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  2. Dopaminergic pathways - Wikipedia

    en.wikipedia.org/wiki/Dopaminergic_pathways

    The dopamine neurons of the dopaminergic pathways synthesize and release the neurotransmitter dopamine. [2] [3] Enzymes tyrosine hydroxylase and dopa decarboxylase are required for dopamine synthesis. [4] These enzymes are both produced in the cell bodies of dopamine neurons. Dopamine is stored in the cytoplasm and vesicles in axon terminals.

  3. Dopamine receptor - Wikipedia

    en.wikipedia.org/wiki/Dopamine_receptor

    Dopamine receptors can also transactivate Receptor tyrosine kinases. [19] Beta Arrestin recruitment is mediated by G-protein kinases that phosphorylate and inactivate dopamine receptors after stimulation. While beta arrestin plays a role in receptor desensitization, it may also be critical in mediating downstream effects of dopamine receptors.

  4. Conditioned avoidance response test - Wikipedia

    en.wikipedia.org/wiki/Conditioned_avoidance...

    The test can detect antipsychotic-like activity both in the case of dopamine D 2 receptor antagonists and in the case of drugs lacking D 2 receptor antagonism. [1] [2] [6] The occupancy of the D 2 receptor by antagonists of this receptor required to inhibit the CAR is around 65 to 80%, which is similar to the occupancy at which therapeutic antipsychotic effects occur in humans with these drugs.

  5. Dopamine antagonist - Wikipedia

    en.wikipedia.org/wiki/Dopamine_antagonist

    Dopamine receptor flow chart. Dopamine receptors are all G protein–coupled receptors, and are divided into two classes based on which G-protein they are coupled to. [1] The D 1-like class of dopamine receptors is coupled to Gα s/olf and stimulates adenylate cyclase production, whereas the D 2-like class is coupled to Gα i/o and thus inhibits adenylate cyclase production.

  6. Dopamine receptor D5 - Wikipedia

    en.wikipedia.org/wiki/Dopamine_receptor_D5

    D 5 receptor is a subtype of the dopamine receptor that has a 10-fold higher affinity for dopamine than the D 1 subtype. [6] The D 5 subtype is a G-protein coupled receptor, which promotes synthesis of cAMP by adenylyl cyclase via activation of Gα s/olf family of G proteins. [7] [8] Both D 5 and D 1 subtypes activate adenylyl cyclase.

  7. Dopaminergic - Wikipedia

    en.wikipedia.org/wiki/Dopaminergic

    Also, any endogenous or exogenous chemical substance that acts to affect dopamine receptors or dopamine release through indirect actions (for example, on neurons that synapse onto neurons that release dopamine or express dopamine receptors) can also be said to have dopaminergic effects, two prominent examples being opioids, which enhance ...

  8. D2-like receptor - Wikipedia

    en.wikipedia.org/wiki/D2-like_receptor

    The D 2-like receptors [1] are a subfamily of dopamine receptors that bind the endogenous neurotransmitter dopamine. The D 2-like subfamily consists of three G-protein coupled receptors that are coupled to G i /G o and mediate inhibitory neurotransmission, of which include D 2, D 3, and D 4. For more information, please see the respective main ...

  9. Dopamine receptor D1 - Wikipedia

    en.wikipedia.org/wiki/Dopamine_receptor_D1

    D 1 receptor has a high degree of structural homology to another dopamine receptor, D 5, and they both bind similar drugs. [13] As a result, none of the known orthosteric ligands is selective for the D 1 vs. the D 5 receptor, but the benzazepines generally are more selective for the D 1 and D 5 receptors versus the D 2 -like family. [ 12 ]