La. Lyapina et al., The effect of prolil-glycil-proline (PGP) peptide and PGP-rich substances on haemostatic parameters of rat blood, BL COAG FIB, 11(5), 2000, pp. 409-414
The effect of intravenous and intranasal administration of proline-containi
ng peptide, especially prolil-glycil-proline (PGP), on the haemostatic syst
em of rats was investigated. Tripeptide PGP after single intravenous (0.2,
1.0 and 1.5 mg/kg) or intranasal (0.5 mg/kg) administration increased (P <
0.05) total fibrinolytic and fibrin depolymerizating (FDA) activities, and
tissue plasminogen activator levels (t-PA), and decreased the plasmin inhib
itors (PI) and activated factor XIII (factor XIIIa) levels in blood plasma.
Repeated daily intranasal administration (5 days) of PGP produced a signif
icant increase of anticoagulant and fibrinolytic activities (P < 0.05), and
a decrease of platelet aggregation, PI and factor XIIIa levels in blood pl
asma. Fibrinogen concentrations remained practically unchanged. Chronic per
oral administration of gelatin (protein particularly rich of PGP, prolil-gl
ycil, glycil-proline) as a food supplement significantly increased t-PA lev
el (by 120%) at day 10 and FDA (by 290%) at day 14 in blood plasma. We also
observed potent suppression of thrombus formation (venous thrombosis model
) by intranasal PGP administration. Therefore, PGP and some PGP-rich substa
nces can be qualified as potent anticoagulant and antithrombotic agents. (C
) 2000 Lippincott Williams & Wilkins.