Adenosine and cerebral ischemia: therapeutic future or death of a brave concept?

• Published in: European Journal of Pharmacology Vol. 365; no. 1; pp. 9 - 25
• Main Author: Von Lubitz, Dag K.J.E.
• Format: Book Review Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 15.01.1999; Elsevier
• Subjects: Adenosine; Adenosine - pharmacology; Adenosine - therapeutic use; Adenosine receptor; Animals; Biological and medical sciences; Brain Ischemia - drug therapy; Brain Ischemia - metabolism; Cardiovascular Agents - pharmacology; Cardiovascular Agents - therapeutic use; Cerebral ischemia; Humans; Medical sciences; Neuropharmacology; Neuroprotective agent; Pharmacology. Drug treatments; Purinergic P1 Receptor Agonists; Stroke; Treatment; Adenosine; Cerebral ischemia; Stroke; Treatment; Adenosine receptor; Human; Nervous system diseases; Agonist; Pathophysiology; Treatment efficiency; A1 Adenosine receptor; Cardiovascular disease; Neuroprotective agent; Review; Biological activity; Cerebral disorder; Vascular disease; Chemotherapy; Ischemia; Animal; Central nervous system disease; Antiïschemic; Cerebrovascular disease; Brain (vertebrata)
• ISSN: 0014-2999; 1879-0712
• DOI: 10.1016/S0014-2999(98)00788-2

Numerous studies have consistently shown that agonist stimulation of adenosine A 1 receptors results in a significant reduction of morbidity and mortality associated with global and focal brain ischemia in animals. Based on these observations, several authors have suggested utilization of adenosine A 1 receptors as targets for the development of clinically viable drugs against ischemic brain disorders. Recent advent of adenosine A 1 receptor agonists characterized by lowered cardiovascular effects added additional strength to this argument. On the other hand, although cardioprotective, adenosine A 3 receptor agonists proved severely cerebrodestructive when administered prior to global ischemia in gerbils. Moreover, stimulation of adenosine A 3 receptors appears to reduce the efficacy of some of the neuroprotective actions mediated by adenosine A 1 receptors. The review discusses the possible role of adenosine receptor subtypes (A 1, A 2, and A 3) in the context of their involvement in the pathology of cerebral ischemia, and analyzes putative strategies for the development of clinically useful strategies based on adenosine and its receptors. It also stresses the need for further experimental studies before definitive conclusions on the usefulness of the adenosine concept in the treatment of brain ischemia can be made.