SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Maria A) ;lar1:(gih)"

Sökning: WFRF:(Maria A) > Gymnastik- och idrottshögskolan

  • Resultat 1-10 av 21
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Fakhrai-Rad, H, et al. (författare)
  • Insulin-degrading enzyme identified as a candidate diabetes susceptibility gene in GK rats.
  • 2000
  • Ingår i: Human Molecular Genetics. - : Oxford University Press (OUP). - 0964-6906 .- 1460-2083. ; 9:14, s. 2149-58
  • Tidskriftsartikel (refereegranskat)abstract
    • Genetic analysis of the diabetic GK rat has revealed several diabetes susceptibility loci. Congenic strains have been established for the major diabetes locus, Niddm1, by transfer of GK alleles onto the genome of the normoglycemic F344 rat. Niddm1 was dissected into two subloci, physically separated in the congenic strains Niddm1b and Niddm1i, each with at least one disease susceptibility gene. Here we have mapped Niddm1b to 1 cM by genetic and pathophysiological characterization of new congenic substrains for the locus. The gene encoding insulin-degrading enzyme (IDE:) was located to this 1 cM region, and the two amino acid substitutions (H18R and A890V) identified in the GK allele reduced insulin-degrading activity by 31% in transfected cells. However, when the H18R and A890V variants were studied separately, no effects were observed, demonstrating a synergistic effect of the two variants on insulin degradation. No effect on insulin degradation was observed in cell lysates, indicating that the effect is coupled to receptor-mediated internalization of insulin. Congenic rats with the IDE: GK allele displayed post-prandial hyperglycemia, reduced lipogenesis in fat cells, blunted insulin-stimulated glucose transmembrane uptake and reduced insulin degradation in isolated muscle. Analysis of additional rat strains demonstrated that the dysfunctional IDE: allele was unique to GK. These data point to an important role for IDE: in the diabetic phenotype in GK.
  •  
2.
  • Schaumberg, Katherine, et al. (författare)
  • The Science Behind the Academy for Eating Disorders' Nine Truths About Eating Disorders
  • 2017
  • Ingår i: European eating disorders review. - : WILEY. - 1072-4133 .- 1099-0968. ; 25:6, s. 432-450
  • Forskningsöversikt (refereegranskat)abstract
    • ObjectiveIn 2015, the Academy for Eating Disorders collaborated with international patient, advocacy, and parent organizations to craft the Nine Truths About Eating Disorders'. This document has been translated into over 30 languages and has been distributed globally to replace outdated and erroneous stereotypes about eating disorders with factual information. In this paper, we review the state of the science supporting the Nine Truths'. MethodsThe literature supporting each of the Nine Truths' was reviewed, summarized and richly annotated. ResultsMost of the Nine Truths' arise from well-established foundations in the scientific literature. Additional evidence is required to further substantiate some of the assertions in the document. Future investigations are needed in all areas to deepen our understanding of eating disorders, their causes and their treatments. ConclusionsThe Nine Truths About Eating Disorders' is a guiding document to accelerate global dissemination of accurate and evidence-informed information about eating disorders. Copyright (c) 2017 John Wiley & Sons, Ltd and Eating Disorders Association.
  •  
3.
  • Xuan, Xing, et al. (författare)
  • Fully Integrated Wearable Device for Continuous Sweat Lactate Monitoring in Sports.
  • 2023
  • Ingår i: ACS Sensors. - : American Chemical Society (ACS). - 2379-3694. ; 8:6, s. 2401-2409
  • Tidskriftsartikel (refereegranskat)abstract
    • The chemical digitalization of sweat using wearable sensing interfaces is an attractive alternative to traditional blood-based protocols in sports. Although sweat lactate has been claimed to be a relevant biomarker in sports, an analytically validated wearable system to prove that has not yet been developed. We present a fully integrated sweat lactate sensing system applicable to in situ perspiration analysis. The device can be conveniently worn in the skin to monitor real-time sweat lactate during sports, such as cycling and kayaking. The novelty of the system is threefold: advanced microfluidics design for sweat collection and analysis, an analytically validated lactate biosensor based on a rational design of an outer diffusion-limiting membrane, and an integrated circuit for signal processing with a custom smartphone application. The sensor covering the range expected for lactate in sweat (1-20 mM), with appropriate sensitivity (-12.5 ± 0.53 nA mM-1), shows an acceptable response time (<90 s), and the influence of changes in pH, temperature, and flow rate are neglectable. Also, the sensor is analytically suitable with regard to reversibility, resilience, and reproducibility. The sensing device is validated through a relatively high number of on-body tests performed with elite athletes cycling and kayaking in controlled environments. Correlation outcomes between sweat lactate and other physiological indicators typically accessible in sports laboratories (blood lactate, perceived exhaustion, heart rate, blood glucose, respiratory quotient) are also presented and discussed in relation to the sport performance monitoring capability of continuous sweat lactate.
  •  
4.
  • Andersson, Eva A, et al. (författare)
  • Improving Strength, Power, Muscle Aerobic Capacity, and Glucose Tolerance through Short-term Progressive Strength Training Among Elderly People.
  • 2017
  • Ingår i: Journal of Visualized Experiments. - : MyJove Corporation. - 1940-087X. ; :125
  • Tidskriftsartikel (refereegranskat)abstract
    • This protocol describes the simultaneous use of a broad span of methods to examine muscle aerobic capacity, glucose tolerance, strength, and power in elderly people performing short-term resistance training (RET). Supervised progressive resistance training for 1 h three times a week over 8 weeks was performed by RET participants (71±1 years, range 65-80). Compared to a control group without training, the RET showed improvements on the measures used to indicate strength, power, glucose tolerance, and several parameters of muscle aerobic capacity. Strength training was performed in a gym with only robust fitness equipment. An isokinetic dynamometer for knee extensor strength permitted the measurement of concentric, eccentric, and static strength, which increased for the RET group (8-12% post- versus pre-test). The power (rate of force development, RFD) at the initial 0-30 ms also showed an increase for the RET group (52%). A glucose tolerance test with frequent blood glucose measurements showed improvements only for the RET group in terms of blood glucose values after 2 h (14%) and the area under the curve (21%). The blood lipid profile also improved (8%). From muscle biopsy samples prepared using histochemistry, the amount of fiber type IIa increased, and a trend towards a decrease in IIx in the RET group reflected a change to a more oxidative profile in terms of fiber composition. Western blot (to determine the protein content related to the signaling for muscle protein synthesis) showed a rise of 69% in both Akt and mTOR in the RET group; this also showed an increase in mitochondrial proteins for OXPHOS complex II and citrate synthase (both ~30%) and for complex IV (90%), in only the RET group. We demonstrate that this type of progressive resistance training offers various improvements (e.g., strength, power, aerobic capacity, glucose tolerance, and plasma lipid profile).
  •  
5.
  • Bergström, Göran, et al. (författare)
  • Prevalence of Subclinical Coronary Artery Atherosclerosis in the General Population
  • 2021
  • Ingår i: Circulation. - : Wolters Kluwer. - 0009-7322 .- 1524-4539. ; 144:12, s. 916-929
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Early detection of coronary atherosclerosis using coronary computed tomography angiography (CCTA), in addition to coronary artery calcification (CAC) scoring, may help inform prevention strategies. We used CCTA to determine the prevalence, severity, and characteristics of coronary atherosclerosis and its association with CAC scores in a general population.Methods: We recruited 30 154 randomly invited individuals age 50 to 64 years to SCAPIS (the Swedish Cardiopulmonary Bioimage Study). The study includes individuals without known coronary heart disease (ie, no previous myocardial infarctions or cardiac procedures) and with high-quality results from CCTA and CAC imaging performed using dedicated dual-source CT scanners. Noncontrast images were scored for CAC. CCTA images were visually read and scored for coronary atherosclerosis per segment (defined as no atherosclerosis, 1% to 49% stenosis, or ≥50% stenosis). External validity of prevalence estimates was evaluated using inverse probability for participation weighting and Swedish register data.Results: In total, 25 182 individuals without known coronary heart disease were included (50.6% women). Any CCTA-detected atherosclerosis was found in 42.1%; any significant stenosis (≥50%) in 5.2%; left main, proximal left anterior descending artery, or 3-vessel disease in 1.9%; and any noncalcified plaques in 8.3% of this population. Onset of atherosclerosis was delayed on average by 10 years in women. Atherosclerosis was more prevalent in older individuals and predominantly found in the proximal left anterior descending artery. Prevalence of CCTA-detected atherosclerosis increased with increasing CAC scores. Among those with a CAC score >400, all had atherosclerosis and 45.7% had significant stenosis. In those with 0 CAC, 5.5% had atherosclerosis and 0.4% had significant stenosis. In participants with 0 CAC and intermediate 10-year risk of atherosclerotic cardiovascular disease according to the pooled cohort equation, 9.2% had CCTA-verified atherosclerosis. Prevalence estimates had excellent external validity and changed marginally when adjusted to the age-matched Swedish background population.Conclusions: Using CCTA in a large, random sample of the general population without established disease, we showed that silent coronary atherosclerosis is common in this population. High CAC scores convey a significant probability of substantial stenosis, and 0 CAC does not exclude atherosclerosis, particularly in those at higher baseline risk.
  •  
6.
  • Gago, Paulo, 1984-, et al. (författare)
  • Effects of post activation potentiation on electromechanical delay
  • 2019
  • Ingår i: Clinical Biomechanics. - : Elsevier. - 0268-0033 .- 1879-1271. ; 70, s. 115-122
  • Tidskriftsartikel (refereegranskat)abstract
    • Electromechanical delay (EMD) presumably depends upon both contractile and tensile factors. It has recently been used as an indirect measure of muscle tendon stiffness to study adaptations to stretching and training. The aim of the present study was to investigate whether contractile properties induced by a 6 s maximum voluntary isometric contraction (MVIC) could affect EMD without altering passive muscle tendon stiffness or stiffness index. Plantar flexor twitches were evoked via electrical stimulation of the tibial nerve in eight highly trained male sprinters before and after a 6 s MVIC in passive isometric or passively shortening or lengthening muscles. For each twitch, EMD, twitch contractile properties and SOLM-Wave were measured. Passive muscle tendon stiffness was measured from the slope of the relation between torque and ankle angle during controlled passive dorsal flexion and stiffness index by curve-fitting the torque angle data using a second-order polynomial function. EMD did not differ between isometric, lengthening or shortening movements. EMD was reduced by up to 11.56 ± 5.64% immediately after the MVIC and stayed depressed for up to 60 s after conditioning. Peak twitch torque and rate of torque development were potentiated by up to 119.41 ± 37.15% and 116.06 ± 37.39%, respectively. Rising time was reduced by up to 14.46 ± 7.22%. No significant changes occurred in passive muscle tendon stiffness or stiffness index. Using a conditioning MVIC, it was shown that there was an acute enhancement of contractile muscle properties as well as a significant reduction in EMD with no corresponding changes in stiffness. Therefore, caution should be taken when using and interpreting EMD as a proxy for muscle tendon stiffness.
  •  
7.
  • Gago, Paulo, et al. (författare)
  • Passive Muscle Length Changes Affect Twitch Potentiation in Power Athletes.
  • 2014
  • Ingår i: Medicine & Science in Sports & Exercise. - 0195-9131 .- 1530-0315. ; 46:7, s. 1334-1342
  • Tidskriftsartikel (refereegranskat)abstract
    • INTRODUCTION: A conditioning maximal voluntary muscle action (MVC) has been shown to induce post-activation potentiation, i.e. improved contractile muscle properties, when muscles are contracted isometrically. It is still uncertain how the contractile properties are affected during ongoing muscle length changes. The purpose of this study was to investigate the effects of a 6 s conditioning MVC on twitch properties of the plantar flexors during ongoing muscle length changes.METHODS: Peak twitch, rate of torque development (RTD) and relaxation (RTR), rising time and half relaxation time (HRT) were measured from supramaximal twitches evoked in the plantar flexors of 11 highly trained athletes. Twitches were evoked prior to a 6 s MVC and subsequently on 8 different occasions during a 10-minute recovery, for five different modes: fast lengthening, slow lengthening, isometric, fast shortening and slow shortening of the plantar flexors.RESULTS: The magnitude and duration of effects from the conditioning MVC were significantly different between modes. Peak twitch, RTD and RTR significantly increased for all modes but more so for twitches evoked during fast and slow shortening as compared to lengthening. Rising time was reduced in the lengthening modes, but slightly prolonged in the shortening modes. HRT was significantly reduced for all modes except fast lengthening.CONCLUSION: The findings show that the effects of a conditioning MVC on twitch contractile properties are dependent on direction and velocity of ongoing muscle length changes. This may imply that functional enhancements from a conditioning MVC might be expected to be greatest for concentric muscle actions, but are still present in isometric and eccentric parts of a movement.
  •  
8.
  • Gago, Paulo, et al. (författare)
  • Post Activation Potentiation of the Plantarflexors: Implications of Knee Angle Variations
  • 2017
  • Ingår i: Journal of Human Kinetics. - : Walter de Gruyter GmbH. - 1640-5544 .- 1899-7562. ; 57, s. 29-38
  • Tidskriftsartikel (refereegranskat)abstract
    • Flexing the knee to isolate the single joint soleus from the biarticular gastrocnemius is a strategy forinvestigating individual plantarflexor's post activation potentiation (PAP). We investigated the implications of testingplantarflexor PAP at different knee angles and provided indirect quantification of the contribution of gastrocnemiuspotentiation to the overall plantarflexor enhancements post conditioning. Plantarflexor supramaximal twitches weremeasured in ten male power athletes before and after a maximal isometric plantarflexion (MVIC) at both flexed andextended knee angles. Mean torque and soleus (SOLRMS) and medial gastrocnemius (MGRMS) activity were measuredduring the MVIC. The mean torque and MGRMS of the MVIC were lower (by 33.9 and 42.4%, respectively) in the flexedcompared to the extended position, with no significant difference in SOLRMS. After the MVIC, twitch peak torque (PT)and the rate of torque development (RTR) potentiated significantly more (by 17.4 and 14.7% respectively) in theextended as compared to the flexed knee position, but only immediately (5 s) after the MVIC. No significant differenceswere found in the twitch rate of torque development (RTD) potentiation between positions. It was concluded that kneejoint configuration should be taken into consideration when comparing studies of plantarflexor PAP. Furthermore,results reflect a rather brief contribution of the gastrocnemius potentiation to the overall plantarflexor twitchenhancements.
  •  
9.
  • Hjeltnes, N, et al. (författare)
  • Regulation of UCP2 and UCP3 by muscle disuse and physical activity in tetraplegic subjects.
  • 1999
  • Ingår i: Diabetologia. - : Springer Science and Business Media LLC. - 0012-186X .- 1432-0428. ; 42:7, s. 826-30
  • Tidskriftsartikel (refereegranskat)abstract
    • AIMS/HYPOTHESIS: The regulation of uncoupling protein 2 and uncoupling protein 3 gene expression in skeletal muscle has recently been the focus of intense interest. Our aim was to determine expression of uncoupling protein 2 and 3 in skeletal muscle from tetraplegic subjects, a condition representing profound muscle inactivity. Thereafter we determined whether exercise training would modify expression of these genes in skeletal muscle.METHODS: mRNA expression of uncoupling protein 2 and 3 was determined using quantitative reverse transcription-polymerase chain-reaction.RESULTS: Expression of uncoupling protein 2 and 3 mRNA was increased in skeletal muscle from tetraplegic compared with able-bodied subjects (3.7-fold p < 0.01 and 4.1-fold, p < 0.05, respectively). A subgroup of four tetraplegic subjects underwent an 8-week exercise programme consisting of electrically-stimulated leg cycling (ESLC, 7 ESLC sessions/week). This training protocol leads to increases in whole body insulin-stimulated glucose uptake and expression of genes involved in glucose metabolism in skeletal muscle from tetraplegic subjects. After ESLC training, uncoupling protein 2 expression was reduced by 62% and was similar to that in able-bodied people. Similarly, ESLC training was associated with a reduction of uncoupling protein 3 expression in skeletal muscle from three of four tetraplegic subjects, however, post-exercise levels remained increased compared with able-bodied subjects.CONCLUSION/INTERPRETATION: Tetraplegia is associated with increased mRNA expression of uncoupling protein 2 and 3 in skeletal muscle. Exercise training leads to normalisation of uncoupling protein 2 expression in tetraplegic subjects. Muscle disuse and physical activity appear to be powerful regulators of uncoupling protein 2 and 3 expression in human skeletal muscle.
  •  
10.
  • Kuster, Roman P, et al. (författare)
  • Detecting Prolonged Sitting Bouts with the ActiGraph GT3X.
  • 2020
  • Ingår i: Scandinavian Journal of Medicine and Science in Sports. - Stockholm : Wiley-Blackwell. - 0905-7188 .- 1600-0838. ; 30:3, s. 572-582
  • Tidskriftsartikel (refereegranskat)abstract
    • The ActiGraph has a high ability to measure physical activity, however, it lacks an accurate posture classification to measure sedentary behaviour. The aim of the present study was to develop an ActiGraph (waist-worn, 30Hz) posture classification to detect prolonged sitting bouts, and to compare the classification to proprietary ActiGraph data. The activPAL, a highly valid posture classification device, served as reference criterion.1 Both sensors were worn by 38 office workers over a median duration of 9 days. An automated feature selection extracted the relevant signal information for a minute based posture classification. The machine-learning algorithm with optimal feature number to predict the time in prolonged sitting bouts (≥5 and ≥10 minutes) was searched and compared to the activPAL using Bland-Altman statistics. The comparison included optimised and frequently used cut-points (100 and 150 counts-per-minute (cpm), with and without low-frequency-extension (LFE) filtering). The new algorithm predicted the time in prolonged sitting bouts most accurate (bias ≤7 minutes/day). Of all proprietary ActiGraph methods, only 150 cpm without LFE predicted the time in prolonged sitting bouts non-significantly different from the activPAL (bias ≤18 minutes/day). However, the frequently used 100 cpm with LFE accurately predicted total sitting time (bias ≤7 minutes/day). To study the health effects of ActiGraph measured prolonged sitting, we recommend using the new algorithm. In case a cut-point is used, we recommend 150 cpm without LFE to measure prolonged sitting, and 100 cpm with LFE to measure total sitting time. However, both cpm cut-points are not recommended for a detailed bout analysis.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-10 av 21
Typ av publikation
tidskriftsartikel (20)
forskningsöversikt (1)
Typ av innehåll
refereegranskat (21)
Författare/redaktör
Mehlig, Kirsten, 196 ... (3)
Åberg, Maria A I, 19 ... (3)
Lissner, Lauren, 195 ... (3)
Zierath, J. R. (3)
Hagströmer, Maria (3)
Lebedev, A. (2)
visa fler...
Börjesson, Mats, 196 ... (2)
af Geijerstam, Agnes (2)
Engström, Gunnar (1)
Krook, A (1)
Ahlström, Håkan (1)
Gisslén, Magnus, 196 ... (1)
Magnusson, Martin (1)
Eriksson, Mats (1)
Lind, Lars (1)
Lindqvist, Per (1)
Persson, Margaretha (1)
Rosengren, Annika, 1 ... (1)
Adiels, Martin, 1976 (1)
Bolam, Kate A. (1)
Erlinge, David (1)
Kuhn, Hans-Georg, 19 ... (1)
Persson, Anders (1)
Robertson, Josefina (1)
Crespo, Gaston A., 1 ... (1)
Galli, J. (1)
Rosengren, Annika (1)
Berglund, Göran (1)
Engvall, Jan E. (1)
Hagström, Emil (1)
Wallberg-Henriksson, ... (1)
Goncalves, Isabel (1)
Chen, Chen (1)
Rundqvist, H (1)
Lindberg, Eva (1)
Luthman, H (1)
Hjeltnes, N (1)
Norgren, S (1)
Ostenfeld, Ellen (1)
Alfredsson, Joakim (1)
Jernberg, Tomas (1)
Sundström, Johan (1)
Söderberg, Stefan (1)
Lindgren, Martin (1)
Ghaderi, Ata (1)
Swahn, Eva (1)
Östgren, Carl Johan (1)
de Faire, Ulf (1)
Olivo, Gaia (1)
Hjelmgren, Ola (1)
visa färre...
Lärosäte
Karolinska Institutet (15)
Göteborgs universitet (5)
Umeå universitet (2)
Stockholms universitet (2)
Kungliga Tekniska Högskolan (1)
visa fler...
Jönköping University (1)
Högskolan i Skövde (1)
Högskolan Dalarna (1)
Sophiahemmet Högskola (1)
visa färre...
Språk
Engelska (21)
Forskningsämne (UKÄ/SCB)
Medicin och hälsovetenskap (20)
Naturvetenskap (1)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy