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Biomedical subjects

A Bonen

Publications and source records attributed to A Bonen.

At least 127 records · Page 7Linked to original sources

Insulin binding and 2-deoxy-D-glucose uptake in fast- and slow-twitch mouse skeletal muscle at 18 and 37 degrees C.

Insulin binding, insulin degradation, and 2-deoxyglucose uptake were examined at 18 and 37 degrees C in soleus and extensor digitorum longus muscles of mice. Insulin binding and degradation were greater in the soleus than in the extensor digitorum longus at both temperatures (p less than 0.05). At 37 degrees C, binding was decreased in both muscles while percentage degradation was increased in comparison with 18 degrees C (p less than 0.05). Dose--response curves (percentage of binding at 4 nM of insulin) remained the same for both muscles at the two temperatures. Basal (no insulin) 2-deoxyglucose uptake was increased at 37 degrees C in the extensor digitorum longus but not the soleus. Insulin responsiveness in terms of the amount of 2-deoxyglucose taken up per femtomole of insulin bound was almost identical for the two muscles at 18 degrees C, whereas at 37 degrees C it was increased more in the soleus than in the extensor digitorum longus. The results indicate that in the presence of physiological concentrations of insulin (0.2-4 nM), insulin binding trends are minimally affected by increased temperature. In contrast, the ability of insulin to stimulate 2-deoxyglucose uptake varies between the two temperatures, and at the higher temperature between fast- and slow-twitch muscle.

Animals↗

Effects of exercise on insulin binding and glucose metabolism in muscle.

To elucidate the mechanism of enhanced insulin sensitivity by muscle after exercise, we studied insulin binding, 2-deoxy-D-[1-14C]glucose (2-DOG) uptake and [5-3H]glucose utilization in glycolysis and glycogenesis in soleus and extensor digitorum longus (EDL) muscles of mice after 60 min of treadmill exercise. In the soleus, glycogenesis was increased after exercise (P less than 0.05) and remained sensitive to the action of insulin. Postexercise insulin-stimulated glycolysis was also increased in the soleus (P less than 0.05). In the EDL, glycogenesis was increased after exercise (P less than 0.05). However, this was already maximal in the absence of insulin and was not further stimulated by insulin (0.1-4 nM). The disposal of glucose occurred primarily via the glycolytic pathway (greater than 60%) in the soleus and EDL at rest and after exercise. The uptake of 2-DOG uptake was not altered in the soleus after exercise (4 h incubation at 18 degrees C). However, with 1-h incubations at 37 degrees C, a marked increase in 2-DOG uptake after exercise was observed in the soleus (P less than 0.05) in the absence (0 nM) and presence of insulin (0.2-4 nM) (P less than 0.05). A similar postexercise increase in 2-DOG uptake occurred in EDL. Despite the marked increase in glucose uptake and metabolism, no changes in insulin binding were apparent in either EDL or soleus at 37 degrees C or 18 degrees C. This study shows that the postexercise increase of glucose disposal does not appear to be directly attributable to increments in insulin binding to slow-twitch and fast-twitch muscles.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Muscle glycogen repletion after exercise in trained normal and diabetic rats.

We hypothesize that training results in a faster and greater repletion of glycogen in skeletal muscles of normal and diabetic rats. Normal male Sprague-Dawley rats (100-140 g) were divided into two groups--one to train by treadmill running for 10 wk and the other to remain sedentary. Forty-eight hours after the last training session the rats of both groups were exercised to exhaustion. One subgroup of each was fed oral glucose (3 g/kg) at exhaustion and killed 60 min later. The other was killed at exhaustion. The glycogen concentration of soleus, plantaris, and red and white gastrocnemius was determined in all rats. The trained group had higher glycogen levels after glucose feeding in all muscles (P less than 0.002) and repleted their muscle glycogen more rapidly (P less than 0.05). However, in diabetic rats (45 mg streptozotocin/kg body wt) the trained and sedentary rats have similar glycogen levels and glycogen repletion rates in all muscles. Compared with the normal trained rats, the diabetic trained rats had slower glycogen repletion rates (P less than 0.05).

Animals↗

Effects of menstrual cycle on metabolic responses to exercise.

Selected substrate and hormonal responses to exercise were compared in two phases of the menstrual cycle. Exercise-induced changes in substrate [glucose, lactate, free fatty acids (FFA), glycerol] and hormonal patterns [luteinizing hormone (LH), follicle-stimulating hormone (FSH), insulin, progesterone (P), growth hormone (GH), cortisol] were compared in the follicular and luteal phases of the menstrual cycle in 24-h-fasted (n = 5), glucose-loaded (n = 6; 1.50 g/kg, 20% solution), and control subjects (n = 8). A treadmill walk was maintained for 60 min (30 min, 40% VO2 max; 30 min, 80% VO2 max). Blood samples were obtained 5 min before, 15, 30, 45, and 60 min during, and 30 min after exercise. In the glucose group a blood sample was also taken 20 min before exercise, and glucose was ingested 15 min before exercise. Within each nutritional group the metabolic and endocrine responses to exercise were similar in the two phases for glucose, lactate, glycerol, LH, FSH, and cortisol (P greater than 0.05). In the glucose group the FFA response was lower in the luteal phase (P less than 0.05). In the fasted subjects insulin and GH responses were elevated in the luteal phase (P less than 0.05). P responses in the control and glucose groups were markedly greater in the luteal phase (P less than 0.05). In the fasted subjects no alteration in P occurred in either phase (P less than 0.05), and the LH concentration was lower in these subjects relative to the control groups (P less than 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗

Physical training in diabetic rats: effect on glucose tolerance and serum lipids.

The effect of 10 wk of treadmill training on glucose tolerance, serum lipids, tissue lipoprotein lipase (LPL) activities, and triglyceride secretion rates (TGSR) were studied in normal and diabetic rats. Training had little effect on the glucose tolerance of the normal rats but ameliorated the deterioration of glucose intolerance seen in the sedentary diabetic rats. Trained diabetic and normal rats had lower serum triglycerides than their sedentary counterparts [diabetic 34 +/- 5 vs. 61 +/- 4 (means +/- SE); normal 34 +/- 3 vs. 50 +/- 3 mg/dl]. This hypotriglyceridemic effect was associated with a reduction in the TGSR in the trained rats (diabetics 0.34 +/- 0.05 vs. 0.51 +/- 0.02; normal 0.48 +/- 0.05 vs. 0.53 +/- 0.04 mg/min). There were no differences in the tissue LPL activities (soleus, gastrocnemius, epididymal fat, and heart) between the trained and sedentary rats in both groups. Training also did not affect the serum cholesterol and the high-density lipoprotein cholesterol levels in both groups of rats.

Animals↗

The effects of immobilization and of electrical stimulation on muscle glycogen and myofibrillar ATPase.

This study observed biochemical changes that occur when an athlete's limb is immobilized for six weeks, and determined if electrical stimulation could alter any of these changes. A control group (n = 3) and a stimulation group (n = 6) who had undergone major knee surgery, consented to a series of muscle biopsies of the vastus lateralis muscle. Both groups engaged in standard rehabilitative procedures following cast removal. The stimulation group's therapy also consisted of electrical stimulation (f = 2500 Hz.) of the quadricep group. The results indicate that ATPase activity decreased in the control group during the immobilization period (from 0.321 +/- 0.095 mumoles Pi/mg./min. to 0.205 +/- 0.032 mumoles Pi/mg./min.) but not in the stimulation group (from 0.268 +/- 0.022 mumoles Pi/mg./min. to 0.296 +/- 0.073 mumoles Pi/mg./min.), p less than 0.05. The stimulation did not appear to have any effect on glycogen concentrations. It is suggested that electrical stimulation retards the decrements in biochemical characteristics of human muscle due to immobilization.

Adenosine Triphosphatases↗

Needle muscle biopsy: techniques to increase sample sizes, and complications.

Muscle biopsy samples of the vastus lateralis (444) using Bergström needles were obtained under local anesthesia from 43 normal athletes and 17 patients with suspected muscle disease. Five biopsy techniques were used and sample weights were compared. Biopsy during isometric muscle contraction was the most effective technique, yielding a mean sample weight 3.2 times that obtained by simple needle insertion, the least effective method (p less than 0.001). Use of a 5mm rather than 4mm diameter needle raised the mean (+/- 1 SD) sample weight to 35mg (+/- 7.3) from 13.7mg (+/- 5.2) (p less than 0.001), and total yields of 150-200mg were easily obtained by resampling. No difficulties were encountered in the biochemical, histochemical, or immunofluroescent evaluations of these samples. Several subjects were assessed for complications at various times following biopsy. Mild to moderate symptoms, signs, and investigative findings were noted in some subjects within the first few days. Only one person reported subsequent persistent symptoms at the biopsy site-a mild "awareness" during athletic exertion. The higher-yield techniques were generally safe, well tolerated, and provided samples of sufficient size and quality for multiple simultaneous studies. Needle biopsy appears to warrant increased use in physiatric research and clinical practice.

Adolescent↗

Profiles of selected hormones during menstrual cycles of teenage athletes.

Concentrations of luteinizing hormone (LH), follicle-stimulating hormone (FSH), progesterone (P), 17 alpha-hydroxyprogesterone (17 alpha OHP), 17 beta-estradiol (E2), and prolactin (HPr) were monitored for one complete menstrual cycle in teenage swimmers, a gynecologically age-matched control group, and a group of fertile adult women. The swimmers experienced anovulatory menstrual cycles. The time from the LH surge to the onset of menses ("luteal" phase) was very short in the swimmers (4.5 +/- 0.6 days) in comparison with the lengths of these phases in the adults (13.4 +/- 1.7 days; P less than 0.05) and in the control group (7.8 +/- 3.0 days; P less than 0.05). In the follicular phase the swimmers' LH concentration was elevated and their FSH concentration was depressed in comparison with each of the other groups (P less than 0.05). Luteal phase FHS, P, E2, and 17 alpha OHP were also lower in the swimmers (P less than 0.05), as was HPr (0.05 greater than P less than 0.10). Gonadotropin concentrations and luteal phase P concentrations were not different (P greater than 0.05) in the adults and the control group. The present findings indicate that the corpora lutea in the swimmers were not functioning properly. It is likely that the swimmers' strenuous daily 2-4 h training regimen is implicated.

Adolescent↗

Glucose ingestion before and during intense exercise.

Glucose and insulin responses were compared in glycogen depleted subjects when glucose (1.5 g/kg) was ingested 15 min before (n = 7) or during (min 3-5) intense exercise (80% VO2 max; n = 8). A nonexercise group (n = 8) and a no-glucose group (n = 8) were also included for comparisons. A 36- to 44-h fast, combined with exhaustive exercise to deplete muscle glycogen, (congruent to 80% in pilot studies) suggested that the subjects initiated exercise with substantially depleted hepatic and muscle glycogen reserves. With no glucose ingestion, blood glucose decreased during exercise (P less than 0.05) and blood lactate (HLa congruent to 3.8 mM) and the respiratory exchange ratio (R) remained low (0.83); with glucose ingestion before or during exercise, HLa concentrations were doubled (7.3 mM) and R was greater (0.90-0.92; P less than 0.05). Although insulin concentrations decreased rapidly to basal levels within 10 min after the onset of exercise in the preexercise glucose group (P less than 0.05), blood glucose continued to decrease throughout exercise. No such decrease occurred in the subjects who ingested glucose during exercise, nor did insulin concentrations change markedly in this group (P greater than 0.05). The HLa and R data indicated that a considerable portion of glucose was metabolized during exercise. Differences in the preexercise insulin environment appear to exert a persistent effect on glucose uptake throughout exercise.

Blood Glucose↗

Insulin binding and glucose uptake differences in rodent skeletal muscles.

Insulin binding and 2-deoxy-d-glucose uptake were compared in the soleus, plantaris, and extensor digitorum longus (EDL) muscles, in vitro, since the known biochemical profile of the soleus differs markedly from the other two. The present study showed that insulin binding increased in all three muscles with increasing concentrations of insulin in the range of 0.2-30 nM. However, the increase in binding of insulin to soleus at each insulin concentration exceeded that observed in the other two muscles (P less than 0.05). Differences between the plantaris and EDL were not significant. The quantity of insulin bound at each concentration also increased more rapidly in the soleus than in either the plantaris (P less than 0.05) or EDL (P less than 0.05). Basal and insulin-stimulated uptake of 2-deoxy-d-glucose was also greater in the soleus than in the other muscles (P less than 0.05). Maximal 2-deoxy-d-glucose uptake occurred at 1 nM insulin in each of the three muscles. These results indicate that in metabolically distinct types of skeletal muscles glucose uptake can differ markedly, and this is related to differences in the insulin binding capacities of these muscles.

Animals↗

Maximal oxygen uptake during free, tethered, and flume swimming.

The purpose of this study was 1) to compare the maximal oxygen uptake (VO2max) obtained in swimmers during tethered swimming, free swimming, and flume swimming, and 2) to determine whether an arm-ergometer test would provide comparable results. In the first experiments the VO2max for tethered swimming (2.67 +/- 0.26 l/min) and flume swimming (2.62 +/- 0.26 l/min) were not different (P greater than 0.05) and were highly correlated (r = 0.99). However, with arm ergometry a significantly lower VO2max (2.36 +/- 0.24 l/min) occurred from those found in the two swimming tests (P less than 0.05). Other experiments demonstrated that the tethered swimming VO2max (3.53 +/- 0.27 l/min) and the free swimming VO2max (3.55 +/- 0.28 l/min) also provide results that were similar (P greater than 0.05) and highly correlated with each other (r = 0.99). Differences between tethered and flume swimming, and tethered and free swimming were small, being 1.2 +/- 1.6% and 0.6 +/- 0.9%, respectively. Differences between tethered swimming and arm ergometry VO2max were large, 14.7 +/- 2.4%, despite the high correlation (r = 0.97) between these measurements. Predictions of a swimming VO2max from the arm-ergometer data yielded a considerable error (+/-7.1% and +/-7.4%). The present results indicate that flume swimming, free swimming, and tethered swimming yield essentially identical VO2max results.

Adolescent↗

Functional overload of rat fast-twitch skeletal muscle during development.

The intent of this study was observe the effects of different training programs on selected biochemical properties in lantaris muscle of young rats. Littermates (10 days old) were assigned to endurance (E), sprint (S), and control (C) groups. Animals in each group were partitioned into either 21- or 51-day groups and 10-day controls. Myofibrillar ATPase activities at 21 and 51 days (0.720 +/- 0.028 and 0.719 +/- 0.012 mumol Pi.mg-1.min-1) were higher than the 10-day activity (0.191 +/- 0.022 mumol Pi.mg-1.min) for C animals (P less than or equal to 0.05). At 51 days, E training resulted in a lower ATPase activity than both the 21-day E and 51-day C animals (P less than or equal to 0.05). Sarcoplasmic reticulum protein yield and Ca2+ binding and uptake increased from 10 to 51 days for C animals (P less than or equal to 0.05). The Ca2+-binding ability for 51-day E animals (26.1 +/- 3.4 nmol Ca2+/mg) was greater than for the 51-day C animals (20.0 +/- 1.69 nmol Ca2+/mg) (P less than or equal to 0.05). The plantaris muscle of S animals were not altered at 21 and 51 days compared to C animals were not altered at 21 and 51 days compared to C animals (all variables). The results suggest that exercise training alters the biochemical characteristics of skeletal muscle during growth.

Adenosine Triphosphatases↗

The effects of hypercapnia on metabolic responses to progressive exhaustive work.

Altering CO2 storage has been shown to influence lactate metabolism. However, the metabolic effects on man during physical activity have not been well documented. Subjects (n = 8) performed a progressive bicycle test (beginning at 0 and increasing 30 W every 4 min to exhaustion) on two occasions (once inspiring compressed air and once 4% CO2 and 21% O2). The work time, peak Vo2, VCO2, and HR achieved were the same in the two trials for each subject. The VI was significantly (p less than or equal to 0.05) elevated throughout the CO2 work and the recovery. The O2 debt increased from a mean of 5.87 to 7.761 with CO2, although the difference was not significant. Blood lactate was lower (p less than or equal to 0.05) from the onset of the work and throughout both the exercise and the 30 min. recovery period. Peak lactate was decreased from a mean of 9.59 to 6.99mM.1(-1). The oxygen cost of the work was not altered but the blood lactate response to the activity was significantly depressed. The reduction in lactate could be due to glycolytic inhibition and enhanced fat metabolism. The data support, but do not prove, this hypothesis.

Adult↗

Hormonal responses during intense exercise preceded by glucose ingestion.

In this study the metabolic and endocrine responses during and after intense exercise (80% VO2max) were investigated under a) normal conditions b) diminished intra-muscular carbohydrate supplies, and c) an augmented supply of blood glucose. For this purpose four experimental conditions were employed, rest (R), rest with glucose ingestion (RG), exercise (E), and exercise with glucose ingestion (EG). On the exercise days the subjects exercised twice for 30 min with 2 hour rest between each bout. When glucose was ingested 15 min prior to exercise an accelerated glucose decrease occurred in the first 15 min of exercise (-35 mg/100 ml) (P less than 0.05). Insulin concentrations also decreased sharply throughout this exercise period (EG) (P less than 0.05). After exercise, an insulin rebound occurred in EG that was not observed after exercise in E. In EG, min (180-210) the exercise-induced GH increase was diminished (P less than 0.05) in comparison to the response observed during E. No differences were found in the cortisol responses during or after E and EG. (P greater than 0.05). It is concluded that moderate muscle and hepatic glycogen loss, induced several hours prior to exercise, does not alter the responses of cortisol, GH and insulin during exercise. Increasing the available glucose prior to exercise does not alter the cortisol or insulin responses during exercise but the diminished GH concentrations suggest that the release of this hormone is attenuated directly or indirectly by glucose and/or insulin.

Adult↗

Effects of exercise on the serum concentrations of FSH, LH, progesterone, and estradiol.

The effects of 30 min of exercise (74.1 +/- 3.0% (VO2), on the responses of progesterone (P), estradiol (E2), follicle stimulating hormone (FSH), and luteinizing hormone (LH) were investigated in 10 women. With such exercise significant increments occurred in P (37.6 +/- 9.5%) and E2 (13.5 +/- 7.5%) (P less than 0.05), whereas no changes were observed in FSH and LH (p greater than 0.05). Exercise in the luteal phase and during menses provoked similar changes in P, but E2 concentrations remained unchanged when exercise occurred during menses (p greater than 0.05). With 8-11 weeks of training the menstrual cycles were quite irregular and retesting of subjects in the same phase of the cycle was not possible. Yet, when subjects were retested after training, no changes occurred in P, E2 or LH (p greater than 0.05) but a decrement did occur in FSH (p less than 0.10). Thus, heavy exercise in untrained subjects provokes significant increments in ovarian hormones, whereas no such increments are observed in trained subjects exercising at the same absolute workload.

Adult↗

A multiple regression model for blood lactate removal in man.

After exercise the lactate (La) removal from blood occurs significantly faster during moderate exercise than at rest. However, under both conditions there are considerable inter-individual differences in La removal. These differences in man may depend on the slow-twitch (ST) fiber content of muscle (X1), the La concentration in blood (X2), and the intensity of the recovery exercise (X3). Therefore, multiple regression models were obtained to describe La removal rates with these variables. In 10 women La concentrations were increased via a 6 min bicycle ergometer ride (87% VO2max) and blood La concentrations were measured every 5 min during 20 min resting and active recovery periods (29--49% VO2max). For resting recovery only the initial La concentration after the 6 min exercise provided a significant description for La removal in 8 subjects (P = 0.03). However, for the active recovery a highly significant description for La removal was obtained: La removal rate (mM/1 . min) = 0.773 x 10-2X1 + 0.321 x 10-1X2 - 0.120 x 10-1X3 + 0.202 (R = 0.91; P = 0.01). The statistical independence (P greater than 0.010) of each of these variables in the model suggests that each is contributing uniquely to the total removal rate of La observed during an active recovery period. The relationship between La removal and %ST fibers may be related to the metabolic and anatomical features of these fibers, the La concentration probably reflects the significance of the mass action effect of La, and the intensity of exercise reflects the role of the muscle's metabolic rate. The present results illustrate that the removal of blood lactate is influenced by the interactive effects of the intensity of the recovery exercise, blood lactate concentration and the ST fiber content of muscle.

Adult↗