Erfurth A, Schmauss M
Neurologisches Zentrum, Segeberger Kliniken, Bad Segeberg.
Fortschr Neurol Psychiatr. 1995 Mar;63(3):93-8. doi: 10.1055/s-2007-996607.
The function of the neuromodulator, adenosine, has been thoroughly examined during the last two decades. Adenosine inhibits the release of several neurotransmitters and endogenous adenosine is supposed to have sedative and anticonvulsive properties. Lately, it has been discussed whether neuropsychiatric disorders could be treated with adenosynergic drugs. In patients with anxiety disorder a first clinical trial with the reuptake inhibitor dipyridamole was not successful. Disorders of the basal ganglia and schizophrenia might be positively influenced by newly developed A2-receptor ligands. A1-receptor agonists might prove to be neuroprotective; they also could be of importance in the treatment of epilepsy. Selective A1-receptor antagonists might be used in the treatment of depressive disorders and of neurodegenerative disorders such as Alzheimer's disease. The adenosine receptor antagonist, caffeine, is widely used in the treatment of migraine; more selective antagonists would provide a more powerful treatment.
在过去二十年中,对神经调质腺苷的功能进行了深入研究。腺苷可抑制多种神经递质的释放,内源性腺苷被认为具有镇静和抗惊厥特性。最近,人们讨论了神经精神疾病是否可用腺苷协同药物治疗。在焦虑症患者中,使用再摄取抑制剂双嘧达莫的首次临床试验并不成功。基底神经节疾病和精神分裂症可能会受到新开发的A2受体配体的积极影响。A1受体激动剂可能具有神经保护作用;它们在癫痫治疗中也可能具有重要意义。选择性A1受体拮抗剂可用于治疗抑郁症和神经退行性疾病,如阿尔茨海默病。腺苷受体拮抗剂咖啡因广泛用于偏头痛治疗;更具选择性的拮抗剂将提供更有效的治疗。