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・ Vesicle-fusing ATPase
・ Vesico-uterine pouch
・ Vesicointestinal fistula
・ Vesicomyidae
・ Vesicopustular dermatosis
・ Vesicoureteral reflux
・ Vesicovaginal fistula
・ Vesiculaphis caricis
・ Vesicular acetylcholine transporter
・ Vesicular appendages of epoophoron
・ Vesicular exanthema of swine virus
・ Vesicular film
・ Vesicular glutamate transporter 1
・ Vesicular monoamine transporter
・ Vesicular monoamine transporter 1
Vesicular monoamine transporter 2
・ Vesicular pemphigoid
・ Vesicular stomatitis virus
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・ Vesicular transport protein
・ Vesicular-tubular cluster
・ Vesicularia montagnei
・ Vesiculentomon
・ Vesiculo-vacuolar organelle
・ Vesiculobullous disease
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・ Vesiculopustular eruption and leukemoid reaction in Down syndrome
・ Vesiculovirus
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Vesicular monoamine transporter 2 : ウィキペディア英語版
Vesicular monoamine transporter 2

The vesicular monoamine transporter 2 (VMAT2) also known as solute carrier family 18 member 2 (SLC18A2) is a protein that in humans is encoded by the ''SLC18A2'' gene. VMAT2 is an integral membrane protein that transports monoamines—particularly neurotransmitters such as dopamine, norepinephrine, serotonin, and histamine—from cellular cytosol into synaptic vesicles. In nigrostriatal pathway and mesolimbic pathway dopamine-releasing neurons, VMAT2 function is also necessary for the vesicular release of the neurotransmitter GABA.
==Binding sites and ligands==
One binding site is that of dihydrotetrabenazine (DTBZ) and reserpine. Lobeline binds at this site. Amphetamine (TBZ site) and methamphetamine (reserpine site) bind at distinct sites to on VMAT2 to inhibit its function. Although the amphetamines inhibit VMAT2 presynaptically leading to diminished neurotransmitter, the primary mechanism for the enhancement of extracellular monoamines, like dopamine, is reversal of the dopamine transporter (DAT). Other VMAT2 inhibitors such as GZ-793A inhibit the reinforcing effects of methamphetamine, but without producing stimulant or reinforcing effects themselves.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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