Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Skating”

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 109 records · Page 6Linked to original sources

On the duplex nature of the skate retina.

The skate retina contains only one type of photoreceptor which has rod-like properties in the dark-adapted state. In the presence of background illumination, the receptors take on cone-like properties, i.e., their photoresponses become much faster, are less sensitive to light, and can be elicited in the presence of very bright backgrounds. Although the transformation is an extremely slow process, the skate retina performs like that of animals with mixed, rod-cone retinae. In this report we examine some postreceptoral features which may relate to this remarkable behavior. We show, for example, that the skate photoreceptor terminals make two kinds of junctions (ribbon synapses and basal junctions) that appear analogous to the two kinds of synaptic contacts made by cone terminals in other species. Furthermore, two types of horizontal cells are seen in the skate retina. Although the light-evoked responses of these horizontal cells are similar, there are differences in their current profiles recorded under voltage clamp, and in the nature of their dendritic processes. We have also observed several unusual postreceptoral structural features that may have some bearing on the response properties of the skate retina. In addition, a comparison of the adaptive properties of the receptor potential with those of intraretinal responses (b-wave, PNR) reveals differences that suggest strongly the presence of a network adaptive mechanism originating within the proximal retina. The network mechanism appears to be controlled to a large extent by the extracellular concentration of potassium [K+]0; i.e., changes in [K+]0 affect significantly the sensitivities of the b-wave and PBR, but have little effect on responses arising in the distal retina.

Adaptation, Ocular↗

Stretch-shortening cycle in roller ski skating: effects of technique.

The purposes of this study were 1) to examine the occurrence of the stretch-shortening cycle (SSC) in the three principal techniques of ski skating and 2) to test the hypothesis that differences in SSC behaviour may explain the choice of a technique when the grade is altered. Ten highly skilled male cross-country skiers roller skied at 5.3+/-0.1 m x s(-1) using the V1 skate (V1), V2-alternate (V2A), and V2 skate (V2) techniques. Knee and ankle joint kinematics, EMG of the vastus lateralis (VL) and gastrocnemius lateralis (GL) muscles, and roller ski velocity were recorded during the last 40 s of each bout of roller skiing. The existence of an EMG signal during the eccentric phase prior to the thrust, as well as the lack of significant delay between the two phases, showed that SSC occurs in the three techniques of roller ski skating with the exception of 50% of the subjects at the weak side knee with V1. The VL stretching velocity over the eccentric phase was higher (p < 0.005) with V2 and V2A than V1, indicating that less elastic energy was stored in the lower limbs extensor muscles with V1. This could partly explain why this technique is not used on flat terrains during races. However, no differences of average EMG activity or IEMG existed between techniques for either GL or VL during the concentric phase, suggesting that the theoretical advantage due to the SSC behaviour is minor in roller ski skating.

Adult↗

Prediction of ice skating performance with off-ice testing in women's ice hockey players.

Off-ice predictors of skating performance have not been investigated for women's hockey players. The purpose of this study was to identify the off-ice variables associated with high-performance skating acceleration, speed, agility, and on-ice anaerobic capacity and power in women's ice hockey players. Sixty-one women's ice hockey players between the ages of 8 and 16 years (x age = 12.18 +/- 2.05 years, x playing experience = 4.68 +/- 2.69 years) participated in the study. Subjects were 1-4 months postseason. Some players were continuing to play once per week during the off-season. Skating tests (ST) included (a) 6.10-m acceleration, (b) 47.85-m speed, (c) agility cornering S turn, and (d) modified repeat skate test (MRS). Two trials of each ST were measured with a photoelectric timing system (except MRS, which was measured with 1 trial). The off-ice variables that were evaluated included age, years of playing experience, height, body mass, predicted fat percentage, sit-and-reach flexibility, vertical jump height, 40-yd dash time, and 1-minute timed sit-ups and push-ups. The results of this study show that 40-yd dash time is the strongest predictor of skating speed in women's hockey players ages 8-16 years old. From the regression procedure the best prediction equation was speed = 4.913 - (0.0107 x kilograms) + (0.4356 x 40-yd dash time).

Adolescent↗

Erythropoietin stimulates tyrosine phosphorylation and taurine transport in skate erythrocytes.

Taurine, a beta amino acid, is a primary osmolyte in nucleated skate erythrocytes and is involved in the regulation of cell volume. Growth factors may be involved in the regulation of cell volume which occurs during cell division. Erythropoietin (EPO) is the primary growth factor controlling erythropoiesis. To investigate its mechanism of action, we used nucleated skate erythrocytes. EPO stimulates Na(+)-independent uptake of taurine in a concentration-dependent manner. The uptake was inhibited by the tyrosine kinase inhibitor genistein. Concomitantly, EPO stimulates tyrosine phosphorylation of a number of proteins, particularly ones of molecular masses 145, 120, 100, 80, 65, and 35 kDa. Using specific antibodies, the 145 kDa protein is identified as phospholipase C gamma-1 (PLC gamma-1) and the 100 kDa protein as the skate homolog of the anion exchanger band 3. Since PLC gamma-1 is activated, turnover of membrane lipids was determined. EPO increased 1,2-diacylglycerol formation from phosphatidylinositols (phosphatidylinositol-4-monophosphate and 4,5-biphosphate) during an early phase and later preferentially from phosphatidylcholine. The early hydrolysis of phosphoinositides was confirmed measuring generation of inositol-1,4,5-trisphosphate, demonstrating an activation of PLC gamma-1 activity. To determine if phospholipase D (PLD) stimulation also occurred, ethanol was included in the reactions. Phosphatidylethanol, synthesized by PLD-mediated transphosphatidylation, appeared at times longer than 5 min, suggesting delayed activation of PLD. These results demonstrate that EPO, via simulation of tyrosine phosphorylation, stimulates taurine transport in skate erythrocytes.

Animals↗

Localization and partial characterization of melatonin receptors in amphioxus, hagfish, lamprey, and skate.

Through its secretion of melatonin, the pineal complex of vertebrates exerts a range of physiological effects including regulation of circadian rhythms, seasonal reproduction, metamorphosis, and body color change. Little is known about phylogenetic differences in the distribution and characteristics of melatonin binding sites in fishes. We used in vitro autoradiography to examine binding of [2-125I]iodomelatonin (IMEL) in 20-micron frozen sections of amphioxus (Branchiostoma lanceolatum), Atlantic hagfish (Myxine glutinosa), larval and adult lamprey (Petromyzon marinus), little skate (Raja erinacea), and rainbow trout (Oncorhynchus mykiss). Tissue was incubated with IMEL in the presence or absence of unlabeled melatonin (1 muM, in order to assess nonspecific binding). A concentration of 32 pM IMEL was used for single point assays and competition studies. No specific binding was found in hagfish or amphioxus, which lack a pineal complex. In the optic tecta of lamprey, skate, and trout, IMEL binding is highly specific (melatonin >> N-acetylserotonin > 5- methoxytryptophol >> serotonin). Scatchard analysis revealed that the tectal binding sites are of high affinity (Kd = 36, 38, and 50 pM) and low capacity (Bmax = 8.1, 19.8, and 21.8 fmol/mg protein) in lamprey, skate, and trout, respectively. In adult lampreys, intense specific IMEL binding is found in the optic tectum (layer I > II > III) and preoptic nucleus (pars parvocellularis > magnocellularis). Binding was less intense and consistent in the same areas of ammocoete brain. In skates and trout, intense specific binding is found in optic tectum, lateral geniculate body, diencephalic preoptic and suprachiasmatic nuclei, basal hypothalamus, and the medial pallium. These results indicate that specific melatonin binding sites are present in all craniate taxa examined except in hagfish. Although we cannot rule out the possibility that melatonin receptors are secondarily lost in hagfish, their absence in amphioxus makes this unlikely. We speculate that melatonin actions in early vertebrates may have included regulation of visual and endocrine responses to light.

Animals↗

Disruption of cell volume regulation by mercuric chloride is mediated by an increase in sodium permeability and inhibition of an osmolyte channel in skate hepatocytes.

The mechanism by which mercury leads to cell swelling and impairs the normal regulatory volume decrease (RVD) in cells swollen in hypotonic media was examined in hepatocytes isolated from the little skate, Raja erinacea, an osmoconforming marine elasmobranch. Skate hepatocytes treated with 50 microM HgCl2 in isotonic medium swelled to volumes double those of control cells, and this was associated with an increase in Na+ and K+ permeability. The gain in intracellular Na+ exceeded the K+ loss by 0.27 microEq/mg protein, accounting in large part for the observed cell swelling. The effects of mercury were blunted when hepatocytes were incubated in medium in which the Na+ was replaced with K+, and were essentially absent when Na+ was replaced with choline+, indicating an important role of Na+ influx in mediating mercury's effects on cell volume regulation. The inhibition of RVD by mercury was prevented if the metal was administered as a mercaptide with dithiothreitol or glutathione. However, when these chelating agents were added after the mercury, only the membrane permeant dithiothreitol was able to reverse the inhibition of RVD, suggesting an intracellular site of action. Mercuric chloride also produced a concentration-dependent inhibition of the ATP-sensitive volume-regulatory osmolyte channel in skate hepatocytes, as assessed by inhibition of swelling-activated [14C]taurine efflux. [14C]Taurine efflux was inhibited at mercury concentrations (20-40 microM) that had no effect on intracellular ATP levels or ATP/ADP ratios, consistent with a direct interaction with the channel. These findings indicate that mercury impairs cell volume regulation in skate hepatocytes at multiple sites, including the volume-regulatory osmolyte channels, and Na+ and K+ permeability pathways. The combined effects of increased Na+ influx and the inability to extrude organic osmolytes may account for the inhibition of RVD.

Animals↗

Inhibition of volume-stimulated taurine efflux and tyrosine kinase activity in the skate red blood cell.

Phosphorylation of the band 3 anion exchange protein by the tyrosine kinases p72syk and p56lyn is thought to play a role in the pathway that regulates swelling-activated taurine efflux from the skate red blood cell. In this study, the protein tyrosine kinase (PTK) inhibitors piceatannol and tyrphostin A23 both inhibited taurine efflux and the activities of the tyrosine kinases p72syk and p56lyn in the skate erythrocyte. However, the PTK inhibitors genistein and tyrphostin A46 had only small effects on taurine efflux and PTK activities. In general, a strong correlation between the extent of inhibition of taurine efflux and of tyrosine kinase activity was observed. PTK inhibitors showed a similar pattern of inhibition of band 3 phosphorylation, with the greatest inhibition observed in cells treated with piceatannol. The protein kinase C inhibitors staurosporine and bisindolylmaleimide tested alone or in combination with piceatannol had little or no significant effect on swelling-activated taurine efflux. Overall the results support the hypothesis that phosphorylation of the skate band 3 protein by p72syk and p56lyn contributes to the regulation of volume-activated taurine efflux in skate red cells, and suggest that protein kinase C may not be involved in this regulation.

Animals↗

Retention of structural and functional polarity in cultured skate hepatocytes undergoing in vitro morphogenesis.

The present study characterized a primary culture model of hepatocytes isolated from the little skate, Leucoraja erinacea, that maintain remarkable structural and functional polarity over 7 days in culture. Skate hepatocytes were isolated as clusters of 3-20 hepatocytes surrounding a bile canaliculus, rather than as single cells. Trypan blue and propidium iodide exclusion was found to be >98%, and the cells maintained high intracellular concentrations of K+, ATP, and reduced glutathione (GSH), and high ratios of ATP/ADP and GSH/GSSG. Glutathione S-transferase activity remained constant, whereas cytochrome P450 activity declined to 16% of initial levels after 7 days. Quantitative RT-PCR analysis revealed that the mRNA levels of several genes remained constant over the 7-day period, whereas Bsep, the canalicular bile salt export pump, levels declined slowly to 30% of initial values. In the presence of dexamethasone, the cells underwent a morphogenesis in which the clusters reannealed into a three-dimensional network of chords. During this morphogenesis, skate hepatocytes clusters maintained a polarized distribution of actin filaments and microtubules, as well as apical and basolateral membrane domains. Polarity of membrane transport systems was confirmed both morphologically, using antibodies raised against Bsep and Mrp2, the canalicular multispecific organic anion transporter, and functionally, by monitoring secretion of the fluorescent organic anions NBD-taurocholate, a Bsep substrate, and fluorescein-methotrexate, an Mrp2 substrate, into the bile canalicular spaces. Overall, the results indicate that in contrast with mammalian hepatocytes, isolated skate hepatocyte clusters retain polarity in culture, and provide an excellent system for investigating long-term effects of drugs and xenobiotics on hepatobiliary functions, and for studying in vitro morphogenesis.

Animals↗

The organic anion transport polypeptide 1d1 (Oatp1d1) mediates hepatocellular uptake of phalloidin and microcystin into skate liver.

Organic anion transporting polypeptides (rodent Oatp; human OATP) mediate cellular uptake of numerous organic compounds including xenobiotic toxins into mammalian hepatocytes. In the little skate Leucoraja erinacea a liver-specific Oatp (Oatp1d1, also called sOatp) has been identified and suggested to represent an evolutionarily ancient precursor of the mammalian liver OATP1B1 (human), Oatp1b2 (rat), and OATP1B3 (human). The present study tested whether Oatp1d1 shares functional transport activity of the xenobiotic oligopeptide toxins phalloidin and microcystin with the mammalian liver Oatps/OATPs. The phalloidin analogue [(3)H]-demethylphalloin was taken up into skate hepatocytes with high affinity (Km approximately 0.4 microM), and uptake could be inhibited by phalloidin and a variety of typical Oatp/OATP substrates such as bromosulfophthalein, bile salts, estrone-3-sulfate, cyclosporine A and high concentrations of microcystin-LR (Ki approximately 150 microM). When expressed in Xenopus laevis oocytes Oatp1d1 increased uptake of demethylphalloin (Km approximately 2.2 microM) and microcystin-LR (Km approximately 27 microM) 2- to 3-fold over water-injected oocytes, whereas the alternative skate liver organic anion transporter, the dimeric Ostalpha/beta, exhibited no phalloidin and only minor microcystin-LR transport. Also, the closest mammalian Oatp1d1 orthologue, the human brain and testis OATP1C1, did not show any phalloidin transport activity. These results demonstrate that the evolutionarily ancient Oatp1d1 is able to mediate uptake of cyclic oligopeptide toxins into skate liver. The findings support the notion that Oatp1d1 is a precursor of the liver-specific mammalian Oatps/OATPs and that its transport properties are closely associated with certain forms of toxic liver injury such as for example protein phosphatase inhibition by the water-borne toxin microcystin.

Animals↗

Injuries and small-wheel skates.

STUDY OBJECTIVE: To determine the types of injuries sustained during the use of in-line skates and to compare them with injuries sustained during the use of roller skates and skateboards, which have similar riding mechanics; and to assess the protection afforded by wrist, elbow, and knee guards. METHODS: The study population was a consecutive series of injured patients who presented to the emergency department of a Level 1 trauma center between May 1992 and October 1993. RESULTS: Of the 137 patients with skating injuries evaluated in the ED during the study period, 63 (46%) were in-line skaters, 36 (26%) were roller skaters, and 38 (28%) were skateboarders. Minor injuries (sprains, bruises, lacerations) were more common than fractures, and there was no statistical difference in the types of injury between skate groups (P=NS). The most common serious injury was fracture of the distal arm, which occurred in each of the three skater groups (43%, n=59). Of these patients 37% (n=21) required open or closed orthopedic reduction. More fractures of the distal forearm or elbow occurred among skaters who had not been wearing wrist guards (P=.013; risk ratio, 2.07; 95% confidence interval, 1.37 to 3.13). Only 25% of skaters used any protective equipment. In-line skaters owned and used protective equipment more often than did roller-skaters or skateboarders. Most injuries occurred while the patient was travelling in the street or on the sidewalk. Injuries occurred more commonly because the skater was going too fast (35%), because the skater struck an object in the pavement (20%), or because the skater was unable to brake (19%) than because of equipment failure (2%) or interference from motor vehicles (3%). CONCLUSION: Injuries sustained by in-line skaters were similar to those sustained by roller skaters and skateboarders. The risk of wrist or elbow fracture is greater when wrist guards are not worn.

Adolescent↗

A closed pelvic fracture from wheels-in-line skating.

Wheels-in-line skating is the fastest growing recreational sport in the United States. An estimated 105,000 in-line skating injuries received treatment in emergency departments in 1995. This article reports an unusual in-line skating injury: a closed pelvic fracture requiring hospitalization. More commonly encountered injuries are also reviewed. Although there is increasing evidence that in-line skating is associated with a significant number of injuries, protective gear remains greatly underused. It is prudent to promote the use of protective gear, which should include a helmet, wrist guards, and knee and elbow protectors.

Accidental Falls↗

Physiological comparison of roller skating, treadmill running and ergometer cycling.

This study was undertaken to determine the metabolic and cardiorespiratory differences between treadmill running, ergometer cycling and roller skating in top level roller skaters. The subjects performed 3 discontinuous graded tests until exhaustion. The protocol was established so that heart rate kinetics during exercise were similar in all the tests. Maximal oxygen uptake (VO2max), maximal heart rate and exercise time to exhaustion were higher during running (p < 0.05) than during cycling. Blood lactate during submaximal and maximal running exercise was significantly lower (p < 0.05) than during cycling or roller skating. There were no differences between cycling and roller skating in any of the variables studied. These results seem to suggest that, compared with running, VO2max during cycling is limited more by local muscle fatigue than by cardiac factors. The similar response found during roller skating and cycling supports the concept that cycloergometer testing is a valid simple laboratory test for testing physical fitness in top level roller skaters.

Adolescent↗

Moments of force, power, and muscle coordination in speed-skating.

Two well-trained speed-skaters were subjected to a biomechanical analysis incorporating push-off forces, cinematographic data, and link segment modeling. To gain knowledge on the backgrounds on technique and performance in speed-skating, the muscle coordination was studied by EMG and muscle contraction velocities. In speed-skating during the push-off, the body center of gravity (cg) is accelerated with respect to the point of application of the push-off force, with a forward gliding skate. The velocity of cg is a result of rotation of segments. Due to the absence of plantar flexion of the foot, the knee extension range is limited. The short and explosive push-off can be considered as a catapult-like action. The knee extensor muscles vastus medialis and rectus femoris are prestretched in the gliding phase by the antagonistic action of gastrocnemius and biceps femoris. In this phase the skater rotates his cg from the lateral to the medial side of the skate to reach an optimal push-off angle. The power output in the push-off phase is mainly generated by the monoarticular extensor muscles gluteus maximus and vastus medialis.

Ankle Joint↗

Measurement in speed skating tournaments.

Twenty principal components analyses were performed on the results of 10 European and 10 World male speed skating championships. The first principal component obtained was defined as 'the ability to skate well at all tournament distances'. Therefore the rank order of the participants' skating ability could be estimated in an alternative way to allow validation of the scoring method currently in force. This validity coefficient turned out to be so high (r = 0.967) that it does not seem necessary to adopt a more sophisticated method, despite a few demonstrable shortcomings of the one in use. However, there remains a considerable proportion of variance (10-34%) that can not be explained by systematic aspects of skating ability.

Humans↗

Applied physiology of speed skating.

Speed skating exercise can be better understood by taking account of physiological and biomechanical considerations. Comparison with other sports shows the unique and peculiar way of skating propulsion. The relatively long lasting isometric muscle contractions during the gliding phase, alternated with high power output push-offs, place unusual demands on the (local) energy delivering systems. The short and explosive push-off needs a specific pattern of motor unit recruitment. Some mixture of slow twitch (to sustain skating posture) and fast twitch fibres (to effect push off) in the hip and knee extensors seems necessary for optimal skating performance.

Biomechanical Phenomena↗

The little skate Raja erinacea exhibits an extrahepatic ornithine urea cycle in the muscle and modulates nitrogen metabolism during low-salinity challenge.

Urea synthesis via the hepatic ornithine urea cycle (OUC) has been well described in elasmobranchs, but it is unknown whether OUC enzymes are also present in extrahepatic tissues. Muscle and liver urea, trimethylamine oxide (TMAO), and other organic osmolytes, as well as selected OUC enzymes (carbamoyl phosphate synthetase III, ornithine transcarbamoylase, arginase, and the accessory enzyme glutamine synthetase), were measured in adult little skates (Raja erinacea) exposed to 100% or 75% seawater for 5 d. Activities of all four OUC enzymes were detected in the muscle. There were no changes in muscle OUC activities in skates exposed to 75% seawater; however, arginase activity was significantly lower in the liver, compared to controls. Urea, TMAO, and several other osmolytes were significantly lower in the muscle of little skates exposed to 75% seawater, whereas only glycerophosphorylcholine was significantly lower in the liver. Urea excretion rates were twofold higher in skates exposed to 75% seawater. Taken together, these data suggest that a functional OUC may be present in the skeletal muscle tissues of R. erinacea. As well, enhanced urea excretion rates and the downregulation of the anchor OUC enzyme, arginase, in the liver may be critical in regulating tissue urea content under dilute-seawater stress.

Analysis of Variance↗

Roller skating accidents and injuries.

A consecutive series of 65 fractures, dislocations, and ligament tears produced by roller skating accidents treated by the Orthopaedic Department of the Mt. Sinai Services at City Hospital Center of Elmhurst, New York, is reviewed. It was learned that the injuries resulting from collisions occurring in a skating rink were more serious than those resulting from street accidents. Data indicated that lack of expertise is a prominent factor in the production of serious injury. However, the sport has inherent risk which is not eliminated by expertise. It was concluded that roller skating can and does produce disabling injuries. In order to reduce the number of injuries it will be required to reduce crowding in rinks, designate separate beginners' areas, use training wheels or clampon-type of skates when learning, encourage lessons, and separate beginners in the rinks.

Accident Prevention↗

Compromised oxygen uptake in speed skaters during treadmill in-line skating.

The "sitting" posture of speed skating may result in compromised blood flow to the working muscles, thus limiting oxygen uptake. To examine this metabolic problem, male (N = 7) short track speed skaters performed running (TR), in-line skating upright (US), and in-line skating in the "sitting" position (LS) on a motor driven treadmill on randomized days. Each test consisted of four 4-min stages at 2.24, 2.68, 3.13, and 3.58 m.s-1 (5, 6, 7, and 8 mph) at 5% incline. After a brief rest, athletes performed at 4.03 m.s-1 (9 mph) with elevation increasing 1% each minute to exhaustion. Two on-ice 1000-m time trials (TT) were performed to assess the relationship between performance and laboratory measurements. Peak VO2 was lower during LS (57.2 +/- 2.7, 62.3 +/- 4.0, and 64.3 +/- 1.6; for LS, US, and TR, respectively; P < 0.05). At equivalent speeds, submaximal O2 uptake was lower for LS and blood lactate was higher (P < 0.05). LS peak VO2 (ml.kg-1.min-1) was strongly related to TT (P < 0.05). The depressed VO2 and higher blood lactate during LS may be related to decreased knee or trunk angle. Peak VO2 values during skating did not approach values during running. Evaluation of speed skaters in a sports-specific test is congruent with performance and demonstrates potential in addressing the unique physiological demands of the sport.

Adolescent↗