Riekkinen P, Soininen H, Partanen J, Pääkkönen A, Helisalmi S, Riekkinen P
Department of Neurology, University Hospital of Kuopio, Finland.
Psychopharmacology (Berl). 1997 Feb;129(3):285-8. doi: 10.1007/s002130050192.
In a previous study, we reported that Alzheimer disease (AD) patients with an apolipoprotein E (APOE) epsilon 4 allele (+ APOE4) show more severe loss of nucleus basalis (NB) cholinergic cells than patients without epsilon 4 alleles (-APOE4). The present study investigates the effects of a single oral administration of THA 25 or 50 mg on cortical spectral EEG activity in + (five APOE4/4, six APOE4/3) and -APOE4 (eight APOE3/3) AD patients. THA 25 mg had no significant effect on EEG activity in any AD patients. However, THA 50 mg increased alpha activity and alpha/theta ratio in -APOE4 patients. In contrast, THA 50 mg had no effect on EEG activity in + APOE4 patients. This result tentatively suggests that in AD patients APOE genotype may affect the response of cortical electrical arousal to cholinergic therapy that enhances the efficacy of presynaptic NB axons.
在之前的一项研究中,我们报告称,携带载脂蛋白E(APOE)ε4等位基因(+APOE4)的阿尔茨海默病(AD)患者比不携带ε4等位基因(-APOE4)的患者,基底核(NB)胆碱能细胞的损失更为严重。本研究调查了单次口服25毫克或50毫克THA对携带+(5名APOE4/4、6名APOE4/3)和-APOE4(8名APOE3/3)的AD患者皮层脑电图频谱活动的影响。25毫克THA对任何AD患者的脑电图活动均无显著影响。然而,50毫克THA增加了-APOE4患者的α波活动和α/θ比值。相比之下,50毫克THA对+APOE4患者的脑电图活动没有影响。这一结果初步表明,在AD患者中,APOE基因型可能会影响皮层电觉醒对胆碱能治疗的反应,而胆碱能治疗可增强突触前NB轴突的功效。