scholarly journals How Prof. Burnstock’s enthusiasm supported P2 receptor research in Germany

Author(s):  
Ralf Hausmann ◽  
Heike Franke ◽  
Günther Schmalzing
1998 ◽  
pp. 427-428
Author(s):  
Jeffrey S. Fedan ◽  
Gary A. Weisman ◽  
John T. Turner

10.2741/s214 ◽  
2011 ◽  
Vol S3 (3) ◽  
pp. 1101-1118
Author(s):  
S. Jeffrey Dixon

2018 ◽  
Vol 43 (3) ◽  
pp. 312-315
Author(s):  
Naoto Fujii ◽  
Robert D. Meade ◽  
Jeffrey C. Louie ◽  
Pegah Akbari ◽  
Pierre Boulay ◽  
...  

We assessed the role of purinergic P2 receptors in the regulation of cutaneous vasodilation in young adults at rest and during intermittent moderate-intensity exercise in the heat (35 °C). P2 receptor blockade augmented resting cutaneous vasodilation but had no influence during and following exercise. This increase was partly diminished by nitric oxide synthase inhibition. These results suggest a functional role of P2 receptors in the regulation of cutaneous vascular tone during ambient heat exposure at rest.


2005 ◽  
Vol 26 (11) ◽  
pp. 1281-1287 ◽  
Author(s):  
Zhong-jian CHEN ◽  
Kenneth P MINNEMAN

2003 ◽  
Vol 59 (1) ◽  
pp. 175-189 ◽  
Author(s):  
Heike Franke ◽  
Ute Krügel ◽  
Jens Grosche ◽  
Peter Illes

1997 ◽  
Vol 272 (33) ◽  
pp. 20402-20407 ◽  
Author(s):  
Eduardo R. Lazarowski ◽  
László Homolya ◽  
Richard C. Boucher ◽  
T. Kendall Harden

2010 ◽  
Vol 299 (6) ◽  
pp. H1762-H1771 ◽  
Author(s):  
Liang-Wu Fu ◽  
John C. Longhurst

Myocardial ischemia activates cardiac sympathetic afferents leading to chest pain and reflex cardiovascular responses. Brief myocardial ischemia leads to ATP release in the interstitial space. Furthermore, exogenous ATP and α,β-methylene ATP (α,β-meATP), a P2X receptor agonist, stimulate cutaneous group III and IV sensory nerve fibers. The present study tested the hypothesis that endogenous ATP excites cardiac afferents during ischemia through activation of P2 receptors. Nerve activity of single unit cardiac sympathetic afferents was recorded from the left sympathetic chain or rami communicates (T2-T5) in anesthetized cats. Single fields of 45 afferents (conduction velocities = 0.25–4.92 m/s) were identified in the left ventricle with a stimulating electrode. Five minutes of myocardial ischemia stimulated 39 of 45 cardiac afferents (8 Aδ, 37 C fibers). Epicardial application of ATP (1–4 μmol) stimulated six ischemically sensitive cardiac afferents in a dose-dependent manner. Additionally, epicardial ATP (2 μmol), ADP (2 μmol), a P2Y agonist, and α,β-meATP (0.5 μmol) significantly activated eight other ischemically sensitive afferents. Third, pyridoxal phosphate-6-azophenyl-2′,4′-disulfonic acid, a P2 receptor antagonist, abolished the responses of six afferents to epicardial ATP (2 μmol) and attenuated the ischemia-related increase in activity of seven other afferents by 37%. In the absence of P2 receptor blockade, cardiac afferents responded consistently to repeated application of ATP ( n = 6) and to recurrent myocardial ischemia ( n = 6). Finally, six ischemia-insensitive cardiac spinal afferents did not respond to epicardial ATP (2–4 μmol), although these afferents did respond to epicardial bradykinin. Taken together, these data indicate that, during ischemia, endogenously released ATP activates ischemia-sensitive, but not ischemia-insensitive, cardiac spinal afferents through stimulation of P2 receptors likely located on the cardiac sensory neurites.


2014 ◽  
Vol 114 (10) ◽  
pp. 2147-2155 ◽  
Author(s):  
S. P. Mortensen ◽  
R. M. McAllister ◽  
H. T. Yang ◽  
Y. Hellsten ◽  
M. H. Laughlin

2000 ◽  
Vol 129 (2) ◽  
pp. 291-298 ◽  
Author(s):  
Satoko Ohkubo ◽  
Junko Kimura ◽  
Hironori Nakanishi ◽  
Isao Matsuoka

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