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CONCEPT OF DEPRESSION
&
ANTIDEPRESSANT DRUGS
Noem Dawood
Lecturer
Dow Institute of Nursing And Midwifery ,
DUHS.
1
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INTRODUCTION OF TEACHER
AND ROLE IN INSTITUTE
Noem Dawood
Lecture – DIONAM,DUHS
RN, Post RN BSN, MSN, PB, Psych
Specialization.
In BSN Semester VI- I will teach and facilitates
mental health nursing theory as well as clinical
rotation in different psychiatric setting at both private
and public sectors hospitals of Karachi .
2
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AGENDA
3
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INTRODUCTION OF THE
TOPIC
While no single person can be
credited with the discovery of
depression, there are many
great thinkers whose ideas
contributed—and continue to
contribute—to our growing
knowledge of what this illness
really is .
4
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MECHANISM OF DEPRESSION AND ANTIDEPRESSANT DRUGS
Subtitle
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DEPRESSION
6
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MONOAMINE HYPOTHESIS
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MECHANISM OF DEPRESSION
8
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IMAGE BASE QUESTION
9
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IMAGE BASE QUESTION
WHAT SPEAKS LEFT AND RIGHT SIDE FACES
10
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ANTIDEPRESSANTS
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SYNAPTIC TRANSMISSION
15
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MODE OF ACTIONS
 All antidepressant functions by increasing availability of monoamines (5-HT ,
NA or DA) by one of the following methods
 Presynaptic inhibition of reuptake of 5-HT, NA or DA.
 Antagonist activity at presynaptic inhibitory 5HT or NA receptors which
enhances neurotransmitter release.
 Inhibitions of monoamines oxides, reducing NT breakdown
 Initial regulation of depressive symptoms takes minimum of 2+4 Weeks.
16
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CLASSIFICATION
17
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ALL ANTIDEPRESSANTS (EXCEPT MAO'S INHIBITORS) BLOCK
MONOAMINE TRANSPORTER PROTEINS
 Serotonin transporter (SERT)
 Norepinephrine Transporter (NET)
 Dopamine Transporter (DAT)
18
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PLASMA MEMBRANE MONOAMINE TRANSPORTERS: STRUCTURE,
REGULATION AND FUNCTION
19
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ANTIDEPRESSANT
20
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TCA'S ANTI HAM EFFECTS
 TCAs Inhibit axonal reuptake of NA and 5HT in neurons –and increase concentration of these
neurotransmitters in brain.
 Classification of TCAs
 Potent anti cholinergic, more sedative.
 Imipramine
 Clomipramine
 Amitryptyline
 Less Sedative
 Desipramine
 Amoxapine
 Nortriptyline
22
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TRICYCLIC ANTIDEPRESSANT TOXICITY
 Fatal in toxicity
 Most important toxic effect is
 Slowing od depolarization of the cardiac action potential by blocking fast
sodium channels (Quinidine- like effect)
 Delays propagation of depolarization through both myocardium and
conducting tissue
 Cardiac arrhythmias
23
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USE OF TRICYCLIC ANTIDEPRESSANT
 Tricyclic antidepressant are approved by the food and drug administration
(FDA) for treating
 Several types of depression , (Primary drug for depression)
 OCD ( Primary SSRIs)
 Bedwetting (nocturnal enuresis)
 Imipramine at low dose.
24
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MONOAMINE OXIDASE INHIBITORS
 Monoamine Oxidase Inhibitors (MAOIs) are a class of powerful
antidepressant drugs. They are particular effective in treating
atypical depression, panic disorders, social phobia.
 Due to potentially lethal dietary and drug integrations , MAOIs had
been reserved as a last line of Rx, used only when other classes
of antidepressant drugs (eg. SSRIs and TCAs) have failed
25
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Attribution-NonCommercial-NoDerivatives 4.0
MONOAMINE OXIDASE?
 MAO is a mitochondrial enzyme found in most tissue; liver, gut (presynaptic
nerves)
 The enzyme is responsible for the degradation of monoamine
neurotransmitters
 There are two forms of monoamine oxidase.
 MAO-A and MOA-B
 MAO-A is responsible for NE, 5-HT and Tyramine metabolism
 MAO-B is more selective for dopamine metabolism
26
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QUESTION TIME
 Anti depressant having both high sedative and high anticholinergic
activity
27
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SSRI BLOCK REUPTAKE OF SEROTONIN INTO PRESYNAPTIC NEURON
28
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OTHER INDICATOIN FOR SSRI
 Sertraline
 Fluoxetine
 Citalopram
 Escitalopram
 Paroxetine
29
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SELECTIVE SEROTONIN REUPTAKE INHIBITORS
ADVERSE DRUG REACTIONS
30
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SELECTIVE SEROTONIN REUPTAKE INHIBITORS
ADVERSE EFFECT
31
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HALF-LIVES OF THE SSRI
32
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 ___________ has the lower risk of causing an
SSRIs discontinuation syndrome?
33
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 Venlafaxine
 Desvenlafaxine
 Duloxetine
34
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SEROTONIN /NE REUPTAKE INHIBITORS
 Selectively inhibit the reuptake of both serotonin and NE
 SNRIs unlike the TCAs, have no activity at adrenergic
,muscarinic, or histamine receptors and thus have fewer side
effects than the TCAs.
35
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Attribution-NonCommercial-NoDerivatives 4.0
ATYPICAL ANTIDEPRESSANT
 Bupropion (DAT+NET)
 Nicotine withdraw and smoking
 Mirtazapine (Alpha2 Antagonist & 5HT2A)
 Antihistamine
 Trazodone (SERT+5HT2A)
 Anti alpha 1, Antihistamine
36
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Attribution-NonCommercial-NoDerivatives 4.0
Noem Dawood
Noem.dawood@duhs,edu.pk
DIONAM-DUHS
+92 343 3057812

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Antidepressant_Pharmacology (LMS).pptx mental health

  • 1. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 CONCEPT OF DEPRESSION & ANTIDEPRESSANT DRUGS Noem Dawood Lecturer Dow Institute of Nursing And Midwifery , DUHS. 1
  • 2. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 INTRODUCTION OF TEACHER AND ROLE IN INSTITUTE Noem Dawood Lecture – DIONAM,DUHS RN, Post RN BSN, MSN, PB, Psych Specialization. In BSN Semester VI- I will teach and facilitates mental health nursing theory as well as clinical rotation in different psychiatric setting at both private and public sectors hospitals of Karachi . 2
  • 3. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 AGENDA 3
  • 4. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 INTRODUCTION OF THE TOPIC While no single person can be credited with the discovery of depression, there are many great thinkers whose ideas contributed—and continue to contribute—to our growing knowledge of what this illness really is . 4
  • 5. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 MECHANISM OF DEPRESSION AND ANTIDEPRESSANT DRUGS Subtitle
  • 6. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 DEPRESSION 6
  • 7. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 7 MONOAMINE HYPOTHESIS
  • 8. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 MECHANISM OF DEPRESSION 8
  • 9. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 IMAGE BASE QUESTION 9
  • 10. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 IMAGE BASE QUESTION WHAT SPEAKS LEFT AND RIGHT SIDE FACES 10
  • 11. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 11
  • 12. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 12
  • 13. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 13
  • 14. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 14 ANTIDEPRESSANTS
  • 15. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 SYNAPTIC TRANSMISSION 15
  • 16. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 MODE OF ACTIONS  All antidepressant functions by increasing availability of monoamines (5-HT , NA or DA) by one of the following methods  Presynaptic inhibition of reuptake of 5-HT, NA or DA.  Antagonist activity at presynaptic inhibitory 5HT or NA receptors which enhances neurotransmitter release.  Inhibitions of monoamines oxides, reducing NT breakdown  Initial regulation of depressive symptoms takes minimum of 2+4 Weeks. 16
  • 17. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 CLASSIFICATION 17
  • 18. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 ALL ANTIDEPRESSANTS (EXCEPT MAO'S INHIBITORS) BLOCK MONOAMINE TRANSPORTER PROTEINS  Serotonin transporter (SERT)  Norepinephrine Transporter (NET)  Dopamine Transporter (DAT) 18
  • 19. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 PLASMA MEMBRANE MONOAMINE TRANSPORTERS: STRUCTURE, REGULATION AND FUNCTION 19
  • 20. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 ANTIDEPRESSANT 20
  • 21. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 21
  • 22. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 TCA'S ANTI HAM EFFECTS  TCAs Inhibit axonal reuptake of NA and 5HT in neurons –and increase concentration of these neurotransmitters in brain.  Classification of TCAs  Potent anti cholinergic, more sedative.  Imipramine  Clomipramine  Amitryptyline  Less Sedative  Desipramine  Amoxapine  Nortriptyline 22
  • 23. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 TRICYCLIC ANTIDEPRESSANT TOXICITY  Fatal in toxicity  Most important toxic effect is  Slowing od depolarization of the cardiac action potential by blocking fast sodium channels (Quinidine- like effect)  Delays propagation of depolarization through both myocardium and conducting tissue  Cardiac arrhythmias 23
  • 24. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 USE OF TRICYCLIC ANTIDEPRESSANT  Tricyclic antidepressant are approved by the food and drug administration (FDA) for treating  Several types of depression , (Primary drug for depression)  OCD ( Primary SSRIs)  Bedwetting (nocturnal enuresis)  Imipramine at low dose. 24
  • 25. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 MONOAMINE OXIDASE INHIBITORS  Monoamine Oxidase Inhibitors (MAOIs) are a class of powerful antidepressant drugs. They are particular effective in treating atypical depression, panic disorders, social phobia.  Due to potentially lethal dietary and drug integrations , MAOIs had been reserved as a last line of Rx, used only when other classes of antidepressant drugs (eg. SSRIs and TCAs) have failed 25
  • 26. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 MONOAMINE OXIDASE?  MAO is a mitochondrial enzyme found in most tissue; liver, gut (presynaptic nerves)  The enzyme is responsible for the degradation of monoamine neurotransmitters  There are two forms of monoamine oxidase.  MAO-A and MOA-B  MAO-A is responsible for NE, 5-HT and Tyramine metabolism  MAO-B is more selective for dopamine metabolism 26
  • 27. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 QUESTION TIME  Anti depressant having both high sedative and high anticholinergic activity 27
  • 28. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 SSRI BLOCK REUPTAKE OF SEROTONIN INTO PRESYNAPTIC NEURON 28
  • 29. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 OTHER INDICATOIN FOR SSRI  Sertraline  Fluoxetine  Citalopram  Escitalopram  Paroxetine 29
  • 30. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 SELECTIVE SEROTONIN REUPTAKE INHIBITORS ADVERSE DRUG REACTIONS 30
  • 31. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 SELECTIVE SEROTONIN REUPTAKE INHIBITORS ADVERSE EFFECT 31
  • 32. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 HALF-LIVES OF THE SSRI 32
  • 33. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0  ___________ has the lower risk of causing an SSRIs discontinuation syndrome? 33
  • 34. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0  Venlafaxine  Desvenlafaxine  Duloxetine 34
  • 35. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 SEROTONIN /NE REUPTAKE INHIBITORS  Selectively inhibit the reuptake of both serotonin and NE  SNRIs unlike the TCAs, have no activity at adrenergic ,muscarinic, or histamine receptors and thus have fewer side effects than the TCAs. 35
  • 36. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 ATYPICAL ANTIDEPRESSANT  Bupropion (DAT+NET)  Nicotine withdraw and smoking  Mirtazapine (Alpha2 Antagonist & 5HT2A)  Antihistamine  Trazodone (SERT+5HT2A)  Anti alpha 1, Antihistamine 36
  • 37. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 37
  • 38. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 Noem Dawood Noem.dawood@duhs,edu.pk DIONAM-DUHS +92 343 3057812