Selective attenuation of norepinephrine release and stress-induced heart rate increase by partial adenosine A1 agonism.
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Selective attenuation of norepinephrine release and stress-induced heart rate increase by partial adenosine A1 agonism. / Bott-Flügel, Lorenz; Bernshausen, Alexandra; Schneider, Heike; Luppa, Peter; Zimmermann, Katja; Albrecht-Küpper, Barbara; Kast, Raimund; Laugwitz, Karl-Ludwig; Ehmke, Heimo; Knorr, Andreas; Seyfarth, Melchior.
in: PLOS ONE, Jahrgang 6, Nr. 3, 3, 2011, S. 18048.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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TY - JOUR
T1 - Selective attenuation of norepinephrine release and stress-induced heart rate increase by partial adenosine A1 agonism.
AU - Bott-Flügel, Lorenz
AU - Bernshausen, Alexandra
AU - Schneider, Heike
AU - Luppa, Peter
AU - Zimmermann, Katja
AU - Albrecht-Küpper, Barbara
AU - Kast, Raimund
AU - Laugwitz, Karl-Ludwig
AU - Ehmke, Heimo
AU - Knorr, Andreas
AU - Seyfarth, Melchior
PY - 2011
Y1 - 2011
N2 - The release of the neurotransmitter norepinephrine (NE) is modulated by presynaptic adenosine receptors. In the present study we investigated the effect of a partial activation of this feedback mechanism. We hypothesized that partial agonism would have differential effects on NE release in isolated hearts as well as on heart rate in vivo depending on the genetic background and baseline sympathetic activity. In isolated perfused hearts of Wistar and Spontaneously Hypertensive Rats (SHR), NE release was induced by electrical stimulation under control conditions (S1), and with capadenoson 6 · 10(-8) M (30 µg/l), 6 · 10(-7) M (300 µg/l) or 2-chloro-N(6)-cyclopentyladenosine (CCPA) 10(-6) M (S2). Under control conditions (S1), NE release was significantly higher in SHR hearts compared to Wistar (766+/-87 pmol/g vs. 173+/-18 pmol/g, p
AB - The release of the neurotransmitter norepinephrine (NE) is modulated by presynaptic adenosine receptors. In the present study we investigated the effect of a partial activation of this feedback mechanism. We hypothesized that partial agonism would have differential effects on NE release in isolated hearts as well as on heart rate in vivo depending on the genetic background and baseline sympathetic activity. In isolated perfused hearts of Wistar and Spontaneously Hypertensive Rats (SHR), NE release was induced by electrical stimulation under control conditions (S1), and with capadenoson 6 · 10(-8) M (30 µg/l), 6 · 10(-7) M (300 µg/l) or 2-chloro-N(6)-cyclopentyladenosine (CCPA) 10(-6) M (S2). Under control conditions (S1), NE release was significantly higher in SHR hearts compared to Wistar (766+/-87 pmol/g vs. 173+/-18 pmol/g, p
KW - Animals
KW - Female
KW - Rats
KW - Rats, Wistar
KW - Stress, Physiological/drug effects
KW - Blood Pressure/drug effects
KW - Adenosine A1 Receptor Agonists/pharmacology
KW - Heart Rate/drug effects
KW - Norepinephrine/secretion
KW - Rats, Inbred SHR
KW - Receptor, Adenosine A1/metabolism
KW - Restraint, Physical
KW - Animals
KW - Female
KW - Rats
KW - Rats, Wistar
KW - Stress, Physiological/drug effects
KW - Blood Pressure/drug effects
KW - Adenosine A1 Receptor Agonists/pharmacology
KW - Heart Rate/drug effects
KW - Norepinephrine/secretion
KW - Rats, Inbred SHR
KW - Receptor, Adenosine A1/metabolism
KW - Restraint, Physical
U2 - 10.1371/journal.pone.0018048
DO - 10.1371/journal.pone.0018048
M3 - SCORING: Journal article
VL - 6
SP - 18048
JO - PLOS ONE
JF - PLOS ONE
SN - 1932-6203
IS - 3
M1 - 3
ER -