Shinotoh H, Asahina M, Inoue O, Suhara T, Hirayama K, Tateno Y
Department of Neurology, School of Medicine, Chiba University, Japan.
J Neural Transm Park Dis Dement Sect. 1994;7(1):35-46. doi: 10.1007/BF02252661.
The effects of pharmacological intervention on brain muscarinic cholinergic receptor (mAChR) binding were assessed in seven patients with Parkinson's disease by positron emission tomography and carbon-11 labelled N-methyl-4-piperidyl benzilate ([11C]NMPB). [11C]NMPB was injected twice, approximately 2 hours apart, in each patient, to assess the effect of single doses of 4 mg of trihexyphenidyl (n = 5) or 400 mg of L-dopa with 57 mg of benserazide (n = 2) on the binding parameter of mAChRs (K3). There was a mean 28% inhibition of K3 values in the brain in the presence of trihexyphenidyl, which was assumed to reflect mAChR occupancy. No significant change in K3 was observed in the presence of L-dopa. This study demonstrates the feasibility of measuring mAChR occupancy by an anticholinergic medication with PET.
通过正电子发射断层扫描和碳-11标记的N-甲基-4-哌啶基苯甲酸苄酯([11C]NMPB),对7例帕金森病患者进行了药物干预对脑毒蕈碱胆碱能受体(mAChR)结合的影响评估。在每位患者中,[11C]NMPB大约间隔2小时注射两次,以评估单剂量4毫克苯海索(n = 5)或400毫克左旋多巴与57毫克苄丝肼(n = 2)对mAChRs结合参数(K3)的影响。在苯海索存在的情况下,大脑中K3值平均有28%的抑制,这被认为反映了mAChR的占有率。在左旋多巴存在的情况下,未观察到K3有显著变化。本研究证明了用正电子发射断层扫描通过抗胆碱能药物测量mAChR占有率的可行性。