By the end of this lecture you will be able to: Recognize the possible causes in mood swing in bipolar depression Classify mood stabilizing drugs Focus.

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Presentation transcript:

By the end of this lecture you will be able to: Recognize the possible causes in mood swing in bipolar depression Classify mood stabilizing drugs Focus on the mechanism of action of lithium as a mood stabilizer Expand on its pharmacological actions, kinetics, indications, side effects, contraindications & toxicity

Is a psychiatric medication used for treatment of mood disorders characterized by intense & sustained mood shifts typically in bipolar depression A MOOD STABILIZER i.e. Suppress Swings between MANIA & DEPRESSION BIPOLAR DEPRESSION = Elevated energy levels, moods & cognition = depressed energy levels, moods & cognition Separated by periods of "normal“ mood

An affective health disorder, characterized by cycling from depression to mania [hypomania] and back again over time; so there are switch in person’s mood, energy levels and ability to function CYCLING Rapid Cycles back & forth in the course of a day or multiple times a week Stuck in one mood or the other for weeks or months at a time Slow a spectrum or continuous range

Biological Symptoms Emotional Symptoms Thinking Patterns Full of new, exciting ideas Moving quickly from one to another (flight of ideas) Lack of judgment Full of new, exciting ideas Moving quickly from one to another (flight of ideas) Lack of judgment Hyperactive & full of energy Unable or unwilling to sleep More interested in sex Hyperactive & full of energy Unable or unwilling to sleep More interested in sex Happy, excited, euophoric Unwarranted optimism Irritated with those who do not share same feeling Happy, excited, euophoric Unwarranted optimism Irritated with those who do not share same feeling Very active, behaving unusually Less inhibited in general Plans are grandiose & unrealistic Excessive rapid talking Sudden odd decisions, that are mostly of disastrous consequences Recklessly spending of money Over-familiar with other people Sudden irritability, rage or paranoia Very active, behaving unusually Less inhibited in general Plans are grandiose & unrealistic Excessive rapid talking Sudden odd decisions, that are mostly of disastrous consequences Recklessly spending of money Over-familiar with other people Sudden irritability, rage or paranoia CHARACTERS OF MANIA Behavioral Patterns

TYPES OF BD BIPOLAR I One or more manic episodes alternating with major depression, with or without psychosis Average length of time either depressed or manic is about 13 weeks Seasonal; depression >winter & mania >summer/change of seasons One or more hypomanic episodes & one or more major depressive episode, without psychosis BIPOLAR II Brief & attenuated episodes of depression & hypomania, some times known as minor cyclic mood disorder CYCLOTHYMIC MECHANISM OF BD Because of its cyclical nature, BD has been tied to the disruption of circadian rhythm  i.e. master clock can no longer be reset appropriate in response to light / dark signals  so circadian cycle becomes faster & circadian period becomes shorter  disruption of the routine schedules of many functions in the body  metabolism, hormones, transmitters, sleep- wake patterns……. BECOME DISRUPTED

A MOOD STABILIZER Reset Back the Master Clock Circadian cycle becomes slower Circadian period becomes longer Metabolism, Hormones, Transmitters, Sleep- Wake patterns …. Become Adjusted

Classification of MOOD STABILIZING DRUGS  Valproic acid  Carbamazepine  Gabapentin  Lamotrigine  Topiramate Lithium CarbonateBenzodiazepines  Olanzapine  Risperidone  Quetiapine  Clozapine AntiepilepticsAtypical antipsychotics Prophylaxis in bipolar disorder  therapeutic effects more predominates, either for prevention of depression or mania Mono or in combination therapy with lithium in acute mania. Are used for;

Lithium [ Li + ] As salts carbonate or citrate are used as drugs Mechanism Can substitute ions as Na  alter excitability thresholds, conductivity potentials, ….etc. Can compete for Mg binding sites that activate many key cellular enzymes that signal the effects of many transmitters i.e altering cAMP, AA, PI turn over & DAG production  specially  myoinositol, PKC…..etc. Genes Responsible for Neuroplasticity & Neuroprotection Implicated in long term modulation of Genes Responsible for Neuroplasticity & Neuroprotection Circadian Cycle Gene Expression  glycogen synthase kinase-3 (GSK-3)  affects Circadian Cycle Gene Expression Adjusting neuronal morphology, neurotransmission, synaptogenesis, axonogenesis, survival & apoptosis) Circadian cycle becomes slower Circadian period becomes longer Valproic acid & Lamotrigine MANIA DA

Completely absorbed from GIT. Peak plasma levels within 30 minutes to 2 hours Long plasma half-life (20 hr). Not bound to plasma proteins. Not metabolized in the body. Distributed in all body fluids Slow entry into intracellular compartment. Has a slow onset of action (takes 3-4 days to act, so sedative drugs should be given as haloperidol I.V.). Pharmacokinetics

Excretion mostly in urine. Lithium clearance is about 20% of creatinine. Less is via, in feces, sweat, breast milk Has a narrow therapeutic range. Its concentration can be detected in plasma, saliva, urine. Monitoring of plasma level is essential. Target plasma concentration: 0.6–1.4 mEq/L Pharmacokinetics

Treatment of bipolar affective disorders. Prophylactic of manic-depressive disorders. Schizoaffective disorders. Acute mania. Aggressive behavior in children. Premenstrual dysphoria. Leucopenia [ make use of ADRs inducing leukocytosis ] CLINICAL USES

Neurologic effects mainly tremors. Psychotic effect as mental confusion. Renal effects:  Polydipsia & polyuria (diabetes insipidus).  Prolonged use cause chronic interstitial nephritis, nephrotic syndrome. Edema, Hypernatremia, Increase body weight. Disturbance in thyroid function (>hypothyroidism) Cardiac effects:  Bradycardia-tachycardia (“sick sinus”) syndrome  T wave flattening in ECG. Transient acne eruption & folliculitis. Leucocytosis. Teratogenic effects. ADVERSE EFFECTS

How  (GSK-3) by lithium  can lead to ADRs in kidney Li +

Drug Interactions Diuretics e.g. thiazides  25% renal clearance of Li NSAIDs decrease renal clearance of lithium. Antipsychotic drugs mainly typical drugs causing severe extrapyramidal adverse effects. Pregnancy   plasma level of lithium Post partum  plasma level of lithium suddenly Breast milk  1 / 3 – ½ concentration of serum. If toxicity  cyanosis, poor suckling & hepato- megaly. PREGNANCY NEWBORN

Toxicity develops when given in the following cases : Renal dysfunction Postpartum Dehydation or low salt diet Concomittent drugs; diuretics, NSAIDs… Lithium Toxicity Therapeutic over dose is more common than accidental Values over 2 mEq/L  considered as  likely toxicity Treatment of toxicity  Peritoneal or Hemodialysis