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Role of Adenosine A2 Receptors in Regulation of Cerebral Blood Flow during Induced Hypotension
Author(s) -
Yoshikazu Kusano,
Germán Echeverry,
Grzegorz Miękisiak,
Tobias Kulik,
Shimon Aronhime,
JiangFan Chen,
H. Richard Winn
Publication year - 2009
Publication title -
journal of cerebral blood flow and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.167
H-Index - 193
eISSN - 1559-7016
pISSN - 0271-678X
DOI - 10.1038/jcbfm.2009.244
Subject(s) - adenosine , autoregulation , vasodilation , adenosine receptor , adenosine a2a receptor , medicine , endocrinology , cerebral blood flow , knockout mouse , cerebral autoregulation , receptor , chemistry , pharmacology , anesthesia , blood pressure , agonist
The mechanisms responsible for vascular autoregulation in the brain during changes in mean arterial blood pressure are ambiguous. Potentially, adenosine, a purine nucleoside and potent vasodilator, may be involved as earlier studies have documented an increase in brain adenosine concentrations with cerebral ischemia and hypotension. Consequently, we tested the hypothesis that adenosine is involved in vasodilatation during hypotension within the autoregulatory range (>50 mm Hg) by exposing adenosine 2a receptor (A2aR) knockout and wild type (WT) mice to short (2 to 5 mins) periods of hypotension. We found that autoregulation was significantly ( P A2b:10–85>1), ZM-241385, in a dose (1, 5, 10 mg/kg, intraperitoneally)-related manner, attenuated autoregulation in WT mice. In knockout mice treated with ZM-2413585 (5 and 10 mg/kg), autoregulation was further impaired indicating that A2b receptors also participated in cerebral vasodilatation. Treatment with dipyridamole (1.0 mg/kg) that increases extracellular concentrations of adenosine improved autoregulation in the A2aR knockout mice. We would conclude that adenosine through both A2a and A2b receptors is involved in physiologic vascular regulation during hypotension even within the autoregulatory range.

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