| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
|
|
|
|||||||
|
|||||||||
Nutrition, Metabolism, and Exercise Laboratory, Donald W. Reynolds Center on Aging, Slot 806, University of Arkansas for Medical Sciences, Little Rock, Arkansas
Address reprint requests to: William J. Evans, Ph.D., Director, Nutrition, Metabolism, and Exercise Laboratory, Donald W. Reynolds Center on Aging, Slot 806, University of Arkansas for Medical Sciences, Little Rock, AR 72205. E-mail: evanswilliamj{at}uams.edu
 |
ABSTRACT |
|---|
 TOP ABSTRACT INTRODUCTIONREFERENCES |
|---|
One important strategy that counters sarcopenia is strength conditioning. Strength conditioning will result in an increase in muscle size and this increase in size is largely the result of increased contractile proteins. The mechanisms by which the mechanical events stimulate an increase in RNA synthesis and subsequent protein synthesis are not well understood. Lifting weight requires that a muscle shorten as it produces force (concentric contraction). Lowering the weight, on the other hand, forces the muscle to lengthen as it produces force (eccentric contraction). These lengthening muscle contractions have been shown to produce ultrastructural damage (microscopic tears in contractile proteins muscle cells) that may stimulate increased muscle protein turnover. This muscle damage produces a cascade of metabolic events which is similar to an acute phase response and includes complement activation, mobilization of neutrophils, increased circulating an skeletal muscle interleukin-1, macrophage accumulation in muscle, and an increase in muscle protein synthesis and degradation. While endurance exercise increases the oxidation of essential amino acids and increases the requirement for dietary protein, resistance exercise results in a decrease in nitrogen excretion, lowering dietary protein needs. This increased efficiency of protein use may be important for wasting diseases such as HIV infection and cancer and particularly in elderly people suffering from sarcopenia. Research has indicated that increased dietary protein intake (up to 1.6 g protein · kg–1 · d–1) may enhance the hypertrophic response to resistance exercise. It has also been demonstrated that in very old men and women the use of a protein-calorie supplement was associated with greater strength and muscle mass gains than did the use of placebo.
Key words: aging, elderly, sarcopenia, muscle mass, diet, protein, strength conditioning
Key teaching points:
•Sarcopenia is the loss of skeletal muscle in the aging process.
•As the body ages, there is a natural loss of skeletal muscle and gains in total body fat and visceral fat.
•The elderly can benefit from aerobic conditioning and strength training, only strength training can stop or reverse sarcopenia.
•The current RDA of .8 grams/KG body weight per day is insufficient to meet the protein needs of most elderly people.
•Research shows that the use of a protein and calorie supplement was associated with greater strength and muscle mass gains than did the use of placebo.
|
INTRODUCTION |
|---|
|
TOPABSTRACTINTRODUCTIONREFERENCES |
|---|
Dietary Protein Needs of Elderly People
The current Recommended Dietary Allowance for protein to meet the needs of adults over the age of 19 years (unless pregnant or lactating) is 0.8 grams · kg–1 · d–1 [26]. This estimate should meet the needs of virtually all health people regardless of age of level of physical activity. However, the information concerning the dietary protein requirements of elderly people is limited. Campbell et al. [8,11] examined studies in the literature examining nitrogen-balance in elderly people and recalculated the balance data using currently accepted values for miscellaneous losses. The conclusion of this retrospective analysis and new balance data presented was that the current RDA is inadequate to meet the dietary protein needs of most elderly people. This conclusion was confirmed by our laboratory [13] in a study that examined the long-term consequences of consumption of the protein RDA. This study enrolled health, elderly men and women and provided the 0.8 g protein · kg–1 · d–1 over 14-week period in a metabolic ward. The subjects in this study demonstrated a classic accommodation response described by Waterlow [75] with a continued decrease in urinary nitrogen excretion over the 14-week period of the study. The accommodated tissue was skeletal muscle. Using computerized tomography, we demonstrated a significant reduction in the cross-sectional area of thigh muscle. Thus, these data suggest that the protein RDA for elderly people is not adequate, even while consuming a weight maintenance diet.
The etiology of this increased need for dietary protein is not well understood. While some have demonstrated that the rate muscle protein synthesis is reduced in elderly people [76], it appears that basal rate of muscle protein synthesis is not depressed in this population compared to that of young people [74]. There is evidence that post-prandial rise in amino acids results in a greater rise in muscle protein synthesis in young people compared to old. There is also a greater extraction of essential amino acid during the first pass through the liver, potentially diminishing the amount of amino acids presented to muscle. In addition, glucose intolerance may also play an important role in a reduced post-prandial increase in muscle protein synthesis in elderly people [73].
The fact that elderly people require more dietary protein than the RDA has important implications. Surveys of the nutrition status of older people have shown that a large number (up to 30%) consume the RDA or less each day. Inadequate intake of protein over a prolonged period of time results in a decrease in the rate of whole body protein turnover and an accelerated loss of muscle mass in elderly people [19,20]. Indeed, epidemiological evidence of increased dietary protein shows that elderly people who consume the RDA for protein are at greater risk of health problems than those older people who consume a greater amount of protein [72]. These investigators [72] suggested that "the mean protein requirement in elderly adults is greater than that established by the 1985 joint WHO/FAO/UNU expert committee." Dietary energy needs of elderly people are generally lower than those of young men and women [63]. This means that older people may need a greater amount of dietary protein as a percentage of their total energy intake. Because of their decreased energy requirements and decreased intake compared to young, elderly people should increase their intake of high quality but low fat protein, such as eggs, low fat meat and fish, and whey or casein.
These estimates of increased dietary protein needs of elderly people were made under eucaloric conditions. During periods of decreased energy intake, dietary protein needs increase. Certainly, strong consideration for increased intake of low fat, high quality protein should be made for those older people who voluntarily attempt to lose weight. In addition, appetite regulation has been demonstrated to be impaired in the elderly [62]. While energy intake increases in young people after a period of decreased energy intake, Roberts et al. [62] demonstrated that older people remain hypophagic after reduced energy intake and weight loss. This may help to explain why many older people experience involuntary weight loss with no increase in appetite. Indeed, use of protein/calorie supplements in very old men and women have not been shown to increased dietary energy intake or body weight [34]. In this population, dietary protein intake may be critical to the preservation of skeletal muscle mass.
Strength Training
Progressive resistance exercise or strength training has been demonstrated to result in an increase in muscle size and strength. Strength conditioning or progressive resistance training is generally defined as training in which the resistance against which a muscle generates force is progressively increased over time. Progressive resistance training involves few contractions against a heavy load. While endurance exercise has been the more traditional means of increasing cardiovascular fitness, the American College of Sports Medicine currently recommends strength or resistance training as an important component of an overall fitness program. This is particularly important in the elderly where loss of muscle mass and weakness are prominent deficits.
Resistance Exercise and Muscle Damage
The metabolic and morphological adaptations resulting from resistance and endurance exercise are quite different. Muscle strength has been shown to increase in response to training between 60 and 100% of the 1 repetition maximum (1 RM) [54]. 1 RM is the maximum amount of weight that can be lifted with one contraction. Strength conditioning will result in an increase in muscle size and this increase in size is largely the result of increased contractile proteins. The mechanisms by which the mechanical events stimulate an increase in RNA synthesis and subsequent protein synthesis are not well understood. Lifting weight requires that a muscle shorten as it produces force (concentric contraction). Lowering the weight, on the other hand, forces the muscle to lengthen as it produces force (eccentric contraction). These lengthening muscle contractions have been shown to produce ultrastructural damage (microscopic tears in contractile proteins muscle cells) that may stimulate increased muscle protein turnover [31].
High intensity strength training has been shown to increase skeletal muscle mass despite resulting in increased myofibrillar proteolysis [40], suggesting a disproportionate increase in myofibrillar protein synthesis. Our laboratory has demonstrated that eccentric exercise (a large component of high intensity strength training) results in ultrastructural damage to skeletal muscle, which results in a prolonged increase in the rate of protein degradation. Our data also implicate the exercise-induced increase in skeletal muscle interleukin-1ß as a mediator of these changes. Interleukin-1ß is a peptide derived from mononuclear cells which has been implicated as the substance responsible for the so-called acute phase response to infection that includes fever, mobilization of neutrophils, redistribution of trace metals and increased skeletal muscle proteolysis. In addition, we have demonstrated that many of the components of this acute phase response to exercise are reduced in older compared to younger subjects. For example, we have shown that complement activation is similar between older and younger subjects, but neutrophil mobilization (presumably stimulated by complement) is greatly reduced or not apparent in old vs. young subjects. The release of creatine kinase from damaged muscle is also attenuated in older subjects compared to young. These age-related differences in the acute phase response to damaging exercise may result in an attenuated response in alterations in muscle protein metabolism and reduced amount of muscle hypertrophy in older compared to younger subjects.
Skeletal muscle undergoes well-established adaptations following repeated bouts of resistance exercise in animals and humans [5]. In particular muscle size and strength increase significantly following high-intensity resistance [22,40]. Contributing to these adaptations are temporary adjustments in whole body [67] and muscle protein synthesis [23,83] that exist for several days following acute exercise. While we have demonstrated that resistance training results in an increase in muscle size in older subjects, our results have been variable. While two studies demonstrated a significant increase in muscle size resulting from strength training [32,40], two other studies using the same intervention showed no change [10,33].
Exercises that involve eccentric (lengthening) contractions elicit the most rapid and largest improvements in muscle strength and size [24,25]. Seemingly events associated with muscle hypertrophy are more apparent following eccentric than concentric resistance exercise. For example, repeated eccentric contractions induce local accumulation of several peptide growth factors, including insulin like growth factor (IGF) [82], fibroblast growth factor (FGF) [81], and potentially platelet-derived growth factor (PDGF). All three growth factors stimulate satellite cell proliferation in vitro; processes which require an enhanced rate of protein synthesis. In-vivo effects of these growth factors on protein synthesis are scarce, but it has been shown that infusion of IGF-I increases whole-body protein synthesis in man [64].
Since a major source of these growth factors are macrophages [57], muscle hypertrophy may be linked with the body’s inflammatory response to exercise-induced muscle injury [18,78]. Various indices of inflammation are apparent after damaging-type (eccentric) exercise, including leukocyte mobilization and infiltration, muscle proteolysis, complement activation and fever. Although eccentric exercise causes local inflammation [6,14–17,35] there is no in-vivo evidence that the inflammatory response induces protein synthesis and muscle hypertrophy.
We have recently demonstrated that a single bout of high intensity eccentric exercise performed by sedentary men resulted in a significant increase in skeletal muscle prostaglandin levels (PGE2 and PGF2
) [69]. Previous studies have demonstrated that PGE2 and PGF2 have a [3,41,42]. Because cyclooxygenase inhibitors may effect the post-exercise rise in muscle prostaglandin, we examined the effect of two commonly consumed over-the-counter analgesics, ibuprofen and acetaminophen, on muscle protein metabolism following high intensity eccentric exercise. Twenty four men (age: 25 ± 3 yr, height: 180 ± 6 cm, weight: 81 ± 6 kg, body fat: 17 ± 8%) were randomly assigned to one of 3 groups that received either the maximal over-the-counter dose of ibuprofen (IBU; 1200 mg/d), acetaminophen (ACET; 4000 mg/d), or a placebo (PLA) following 10–14 sets of 10 repetitions at 120% of concentric 1 repetition maximum using the knee extensors. Post-exercise (24 h) skeletal muscle fractional synthesis rate (FSR, measured by incorporation of phenylalanine into muscle protein) was increased 71 ± 20% (p < 0.05) in PLA (0.037 ± 0.009 %/h), and was unchanged (p > 0.05) in IBU (38 ± 22%; 0.015 ± 0.009%/h) and ACET (23 ± 26%; 0.006 ± 0.014%/h) [70]. Exercise induced a significant increase in skeletal muscle prostaglandin levels (PGE2 & PGF2) that was completely suppressed by ibuprofen and acetaminophen. These results suggest that both ibuprofen and acetaminophen suppress the protein metabolic response to eccentric exercise. These are the first data to demonstrate an anti-inflammatory effect of acetaminophen in skeletal muscle. Thus, these two analgesics may work through a common mechanism to influence protein metabolism in skeletal muscle. These data also indicate that the common practice of treating delayed onset muscle soreness that may result from exercise may have a strong effect on muscle hypertrophy by greatly decreasing the rate of protein synthesis.
Effects of Resistance Exercise and Insulin on Protein Metabolism
Hormonal and nutritional factors, particularly the availability of insulin and amino acids, have important effects in the control of muscle protein synthesis [47,61]. For example, starvation reduces the rate of protein synthesis in skeletal muscle by more than 50% compared to the rate seen in fed animals. This inhibition of protein synthesis (also seen in muscle from diabetic animals) is a result of an impairment in the initiation phase of protein synthesis [47,61]. The mechanism through which insulin regulates protein synthesis initiation involves phosphorylation of the translational regulator eukaryotic initiation factor 4E (eIF-4E)-binding protein 1 (4E-PB1) [38]. Insulin-like growth factor 1 (IGF-I) results in the phosphorylation of 4E-BP1 and dissociation of the 4E-BP1 · eIF-4E complex in [43] cells in culture (muscle cells that are grown in a medium containing appropriate nutrients and growth factors). IGF-I has also been shown to stimulate protein synthesis in rats in vivo [45] and in muscle in perfused hindlimb preparations [46]. These studies also suggest that insulin plays a permissive role in the effect of IGF-I in stimulating muscle protein synthesis.
Studies of insulin secretion after resistance but not endurance exercise provide evidence for insulin’s role in maintaining muscle mass. King et al. [48] and Dela et al. [27] showed that arginine-stimulated insulin secretion is decreased with endurance training. In contrast, acute resistance exercise in rats has been shown to increase insulin secretion [37]. As reviewed above, regular aerobic exercise is known to increase insulin sensitivity and glucose tolerance. In addition to its effects on insulin action, aerobic exercise training results in decreased insulin secretion [28]. Regularly performed endurance exercise in young men is associated with an insulin pulse profile in the resting fasted state characterized by less insulin secreted per burst but a similar number of bursts over a 90-min period. They suggested that training-induced elevations in target-tissue sensitivity to insulin reduce the requirement for pulsatile insulin secretion. This coordinated response keeps glucose concentrations constant. Dela et al. [27] demonstrated that aerobic exercise training decreases both arginine and glucose stimulated insulin secretion, indicating, they conclude, a profound ß-cell adaptation.
A single bout of concentric exercise is a recognized enhancer of insulin action, while eccentric exercise transiently impairs whole body insulin action for at least 2 days after the bout [49]. We have demonstrated that eccentric exercise can result in a long-term delay in the rate of glycogen synthesis [59]. This decrease insulin action and delayed glycogen synthetic rate has been shown to result from decreased rate of glucose transport rather than decrease glycogen synthase activity [2]. This transient resistance to insulin and impaired resynthesis of glycogen can result in a systemic hyperinsulinemia that may result in an increase in the rate of muscle protein synthesis. Our laboratory [50] has demonstrated age-related differences in the insulin response to hyperglycemia following a single bout of eccentric exercise. Two days following upper and lower body eccentric exercise younger subjects demonstrated a pronounced pancreatic insulin response during a hyperglycemic clamp while this response was blunted in healthy elderly men.
The effects of resistance exercise on insulin availability appear to be opposite those of endurance exercise and thus stimulate net protein accretion. Insulin has been demonstrated to have profoundly anabolic effects on skeletal muscle. In the resting state, insulin has been demonstrated to decrease the rate of muscle protein degradation. Stable isotope amino acid studies in humans [21,68] clearly demonstrate that insulin inhibits whole body protein breakdown in vivo and stimulates muscle protein synthetic rate [4].
Insulin has been demonstrated to increase the rate of muscle protein synthesis in insulin deficient rats. However, in non-diabetic animals this effect was not seen. Fluckey et al. have argued [36,37] that insulin is not likely to stimulate muscle protein synthesis in quiescent muscle. We have demonstrated that an insulin infusion does not increase the rate of protein synthesis in non-exercised muscle. However, using a resistance exercise model, we have demonstrated that resistance exercise did not stimulate an increase in the rate of protein synthesis. It was only with the addition of insulin that an exercise induced increase in the rate of soleus and gastrocnemius protein synthesis was seen. This effect of insulin stimulation of the rate of protein synthesis was preserved with advancing age.
Protein Requirements and Exercise
High intensity resistance training is clearly anabolic in both young and older individuals. Data from our laboratory [10] demonstrated a 10 to 15 percent decrease in N-excretion at the initiation of training that persists for 12 weeks. That is, progressive resistance training improved N-balance, thus older subjects performing resistance training have a lower mean protein requirement than do sedentary subjects. This effect was seen at a protein intake of 0.8 and 1.6 g protein · kg–1 · d–1, indicating that the effect of resistance training on protein retention may not be related to dietary protein intake. These results are somewhat at variance to our previous research [56] demonstrating that regularly performed aerobic exercise causes an increase in the mean protein requirement of middle-aged and young endurance athletes (mean of 0.93 g · kg–1 · d–1). This difference likely results from increased oxidation of amino acids during aerobic exercise that may not be present during resistance training.
Strawford et al. [66] also demonstrated similar effects of resistance exercise training on nitrogen balance in patients with HIV-related weight loss. The investigators examined the effects of an anabolic steroid (oxandrolone, 20 mg/d and placebo) and high intensity resistance exercise training in 24 eugonadal men with HIV-associated weight loss (mean, 9% body weight loss). Both groups showed significant nitrogen retention and increases in LBM, weight, and strength. The mean gains were significantly greater in the oxandrolone group than in the placebo group in nitrogen balance, accrual of FFM, and strength. Results were similar whether or not patients were taking protease inhibitors. These results confirm the positive effects of resistance exercise on nitrogen retention and protein requirements.
These studies, taken as a whole demonstrate the powerful effects of resistance exercise training on protein nutriture. The anabolic effects have important implications in the treatment of many wasting diseases and conditions such as cancer, HIV infection, aging, chronic renal failure, and undernutrition seen in many very old men and women. By effectively lowering dietary protein needs, resistance exercise can limit further losses of skeletal muscle mass while simultaneously increase muscle strength and functional capacity.
Resistance Exercise, Protein Intake, and Aging
A number of investigators have demonstrated that resistance exercise can result in a substantial increase in muscle size and strength in elderly people. However, it is clear that when the intensity of the exercise is low, only modest increases in strength are achieved by elderly subjects [1,53]. A number of studies have demonstrated that, given an adequate training stimulus, older men and women show similar or greater strength gains compared to young individuals as a result of resistance training.
Frontera et al. [39,40] showed that older men responded to a 12 week progressive resistance training program (80% of the 1 repetition maximum, 3 sets of 8 repetition of the knee extensor and flexors, 3 days per week) by more than doubling extensor strength and more than tripling of flexor strength. The increases in strength averaged approximately 5% per training session, similar to strength gains observed by younger men. Total muscle area estimated by computerized tomography (CT) increased by 11.4%. Biopsies of the vastus lateralis muscle revealed similar increases in type I fiber area (33.5%) and type II fiber area (27.6%). Daily excretion of urinary 3-methyl-L-histidine increased with training (p < 0.05) by an average of 40.8%, indicating that increased muscle size and strength resulting from PRT is associated with an increased rate of myofibrillar protein turnover. Half of the men who participated in this study were given a daily protein-calorie supplement (S) providing an extra 560 ± 16 kcal/d (16.6% as protein, 43.3% as carbohydrate, and 40.1% as fat) in addition to their normal ad lib diet. The rest of the subjects received no supplement (NS) and consumed an ad lib diet. By the twelfth week of the study, dietary energy (2960 ± 230 in S vs. 1620 ± 80 kcal in NS) and protein (118 ± 10 in S vs. 72 ± 11 g/d in NS) intake were significantly different between the S and NS groups. Composition of the midthigh was estimated by computerized tomography and showed that the S group had greater gains in muscle than did the NS men [55]. In addition, urinary creatinine excretion was greater at the end of the training in the S group when compared to that of the men in the NS group, indicating a greater muscle mass in the S group at the end of the 12 weeks of training. The change in energy and protein intake (beginning vs. 12 weeks) was correlated with the change in midthigh muscle area (r = 0.69, p = 0.019; r = 0.63, p = 0.039, respectively). There were no differences in the strength gains between the two groups. These data suggest that a change in total food intake, or perhaps, selected nutrients, in subjects beginning a strength-training program can affect muscle hypertrophy.
We applied this same training program to a group of frail, institutionalized elderly men and women (mean age 90 ± 3 years, range 87–96) [32]. After 8 weeks of training, the 10 subjects in this study increased muscle strength by almost 180% and muscle size by 11%. We also used [33] a similar intervention on frail nursing home residents and demonstrated not only increases in muscle strength and size, but increased gait speed, stair climbing power, and balance. In addition, spontaneous activity levels increased significantly while the activity of a non-exercised control group was unchanged. In this study the effects of a protein/calorie supplement combined with exercise was also examined. The supplement consisted of a 240-ml liquid supplying 360 kcal in the form of carbohydrate (60%), fat (23%), and soy-based protein (17%), and was designed to augment caloric intake by about 20%, and provide one third of the RDA for vitamins and minerals. The men and women who consumed the supplement and exercised gained weight compared to the three other groups examined (exercise/control, non-exercise supplemented, and non-exercise control). The non-exercising subjects who received the supplement reduced their habitual dietary energy intake so that total energy intake was unchanged. In other words, the supplement did not add to total energy intake, but rather substituted one source of energy (the supplement) for another (their meals). More recently (in the same study population), we [65] demonstrated that the combined weight lifting and nutritional supplementation increased strength by 257 ± 62% (p = 0.0001) and type II fiber area by 10.1 ± 9.0% (p = 0.033), with a similar trend for type I fiber area (+12.8 ± 22.2%). Exercise was associated with a 2.5-fold increase in neonatal myosin (a form of myosin found in growing muscle) staining (p = 0.0009) and an increase of 491 ± 137% (p < 0.0001) in IGF-I staining. Ultrastructural damage increased by 141 ± 59% after exercise training (p = 0.034). Strength increases were largest in those with the greatest increases in myosin, IGF-I, damage, and caloric intake during the trial. Frail, very old, elders respond robustly to resistance training with musculoskeletal remodeling, and significant increases in muscle area are possible with resistance training in combination with adequate energy intakes. It should be pointed out that this was a very old, very frail population with diagnoses of multiple chronic diseases. The increase in overall levels of physical activity have been a common observation in our studies [33,39,58]. Since muscle weakness is a primary deficit in many older individuals, increased strength may stimulate more aerobic activities like walking and cycling.
We examined the influence of increased dietary protein on the hypertrophic response to resistance exercise in a group of healthy older people [10]. These men and women were randomly assigned to a RDA group consuming 0.8 or 1.6 g protein · kg–1 · d–1. All of the subjects in this study were asked to participate in a high intensity resistance exercise training program (3 d/wk, 80% 1 RM) for three months. The subjects who consumed the higher protein level tended to show a greater hypertrophic response to the training. More recently we compared the effects of a meat-free, lacto-ovo vegetarian diet vs. a diet with meat on gains in muscle size from resistance exercise [7]. This study demonstrated that those subjects who consumed meat (as part of normal dietary intake) gained more muscle than those who excluded meat did.
Strength Training Effects in Older People
Strength training may increase balance through the improvement in strength of muscle involved in walking. Indeed ankle weakness has been demonstrated to be associated with increased risk of falling in nursing home patients [77]. However, balance training, which may demonstrate very little improvement in muscle strength, size, or cardiovascular changes has also been demonstrated to decrease the risk of falls in older people [80]. Tai Chi, a form of dynamic balance training that requires no new technology or equipment, has been demonstrated to reduce the risk of falling in older people by almost 50% [79]. As a component of the National Institute on Aging FICSIT trials (Frailty and Injuries: Cooperative Studies of Intervention Techniques), individuals aged 70+ were randomized to Tai Chi (TC), individualized balance training (BT), and exercise control education (ED) groups for 15 weeks [52]. In a follow-up assessment 4 months post-intervention, 130 subjects responded to exit interview questions asking about perceived benefits of participation. Both TC and BT subjects reported increased confidence in balance and movement, but only TC subjects reported that their daily activities and their overall life had been affected; many of these subjects had changed their normal physical activity to incorporate ongoing TC practice. The data suggest that when mental as well as physical control is perceived to be enhanced, with a generalized sense of improvement in overall well-being, older persons’ motivation to continue exercising also increases. Province et al. [60] examined the overall effect of many different exercise interventions in the FICSIT trials on reducing falls. While each these separate interventions were not powered to make conclusions about their effects on the incidence of falls in and elderly population, they did conclude that "all training domains, taken together under the heading of "general exercise" showed and effect on falls, this probably demonstrates the "rising tide raises all boats" principle, in which training that targets one domain may improve performance somewhat in other domains as a consequence. If this is so, then the differences seen on fall risk due to the exact nature of the training may not be as critical compared with the differences in not training at all." The use of a community-based exercise program for frail older people was examined [44] in a group of predominantly sedentary women over age 70 with multiple chronic conditions. The program was conducted with peer leaders to facilitate its continuation after the research demonstration phase. In addition to positive health outcomes related to functional mobility, blood pressure maintenance, and overall well-being, this intervention was successful in sustaining active participation in regular physical activity through the use of peer leaders selected by the program participants.
In addition to its effect on increasing muscle mass and function, resistance training can also have an important effect on energy balance [9]. Men and women participating in a resistance training program of the upper and lower body muscles required approximately 15% more calories to maintain body weight after 12 weeks of training when compared to their pretraining energy requirements. This increase in energy needs came about as a result of an increased resting metabolic rate, the small energy cost of the exercise, and what was presumed to be an increase in activity levels. While endurance training has been demonstrated to be an important adjunct to weight loss programs in young men and women by increasing their daily energy expenditure, its utility in treating obesity in the elderly may not be great. This is because many sedentary older men and women do not spend many calories when they perform endurance exercise, due to their low fitness levels. Thirty to forty minutes of exercise may increase energy expenditure by only 100 to 200 kcals with very little residual effect on calorie expenditure. Aerobic exercise training will not preserve lean body mass to any great extent during weight loss. Because resistance training can preserve or even increase muscle mass during weight loss, this type of exercise for those older men and women who must lose weight may be of genuine benefit.
In conclusion, progressive resistance exercise results in decreased nitrogen excretion and, thus, lower dietary protein needs. This has important implications for treatment of individuals with a wasting syndrome or cachexia, and particularly older men and women who experience involuntary weight loss. There is evidence that and increase in dietary protein intake will result in enhanced muscle hypertrophy when combined with high intensity resistance exercise training. Muscle strength training can be accomplished by virtually anyone. Many health care professionals have directed their patients away from strength training in the mistaken belief that it can cause undesirable elevations in blood pressure. With proper technique, the systolic pressure elevation during aerobic exercise is far greater than that seen during resistance training. Muscle strengthening exercises are rapidly becoming a critical component to cardiac rehabilitation programs as clinicians realize the need for strength as well as endurance for many activities of daily living. There is no other group in our society that can benefit more from regularly performed exercise, than the elderly. While both aerobic and strength conditioning are highly recommended, only strength training can stop or reverse sarcopenia. Increased muscle strength and mass in the elderly can be the first step towards a lifetime of increased physical activity and a realistic strategy for maintaining functional status and independence.
|
REFERENCES |
|---|
|
TOPABSTRACTINTRODUCTIONREFERENCES |
|---|
This article has been cited by other articles:
|
|
 |
|
  R. Hasegawa, M. M Islam, Sung Chul Lee, D. Koizumi, M. E Rogers, and N. Takeshima Threshold of lower body muscular strength necessary to perform ADL independently in community-dwelling older adults Clinical Rehabilitation, October 1, 2008; 22(10-11): 902 - 910. [Abstract] [PDF]
|
|
|
|
 |
|
 S. Al-Majid and H. Waters The biological mechanisms of cancer-related skeletal muscle wasting: the role of progressive resistance exercise. Biol Res Nurs, July 1, 2008; 10(1): 7 - 20. [Abstract] [PDF]
|
|
|
|
 |
|
 R. J. Manders, R. Koopman, M. Beelen, A. P. Gijsen, W. K. Wodzig, W. H. Saris, and L. J. van Loon The Muscle Protein Synthetic Response to Carbohydrate and Protein Ingestion Is Not Impaired in Men with Longstanding Type 2 Diabetes J. Nutr., June 1, 2008; 138(6): 1079 - 1085. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 D. K Houston, B. J Nicklas, J. Ding, T. B Harris, F. A Tylavsky, A. B Newman, J. S. Lee, N. R Sahyoun, M. Visser, S. B Kritchevsky, et al. Dietary protein intake is associated with lean mass change in older, community-dwelling adults: the Health, Aging, and Body Composition (Health ABC) Study Am. J. Clinical Nutrition, January 1, 2008; 87(1): 150 - 155. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 S. Bhashyam, P. Parikh, H. Bolukoglu, A. H. Shannon, J. H. Porter, Y.-T. Shen, and R. P. Shannon Aging is associated with myocardial insulin resistance and mitochondrial dysfunction Am J Physiol Heart Circ Physiol, November 1, 2007; 293(5): H3063 - H3071. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
R. Koopman, L. Verdijk, R. J. Manders, A. P Gijsen, M. Gorselink, E. Pijpers, A. J. Wagenmakers, and L. J. van Loon Co-ingestion of protein and leucine stimulates muscle protein synthesis rates to the same extent in young and elderly lean men. Am. J. Clinical Nutrition, September 1, 2006; 84(3): 623 - 632. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
