Kilbourn M, Lee L, Vander Borght T, Jewett D, Frey K
Department of Internal Medicine, University of Michigan Medical School, Ann Arbor 48109, USA.
Eur J Pharmacol. 1995 May 24;278(3):249-52. doi: 10.1016/0014-2999(95)00162-e.
The two enantiomers of alpha-dihydrotetrabenazine were separated using chiral high performance liquid chromatography. The (+)-isomer showed high affinity in vitro (Ki = 0.97 +/- 0.48 nM) for the vesicular monoamine transporter (VMAT2) in rat brain striatum, whereas the (-)-isomer was inactive (Ki = 2.2 +/- 0.3 microM). Each isomer was then synthesized in carbon-11 labeled form, and regional brain biodistributions in mice determined after intravenous injection. Only (+)-alpha-dihydrotetrabenazine showed selective and specific accumulations in regions of dense monoaminergic innervation (e.g., striatum, hypothalamus), which could be blocked by coinjection of unlabeled tetrabenazine. Binding of alpha-dihydrotetrabenazine to the vesicular monoamine transporter is thus stereospecific.
使用手性高效液相色谱法分离了α-二氢丁苯那嗪的两种对映体。(+)-异构体在体外对大鼠脑纹状体中的囊泡单胺转运体(VMAT2)表现出高亲和力(Ki = 0.97±0.48 nM),而(-)-异构体无活性(Ki = 2.2±0.3 μM)。然后将每种异构体合成碳-11标记形式,并在静脉注射后测定小鼠脑内区域的生物分布。只有(+)-α-二氢丁苯那嗪在密集单胺能神经支配区域(如纹状体、下丘脑)表现出选择性和特异性积累,这种积累可通过注射未标记的丁苯那嗪来阻断。因此,α-二氢丁苯那嗪与囊泡单胺转运体的结合具有立体特异性。