Research Service, VA Portland Health Care System, Portland, Oregon (N.B.M., T.J.P., A.J.); and Departments of Behavioral Neuroscience (N.B.M., T.J.P., A.J.) and Psychiatry (A.J.), and The Methamphetamine Abuse Research Center (T.J.P., A.J.), Oregon Health & Science University, Portland, Oregon.
Research Service, VA Portland Health Care System, Portland, Oregon (N.B.M., T.J.P., A.J.); and Departments of Behavioral Neuroscience (N.B.M., T.J.P., A.J.) and Psychiatry (A.J.), and The Methamphetamine Abuse Research Center (T.J.P., A.J.), Oregon Health & Science University, Portland, Oregon
J Pharmacol Exp Ther. 2019 Oct;371(1):36-44. doi: 10.1124/jpet.119.258970. Epub 2019 Jul 18.
Methamphetamine (MA) impairs vesicular monoamine transporter 2 (VMAT2) and dopamine transporter (DAT) function and expression, increasing intracellular DA levels that lead to neurotoxicity. The trace amine-associated receptor 1 (TAAR1) is activated by MA, but when the receptor is not activated, MA-induced neurotoxicity is increased. To investigate interactions among TAAR1, VMAT2, and DAT, transporter function and expression were measured in transgenic knockout (KO) and wild-type (WT) mice 24 hours following a binge-like regimen (four intraperitoneal injections, 2 hours apart) of MA (5 mg/kg) or the same schedule of saline treatment. Striatal synaptosomes were separated by fractionation to examine the function and expression of VMAT2 localized to cytosolic and membrane-associated vesicles. DAT was measured in whole synaptosomes. VMAT2-mediated [H]DA uptake inhibition was increased in KO mice in synaptosomal and vesicular fractions, but not the membrane-associated fraction, compared with WT mice. There was no difference in [H]dihydrotetrabenazine binding to the VMAT2 or [I]RTI-55 binding to the DAT between genotypes, indicating activation of TAAR1 does not affect VMAT2 or DAT expression. There was also no difference between WT and KO mice in DAT-mediated [H]DA uptake inhibition following in vitro treatment with MA. These findings provide the first evidence of a TAAR1-VMAT2 interaction, as activation of TAAR1 mitigated MA-induced impairment of VMAT2 function, independently of change in VMAT2 expression. Additionally, the interaction is localized to intracellular VMAT2 on cytosolic vesicles and did not affect expression or function of DAT in synaptosomes or VMAT2 at the plasmalemmal surface, i.e., on membrane-associated vesicles. SIGNIFICANCE STATEMENT: Methamphetamine stimulates the G protein-coupled receptor TAAR1 to affect dopaminergic function and neurotoxicity. Here we demonstrate that a functional TAAR1 protects a specific subcellular fraction of VMAT2, but not the dopamine transporter, from methamphetamine-induced effects, suggesting new directions in pharmacotherapeutic development for neurodegenerative disorders.
甲基苯丙胺(MA)会损害囊泡单胺转运体 2(VMAT2)和多巴胺转运体(DAT)的功能和表达,增加细胞内 DA 水平,从而导致神经毒性。微量胺相关受体 1(TAAR1)被 MA 激活,但当受体未被激活时,MA 诱导的神经毒性会增加。为了研究 TAAR1、VMAT2 和 DAT 之间的相互作用,在 MA(5mg/kg)或相同盐疗方案的 binge-like 方案(4 次腹腔注射,每 2 小时一次)后 24 小时,用转基因敲除(KO)和野生型(WT)小鼠测量转运体功能和表达。通过分级分离分离纹状体突触小体,以检查定位于细胞质和膜相关囊泡的 VMAT2 的功能和表达。在整个突触小体中测量 DAT。与 WT 小鼠相比,在突触小体和囊泡部分,而不是膜相关部分,KO 小鼠中的 VMAT2 介导的[H]DA 摄取抑制增加。在基因型之间,[H]二氢四苯嗪与 VMAT2 的结合或[I]RTI-55 与 DAT 的结合没有差异,表明 TAAR1 的激活不会影响 VMAT2 或 DAT 的表达。WT 和 KO 小鼠之间在体外用 MA 处理后 DAT 介导的[H]DA 摄取抑制也没有差异。这些发现首次提供了 TAAR1-VMAT2 相互作用的证据,因为 TAAR1 的激活减轻了 MA 诱导的 VMAT2 功能障碍,而与 VMAT2 表达的变化无关。此外,这种相互作用定位于细胞质囊泡上的细胞内 VMAT2,并且不会影响突触小体中 DAT 的表达或功能,也不会影响质膜表面(即膜相关囊泡上)的 VMAT2。意义陈述:甲基苯丙胺刺激 G 蛋白偶联受体 TAAR1 影响多巴胺能功能和神经毒性。在这里,我们证明了功能性 TAAR1 可保护 VMAT2 的特定亚细胞部分免受 MA 诱导的影响,但不影响多巴胺转运体,这表明在神经退行性疾病的药物治疗开发方面有了新的方向。