Kim Sang Eun, Choi Joon Young, Choe Yearn Seong, Choi Yong, Lee Won Yong
Department of Nuclear Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
J Nucl Med. 2003 Jun;44(6):870-6.
In Parkinson's disease (PD), both neuropathologic and biochemical studies suggest that serotonin (5-hydroxytryptamine [5-HT]) neurons are affected by the disease process. The integrity of 5-HT transporters was assessed in PD patients with SPECT using 2beta-carbomethoxy-3beta-(4-(123)I-iodophenyl)tropane ((123)I-beta-CIT), which binds with high affinity to both dopamine (DA) and 5-HT transporters.
Forty-five PD patients at relatively early stages (mean Hoehn-Yahr stage, 2.0 +/- 0.7; range, 1-3) and 7 age-matched healthy control subjects had 15 scans over a 24-h period after injection of (123)I-beta-CIT using a 3-head SPECT system. In the midbrain, the 5-HT transporter parameter k(3)/k(4) was estimated by 3 noninvasive methods: pseudoequilibrium ratio (R(PE)) method, area ratio (R(A)) method, and a modified graphic method that derives the ratio of ligand distribution volumes (R(V)). Striatal V(3)", the DA transporter parameter that is equivalent to k(3)/k(4), was measured using the images acquired at 24 h after tracer injection. All measures were derived using the cerebellum as the reference region.
In control subjects, the (123)I-beta-CIT activity in the midbrain reached a peak at 91 +/- 21 min after injection and then washed out at a slow rate (1.1%/h +/- 0.5%/h). The peak specific uptake in the midbrain occurred at 315 +/- 46 min. In PD patients, the temporal patterns of the midbrain and cerebellar activity were not significantly different from those in control subjects. None of midbrain R(PE), R(A), and R(V) was significantly different between control subjects and PD patients, whereas striatal V(3)" was bilaterally reduced in all patients, being 32% lower than that of the control subjects (P = 0.002). In PD patients, none of the midbrain outcome measures was significantly correlated with either striatal V(3)" or motor or nonmotor symptom ratings, including the Hoehn-Yahr stage and the Unified Parkinson's Disease Rating Scale scores. When the studies of 7 PD patients with depression were analyzed separately, none of the midbrain outcome measures in these patients either was different significantly from control values or correlated with the Hamilton Depression Rating Scale score.
These results suggest that DA and 5-HT transporters are differentially affected in PD, and 5-HT transporters in the midbrain region may not be affected in relatively early stages of PD. Alternatively, 5-HT transporters in the remaining neurons may be upregulated, thus raising the midbrain 5-HT transporter density to almost normal levels.
在帕金森病(PD)中,神经病理学和生物化学研究均表明血清素(5-羟色胺[5-HT])神经元受疾病进程影响。使用2β-甲氧基羰基-3β-(4-(¹²³I)碘苯基)托烷(¹²³I-β-CIT),通过单光子发射计算机断层扫描(SPECT)评估PD患者中5-HT转运体的完整性,¹²³I-β-CIT与多巴胺(DA)和5-HT转运体均具有高亲和力。
45例相对早期的PD患者(平均Hoehn-Yahr分期为2.0±0.7;范围为1 - 3期)和7名年龄匹配的健康对照者,在注射¹²³I-β-CIT后24小时内使用三头SPECT系统进行15次扫描。在中脑,通过3种非侵入性方法估计5-HT转运体参数k(3)/k(4):伪平衡比(R(PE))法、面积比(R(A))法以及推导配体分布容积比(R(V))的改良图像法。纹状体V(3)",即等同于k(3)/k(4)的DA转运体参数,使用注射示踪剂后24小时采集的图像进行测量。所有测量均以小脑作为参考区域得出。
在对照者中,中脑的¹²³I-β-CIT活性在注射后91±21分钟达到峰值,然后以缓慢速率清除(1.1%/小时±0.5%/小时)。中脑的峰值特异性摄取发生在315±46分钟。在PD患者中,中脑和小脑活性的时间模式与对照者无显著差异。对照者与PD患者之间,中脑的R(PE)、R(A)和R(V)均无显著差异,而所有患者的纹状体V(3)"双侧降低,比对照者低32%(P = 0.002)。在PD患者中,中脑的所有测量结果与纹状体V(3)"或运动及非运动症状评分均无显著相关性,包括Hoehn-Yahr分期和统一帕金森病评定量表评分。当单独分析7例伴有抑郁的PD患者的研究时,这些患者中脑的所有测量结果与对照值均无显著差异,也与汉密尔顿抑郁评定量表评分无相关性。
这些结果表明,在PD中DA和5-HT转运体受到不同影响,并且在PD相对早期阶段中脑区域的5-HT转运体可能未受影响。或者,剩余神经元中的5-HT转运体可能上调,从而使中脑5-HT转运体密度提高至几乎正常水平。