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At least 577 records · Page 32Linked to original sources

PubMed1999

Behaviour of house mice artificially selected for high levels of voluntary wheel running.

We have developed a novel model to study the correlated evolution of behavioural and morphophysiological traits in response to selection for increased locomotor activity. We used selective breeding to increase levels of voluntary wheel running in four replicate lines of laboratory house mice, Mus domesticus, with four random-bred lines maintained as controls. The experiment presented here tested for correlated behavioural responses in the wheel-cage complex, with wheels either free to rotate or locked (environmental factor). After 13 generations, mice from selected lines ran 2.2 times as many revolutions/day as controls on days 5 and 6 of initial exposure to wheels (10 826 versus 4890 revolutions/day, corresponding to 12.1 and 5.5 km/day, respectively). This increase was caused primarily by mice from selected lines running faster, not more minutes per day. Focal-animal observations confirmed that the increase in revolutions/day involved more actual running (or climbing in locked wheels), not an increase in coasting (or hanging). Not surprisingly, access to free versus locked wheels had several effects on behaviour, including total time spent in wheels, sniffing and biting. However, few behaviours showed statistically significant differences between the selected and control lines. Selection did not increase the total time spent in wheels (either free or locked), the frequency of nonlocomotor activities performed in the wheels, nor the amount of locomotor activity in cages attached to the wheels; as well, selection did not decrease the amount of time spent sleeping. Thus, wheel running is, at the genetic level, a largely independent axis of behaviour. Moreover, the genetic architecture of overall wheel running and its components seem conducive to increasing total distance moved without unduly increasing energy or time-related costs. The selection experiment also offers a new approach to study the proximate mechanisms of wheel-running behaviour itself. For example, frequencies of sniffing and wire biting were reduced in selected females but not males. This result suggests that motivation or function of wheel running may differ between the sexes. Copyright 1999 The Association for the Study of Animal Behaviour.

Journal Article↗

PubMed1993

A new method for the evaluation of anaerobic running power in athletes.

A new maximal anaerobic running power (MARP) test was developed. It consisted of n.20-s runs on a treadmill with a 100-s recovery between the runs. During the first run the treadmill speed was 3.97 m.s-1 and the gradient 5 degrees. The speed of the treadmill was increased by 0.35 m.s-1 for each consecutive run until exhaustion. The height of counter-movement jumps and blood lactate concentration ([la-]b) were measured after each run. Submaximal ([la-]b = 3 mmol.l-1 and 10 mmol.l-1) and maximal speed and power (W3mmol, W10mmol and Wmax, respectively) were calculated and W was expressed in oxygen equivalents according to the American College of Sports Medicine equation. Thirteen male athletes whose times over 400 m ranged from 47.98 s to 54.70 s served as subjects. In the MARP-test the speed at exhaustion was 6.89 (SD 0.28) m.s-1 corresponding to a Wmax of 118 (SD 5) ml.kg-1 x min-1. The peak [la-]b after exhaustion was 17.0 (SD 1.6) mmol.l-1. A significant correlation (r = 0.89, P < 0.001) was observed between the Wmax and the average speed in the 400-m sprint. The maximal 20-m sprinting speed on a track and W10mmol correlated with both the Wmax and the 400-m speed. It was concluded that the new method allows the evaluation of several determinants of maximal anaerobic performance including changes in the force-generating capacity of leg muscles and [la-]b relative to the speed of the sprint running. the [la-]b at submaximal sprinting speed was suggested as describing the anaerobic sprinting economy.

Adult↗

PubMed2001

Differential sensitivity to acute administration of cocaine, GBR 12909, and fluoxetine in mice selectively bred for hyperactive wheel-running behavior.

RATIONALE: To study the neural basis of genetic hyperactivity, we measured acute drug responses of mice (Mus domesticus) from four replicate lines that had been selectively bred (23-24 generations) for increased running-wheel activity. OBJECTIVES: We tested the hypothesis that the high-running lines would respond differently to cocaine, GBR 12909, and fluoxetine (Prozac) compared with four replicate, random-bred, control lines. We also tested the hypothesis that the high-running lines would display hyperactivity in cages without wheels. METHODS: Drug trials were conducted at night, during peak activity, after animals were habituated (3 weeks) to their cages with attached wheels. Revolutions on wheels 10-40 min post-injection were used to quantify drug responses. In a separate study, total photobeam breaks (produced on the first and second 24-h period of exposure) were used to quantify basal activity in animals deprived of wheels. RESULTS: Cocaine and GBR 12909 decreased wheel running in selected lines by reducing the average speed but not the duration of running, but these drugs had little effect in control lines. Fluoxetine reduced running speed and duration in both selected and control animals, and the magnitude of the reduction was proportional to baseline activity. Basal activity in animals deprived of wheels (quantified using photobeam breaks) was significantly higher in selected than control lines on the second day of testing. CONCLUSIONS: These results suggest an association between genetically determined hyperactive wheel-running behavior and dysfunction in the dopaminergic neuromodulatory system. Our selected lines may prove to be a useful genetic model for attention deficit hyperactivity disorder.

Animals↗

PubMed2000

Running wheel size influences circadian rhythm period and its phase shift in mice.

Running wheels are widely used in studies on biological rhythms. In mice wheel diameters have ranged from 11 cm to 23 cm. We provided mice with running wheels of two different sizes: 15 cm diameter and 11 cm diameter. The amount of running in the 12-h light:12-h dark condition and the endogenous period of wheel running in constant darkness was determined over 40 days. On the 1st day in constant darkness all animals were exposed to a 15-min light pulse at circadian time 13. The animals in the small wheel ran significantly less both in 12 h light: 12 h dark and constant darkness, and showed a longer endogenous period in constant darkness compared to animals in the large wheel. Moreover, after the light pulse at circadian time 13, mice in the small wheel showed a significantly smaller phase delay in running wheel activity than mice in the larger wheels. The data suggest that the magnitude of a photic phase shift depends on the amount and timing of activity the animals display in relation to this stimulus. It can be concluded that technical features of the running wheel can influence the circadian period of wheel running.

Animals↗

PubMed1999

Loosening of single versus double running sutures in penetrating keratoplasty for keratoconus.

PURPOSE: Purpose of the study was to evaluate single versus double running sutures in penetrating keratoplasty for keratoconus with respect to suture loosening. METHODS: Eighty-eight patients were consecutively operated for keratoconus by the same surgeon with the same surgical technique. For the first 45 patients, a single running 10-0 nylon suture was used. For the remaining 43 patients, double running 10-0 nylon sutures were taken. RESULTS: Suture loosening was observed significantly (P<0.001; Chi-Square test) more often in the patients with a single running suture (12/45=27%) than in the patients with double running sutures (0/43=0%). CONCLUSIONS: The results indicate that double running sutures in comparison to a single running suture may be helpful in preventing suture loosening in penetrating keratoplasty for keratoconus.

Corneal Transplantation↗

PubMed1999

Complete reversal of run-down in rabbit cardiac Ca2+ channels by patch-cramming in Xenopus oocytes; partial reversal by protein kinase A.

The rabbit cardiac Ca2+ channel (alpha1C) expressed in Xenopus oocytes exhibited a complete run-down of ionic currents when cell-attached patches were excised. The alpha1C channel was expressed alone or was coexpressed with the accessory beta2a or beta1b subunit. The catalytic subunit of protein kinase A (PKAc) and MgATP were capable of delaying the run-down of single-channel currents. In 33% of the alpha1C patches, and 26% of the alpha1C+beta2a patches, inclusion of PKAc in the bath solution delayed the run-down for a maximum of 20 min. In experiments where PKAc in the bath was not sufficient to delay the run-down of channel activity, insertion of the patch back into the oocyte (patch-cramming) could restore channel activity. Gating currents were also measured in the alpha1C+beta1b channel and were not subject to any run-down, even after the complete run-down of ionic currents. The results presented here reveal that PKAc is capable of delaying the run-down of currents in a subset of patches. The patch-cramming results suggest that a cytoplasmic factor, in addition to phosphorylation of the channel (by PKAc), may be involved in the maintenance of channel activity.

Adenosine Triphosphate↗

PubMed1986

Effects of rate and distance of procurement wheel-running on saccharin-and-sucrose solution drinking by non-deprived rats.

Four non-deprived rats received daily sessions of 20 min access to a saccharin-and-sucrose solution following various prior activities, in an attempt to disentangle the normally confounded roles of time spent, amount and rate of procurement responding in causing an increase in consumption once access is gained. After the normal rate of running (approx 35 m/min) was established, six conditions were run in random order, involving waiting zero and 2.5 min in an immobilised running-wheel, and running, with the wheel rotated by a motor, in four conditions formed by combining two speeds (12 and 30 m/min) with two distances (12 and 30 m), prior to access to the solution. Drinking increased with the speed of prior running, and to a lesser extent with the distance run, but was not related systematically to the time spent running. It is suggested that information from the animal's own behavior in gaining access to a commodity, particularly the rate of energy expenditure, may influence its utilisation of the commodity by affecting the rate of subsequent consummatory responding.

Animals↗

PubMed1992

Use of running wheels regulates the effects of the ovaries on circadian rhythms.

Free-running circadian rhythms in core temperature, wheel-running and general locomotor activity were studied in ovariectomized or intact female rats housed with or without access to a running wheel. No differences in the monitored parameters were found between the intact and ovariectomized rats without a wheel. In the presence of a wheel, however, the intact rats differed from those that had been ovariectomized by displaying a shorter circadian period, an increased amplitude of the temperature rhythm, and strikingly higher rates of wheel-running and general locomotor activity. After estradiol treatment, the ovariectomized rats with a wheel developed a small increase in the temperature amplitude, and also in the correlation between wheel-running and general locomotor activity; these changes were not associated with a significant increase in wheel-running or a shortening of the circadian period. We conclude that some of the differences in circadian function between intact and ovariectomized rats are due to the differential use they make of running wheels, when available, and not directly attributable to the absence or presence of gonadal steroids.

Animals↗

PubMed1992

The effects of wheel running, a light/dark cycle, and the instrumental cost of food on the intake of food in a closed economy.

The effects of wheel running on the food intake of rats, and on the extent to which rats defend their daily food intake against increases in the instrumental cost of food, were studied in a closed economy. Rats lived in cages that were attached to running wheels. Within each cage, water was freely available and lever pressing was required for access to food; a fixed number of presses was required for the delivery of a single food pellet. All cages were located in an environmental chamber where a 12-h light/dark cycle was continuously maintained. During stage I, the entrance to each running wheel was blocked and two series (series 1 and 2) of progressively increasing fixed ratios (FRs) of presses per pellet were imposed. Each FR was used for a single day. During stage II, the entrance to each wheel was unblocked and wheel running and food intake were allowed to stabilize. During stage III, the running wheels remained available and the FR was again increased (series 3). In stage I, increases in the FR reduced food intake proportionally more rapidly during the light than during the dark, and this reduction in the light was greater during series 1 than series 2. During stage II, food intake was transiently reduced during the first week of access to running wheels, but recovered by the end of the second week. During stage III, increases in the FR again reduced food intake proportionally more rapidly during the light than during the dark. Wheel running did not affect the extent to which food intake was reduced within light and dark periods.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1985

Operantly conditioned running: effects on brain catecholamine concentrations and receptor densities in the rat.

It was hypothesized that endurance exercise results in an alteration in the brain monoamine systems. Rats were trained to run for food reinforcement on a variable ratio schedule in running wheels. Yoked control rats were also allowed to run but were not specifically reinforced for running. The animals ran 5 days per week for 8 weeks and were sacrificed 48 hours after the last endurance training session. The brains were assayed for norepinephrine and dopamine concentrations and beta-adrenergic (3H-dihydroalprenolol binding) and dopaminergic (3H-spiroperidol binding) receptor densities. Changes in norepinephrine concentration and beta-adrenergic receptor densities were not significantly different between reinforced running and yoked control groups. Dopamine concentrations were significantly higher while dopamine receptor densities were significantly lower in the reinforced running group. These results suggest that chronic running elevates dopamine secretion and consequently produces a compensatory down-regulation of dopaminergic receptor sites. The relationship of these changes to motor activity and to the antidepressant effects of exercise are discussed.

Animals↗

PubMed1987

Opioid-induced linear running in obese (ob/ob) and lean mice.

Earlier research has shown that opioids stimulate behavioral activation in mice whereas opioid antagonists attenuate this activation. We conducted an experiment to determine the dose-response curve of FK33824, a potent Met-enkephalin analogue. FK33824 produced an unusual form of behavioral activation we called "linear running" in which the mice ran continuously in one direction and were nearly oblivious to environmental stimuli. This may be the kind of running that occurs naturally during migration. Wheel running activity of genetically obese (ob/ob) and lean (C57BL/6J ?/+) mice was measured following the intracerebroventricular infusion of 0.1, 1.0, 10.0 and 100.0 ng of FK33824. The lowest dose did not alter baseline running, whereas the 1.0 and 10.0 ng doses significantly increased running in both genotypes. We found a genotype difference with the highest dose tested, the lean mice ran at baseline levles and displayed ataxia whereas the obese mice continued to show increased running without ataxia. We hypothesize that genetic differences in the enkephalin mechanisms of C57 lean and obese mice are responsible for linear running.

Animals↗

PubMed2004

Comparison of social ranks based on worm-running and aggressive behaviour in young domestic fowl.

Worm-running is behaviour in which a chick runs carrying a worm-like object while flock mates follow and attempt to grab the object from its beak. We hypothesised that social ranks based on worm-running frequency are stable over time and are positively correlated with social ranks based on success in aggressive interactions when older. At 8-12 days of age, we scored worm-running in 17 groups of 12 female White Leghorn chicks during three 10-min tests. Based on instantaneous scans at 5-s intervals, the bird carrying the 'worm' most often was placed in rank one and so on down the rank order. These tests were repeated at 68-70 days of age. An aggression index for each bird was calculated as the number of aggressive acts given, divided by the number given and received, during three 1-h observation periods when the birds were 68-70 days. Ranks obtained in worm-running tests were positively correlated over the two age periods (P < 0.05) but were not correlated with ranks based on the aggression index (P > 0.05). Our results indicate that worm-running ranks are not predictive of success in aggressive interactions. Instead, worm-running fits some criteria for play.

Aggression↗

PubMed2004

Endurance treadmill training in rats alters CRH activity in the hypothalamic paraventricular nucleus at rest and during acute running according to its period.

Running training on the treadmill increases the resting hypothalamic corticotropin-releasing hormone (CRH) content in rats, though is still unknown whether and how it occurs in the parvocellular region of the hypothalamic paraventricular nucleus (PVN) where is a predominant region of pituitary-adrenal activity and where CRH and arginine vasopressin (AVP) are colocalized. We thus aimed at examining whether treadmill training would alter the CRH and AVP mRNA levels in the PVN at rest and during acute running with different lengths of a training regime. Male Wistar rats were subjected to treadmill running (approximately 25 m/min, 60 minutes/day, 5 times/week) for training regimes of 0, 1, 2 or 4 weeks. All training regimes induced an adrenal hypertrophy. Plasma corticosterone levels before acute running increased with lengthening the training period. Four weeks of training produced a significant increase in the resting CRH, but not AVP, mRNA levels in the PVN though relatively shorter training regimes did not. Acute responses of lactate and ACTH release were reduced after 2 and 4 weeks of training, respectively. The responsive PVN CRH mRNA level to acute running decreased with 4 weeks of training but increased with relatively shorter training regimes. These results indicate that running training changes the PVN CRH biosynthetic activity with the regime lasting for 4 weeks, which follows adaptive changes in adrenal functions. Thus, running training-induced changes in hypothalamic CRH activity would originate from the PVN and be induced according to the training period.

Adrenal Glands↗

PubMed2006

Wheel running and fluoxetine antidepressant treatment have differential effects in the hippocampus and the spinal cord.

Exercise and antidepressants used independently have been shown to increase hippocampal brain-derived neurotrophic factor (BDNF) and neurogenesis. Despite the fact that patients with depression are often prescribed both, the effects of the exercise and fluoxetine antidepressant treatment used in combination are unknown. Using C57Bl/10 female mice, BDNF protein, insulin-like growth factor 1 (IGF-1) protein and neurogenesis were measured in the hippocampus after 21 days of wheel running, 21 days of fluoxetine antidepressant therapy (daily i.p. injections of 5 mg/kg, 10 mg/kg or 25 mg/kg) and the combination of the two. BDNF protein and cytogenesis/neurogenesis increased in the hippocampus with fluoxetine (high dose), but not wheel running. Hippocampal IGF-1 protein did not change with either treatment. There were no synergistic effects of combining exercise and fluoxetine treatment. Recent reports have also shown that exercise induces molecular mechanisms that benefit the spinal cord and can improve recovery after spinal cord injury (SCI); therefore, we repeated the assays in the spinal cord. Results showed that BDNF, IGF-1 and neurogenesis behave independently in the hippocampus and spinal cord. BDNF protein did not change in the spinal cord with either wheel running or fluoxetine treatment. Spinal cord IGF-1 protein did not change with wheel running, but it decreased with fluoxetine (high dose). Furthermore, spinal cord cytogenesis decreased with fluoxetine treatment. The combined wheel running and fluoxetine groups did not show synergistic results. Thus, the hippocampus and the spinal cord respond in distinct ways to wheel running and fluoxetine, and a prior induction of BDNF, IGF-1 or cytogenesis is unlikely to be the mechanism for wheel running providing a margin of protection against SCI.

Animals↗

PubMed1999

Prevalence and characteristics of red light running crashes in the United States.

About 40% of motor vehicle crashes occur at intersections. In recent years, the number of crashes at traffic signals has increased considerably. A major cause of such crashes is drivers disregarding traffic signals. Despite concerns about the frequent occurrence of red light violations and the significant crash consequences, relatively little is known about the overall prevalence and characteristics of red light running crashes. The present study examines the prevalence of red light running crashes on a national basis and identifies the characteristics of such crashes and the drivers involved. Cities with especially high rates of fatal red light running crashes are identified. Countermeasures to reduce red light running crashes based on collision patterns and characteristics of drivers involved are discussed. It was estimated that about 260000 red light running crashes occur annually in the United States, of which approximately 750 result in fatalities. Comparisons were made between red light running drivers and drivers deemed not to have run red lights in these same crashes. As a group, red light runners were more likely than other drivers to be younger than age 30, male, have prior moving violations and convictions for driving while intoxicated, have invalid driver's licenses, and have consumed alcohol prior to the crash. Comparisons also were made between characteristics of red light runners involved in daytime and nighttime crashes. Nighttime red light runners were more likely than daytime runners to be young, male, and have more deviant characteristics, 53% having high blood alcohol concentrations.

Accidents, Traffic↗

PubMed1980

Nonivasive detection of retrograde descending aortic flow in infants using continuous wave doppler ultrasonography. Implications for diagnosis of aortic run-off lesions.

Continuous wave Doppler ultrasonography was utilized to detect and characterize descending aortic blood flow velocity patterns in 27 preterm and term infants with or without an aortic run-off lesion proximal to the descending aorta. The effects of coexistent intracardiac defects on the velocity time profiles were evaluated by comparing records from patients with no intracardiac defects or systemic run-off lesions to those with a variety of intracardiac defects but no systemic run-off lesion. No significant alterations were noted. In all patients, the velocity tracing in systole was triangular in shape. During diastole, however, there were qualitative and quantitative differences between patients with and without a proximal run-off lesion. In those without a run-off lesion, retrograde descending aortic flow was present only in early diastole, and aortic flow velocity oscillated around the zero baseline during mid and late diastole. In those with a run-off lesion, retrograde flow present in early diastole continued throughout diastole. Quantitatively, the ratio of the area under the retrograde flow portion of the tracing to the forward flow portion was significantly greater in those with a run-off lesion. The velocity time profiles obtained with CW Doppler were similar to those previously obtained invasively with electromagnetic flow probes of catheter-mounted velocitometers. CW Doppler ultrasonograpy provides a reliable, noninvasive method for describing descending aortic blood flow velocity in infants.

Aorta, Thoracic↗

PubMed2001

Naloxone attenuates the conditioned place preference induced by wheel running in rats.

Pairings, during which an episode of wheel running is followed by confinement in a distinctive place, produce conditioned place preference (CPP) in rats. This finding indicates that wheel running has a rewarding effect that outlasts the activity itself. In two similar experiments, we tested the hypothesis that this rewarding effect of wheel running is mediated by endogenous opioids. During a paired trial, the rats in the naloxone group were first allowed to wheel run for 2 h, then injected with naloxone (0.5 or 0.1 mg/kg in Experiments 1 and 2, respectively), and 10 min later placed in a distinctive chamber. During an unpaired trial, these rats were confined in an adjoining chamber without wheel running. Naloxone was injected before placement in both chambers, so that if naloxone-induced conditioned place aversion occurred, it would have counteracting effects on performance during the preference test. The rats in the saline group were similarly treated, except that saline was injected instead of naloxone. CPP occurred in the saline group, but not in the naloxone group. Thus, naloxone attenuated the CPP induced by wheel running. This finding supports the hypothesis that the rewarding effect of wheel running is mediated by endogenous opioids.

Animals↗

PubMed1999

Effects of short- and long-term wheel deprivation on running.

The effects of wheel deprivation on running were explored. Eight male rats, well habituated to wheels, were each deprived of wheels for periods of 0, 1, 3, and 10 h during the night (Experiment 1) and 0, 1, 3, and 10 days (Experiment 2). In Experiment 1, as wheel deprivation lengthened, wheel running in the first 24 h of access increased. After 10 days of wheel deprivation subsequent daily running decreased (by 70%), and feeding was suppressed for several days. This temporary decline may be due to detraining and the rats physical inability to run more. Experiment 3 with 12 rats found that the running increase after 3-h wheel deprivation was proportional to the amount of running normally occurring during the deprivation period. Over the short-term, running appears to be regulated like other appetitive behaviors.

Animals↗