Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “SWIMMING”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 433 records · Page 24Linked to original sources
PubMed1996

Lamprey spinal interneurons and their roles in swimming activity.

An isolated lamprey spinal cord generates rhythmic ventral root bursting that closely resembles swimming activity: ventral roots on opposite sides of the spinal cord burst in alternation, and rostral ventral roots lead caudal ventral roots. This rhythmic activity is induced by superfusion of the spinal cord with an excitatory amino acid and is called 'fictive' swimming. Three main types of spinal interneurons that are active during fictive swimming have been characterized: small excitatory interneurons with ipsilateral axons, large inhibitory interneurons with ipsilateral descending axons (lateral interneurons), and inhibitory commissural interneurons. The synaptic connectivities of these inter-neurons can account for the pattern of motoneuron excitation and inhibition occurring during fictive swimming, and it has been proposed that the synaptic interactions of these spinal neurons form the unit segmental oscillators of the swim network. Computer modeling has confirmed that this network can generate rhythmic activity resembling fictive swimming. The core of the model is the reciprocal inhibition between commissural interneurons on opposite sides of the cord. Evidence that the commissural interneurons are essential to rhythm generation comes from lesion studies in which the spinal cord was split down the midline and also from photo-ablation studies in which commissural interneurons were inactivated by illumination after retrograde labeling with a photo-toxic tracer. In both types of experiments, rhythmic activity of fictive swimming can be abolished, supporting the view that the commissural interneurons are necessary for rhythmogenesis.

Action Potentials↗
PubMed1999

Evolution and development of a central pattern generator for the swimming of a lamprey.

This article describes the design of neural control architectures for locomotion using an evolutionary approach. Inspired by the central pattern generators found in animals, we develop neural controllers that can produce the patterns of oscillations necessary for the swimming of a simulated lamprey. This work is inspired by Ekeberg's neuronal and mechanical model of a lamprey [11] and follows experiments in which swimming controllers were evolved using a simple encoding scheme [25, 26]. Here, controllers are developed using an evolutionary algorithm based on the SGOCE encoding [31, 32] in which a genetic programming approach is used to evolve developmental programs that encode the growing of a dynamical neural network. The developmental programs determine how neurons located on a two-dimensional substrate produce new cells through cellular division and how they form efferent or afferent interconnections. Swimming controllers are generated when the growing networks eventually create connections to the muscles located on both sides of the rectangular substrate. These muscles are part of a two-dimensional mechanical simulation of the body of the lamprey in interaction with water. The motivation of this article is to develop a method for the design of control mechanisms for animal-like locomotion. Such a locomotion is characterized by a large number of actuators, a rhythmic activity, and the fact that efficient motion is only obtained when the actuators are well coordinated. The task of the control mechanism is therefore to transform commands concerning the speed and direction of motion into the signals sent to the multiple actuators. We define a fitness function, based on several simulations of the controller with different commands settings, that rewards the capacity of modulating the speed and the direction of swimming in response to simple, varying input signals. Central pattern generators are thus evolved capable of producing the relatively complex patterns of oscillations necessary for swimming. The best solutions generate traveling waves of neural activity, and propagate, similarly to the swimming of a real lamprey, undulations of the body from head to tail propelling the lamprey forward through water. By simply varying the amplitude of two input signals, the speed and the direction of swimming can be modulated.

Algorithms↗
PubMed2003

The hydrodynamics of locomotion at intermediate Reynolds numbers: undulatory swimming in ascidian larvae (Botrylloides sp.).

Understanding how the shape and motion of an aquatic animal affects the performance of swimming requires knowledge of the fluid forces that generate thrust and drag. These forces are poorly understood for the large diversity of animals that swim at Reynolds numbers (Re) between 10(0) and 10(2). We experimentally tested quasi-steady and unsteady blade-element models of the hydrodynamics of undulatory swimming in the larvae of the ascidian Botrylloides sp. by comparing the forces predicted by these models with measured forces generated by tethered larvae and by comparing the swimming speeds predicted with measurements of the speed of freely swimming larvae. Although both models predicted mean forces that were statistically indistinguishable from measurements, the quasi-steady model predicted the timing of force production and mean swimming speed more accurately than the unsteady model. This suggests that unsteady force (i.e. the acceleration reaction) does not play a role in the dynamics of steady undulatory swimming at Re approximately 10(2). We explored the relative contribution of viscous and inertial force to the generation of thrust and drag at 10(0) 10(2)) and low (<10(0)) Re, the fluid forces that generate thrust cannot be assumed to be the same as those that generate drag at intermediate Re.

Acceleration↗
PubMed2003

Escape from viscosity: the kinematics and hydrodynamics of copepod foraging and escape swimming.

Feeding and escape swimming in adult females of the calanoid copepod Temora longicornis Müller were investigated and compared. Swimming velocities were calculated using a 3-D filming setup. Foraging velocities ranged between 2 and 6 mm s(-1), while maximum velocities of up to 80 mm s(-1) were reached during escape responses. Foraging took place at Reynolds numbers between 2 and 6, indicating that viscous forces are considerable during this swimming mode. Inertial forces are much more important during escape responses, when Reynolds numbers of more than 100 are reached. High-speed film recordings at 500 frames s(-1) of the motion pattern of the feeding appendages and the escape movement of the swimming legs revealed that the two swimming modes are essentially very different. While foraging, the first three mouth appendages (antennae, mandibular palps and maxillules) create a backwards motion of water with a metachronal beating pattern. During escape movements the mouth appendages stop moving and the swimming legs beat in a very fast metachronal rhythm, accelerating a jet of water backwards. The large antennules are folded backwards, resulting in a streamlined body shape. Particle image velocimetry analysis of the flow around foraging and escaping copepods revealed that during foraging an asymmetrical vortex system is created on the ventral side of the animal. The feeding motion is steady over a long period of time. The rate of energy dissipation due to viscous friction relates directly to the energetic cost of the feeding current. During escape responses a vortex ring appears behind the animal, which dissipates over time. Several seconds after cessation of swimming leg movements, energy dissipation can still be measured. During escape responses the rate of energy dissipation due to viscous friction increases by up to two orders of magnitude compared to the rate when foraging.

Animals↗
PubMed2003

The Kármán gait: novel body kinematics of rainbow trout swimming in a vortex street.

Most fishes commonly experience unsteady flows and hydrodynamic perturbations during their lifetime. In this study, we provide evidence that rainbow trout Oncorhynchus mykiss voluntarily alter their body kinematics when interacting with vortices present in the environment that are not self-generated. To demonstrate this, we measured axial swimming kinematics in response to changes in known hydrodynamic wake characteristics. We compared trout swimming in the Kármán street behind different diameter cylinders (2.5 and 5 cm) at two flow speeds (2.5 and 4.5 L s(-1), where L is total body length) to trout swimming in the free stream and in the cylinder bow wake. Trout swimming behind cylinders adopt a distinctive, previously undescribed pattern of movement in order to hold station, which we term the Kármán gait. During this gait, body amplitudes and curvatures are much larger than those of trout swimming at an equivalent flow velocity in the absence of a cylinder. Tail-beat frequency is not only lower than might be expected for a trout swimming in the reduced flow behind a cylinder, but also matches the vortex shedding frequency of the cylinder. Therefore, in addition to choosing to be in the slower flow velocity offered behind a cylinder (drafting), trout are also altering their body kinematics to synchronize with the shed vortices (tuning), using a mechanism that may not involve propulsive locomotion. This behavior is most distinctive when cylinder diameter is large relative to fish length. While tuning, trout have a longer body wavelength than the prescribed wake wavelength, indicating that only certain regions of the body may need to be oriented in a consistent manner to the oncoming vortices. Our results suggest that fish can capture energy from vortices generated by the environment to maintain station in downstream flow. Interestingly, trout swimming in front of a cylinder display lower tail-beat amplitudes and body wave speeds than trout subjected to any of the other treatments, implying that the bow wake may be the most energetically favorable region for a fish to hold station near a cylinder.

Animals↗
PubMed2003

The ontogenetic scaling of hydrodynamics and swimming performance in jellyfish (Aurelia aurita).

It is not well understood how ontogenetic changes in the motion and morphology of aquatic animals influence the performance of swimming. The goals of the present study were to understand how changes in size, shape and behavior affect the hydrodynamics of jet propulsion in the jellyfish Aurelia aurita and to explore how such changes affect the ontogenetic scaling of swimming speed and cost of transport. We measured the kinematics of jellyfish swimming from video recordings and simulated the hydrodynamics of swimming with two computational models that calculated thrust generation by paddle and jet mechanisms. Our results suggest that thrust is generated primarily by jetting and that there is negligible thrust generation by paddling. We examined how fluid forces scaled with body mass using the jet model. Despite an ontogenetic increase in the range of motion by the bell diameter and a decrease in the height-to-diameter ratio, we found that thrust and acceleration reaction scaled with body mass as predicted by kinematic similarity. However, jellyfish decreased their pulse frequency with growth, and speed consequently scaled at a lower exponential rate than predicted by kinematic similarity. Model simulations suggest that the allometric growth in Aurelia results in swimming that is slower, but more energetically economical, than isometric growth with a prolate bell shape. The decrease in pulse frequency over ontogeny allows large Aurelia medusae to avoid a high cost of transport but generates slower swimming than if they maintained a high pulse frequency. Our findings suggest that ontogenetic change in the height-to-diameter ratio and pulse frequency of Aurelia results in swimming that is relatively moderate in speed but is energetically economical.

Acceleration↗
PubMed2004

Does condition of Atlantic cod (Gadus morhua) have a greater impact upon swimming performance at Ucrit or sprint speeds?

To compare the sensitivity of sprint and critical (Ucrit) swimming speeds to the condition of Atlantic cod (Gadus morhua) and to identify the best anatomic, behavioural and biochemical correlates of these types of swimming, we established two groups of cod that were fed or starved for 12 weeks. We evaluated sprint swimming and Ucrit performance as well as the speed at which repeated burst-coast movements began in the Ucrit test before measuring the metabolic capacities of red and white muscle sampled caudally, centrally and rostrally and the anatomic characteristics of the cod. White muscle lactate was measured directly after the Ucrit test. As expected, the twofold difference in Fulton's condition factor (0.5+/-0.04 for starved and 1.0+/-0.1 for fed cod) was accompanied by large differences in the anatomic and biochemical parameters measured. Despite the relative sparing of muscle aerobic capacity during starvation and despite the greater use of oxidative fibres during Ucrit compared with sprint swimming, these types of swimming differed by much the same extent between starved and fed cod. In the Ucrit tests, white muscle lactate levels and lactate accumulation per burst-coast movement were considerably higher in fed than starved cod, suggesting more intensive use of fast muscle fibres in cod in good condition. Multiple regression analysis indicated strong correlations between Ucrit, the speed at which regular burst-coasting began and the activity of pyruvate dehydrogenase (PDH) in red muscle (both caudal and central positions). PDH activity may limit the rate of oxidative ATP production by red muscle. The activity of cytochrome c oxidase in rostral white muscle was the strongest correlate of sprint swimming, suggesting that aerobic preparation of white muscle facilitates rapid contraction. The correlation between Ucrit and sprint swimming was weak, perhaps due to inter-individual differences in sensitivity during sprint tests.

Adenosine Triphosphate↗
PubMed2004

Hydrodynamics of surface swimming in leopard frogs (Rana pipiens).

The kinematics of swimming frogs have been studied extensively in the past and, based on these results, hypotheses regarding the hydrodynamics of frog swimming can be generated. To test these hypotheses we used digital particle image velocimetry (DPIV) to quantify the flow structure of the wake produced by the feet during the propulsion phase of the kick of surface swimming frogs (Rana pipiens). These frogs use two different gaits, asynchronous and synchronous kicking, and the magnitude of the thrust produced by the feet differs between asynchronous (34+/-5.4 mN foot(-1)) and synchronous kicking (71+/-13.3 mN foot(-1)), as does maximum swimming speed, with higher swimming speed and forces produced during the synchronous kicks. Previous studies have suggested that an interaction between the feet, resulting in a single posteriorly directed fluid jet, as the feet come together at the end of synchronous kicks, may augment force production. Our results show, however, that each foot produces its own distinct vortex ring, in both asynchronous and synchronous kicking of the feet. There is no evidence of a central jet being produced even during powerful synchronous kicks (maximum thrust calculated was 264 mN foot(-1)). An alternative mechanism of force production could be the lift-based paddling recently suggested for delta-shaped feet of swimming birds. However, the orientation of the vortex rings generated by the feet is almost perpendicular to the swimming direction for both gaits and there is only a slight asynchrony of the shedding of the distal (start) and proximal (stop) vortex rings, which is different from what would be expected by a dominantly lift-based mechanism. Thus, our results do not support lift as a major mechanism contributing to thrust. Instead, our data support the hypothesis that propulsion is based on drag and acceleration reaction forces where the thrust is generated by separated, but attached, vortex rings on the suction side of the feet, resulting in vortices that are shed behind the frogs during both asynchronous and synchronous kicking.

Acceleration↗
PubMed1984

Mechanics, power output and efficiency of the swimming muskrat (Ondatra zibethicus).

The surface swimming of muskrats (Ondatra zibethicus Linnaeus) was studied by forcing individual animals to swim against a constant water current, of velocity ranging from 0.2 to 0.75 m s-1, in a recirculating water channel. Lateral and ventral views of the swimming muskrats were filmed simultaneously for analysis of thrust by the propulsive appendages. Drag measurements and flow visualization on dead muskrats demonstrated that these animals experience large resistive forces due to the formation of waves and a turbulent wake, because of the pressure and gravitational components which dominate the drag force. Biomechanical analysis demonstrated that thrust is mainly generated by alternating strokes of the hindfeet in the paddling mode. A general lengthening of the hindfeet and presence of lateral fringe hairs on each digit increase the surface area of the foot to produce thrust more effectively during the power phase of the stroke cycle. Increased energy loss from drag on the foot during the recovery phase is minimized by configural and temporal changes of the hindfoot. Employing the models developed by Blake (1979, 1980a,b) for paddle propulsion, it was found that as the arc through which the hindfeet were swept increased with increasing velocity the computed thrust power increased correspondingly. However, the frequency of the stroke cycle remained relatively constant across all velocities at a level of 2.5 Hz. Both mechanical and aerobic efficiencies rose to a maximum with increasing swimming velocity. The aerobic efficiency, which examined the transformation of metabolic power input to thrust power output reached a value of 0.046 at 0.75 m s-1. The mechanical efficiency expressing the relationship of the thrust power generated by the paddling hindfeet and laterally compressed tail (Fish, 1982a,b) to the total mechanical power developed by the propulsive appendages increased to a maximum of 0.33 at 0.75 m s-1. I conclude that the paddling mode of swimming in the muskrat is relatively inefficient when compared to swimming modes which maintain a nearly continuous thrust force over the entire propulsive cycle. However, the paddling mode permits the muskrat to generate propulsive forces effectively while swimming at the surface. The evolution of this mode for semi-aquatic mammals represents only a slight modification from a terrestrial type of locomotion.

Animals↗
PubMed1999

Energetics of locomotion by the Australian water rat (Hydromys chrysogaster): a comparison of swimming and running in a semi-aquatic mammal.

Semi-aquatic mammals occupy a precarious evolutionary position, having to function in both aquatic and terrestrial environments without specializing in locomotor performance in either environment. To examine possible energetic constraints on semi-aquatic mammals, we compared rates of oxygen consumption for the Australian water rat (Hydromys chrysogaster) using different locomotor behaviors: swimming and running. Aquatic locomotion was investigated as animals swam in a water flume at several speeds, whereas water rats were run on a treadmill to measure metabolic effort during terrestrial locomotion. Water rats swam at the surface using alternate pelvic paddling and locomoted on the treadmill using gaits that included walk, trot and half-bound. Water rats were able to run at twice their maximum swimming velocity. Swimming metabolic rate increased with velocity in a pattern similar to the 'humps' and 'hollows' for wave drag experienced by bodies moving at the water surface. Metabolic rate increased linearly during running. Over equivalent velocities, the metabolic rate for running was 13-40 % greater than for swimming. The minimum cost of transport for swimming (2.61 J N-1 m-1) was equivalent to values for other semi-aquatic mammals. The lowest cost for running (2.08 J N-1 m-1) was 20 % lower than for swimming. When compared with specialists at the extremes of the terrestrial-aquatic continuum, the energetic costs of locomoting either in water or on land were high for the semi-aquatic Hydromys chrysogaster. However, the relative costs for H. chrysogaster were lower than when an aquatic specialist attempts to move on land or a terrestrial specialist attempts to swim.

Animals↗
PubMed2000

Locomotor repertoire of the larval zebrafish: swimming, turning and prey capture.

Larval zebrafish (Brachydanio rerio) are a popular model system because of their genetic attributes, transparency and relative simplicity. They have approximately 200 neurons that project from the brainstem into the spinal cord. Many of these neurons can be individually identified and laser-ablated in intact larvae. This should facilitate cellular-level characterization of the descending control of larval behavior patterns. Towards this end, we attempt to describe the range of locomotor behavior patterns exhibited by zebrafish larvae. Using high-speed digital imaging, a variety of swimming and turning behaviors were analyzed in 6- to 9-day-old larval fish. Swimming episodes appeared to fall into two categories, with the point of maximal bending of the larva's body occurring either near the mid-body (burst swims) or closer to the tail (slow swims). Burst swims also involved larger-amplitude bending, faster speeds and greater yaw than slow swims. Turning behaviors clearly fell into two distinct categories: fast, large-angle escape turns characteristic of escape responses, and much slower routine turns lacking the large counterbend that often accompanies escape turns. Prey-capture behaviors were also recorded. They were made up of simpler locomotor components that appeared to be similar to routine turns and slow swims. The different behaviors observed were analyzed with regard to possible underlying neural control systems. Our analysis suggests the existence of discrete sets of controlling neurons and helps to explain the need for the roughly 200 spinal-projecting nerve cells in the brainstem of the larval zebrafish.

Animals↗
PubMed2000

Energetics of surface swimming in Brandt's cormorants (Phalacrocorax penicillatus brandt).

The energy requirements of Brandt's cormorants (Phalacrocorax penicillatus) during surface swimming were measured in birds swimming under a metabolic chamber in a water flume. From the oxygen consumption recordings, we extrapolated the metabolic rate and cost of transport at water speeds ranging from 0 to 1.3 m s(-)(1). In still water, the birds' mean mass-specific rate of oxygen consumption ( V(O2)) while floating at the surface was 20.2 ml O(2 )min(-)(1 )kg(-)(1), 2.1 times the predicted resting metabolic rate. During steady-state voluntary swimming against a flow, their V(O2) increased with water speed, reaching 74 ml O(2 )min(-)(1 )kg(-)(1) at 1.3 m s(-)(1), which corresponded to an increase in metabolic rate from 11 to 25 W kg(-)(1). The cost of transport decreased with swimming velocity, approaching a minimum of 19 J kg(-)(1 )m(-)(1) for a swimming speed of 1.3 m s(-)(1). Surface swimming in the cormorant costs approximately 18 % less than sub-surface swimming. This confirms similar findings in tufted ducks (Aythya fuligula) and supports the hypothesis that increased energy requirements are necessary in these birds during diving to overcome buoyancy and heat loss during submergence.

Air Movements↗
PubMed2002

Modulation of swimming in the gastropod Melibe leonina by nitric oxide.

Nitric oxide (NO) is a gaseous intercellular messenger produced by the enzyme nitric oxide synthase. It has been implicated as a neuromodulator in several groups of animals, including gastropods, crustaceans and mammals. In this study, we investigated the effects of NO on the swim motor program produced by isolated brains and by semi-intact preparations of the nudibranch Melibe leonina. The NO donors sodium nitroprusside (SNP, 1 mmol x l(-1)) and S-nitroso-N-acetylpenicillamine (SNAP, 1 mmol x l(-1)) both had a marked effect on the swim motor program expressed in isolated brains, causing an increase in the period of the swim cycle and a more erratic swim rhythm. In semi-intact preparations, the effect of NO donors was manifested as a significant decrease in the rate of actual swimming. An NO scavenger, reduced oxyhemoglobin, eliminated the effects of NO donors on isolated brains, supporting the assumption that the changes in swimming induced by donors were actually due to NO. The cGMP analogue 8-bromoguanosine 3',5'-cyclic monophosphate (1 mmol x l(-1)) produced effects that mimicked those of NO donors, suggesting that NO is working via a cGMP-dependent mechanism. These results, in combination with previous histological studies indicating the endogenous presence of nitric oxide synthase, suggest that NO is used in the central nervous system of Melibe leonina to modulate swimming.

8-Bromo Cyclic Adenosine Monophosphate↗
PubMed1995

Thermal responses to swimming in three water temperatures: influence of a wet suit.

The primary objective of this investigation was to determine the thermal and metabolic effects of wearing a rubberized wet suit (WS) while swimming for 30 min in 20.1, 22.7, and 25.6 degrees C water. Metabolic and body temperature measurements were recorded in each water temperature with subjects wearing either a WS or a competitive swimming suit (SS). Immediately after each swim the subjects cycled for 15 min on a stationary cycle ergometer. Energy expenditure (VO2), heart rate, post-swim blood lactate, work completed on the cycle ergometer, and rating of perceived exertion (RPE) were similar in all trials. Mean (+/- SE) core temperature (Tc) during swimming in the SS trials increased 0.56 (+/- 0.33), 0.48 (+/- 0.20), and 1.22 (+/- 0.24) degrees C, whereas in the WS trial Tc rose 0.62 (+/- 0.22), 1.02 (+/- 0.15), and 0.89 (+/- 0.13) degrees C in the 20.1, 22.7, and 25.6 degrees C treatments, respectively. Following swimming many of the subjects experienced a decrease in Tc, but it was significantly elevated above preimmersion by the end of cycling in all trials except the SS 20.1 degrees C trial. Mean trunk temperatures (Ttr) during swimming in the WS trials were 4.32 +/- 0.16 (20.1 degrees C), 3.90 +/- 0.25 (22.7 degrees C), and 3.21 +/- 0.20 (25.6 degrees C) degrees C warmer than in the SS. Ttr rose after the subjects exited the water, but remained significantly below baseline throughout cycling in all trials.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed2000

Biological effects of single and repeated swimming stress in male rats: beneficial effects of glucocorticoids.

We have examined the biological effects of single (45 min at 22 degrees C) and repeated swimming stress (45 min at 22 degrees C for 7 d) using male Sprague-Dawley rats. Repeated swimming for a week resulted in a significant inhibition in total body weight (25%) as compared to control unstressed animals. There was significant increase in adrenal and kidney relative weight and decreases in relative thymus weight in repeated swimming-stressed animals as compared to control animals. Repeated swimming stress resulted in almost threefold increase in plasma corticosterone levels with concomitant dramatic decrease in total glucocorticoid receptor (GR) levels in liver, thymus, and heart as compared to control unstressed animals. Interestingly, single swimming stress resulted in a significant elevation in lipid peroxidation levels in the liver and heart. In contrast, there was no change in the lipid per oxidation levels in the liver and heart between chronic stressed and control unstressed animals. Finally, both single and repeated swimming-stress animals had almost 50% reduction in plasma triglyceride levels as compared to control unstressed animals. It is concluded that elevated plasma corticosterone levels by downregulating GR during repeated swimming stress exerts beneficial effects in rats by retarding the total body weight gain and lowering plasma triglyceride levels without affecting free-radicals-induced oxidative stress.

Adrenal Glands↗
PubMed2004

Combined creatine and sodium bicarbonate supplementation enhances interval swimming.

This study examined the effect of simultaneous supplementation of creatine and sodium bicarbonate on consecutive maximal swims. Sixteen competitive male and female swimmers completed, in a randomized order, 2 different treatments (placebo and a combination of creatine and sodium bicarbonate) with 30 days of washout period between treatments in a double-blind crossover procedure. Both treatments consisted of placebo or creatine supplementation (20 g per day) in 6 days. In the morning of the seventh day, there was placebo or sodium bicarbonate supplementation (0.3 g per kg body weight) during 2 hours before a warm-up for 2 maximal 100-m freestyle swims that were performed with a passive recovery of 10 minutes in between. The first swims were similar, but the increase in time of the second versus the first 100-m swimming time was 0.9 seconds less (p < 0.05) in the combination group than in placebo. Mean blood pH was higher (p < 0.01-0.001) in the combination group than in placebo after supplementation on the test day. Mean blood pH decreased (p < 0.05) similarly during the swims in both groups. Mean blood lactate increased (p < 0.001) during the swims, but there were no differences in peak blood lactate between the combination group (14.9 +/- 0.9 mmol.L(-1)) and placebo (13.4 +/- 1.0 mmol.L(-1)). The data indicate that simultaneous supplementation of creatine and sodium bicarbonate enhances performance in consecutive maximal swims.

Adolescent↗
PubMed1992

[Comparison of submaximal front crawl and breast stroke swimming in relation to energy expenditure].

The purpose of this study was to compare the energy expenditure during submaximal front crawl (Fr) and breast stroke (Br) swimming. Six male college swimmers performed submaximal and maximal exercise tests in both styles in a swimming flume. In submaximal exercise tests, they swam at the following given velocities for 5 min, Br: 0.3, 0.5 and 0.7 m/sec; Fr: 0.3, 0.5, 0.7 and 0.9 m/sec. In maximal exercise tests, following submaximal swimming at 0.9 m/sec in Br and 1.1 m/sec in Fr, swimming velocity was increased progressively by 0.1 m/sec every 1 min until the subjects reached to voluntary exhaustion. VO2max obtained from the maximal swimming tests in Br and Fr were 4.27 and 4.18 l/min, respectively. And there was no significant difference between these two values. VO2 during Br and Fr swimming at four and five submaximal velocities were 1.06, 1.30, 1.79, 2.65 l/min and 1.17, 1.34, 1.63, 2.04, 3.05 l/min, respectively. And, it was found that VO2 at 0.3 and 0.9 m/sec were significantly different (p < 0.05 and p < 0.01) between Fr and Br. VO2 in both styles curvilinearly increased with swimming velocity, and these relationships were well fitted for the regression equation of the second order (Br: y = 3.84625x2 - 1.95914x + 1.310463,r2 = 0.999 (p < 0.05), Fr: y = 3.233446x2 - 2.28136x + 1.611524, r2 = 0.979 (p < 0.05)). It was calculated that the two curves crossed at a point on 0.49 m/sec, and that VO2 at this point was 1.27 l/min. This value equivalented to 30.4% VO2max in Br and 29.7% VO2max in Fr.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed1992

Swimming and asthma. Benefits and deleterious effects.

Swimming is a common pastime activity and competitive sport for patients with asthma. One reason for such popularity may be the low asthmogenicity of swimming compared with landbased activities. Review of available evidence suggests that swimming induces less severe bronchoconstriction than other sports. The mechanisms for this protective effect of swimming are not clear, but there is some experimental evidence intimating that it results in part from the high humidity of inspired air at water level, which reduces respiratory heat loss (and possibly osmolarity of airways mucus). Beneficial roles of horizontal posture and of water immersion have been tested but not confirmed. Swimming poses two potentially deleterious effects to the patient with asthma. One is the exaggerated parasympathetic tone due to the 'diving reflex', that has been shown to trigger bronchoconstriction. The other is airway irritation because of chlorine and its derivatives. Swimming as a training modality has definite benefits for the patient with asthma. These include an increase in aerobic fitness and a decrease in asthma morbidity. There is no conclusive evidence, however, that swim training causes a decrease in the severity or frequency of exercise-induced bronchoconstriction.

Asthma↗