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Interference of norepinephrine transporter trafficking motif attenuates amphetamine-induced locomotor hyperactivity and conditioned place preference

机译:Norepinephrine运输贩运基序的干扰衰减anphetamine诱导的机车多动症和条件的地方偏好

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Abstract Amphetamine (AMPH)-mediated norepinephrine transporter (NET) downregulation requires NET-T258/S259 trafficking motif. The present study utilizes cell permeable NET-T258/S259 motif interfering peptide, which blocks AMPH-induced NET downregulation, to explore the role of this form of NET regulation in AMPH-mediated behaviors. In rats receiving intra-accumbal microinjections of TAT-conjugated peptides encompassing NET-T258/S259 motif, acute systemic AMPH failed to inhibit NE transport in the TAT-NET-T258/S259 wild-type (WT) peptide injected hemisphere but not in the vehicle or scrambled peptide injected hemisphere. Acute AMPH-induced hyperactivity was significantly reduced in rats receiving intra-accumbal TAT-NET-T258/S259 WT peptide compared to those receiving intra-accumbal vehicle or TAT-NET-T258A/S259A mutant peptide or corresponding TAT-conjugated scrambled peptide. Basal locomotor activity was not altered by peptide infusions alone. Similarly AMPH-induced locomotor sensitization was significantly reduced in rats receiving intra-accumbal TAT-NET-T258/S259 WT peptide prior to AMPH challenge and not in rats receiving the mutant or scrambled peptide. In conditioned place preference (CPP) paradigm, a single bilateral intra-accumbal microinjection of TAT-NET-T258/S259 WT peptide prior to CPP testing significantly reduced AMPH-induced CPP expression. Likewise, a single bilateral intra-accumbal microinjection of TAT-NET-T258/S259 WT peptide prior to drug-challenge significantly attenuated AMPH-primed CPP reinstatement. On the other hand, bilateral intra-accumbal microinjection of scrambled peptide did not affect AMPH-induced CPP expression or reinstatement. These data demonstrate a role for T258/S259-dependent NET regulation in AMPH-induced hyperactivity and sensitization as well as AMPH-induced CPP expression and reinstatement. Highlights ? Amphetamine targets norepinephrine transporter contributing to drug-abuse potential. ? NET-T258/S259 trafficking motif is required for AMPH mediated NET downregulation. ? Intra-accumbal TAT-NET-T258/S259 peptide infusion blocks NET inhibition by AMPH. ? In-vivo interference of NET-T258/S259 motif attenuates AMPH-induced behaviors.
机译:摘要amphetamine(AMPH)介导的去甲肾上腺素转运蛋白(净)下调需要NET-T258 / S259贩运主题。本研究利用细胞可渗透的NET-T258 / S259基序干扰肽,其阻断AMPH诱导的净下调,探讨这种形式的净调控在AMPH介导的行为中的作用。在大鼠接受包含网T258 / S259基序的TAT缀合肽的宫内显微注射的大鼠中,急性全身AMPph未能抑制TAT-NET-T258 / S259野生型(WT)肽注射半球的NE转运,但不抑制载体或加糖肽注射半球。与接受内骨内载体或TAT-NET-T258A / S259A突变肽或相应的TAT缀合的丙哒肽相比,在接受宫内TAT-NET-T258 / S259WT肽的大鼠中,急性AMPH诱导的多动显着降低。单独的肽输注没有改变基础运动活性。在AMPH攻击之前,在AMPH攻击之前,在接受ABS-TAT-NET-T258 / S259WT肽的大鼠中,同样地减少了同样的AMPH诱导的运动致敏化。在条件下偏好(CPP)范式中,在CPP测试之前,TAT-NET-T258 / S259 WT肽的单侧双侧内部分子显微注射显着降低了AMPH诱导的CPP表达。同样地,在药物攻击之前,TAT-NET-T258 / S259 WT肽的单侧双侧内部分子显微注射显着减弱了AMPH引发的CPP恢复。另一方面,糖浆的双侧内骨内显微注射蛋白癌肽不影响AMPH诱导的CPP表达或恢复。这些数据表明了在AMPH诱导的血清活动和敏化中的T258 / S259依赖性净调控的作用以及AMPH诱导的CPP表达和恢复。强调 ? amphetamine靶向去甲肾上腺素转运蛋白,有助于药物滥用潜力。还AMPH介导的净下调需要NET-T258 / S259贩运主题。还宫内TAT-NET-T258 / S259肽输注通过AMPph进行净抑制。还NET-T258 / S259主题的体内干扰衰减了AMPH诱导的行为。

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