Disclaimer: The information contained herein should NOT be used as a substitute for the advice of an appropriately qualified and licensed physician or other health care provider. The tool is not a substitute for the care provided… (more)
“An essentially different interpretation after beta blocker discontinuation was found in two cases (10%).ConclusionA beta blocker withdrawal induces an increase in adenosine MBF.”
Naunyn-Schmiedeberg's Archives of Pharmacology • 2000 | View Paper
“Besides the established use of beta-blockers there are some beneficial perspectives for myocardial protection by blockade of the Na(+)-H(+)-exchange or by adenosine.”
The American journal of cardiology • 1997 | View Paper
“The purinoceptor P2 blockers , suramin and pyridoxal-phosphate-6-azophenyl-2',4'-disulphonic acid (PPADS), inhibited the diadenosine polyphophate-induced [Ca2+]i increase, whereas the P2y purinoceptor blocker, reactive blue, had no effect.”
“Segments … on beta-blockers that contracted normally at … increased blood flow with adenosine (0.78 +/- 0.31 to 1.10 +/- 0.70 mL.g-1.min-1; P < .05), as did … became abnormal (0.74 +/- 0.34 to 1.06 +/- 0.82 mL.g-1.min-1; P = NS).”
“By competitive inhibition of the enzyme phosphodiesterase, they prevent the breakdown of cyclic 39,59—AMP adenosine monophosphate ) to 59—AMP and act synergistically with beta-adrenergic agents to increase the intracellular concentration of 39 5 cyclic AMP.”
Polish journal of pharmacology • 2001 | View Paper
“Glibenclamide-sensitive currents induced by adenosine and CGS-21680 were largely reduced by blockers of the cAMP-dependent protein kinase (Rp-cAMP[S], H-89, protein kinase A inhibitor peptide).”
Proceedings of the National Academy of Sciences of the United States of America • 1995 | View Paper
“It is, therefore, likely that adenosine (and its analogs) and Ca2+ entry blockers have different mechanisms for the relaxation of coronary smooth muscle and that adenosine probably relaxes the vessels through A2 receptor.”