Influence of aspirin on platelet activation during vascular endothelial injury induced by high blood glucose fluctuations
10.3969/j.issn.1001-1978.2018.01.012
- VernacularTitle:阿司匹林对波动高糖诱导内皮损伤过程中血小板活化的影响
- Author:
shang Jing WANG
1
;
yue Ming SUN
;
jun Hui YIN
;
Ye HUANG
Author Information
1. 首都医科大学附属北京妇产医院中医科
- Keywords:
aspirin;
high blood glucose fluctuations;
endothelial injury;
platelet activation;
human umbilical vein endothelial cell;
type 2 diabetes mellitus rat
- From:
Chinese Pharmacological Bulletin
2018;34(1):50-54
- CountryChina
- Language:Chinese
-
Abstract:
Aim To investigate the influence of aspirin on platelet activation during vascular endothelial injury induced by high blood glucose fluctuations .Methods In this study , "fluctuant high blood glucose cultured human umbilical vein endothelial cell ( HUVEC ) mod-el" and "human platelet-HUVEC supernate experi-mental system" were established in vitro, as well as type 2 diabetes mellitus ( T2DM) rat model with high blood glucose fluctuation in vivo. There were four groups: normal glucose ( N ) , steady high glucose (W), fluctuant high glucose ( B), and aspirin group ( ASA) .At the end of the study , the peripheral blood platelet maximum aggregation rate , levels of sE-selec-tin, von Willebrand factor ( vWF ) and platelet mem-brane protein level of CD62p were determined.Results In comparison with N group, levels of sE-selectin,vWF, the platelet maximum aggregation rate and plate-let membrane protein level of CD 62 p in W group and B group all significantly increased ( P <0.01 ) , mean-while B group significantly increased further compared with W group ( P <0.05 or P <0.01 ) .Pretreatment with ASA significantly decreased the elevated levels of sE-selectin, vWF, the platelet maximum aggregation rate and CD62p induced by high glucose fluctuations (P<0.01).Conclusions High blood glucose fluctu-ations can not only aggravate endothelial injury , but al-so promote platelet aggregation obviously , while aspirin has obvious antagonistic effects on these effects .
