Abstract
There are insufficient data about the effects of melatonin on hemostasis. The purpose of the study is to investigate the effect of melatonin and of luzindole, an inhibitor of melatonin receptors MT 1 and MT 2, on the count and functional activity of thrombocytes, as estimated according to the changes in the plasma levels of beta-thromboglobulin (β-TG) and platelet factor 4 (PF 4).
The study included 52 white male Wistar rats weighing 200-220 g on a 12/12 h light/dark regimen. Daily doses of melatonin of 0.2 mg/kg b.m. and luzindole of 0.4 mg/kg b.m. were applied. Melatonin was administered s.c. twice daily at intervals of 12 h, for three consecutive days.
The animals were divided into 4 equal groups (n = 13) and injected as follows: group one-with saline, group two-with melatonin, group three -with luzindole, and group four-with luzindole and 1 h later-with melatonin.
The results demonstrated that melatonin significantly increased the thrombocyte count (p < 0.001) and plasma levels of β-TG (p < 0.001) and PF 4 (p < 0.001) known as markers of platelet functional activity. When applied independently, luzindole significantly reduced (p < 0.001) thrombocyte count, β-TG and PF 4, which allowed for the assumption that it probably inhibited the effect of endogenous melatonin to a significant extent. Luzindole pretreatment suppressed the effects of both endogenous and exogenous melatonin.
Melatonin represents an important non-specific regulator of platelet homeostasis. It significantly increases the count and functional activity of thrombocytes, as estimated by means of the plasma concentrations of β-TG and PF 4.
NOTE: This publication mentions (Ref. N.13): Di Bella L, Gualano L (2006). Key aspects of melatonin physiology: thirty years of research. Neuro Endocrinol Lett. 27(4): 425–32.
See also:
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