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[DOC File]iums.ac.ir
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Dynamic 10-minute PET measurements were started with an administration of 13N-NH3 over 20 seconds (approximately 20 and 80 MBq for the rest and stress study, respectively).5 The stress study was performed 5 minutes after bolus injection of CGS-21680 (5 µg/kg), a selective adenosine A2A agonist that induced coronary vasodilatation and increases ...

[DOC File]PREVALENCE AND SIGNIFICANCE OF …
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In 1991 and 1992 we proposed the introduction of A2A antagonists in the treatment of Parkinson’s disease and in 1994 the use of A2A agonists in the treatment of schizophrenia. We believe that we will develop many new drugs for neuropsychopharmacology based on the receptor-receptor interactions taking place via the interface of receptor ...

[DOC File]Curriculum Vitae
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, which shows how the G protein-coupling affects inverse agonist binding, is described in the main text. Section. S3. The ensemble of low-lying energy conformations of the seven-helix TM bundle. The predicted ensemble of low energy structures of WT CB1 and its two mutants, T3.46A and T3.46I, are shown in . Table SIIA

Adenosine A2A receptor antagonist - Wikipedia
Regadenoson is a coronary vasodilator that induces its effects through selective activation of the A2A adenosine receptor. Regadenoson is a low affinity but potent agonist of the A2A receptor, with at least a 10-fold reduced affinity for the A1 receptor, and weak if any affinity for the A2B and A3 receptors. Table 1.

[DOCX File]California Institute of Technology
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Haemodynamic effects of a selective adenosine A2A receptor agonist, CGS 21680, in chronic heart failure in anaesthetized rats. British Journal Pharmacology. 125(4): 651-658. Nekooeian A.A., Tabrizchi R. (1998) Effects of adenosine A(2A) receptor agonist, CGS 21680, on blood pressure, cardiac index and arterial conductance in anaesthetized rats.

[DOC File]Cell
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Background: Regadenoson is an adenosine A2a receptor selective agonist that has been rapidly adopted into clinical use. Prevalence and implication of electrocardiogram (ECG) changes associated with it are unknown.

[DOC File]National PBM Monograph Template
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. a2A- and a2C adrenergic receptors form homo- and heterodimers: the heterodimeric state impairs agonist-promoted GRK phosphorylation and b-arrestin recruitment. Biochemistry. 45:4760-4767, 2006. Small KM, Brown KM, Seman CA, Theiss CT, Liggett SB

[DOCX File]Research Explorer | The University of Manchester
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The results of these tests are presented in Table 1. TI-299423 is a partial agonist for α6β2*-nAChRs and is extremely potent, with an EC 50 in the low tens of nanomolar range. For α4β2*-nAChRs, TI-299423 is a full agonist of the high sensitivity and a partial agonist of the low sensitivity receptors.

[DOC File]Kjell Fuxe received his MD degree in 1965 from the ...
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In contrast, activation of adenosine receptor A2A by a selective agonist CGS21680 increased ILC3 production of IL-22 in a concentration-dependent manner (Fig. ure. s. 4. e,f). This is in agreement with our observation that ILC3s highly express the A2A gene (encoded by . Adora2a), rather than other adenosine receptors (Supplementary Fig. ure . 6

health.usf.edu
Journal of Gorgan University of Medical Sciences 15 (1), 12-18, 2013 2013 Effects of adenosine A2a receptor agonist and antagonist on hippocampal nuclear factor-kB expression preceded by MDMA toxicity. F Kermanian, M Soleimani, A Ebrahimzadeh, H Haghir, M …

A2a agonist