Dose and Time Effects of Caffeine Intake on Human Platelet Adenosine A2A Receptors
Functional and Biochemical Aspects
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Background—We determined whether repeated caffeine administration at different dosages and for different periods of time (400 or 600 mg/d for 1 week or 400 mg/d for 2 weeks) upregulates human platelet adenosine A2A receptors and is accompanied by increases in cAMP accumulation and decreases in aggregation and calcium levels after stimulation of A2A receptors by the selective agonist 2-hexynyl-5′-N-ethylcarboxamidoadenosine (HE-NECA).
Methods and Results—Platelets were obtained from peripheral venous blood of 45 healthy human volunteers at the end of 2 weeks of caffeine abstinence and at 12, 60, and 108 hours after the last dose of caffeine. The lowest dose of caffeine, when given for only 7 days, had no effect. Increasing the total dose, either by giving 400 mg/d for 14 days or giving 600 mg/d, resulted in binding assays performed with the adenosine A2A receptor radioligand [3H]SCH 58261 [5-amino-7(phenylethyl)-2-(2-furyl)-pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine], in the upregulation of A2A receptors. Moreover, the potency of HE-NECA to produce antiaggregatory effects, a rise in cAMP accumulation, and a decrease in calcium levels was significantly increased.
Conclusions—Chronic caffeine intake can lead to upregulation of adenosine A2A receptors, which is accompanied by sensitization, in a time- and dose-dependent manner, to the actions of the agonist HE-NECA.
- Received November 1, 1999.
- Revision received January 21, 2000.
- Accepted February 15, 2000.
- Copyright © 2000 by American Heart Association