EFFECTS OF VINCRISTINE AND PREDNISONE ON PLATELET NUMBERS AND FUNCTION IN CLINICALLY NORMAL DOGS

Citation
Aj. Mackin et al., EFFECTS OF VINCRISTINE AND PREDNISONE ON PLATELET NUMBERS AND FUNCTION IN CLINICALLY NORMAL DOGS, American journal of veterinary research, 56(1), 1995, pp. 100-108
Citations number
76
Categorie Soggetti
Veterinary Sciences
ISSN journal
00029645
Volume
56
Issue
1
Year of publication
1995
Pages
100 - 108
Database
ISI
SICI code
0002-9645(1995)56:1<100:EOVAPO>2.0.ZU;2-N
Abstract
Effects of a single Iv administered therapeutic dose of vincristine su lfate on platelet numbers and function were evaluated in 16 clinically normal dog; over the 2 weeks after drug administration. Results were statistically compared with those of a previous control study in which the same 16 dogs were administered saline solution (IV), instead of v incristine. Of the 16 dogs, 8 were orally administered daily immunosup pressive doses of prednisone concurrently throughout the saline-contro l and vincristine study periods. Platelet numbers and mean platelet vo lume were measured, using an automated hematology analyzer. Platelet f unction was evaluated by turbidimetric measurement of platelet aggrega tion in response to collagen, platelet-activating factor, and adenosin e diphosphate (ADP), and by dot retraction (diluted whole-blood method ) and buccal mucosa bleeding time. Vincristine had a significant (P < 0.05) effect on circulating platelet numbers. Vincristine induced a tr ansient mild decrease in platelet numbers, followed by a moderate incr ease in numbers, with peak platelet count observed 8 days after drug a dministration. Mean platelet volume was not significantly affected by administration of vincristine. Vincristine had no significant effects on platelet aggregation in response to collagen, low or high doses of platelet-activating factor, and a high dose of ADP. The maximal degree of platelet aggregation attained in response to a low dose of ADP was not significantly affected by prior administration of vincristine. Th e maximal rate of platelet aggregation induced by a low dose of ADP af ter vincristine administration, however, was significantly (P < 0.05) lower than the rate of aggregation induced by a similar dose of ADP in the previous control study. Vincristine had no significant effects on clot retraction and bleeding time. Prednisone did not significantly a ffect platelet numbers and function, and did not modify vincristine's effects on the same variables.