Selective serotonin reuptake inhibitors ( SSRIs ) are the class of antidepressants commonly used as the first-line treatment for depression because they have a favorable side effect profile and low toxicity.

Selective serotonin reuptake inhibitors or serotonin-specific reuptake inhibitor ( SSRIs ) are a class of compounds typically used as antidepressants in the treatment of depression, anxiety disorders, and some personality disorders.

Selective serotonin reuptake inhibitors are likely to be the best choice of pharmacotherapy for many patients with panic disorder, but benzodiazepines are also often used, and some studies suggest that these medications are still used with greater frequency than the SSRIs.

# REDIRECT Selective serotonin reuptake inhibitor

# REDIRECT Selective serotonin reuptake inhibitor

** Selective serotonin reuptake inhibitors

Selective serotonin reuptake inhibitors ( SSRIs ) selectively block the reuptake of serotonin ( 5-HT ) through their inhibiting effects on the sodium / potassium ATP-dependent serotonin transporter in presynaptic neurons.

# REDIRECT Selective serotonin reuptake inhibitor

Category: Selective serotonin reuptake inhibitors

# REDIRECT Selective serotonin reuptake inhibitor

Selective serotonin reuptake inhibitor ( SSRI ) antidepressants might be indicated for use in men with small penis syndrome.

During investigation, it was revealed that Nishizawa had taken a large dose of SSRI medication ( SSRI ( Selective serotonin reuptake inhibitors ) are antidepressants used in the treatment of depression ) before the episode, and he said that he hijacked the plane because he wanted to fly it under the Rainbow Bridge in Tokyo.

Category: Selective serotonin reuptake inhibitors

* Selective serotonin reuptake inhibitor anti-depressants ( SSRIs ), because of their serotonergic effect, would seem to help IBS, especially patients who are constipation predominant.

Category: Selective serotonin reuptake inhibitors

* Selective serotonin reuptake inhibitor ( SSRI )

Selective serotonin reuptake inhibitor ( SSRI ) antidepressants are believed to act in these nuclei, as well as at their targets.

Selective serotonin reuptake inhibitors ( SSRIs ) have emerged as first-line therapy.

* Selective dopamine reuptake inhibitors

** Selective serotonin reuptake inhibitors ( SSRIs, a class of antidepressants )

* Selective serotonin reuptake inhibitors ( Prozac, Zoloft, and Paxil )

Selective serotonin reuptake inhibitor ( SSRI ) antidepressants are believed to act at these nuclei.

Selective inhibitors can distinguish the two activities.

** Selective MAO-B inhibitors

Selective serotonin re-uptake inhibitors, SSRI's, frequently prescribed for panic and / or anxiety disorder and depression, affect serotonin in the gut as well as the brain.

Selective JAK2 inhibitors are being investigated in vitro and in clinical trials.

Selective serotonin re-uptake inhibitors ( SSRIs ) are used to treat major depression.

: Selective cyclic nucleotide phosphodiesterase inhibitors as potential therapeutic agents.

Tramadol is structurally closer to venlafaxine than to codeine and delivers analgesia by not only delivering " opiate-like " effects ( through mild agonism of the mu receptor ) but also by acting as a weak but fast-acting serotonin releasing agent and norepinephrine reuptake inhibitor.

Serotonin-norepinephrine reuptake inhibitors ( SNRIs ) are a newer form of antidepressants that work on both norepinephrine and 5-HT.

Changing the balance of serotonin and norepinephrine would help the brain cells send and receive messages, therefore boosting the mood, which also is the main reason why these types of medications are called dual reuptake inhibitors.

Norepinephrine reuptake inhibitors ( NRIs ) act via norepinephrine ( noradrenaline ).

Norepinephrine-dopamine reuptake inhibitors inhibit the neuronal reuptake of dopamine and norepinephrine.

Tricyclics block the reuptake of certain neurotransmitters such as norepinephrine and serotonin.

The choice of treatment between benzodiazepines, SSRIs, serotonin – norepinephrine reuptake inhibitors, tricyclic antidepressants, and psychotherapy should be based on the patient's history, preference, and other individual characteristics.

The TCAs include the following agents which are predominantly serotonin and / or norepinephrine reuptake inhibitors:

Most of the TCAs inhibit the reuptake of norepinephrine, though not dopamine, and as a result, they show some efficacy in remedying the disorder.

The majority of the TCAs act primarily as serotonin-norepinephrine reuptake inhibitors ( SNRIs ) by blocking the serotonin transporter ( SERT ) and the norepinephrine transporter ( NET ), respectively, which results in an elevation of the synaptic concentrations of these neurotransmitters, and therefore an enhancement of neurotransmission.

Tricyclic antidepressants ( TCAs ) work through binding to the presynaptic transporter proteins and blocking the reuptake of norepinephrine or 5-HT into the presynaptic terminal, prolonging the duration of transmitter action at the synapse.

Most of the behavioral and physiological actions of cocaine can be explained by its ability to block the reuptake of the two catecholamines, dopamine and norepinephrine, as well as serotonin.

In the prefrontal cortex, however, there are very few DAT proteins, and dopamine is inactivated instead by reuptake via the norepinephrine transporter ( NET ), presumably on neighboring norepinephrine neurons, then enzymatic breakdown by COMT into 3-MT.

The action of cathine and cathinone on the reuptake of epinephrine and norepinephrine has been demonstrated in lab animals, showing that one or both of these chemicals cause the body to recycle these neurotransmitters more slowly, resulting in the wakefulness and insomnia associated with khat use.

Like NDRIs, amphetamine increases the levels of norepinephrine and dopamine in the brain via reuptake inhibition ; however, the more important mechanism by which amphetamines cause stimulation is through the direct release of these catecholamines from storage vesicles in cells.

These drugs inhibit the reuptake of norepinephrine and / or dopamine, resulting in increased extracellular levels and therefore enhanced neurotransmission, ultimately producing a stimulant effect.

It belongs to the piperidine class of compounds and increases the levels of dopamine and norepinephrine in the brain through reuptake inhibition of the monoamine transporters.

A three-way comparison of sertraline, norepinephrine reuptake inhibitor tricyclic antidepressant desipramine, and placebo demonstrated the superiority of sertraline, while desipramine fared no better than placebo.

Further work on these compounds led to tametraline, a norepinephrine and weaker dopamine reuptake inhibitor.

Welch generated a number of potent norepinephrine and triple reuptake inhibitors, but to the surprise of the scientists, one representative of the generally inactive cis-analogs was a serotonin reuptake inhibitor.

The psychoactive drug cocaine potently inhibits the normal reuptake of norepinephrine into presynaptic nerve terminals, resulting in an increased level of extracellular norepinephrine.