Antidepressant Drugs Depression is a disease characterized by feelings of sadness and hopelessness, as well as the inability to experience pleasure in.

Slides:



Advertisements
Similar presentations
Drugs acting on the CNSI
Advertisements

Other Medicines. Andrenergic Antagonists (Blockers) Bind to receptor site but do not cause an action Bind to receptor site but do not cause an action.
Waqas Tahir GPST2. Overview Introduction Introduction Mechanism of action Mechanism of action Therapeutic uses Therapeutic uses Pharmacokinetics Pharmacokinetics.
Drugs used to Treat Depression
Overview of Mental Health Medications for Children and Adolescents Module 2 Depressive Disorders 1.
Monoamine oxidase inhibitors Monoamine Oxidase Inhibitors (MAOIs) are a class of powerful antidepressant drugs. They are particularly effective in treating.
Anti-depressants Depression is considered to be due to functional deficit of neurotransmitters like norepinephrine and / or serotonin. Antidepressants.
Copyright © 2013, 2010 by Saunders, an imprint of Elsevier Inc. Chapter 32 Antidepressants.
Antidepressant agents By Bohlooli S., Ph.D. School of Medicine, Ardabil University of Medical Sciences.
Depression Ibrahim Sales, Pharm.D. Associate Professor of Clinical Pharmacy King Saud University
Drugs used in affective disorders: antidepressants
Joseph De Soto MD, PhD, FAIC
Pharmacology – II PHL-322 CNS Pharmacology
Antidepressant. Management of psychological disorders Medical treatment Psychotherapy Support groups.
for the Psychiatry Clerkship is proud to present And Now Here Is The Host... Insert Name Here.
1 ANTI DEPRESSANT DRUGS. 2 3 DEPRESSION INTENSE FEELINGS OF SADNESS INTENSE FEELINGS OF SADNESS HOPELESSNESS HOPELESSNESS DESPAIR DESPAIR INABILITY TO.
Antidepressants & Neuroleptics Lesson 20. Unipolar Depression n Major Depressive Disorder n Extreme sadness & despair l extent & duration important n.
Management Of Depressive Disorders Pharmacologic Treatments For Depression Copyright © World Psychiatric Association.
PIPC ® Psychiatry In Primary Care Medications Robert K. Schneider, MD Departments of Psychiatry, Internal Medicine and Family Practice The Medical College.
Treating Behavioral and Psychological Symptoms of Dementia (BPSD) Kuang-Yang Hsieh, M.D. ph.D. Department of Psychiatry Chimei Medical Center.
Anxiety A state of tension in response to real or imagined stress or danger situations. Anxiety may manifest itself as Psychic or mental state. Somatic.
ANTIDEPRESSANTS New Antidepressants.
Drugs used in Anxiety & Panic Disorders
By S.Bohlooli, Ph.D..  “An affective disorder characterized by loss of interest or pleasure in almost all a person’s usual activities or pastimes.”
Mood Disorders Lesson 24.
Copyright © 2008 Lippincott Williams & Wilkins. Introductory Clinical Pharmacology Chapter 24 Antidepressant Drugs.
Trazodone Mianserin Mirtazapine Tetracyclic Antidepressants Noradrenergic & Specific Serotonergic Antidepressants (NaSSAs) Serotonin Antagonists & Reuptake.
Isahel N. Alfonso, R.N.  Selective Serotonin Reuptake Inhibitor (SSRI) Fluoxetine Fluvoxamine Paroxetine Sertraline Citalopram  Tricyclic Compound (TCA)
Psychopharmacology in Psychiatry
Drugs used in Depression- New groups By Prof. Yieldez Bassiouni.
Antidepressant drugs. Mood Disorder  The most common mood disorders are: 1. Major depression (unipolar depression). 2. Manic-depressive illness (bipolar.
Dr. Laila M. Matalqah Ph.D. Pharmacology PHARMACOLOGY OF CNS 4 Antidepressant General Pharmacology M212.
for MHD & Therapeutics is proud to present And Now Here Is The Host... Insert Name Here.
PHARMACOLOGY TUTORING FOR ANTIDEPRESSANTS By Alaina Darby.
Antidepressant drugs. Depression: is a disorder of mood rather than disturbance of thought or cognition. It is postulated that depression is due to deficiency.
Anti-depressants Dr. Sanjita Das Range Tricyclics Tetracyclics Selective serotonin reuptake inhibitorsSelective serotonin reuptake inhibitors SSRI Serotonin.
Antidepressants: Prof. Riyadh Al_Azzawi F.R.C.Psych.
Drugs used in the treatment of affective disorders Dr. Vidumini De Silva.
 : Monoamine hypothesis of depression asserts that depression is caused by functional insufficiency of monoamine neurotransmitter (norepinephrine, serotonin.
ANTIDEPRESSANTS Drugs which can Elevate Mood (Mood Elevators)
Chapter 12: Antidepressants
By dr.safeyya alchalabi
Drugs used for anxiety and panic disorders
Management of Depression
Drugs used for anxiety and panic disorders
Antidepressants.
Antidepressants The optimal use of antidepressant required a clear understanding of their mechanism of action, pharmacokinetics, potential drug interaction.
Antidepressants The optimal use of antidepressant required a clear understanding of their mechanism of action, pharmacokinetics, potential drug interaction.
Drugs used in Depression- Prof. Yieldez Bassiouni
Anti depressants.
Drugs used in Depression- Prof. Yieldez Bassiouni
AFFECTIVE DISORDERS Anxiety----uneasiness from apprehension and worry about possible events. Try psychotherapy first. benzodiazepenes: xanax/alprazolam.
Antidepressants.
ANTIDEPRESSANTS 22 Dr. Hiwa K. Saaed 9/19/2018
PHARMACOTHERAPY - I PHCY 310
Antidepressant agents
Antidepressants: pharmacokinetics
Antidepressants: pharmacodynamics
School of Pharmacy, University of Nizwa
School of Pharmacy, University of Nizwa
PHARMACOTHERAPY - I PHCY 310
Antidepressants The optimal use of antidepressant required a clear understanding of their mechanism of action, pharmacokinetics, potential drug interaction.
Antidepressant drugs.
Tricyclic and Tetracyclic Antidepressants Adverse Effects and Pharmacokinetics In this presentation we discuss adverse effects and pharmacokinetics of.
Drugs used in Depression- Prof. Yieldez Bassiouni
Antidepressants.
Drugs used in Depression-
Antidepressants The optimal use of antidepressant required a clear understanding of their mechanism of action, pharmacokinetics, potential drug interaction.
Drugs Used in Depression (New group)
Drugs Used in Depression (Old Group)
Presentation transcript:

Antidepressant Drugs Depression is a disease characterized by feelings of sadness and hopelessness, as well as the inability to experience pleasure in usual activities, changes in sleep patterns and appetite, loss of energy, and suicidal thoughts.

Biogenic Amine Hypothesis 1950: Reserpine  Induce depression ( Reserpine depletes storage or amine neurotransmitters such as serotonin and norepinephrine Depression  Amine (serotonin and norepinephrine )-dependent synaptic transmission (Antidepressants  Amine by inhibition of their reuptake and metabolism) mania is caused by an overproduction of these neurotransmitters.

Classification of antidepressants: I Classification of antidepressants: I . Monoamine oxidase inhibitors MAO-I: Phenelzine, Tranylcypromine, Isocarboxazid and Selegiline I I . Tricyclic antidepressants (TCAs) A) NA + 5-HT reuptake inhibitors: Imipramine, Amitriptyline, Trimipramine, Doxepin, Dothiepin, Clomipramine B) Predominantly NA reuptake inhibitors: Desipramine, Nortriptyline, Amoxapine, Reboxetine I l l . Selective serotonin reuptake inhibitors (SSRis): Fluoxetine, Fluvoxamine, Paroxetine, Sertraline, Citalopram, Escitalopram IV. Atypical antidepressants Trazodone, Mianserin, Mirtazapine, Venlafaxine, Duloxetine, Tianeptine, Amineptine, Bupropion and others.

Monoamino oxidase inhibitors (MAOIs): phenelzine, tranylcypromine, isocarboxazid and selegiline [ Selegiline is also used for the treatment of Parkinson’s disease. It is the only antidepressant available in a transdermal delivery system.] Action: inhibit  monoamine oxidase, thus preventing the breakdown of monoamine neurotransmitters and thereby increasing their availability. There are two isoforms of monoamine oxidase, MAO-A and MAO-B. MAO-A preferentially deaminates serotonin, melatonin, epinephrine, and norepinephrine. MAO-A preferentially deaminates other trace amines, like tyramine, dopamine  is equally deaminated by both types. Use of MAOIs is limited due to the complicated dietary restrictions required while taking these agents. These drugs inhibit not only MAO in the brain but also MAO in the liver and gut that catalyzes oxidative deamination of drugs and toxic substances, such as tyramine, which is found in certain foods. The MAOIs, therefore, show a high incidence of drug–drug and drug–food interactions. Selegiline administered as the transdermal patch may produce less inhibition of gut and hepatic MAO at low doses because it avoids first-pass metabolism. Although MAO is fully inhibited after several days of treatment, the antidepressant action of the MAOIs, (like that of the SSRIs, SNRIs, and TCAs) is delayed several weeks. Selegiline and tranylcypromine have an amphetamine-like stimulant effect that may produce agitation or insomnia.

Indications: -used in depressed patients who are unresponsive or allergic to TCA or who are experience strong anxiety. -Patients with low psychomotor activity may benefit from the stimulant properties of MAOIs. -Treatment of phobic states. -Atypical depression. -Because of their risk for drug–drug and drug–food interactions, the MAOIs are considered last-line agents in many treatment settings.

Pharmacokinetics These drugs are well absorbed after oral administration, hepatically metabolized and excreted rapidly in urine. Enzyme regeneration, when irreversibly inactivated, varies, but it usually occurs several weeks after termination of the drug. Thus, when switching antidepressant agents, a minimum of 2 weeks of delay must be allowed after termination of MAOI therapy and the initiation of another antidepressant from any other class.

Adverse effects Side effects include: Dry mouth, Nausea, diarrhea or constipation, Headache, Drowsiness, Insomnia, Dizziness or light headedness, Skin reaction at the patch site, Involuntary muscle jerks, Low blood pressure Reduced sexual desire or difficulty reaching orgasm, Weight gain, Difficulty starting a urine flow, Muscle cramps, Prickling or tingling sensation in the skin (paresthesia) Severe and often unpredictable side effects, due to drug–food and drug–drug interactions, limit the widespread use of MAOIs. For example, tyramine, which is contained in foods, such as aged cheeses and meats, chicken liver, pickled or smoked fish, and red wines, is normally inactivated by MAO in the gut. Individuals receiving a MAOI are unable to degrade tyramine obtained from the diet. Tyramine causes the release of large amounts of stored catecholamines from nerve terminals, resulting in a hypertensive crisis. Patients must, therefore, be educated to avoid tyramine-containing foods. Due to the risk of serotonin syndrome, the use of MAOIs with other antidepressants is contraindicated. For example, SSRIs should not be coadministered with MAOIs. Both SSRIs and MAOIs require a washout period of at least 2 weeks before the other type is administered, with the exception of fluoxetine, which should be discontinued at least 6 weeks before a MAOI is initiated.

Tricyclic antidepressants: 1 Tricyclic antidepressants: 1. Block NE & 5-HT reuptake, Desipramine, Nortriptyline, Amoxapine, Reboxetine are selective NE reuptake inhibitors. 2. Block α-adrenergic, histaminic, & muscarinic receptors which results in many of TCAs adverse effects. Amoxapine also blocks D2 receptors.

Indications: 1. depression & panic disorder. 2 Indications: 1. depression & panic disorder. 2. Imipramine is used to control bed-wetting in children  3. Amitriptyline is used to treat migraine & chronic pain syndromes (eg. neuropathic pain)  4. Doxepin, can be used to treat insomnia.

Pharmacokinetics - high lipid solubility - large volume of distribution (Vd) - rapid absorption - serum concentrations peak within a few hours - significant first pass metabolism - high protein binding - half-life of 8-36 hours (active metabolites of imipramine and amitriptyline) - metabolized by the liver, excreted by kidney

Adverse effects In addition to blocking monoamine transporters, the tricyclic antidepressants produce prominent antagonist effects at: alpha-1 adrenergic, muscarinic M1 and H-1 histamine receptors. - Antimuscarinic adverse effects.  -Orthostatic hypotension (most likely with imipramine & least likely with nortriptyline). - cardiotoxicity, quinidine like life-threatening arrhythmias.  -confusion with memory dysfunction - excessive sedation and fatigue - weight gain. - Sexual dysfunction ( but lower than that associated with SSRIs). Tricyclic antidepressants are not recommended for elderly patients (65+ years) because of their liability for inducing a toxic and confused state.

Drug interactions: TCAs & MAOIs concomitant use result in HT, hyperpyrexia, convulsion & coma. TCAs potentiate effects of direct-acting adrenergic drugs. TCAs prevent indirect-acting sympathomimetic from reaching their sites of action. TCAs used with ethanol or other CNS depressants may result in toxic sedation.  Precautions :  TCAs (like all antidepressants) should be used with caution in patients with manic-depressive disorder (bipolar), since switch to manic behavior may occur . TCAs have a narrow therapeutic index  Suicidal depressed patients should be given only limited quantities of TCAs with close monitoring.  TCAs may exacerbate unstable angina, BPH, epilepsy and preexisting arrhythmias. 

Selective serotonin reuptake inhibitors (SSRIs): fluoxetine, citalopram, fluvoxamine, sertraline, paroxetine and escitalopram The selective serotonin reuptake inhibitors (SSRIs) having 300- to 3000-fold greater selectivity for the serotonin transporter, as compared to the norepinephrine transporter. Moreover, the SSRIs have little blocking activity at muscarinic, α-adrenergic, and histaminic H1 receptors. Therefore, common side effects associated with TCAs, such as orthostatic hypotension, sedation, dry mouth, and blurred vision, are not commonly seen with the SSRIs. Because they have different adverse effects and are relatively safe even in overdose, the SSRIs have largely replaced TCAs and monoamine oxidase inhibitors (MAOIs) as the drugs of choice in treating depression. Antidepressants, including SSRIs, typically take at least 2 weeks to produce significant improvement in mood, and maximum benefit may require up to 12 weeks or more.

Therapeutic uses -As effective as the TCAs is depression Therapeutic uses -As effective as the TCAs is depression. -A number of other psychiatric disorders also respond favorably to SSRIs, including obsessive–compulsive disorder, panic disorder, generalized anxiety disorder, posttraumatic stress disorder, social anxiety disorder, premenstrual dysphoric disorder, and bulimia nervosa (only fluoxetine is approved for bulimia).

Pharmacokinetics All of the SSRIs are well absorbed after oral administration. Food has little effect on absorption (except with sertraline, for which food increases its absorption). Bioavailability - ranges from 50%- > 90% Peak levels are seen in approximately 2 to 8 hours on average. Protein Binding - ranges from 50% (escitalopram) to 95 % (sertraline) The majority of SSRIs have plasma half-lives that range between 16 and 36 hours, except for fluoxetine (1-4days) and its active metabolite S-norfluoxetine (7-15 days). It is available as a sustained-release preparation allowing once-weekly dosing. Metabolism by cytochrome P450 (CYP450)–dependent enzymes and glucuronide or sulfate conjugation occur extensively. Dosages of the SSRIs should be reduced in patients with hepatic impairment.

Adverse effects Include: Drowsiness, Insomnia (Paroxetine and fluvoxamine are generally more sedating), Sexual dysfunction (loss of libido, delayed ejaculation, and anorgasmia), Nausea, Dry mouth, Diarrhea, Nervousness, agitation or restlessness, Dizziness, Headache and Blurred vision Use in children and teenagers: Antidepressants should be used cautiously in children and teenagers, because about 1 out of 50 children report suicidal ideation as a result of SSRI treatment. Pediatric patients should be observed for worsening depression and suicidal thinking with initiation or dosage change of any antidepressant. Fluoxetine, sertraline, and fluvoxamine are approved for use in children to treat obsessive–compulsive disorder, and fluoxetine and escitalopram are approved to treat childhood depression. Overdose: Overdose with SSRIs does not usually cause cardiac arrhythmias, with the exception of citalopram, which may cause QT prolongation. Discontinuation syndrome: All of the SSRIs have the potential to cause a discontinuation syndrome after their abrupt withdrawal, particularly the agents with shorter half-lives and inactive metabolites. Fluoxetine has the lowest risk of causing an SSRI discontinuation syndrome due to its longer half-life and active metabolite.

Atypical antidepressants: bupropion, mirtazapine, nefazodone, trazodone, vilazodone], and vortioxetine

Bupropion Bupropion is a weak dopamine and norepinephrine reuptake inhibitor that is used to alleviate the symptoms of depression. Bupropion is also useful for decreasing cravings and attenuating withdrawal symptoms of nicotine in patients trying to quit smoking. Side effects may include dry mouth, sweating, nervousness, tremor, and a dose dependent increased risk for seizures. It has a very low incidence of sexual dysfunction. Bupropion is metabolized by the CYP2B6 pathway and has a relatively low risk for drug–drug interactions, given the few agents that inhibit/induce this enzyme. However, bupropion may inhibit CYP2D6 and, thus, increase exposure to substrates of this isoenzyme. Use of bupropion should be avoided in patients at risk for seizures or those who have eating disorders such as bulimia.

Mirtazapine Mirtazapine enhances serotonin and norepinephrine neurotransmission by serving as an antagonist at presynaptic α2 receptors. Additionally, some of the antidepressant activity may be related to antagonism at 5-HT2 receptors. It is sedating because of its potent antihistaminic activity, but it does not cause the antimuscarinic side effects of the TCAs, or interfere with sexual function like the SSRIs. Increased appetite and weight gain frequently occur. Mirtazapine is markedly sedating, which may be an advantage in depressed patients having difficulty sleeping.

Nefazodone and trazodone These drugs are weak inhibitors of serotonin reuptake. Their therapeutic benefit appears to be related to their ability to block postsynaptic 5-HT2a receptors. Both agents are sedating, probably because of their potent histamine H1-blocking activity. Trazodone is commonly used off-label for the management of insomnia. Trazodone has been associated with priapism, and nefazodone has been associated with a risk for hepatotoxicity. Both agents also have mild to moderate α1 receptor antagonism, contributing to orthostasis and dizziness.

Vilazodone Vilazodone is a serotonin reuptake inhibitor and a 5-HT1a partial agonist. Although the extent to which the 5-HT1a receptor activity contributes to its therapeutic effects is unknown, this possible mechanism of action renders it unique from that of the SSRIs. The adverse effect profile of vilazodone is similar to the SSRIs, including a risk for discontinuation syndrome if abruptly stopped.

Vortioxetine Vortioxetine utilizes a combination of serotonin reuptake inhibition, 5-HT1a agonism, and 5-HT3 and 5-HT7 antagonism as its suggested mechanisms of action to treat depression. It is unclear to what extent the activities other than inhibition of serotonin reuptake influence the overall effects of vortioxetine. The common adverse effects include nausea, vomiting, and constipation, which may be expected due to its serotonergic mechanisms.

Side effects of atypical antidepressants Because of the different ways atypical antidepressants work, each has unique characteristics and varying possible side effects. For example: Most of the atypical antidepressants caused dry mouth, dizziness or lightheadedness Some antidepressants may help you sleep and are best taken at night, while others may cause insomnia. Some antidepressants may cause constipation, while others may increase the risk of diarrhea. Some antidepressants may increase your appetite, resulting in weight gain, while others may cause nausea. Some antidepressants are less likely than others to cause sexual side effects.

Antidepressant Usual starting dose mg/day Usual therapeutic dose (mg/day) Monoamine oxidase inhibitors Isocarboxazid 10 10-40 Phenelzine 15 15-90 Tranylcypromine 10 30-60 Tricyclic antidepressants Amitriptyline 25 150-300 Clomipramine 25 100-250 Desipramine 25 150-300 Imipramine 25 150-300 Nortriptyline 25 50-150 Selective serotonin re-uptake inhibitors Citalopram 20 20-40 Escitalopram 10 10-20 Fluoxetine 20 20-60 Fluvoxamine 50 50-200 Sertraline 50 50-200 Atypical agents Agomelatine  25 25-50 Bupropion 200 300 (maximum single dose 150 mg) Bupropion XL 24 hour 150 300 Mirtazapine 15 15-45 Duloxetine 30-60 30-120 Venlafaxine 37.5-75.0 75-375