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  2. Catecholamine - Wikipedia

    en.wikipedia.org/wiki/Catecholamine

    Catecholamines are produced mainly by the chromaffin cells of the adrenal medulla and the postganglionic fibers of the sympathetic nervous system. Dopamine, which acts as a neurotransmitter in the central nervous system, is largely produced in neuronal cell bodies in two areas of the brainstem: the ventral tegmental area and the substantia nigra, the latter of which contains neuromelanin ...

  3. Catecholaminergic cell groups - Wikipedia

    en.wikipedia.org/wiki/Catecholaminergic_cell_groups

    Some authors include in this category 'putative' adrenergic cell groups, collections of neurons that stain for PNMT, the enzyme that converts norepinephrine to epinephrine (adrenaline). [2] Catecholaminergic cell groups and Parkinson's disease have an interactive relationship. Catecholaminergic neurons containing neuromelanin are more ...

  4. L-DOPA - Wikipedia

    en.wikipedia.org/wiki/L-DOPA

    l-DOPA can be directly metabolized by catechol-O-methyl transferase to 3-O-methyldopa, and then further to vanillactic acid. This metabolic pathway is nonexistent in the healthy body, but becomes important after peripheral l-DOPA administration in patients with Parkinson's disease or in the rare cases of patients with AADC enzyme deficiency. [11]

  5. Neurotransmitter - Wikipedia

    en.wikipedia.org/wiki/Neurotransmitter

    The cell receiving the signal, or target cell, may be another neuron, but could also be a gland or muscle cell. [1] Neurotransmitters are released from synaptic vesicles into the synaptic cleft where they are able to interact with neurotransmitter receptors on the target cell. Some neurotransmitters are also stored in large dense core vesicles. [2]

  6. Norepinephrine - Wikipedia

    en.wikipedia.org/wiki/Norepinephrine

    Norepinephrine is a catecholamine and a phenethylamine. [4] Its structure differs from that of epinephrine only in that epinephrine has a methyl group attached to its nitrogen, whereas the methyl group is replaced by a hydrogen atom in norepinephrine. [4]

  7. Tyrosine hydroxylase - Wikipedia

    en.wikipedia.org/wiki/Tyrosine_hydroxylase

    The enzyme is highly specific, not accepting indole derivatives - which is unusual as many other enzymes involved in the production of catecholamines do. Tryptophan is a poor substrate for tyrosine hydroxylase, however it can hydroxylate L -phenylalanine to form L -tyrosine and small amounts of 3-hydroxyphenylalanine.

  8. Catechol-O-methyltransferase - Wikipedia

    en.wikipedia.org/wiki/Catechol-O-methyltransferase

    Catechol-O-methyltransferase is involved in the inactivation of the catecholamine neurotransmitters (dopamine, epinephrine, and norepinephrine). The enzyme introduces a methyl group to the catecholamine, which is donated by S-adenosyl methionine (SAM). Any compound having a catechol structure, like catecholestrogens and catechol-containing ...

  9. 3-Methoxytyramine - Wikipedia

    en.wikipedia.org/wiki/3-Methoxytyramine

    3-Methoxytyramine (3-MT), also known as 3-methoxy-4-hydroxyphenethylamine, is a human trace amine and the major metabolite of the monoamine neurotransmitter dopamine. [1] [2] It is formed by the introduction of a methyl group to dopamine by the enzyme catechol-O-methyltransferase (COMT). 3-MT can be further metabolized by the enzyme monoamine oxidase (MAO) to form homovanillic acid (HVA ...