Antipsychotic Drugs and Their Classification

 
Shaymaa F. Abbas
Msc Pharmacology
 
Antipsychotic
drugs
 
1. Dopamine- serotonin hypothesis of
schizophrenia
2. Classification of antipsychotic drugs
3. Basic concepts about their receptors action
4. Basic concepts about their related effects/
side effects and how to manage them
 
Learning
objectives
Dopamine
 
Chemoreceptor
trigger zone
 
Dopamine= vomiting
 
Mesolimbic
pathway
 
Dopamine= Psychosis
 
Pituitary gland
 
Dopamine=       Prolactin
 
Basal ganglia
 
  Dopamine= Extrapyramidal
symptoms (eg: parkinsonism)
The antipsychotic drugs
The antipsychotic drugs
 
Psychosis (from the Greek , psyche, "mind ", and -osis,
"abnormal condition or derangement") refers to an abnormal
condition of the mind
 
The antipsychotic drugs (also called neuroleptics or major
tranquilizers) are used primarily to treat schizophrenia, but
they are also effective in other psychotic and manic states.
 
 
Schizophrenia is a type of chronic psychosis characterized by:
1.
Positive symptoms: Thought disorders, Delusions,
Hallucinations, Paranoia
2.
 Negative symptoms: loss of motivation, Social withdrawal,
Flat affect, Poverty of speech
3.
Cognitive impairment
"Dopamine hypothesis": Symptoms arise because of
excessive dopaminergic activity in mesolimbic system.
Serotonin is increasingly seen as a part of the etiology of
schizophrenia. May be linked to negative symptoms
 
1- Typical antipsychotics: 1
st
 generation
Phenothiazines: Chlorpromazine, Thioridazine, Promethazine
Haloperidol: Most likely cause of neuroleptic malignant
syndrome (NMS) and Tardive dyskinesia
 
2- Atypical antipsychotics: 2nd generation
Clozapine: 
Agranulocytosis
-requirement for frequent blood test
Olanzapine, Risperidone
 
 
Classification of antipsychotics
Classification of antipsychotics
 
 
1
st
 generation antipsychotics are more likely to be
associated with movement disorders known as
extrapyramidal symptoms (EPS), particularly drugs that
bind tightly to D2 receptors, such as 
haloperidol
 
Movement disorders are less likely with medications that
bind weakly, such as chlorpromazine.
Mechanism of action of antipsychotics
Mechanism of action of antipsychotics
 
All
 of the 1
st
 generation and 
most
 of the 2
nd
 generation
antipsychotic  drugs  block  D2 receptors in the brain &
periphery.
Atypical antipsychotics exert part of their action through
blocking of serotonin  receptors  ((5-HT2A )) receptors
 
Some of 
atypical
 antipsychotics blocks D1,D4 receptors, with
weak affinity to D2 receptors
 
Additional mechanisms for both typical and atypicals:
antagonism on  α1, Muscarinic , H1
 
Clinical uses
Clinical uses
 
1.
Schizophrenia and schizoaffective states
2.
 Bipolar disorder
3.
Drug or radiation emesis
4.
Intractable hiccup—chlorpromazine
5.
Pruritus —promethazine
6.
Co-analgesic in chronic pain and terminal illness
7.
Others
 
Side effects of antipsychotics
Side effects of antipsychotics
 
Side effects from dopamine blockade:
1- 
Dyskinesias
 (extrapyramidal symptoms [EPS]) mainly
with 
typical(1
st
 generation)
1.
Reversible EPS: Pseudoparkinsonism (drug-induced
parkinsonism), dystonia, akathisia
2.
Chronic EPS: Tardive dyskinesia (TD)
 
Side effects of antipsychotics
Side effects of antipsychotics
 
Tardive dyskinesia—this important toxicity includes
choreoathetoid movements of the muscles of the lips and
buccal cavity and may be irreversible.
It tends to develop after several years of antipsychotic
drug therapy but may appear as early as 6 months
 
Antimuscarinic drugs generally
 increase 
the severity of
tardive dyskinesia symptoms.
 
 
2- Endocrine dysfunction
Hyper prolactinemia (galactorrhea, amenorrhea,
gynecomastia), sexual dysfunction
Metabolic disorders: eating disorders (weight gain),
glucose intolerance, dyslipidemia : mainly with 
atypical
3-Temperature regulation problems (Poikilothermia)
Side effects –dopamine blockade –continue
Side effects –dopamine blockade –continue
4. Neuroleptic malignant syndrome
4. Neuroleptic malignant syndrome
 
Rare but fatal adverse effect that can occur at any time during treatment
The onset of symptoms is rapid with increased temperature, severe
muscular rigidity, confusion, agitation, elevation in WBC count, elevated
CPK concentrations, elevated liver enzymes, myoglobinuria, and acute
renal failure.
 The antipsychotic should be immediately discontinued
Adequate hydration, cooling, and close monitoring of vital signs and serum
electrolytes.
Treated with dantrolene and bromocriptine
The risk of neuroleptic malignant syndrome is higher with first-generation
antipsychotics,
Second-generation antipsychotics also cause this adverse effect
 
Side effects from 
muscarinic blockade
All cause dry mouth except clozapine causes 
hyper
salivation
Side effects from 
α
-
blockade (particularly hypotension)
Side effects from H1 blockade: sedation
Cardiotoxicity: prolongation of QT interval, myocarditis,
sudden death
Other side effects
1.
Seizure: chlorpromazine, clozapine
2.
Immune mediated reactions: Photosensitivity, Cholestatic
jaundice-especially with chlorpromazine, agranulocytosis
(clozapine)
 
Parenteral forms of many agents (e.g. Fluphenazine
decanoate, haloperidol decanoate and olanzapine pamoate)
are long-acting injectable (LAI) formulations of
antipsychotics.
These formulations have a therapeutic duration of action of
up to 2 to 4 weeks and, therefore, are often used to treat
out- patients and individuals who are non-adherent with
oral medications
Long acting formulations
Long acting formulations
 
Typical               Vs.                Atypical
Typical               Vs.                Atypical
     
     


 
Mainly DA
Mainly DA
Mainly D2
Mainly D2
Treat mostly POSITIVE
Treat mostly POSITIVE
symptoms
symptoms
More EPS adverse effects
More EPS adverse effects
Less useful in refractory
Less useful in refractory
disease
disease
 
DA and 5HT
DA and 5HT
D1+D2+D4+5HT
D1+D2+D4+5HT
Treat POSITIVE and
Treat POSITIVE and
NEGATIVE
NEGATIVE
 symptoms
 symptoms
Lesser EPS
Lesser EPS
Useful in refractory
Useful in refractory
disease
disease
 
 
 
 A woman taking haloperidol developed a spectrum of adverse
effects that included the amenorrhea-galactorrhea syndrome and
extrapyramidal dysfunction. Another, newer, antipsychotic drug was
prescribed which however caused weight gain and hyperglycemia due to
a diabetogenic action. The drug prescribed was
(A) Bupropion
(B) Chlorpromazine
(C) Fluoxetine
(D) Lithium
(E) Olanzapine
 
 
The reason why clozapine causes less extrapyramidal
dysfunction than haloperidol when used in schizophrenia is
that in the CNS, clozapine
(A) Activates GABA receptors
(B) Blocks dopamine release
(C) Has greater antagonism at muscarinic receptors
(D) Has a low affinity for dopamine D2 receptors
(E) Is an 
α-
receptor agonist
 
 
 A young male patient recently diagnosed as schizophrenic
develops severe muscle cramps with torticollis a short time
after drug therapy is initiated with haloperidol. The best
course of action would be to
(A) Add risperidone to the drug regimen
(B) Discontinue haloperidol and observe the patient
(C) Give oral diphenhydramine
(D) Inject benztropine
(E) Switch the patient to fluphenazine
 
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Antipsychotic drugs, also known as neuroleptics, are essential in treating schizophrenia and other psychotic disorders. They work by targeting dopamine and serotonin receptors in the brain, managing symptoms like hallucinations and delusions. Learn about the dopamine-serotonin hypothesis of schizophrenia, classification of antipsychotic drugs (typical and atypical), their side effects, and how to manage them effectively.

  • Antipsychotic drugs
  • Schizophrenia treatment
  • Dopamine hypothesis
  • Serotonin receptors
  • Mental health

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  1. Antipsychotic Antipsychotic drugs drugs Shaymaa F. Abbas MscPharmacology

  2. Learning objectives 1. Dopamine- serotonin hypothesis of schizophrenia 2. Classification of antipsychotic drugs 3. Basic concepts about their receptors action 4. Basic concepts about their related effects/ side effects and how to manage them

  3. Dopamine Chemoreceptor trigger zone Mesolimbic pathway Dopamine= vomiting Dopamine= Psychosis Basal ganglia Pituitary gland Dopamine= Prolactin Dopamine= Extrapyramidal symptoms (eg: parkinsonism)

  4. The antipsychotic drugs Psychosis (from the Greek , psyche, "mind ", and -osis, "abnormal condition or derangement") refers to an abnormal condition of the mind The antipsychotic drugs (also called neuroleptics or major tranquilizers) are used primarily to treat schizophrenia, but they are also effective in other psychotic and manic states.

  5. Schizophrenia is a type of chronic psychosis characterized by: 1. Positive symptoms: Thought disorders, Delusions, Hallucinations, Paranoia 2. Negative symptoms: loss of motivation, Social withdrawal, Flat affect, Poverty of speech 3. Cognitive impairment "Dopamine hypothesis": Symptoms arise because of excessive dopaminergic activity in mesolimbic system. Serotonin is increasingly seen as a part of the etiology of schizophrenia. May be linked to negative symptoms

  6. Classification of antipsychotics 1- Typical antipsychotics: 1stgeneration Phenothiazines: Chlorpromazine, Thioridazine, Promethazine Haloperidol: Most likely cause of neuroleptic malignant syndrome (NMS) and Tardive dyskinesia 2-Atypical antipsychotics: 2nd generation Clozapine: Agranulocytosis-requirement for frequent blood test Olanzapine, Risperidone

  7. 1stgeneration antipsychotics are more likely to be associated with movement disorders known as extrapyramidal symptoms (EPS), particularly drugs that bind tightly to D2 receptors, such as haloperidol Movement disorders are less likely with medications that bind weakly, such as chlorpromazine.

  8. Mechanism of action of antipsychotics All of the 1stgeneration and most of the 2ndgeneration antipsychotic drugs block D2 receptors in the brain & periphery. Atypical antipsychotics exert part of their action through blocking of serotonin receptors ((5-HT2A )) receptors Some of atypical antipsychotics blocks D1,D4 receptors, with weak affinity to D2 receptors Additional mechanisms for both typical and atypicals: antagonism on 1, Muscarinic , H1

  9. Clinical uses 1. Schizophrenia and schizoaffective states Bipolar disorder 3. Drug or radiation emesis 4. Intractable hiccup chlorpromazine 5. Pruritus promethazine 6. Co-analgesic in chronic pain and terminal illness 7. Others 2.

  10. Side effects of antipsychotics Side effects from dopamine blockade: 1- Dyskinesias (extrapyramidal symptoms [EPS]) mainly with typical(1stgeneration) 1. Reversible EPS: Pseudoparkinsonism (drug-induced parkinsonism), dystonia, akathisia 2. Chronic EPS: Tardive dyskinesia (TD)

  11. Dyskinesias [EPS] Reversible EPS Chronic Drug-induced parkinsonism Dystonia Akathisia Tardive dyskinesia B-blockers or benzodiazepines Discontinuation switch to atypical valbenazine Antimuscarinic drugs (benztropine or diphenhydramine)

  12. Side effects of antipsychotics Tardive dyskinesia this important toxicity includes choreoathetoid movements of the muscles of the lips and buccal cavity and may be irreversible. It tends to develop after several years of antipsychotic drug therapy but may appear as early as 6 months Antimuscarinic drugs generally increase the severity of tardive dyskinesia symptoms.

  13. Side effects dopamine blockade continue 2- Endocrine dysfunction Hyper prolactinemia (galactorrhea, amenorrhea, gynecomastia), sexual dysfunction Metabolic disorders: eating disorders (weight gain), glucose intolerance, dyslipidemia : mainly with atypical 3-Temperature regulation problems (Poikilothermia)

  14. 4. Neuroleptic malignant syndrome Rare but fatal adverse effect that can occur at any time during treatment The onset of symptoms is rapid with increased temperature, severe muscular rigidity, confusion, agitation, elevation in WBC count, elevated CPK concentrations, elevated liver enzymes, myoglobinuria, and acute renal failure. The antipsychotic should be immediately discontinued Adequate hydration, cooling, and close monitoring of vital signs and serum electrolytes. Treated with dantrolene and bromocriptine The risk of neuroleptic malignant syndrome is higher with first-generation antipsychotics, Second-generation antipsychotics also cause this adverse effect

  15. Side effects from muscarinic blockade All cause dry mouth except clozapine causes hyper salivation Side effects from -blockade (particularly hypotension) Side effects from H1 blockade: sedation Cardiotoxicity: prolongation of QT interval, myocarditis, sudden death Other side effects 1. Seizure: chlorpromazine, clozapine 2. Immune mediated reactions: Photosensitivity, Cholestatic jaundice-especially with chlorpromazine, agranulocytosis (clozapine)

  16. Long acting formulations Parenteral forms of many agents (e.g. Fluphenazine decanoate, haloperidol decanoate and olanzapine pamoate) are long-acting injectable (LAI) formulations of antipsychotics. These formulations have a therapeutic duration of action of up to 2 to 4 weeks and, therefore, are often used to treat out- patients and individuals who are non-adherent with oral medications

  17. Typical Vs. Atypical DA and 5HT D1+D2+D4+5HT Treat POSITIVE and NEGATIVE symptoms Lesser EPS Useful in refractory disease Mainly DA Mainly D2 Treat mostly POSITIVE symptoms More EPS adverse effects Less useful in refractory disease

  18. A woman taking haloperidol developed a spectrum of adverse effects that included the amenorrhea-galactorrhea syndrome and extrapyramidal dysfunction. Another, newer, antipsychotic drug was prescribed which however caused weight gain and hyperglycemia due to a diabetogenic action. The drug prescribed was (A) Bupropion (B) Chlorpromazine (C) Fluoxetine (D) Lithium (E) Olanzapine

  19. The reason why clozapine causes less extrapyramidal dysfunction than haloperidol when used in schizophrenia is that in the CNS, clozapine (A) Activates GABA receptors (B) Blocks dopamine release (C) Has greater antagonism at muscarinic receptors (D) Has a low affinity for dopamine D2 receptors (E) Is an -receptor agonist

  20. A young male patient recently diagnosed as schizophrenic develops severe muscle cramps with torticollis a short time after drug therapy is initiated with haloperidol. The best course of action would be to (A) Add risperidone to the drug regimen (B) Discontinue haloperidol and observe the patient (C) Give oral diphenhydramine (D) Inject benztropine (E) Switch the patient to fluphenazine

  21. Thank you Thank you

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