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Am J Physiol Heart Circ Physiol 290: H1271-H1277, 2006. First published November 4, 2005; doi:10.1152/ajpheart.00883.2005
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Evidence of preserved endothelial function and vascular plasticity with age

D. Walter Wray, Abhimanyu Uberoi, Lesley Lawrenson, and Russell S. Richardson

Physiology Division, Department of Medicine, University of California, San Diego, La Jolla, California

Submitted 18 August 2005 ; accepted in final form 26 October 2005


    ABSTRACT
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
We sought to identify the relationship between shear stimuli and flow-mediated vasodilation and to determine whether small muscle mass exercise training could provoke limb-specific improvements in endothelial function in older subjects. In five young (22 ± 1 yr old) and six old (71 ± 2 yr old) subjects, ultrasound Doppler measurements were taken in the arm (brachial artery) and leg (deep and superficial femoral arteries) after suprasystolic cuff occlusion with and without ischemic exercise to evaluate flow-mediated dilation (FMD) in both limbs. Older subjects were reevaluated after 6 wk of single-leg knee extensor exercise training. Before the training, a significant FMD was observed in the arm of young (3 ± 1%) but not old (1 ± 1%) subjects, whereas a significant leg FMD was observed in both groups (5 ± 1% old vs. 3 ± 1% young). However, arm vasodilation was similar between young and old when normalized for shear rate, and cuff occlusion with superimposed handgrip exercise provoked additional shear, which proportionately improved the FMD response in both groups. Exercise training significantly improved arm FMD (5 ± 1%), whereas leg FMD was unchanged. However, ischemic handgrip exercise did not provoke additional arm vasodilation after training, which may indicate an age-related limit to shear-induced vasodilation. Together, these data demonstrate that vascular reactivity is dependent on limb and degree of shear stimuli, challenging the convention of diminished endothelial function typically associated with age. Likewise, exercise training improved arm vasodilation, indicating some preservation of vascular plasticity with age.

exercise; shear rate; vasodilation; flow-mediated dilation


ENDOTHELIUM-DEPENDENT VASODILATION has been reported to decline with age (6, 21, 46), and there is mounting evidence implicating endothelial dysfunction in the pathogenesis of cardiovascular disease (6, 8, 25, 37). Despite this evidence for endothelial dysfunction as a significant cardiovascular risk factor, few nonpharmacological therapeutic interventions have been identified. Aerobic exercise represents one such approach, because regular intervals of increased blood flow and accompanying shear stimuli have been shown to evoke positive changes in vascular health (11, 19, 28). Furthermore, regular exercise has been shown to increase endothelial nitric oxide (NO) synthase protein (43) and NO synthesis (41, 44) in animals and to upregulate endothelial NO synthase protein expression in humans (20). Thus, through enhanced bioavailability of NO, exercise training represents a noninvasive means of addressing the apparent age-related decline in endothelium-dependent vasodilation. Others (11) have demonstrated the efficacy of this intervention, showing that whole body exercise training significantly improved blood flow in response to acetylcholine administration in the arm of old subjects. Cross-sectional studies have also identified a greater vasodilation in response to forearm ischemia (39) and acetylcholine infusion (11, 45) in old athletes compared with sedentary, age-matched controls. However, no longitudinal studies have evaluated the capacity of isolated limb exercise training to affect limb-specific vascular reactivity in the aged.

The postischemia flow-mediated dilation (FMD) technique has become a common clinical research tool for noninvasive assessment of endothelial function, and several clinical studies (15, 31, 47) have reported that a diminished FMD in the brachial artery (BA) correlates with coronary artery endothelial dysfunction. However, previous findings utilizing the FMD technique may require some afterthought, considering the increasingly recognized variability in vascular responsiveness according to shear stimuli and site of measurement (24, 3335, 49). Others (3, 4) have shown that reactive hyperemia after cuff occlusion varies according to the duration of ischemia and amount of tissue that becomes ischemic. Therefore, we propose that a more comprehensive interpretation of endothelial function in older individuals may be achieved by including noninvasive interventions that selectively vary shear stimuli, such as FMD with and without superimposed ischemic exercise (4), and through assessment of conduit vessel vasodilation relative to the degree of shear stimuli (9).

To our knowledge, the effect of wide-ranging shear stimuli on the FMD response in older subjects has not been documented. Furthermore, the capacity of small muscle mass exercise training to improve the age-related decline in systemic vascular function has not been examined. Accordingly, we sought to determine whether varied levels of shear stimuli could further characterize age-related changes in vascular plasticity and whether 6 wk of small muscle mass knee extensor exercise training could alter this relationship and improve FMD in the arms and legs of older subjects. We hypothesized that 1) ischemic exercise during cuff occlusion would elevate shear rate and thus enhance FMD in both young and old; 2) normalization of vasodilation for the degree of hyperemia after cuff occlusion would minimize age-related differences in FMD; and 3) isolated limb exercise training would improve vascular responsiveness (FMD) in both trained and untrained limbs of older subjects.


    METHODS
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
Subjects and General Procedures

A total of 11 [5 young (22 ± 1 yr old) and 6 old (71 ± 2 yr old)] healthy men participated in the current study. All subjects were nonsmokers, normotensive (140/90 mmHg), and free of overt cardiovascular disease. The current study was reviewed and approved by the Institutional Review Board committee of the University of California, San Diego, and informed consent was obtained according to the University of California, San Diego, Human Subjects Protection Program requirements. Subjects reported to the laboratory on a preliminary day to complete health histories and physical examinations and to perform a graded single-leg knee extensor test to determine maximal work rate (WRmax) and a single maximal voluntary contraction by using a hydraulic handgrip dynamometer (Rolyan Ability One, Germantown, WI). Subjects always reported to the laboratory in the fasted state, and during data collection, they were in a semirecumbent position (~60° reclined, with both legs extended) during leg measurements or supine during arm measurements, with the arm at heart level. All studies were performed in a thermoneutral environment.

Arm FMD protocol. Subjects were positioned supine, and a pneumatic cuff was positioned on the upper arm near the elbow, distal to the site of the ultrasound Doppler probe (36). After a 20-min rest period, baseline measurements were made, and the arm cuff was then inflated to suprasystolic pressure (>250 mmHg) for 5 min. Full occlusion of the BA was verified by continuous ultrasound Doppler scanning during occlusion. After a 20-min recovery from the cuff ischemia, this procedure was repeated with light-intensity, intermittent handgrip exercise (20% of maximal voluntary contraction, 0.5 Hz) performed during the last 2 min of the cuff occlusion period.

Leg FMD protocol. Subjects were seated in a semirecumbent position with both legs extended, and a pneumatic cuff was placed on the upper left leg, distal to the site of the ultrasound Doppler probe. As with the arm, after a 20-min rest period and baseline measurements, the leg cuff was inflated to suprasystolic pressure (>250 mmHg) for 5 min. Full occlusion of both the deep femoral artery (DFA) and superficial femoral artery (SFA) was verified by continuous ultrasound Doppler scanning during occlusion. After a 20-min recovery from the cuff ischemia, this procedure was repeated with light-intensity plantar flexion exercise (3 kg, 20-cm excursion, 1 Hz) superimposed during the last 2 min of the cuff occlusion period. To avoid ordering effects, the sequence of arm and leg FMD was randomized, but resting FMD was always performed before the exercising FMD due to the prolonged hyperemia after ischemic exercise.

Training regimen. After the initial test day, the older group reported to the laboratory three times each week for 6 wk to complete single-leg knee extensor exercise training (left leg) of varied 1-h protocols (ranging from 30% to 90% of WRmax), a protocol which has previously resulted in a significant improvement in maximum oxygen consumption in young and old healthy subjects (23). The exercise regimen combined short, high-intensity (5–10 min at 70–95% of WRmax) intervals with longer, low-intensity (15–45 min at 40–65% of WRmax) work bouts. Graded WRmax tests were performed to reevaluate WRmax after weeks 2, 4, and 6 of the 6-wk training protocol, with relative work rates adjusted as improvements in WRmax were achieved.

Measurements

Ultrasound Doppler. The ultrasound system (Logiq 7, GE Medical Systems, Milwaukee, WI) was equipped with two linear array transducers operating at an imaging frequency of 7–8 MHz and 10 MHz. Vessel diameter was determined at a perpendicular angle along the central axis of the scanned area, where the best spatial resolution was achieved. Landmarks and printed ultrasound images were utilized to ensure a similar site of measurement between scans and across experimental days. The DFA and SFA were insonated 4–5 cm distal to the bifurcation of the common femoral artery of the left leg. The BA of the right arm was insonated approximately midway between the antecubital and axillary regions, medial to the biceps brachii muscle (Fig. 1).


Figure 1
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Fig. 1. Illustration of ultrasound images and Doppler velocity spectra in the arm [brachial artery (BA)] and leg [deep and superficial femoral arteries (DFA and SFA)] at rest (A and C) and after cuff release (B and D). FMD, flow-mediated dilation.

 
The blood velocity profile was obtained by using the same transducers with a Doppler frequency of 4.0–5.0 MHz, operated in the high-pulsed repetition frequency mode (2–25 kHz) with a sample volume of 1.5–3.5 cm in depth. Care was taken to avoid aliasing by using scale adjustments, especially after cuff release. In duplex mode, real-time ultrasound imaging and pulse-wave velocity profile were viewed simultaneously (Fig. 1). All blood velocity measurements were obtained with the probe appropriately positioned to maintain an insonation angle of 60° or less. The sample volume was maximized according to vessel size and centered, verified by real-time ultrasound visualization of the vessel. With the use of artery diameter and mean blood velocity (Vmean), blood flow was calculated as

Formula
Ultrasound images and Doppler velocity waveforms were measured continuously, with serial 20-s segments recorded before, during, and after (0–20, 40–60, and 70–90 s postcuff release) release of suprasystolic cuff inflation. For the leg FMD trial, after cuff release, velocity spectra were first obtained in the DFA (0- to 20-s and 40- to 60-s segments) and then in the SFA (70- to 90-s segment). This switch from the DFA to the SFA required only a change in the sample volume velocity gate, with no change in probe position. At all sample points, arterial diameter and angle-corrected, time- and space-averaged, and intensity-weighted Vmean values were calculated by using commercially available software (Logiq 7).

Shear stress has been identified as a mechanism that stimulates the vascular endothelium and results in subsequent vasodilation (32). Blood viscosity was not measured, so shear rate was calculated by using the equation (4, 9, 49)

Formula
Shear rate values are reported as the change ({Delta}) from baseline averaged over the multiple segments of Doppler blood velocity data acquired during the 90 s after cuff release by using the maximal change in vessel diameter. To most effectively evaluate the stimulus-response relationship between shear rate and vasodilation, FMD was normalized for shear rate (%{Delta}diameter/mean {Delta}shear rate) (34).

Arterial blood pressure was measured by using automated radial tonometry (Medwave Vasotrac APM205A; BioPac Systems, Goleta, CA), with one measurement every 8–10 s. Heart rate was recorded from a standard three-lead ECG as an integral part of the Doppler system (Logiq 7).

Data analysis and statistics. For each 20-s ultrasound Doppler segment, Vmean was averaged across the first and last 10 s of the recorded clip, with diameter measurements evaluated during diastole, as described previously (49). For the arm FMD trials, BA diameters during the 70- to 90-s postocclusion interval are reported, because this was the time period during which maximal vasodilation was observed. BA velocity was averaged across the three recorded segments (0–20, 40–60, and 70–90 s postcuff release). For leg FMD trials, DFA diameters during the 40- to 60-s segment are reported, and DFA velocity was averaged across the two recorded segments (0–20 and 40–60 s postcuff release), whereas SFA diameter and velocity from the 70- to 90-s segment are reported. To verify the reproducibility of ultrasound measurements within subjects and across study days, a coefficient of variation [(standard deviation/mean) x 100] was calculated for postocclusion diameters in each vessel at weeks 0, 3, and 6.

Statistics were performed with the use of commercially available software (SigmaStat 3.10, Systat Software, Point Richmond, CA). Repeated-measure ANOVA, ANOVA, and Student's t-tests were used to identify significant changes in measured variables within and between groups, with the Bonferroni test used for post hoc analysis when a significant main effect was found. All group data are expressed as means ± SE. Significance was established at P < 0.05.


    RESULTS
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
Pretraining measurements (week 0). Subject characteristics for both young and old groups are listed in Table 1, and the individual time course for the vascular response to cuff release in the arm is provided in Table 2. In the young subjects, BA diameter increased significantly after cuff occlusion ({approx}3%, from 0.52 ± 0.02 to 0.54 ± 0.02 cm), but BA vasodilation in the old group was not significant ({approx}1%, from 0.54 ± 0.02 to 0.55 ± 0.02 cm). Postocclusion BA peak hyperemia and mean {Delta}shear rate were greater in the young (995 ± 101 ml/min and 249 ± 29 s–1) than the old (608 ± 76 ml/min and 40 ± 12 s–1; Fig. 2). Postocclusion hyperemia was significantly correlated with age (r2 = 0.66), with lower postocclusion shear rates in the older subjects. When BA vasodilation was normalized for mean {Delta}shear rate, responses were similar between young and old during both resting FMD (0.01 ± 0.004% x s–1, young; 0.01 ± 0.007% x s–1, old) and ischemic handgrip exercise FMD (0.02 ± 0.005% x s–1, young; 0.02 ± 0.008% x s–1, old) trials (Fig. 2).


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Table 1. Subject characteristics

 

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Table 2. Temporal response in all subjects (untrained) after ischemic cuff release in the arm (brachial artery)

 

Figure 2
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Fig. 2. Relationship between shear rate and vasodilation in brachial arteries of young (shaded symbols) and older (open symbols) subjects after cuff occlusion at rest (squares) and cuff occlusion with concomitant handgrip exercise (triangles). Note the linear relationship between young and old with varied shear rate (r2 = 0.96). EX, exercise; {Delta}, change.

 
In the leg, cuff release raised blood flow and average {Delta}shear rate in both groups (390 ± 81 ml/min and 69 ± 20 s–1, young; 269 ± 86 ml/min and 73 ± 27 s–1, old) and resulted in significant DFA dilation in the old group ({approx}5%, from 0.54 ± 0.04 to 0.57 ± 0.04 cm), but the DFA vasodilation was not significant in the young group ({approx}3%, from 0.61 ± 0.03 to 0.63 ± 0.03 cm). SFA diameter was not altered by cuff release hyperemia in either group. Ischemic handgrip exercise superimposed on cuff occlusion resulted in a small and statistically insignificant increase in heart rate (from 61 ± 3 to 63 ± 2 beats/min, young; from 60 ± 2 to 65 ± 2 beats/min, old) and mean arterial blood pressure (from 94 ± 5 to 99 ± 6 mmHg, young; from 110 ± 8 to 117 ± 7 mmHg, old). BA peak blood flow and average {Delta}shear rate also increased in both young (1,001 ± 91 ml/min and 396 ± 67 s–1) and old (878 ± 176 ml/min and 255 ± 37 s–1) and subsequently resulted in a significant BA vasodilation in both groups (8.5 ± 2%, young; 4.7 ± 2%, old; Figs. 2 and 4). Ischemic plantar flexion did not significantly increase shear rate or vasodilation in the DFA or SFA in either group.


Figure 4
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Fig. 4. Decay in hyperemic shear stimuli after cuff ischemia (cuff only) and cuff ischemia with superimposed exercise (cuff + EX). Note that shear stimuli were similar before and after training for both conditions.

 
Midtraining measurements (week 3). The older group underwent 6 wk of dynamic knee extensor exercise training, and subjects were reevaluated at both weeks 3 and 6 to characterize temporal aspects of the training on vascular responsiveness. At week 3, a small but statistically insignificant improvement in BA vasodilation could be seen with average {Delta}shear rates that were similar to week 0 (Fig. 3A). Ischemic exercise evoked similar increases in peak hyperemia and average {Delta}shear rate and vasodilation as that seen during week 0. Likewise, in the leg, DFA and SFA shear rate and vasodilation were also similar to the response seen at week 0 (Fig. 3B).


Figure 3
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Fig. 3. Impact of knee extensor exercise training on vasodilation after ischemic cuff (A) and ischemic cuff with superimposed exercise (B) in arm (BA) and leg (DFA and SFA). *Significantly different from pretraining (week 0).

 
Posttraining measurements (week 6). After 6 wk of knee extensor exercise training, significant adaptations in BA vascular reactivity were recorded. When compared with pretraining, BA vasodilation after cuff release was improved, with a statistically significant vasodilation ({approx}5%, from 0.54 ± 0.02 to 0.57 ± 0.02 cm) and a peak hyperemia and average {Delta}shear rate that were similar to week 0 (Fig. 4). After the training, ischemic arm exercise during cuff occlusion resulted in peak hyperemia (616 ± 67 ml/min) and average {Delta}shear rate (228 ± 24 s–1) levels that were similar to week 0 but, unlike week 0, did not further augment the FMD response (Figs. 3B and 4). Despite these improvements in vasodilatory capacity in the arm, training did not improve the shear response or vasodilatory capacity in the trained leg (DFA and SFA; Fig. 3, A and B). However, a {approx}40% improvement in maximal knee extensor exercise capacity was noted after training (from 29 ± 7 to 40 ± 8 W, pre- vs. posttraining). Knee extensor exercise training did not significantly lower resting heart rate but did reduce systolic (–12 ± 8 mmHg) and diastolic (–12 ± 4 mmHg) arterial blood pressure.

Measurement reproducibility. The low variability in ultrasound measurements between experimental days (weeks 0, 3, and 6) was documented by a <5% coefficient of variation for vessel diameter (BA, DFA, and SFA) after cuff release in the older group.


    DISCUSSION
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
The current study utilized small muscle mass exercise training and the application of wide-ranging shear stimuli in both the arm and leg to further characterize the uniformity and plasticity of endothelial function with age. Before the training, an age-related decline in FMD after cuff occlusion was observed in the arm (BA) but not in the leg (DFA) of older subjects. However, a significant correlation between age and postcuff occlusion hyperemia was also observed, so that BA FMD was similar between young and old when normalized to the change in shear rate. In the arm of both young and old, ischemic handgrip exercise during cuff occlusion provoked greater hyperemia and additional shear that proportionally improved the FMD response, further demonstrating a range of vascular reactivity dependent on the shear stimulus. The old group completed 6 wk of moderate intensity single-leg knee extensor exercise training, which resulted in a significant improvement in arm FMD, whereas leg FMD was unchanged. After the training, ischemic handgrip exercise raised shear rate but did not provoke additional vasodilation, which may indicate an age-related limit to shear-induced vasodilation. Together, these data demonstrate that the vascular dysfunction typically associated with age is largely dependent on limb and degree of shear stimuli and also reveal that small muscle mass exercise training can improve vascular function in a distal limb, emphasizing the preservation of vascular plasticity with age.

Limb-specific decline in vascular function. FMD tests are traditionally evaluated in the arm, and this responsiveness is thought to provide an indication of coronary vascular health (47). However, there is increasing evidence supporting the nonuniform nature of the vasculature, with recent reports of heterogeneity between limbs in response to acute exercise (49), endothelium-dependent and -independent vasodilation (26), and sympathomimetics (29). In one of the few studies evaluating leg FMD after cuff release, Black et al. (5) identified significant vasodilation in the lower leg (posterior tibial artery) and concluded that comparison of FMD between the arm and leg could provide a better indication of global vascular health. Others (2, 9) have compared superficial and tibial artery with BA vasodilation in clinical populations. However, to our knowledge, this is the first study to evaluate both arm (BA) and leg (DFA and SFA) FMD in both young and old subjects and to identify a heterogeneous FMD response between limbs (Fig. 3).

An age-related and limb-specific decline in endothelial function has previously been established on the basis of attenuated responses to administration of vasodilatory substances (10, 45). Newcomer et al. (27) recently reported limb differences in aged individuals, showing an attenuation of endothelium-dependent and -independent vasodilation in the arm but not the leg in older sedentary subjects, and the FMD data from the current study support these findings. No aging studies have attempted measurements in the DFA, and, as such, little is currently known about the mechanisms that could be responsible for the observed greater vasodilatory capacity of the DFA in the old than in the young. However, we speculate that the difference could be related to hydrostatic forces and locomotion in the leg vasculature that are not present in the arm (26, 29) or to age-related changes in vascular structure, such as the expansive remodeling, reported by others in the common femoral artery (12).

It is noteworthy that in the present study, postocclusion hyperemia was approximately threefold greater in the arm than the leg due to the bifurcation of the common femoral artery (Fig. 1), and thus the BA was exposed to a greater shear stimulus than the DFA after cuff release. When vasodilation is assessed in proportion to shear rate, the DFA seems quite reactive to shear after cuff occlusion, which contrasts to the modest dilation of this vessel compared with the arm that we (49) recently reported during knee extensor exercise. This apparent dichotomy in leg vascular reactivity seems to exemplify the dissimilarity of hyperemia elicited by steady-state, dynamic exercise versus the "bolus" and subsequent decay of the shear stimulus that follow ischemic cuff release (Table 2 and Fig. 4).

Impact of varied shear rate on vasodilation in young and old. Whereas the ischemic cuff occlusion technique provides a noninvasive, physiological approach for evoking FMD, the stimulus does not allow titration of the vascular response. Therefore, we superimposed exercise during the last 2 min of ischemia, further increasing metabolism in the ischemic tissue and thus fostering a greater hyperemia (and shear stimulus in the BA) on cuff release (4, 48). Indeed, ischemic arm exercise significantly increased BA shear rate and subsequent vasodilation proportionally in both the young and old groups. It is interesting to note the linear relationship between shear and vasodilation for both groups across two different levels of shear (Fig. 2) and the correlation between age and cuff-induced hyperemia, which together suggest that the apparent age-related diminution in FMD could be at least partially attributed to decreased postocclusion hyperemia rather than simply a decline in vascular responsiveness. Together, these findings emphasize the importance of considering the degree of shear stimulus when interpreting FMD results, as noted by others (33, 34), which may serve to better define the conventional view of an age-related decline in vasodilatory capacity.

Exercise training improves vascular function. The impact of activity level on endothelial function has been well described, with evidence for enhanced arm vasodilation in response to cuff occlusion hyperemia (39) and endothelium-dependent drug infusion (11, 27) in older endurance-trained subjects compared with age-matched sedentary controls. However, few investigations have utilized a longitudinal experimental design to demonstrate the restorative capacity of exercise training with age. DeSouza et al. (11) reported a significant improvement in endothelium-dependent vasodilation to acetylcholine in the arm after 3 mo of aerobic exercise training. Data from the current study extend these findings, demonstrating a significant, limb-specific improvement in BA FMD after only 6 wk of isolated quadriceps muscle training, which may be advantageous for pathologies and general training compliance, considering that this exercise is minimally taxing on the cardiovascular system (40). This improved vasodilation is especially significant, considering that the shear stimulus was similar between pre- and posttraining FMD tests (Fig. 4). It is also interesting to note that BA vasodilation was not significant after 3 wk of exercise training, providing insight into the temporal nature of this vascular adaptation (Fig. 3). Thus this improvement in vasodilatory capacity with exercise training appears to support some preservation of vascular plasticity with age, presenting physical activity as an effective, noninvasive means of addressing the age-related decline in vascular health.

The improvement of BA vasodilation after single-leg knee extensor exercise training raises the question of how isolated limb training may produce improvements in vascular beds that do not experience direct, exercise-induced hyperemia. Others (11, 17, 22) have explored this topic, noting improved vasodilatory capacity in untrained limbs after whole body exercise training, which has been attributed to improved NO bioactivity. Particularly germane to the present study is a recent report by Green et al. (18), who contrasted changes in the anterograde and retrograde portions of the Doppler blood velocity waveform in the BA during handgrip and cycling exercise. The authors suggest that the substantial anterograde and retrograde oscillations in the arm during leg exercise may serve as a potent shear stimulus to the endothelium of the resting limb during exercise. On the basis of these findings, it is conceivable that in the present study, anterograde/retrograde oscillations in the resting arm BA, coupled with the largely anterograde flow in the exercising leg DFA, may explain why knee extensor training improved arm, but not leg, vasodilation.

Clinical implications. To our knowledge, this is the first study to report an improvement in vascular reactivity with such a modest and localized exercise training regimen. This may represent a more manageable therapeutic approach for older individuals unable to perform rigorous whole body aerobic exercise, which may be especially pertinent for patient compliance and safety when exercise is prescribed as treatment for cardiopulmonary disease (30, 38, 42). In addition, the finding of differential responses to shear stimuli between limbs with the use of a clinical test of endothelial function may denote a need for caution when relating regional peripheral limb vascular function to whole body cardiovascular health.

Experimental considerations. Any longitudinal exercise training study with multiple experimental days inherently limits sample size, but in return it allows the advantage of multiple measurements on the same individual and effectively allows the subject to serve as his or her own control. In the present study, a sufficient number of subjects were enrolled to achieve adequate statistical power (beta ≥ 0.8) in the major variables while ensuring compliance of all subjects for the duration of the training regimen. In addition, we recognize that ischemic exercise during cuff occlusion is complicated by the fact that it may activate the metaboreflex, provoke turbulent flow during cuff release, and evoke non-NO-dependent mechanisms that further increase shear rate (1, 34), but this approach nonetheless effectively increased BA shear rate and allowed further evaluation of shear stimulus-response. Others (10, 13, 16) have failed to identify an age-related decline in endothelium-independent vasodilation, and thus this parameter was not evaluated in the present study. Whereas the values are aligned with the current literature demonstrating an age-related decline in FMD, it is noteworthy that the range of values for peak change in BA diameter in the present study is somewhat modest (1–5%) but with a small coefficient of variation for diameter measurements. The peak percent change in BA diameters reported elsewhere varies widely, from as little as 2% (7) to as great as 19% (14), a variability that may be related to differences in cuff placement, ultrasound Doppler probe position, and duration of ischemia, as noted in a recent and timely review (34). Young subjects of a somewhat sedentary nature were recruited to provide an appropriate pretraining control group for the older subjects, and this fitness component may have contributed to the modest FMD response (11).

In conclusion, we have shown that FMD differs according to limb, age, and the degree of shear stimuli, and that the FMD response may be improved by small muscle mass exercise training. Application of wide-ranging shear stimuli (cuff occlusion with and without concomitant ischemic exercise) characterized the BA FMD response in both young and old subjects, demonstrating a range of vascular reactivity that was dependent on age and shear stimuli, with no apparent age-related decline in BA FMD when vasodilation was normalized for shear rate. Training of the older group did not change leg vascular reactivity but improved BA FMD. However, after training, BA vasodilation was not further increased with additional shear stimuli, suggestive of a possible ceiling effect in the older subjects.


    GRANTS
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
This study was funded in part by National Heart, Lung, and Blood Institute Grant HL-17731 and the Sam and Rose Stein Institute for Research on Aging.


    ACKNOWLEDGMENTS
 
We express our sincere thanks to the subjects who participated in the study.


    FOOTNOTES
 

Address for reprint requests and other correspondence: D. Walter Wray, Physiology Division, Dept. of Medicine, Univ. of California San Diego, 9500 Gilman Dr., La Jolla, CA 92093-0623 (e-mail: dwray{at}ucsd.edu)

The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.


    REFERENCES
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 

  1. Agewall S, Hulthe J, Fagerberg B, Gottfridsson B, and Wikstrand J. Post-occlusion brachial artery vasodilatation after ischaemic handgrip exercise is nitric oxide mediated. Clin Physiol Funct Imaging 22: 18–23, 2002.[CrossRef][Web of Science][Medline]
  2. Angerer P, Negut C, Stork S, and von Schacky C. Endothelial function of the popliteal artery in patients with coronary artery disease. Atherosclerosis 155: 187–193, 2001.[CrossRef][Web of Science][Medline]
  3. Berry KL, Skyrme-Jones RA, and Meredith IT. Occlusion cuff position is an important determinant of the time course and magnitude of human brachial artery flow-mediated dilation. Clin Sci (Lond) 99: 261–267, 2000.[Medline]
  4. Betik AC, Luckham VB, and Hughson RL. Flow-mediated dilation in human brachial artery after different circulatory occlusion conditions. Am J Physiol Heart Circ Physiol 286: H442–H448, 2004.[Abstract/Free Full Text]
  5. Black CD, Vickerson B, and McCully KK. Noninvasive assessment of vascular function in the posterior tibial artery of healthy humans. Dyn Med 2: 1–7, 2003.[Medline]
  6. Celermajer DS, Sorensen KE, Spiegelhalter DJ, Georgakopoulos D, Robinson J, and Deanfield JE. Aging is associated with endothelial dysfunction in healthy men years before the age-related decline in women. J Am Coll Cardiol 24: 471–476, 1994.[Abstract]
  7. Clarkson P, Montgomery HE, Mullen MJ, Donald AE, Powe AJ, Bull T, Jubb M, World M, and Deanfield JE. Exercise training enhances endothelial function in young men. J Am Coll Cardiol 33: 1379–1385, 1999.[Abstract/Free Full Text]
  8. Cosentino F and Volpe M. Hypertension, stroke, and endothelium. Curr Hypertens Rep 7: 68–71, 2005.[CrossRef][Web of Science][Medline]
  9. De Groot PC, Poelkens F, Kooijman M, and Hopman MT. Preserved flow-mediated dilation in the inactive legs of spinal cord-injured individuals. Am J Physiol Heart Circ Physiol 287: H374–H380, 2004.[Abstract/Free Full Text]
  10. DeSouza CA, Clevenger CM, Greiner JJ, Smith DT, Hoetzer GL, Shapiro LF, and Stauffer BL. Evidence for agonist-specific endothelial vasodilator dysfunction with aging in healthy humans. J Physiol 542: 255–262, 2002.[Abstract/Free Full Text]
  11. DeSouza CA, Shapiro LF, Clevenger CM, Dinenno FA, Monahan KD, Tanaka H, and Seals DR. Regular aerobic exercise prevents and restores age-related declines in endothelium-dependent vasodilation in healthy men. Circulation 102: 1351–1357, 2000.[Abstract/Free Full Text]
  12. Dinenno FA, Jones PP, Seals DR, and Tanaka H. Age-associated arterial wall thickening is related to elevations in sympathetic activity in healthy humans. Am J Physiol Heart Circ Physiol 278: H1205–H1210, 2000.[Abstract/Free Full Text]
  13. Eskurza I, Monahan KD, Robinson JA, and Seals DR. Effect of acute and chronic ascorbic acid on flow-mediated dilatation with sedentary and physically active human ageing. J Physiol 556: 315–324, 2004.[Abstract/Free Full Text]
  14. Esper RJ, Vilarino J, Cacharron JL, Machado R, Ingino CA, Garcia Guinazu CA, Bereziuk E, Bolano AL, Suarez DH, and Kura M. Impaired endothelial function in patients with rapidly stabilized unstable angina: assessment by noninvasive brachial artery ultrasonography. Clin Cardiol 22: 699–703, 1999.[Web of Science][Medline]
  15. Faulx MD, Wright AT, and Hoit BD. Detection of endothelial dysfunction with brachial artery ultrasound scanning. Am Heart J 145: 943–951, 2003.[CrossRef][Web of Science][Medline]
  16. Franzoni F, Ghiadoni L, Galetta F, Plantinga Y, Lubrano V, Huang Y, Salvetti G, Regoli F, Taddei S, Santoro G, and Salvetti A. Physical activity, plasma antioxidant capacity, and endothelium-dependent vasodilation in young and older men. Am J Hypertens 18: 510–516, 2005.[CrossRef][Web of Science][Medline]
  17. Goto C, Higashi Y, Kimura M, Noma K, Hara K, Nakagawa K, Kawamura M, Chayama K, Yoshizumi M, and Nara I. Effect of different intensities of exercise on endothelium-dependent vasodilation in humans: role of endothelium-dependent nitric oxide and oxidative stress. Circulation 108: 530–535, 2003.[Abstract/Free Full Text]
  18. Green DJ, Bilsborough W, Naylor LH, Reed C, Wright J, O'Driscoll G, and Walsh JH. Comparison of forearm blood flow responses to incremental handgrip and cycle ergometer exercise: relative contribution of nitric oxide. J Physiol 562: 617–628, 2005.[Abstract/Free Full Text]
  19. Green DJ, Maiorana A, O'Driscoll G, and Taylor R. Effect of exercise training on endothelium-derived nitric oxide function in humans. J Physiol 561: 1–25, 2004.[Abstract/Free Full Text]
  20. Hambrecht R, Adams V, Erbs S, Linke A, Krankel N, Shu Y, Baither Y, Gielen S, Thiele H, Gummert JF, Mohr FW, and Schuler G. Regular physical activity improves endothelial function in patients with coronary artery disease by increasing phosphorylation of endothelial nitric oxide synthase. Circulation 107: 3152–3158, 2003.[Abstract/Free Full Text]
  21. Kimura Y, Matsumoto M, Den YB, Iwai K, Munehira J, Hattori H, Hoshino T, Yamada K, Kawanishi K, and Tsuchiya H. Impaired endothelial function in hypertensive elderly patients evaluated by high resolution ultrasonography. Can J Cardiol 15: 563–568, 1999.[Web of Science][Medline]
  22. Kingwell BA, Sherrard B, Jennings GL, and Dart AM. Four weeks of cycle training increases basal production of nitric oxide from the forearm. Am J Physiol Heart Circ Physiol 272: H1070–H1077, 1997.[Abstract/Free Full Text]
  23. Lawrenson L, Hoff J, and Richardson RS. Aging attenuates vascular and metabolic plasticity but does not limit improvement in muscle VO2max. Am J Physiol Heart Circ Physiol 286: H1565–H1572, 2004.[Abstract/Free Full Text]
  24. Levenson J, Pessana F, Gariepy J, Armentano R, and Simon A. Gender differences in wall shear-mediated brachial artery vasoconstriction and vasodilation. J Am Coll Cardiol 38: 1668–1674, 2001.[Abstract/Free Full Text]
  25. Luscher TF and Noll G. Endothelial function as an end-point in interventional trials: concepts, methods and current data. J Hypertens Suppl 14: S111–S119, 1996.[CrossRef][Medline]
  26. Newcomer SC, Leuenberger UA, Hogeman CS, Handly BD, and Proctor DN. Different vasodilator responses of human arms and legs. J Physiol 556: 1001–1011, 2004.[Abstract/Free Full Text]
  27. Newcomer SC, Leuenberger UA, Hogeman CS, and Proctor DN. Heterogeneous vasodilator responses of human limbs: influence of age and habitual endurance training. Am J Physiol Heart Circ Physiol 289: H308–H315, 2005.[Abstract/Free Full Text]
  28. Niebauer J and Cooke JP. Cardiovascular effects of exercise: role of endothelial shear stress. J Am Coll Cardiol 28: 1652–1660, 1996.[Abstract]
  29. Pawelczyk JA and Levine BD. Heterogeneous responses of human limbs to infused adrenergic agonists: a gravitational effect? J Appl Physiol 92: 2105–2113, 2002.[Abstract/Free Full Text]
  30. Perri MG, Anton SD, Durning PE, Ketterson TU, Sydeman SJ, Berlant NE, Kanasky WF Jr, Newton RL Jr, Limacher MC, and Martin AD. Adherence to exercise prescriptions: effects of prescribing moderate versus higher levels of intensity and frequency. Health Psychol 21: 452–458, 2002.[CrossRef][Web of Science][Medline]
  31. Playford DA and Watts GF. Special article: non-invasive measurement of endothelial function. Clin Exp Pharmacol Physiol 25: 640–643, 1998.[Web of Science][Medline]
  32. Pohl U, Holtz J, Busse R, and Bassenge E. Crucial role of endothelium in the vasodilator response to increased flow in vivo. Hypertension 8: 37–44, 1986.[Abstract/Free Full Text]
  33. Pyke KE, Dwyer EM, and Tschakovsky ME. Impact of controlling shear rate on flow-mediated dilation responses in the brachial artery of humans. J Appl Physiol 97: 499–508, 2004.[Abstract/Free Full Text]
  34. Pyke KE and Tschakovsky ME. The relationship between shear stress and flow-mediated dilation: implications for the assessment of endothelial function. J Physiol 568: 357–369, 2005.[Abstract/Free Full Text]
  35. Rakobowchuk M, McGowan CL, de Groot PC, Hartman JW, Phillips SM, and Macdonald MJ. Endothelial function of young healthy males following whole body resistance training. J Appl Physiol 98: 2185–2190, 2005.[Abstract/Free Full Text]
  36. Ramsey M, Goodfellow J, Bellamy M, Lewis M, and Henderson A. Non-invasive detection of endothelial dysfunction. Lancet 348: 128–129, 1996.[Web of Science][Medline]
  37. Reddy KG, Nair RN, Sheehan HM, and Hodgson JM. Evidence that selective endothelial dysfunction may occur in the absence of angiographic or ultrasound atherosclerosis in patients with risk factors for atherosclerosis. J Am Coll Cardiol 23: 833–843, 1994.[Abstract]
  38. Richardson RS, Leek BT, Gavin TP, Haseler LJ, Mudaliar SR, Henry R, Mathieu-Costello O, and Wagner PD. Reduced mechanical efficiency in chronic obstructive pulmonary disease but normal peak VO2 with small muscle mass exercise. Am J Respir Crit Care Med 169: 89–96, 2004.[Abstract/Free Full Text]
  39. Rinder MR, Spina RJ, and Ehsani AA. Enhanced endothelium-dependent vasodilation in older endurance-trained men. J Appl Physiol 88: 761–766, 2000.[Abstract/Free Full Text]
  40. Saltin B, Radegran G, Koskolou MD, and Roach RC. Skeletal muscle blood flow in humans and its regulation during exercise. Acta Physiol Scand 162: 421–436, 1998.[CrossRef][Web of Science][Medline]
  41. Sessa WC, Pritchard K, Seyedi N, Wang J, and Hintze TH. Chronic exercise in dogs increases coronary vascular nitric oxide production and endothelial cell nitric oxide synthase gene expression. Circ Res 74: 349–353, 1994.[Abstract/Free Full Text]
  42. Shephard RJ. Exercise for patients with congestive heart failure. Sports Med 23: 75–92, 1997.[Web of Science][Medline]
  43. Spier SA, Delp MD, Meininger CJ, Donato AJ, Ramsey MW, and Muller-Delp JM. Effects of ageing and exercise training on endothelium-dependent vasodilatation and structure of rat skeletal muscle arterioles. J Physiol 556: 947–958, 2004.[Abstract/Free Full Text]
  44. Sun D, Huang A, Koller A, and Kaley G. Short-term daily exercise activity enhances endothelial NO synthesis in skeletal muscle arterioles of rats. J Appl Physiol 76: 2241–2247, 1994.[Abstract/Free Full Text]
  45. Taddei S, Galetta F, Virdis A, Ghiadoni L, Salvetti G, Franzoni F, Giusti C, and Salvetti A. Physical activity prevents age-related impairment in nitric oxide availability in elderly athletes. Circulation 101: 2896–2901, 2000.[Abstract/Free Full Text]
  46. Taddei S, Virdis A, Mattei P, Ghiadoni L, Gennari A, Fasolo CB, Sudano I, and Salvetti A. Aging and endothelial function in normotensive subjects and patients with essential hypertension. Circulation 91: 1981–1987, 1995.[Abstract/Free Full Text]
  47. Takase B, Uehata A, Akima T, Nagai T, Nishioka T, Hamabe A, Satomura K, Ohsuzu F, and Kurita A. Endothelium-dependent flow-mediated vasodilation in coronary and brachial arteries in suspected coronary artery disease. Am J Cardiol 82: 1535–1539, 1998.[CrossRef][Web of Science][Medline]
  48. Wendelhag I, Fagerberg B, and Wikstrand J. Adding ischaemic hand exercise during occlusion of the brachial artery increases the flow-mediated vasodilation in ultrasound studies of endothelial function. Clin Physiol 19: 279–283, 1999.[CrossRef][Web of Science][Medline]
  49. Wray DW, Uberoi A, Lawrenson L, and Richardson RS. Heterogeneous limb vascular responsiveness to shear stimuli during dynamic exercise in humans. J Appl Physiol 99: 81–86, 2005.[Abstract/Free Full Text]



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