Pharmacology Of A Unique Adenosine Binding Site In Rat Brain Using A Selective Ligand-Reference-Cited by-同舟云学术

Pharmacology Of A Unique Adenosine Binding Site In Rat Brain Using A Selective Ligand

Published:2001-04 Issue:4 Volume:28 Page:278-284
ISSN:0305-1870
Container-title:Clinical and Experimental Pharmacology and Physiology
language:en
Short-container-title:Clin Exp Pharmacol Physiol

Author:

Yoshioka Kazuaki,Matsuda Akira,Nakata Hiroyasu

Publisher

Wiley

Subject

Physiology (medical),Pharmacology,Physiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1440-1681.2001.03438.x/fullpdf

Reference24 articles.

1. 2. G. Burnstock A basis for distinguishing two types of purinoceptors. In: Staub RW, Bolis L (eds).Cell Membrane Receptors for Drugs and Hormones: A Multidisciplinary Approach. Raven Press, New York. 1978; 107-18.

2. Adenosine activates the K+ channel and enhances cytosolic Ca2+ release via a P2Y purinoceptor in hippocampal neurons

3. Dependence of P2-nucleotide receptor agonist-mediated endothelium-independent relaxation on ectonucleotidase activity and A2A -receptors in rat portal vein

4. Characterization of prejunctional purinoceptors on adrenergic nerves of the rat caudal artery

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