Abstract
Responses to vasopressin were studied in human platelets loaded with the fluorescent Ca2+ indicator, quin2. In the presence of 1 mM external Ca2+, vasopressin caused a transient rise in [Ca2+]i from the basal level near 100nM to about 700 nM; peak [Ca2+]i was reached in a few seconds and the level then declined towards resting over several minutes. In the absence of external Ca2+ there was a much smaller rise of similar time-course, suggesting that vasopressin increases [Ca2+]i mainly by stimulated-influx across the plasma membrane but also by partly releasing internal Ca2+. Inhibition of thromboxane A2 formation somewhat reduced the peak [Ca2+]i in the presence of external Ca2+, but had no effect on the response attributed to release of internal Ca2+. With external Ca2+, vasopressin stimulated shape-change, secretion and aggregation. Secretion and aggregation were decreased by about half following blockage of thromboxane production. The ability of vasopressin to induce shape-change and secretion even at near basal [Ca2+]i suggests that activators other than Ca2+ are involved.
MeSH Terms
Aminoquinolines
Blood Platelets/drug effects,metabolism
Calcium/blood
Cyclooxygenase Inhibitors
Humans
Male
Platelet Aggregation/drug effects
Prostaglandin-Endoperoxide Synthases/blood
Vasopressins/pharmacology
Chemicals
Aminoquinolines
Cyclooxygenase Inhibitors
Vasopressins
Quin2-acetoxymethyl ester
Prostaglandin-Endoperoxide Synthases
Calcium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hallam T J
Thompson N T
Scrutton M C
Rink T J
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