Impact of acute dynamic exercise and arterial shear rate modification on radial artery low-flow mediated constriction in young men

Purpose Leg cycling exercise acutely augments radial artery low-flow mediated constriction (L-FMC). Herein, we sought to determine whether this is associated with exercise-induced changes in arterial shear rate (SR). Methods Ten healthy and recreationally active young men (23 ± 2 years) participated in 30 min of incremental leg cycling exercise (50, 100, 150 Watts). Trials were repeated with (Exercise + WC) and without (Exercise) the use of a wrist cuff (75 mmHg) placed distal to the radial artery to increase local retrograde SR while reducing mean and anterograde SR. Radial artery characteristics were measured throughout the trial, and L-FMC and flow mediated dilatation (FMD) were assessed before and acutely (~ 10 min) after leg cycling. Results Exercise increased radial artery mean and anterograde SR, along with radial artery diameter, velocity, blood flow and conductance (P  0.05) but also increased retrograde SR (P  0.05). In contrast, no change in FMD was observed in either Exercise or Exercise + WC trials (P > 0.05). Conclusions These findings indicate that increases in L-FMC following exercise are abolished by the prevention of increases radial artery diameter, mean and anterograde SR, and by elevation of retrograde SR, during exercise in young men

Impact of whole-body passive heat stress and arterial shear rate modification on radial artery function in young men

We sought to determine how whole-body heating acutely influences radial artery function, characterized using flow mediated dilation (FMD) and low-flow mediated constriction (L-FMC), and the mechanistic role of shear rate modification on radial artery functional characteristics during heating. Eleven young healthy men underwent whole-body heating (water-perfused suit) sufficient to raise core temperature +1°C. Trials were repeated with (Heat+WC) and without (Heat) the application of a wrist cuff located distal to the radial artery examined, known to prevent increases in mean and anterograde shear rate but increase retrograde shear. Radial artery characteristics were assessed throughout each trial, with FMD and L-FMC assessed prior to and upon reaching the target core temperature. Heat markedly increased radial artery mean and anterograde shear rate, along with radial artery diameter and blood flow (P<0.05). Heat+WC abolished the heat-induced increase mean and anterograde shear rate (P>0.05), but markedly increased retrograde shear (P<0.05). Concomitantly, increases in radial artery diameter and blood flow were decreased (Heat+WC vs Heat,P<0.05). Heat attenuated FMD (8.6±1.2 vs. 2.2±1.4%, P<0.05), whereas no change in FMD was observed in Heat+WC (7.8±1.2 vs. 10.8±1.2%,P>0.05). In contrast, L-FMC was not different in either trial (P>0.05). In summary, acute whole-body heating markedly elevates radial artery shear rate, diameter and blood flow, and diminishes FMD. However, marked radial artery vasodilation and diminished FMD are absent when these shear rate changes are prevented. Shear rate modifications underpinthe radial artery response to acute whole-body heat-stress, but further endothelial-dependent vasodilation (FMD) is attenuated likely as the vasodilatory range limit is approached

Finishing the euchromatic sequence of the human genome

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead