Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei, Taiwan; Department of Pharmacy Practice, Tri-Service General Hospital, Taipei, Taiwan; School of Pharmacy, National Defense Medical Center, Taipei, Taiwan.
Department of Pharmacy Practice, Tri-Service General Hospital, Taipei, Taiwan; Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan; School of Public Health, National Defense Medical Center, Taipei, Taiwan.
Eur J Pharmacol. 2019 Nov 5;862:172639. doi: 10.1016/j.ejphar.2019.172639. Epub 2019 Sep 3.
This study investigated the effect of dextromethorphan (DXM) against Parkinson's disease (PD) in rats and explored the association between DXM dose and PD risk in elderly patients 65 years and older using a population-based database. The PD rat model (Sprague Dawley rats) was induced by injecting 6-hydroxydopamine (6-OHDA) into the unilateral medial forebrain bundle of the rat brain. DXM (20 mg/kg) was administered intraperitoneally twice daily from 7 days before the appearance of a 6-OHDA lesion to 28 days after the lesion appeared. The availability of dopamine transporter (DAT) and serotonin transporter (SERT) in the striatum of the rat brain was measured using positron emission tomography. The apomorphine-induced rotation test was performed to study the hypersensitivity of the brain regions with lesions. This animal study demonstrated that DXM significantly attenuated 6-OHDA-induced DAT and SERT loss, correlating to rotational behaviors. The population-based human study analyzed the data from the Taiwan Longitudinal Health Insurance Database 2005 between January 2005 and December 2013 and then used the DXM dose-response curve to investigate the trend of its protective effect against PD. In the human study, low cumulative doses of DXM may potentially achieve a protective effect for PD; however, high cumulative doses seem to be a risk for PD.
本研究旨在探讨右美沙芬(DXM)对大鼠帕金森病(PD)的影响,并利用基于人群的数据库探讨老年患者(65 岁及以上)中 DXM 剂量与 PD 风险之间的关联。通过向大鼠大脑内侧前脑束单侧注射 6-羟多巴胺(6-OHDA)诱导 PD 大鼠模型(Sprague Dawley 大鼠)。DXM(20mg/kg)于 6-OHDA 损伤出现前 7 天至损伤出现后 28 天每天两次腹腔内给药。使用正电子发射断层扫描测量大鼠纹状体中多巴胺转运体(DAT)和血清素转运体(SERT)的可用性。通过阿扑吗啡诱导旋转试验研究损伤区域的大脑敏感性。这项动物研究表明,DXM 显著减轻了 6-OHDA 诱导的 DAT 和 SERT 丢失,与旋转行为相关。基于人群的人类研究分析了 2005 年 1 月至 2013 年 12 月期间来自台湾长期健康保险数据库的数据,然后使用 DXM 剂量-反应曲线来研究其对 PD 的保护作用趋势。在人类研究中,低累积剂量的 DXM 可能对 PD 具有潜在的保护作用;然而,高累积剂量似乎对 PD 有风险。