腺苷A1受体
嘌呤能信号
药理学
化学
腺苷A3受体
腺苷A2B受体
出处
期刊:Drug News & Perspectives
[Thomson Reuters (Prous Science)]
日期:2007-01-01
卷期号:20 (10): 607-607
被引量:70
标识
DOI:10.1358/dnp.2007.20.10.1181353
摘要
The endogenous neuromodulator adenosine controls and integrates a wide range of brain functions. Consequently, dysfunction of the adenosine system is involved in pathologies ranging from epilepsy to neurodegenerative disorders and psychiatric conditions. The adenosine system has therefore been recognized as a prime target for the development of new therapeutics for neurological diseases. This review covers the upstream and downstream targets of adenosinergic neurotransmission and provides the neurochemical rationale for the development of adenosine receptor modulating drugs (downstream) and inhibitors of adenosine kinase, the key upstream regulator of ambient levels of adenosine. Due to the unique role of adenosine to integrate and fine-tune glutamatergic and dopaminergic neurotransmission, adenosine-regulating agents have the potential to modify a wide range of downstream effects. Thus, adenosine-based therapies are rapidly evolving in preclinical and clinical studies.
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