Lack of evidence for voltage dependent calcium channels on platelets

Biochem Biophys Res Commun. 1985 Feb 28;127(1):161-7. doi: 10.1016/s0006-291x(85)80139-x.

Abstract

Intracellular calcium was measured in human platelets using the fluorescent calcium indicator Quin 2. A concentration dependent increase was observed with thrombin. Depolarisation induced by high KCl concentrations did not alter [Ca++]i. The calcium agonist Bay K 8644 did not affect resting levels or thrombin stimulated elevation of intracellular calcium. The calcium antagonists diltiazem, verapamil and PN 200-110 did not inhibit the thrombin stimulated elevation in [Ca++]i. Pretreatment of platelets with adenylate cyclase stimulants reduced the rate and magnitude of the maximal [Ca++]i elevation due to thrombin. In addition, thrombin stimulation of 45Ca++ influx was insensitive to Bay K 8644, verapamil, diltiazem and Pn 200-110. We conclude that functional voltage sensitive calcium channels are not present on human platelets.

MeSH terms

  • 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester
  • Aminoquinolines
  • Blood Platelets / analysis*
  • Blood Platelets / drug effects
  • Calcium / blood*
  • Diltiazem / pharmacology
  • Humans
  • Ion Channels / analysis*
  • Nifedipine / analogs & derivatives
  • Nifedipine / pharmacology
  • Sodium / metabolism
  • Thrombin / pharmacology
  • Time Factors

Substances

  • Aminoquinolines
  • Ion Channels
  • 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester
  • Sodium
  • Thrombin
  • Diltiazem
  • Nifedipine
  • Quin2
  • Calcium