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Anxiolytic

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Anxiolytic
Drug class
Class identifiers
SynonymsSedative, minor tranquilizer
UseAnxiety disorders
Clinical data
Drugs.comDrug Classes
Legal status
In Wikidata

An anxiolytic (/ˌæŋksiəˈlɪtɪk, ˌæŋksioʊ-/; also antipanic or anti-anxiety agent)[1] is a medication or other intervention that reduces anxiety. This effect is in contrast to anxiogenic agents which increase anxiety. Anxiolytic medications are used for the treatment of anxiety disorders and their related psychological and physical symptoms.

Nature of anxiety

[edit]

Anxiety is a naturally-occurring emotion and response. When anxiety levels exceed the tolerability of a person, anxiety disorders may occur. People with anxiety disorders can exhibit fear responses, such as defensive behaviors, high levels of alertness, and negative emotions. Those with anxiety disorders may have concurrent psychological disorders, such as depression. Anxiety disorders are classified using six possible clinical assessments:[2]

Type Description
Generalized anxiety disorders (GAD) The anxiety symptoms are usually persistent and constant. Patients of this disorder could experience excessive anxiety for a long duration, commonly over six months and the symptoms could occur without any specific triggers.
Panic disorder This disorder specifically refers to the suffering from panic attacks and also the fear of repetitive attacks. Commonly found in agoraphobia patients (the fear of difficulty in leaving a confined venue). Panic attacks are sudden upsurges in anxiety level usually with unexplained reasons.
Social phobia This refers to the fear of staging in social situations where one experiences public observation among people or performs in front of the public. The fears are often unexplained and persistent. The fear could also be attributed to the possible humiliation in front of others due to poor performance or awkward social interactions.
Specific phobias Persistent fear towards a specific object, either tangible or intangible. This leads to undeniable avoidance or thought of escape from the object or endurance of the object in immense levels of anxiety.
Posttraumatic stress disorder (PTSD) PTSDs develop due to experience of severe trauma or life-threatening events. Specific symptoms include flashbacks to traumatic events triggered during similar situations, as well as avoidance of these situations. The fear of re-experiencing the event is also associated with feelings of helplessness or horror.
Obsessive–compulsive disorder (OCD) Person with OCD would experience compulsive impulses of removing an obsession. One common example is the obsession with impurities or contamination. The person would have compulsion or urge in sterilizing the environment to remove the contamination. Another example is the obsession with orderliness. The person would manipulate the surroundings including visual presentations to ease their obsession.

Different types of anxiety disorders will share some general symptoms while having their own distinctive symptoms. This explains why people with different types of anxiety disorders will respond differently to different classes of anti-anxiety medications.

Etiology

[edit]

The etiology of anxiety disorder remains unknown. There are several contributing factors that are still yet to be proved to cause anxiety disorders.[2] These factors include childhood anxiety, drug induction by central stimulant drugs, metabolic diseases or having depressive disorder.

Medications

[edit]

Anti-anxiety medication is any drug that can be taken or prescribed for the treatment of anxiety disorders, which may be mediated by neurotransmitters like norepinephrine, serotonin, dopamine, and gamma-aminobutyric acid (GABA) in the central nervous system.[3] Anti-anxiety medication can be classified into six types according to their different mechanisms: antidepressants, benzodiazepines, azapirones, antiepileptics, antipsychotics, and beta blockers.[3][4]

Antidepressants include selective serotonin reuptake inhibitors (SSRIs), serotonin–norepinephrine reuptake inhibitors (SNRIs), tricyclic antidepressants (TCAs), and monoamine oxidase inhibitors (MAOIs). SSRIs are used in all types of anxiety disorders while SNRIs are used for generalized anxiety disorder (GAD). Both of them are considered as first-line anti-anxiety medications. TCAs are second-line treatment as they cause more significant adverse effects when compared to the first-line treatment. Benzodiazepines are effective in emergent and short-term treatment of anxiety disorders due to their fast onset but carry the risk of dependence.[4] Buspirone is indicated for GAD, which has much slower onset but with the advantage of less sedating and withdrawal effects.[5]

History

[edit]

The first monoamine oxidase inhibitor (MAOI), iproniazid, was discovered accidentally when developing the new antitubercular drug isoniazid. The drug was found to induce euphoria and improve the patient's appetite and sleep quality.[6]

The first tricyclic antidepressant, imipramine, was originally developed and studied to be an antihistamine alongside other first-generation antihistamines of the time, such as promethazine.[7] TCAs can increase the level of norepinephrine and serotonin by inhibiting their reuptake transport proteins.[8] The majority of TCAs exert greater effect on norepinephrine, which leads to side effects like drowsiness and memory loss. [citation needed]

In order to be more effective on serotonin agonism and avoid anticholinergic and antihistaminergic side effects, selective serotonin reuptake inhibitors (SSRI) were researched and introduced to treat anxiety disorders. The first SSRI, fluoxetine (Prozac), was discovered in 1974 and approved by FDA in 1987. After that, other SSRIs like sertraline (Zoloft), paroxetine (Paxil), and escitalopram (Lexapro) have entered the market.[7]

The first serotonin norepinephrine reuptake inhibitor (SNRI), venlafaxine (Effexor), entered the market in 1993.[7] SNRIs can target serotonin and norepinephrine transporters while avoiding imposing significant effects on other adrenergic (α1, α2, and β), histamine (H1), muscarinic, dopamine, or postsynaptic serotonin receptors.[citation needed]

Classifications

[edit]

There are six groups of anti-anxiety medications available that have been proven to be clinically significant in treatment of anxiety disorders.[9] The groups of medications are as follows.

Drug Class Examples
Antidepressants (e.g., SSRIs, SNRIs) SSRIs e.g., fluoxetine, sertraline; SNRIs e.g., venlafaxine; MAOIs; TCAs
Benzodiazepines Lorazepam, diazepam, alprazolam
Azapirones Buspirone, gepirone, tandospirone
Antiepileptics Gabapentin, pregabalin, tiagabine and valproate
Antipsychotics Olanzapine, risperidone
Beta-adrenoceptor antagonists Propranolol, atenolol

Antidepressants

[edit]

Medications that are indicated for both anxiety disorders and depression. Selective serotonin reuptake inhibitors (SSRIs) and serotonin–norepinephrine reuptake inhibitors (SNRIs) are new generations of antidepressants. They have a much lower adverse effect profile than older antidepressants like monoamine oxidase inhibitors (MAOIs) and tricyclic antidepressants (TCAs). Therefore, SSRIs and SNRIs are now the first-line agent in treating long term anxiety disorders, given their applications and significance in all six types of disorders.[9]

Benzodiazepines

[edit]

Benzodiazepines are used for acute anxiety and could be added along with current use of SSRIs to stabilize a treatment. Long-term use in treatment plans is not recommended. Different kinds of benzodiazepine will vary in its pharmacological profile, including its strength of effect and time taken for metabolism. The choice of the benzodiazepine will depend on the corresponding profiles.[9]

Benzodiazepines are used for emergent or short-term management. They are not recommended as the first-line anti-anxiety drugs, but they can be used in combination with SSRIs/SNRIs during the initial treatment stage.[4] Indications include panic disorder, sleep disorders, seizures, acute behavioral disturbance, muscle spasm and premedication and sedation for procedures.[10]

Azapirones

[edit]

Buspirone can be useful in GAD but not particularly effective in treating phobias, panic disorder or social anxiety disorders.[2] It is a safer option for long-term use as it does not cause dependence like benzodiazepines.[11]

Antiepileptics

[edit]

Antiepileptics are rarely prescribed as an off-label treatment for anxiety disorders and post-traumatic stress disorders.[12] There have been some suggestions that they may help with anxiety symptoms but there is generally a lack of research on its use.[13]

One antiepileptic, pregabalin, has been found to be better at treating GAD than a placebo, and comparable effects to benzodiazepines. It has also been shown be potentially efficient in treating social anxiety disorder. Gabapentin has been prescribed off-label for anxiety despite a lack of research evidence supporting such use, although some studies have indicated that it may relieve anxiety symptoms. The potential anxiolytic effect of tiagabine has been observed in some pre-clinical trials, but its effectiveness has not yet been proved. Similarly, there is a lack of research on valproate for the treatment of anxiety disorders.[13]

Antipsychotics

[edit]

Olanzapine and risperidone are atypical antipsychotics which are also effective in GAD and PTSD treatment. However, there is a higher chance of experiencing adverse effects than the other anti-anxiety medications.[9]

Beta-adrenoceptor antagonists

[edit]

Propranolol is originally used for high blood pressure and heart diseases. It can also be used to treat anxiety with symptoms like tremor or increased heart rate. They work on the nervous system and alleviate the symptoms as a relief.[9] Propranolol is also commonly used for public speaking when one is nervous.[13]

Mechanism of action

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SSRIs and SNRIs

[edit]

Both selective serotonin reuptake inhibitors (SSRI) and serotonin and norepinephrine reuptake inhibitors (SNRI) are reuptake inhibitors of a class of nerve signal transduction chemical called neurotransmitters. Serotonin and norepinephrine are neurotransmitters that are related to nervous control in mood regulation. The level of these neurotransmitters is regulated by the nerve through reuptake to avoid accumulation of the neurotransmitter at the endings of nerve fibers. By reuptaking the neurotransmitter, the level of neuronal activity will go back down and be ready to go back up upon excitation from a new nerve signal.[9] However the neurotransmitter level of patients with anxiety disorders is usually low or the patients’ nerve fibers are insensitive to the neurotransmitters. SSRIs and SNRIs will then block the channel of reuptake and increase the level of the neurotransmitter. The nerve fibers will inhibit further production of neurotransmitters upon the increase. However the prolonged increase will eventually desensitize the nerve about the change in level. Therefore, the action of both SSRIs and SNRIs will take 4–6 weeks to exert their full effect.[2][9]

Benzodiazepine

[edit]

Benzodiazepines bind selectively to the GABA receptor, which is the receptor protein found in the nervous system and is in control of the nervous response. Benzodiazepine will increase the entry of chloride ions into the cells by improving the binding between GABA and GABA receptors and then the better opening of the channel for chloride ion passage. The high level of chloride ion inside the nerve cells makes the nerve more difficult to depolarize and inhibit further nerve signal transduction. The excitability of the nerves then reduces and the nervous system slows down. Therefore, the drug can alleviate symptoms of anxiety disorder and make the person less nervous.[9]

Clinical use

[edit]

Selective serotonin reuptake inhibitors

[edit]

Selective serotonin reuptake inhibitors (SSRIs) are a class of medications used in the treatment of depression, anxiety disorders, OCD and some personality disorders.[14][15] SSRIs are the first-line anti-anxiety medications.[16] Serotonin is one of the crucial neurotransmitters in mood enhancement, and increasing serotonin level produces an anti-anxiety effect.[17] SSRIs increase the serotonin level in the brain by inhibiting serotonin uptake pumps on serotonergic systems, without interactions with other receptors and ion channels. SSRIs are beneficial in both acute response and long-term maintenance treatment for both depression and anxiety disorder.[16]

SSRIs can increase anxiety initially due to negative feedback through the serotonergic autoreceptors; for this reason a concurrent benzodiazepine can be used until the anxiolytic effect of the SSRI occurs.[18]

The SSRIs paroxetine and escitalopram are USFDA approved to treat generalized anxiety disorder.[13]

Therapeutic use

[edit]
Drug Indication Common side effect
Citalopram
  • Depressive illness[19]
  • Panic disorder[16]
Escitalopram[19]

(active enantiomer of citalopram)

  • Depressive illness
  • Generalized anxiety disorder
  • Obsessive-compulsive disorder
  • Panic disorder
  • Social anxiety disorder
Fluoxetine[19]
  • Chills
  • Feeling abnormal
  • Postmenopausal hemorrhage
  • Uterine disorder
  • Vasodilation
  • Blurred vision

Adverse effect

[edit]

The common early side effects of SSRIs include nausea and loose stool, which can be solved by discontinuing the treatment. Headache, dizziness, insomnia are the common early side effects as well.[21]

Sexual dysfunction, anorgasmia, erectile dysfunction, and reduced libido are common adverse side effects of SSRIs. Sometimes they may persist after the cessation of treatment.[21]

Withdrawal symptoms like dizziness, headache and flu-like symptoms (fatigue/myalgia/loose stool) may occur if SSRI is stopped suddenly. The brain is incapable of upregulating the receptors to sufficient levels especially after discontinuation of the drugs with short half life like paroxetine. Both fluoxetine and its active metabolite have a long half life therefore it causes the least withdrawal symptoms.[16][22]

Serotonin–norepinephrine reuptake inhibitors

[edit]

Serotonin–norepinephrine reuptake inhibitor (SNRIs) include venlafaxine and duloxetine drugs. Venlafaxine, in extended release form, and duloxetine, are indicated for the treatment of GAD. SNRIs are as effective as SSRIs in the treatment of anxiety disorders.[23]

Tricyclic antidepressants

[edit]

Tricyclic antidepressants (TCAs) have anxiolytic effects; however, side effects are often more troubling or severe and overdose is dangerous. They are considered effective, but have generally been replaced by antidepressants that cause different adverse effects. Examples include imipramine, doxepin, amitriptyline, nortriptyline and desipramine.[24][25]

Therapeutic use

[edit]
Drugs Indication Common side effect
Imipramine
  • Nocturnal enuresis for children above six years old
  • Severe depression
  • Antihistamine side effects like sedation, weight gain
  • Anticholinergic side effects like blurred vision, dry mouth, constipation
Clomipramine[19]
  • Depressive illness
  • Phobic and obsessional states
  • Adjunctive treatment of cataplexy associated with narcolepsy

Contraindication

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TCAs may cause drug poisoning in patients with hypotension, cardiovascular diseases and arrhythmias.[26]

Tetracyclic antidepressants

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Mirtazapine has demonstrated anxiolytic effect comparable to SSRIs while rarely causing or exacerbating anxiety. Mirtazapine's anxiety reduction tends to occur significantly faster than SSRIs.[27]

Monoamine oxidase inhibitors

[edit]

Monoamine oxidase inhibitors (MAOIs) are first-generation antidepressants effective for anxiety treatment but their dietary restrictions, adverse effect profile and availability of newer medications have limited their use. MAOIs include phenelzine, isocarboxazid and tranylcypromine. Pirlindole is a reversible MAOI that lacks dietary restriction.[28]

Barbiturates

[edit]

Barbiturates are powerful anxiolytics but the risk of abuse and addiction is high. Many experts consider these drugs obsolete for treating anxiety but valuable for the short-term treatment of severe insomnia, though only after benzodiazepines or non-benzodiazepines have failed.[29]

Benzodiazepines

[edit]

Benzodiazepines are prescribed to quell panic attacks. Benzodiazepines are also prescribed in tandem with an antidepressant for the latent period of efficacy associated with many ADs for anxiety disorder. There is risk of benzodiazepine withdrawal and rebound syndrome if BZDs are rapidly discontinued.[30] Tolerance and dependence may occur.[31] The risk of abuse in this class of medication is smaller than in that of barbiturates. Cognitive and behavioral adverse effects are possible.[32]

Benzodiazepines include: alprazolam (Xanax), bromazepam, chlordiazepoxide (Librium), clonazepam (Klonopin), diazepam (Valium), lorazepam (Ativan), oxazepam, temazepam, and Triazolam.

Therapeutic use

[edit]
Drug Indication Common Side effect
Lorazepam
  • Decreased alertness
  • Ataxia, confusion (more in elderly)
Diazepam
  • Muscle spasm of varied aetiology
  • Anxiety
  • Acute drug-induced dystonic reactions
  • Sedation for minor surgical and medical procedures
  • Abnormal appetite
  • Concentration impairment
  • Gastrointestinal disorder
  • Movement disorder
  • Muscle spasm
  • Vomiting
Alprazolam
  • Short term use in anxiety

Adverse effect

[edit]

Benzodiazepines lead to central nervous system depression, resulting in common adverse effects like drowsiness, oversedation, light-headedness. Memory impairment can be a common adverse effect especially in elderly, hypersalivation, ataxia, slurred speech, psychomotor effects.[2]

Sympatholytics

[edit]

Sympatholytics are a group of anti-hypertensives which inhibit activity of the sympathetic nervous system. Beta blockers reduce anxiety by decreasing heart rate and preventing shaking. Beta blockers include propranolol, oxprenolol, and metoprolol.[33][34] The alpha-1 antagonist prazosin could be effective for PTSD.[35] The alpha-2 agonists clonidine and guanfacine have demonstrated both anxiolytic and anxiogenic effects.[36]

Miscellaneous

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Buspirone

[edit]

Buspirone (Buspar) is a 5-HT1A receptor agonist used to treated generalized anxiety disorder.[37] If an individual has only recently stopped taking benzodiazepines, buspirone will be less effective.[38]

Pregabalin

[edit]

Pregabalin (Lyrica) produces anxiolytic effect after one week of use comparable to lorazepam, alprazolam, and venlafaxine with more consistent psychic and somatic anxiety reduction. Unlike BZDs, it does not disrupt sleep architecture nor does it cause cognitive or psychomotor impairment.[39][40]

Hydroxyzine

[edit]

Hydroxyzine (Atarax) is an antihistamine originally approved for clinical use by the FDA in 1956. Hydroxyzine has a calming effect which helps ameliorate anxiety. Hydroxyzine efficacy is comparable to benzodiazepines in the treatment of generalized anxiety disorder.[41]

Phenibut

[edit]

Phenibut (Anvifen, Fenibut, Noofen) is an anxiolytic[42] used in Russia.[43] Phenibut is a GABAB receptor agonist,[42] as well as an antagonist at α2δ subunit-containing voltage-dependent calcium channels (VDCCs), similarly to gabapentinoids like gabapentin and pregabalin.[44] The medication is not approved by the FDA for use in the United States, but is sold online as a supplement.[45][46]

Temgicoluril

[edit]

Temgicoluril (Mebicar) is an anxiolytic produced in Latvia and used in Eastern Europe. Temgicoluril has an effect on the structure of limbic-reticular activity, particularly on the hypothalamus, as well as on all four basic neuromediator systems – γ aminobutyric acid (GABA), choline, serotonin and adrenergic activity.[47] Temgicoluril decreases noradrenaline, increases serotonin, and exerts no effect on dopamine.[48]

Fabomotizole

[edit]

Fabomotizole (Afobazole) is an anxiolytic drug launched in Russia in the early 2000s. Its mechanism of action is poorly-defined, with GABAergic, NGF and BDNF release promoting, MT1 receptor agonism, MT3 receptor antagonism, and sigma receptor agonism thought to have some involvement.[49][50]

Bromantane

[edit]

Bromantane is a stimulant drug with anxiolytic properties developed in Russia during the late 1980s. Bromantane acts mainly by facilitating the biosynthesis of dopamine, through indirect genomic upregulation of relevant enzymes (tyrosine hydroxylase (TH) and aromatic L-amino acid decarboxylase (AAAD)).[51][52]

Emoxypine

[edit]

Emoxypine is an antioxidant that is also a purported anxiolytic.[53][54] Its chemical structure resembles that of pyridoxine, a form of vitamin B6.

Menthyl isovalerate

[edit]

Menthyl isovalerate is a flavoring food additive marketed as a sedative and anxiolytic drug in Russia under the name Validol.[55][56]

Racetams

[edit]

Some racetam based drugs such as aniracetam can have an antianxiety effect.[57]

Alpidem

[edit]

Alpidem is a nonbenzodiazepine anxiolytic with similar anxiolytic effectiveness as benzodiazepines but reduced sedation and cognitive, memory, and motor impairment.[58] It was marketed briefly in France but was withdrawn from the market due to liver toxicity.[58]

Etifoxine

[edit]

Etifoxine has similar anxiolytic effects as benzodiazepine drugs, but does not produce the same levels of sedation and ataxia.[59] Further, etifoxine does not affect memory and vigilance, and does not induce rebound anxiety, drug dependence, or withdrawal symptoms.[59]

Alcohol

[edit]

Alcohol is sometimes used as an anxiolytic by self-medication. fMRI can measure the anxiolytic effects of alcohol in the human brain.[60]

Alternatives to medication

[edit]

Cognitive behavioral therapy (CBT) is an effective treatment for panic disorder, social anxiety disorder, generalized anxiety disorder, and obsessive–compulsive disorder, while exposure therapy is the recommended treatment for anxiety related phobias. Healthcare providers can guide those with anxiety disorder by referring them to self-help resources.[61] Sometimes medication is combined with psychotherapy but research has not found a benefit of combined pharmacotherapy and psychotherapy versus monotherapy.[62]

If CBT is found ineffective, both the Canadian and American medical associations then suggest the use of medication.[63][verification needed]

See also

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Categories

[edit]
Anxiolytics
Drug classes defined by psychological effects
Drugs by psychological effects
Psychoactive drugs

References

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  1. ^ "Antianxiety agent" at Dorland's Medical Dictionary
  2. ^ a b c d e Whittlesea, Cate; Hodson, Karen, eds. (7 August 2018). Clinical pharmacy and therapeutics. Elsevier. ISBN 978-0-7020-7012-9. OCLC 1084882482.
  3. ^ a b "Anxiolytics and you: How anxiety medications can help". Cleveland Clinic. Retrieved 15 January 2024.
  4. ^ a b c "Anxiety: Pharmacotherapy". CAMH. Retrieved 15 January 2024.
  5. ^ Cassano, Giovanni B.; Rossi, Nicolò Baldini; Pini, Stefano (2002). "Psychopharmacology of anxiety disorders". Dialogues in Clinical Neuroscience. 4 (3): 271–285. doi:10.31887/DCNS.2002.4.3/gcassano. ISSN 1294-8322. PMC 3181684. PMID 22033867.
  6. ^ Van Der Walt, Martie; Keddy, Karen H. (1 June 2021). "The Tuberculosis-Depression Syndemic and Evolution of Pharmaceutical Therapeutics: From Ancient Times to the Future". Frontiers in Psychiatry. 12: 617751. doi:10.3389/fpsyt.2021.617751. ISSN 1664-0640. PMC 8203803. PMID 34140898.
  7. ^ a b c Hillhouse, Todd M.; Porter, Joseph H. (2015). "A brief history of the development of antidepressant drugs: From monoamines to glutamate". Experimental and Clinical Psychopharmacology. 23 (1): 1–21. doi:10.1037/a0038550. ISSN 1936-2293. PMC 4428540. PMID 25643025.
  8. ^ Moraczewski, Jordan; Awosika, Ayoola O.; Aedma, Kapil K. (2023), "Tricyclic Antidepressants", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 32491723, retrieved 15 January 2024
  9. ^ a b c d e f g h "Rang and Dale's Pharmacology 7th Edition Preface", Rang &amp Dale's Pharmacology, Elsevier, pp. xv, 2012, doi:10.1016/b978-0-7020-3471-8.00064-0, ISBN 9780702034718, retrieved 16 March 2022
  10. ^ "Benzodiazepines: What They Are, Uses, Side Effects & Risks". Cleveland Clinic. Retrieved 15 January 2024.
  11. ^ "BuSpar For Anxiety: Is It Right For Me? | Klarity". www.klarityadhd.com. 23 November 2022. Retrieved 19 October 2023.
  12. ^ "What is the Best Anticonvulsant for Anxiety?". Psych Central. 28 October 2014. Retrieved 19 October 2023.
  13. ^ a b c d Garakani, Amir; Murrough, James W.; Freire, Rafael C.; Thom, Robyn P.; Larkin, Kaitlyn; Buono, Frank D.; Iosifescu, Dan V. (2020). "Pharmacotherapy of Anxiety Disorders: Current and Emerging Treatment Options". Frontiers in Psychiatry. 11. doi:10.3389/fpsyt.2020.595584. ISSN 1664-0640. PMC 7786299. PMID 33424664.
  14. ^ Kanba, S. (2004). "Although antidepressants and anxiolytics are frequently used together to treat depression in the acute phase, how effective is the concomitant use of these drugs?". Journal of Psychiatry & Neuroscience. 29 (6): 485. PMC 524966. PMID 15644990.
  15. ^ Barlow, David H.; Durand, Mark V (2009). "Chapter 7: Mood Disorders and Suicide". Abnormal Psychology: An Integrative Approach (Fifth ed.). Belmont, CA: Wadsworth Cengage Learning. p. 239. ISBN 978-0-495-09556-9. OCLC 192055408.[page needed]
  16. ^ a b c d e Lochmann, Dee; Richardson, Tara (2018), Macaluso, Matthew; Preskorn, Sheldon H. (eds.), "Selective Serotonin Reuptake Inhibitors", Antidepressants, vol. 250, Cham: Springer International Publishing, pp. 135–144, doi:10.1007/164_2018_172, ISBN 978-3-030-10948-6, PMID 30838457, retrieved 16 March 2022
  17. ^ "Serotonin: What Is It, Function & Levels". Cleveland Clinic. Retrieved 15 January 2024.
  18. ^ Dunlop, Boadie W.; Davis, Paula G. (2008). "Combination Treatment With Benzodiazepines and SSRIs for Comorbid Anxiety and Depression: A Review". Primary Care Companion to The Journal of Clinical Psychiatry. 10 (3): 222–228. ISSN 1523-5998. PMC 2446479. PMID 18615162.
  19. ^ a b c d Formulary., Committee, Joint (2014). British National Formulary. Pharmaceutical Press. ISBN 978-0-85711-152-4. OCLC 874322467.{{cite book}}: CS1 maint: multiple names: authors list (link)
  20. ^ Stahl, Stephen M. (2011). Stahl's essential psychopharmacology : the prescriber's guide. Meghan M. Grady (4th ed.). Cambridge, UK: Cambridge University Press. ISBN 978-0-521-17364-3. OCLC 701672553.
  21. ^ a b "Side effects - Selective serotonin reuptake inhibitors (SSRIs)". nhs.uk. 15 February 2021. Retrieved 15 January 2024.
  22. ^ Bandelow, Borwin; Michaelis, Sophie; Wedekind, Dirk (June 2017). "Treatment of anxiety disorders". Generalized Anxiety Disorders. 19 (2): 93–107. doi:10.31887/dcns.2017.19.2/bbandelow. ISSN 2608-3477. PMC 5573566. PMID 28867934.
  23. ^ John Vanin; James Helsley (19 June 2008). Anxiety Disorders: A Pocket Guide For Primary Care. Springer Science & Business Media. p. 189.
  24. ^ Post, Jason W.; Migne, Louis J. (2012). Antidepressants : Pharmacology, Health Effects and Controversy. New York: Nova Science Publishers. p. 58. ISBN 9781620815557.
  25. ^ "Tricyclic antidepressants (TCAs)". Mayo Clinic.
  26. ^ Thanacoody, H. K. Ruben; Thomas, Simon H. L. (2005). "Tricyclic antidepressant poisoning : cardiovascular toxicity". Toxicological Reviews. 24 (3): 205–214. doi:10.2165/00139709-200524030-00013. ISSN 1176-2551. PMID 16390222. S2CID 44532041.
  27. ^ Montano, C. Brendan; Jackson, W. Clay; Vanacore, Denise; Weisler, Richard (4 July 2023). "Considerations when selecting an antidepressant: a narrative review for primary care providers treating adults with depression". Postgraduate Medicine. 135 (5): 449–465. doi:10.1080/00325481.2023.2189868. ISSN 0032-5481. PMID 36912037.
  28. ^ Tanghe, A.; Geerts, S.; Van Dorpe, J.; Brichard, B.; Bruhwyler, J.; Géczy, J. (August 1997). "Double-blind randomized controlled study of the efficacy and tolerability of two reversible monoamine oxidase A inhibitors, pirlindole and moclobemide, in the treatment of depression". Acta Psychiatrica Scandinavica. 96 (2): 134–141. doi:10.1111/j.1600-0447.1997.tb09918.x. ISSN 0001-690X. PMID 9272198. S2CID 23485112.
  29. ^ Burchum, Jacqueline Rosenjack; Rosenthal, Laura D. (29 January 2015). Lehne's pharmacology for nursing care (9th ed.). St. Louis, Missouri. ISBN 9780323321907. OCLC 890310283.{{cite book}}: CS1 maint: location missing publisher (link)
  30. ^ Cassano, Giovanni B.; Rossi, Nicolò Baldini; Pini, Stefano (2002). "Psychopharmacology of anxiety disorders". Dialogues in Clinical Neuroscience. 4 (3): 271–285. doi:10.31887/DCNS.2002.4.3/gcassano. ISSN 1294-8322. PMC 3181684. PMID 22033867.
  31. ^ Gelder, M, Mayou, R. and Geddes, J. 2005. Psychiatry. 3rd ed. New York: Oxford. pp236.
  32. ^ Lader M, Tylee A, Donoghue J (2009). "Withdrawing benzodiazepines in primary care". CNS Drugs. 23 (1): 19–34. doi:10.2165/0023210-200923010-00002. PMID 19062773. S2CID 113206.
  33. ^ Hayes, Peggy E.; Schulz, S. Charles (1987). "Beta-blockers in anxiety disorders". Journal of Affective Disorders. 13 (2): 119–30. doi:10.1016/0165-0327(87)90017-6. PMID 2890677.
  34. ^ Jefferson, James W. (1974). "Beta-Adrenergic Receptor Blocking Drugs in Psychiatry". Archives of General Psychiatry. 31 (5): 681–91. doi:10.1001/archpsyc.1974.01760170071012. PMID 4155284.
  35. ^ Koola, M. M.; Varghese, S. P.; Fawcett, J. A. (2013). "High-dose prazosin for the treatment of post-traumatic stress disorder". Therapeutic Advances in Psychopharmacology. 4 (1): 43–7. doi:10.1177/2045125313500982. PMC 3896131. PMID 24490030.
  36. ^ Hoehn-Saric, Rudolf; Merchant, A. F.; Keyser, M. L.; Smith, V. K. (1981). "Effects of Clonidine on Anxiety Disorders". Archives of General Psychiatry. 38 (11): 1278–82. doi:10.1001/archpsyc.1981.01780360094011. PMID 7305609.
  37. ^ Annual Reports in Medicinal Chemistry, Volume 32 p. 319
  38. ^ DeMartinis, N.; Rynn, M.; Rickels, K.; Mandos, L. (February 2000). "Prior benzodiazepine use and buspirone response in the treatment of generalized anxiety disorder". The Journal of Clinical Psychiatry. 61 (2): 91–94. doi:10.4088/jcp.v61n0203. ISSN 0160-6689. PMID 10732655.
  39. ^ Bandelow, Borwin; Wedekind, Dirk; Leon, Teresa (2014). "Pregabalin for the treatment of generalized anxiety disorder: A novel pharmacologic intervention". Expert Review of Neurotherapeutics. 7 (7): 769–81. doi:10.1586/14737175.7.7.769. PMID 17610384. S2CID 6229344.
  40. ^ Owen, R.T. (2007). "Pregabalin: Its efficacy, safety and tolerability profile in generalized anxiety". Drugs of Today. 43 (9): 601–10. doi:10.1358/dot.2007.43.9.1133188. PMID 17940637.
  41. ^ Llorca, Pierre-Michel; Spadone, Christian; Sol, Olivier; Danniau, Anne; Bougerol, Thierry; Corruble, Emmanuelle; Faruch, Michel; Macher, Jean-Paul; Sermet, Eric; Servant, Dominique (2002). "Efficacy and Safety of Hydroxyzine in the Treatment of Generalized Anxiety Disorder". The Journal of Clinical Psychiatry. 63 (11): 1020–7. doi:10.4088/JCP.v63n1112. PMID 12444816.
  42. ^ a b Lapin, Izyaslav (2001). "Phenibut (β-Phenyl-GABA): A Tranquilizer and Nootropic Drug". CNS Drug Reviews. 7 (4): 471–481. doi:10.1111/j.1527-3458.2001.tb00211.x. ISSN 1527-3458. PMC 6494145. PMID 11830761.
  43. ^ журнал», Издание для практикующих врачей «Русский медицинский. "Феномен аминофенилмасляной кислоты". www.rmj.ru. Retrieved 19 December 2018.
  44. ^ Zvejniece, Liga; Vavers, Edijs; Svalbe, Baiba; Veinberg, Grigory; Rizhanova, Kristina; Liepins, Vilnis; Kalvinsh, Ivars; Dambrova, Maija (1 October 2015). "R-phenibut binds to the α2–δ subunit of voltage-dependent calcium channels and exerts gabapentin-like anti-nociceptive effects". Pharmacology Biochemistry and Behavior. 137: 23–29. doi:10.1016/j.pbb.2015.07.014. ISSN 0091-3057. PMID 26234470. S2CID 42606053.
  45. ^ Owen, David R.; Wood, David M.; Archer, John R. H.; Dargan, Paul I. (2016). "Phenibut (4-amino-3-phenyl-butyric acid): Availability, prevalence of use, desired effects and acute toxicity". Drug and Alcohol Review. 35 (5): 591–596. doi:10.1111/dar.12356. hdl:10044/1/30073. ISSN 1465-3362. PMID 26693960.
  46. ^ Cohen, Pieter A.; Ellison, Ross R.; Travis, John C.; Gaufberg, Slava V.; Gerona, Roy (22 September 2021). "Quantity of phenibut in dietary supplements before and after FDA warnings". Clinical Toxicology. 60 (4): 486–488. doi:10.1080/15563650.2021.1973020. PMID 34550038. S2CID 237594860.
  47. ^ "Adaptol. Summary of Product Characteristics" (PDF). Archived from the original (PDF) on 3 December 2015. Retrieved 24 July 2015.
  48. ^ Val'dman AV, Zaikonnikova IV, Kozlovskaia MM, Zimakova IE (1980). "[Characteristics of the psychotropic spectrum of action of mebicar]". Biulleten' Eksperimental'noĭ Biologii I Meditsiny (in Russian). 89 (5): 568–70. PMID 6104993.
  49. ^ Neznamov, GG; Siuniakov, SA; Chumakov, DV; Bochkarev, VK; Seredenin, SB (2001). "Clinical study of the selective anxiolytic agent afobazol". Eksperimental'naia i Klinicheskaia Farmakologiia. 64 (2): 15–9. PMID 11548440.
  50. ^ Silkina, IV; Gan'shina, TC; Seredin, SB; Mirzoian, RS (2005). "Gabaergic mechanism of cerebrovascular and neuroprotective effects of afobazole and picamilon". Eksperimental'naia i Klinicheskaia Farmakologiia. 68 (1): 20–4. PMID 15786959.
  51. ^ Vakhitova IuV, Iamidanov RS, Seredinin SB (2004). "[Ladasten induces the expression of genes regulating dopamine biosynthesis in various structures of rat brain]". Eksp Klin Farmakol (in Russian). 67 (4): 7–11. PMID 15500036.
  52. ^ Vakhitova, Yu. V.; Yamidanov, R. S.; Vakhitov, V. A.; Seredenin, S. B. (2005). "The effect of ladasten on gene expression in the rat brain". Doklady Biochemistry and Biophysics. 401 (1–6): 150–153. doi:10.1007/s10628-005-0057-z. ISSN 1607-6729. PMID 15999825. S2CID 28048257.
  53. ^ Volchegorskii, I. A.; Miroshnichenko, I. Yu.; Rassokhina, L. M.; Faizullin, R. M.; Malkin, M. P.; Pryakhina, K. E.; Kalugina, A. V. (2015). "Comparative Analysis of the Anxiolytic Effects of 3-Hydroxypyridine and Succinic Acid Derivatives". Bulletin of Experimental Biology and Medicine. 158 (6): 756–61. doi:10.1007/s10517-015-2855-3. PMID 25894772. S2CID 6052275.
  54. ^ Rumyantseva, S. A.; Fedin, A. I.; Sokhova, O. N. (2012). "Antioxidant Treatment of Ischemic Brain Lesions". Neuroscience and Behavioral Physiology. 42 (8): 842–5. doi:10.1007/s11055-012-9646-3. S2CID 39971165. INIST 26388033.
  55. ^ "Validol". The Great Soviet Encyclopedia.
  56. ^ "Farmak Product Information - Validol" (PDF). Archived from the original (PDF) on 19 December 2013. Retrieved 9 April 2013.
  57. ^ Malykh, Andrei G.; Sadaie, M. Reza (2010). "Piracetam and Piracetam-Like Drugs". Drugs. 70 (3): 287–312. doi:10.2165/11319230-000000000-00000. PMID 20166767. S2CID 12176745.
  58. ^ a b Skolnick P (November 2012). "Anxioselective anxiolytics: on a quest for the Holy Grail". Trends Pharmacol Sci. 33 (11): 611–20. doi:10.1016/j.tips.2012.08.003. PMC 3482271. PMID 22981367.
  59. ^ a b Nuss, Philippe; Ferreri, Florian; Bourin, Michel (2019). "An update on the anxiolytic and neuroprotective properties of etifoxine: from brain GABA modulation to a whole-body mode of action (Review)". Neuropsychiatric Disease and Treatment. 15: 1781–1795. doi:10.2147/ndt.s200568. ISSN 1178-2021. PMC 6615018. PMID 31308671.
  60. ^ Gilman, J. M.; Ramchandani, V. A.; Davis, M. B.; Bjork, J. M.; Hommer, D. W. (2008). "Why We Like to Drink: A Functional Magnetic Resonance Imaging Study of the Rewarding and Anxiolytic Effects of Alcohol". Journal of Neuroscience. 28 (18): 4583–91. doi:10.1523/JNEUROSCI.0086-08.2008. PMC 2730732. PMID 18448634.
  61. ^ Shearer, Steven L. (2007). "Recent Advances in the Understanding and Treatment of Anxiety Disorders". Primary Care: Clinics in Office Practice. 34 (3): 475–504, v–vi. doi:10.1016/j.pop.2007.05.002. PMID 17868756.
  62. ^ Pull, Charles B (2007). "Combined pharmacotherapy and cognitive-behavioural therapy for anxiety disorders". Current Opinion in Psychiatry. 20 (1): 30–5. doi:10.1097/YCO.0b013e3280115e52. PMID 17143079. S2CID 43737803.
  63. ^ CMA & AMA Home medical guides 2012 & 2014 [full citation needed]
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