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  2. Tryptophan - Wikipedia

    en.wikipedia.org/wiki/Tryptophan

    Low brain serotonin level is induced by administration of tryptophan-poor protein in a technique called acute tryptophan depletion. [68] Studies using this method have evaluated the effect of serotonin on mood and social behavior, finding that serotonin reduces aggression and increases agreeableness. [69]

  3. Acute tryptophan depletion - Wikipedia

    en.wikipedia.org/wiki/Acute_tryptophan_depletion

    For example, a meta-analysis show that the effect size for the effects of tryptophan depletion on mood in depressed people not taking antidepressants was large (Hedge's g = −1.9 (95% CIs −3.02 to −0.78) [3] Hence, a more accurate interpretation is that tryptophan depletion studies suggest a role for 5-HT in people vulnerable to depression ...

  4. Biology of depression - Wikipedia

    en.wikipedia.org/wiki/Biology_of_depression

    This leads to alteration in emotion and cognition related brain regions as well as HPA axis dysfunction. Through the dysfunction, the effects of stress can be exacerbated including its effects on 5-HT. Furthermore, some of these effects are reversed by antidepressant action, which may act by increasing hippocampal neurogenesis.

  5. Serotonin–norepinephrine reuptake inhibitor - Wikipedia

    en.wikipedia.org/wiki/Serotonin–norepinephrine...

    Serotonin is synthesized from an amino acid called L-tryptophan. Active transport system regulates the uptake of tryptophan across the blood–brain barrier . Serotonergic pathways are classified into two main ways in the brain: the ascending projections from the medial and dorsal raphe and the descending projections from the caudal raphe into ...

  6. Kynurenic acid - Wikipedia

    en.wikipedia.org/wiki/Kynurenic_acid

    Kynurenic acid (KYNA or KYN) is a product of the normal metabolism of amino acid L-tryptophan. It has been shown that kynurenic acid possesses neuroactive activity. It acts as an antiexcitotoxic and anticonvulsant, most likely through acting as an antagonist at excitatory amino acid receptors. Because of this activity, it may influence ...

  7. TPH2 - Wikipedia

    en.wikipedia.org/wiki/TPH2

    Tryptophan hydroxylase (TPH; EC 1.14.16.4) is the rate-limiting enzyme in the synthesis of serotonin (5-hydroxytryptamine, or 5HT). 5HT is causally involved in numerous central nervous activities, and it has several functions in peripheral tissues, including the maintenance of vascular tone and gut motility.[supplied by OMIM] [7]

  8. 5-Hydroxytryptophan - Wikipedia

    en.wikipedia.org/wiki/5-Hydroxytryptophan

    5-HTP is produced from the amino acid tryptophan through the action of the enzyme tryptophan hydroxylase. Tryptophan hydroxylase is one of the biopterin-dependent aromatic amino acid hydroxylases. Production of 5-HTP is the rate-limiting step in 5-HT (serotonin) synthesis. 5-HTP is normally rapidly converted to 5-HT by amino acid decarboxylase. [1]

  9. Median raphe nucleus - Wikipedia

    en.wikipedia.org/wiki/Median_raphe_nucleus

    According to one study, it represents the main source of serotonin (5-hydroxytryptamine (5-HT)) in the brain. [3] Stimulation of the MRN significantly increases the amount of 5-HT present in the brain. [5] MRN is the main contributor of 5-HT to the dorsal hippocampus as well as anterior and posterior cortical areas. [5]