Pauli S, Liljequist S, Farde L, Swahn C G, Halldin C, Litton J E, Sedvall G
Department of Psychiatry and Psychology, Karolinska Institute, Stockholm, Sweden.
Psychopharmacology (Berl). 1992;107(2-3):180-5. doi: 10.1007/BF02245135.
Acute alcohol administration to rats has in preliminary studies been reported to drastically increase the binding of the benzodiazepine (BZ) receptor antagonist [3H]flumazenil (Ro 15-1788) to central BZ receptors. In the present study the effect of acute alcohol ingestion on the disposition of [11C]flumazenil in the human brain and plasma was examined by positron emission tomography (PET) in four healthy volunteers. Neocortex, cerebellum and pons (reference region) were delineated using X-ray computerized tomography (CT). Alcohol did not increase either total radioactivity uptake or specific [11C]flumazenil binding in neocortex or cerebellum. However, alcohol had a small but significant effect on [11C]flumazenil in arterial blood. After alcohol the plasma radioactivity peak was higher, more narrow and occurred earlier than in the control experiments. The present experiments contradict the view that alcohol directly affects central BZ receptor binding in man. Thus the dramatic increase of flumazenil binding in rat brain reported previously could not be observed in the human brain.
在初步研究中,据报道,给大鼠急性注射酒精会大幅增加苯二氮䓬(BZ)受体拮抗剂[3H]氟马西尼(Ro 15 - 1788)与中枢BZ受体的结合。在本研究中,通过正电子发射断层扫描(PET)对四名健康志愿者进行了检查,以观察急性摄入酒精对[11C]氟马西尼在人脑中及血浆中分布情况的影响。使用X射线计算机断层扫描(CT)描绘了新皮质、小脑和脑桥(参考区域)。酒精并未增加新皮质或小脑中的总放射性摄取或特异性[11C]氟马西尼结合。然而,酒精对动脉血中的[11C]氟马西尼有微小但显著的影响。饮酒后,血浆放射性峰值比对照实验更高、更窄且出现得更早。本实验与酒精直接影响人体中枢BZ受体结合这一观点相矛盾。因此,先前报道的大鼠脑中氟马西尼结合的显著增加在人脑中并未观察到。