Biomedical subjects

Sally E Brett

Publications and source records attributed to Sally E Brett.

3 recordsLinked to original sources

PubMed2006

Elevation of plasma homocysteine by methionine loading increases the diastolic blood pressure response to exercise.

OBJECTIVE: Exercise blood pressure is elevated in conditions associated with endothelial dysfunction. To determine whether this is a causal association, we examined the effects of endothelial dysfunction induced by methionine loading, on exercise blood pressure. DESIGN: Healthy subjects (18-63 years) participated in randomized, double-blind, cross-over studies receiving methionine and placebo on separate occasions before exercise. METHODS: In study 1 (n = 32), subjects received placebo and methionine 100 mg/kg 4 h before exercise and, in study 2 (n = 11), placebo and methionine 200 mg/kg (given as 100 mg 20 and 12 h before exercise). A further study confirmed that methionine 100 mg/kg impaired brachial artery flow-mediated dilation. Blood pressure was measured by mercury sphygmomanometry at rest and during low workload bicycle ergometry. RESULTS: Plasma homocysteine increased after methionine compared to placebo (22.5 +/- 1.2 versus 7.7 +/- 0.7 mumol/l in study 1, and 50.2 +/- 7.6 versus 12.8 +/- 0.7 mumol/l in study 2, means +/- SE, each P < 0.0001). In both studies resting systolic and diastolic blood pressures and the increases in systolic blood pressure during exercise were similar after methionine and placebo. By contrast, exercise diastolic blood pressure responses (measured as the change from resting values) increased more after methionine than after placebo. In study 1, diastolic blood pressure responses increased relative to placebo by 3.5 +/- 1.0, 3.7 +/- 1.0 and 2.4 +/- 1.0 mmHg at 50, 75 and 100 W, respectively (P < 0.01). In study 2, diastolic blood pressure responses increased by 4.9 +/- 1.0, 5.4 +/- 2.1 and 6.1 +/- 1.1 mmHg at 50, 75 and 100 W, respectively (P < 0.001). CONCLUSION: Endothelial dysfunction produced by methionine loading is associated with an increased exercise diastolic blood pressure response.

Adolescent↗

PubMed2004

Cardiovascular risk factors and endothelial dysfunction.

Endothelial dysfunction is a feature of atherosclerosis and is associated with CHD (coronary heart disease) risk factors. This study aimed to determine the relationship between the degree of endothelial dysfunction and calculated cardiovascular risk. Endothelial function, as determined by the ACh/NP (acetycholine/sodium nitroprusside response) ratio on brachial plethysmography, was compared with cardiovascular risk as calculated from the Framingham, PROCAM (Prospective Cardiovascular Munster) and MRFIT (Multiple Risk Factor Intervention Trial) algorithms in 246 (187 male) patients, including 44 (22%) with established CHD. Endothelial dysfunction correlated with the total number of risk factors (r2=0.22; P=0.002) and was related to LDL (low-density lipoprotein)-cholesterol in men and triacylglycerols (triglycerides) in women. The ACh/NP ratio correlated with the occurrence of diabetes, CHD and the LDL-cholesterol concentration (r2=0.58; P<0.001). Endothelial dysfunction was associated with presence of CHD on receiver-operating characteristic plot analysis (area=0.706+/-0.04; P=0.001). There was no correlation between ACh/NP ratio and CHD risk calculated with the Framingham algorithm in men, although both ACh and NP response correlated separately with risk in women. The endothelial ACh/NP ratio correlated with absolute risk in the PROCAM algorithm (r2=0.41; P<0.005). Intermediate results were obtained with MRFIT. Individual risk factors make different contributions to endothelial dysfunction compared with their role in risk calculators. The stronger relationship of endothelial dysfunction with PROCAM risk reflects the contribution of male sex, LDL-cholesterol and triacylglycerols to risk calculated by this algorithm.

Adult↗

PubMed2002

Acute haemodynamic effects of lipolysis-induced increase of free fatty acids in healthy men.

Circulating free fatty acids (FFA) are elevated in subjects with insulin resistance and Type II diabetes, and increase during myocardial ischaemia, but their haemodynamic effects are incompletely understood. During an investigation of the effects of FFA on endothelial function, we administered lipid emulsion (150 mg x min(-1) of soybean oil) with heparin (0.2 unit x kg(-1) x min(-1)) intravenously to eight healthy men for 2 h. This increased circulating FFA to 3.1+/-0.5 mmol/l. Forearm blood flow was measured by venous occlusion plethysmography during brachial artery infusions of saline, acetylcholine and nitroprusside before, and at 1 and 2 h. Lipid/heparin infusion had no significant effect on vasodilation to nitroprusside but progressively increased responses to acetylcholine (from 6.3+/-2.0 during 30 microg x min(-1) before-lipid infusion to 7.9+/-1.3 at 1 h and 12.2+/-1.1 ml x min(-1) x 100 ml(-1) at 2 h, P<0.001). Basal flow increased from 2.7+/-0.7 to 4.7+/-0.8 ml x min(-1) x 100 ml(-1) from 0 to 2 h. We performed a second study to clarify this effect on basal blood flow. Healthy men (n=8) received, on separate occasions, 4 h intravenous infusions of lipid emulsion with heparin and, as a control, saline with heparin. Lipid with heparin increased mean arterial blood pressure (maximum increment 8.2+/-2.7 mm Hg, P<0.01 compared with saline/heparin control) and forearm blood flow (from 1.7+/-0.2 to 2.9+/-0.3 ml x min(-1) x 100 ml(-1), P<0.01) without a significant effect on heart rate, and reduced calculated forearm vascular resistance (from 49.1+/-5.4 to 31.3+/-3.9 arbitrary units, P<0.01). In conclusion, acute elevation of FFA in healthy men increases arterial blood pressure and reduces vascular resistance. These haemodynamic changes could be clinically relevant.

Adult↗