Efficacy of dual antiplatelet therapy combined with Naoxintong capsules see text following coronary microembolization induced by homologous microthrombi in rats.
- Author:
Huan WANG
1
;
Wen-juan ZHONG
;
Ming-wei HUANG
;
Xiao-ying WU
;
Hui CHEN
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Apoptosis; drug effects; Blood Coagulation; drug effects; Blood Loss, Surgical; physiopathology; Capsules; Drug Therapy, Combination; Drugs, Chinese Herbal; pharmacology; therapeutic use; Embolism; complications; drug therapy; pathology; physiopathology; Male; Myocardium; pathology; Platelet Aggregation Inhibitors; pharmacology; therapeutic use; Rats; Rats, Sprague-Dawley; Survival Analysis; Thrombosis; complications; drug therapy; pathology; physiopathology
- From: Chinese journal of integrative medicine 2011;17(12):917-924
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo evaluate the effificacy of dual antiplatelet therapy combined with Naoxintong Capsule ([see text], NXTC) in a rat model of coronary microembolization (CME).
METHODSA total of 95 rats were randomly divided into 6 groups: control, sham-operation, CME model, NXTC, dual antiplatelet (clopidogrel and aspirin) intervention (DA), and NXTC combined with DA (NDA) groups. The complete data in 69 rats were obtained. The number of CME, myocardial apoptosis rate, bleeding time, clotting time, and adensosine diphosphate (ADP)-induced platelet aggregation were assessed.
RESULTSCompared with the CME group, the number of CME and myocardial apoptosis rates were signifificantly decreased in the NXTC, DA, and NDA groups (P <0.01). Compared with other intervention groups, the number of CME and myocardial apoptosis rates were the least in the NDA group (P <0.01), and the incidence of surgical bleeding was the highest in the DA group (P <0.01). Compared with the CME group, ADP-induced maximum platelet aggregation rate was significantly inhibited in the NXTC, DA, and NDA groups (P <0.01), both bleeding time and clotting time were signifificantly increased in the NXTC, DA, and NDA groups (P <0.01), while the above parameters were the highest in the DA group (P <0.05).
CONCLUSIONThe combination therapy of NXTC and DA enhanced the anti-CME effect of either therapy alone and reduced the risk of the DA therapy-associated bleeding, demonstrating an improved benefifit/ risk ratio in the rat model of CME.