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1.
BMC Cardiovasc Disord ; 17(1): 174, 2017 07 03.
Article in English | MEDLINE | ID: mdl-28673246

ABSTRACT

BACKGROUND: The meta-analysis was aimed to evaluate the effects of AMPD1 gene C34T polymorphism on cardiac function indexes, blood pressure and prognosis in patients with cardiovascular diseases (CVD). METHODS: Eligible studies were retrieved through a comprehensive search of electronic databases and manual search. Then the high-quality studies met the rigorous inclusion and exclusion criteria, as well as related to the subject was selected for the study. Comprehensive data analyses were conducted using STATA software 12.0. RESULTS: The study results revealed that CVD patients with CT + TT genotype of AMPD1 C34T polymorphism presented elevated left ventricular ejection fraction (LVEF) (%) and reduced left ventricular end diastolic dimension (LVEDD) (mm) as compared with CC genotype, moreover, the subgroup analysis found that the LVEF (%) was markedly higher in heart failure (HF) patients carrying CT + TT genotype than CC genotype. Besides, the systolic blood pressure (SBP) (mmHg) in CVD patients with CT + TT genotype was obviously decreased in contrast with the CC genotype. Patients suffered from HF with different genotypes (CT + TT and CC) of AMPD1 C34T polymorphism exhibited no significant differences in total survival rate and cardiac survival rate. CONCLUSIONS: Our current meta-analysis indicated that the T allele of AMPD1 gene C34T polymorphism may be correlated with LVEF, LVEDD and SBP, which plays a protective role in the cardiac functions and blood pressure in CVD patients, but had no effects on total survival rate and cardiac survival rate for HF.


Subject(s)
AMP Deaminase/genetics , Blood Pressure/genetics , Cardiovascular Diseases/genetics , Polymorphism, Genetic , Ventricular Function, Left/genetics , Cardiovascular Diseases/diagnosis , Cardiovascular Diseases/enzymology , Cardiovascular Diseases/physiopathology , Gene Frequency , Genetic Predisposition to Disease , Heterozygote , Homozygote , Humans , Kaplan-Meier Estimate , Linear Models , Phenotype , Prognosis , Protective Factors , Risk Assessment , Risk Factors , Stroke Volume/genetics
2.
Zhongguo Ying Yong Sheng Li Xue Za Zhi ; 29(2): 139-41, 146, 2013 Mar.
Article in Chinese | MEDLINE | ID: mdl-23833968

ABSTRACT

OBJECTIVE: To investigate the protective effects of Shengui tablet (Chinese Traditional Medicine) on experimental cerebral ischemia by acute cerebral ischemia hypoxia in mice and bilateral ligation of the carotid artery in rats. METHODS: In the acute cerebral ischemia hypoxia model, the mice were randomly divided into control group, low-, middle- and high-dose (0.16, 0.33 and 1.00 g/kg) groups of Shengui tablet, after oral treatment for 30 d, gasping time of isolated heads of mice were observed. In bilateral ligation of the carotid artery cerebral ischemia model, the rats were randomly divided into control group, model group and low-, middle-, high-dose (0.072, 0.149 and 0.450 g/kg) groups of Shengui tablet. After oral treatment for 7 d, the cerebral index, superoxide dismutase (SOD) activity and the content of malondialdehyde (MDA) were measured. RESULTS: Compared with the control model, Shengui tablet middle- and high-dose could significantly prolong gasping time of isolate heads of mice. Compared with model group, Shengui tablet low-, middle- and high-dose could significantly decrease the cerebral index and enhance SOD activity in brain tissue; only high-dose could reduce the content of MDA. CONCLUSION: Shengui tablet has significant protective effect on the cerebral ischemia.


Subject(s)
Brain Ischemia/metabolism , Drugs, Chinese Herbal/pharmacology , Animals , Brain/metabolism , Brain Ischemia/prevention & control , Female , Male , Malondialdehyde/metabolism , Mice , Mice, Inbred Strains , Neuroprotective Agents/pharmacology , Rats , Rats, Sprague-Dawley , Superoxide Dismutase/metabolism
3.
Article in Chinese | MEDLINE | ID: mdl-22295539

ABSTRACT

OBJECTIVE: To construct an apparatus for the oxygen uptake measurement of rats exposed to hypobaric hypoxia at different simulated altitude. METHODS: The capacity of this apparatus was about 0.01 m3. It included animal experimental cabin, reference cabin, altimeter, altitude vertical velocity indicator, pressure difference inductor and oxygen compensator, low scale manometer, soda lime and calcium chloride, small fan, thermometer, circulating water system and vacuum pump. The oxygen uptake of the rats at 6 000 m, 4 000 m and 1 000 m simulated altitude was measured using this apparatus. RESULTS: The oxygen uptake of the rats at 50 m, 4 000 m and 6 000 m simulated altitude was (24.4 +/- 2.1), (10.8 +/- 2.0) and (8.8 +/- 1.6) ml O2/(kg x min) respectively (average +/- s, n = 10). The oxygen uptake decreased as altitude increased. CONCLUSION: This apparatus can be used to measure the oxygen uptake of the rats at different simulated altitude.


Subject(s)
Altitude , Hypoxia/physiopathology , Oxygen Consumption/physiology , Oxygen/metabolism , Altitude Sickness/physiopathology , Animals , Computer Simulation , Equipment and Supplies , Male , Rats , Rats, Sprague-Dawley
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