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Stahl's Essential Psychopharmacology Online
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Stahl's Essential Psychopharmacology

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The -icon indicates content; the -icon indicates figures; the -icon indicates tables.

  • l-alpha-acetylmethodol acetate (LAAM),
  • L channel, ,
  • la-do (lamotrigine-Depakote), ,
  • la-li-do (lamotrigine-lithium-Depakote), ,
  • la-li (lamotrigine-lithium), ,
  • lactation,
  • Lami-quel, ,
  • lamotrigine,
  • actions as mood stabilizer,
  • binding site of,
  • for bipolar disorder,
  • with depression,
  • combination of medications with, ,
  • and glutamate reduction,
  • icon,
  • mechanism of action
  • on GABA, glutamate, sigma, and dopamine,
  • VSSCs, synaptic vesicles, and carbonic anhydrase,
  • putative clinical actions,
  • rashes from,
  • for schizophrenia,
  • adding to antipsychotic,
  • sites of action, on glutamate release,
  • and VSSCs,
  • language, odd use of,
  • late gene,
  • lateral fissure,
  • lateral parabrachial nucleus,
  • lazaroids, as free radical scavenger,
  • learning
  • and brain restructuring,
  • constant synaptic revision and,
  • and endogenous growth factors,
  • gene expression and,
  • long-term,
  • and neurogenesis in hippocampus, ,
  • learning disabilities, from improper neuronal migration,
  • learning model, and circuit inefficiency,
  • lecozotan,
  • leptin,
  • leucine zipper transcription factor, , , , ,
  • Leucovorin (folinic acid),
  • levetiracetam, ,
  • icon,
  • mechanism of action
  • on GABA, glutamate, sigma, and dopamine,
  • at SV2A symaptic vesicle sites,
  • VSSCs, synaptic vesicles, and carbonic anhydrase,
  • putative clinical actions,
  • and seizure reduction,
  • levodopa, for Parkinson’s disease, MAO-B inhibition and,
  • Lewy bodies
  • damage to cholinergic neurons,
  • dementia with,
  • li-do (lithium-Depakote/divalproex/valproate), ,
  • libido, decreased,
  • licarbazepine,
  • binding site of,
  • mechanism of action
  • on GABA, glutamate, sigma, and dopamine,
  • VSSCs, synaptic vesicles, and carbonic anhydrase,
  • oxcarbazepine conversion to,
  • putative clinical actions,
  • lidocaine
  • anatomic site of action,
  • molecular site of action,
  • and VSSC block,
  • life cycle, antidepressants over, ,
  • life expectancy, of schizophrenic patients,
  • lifestyle, and stress,
  • ligand-gated ion channels, , ,
  • agonists impact on,
  • different states,
  • GABA receptors as,
  • pentameric subtypes,
  • as psychotropic drug target,
  • states,
  • structure and function, ,
  • subunit of tetrameric,
  • top view,
  • tetrameric structure,
  • limbic cortex, noradrenergic receptor simulation in,
  • limbic CSTC circuit,
  • lipid neurotransmitter,
  • lithium, ,
  • for affective symptoms in schizophrenia,
  • for Alzheimer’s disease,
  • for bipolar disorder,
  • in combos
  • for bipolar disorder,
  • for depression,
  • for depression,
  • in bipolar disorder,
  • for dopamine hyperactivity reduction,
  • and fetal toxicity risk,
  • GSK-3 inhibition by,
  • mechanism of action,
  • as mood stabilizer,
  • side effects of,
  • for suicide reduction, ,
  • liver
  • CYP450 enzymes in,
  • insulin resistance in, ,
  • riluzole impact
  • valproic acid toxicity,
  • local anesthesia, ,
  • and VSSC block,
  • locus coeruleus (LC),
  • connection with amygdala,
  • excessive noradrenergic output from,
  • lofepramine (Deprimyl, Gamanil),
  • long-term outcomes, symptom exacerbation and,
  • long-term potentiation (LTP), , ,
  • Loroxyl (amitriptyline, Elavil, Endep, Tryptizol), , ,
  • Lou Gehrig’s disease. See amyotrophic lateral sclerosis (ALS)
  • lovastatin
  • and CYP 450 3A4,
  • risk of muscle damage,
  • low-potency antipsychotic agents, and dissociation,
  • loxapine (Loxitane),
  • 5HT6-antagonist properties of,
  • pharmacological icon,
  • Loxitane. See loxapine (Loxitane)
  • LSD (d-lysergic acid diethylamide),
  • actions,
  • LTP. See long-term potentiation (LTP)
  • LuAA34893, ,
  • Ludiomil (maprotiline),
  • inhibition of serotonin reuptake pump,
  • luxapine,
  • LY 293558,
  • LY354740,
  • LY379268,
  • LY450139,
  • d-lysergic acid diethylamide (LSD),
  • actions,
  • lysosomes, ,
  • localization of,
  • organelle and protein destruction by, ,

 
 

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