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重复给予单胺再摄取抑制剂BTS 74 398会使6-羟基多巴胺损伤的大鼠出现同侧旋转,且不会使运动行为敏感化。

Repeated administration of the monoamine reuptake inhibitor BTS 74 398 induces ipsilateral circling in the 6-hydroxydopamine lesioned rat without sensitizing motor behaviours.

作者信息

Lane E L, Cheetham S C, Jenner P

机构信息

Neurodegenerative Disease Research Centre, GKT School of Biomedical Sciences, King's College, London SE1 1UL, UK.

出版信息

Eur J Neurosci. 2005 Jan;21(1):179-86. doi: 10.1111/j.1460-9568.2004.03834.x.

Abstract

BTS 74 398 (1-[1-(3,4-dichlorophenyl)cyclobutyl]-2-(3-diaminethylaminopropylthio)ethanone monocitrate) is a monoamine reuptake inhibitor that reverses motor deficits in MPTP-treated (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) common marmosets without provoking established dyskinesia. However, it is not known whether BTS 74 398 primes the basal ganglia for dyskinesia induction. In this study, the ability of BTS 74 398 to sensitize 6-hydroxydopamine (6-OHDA)-lesioned rats for the production of abnormal motor behaviours and the induction of striatal DeltaFosB were determined in comparison with l-3,4-dihydroxyphenylalanine methyl ester (L-dopa). Acute administration of BTS 74 398 induced a dose-dependent ipsilateral circling response in unilaterally 6-OHDA-lesioned rats whereas L-dopa produced dose-dependent contraversive rotation. The ipsilateral circling response to BTS 74 398 did not alter during 21 days of administration. In contrast, L-dopa treatment for 21 days caused a marked increase in rotational response. Repeated administration of both L-dopa and BTS 74 398 increased general motor activity and stereotypic behaviour. In L-dopa-treated rats, orolingual, locomotive, forelimb and axial abnormal movements developed whereas BTS 74 398 produced only locomotion with a side bias but no other abnormal movements. Sensitization of circling responses and the development of abnormal movements in 6-OHDA-lesioned rats have been associated with the potential of dopaminergic drugs to induce dyskinesia. Furthermore, striatal DeltaFosB immunoreactivity, shown to correlate with dyskinesia induction, was increased by L-dopa but was unaffected by repeated BTS 74 398 administration. The lack of such changes following repeated BTS 74 398 treatment suggests that it may be an effective antiparkinsonian therapy that is unlikely to produce involuntary movements.

摘要

BTS 74 398(1-[1-(3,4-二氯苯基)环丁基]-2-(3-二氨基乙基氨基丙基硫代)乙酮单柠檬酸盐)是一种单胺再摄取抑制剂,可逆转经1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)处理的普通狨猴的运动功能障碍,且不会引发已有的运动障碍。然而,尚不清楚BTS 74 398是否会使基底神经节对运动障碍的诱导产生易感性。在本研究中,与左旋多巴(L-多巴)相比,测定了BTS 74 398使6-羟基多巴胺(6-OHDA)损伤大鼠产生异常运动行为以及诱导纹状体DeltaFosB的能力。急性给予BTS 74 398可在单侧6-OHDA损伤大鼠中诱导剂量依赖性的同侧转圈反应,而L-多巴则产生剂量依赖性的对侧旋转。在给药的21天内,对BTS 74 398的同侧转圈反应没有改变。相比之下,L-多巴治疗21天导致旋转反应显著增加。重复给予L-多巴和BTS 74 398均可增加总体运动活动和刻板行为。在L-多巴治疗的大鼠中,出现了口面部、 locomotive(原文此处可能有误,推测为“运动性的”motor)、前肢和轴向异常运动,而BTS 74 398仅产生带有侧偏的运动,但没有其他异常运动。6-OHDA损伤大鼠中转圈反应的敏化和异常运动的发展与多巴胺能药物诱导运动障碍的可能性有关。此外,纹状体DeltaFosB免疫反应性与运动障碍的诱导相关,L-多巴可使其增加,但重复给予BTS 74 398对其没有影响。重复给予BTS 74 治疗后缺乏此类变化表明,它可能是一种有效的抗帕金森病疗法,不太可能产生不自主运动。

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