AJP - Heart Watch the video to learn how APS reaches out to developing nations.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Heart Circ Physiol 290: H1596-H1600, 2006. First published November 11, 2005; doi:10.1152/ajpheart.01054.2005
0363-6135/06 $8.00
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
290/4/H1596    most recent
01054.2005v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (9)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cook, J. N.
Right arrow Articles by Tanaka, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cook, J. N.
Right arrow Articles by Tanaka, H.

Arterial compliance of rowers: implications for combined aerobic and strength training on arterial elasticity

Jill N. Cook, Allison E. DeVan, Jessica L. Schleifer, Maria M. Anton, Miriam Y. Cortez-Cooper, and Hirofumi Tanaka

Department of Kinesiology and Health Education, University of Texas at Austin, Austin, Texas; and Department of Kinesiology, University of Wisconsin-Madison, Madison, Wisconsin

Submitted 5 October 2005 ; accepted in final form 8 November 2005


    ABSTRACT
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
Regular endurance exercise increases central arterial compliance, whereas resistance training decreases it. It is not known how the vasculature adapts to a combination of endurance and resistance training. Rowing is unique, because its training encompasses endurance- and strength-training components. We used a cross-sectional study design to determine arterial compliance of 15 healthy, habitual rowers [50 ± 9 (SD) yr, 11 men and 4 women] and 15 sedentary controls (52 ± 8 yr, 10 men and 5 women). Rowers had been training 5.4 ± 1.2 days/wk for 5.7 ± 4.0 yr. The two groups were matched for age, body composition, blood pressure, and metabolic risk factors. Central arterial compliance (simultaneous ultrasound and applanation tonometry on the common carotid artery) was higher (P < 0.001) and carotid beta-stiffness index was lower (P < 0.001) in rowers than in sedentary controls. There were no group differences for measures of peripheral (femoral) arterial stiffness. The higher central arterial compliance in rowers was associated with a greater cardiovagal baroreflex sensitivity, as estimated during a Valsalva maneuver (r = 0.54, P < 0.005). In conclusion, regular rowing exercise in middle-aged and older adults is associated with a favorable effect on the elastic properties of the central arteries. Our results suggest that simultaneously performed endurance training may negate the stiffening effects of strength training.

rowing; arterial stiffness; cardiovagal baroreflex sensitivity


THE AORTA AND CENTRAL ARTERIES are not simply tubes or conduits; rather, they are highly complex components of the vascular tree that buffer oscillations in blood pressure and blood flow. Reductions in this cushioning function result in increased left ventricular afterload, increased myocardial oxygen demand, and decreased coronary blood flow and eventually lead to coronary ischemia (19, 22). Furthermore, because the vascular structure of the carotid sinus determines the deformation of and strain on the arterial baroreceptor endings during changes in arterial blood pressure, decreased arterial compliance is associated with impaired arterial baroreflex regulation of heart rate (17). Thus, through these mechanisms, stiffening of the central arteries exerts a combined effect on the heart, the arteries, and the autonomic nervous system in older humans.

Regular aerobic exercise and strength training are recommended for the prevention and treatment of cardiovascular disease and frailty associated with aging. Regular aerobic exercise is beneficial for reversing arterial stiffening in middle-aged and older adults (18, 26) and attenuates the age-related decline in cardiovagal baroreflex sensitivity (BRS) (16). In contrast to the beneficial effects of aerobic exercise, resistance training in middle-aged adults is associated with lower, rather than higher, central arterial compliance (14). Therefore, regular aerobic exercise and resistance exercise seem to exert opposite effects on the elastic properties of the arterial wall. It is not known how the elastic properties of the arterial wall will behave when one performs endurance training and strength training simultaneously.

In this regard, rowing exercise is unique, as it includes components of aerobic endurance and muscular strength (23). Rowers require large muscle strength to accelerate the boat at the start of the race and high endurance capacity to maintain this speed during the race (24). Similarly, rowers perform a combination of endurance and strength training during their usual training regimen, as demonstrated by their large maximal aerobic capacity and muscle strength (13, 23, 28, 29). Because more time may be required for development of vascular wall adaptations, a cross-sectional study analyzing arterial compliance in rowers may shed light on this clinically important question.

Accordingly, the primary aim of this study was to determine whether central and peripheral arterial compliance is higher in middle-aged and older rowers than in age-matched sedentary controls. We hypothesized that habitual rowers would demonstrate greater central arterial compliance than sedentary controls. Moreover, we hypothesized that compliance of peripheral (more muscular) arteries would be similar between the two groups, because exercise training has been shown to have no impact on these vascular beds (14, 25, 26). Because a reduction in arterial BRS is one of the important sequela of arterial stiffening (17), we also determined whether the hypothesized higher arterial compliance in rowers would be accompanied by greater BRS.


    METHODS
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
Subjects. A total of 30 healthy middle-aged and older adults (37–71 yr) were studied. They were either rowers (11 men and 4 women) or age-matched sedentary controls (10 men and 5 women). All of the subjects were healthy, nonobese, nonsmoking, normotensive (<140/90 mmHg), normolipidemic, and free of overt cardiovascular and other chronic diseases as assessed by medical history questionnaire. None of the subjects were taking cardiovascular-acting medications, including hormone replacement therapy. Physical activity was documented by a modified Godin physical activity questionnaire (4). Rowers had been training 5.4 ± 1.2 (SD) times/wk, 73 ± 14 min/session for 5.7 ± 4.0 yr, and rowing was their primary form of regular exercise. Approximately 65% of their training sessions were devoted to high-intensity workouts, and 87 ± 8% of rowing was performed on water. Sedentary participants had not exercised for ≥12 mo. All procedures were approved by the Institutional Review Board at the University of Texas at Austin, and written informed consent was obtained from each individual before participation.

Procedures. All laboratory procedures were performed at rest under comfortable laboratory conditions. Subjects abstained from food, alcohol, and caffeine for ≥4 h before laboratory procedures. An overnight 12-h fast was required before the measurements of metabolic risk factors. Premenopausal women were tested during the early follicular phase of the menstrual cycle.

Body composition. Body composition was measured using dual-energy X-ray absorptiometry (Lunar DPX, GE Medical Systems, Fairfield, CT).

Dietary intake analysis. A 3-day diet record was obtained and analyzed by a registered dietitian. Carbohydrate, fat, protein, and alcohol intakes were presented as percentage of the total caloric intake.

Handgrip strength. Handgrip strength was measured using an electrical handgrip dynamometer (model HDM-915, Lode Instruments, Groningen, The Netherlands).

Arterial blood pressure and heart rate at rest. Brachial and ankle blood pressure and heart rate were measured by an automated oscillometric device (model VP-2000, Colin Medical Instruments, San Antonio, TX) after ≥15 min of rest in the supine position (4). Ankle-brachial pressure index was calculated as ankle systolic blood pressure divided by brachial systolic blood pressure and was used to screen for peripheral artery disease.

Blood samples. A blood sample was collected from the antecubital vein after an overnight fast. Plasma concentrations of glucose, lipids, and lipoproteins were determined enzymatically using a Vitros DT60 analyzer (Ortho-Clinical Diagnostics, Raritan, NJ). Plasma norepinephrine concentrations were analyzed by enzyme immunoassay (Labor Diagnostika Nord, Nordhorn, Germany). Hematocrit was measured using a microcapillary reader (Damon/IEC Division, Needham, MA).

Arterial compliance. A combination of ultrasound imaging with simultaneous applanation of tonometrically obtained arterial pressures from the contralateral artery permitted noninvasive determinations of arterial compliance and beta-stiffness index (14, 26). The common carotid artery was imaged using B-mode ultrasound (model HDI 5000CV, Philips, Bothel, WA) equipped with a high-resolution linear-array transducer. Ultrasound images were transferred to digital viewing software (Access Point 2000, Freeland, Westfield, IN). Diameters were measured from the intima of the far wall to the media-adventitia of the near wall. Pulsatile changes in the common carotid artery and common femoral artery diameters were analyzed 1–2 cm proximal to the bifurcation. Blood pressure waveforms were obtained from the contralateral artery using arterial applanation tonometry (model TCB-500, Millar Instruments, Houston, TX) (14, 26) and analyzed by waveform browsing software (WinDaq 2000, Dataq Instruments, Akron, OH). To eliminate interinvestigator variability, one investigator analyzed all ultrasound images and blood pressure waveforms.

Cardiovagal BRS. Cardiovagal BRS was determined using the Valsalva maneuver (16, 17, 20). Briefly, subjects were seated in an upright position and familiarized with the procedure. Subjects performed a Valsalva maneuver and maintained an expiratory mouth pressure of 40 mmHg for 10 s. R-R interval (ECG) and blood pressure (Pilot 9200, Colin Medical, San Antonio, TX) were measured continuously. Subjects performed three Valsalva maneuvers ≥5 min apart to allow heart rate and blood pressure to return to baseline.

Data for cardiovagal BRS were recorded and analyzed by waveform browsing software (WinDaq 2000) during the phase IV overshoot. Systolic blood pressure values were linearly regressed against corresponding (lag 1) R-R intervals from the point where the R-R intervals began to lengthen to the point of maximal systolic blood pressure elevation (16, 17).

Carotid artery intima-media thickness. Carotid artery intima-media thickness was measured from images derived from an ultrasound machine equipped with a high-resolution linear-array transducer (model HDI-5000, Philips) (27). Images were analyzed by use of computerized software (QLab, Philips).

Statistics. One-way ANOVA and analysis of covariance were used for statistical analysis to determine significant group differences. Statistical significance was set a priori at P < 0.05 for all comparisons. Values are means ± SD, except in Figs. 1 and 2, where means ± SE are reported. Initially, univariate correlation and regression analysis were used to assess the strength of the relation between carotid arterial compliance and cardiovagal BRS. Partial correlation analysis and forward stepwise multiple regression analysis were then used to determine an independent association between cardiovagal BRS and arterial compliance.


Figure 1
View larger version (13K):
[in this window]
[in a new window]
 
Fig. 1. Arterial compliance and beta-stiffness index of the carotid and femoral artery. Values are means ± SE. *P < 0.001 vs. sedentary.

 

Figure 2
View larger version (9K):
[in this window]
[in a new window]
 
Fig. 2. Cardiovagal baroreflex sensitivity (BRS). Values are means ± SE. *P < 0.001 vs. sedentary.

 

    RESULTS
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
There were no group differences in age, height, body mass, body mass index, body composition, or waist circumference (Table 1). As expected, physical activity scores assessed by the modified Godin questionnaire and handgrip strength were higher (both P < 0.02) in rowers than in sedentary controls. There were no group differences for total caloric intakes, percent carbohydrate, percent fat, percent alcohol, or sodium intakes. Daily protein intake was higher (P < 0.05) in rowers than in sedentary controls. Fasting plasma glucose, lipid, and lipoprotein concentrations were not different between groups. Plasma norepinephrine concentrations were higher (P < 0.05) in rowers than in sedentary controls. Heart rate at rest was lower (P < 0.05) in rowers than in sedentary controls (Table 2). Brachial blood pressure, carotid blood pressure, carotid artery intima-media thickness, and ankle-brachial pressure index were not different between the groups.


View this table:
[in this window]
[in a new window]
 
Table 1. Selected subject characteristics, dietary intake, and metabolic risk factors

 

View this table:
[in this window]
[in a new window]
 
Table 2. Selected physiological variables at rest

 
Carotid arterial compliance was higher (P < 0.001) and beta-stiffness index was lower (P < 0.001) in rowers than in sedentary controls (Fig. 1). Because of the significant group difference in heart rate at rest, analysis of covariance was performed with heart rate as the covariate. The group difference in carotid arterial compliance remained statistically significant (P = 0.01). Femoral arterial compliance and beta-stiffness index were not different between rowers and sedentary controls. Cardiovagal BRS was greater (P < 0.01) in rowers than in sedentary controls (Fig. 2) and was positively associated with carotid arterial compliance (r = 0.54, P < 0.005). Stepwise regression analysis revealed that, among the variables correlated with cardiovagal BRS (arterial compliance, diastolic blood pressure, and heart rate), carotid arterial compliance was the strongest independent physiological correlate of cardiovagal BRS, inasmuch as it explained 36% of the variance (P < 0.01). Additionally, when the influence of other variables (e.g., diastolic blood pressure and heart rate) was accounted for using a partial correlation analysis, the relation between cardiovagal BRS and carotid arterial compliance remained significant (r = 0.45, P < 0.05).


    DISCUSSION
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
The primary findings of the study are as follows: 1) Central arterial compliance was higher and beta-stiffness index was lower in habitual rowers than in age-matched sedentary controls who were matched for age, body mass, metabolic risk factors, blood pressure, and sodium intake. 2) Measures of peripheral arterial stiffness were not different between the groups. 3) Cardiovagal BRS was higher in rowers than in sedentary controls and was positively related to carotid arterial compliance. These results indicate that regular rowing exercise in middle-aged and older adults is associated with favorable effects on the elastic properties of the central arteries.

Because vascular adaptations may be a long-term process requiring a prolonged follow-up or intervention periods to induce appreciable changes, we used a cross-sectional study design. To minimize the weaknesses of this study design and to isolate the influence of rowing as much as possible, both groups were carefully matched for age, body composition, blood lipids, plasma glucose, blood pressure, and dietary sodium intake. Additionally, to isolate the effect of rowing, we excluded individuals for whom rowing was not their primary form of exercise. Rowers were also excluded if more than two training days per week were exclusively nonrowing exercise, such as running, cycling, or weightlifting. Many rowers were competitive and followed similar training schedules. The majority (>65%) of their training sessions were devoted to high-intensity workouts. We found that central arterial compliance was higher and beta-stiffness index was lower in habitual rowers. Therefore, the results of the present study suggest that chronic rowing exercise is associated with a greater central arterial compliance.

Because of the contrasting effects of endurance and resistance training on the elastic properties of arteries, it is of particular interest to determine how the arteries adapt to a combination of these training modes. To gain insight into this issue, we studied a group of highly trained rowers. Rowing is unique for examination of training adaptations, because it includes the components of endurance training and resistance training (13, 23). Rowers exhibit markedly enlarged left ventricular dimensions as well as left ventricular wall thickness (13, 21). This is thought to be due to a combination of extreme volume load (as seen in endurance training) and extreme pressure overload (as seen in resistance training) during rowing (21). Rowing uses the upper and lower body and utilizes both limbs simultaneously to generate powerful force, causing large fluctuations in blood pressure and pulse pressure (2, 23). As shown in the present study, in regard to the impact of the overall rowing training on the vasculature, the endurance-training component appears to outweigh the resistance-training component, producing a higher arterial compliance in rowers. These results suggest that stiffening of the large arteries may be avoided if endurance training is incorporated into an exercise program that has a strength-training component. Intervention studies are necessary to draw more definite conclusions on this issue.

Endurance training does not influence the compliance of peripheral arteries (25, 26). Similarly, peripheral arterial compliance is not different between sedentary and resistance-trained individuals (14). Consistent with these observations, we found that femoral arterial compliance was not different between groups. A lack of association between exercise training and peripheral arterial compliance is attributed to the fact that the arterial wall components of the femoral artery, which, in contrast to the central elastic arteries, do not act to buffer large fluctuations in blood pressure and blood flow.

The sympathetic nervous system exerts a tonic restraint on the compliance of the common carotid artery (11), and the removal of that restraint produces an immediate increase in its compliance (11). We measured plasma concentrations of norepinephrine, a rough index of sympathetic nervous system activity, in an attempt to gain insight into the physiological mechanisms underlying the effects of rowing training on arterial compliance. Although carotid arterial compliance was greater in rowers than in sedentary controls, plasma norepinephrine levels were also higher in rowers. These results are not consistent with the idea that decreased sympathetic vasoconstrictor activity is responsible for the greater arterial compliance in rowers. A more likely explanation for the greater arterial compliance in rowers is increased nitric oxide bioavailability. Arterial compliance is modulated significantly by endothelial function (7), and regular aerobic exercise improves this important function (5). Other possibilities include increases in vasa vasorum flow (1), decreases in collagen cross-linking (8), and/or decreases in local endothelin-1 action (12). Given that the influence of exercise training manifests only in the central elastic arteries, where beat-by-beat arterial distension is greater, there may be an interaction between these physiological mechanisms and mechanical factors that are inherent in the central arterial wall.

The vascular structure of the carotid sinus determines the deformation of the arterial baroreceptor endings during changes in arterial pressure. A compliant artery acts to augment stimulus transduction and afferent responsiveness of baroreceptors. Endurance training is associated with enhanced cardiovagal BRS (17). However, it is unclear whether resistance training has the same effect (3, 9). Given the lower arterial compliance in strength-trained individuals and the close association between arterial compliance and arterial BRS, it is reasonable to hypothesize that strength training is associated with lower cardiovagal BRS. The higher cardiovagal BRS in rowers was positively and independently associated with carotid arterial compliance. Thus regular rowing exercise appears to enhance arterial BRS arguably via its effects on arterial compliance. Alternatively, rowing exercise itself causes large blood pressure changes that mimic the Valsalva maneuver at the catch of the stroke (23). Therefore, in contrast to sedentary individuals, rowers may have developed a greater capacity to adjust disturbances in blood pressure because of frequent exposure to this stimulus.

In addition to the use of a cross-sectional study design, the present study has other important limitations. Because of the risks associated with the testing and a lack of specific testing procedure, we did not measure maximal aerobic capacity and muscle strength to confirm that rowers were endurance trained as well as strength trained. As alternatives, we used the Godin physical activity questionnaire and handgrip strength. Even though these are indirect measures, the magnitude of the differences in these results between the sedentary controls and rowers clearly shows that rowers in the present study demonstrated greater aerobic fitness and muscular strength.

In conclusion, habitual rowers demonstrate a greater central arterial compliance and higher cardiovagal BRS than sedentary controls who are matched for many potentially confounding factors. Our findings suggest that concurrently performed endurance training may negate the stiffening effects of resistance training on arterial compliance.


    GRANTS
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
This study was supported by National Institute on Aging Grant AG-20966. M. M. Anton was supported by a fellowship award from the Ministerio de Educación y Ciencia (Spain) and M. Y. Cortez-Cooper and A. E. DeVan by National Institutes of Health Grants HL-072729 and DA-018431, respectively.


    ACKNOWLEDGMENTS
 
We thank Rhea Montemayor, Phil Stanforth, and Jill Tanaka for assistance.


    FOOTNOTES
 

Address for reprint requests and other correspondence: H. Tanaka, Dept. of Kinesiology, Univ. of Texas at Austin, 1 University Station, Austin, TX 78712 (e-mail: htanaka{at}mail.utexas.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. Angouras D, Sokolis DP, Dosios T, Kostomitsopoulos N, Boudoulas H, Skalkeas G, and Karayannacos PE. Effect of impaired vasa vasorum flow on structure and mechanics of thoracic aorta: implications for the pathogenesis of aortic dissection. Eur J Cardiothorac Surg 17: 469–473, 2000.
  2. Clifford PS, Hanel B, and Secher NH. Arterial blood pressure response to rowing. Med Sci Sports Exerc 26: 715–719, 1994.[CrossRef][Web of Science][Medline]
  3. Cooke WH and Carter JR. Strength training does not affect vagal-cardiac control or cardiovagal baroreflex sensitivity in young healthy subjects. Eur J Appl Physiol 93: 719–725, 2005.[CrossRef][Web of Science][Medline]
  4. Cortez-Cooper MY, Supak JA, and Tanaka H. A new device for automatic measurements of arterial stiffness and ankle-brachial index. Am J Cardiol 91: 1519–1522, 2003.[CrossRef][Web of Science][Medline]
  5. 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]
  6. Godin G and Shephard RJ. A simple method to assess exercise behavior in the community. Can J Appl Sport Sci 10: 141–146, 1985.[Medline]
  7. Joannides R, Richard V, Haefeli WE, Benoist A, Linder L, Luscher TF, and Thuillez C. Role of nitric oxide in the regulation of the mechanical properties of peripheral conduit arteries in humans. Hypertension 30: 1465–1470, 1997.[Abstract/Free Full Text]
  8. Kass DA, Shapiro EP, Kawaguchi M, Capriotti AR, Scuteri A, deGroof RC, and Lakatta EG. Improved arterial compliance by a novel advanced glycation end-product crosslink breaker. Circulation 104: 1464–1470, 2001.[Abstract/Free Full Text]
  9. Lightfoot TJ, Torok DJ, Journell TW, Turner MJ, and Claytor RP. Resistance training increases lower body negative pressure tolerance. Med Sci Sports Exerc 26: 1003–1011, 1994.[Web of Science][Medline]
  10. Longhurst JC, Kelly AR, Gonyea NJ, and Mitchell JH. Echocardiographic left ventricular masses in distance runners and weight lifters. J Appl Physiol 48: 154–162, 1980.[Abstract/Free Full Text]
  11. Mangoni AA, Mircoli L, Giannattasio C, Mancia G, and Ferrari AU. Effect of sympathectomy on mechanical properties of common carotid and femoral arteries. Hypertension 30: 1085–1088, 1997.[Abstract/Free Full Text]
  12. McEniery CM, Qasem A, Schmitt M, Avolio AP, Cockcroft JR, and Wilkinson IB. Endothelin-1 regulates arterial pulse wave velocity in vivo. J Am Coll Cardiol 42: 1975–1981, 2003.[Abstract/Free Full Text]
  13. Mitchell JH, Haskell W, Snell P, and Van Camp SP. Task Force 8: classification of sports. J Am Coll Cardiol 45: 1364–1367, 2005.[Free Full Text]
  14. Miyachi M, Donato AJ, Yamamoto K, Takahashi K, Gates PE, Moreau KL, and Tanaka H. Greater age-related reductions in central arterial compliance in resistance-trained men. Hypertension 41: 130–135, 2003.[Abstract/Free Full Text]
  15. Miyachi M, Kawano H, Sugawara J, Takahashi K, Hayashi K, Yamazaki K, Tabata I, and Tanaka H. Unfavorable effects of resistance training on central arterial compliance: a randomized intervention study. Circulation 110: 2858–2863, 2004.[Abstract/Free Full Text]
  16. Monahan KD, Dinenno FA, Tanaka H, Clevenger CM, DeSouza CA, and Seals DR. Regular aerobic exercise modulates age-associated declines in cardiovagal baroreflex sensitivity in healthy men. J Physiol 529: 263–271, 2000.[Abstract/Free Full Text]
  17. Monahan KD, Tanaka H, Dinenno FA, and Seals DR. Central arterial compliance is associated with age- and habitual exercise-related differences in cardiovagal baroreflex sensitivity. Circulation 104: 1627–1632, 2001.[Abstract/Free Full Text]
  18. Moreau KL, Donato AJ, Seals DR, DeSouza CA, and Tanaka H. Regular exercise, hormone replacement therapy and the age-related decline in carotid arterial compliance in healthy women. Cardiovasc Res 57: 861–868, 2003.[Abstract/Free Full Text]
  19. Pak PH, Maughan L, Baughman KL, and Kass DA. Marked discordance between dynamic and passive diastolic pressure-volume relations in idiopathic hypertrophic cardiomyopathy. Circulation 94: 52–60, 1996.[Abstract/Free Full Text]
  20. Palmero HA, Caeiro TF, Iosa DJ, and Bas J. Baroreceptor reflex sensitivity index derived from phase 4 of the Valsalva maneuver. Hypertension 12: 134–137, 1981.
  21. Pluim BM, Zwinderman AH, van der Laarse A, and van der Wall EE. The athlete's heart: a meta-analysis of cardiac structure and function. Circulation 100: 336–344, 1999.
  22. Rajkumar C, Cameron JD, Chirstophidus N, Jennings GL, and Dart AM. Reduced systemic arterial compliance is associated with left ventricular hypertrophy and diastolic dysfunction in older people. J Am Geriatr Soc 45: 803–808, 1997.[Web of Science][Medline]
  23. Secher N. Physiological and biomechanical aspects of rowing: implications for training. Sports Med 15: 24–42, 1993.[Web of Science][Medline]
  24. Steinacker JM. Physiological aspects of training in rowing. Int J Sports Med 14: S3–S10, 1993.
  25. Tanaka H, DeSouza CA, and Seals DR. Absence of age-related increase in central arterial stiffness in physically active women. Arterioscler Thromb Vasc Biol 18: 127–132, 1998.[Abstract/Free Full Text]
  26. Tanaka H, Dinenno FA, Monahan KD, Clevenger CM, DeSouza CA, and Seals DR. Aging, habitual exercise, and dynamic arterial compliance. Circulation 102: 1270–1275, 2000.[Abstract/Free Full Text]
  27. Tanaka H, Dinenno FA, Monahan DK, DeSouza CA, and Seals DR. Carotid artery wall hypertrophy with age is related to local systolic blood pressure in healthy men. Arterioscler Thromb Vasc Biol 21: 82–87, 2001.[Abstract/Free Full Text]
  28. Yoshiga CC, Higuchi M, and Oka J. Serum lipoprotein cholesterols in older oarsmen. Eur J Appl Physiol 87: 228–232, 2002.[CrossRef][Web of Science][Medline]
  29. Yoshiga CC, Higuchi M, and Oka J. Rowing prevents muscle wasting in older men. Eur J Appl Physiol 88: 1–4, 2002.[CrossRef][Web of Science][Medline]



This article has been cited by other articles:


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
M. Rakobowchuk, S. Tanguay, K. A. Burgomaster, K. R. Howarth, M. J. Gibala, and M. J. MacDonald
Sprint interval and traditional endurance training induce similar improvements in peripheral arterial stiffness and flow-mediated dilation in healthy humans
Am J Physiol Regulatory Integrative Comp Physiol, July 1, 2008; 295(1): R236 - R242.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
T. Okamoto, M. Masuhara, and K. Ikuta
Combined aerobic and resistance training and vascular function: effect of aerobic exercise before and after resistance training
J Appl Physiol, November 1, 2007; 103(5): 1655 - 1661.
[Abstract] [Full Text] [PDF]


Home page
Br. J. Sports. Med.Home page
P E Gates and D R Seals
Decline in large elastic artery compliance with age: a therapeutic target for habitual exercise
Br. J. Sports Med., November 1, 2006; 40(11): 897 - 899.
[Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
290/4/H1596    most recent
01054.2005v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (9)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cook, J. N.
Right arrow Articles by Tanaka, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cook, J. N.
Right arrow Articles by Tanaka, H.


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2006 by the American Physiological Society.