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“The organic calcium antagonist, nitrendipine, and the inorganic calcium channel blockers (Co2+, Mn2+, Cd2+, La3+) drastically inhibited rat and human platelet aggregation induced by thrombin, ADP or adrenaline in the presence of 0.32 mM Ca2+.”
“The synergistic interaction of …-5 microM) and epinephrine (0.5-2 microM) was inhibited by … blocker (yohimbine; IC50= 0.4 microM), calcium channel blockers (verapamil and diltiazem with IC50 of 10 and 48 mM, respectively), PLC inhibitor (…=6 microM) and nitric oxide (NO) donor, SNAP (IC50=1.6 microM)).”
Experimental & Molecular Medicine • 2009 | View Paper
“Conclusion: A hypertensive response, following systemically absorbed topical vasoconstrictors, including both phenylephrine and epinephrine , can be associated with dire consequences when treated with a beta-adrenergic blocking drug and, possibly, calcium channel blockers.”
“ Calcium channel blockers and dibutyryl cAMP enhanced the activity of the pump, and exerted respectively overlapping and additive effects with epinephrine , when added simultaneously.”
“Studies on the possible involvement of secondary messengers in cell expansion indicated that (i) both 8‐bromo‐CAMP and forskolin caused cell shrinking (…, such as 1,2‐dioctanoyl‐sn‐glycerol, lysophosphatidic acid, and arachidonic acid caused cell expansion; and (iv) EGTA (calcium chelator) and nifedipine calcium channel blocker) … epinephrine.”
The Japanese journal of physiology • 1991 | View Paper
“In preparations with prominent … plateaus, addition of epinephrine resulted in triggered activity; similarly, epinephrine caused automaticity from a depolarized … 8/9 fibers quiescent at ‐50 to ‐60 mV. Thus, the calcium channel blocking drugs bepridil and lidoflazine produced striking repolarization changes at …, but unlike quinidine, triggered activity was rare.”
Pacing and clinical electrophysiology : PACE • 1990 | View Paper
“Interventions to counter the deleterious effects of adrenaline were: calcium antagonism , β-blockade, an antilipolytic agent, and a combination of calcium antagonism and an antilipolytic agent.”