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    • Receptor molecule

      • A chemical substance that binds to a receptor molecule and exhibits a function similar to that of a biological ligand such as a neurotransmitter.
      www.sciencedirect.com/topics/neuroscience/ergoline
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  2. Dec 6, 2019 · Dopamine agonists bind to the D1 and D2 group of dopamine receptors in the brain, copying the effects of the neurotransmitter in order to improve disorders that happen from low levels.

  3. Ergoline are ligands for serotonin receptors and hence have a potential of the dopaminergic, anti-dopaminergic, serotonergic and anti-serotonergic activity. This varied functional profile can be attributed to them having the features of monoamine neurotransmitters 5-HT, noradrenaline and dopamine [ 38 ].

  4. Each neurotrophin binds to a specific tropomyosin receptor kinase receptor (tropomyosin receptor kinase A for nerve growth factor, tropomyosin receptor kinase B for brain-derived neurotrophic factor and neurotrophin-4, and tropomyosin receptor kinase C for neurotrophin-3).

  5. Jun 26, 2023 · Dopamine is an important neurotransmitter regulating voluntary movement, reward and addictive behavior, moods such as mania and depression, cognition, memory, learning, sleep, and food intake. Dopamine also inhibits the synthesis and secretion of prolactin from the pituitary gland.

    • Jaehwa Choi, Kristen Ashley Horner
    • 2023/06/26
  6. Ergoline is an indole alkaloid whose structural skeleton is found in many naturally occurring and synthetic ergolines which are known to bind to neurotransmitter receptors, such as dopamine, noradrenaline and serotonin receptors and function as unselective agonists or antagonists at these receptors. It is an ergoline alkaloid, a diamine, an ...

  7. Jun 16, 2020 · The ergoline nucleus (Fig. 2) of ergot alkaloids is structurally similar to the biogenic amines, dopamine, serotonin and adrenaline and consequently ergot alkaloids are able to act on the ...

  8. The ergoline-derived hallucinogen lysergic acid N, N -diethylamide (LSD). The stereochemistry illustrated here is critical for activity, and if the chirality at either the 5- or the 8-position is reversed, activity is lost.

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