Standard : Methamphetamine (2 mg/kg I.P.) Test : Drug to be evaluated animal placed in jiggle cage for 10 min to observe activity changes • Evaluation : Changes in the movement of animal • Modification : Rat can also be used © SJTPC, Rajkot. 16
17.
© SJTPC, Rajkot.
17
18.
8. Tread wheel
method : • Purpose : Effect of drug on locomotor activity of rat • Procedure : Wistar rats of either sex weighing 250-300 gm are grouped Control : Saline Standard : Methamphetamine (2 mg/kg I.P.) Test : Drug to be evaluated animal placed in tread wheel for 10 min to observe activity changes • Evaluation : Changes in the movement (speed of rotation) of animal • Modification : Rat can also be used © SJTPC, Rajkot. 18
19.
© SJTPC, Rajkot.
19
20.
Tread Wheel
© SJTPC, Rajkot. 20
21.
9. Rota road
test : • Purpose : To evaluate the effect of drug on motor coordination • Procedure : Mice weighing 18-24 gm are grouped Control : saline Standard : Amphetamine (4 mg/kg I.P.) Test : drug to be evaluated After 30 min Animal placed on rotarod • Evaluation :The time for falling of animal is recorded © SJTPC, Rajkot. 21
22.
Rotarod © SJTPC, Rajkot.
22
23.
10.Barbiturate induced sleeping
time : • Purpose : To evaluate the effect of drug on motor coordination • Procedure : Mice weighing 20-30 gm are grouped Control : Distilled water (10 ml/kg I.P) Standard : caffeine (20 mg/kg S.C) Test : drug to be evaluated After 30 min Pentobarbitone (40 mg/kg I.P.) Animal are observed for onset and duration of sleeping • Evaluation :The sleeping time • The sleeping time is the time interval between onset of loss of righting reflex and regain of righting reflex. © SJTPC, Rajkot. 23
24.
REFERENCES : 1. Owolabi
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