1.Effect of Tongxinluo on endothelial function and hypersensitive C-reactive protein in acute coronary syndrome patients undergoing percutaneous coronary intervention.
Qilin MA ; Saidan ZHANG ; Yanggen NING ; Xiaoqun PU ; Guolong YU ; Zhaofen ZHENG ; Xiaobin CHEN ; Ke HU ; Tianlun YANG
Journal of Central South University(Medical Sciences) 2009;34(6):550-554
OBJECTIVE:
To determine the effect of Tongxinluo on the endothelial function and hypersensitive C-reactive protein (hs-CRP) in acute coronary syndrome patients undergoing percutaneous coronary intervention(PCI).
METHODS:
Thirty-three patients with unstable angina pectoris and 6 patients with acute myocardial infarction who underwent PCI for stenotic lesions of the coronary artery were enrolled. The patients were randomly assigned to a conventional group (n = 19) which took routine treatment or a tongxinluo group (n = 20) which took Tongxinluo(4 capsules once, 3 times per day) at the base of routine treatment after PCI. Nitric oxide synthase (NOS), nitric oxide (NO), endothelium-dependent vasodilation which was evaluated in the brachial artery flow mediated diameter(FMD) and hs-CRP were measured before the PCI and 24 hours and 3 months after the PCI. The correlation between NO and hs-CRP was analyzed.
RESULTS:
NOS, NO, and FMD in the 2 groups 24 hours after the PCI were significantly lower than those before the PCI(P < 0.05), but hs- CRP obviously increased (P < 0.05). NOS, NO, and FMD 3 months after the PCI in the 2 groups were significantly higher than those before the PCI (P < 0.05 or P < 0.01), but hs-CRP obviously decreased (P < 0.01).All indexes mentioned above in the Tongxinluo group showed greater changes than those of the conventional group(P < 0.05). NO was negatively correlated with hs-CRP (r = -0.3219, P<0.01).
CONCLUSION
Tongxinluo capsules have obvious beneficial effect on endothelial function and anti-inflammation in acute coronary syndrome patients undergoing PCI, by directly acting on the endothelium and indirectly inhibiting inflammation.
Acute Coronary Syndrome
;
blood
;
physiopathology
;
therapy
;
Aged
;
Angioplasty, Balloon, Coronary
;
methods
;
C-Reactive Protein
;
metabolism
;
Drugs, Chinese Herbal
;
therapeutic use
;
Endothelium, Vascular
;
drug effects
;
physiopathology
;
Female
;
Humans
;
Male
;
Middle Aged
;
Phytotherapy
2.Plasma tissue factor and serum angiotensin II and the therapeutic effect of different dosages of fosinopril on chronic heart failure.
Qilin MA ; Lijie YANG ; Tianlun YANG ; Ming SUN ; Shenbin WU ; Yanggen NING
Journal of Central South University(Medical Sciences) 2009;34(5):448-452
OBJECTIVE:
To determine the relation between plasma tissue factor (TF) and serum angiotensin II(AngII) and the effect of different dosages of fosinopril on chronic heart failure(CHF).
METHODS:
Thirty healthy controls and 35 CHF patients were recruited to observe AngII,TF, left ventricular ejection fractions(LVEF) and left ventricular end-systolic volume index (LVESVI) at baseline and 10 weeks after the treatment. The 35 patients were randomly assigned into 2 groups: A routine dosage fosinopril group received 10 mg once daily and a middle dosage group received 10 mg twice a day for 10 weeks.
RESULTS:
Compared with the healthy controls, AngII,TF,and LVESVI significantly increased (P<0.01) and LVEF significantly decreased (P<0.01) in CHF patients. The TF was positively correlated with AngII(r=0.2491, P<0.01) in the patients. After the 10-week treatment with different dosages of fosinopril, AngII,TF,and LVESVI obviously decreased(P<0.05 or P<0.01) and LVEF significantly increased in the 2 groups (P<0.05 or P<0.01). The middle dosage group changed more than the routine dosage group (P<0.01).
CONCLUSION
TF is positively correlated with AngII in CHF patients. Fosinopril can greatly improve cardiac function and antagonize prethrobotic state,and the therapeutic effect improves with the dosage increase.
Aged
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Angiotensin II
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blood
;
Angiotensin-Converting Enzyme Inhibitors
;
administration & dosage
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Chronic Disease
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Female
;
Fosinopril
;
administration & dosage
;
Heart Failure
;
blood
;
drug therapy
;
Humans
;
Male
;
Middle Aged
;
Thromboplastin
;
metabolism