ライフサイエンスコーパス: treadmill

1 re automated behavior, such as stepping on a treadmill.

2 field potential in mice running on a linear treadmill.

3 rded grid cells as animals ran in place on a treadmill.

4 optimal strategy for walking on a split-belt treadmill.

5 ce during locomotion on the laterally tilted treadmill.

6 oints included walking distances on a graded treadmill.

7 m for head-fixed mice running on a spherical treadmill.

8 the cat and a sustained lateral tilt of the treadmill.

9 waist-pull perturbations while walking on a treadmill.

10 r awake mice were stationary or running on a treadmill.

11 that were free to rest or run on a spherical treadmill.

12 level of work when tested to exhaustion on a treadmill.

13 ons in head-fixed mice placed on a spherical treadmill.

14 train a simple mechanical model of the actin treadmill.

15 rated for each participant using an inclined treadmill.

16 CoM was significantly reduced on the curved treadmill.

17 before the behavioural tasks by running on a treadmill.

18 cts walk on a curved treadmill and on a flat treadmill.

19 ing epochs of rest and walking on a circular treadmill.

20 ll as supported faster speed on a mechanical treadmill.

21 hape) when animals ran on level and inclined treadmills.

22 or 5 d/week or placed control mice on static treadmills.

23 observed when animals locomoted on inclined treadmills.

24 olar filaments, which annealed laterally and treadmilled.

25 lex nucleated TubZ filaments and allowed for treadmilling.

26 ectional polymerization cycle referred to as treadmilling.

27 in equilibrium with the polymer during actin treadmilling.

28 pod development and the rate of pseudopodial treadmilling.

29 We exercised wild-type BALB/c mice on a treadmill (10 m/min for 1 h) for 5 d/week or placed cont

30 Arp2/3 complex is an essential organizer of treadmilling actin filament arrays but has little effect

31 esent work were as follows: (1) to develop a treadmill allowing the assessment of locomotion of intac

32 ions could occur during real locomotion on a treadmill and determined their consequences on the overt

33 py, we show that bacterial mini microtubules treadmill and display dynamic instability, another hallm

34 ity and cognitive impairment across both the treadmill and lipectomy studies, so we manipulated hippo

35 mplished by having subjects walk on a curved treadmill and on a flat treadmill.

36 easured by force sensitive foot soles during treadmill and over ground walking.

37 bearing locomotion of the paralysed leg on a treadmill and overground.

38 serum levels, restored running capacity on a treadmill and reduced muscle membrane leakiness in vivo

39 in the mechanical balance driving the actin treadmill and reproduces the recent experimental observa

40 The combination of treadmill and resistance exercises may result in greater

41 eas 5b and 7 of the PPC of cats walking on a treadmill and stepping over a moving obstacle whose spee

42 nd that to contract, actin filaments have to treadmill and to be sufficiently cross linked, and myosi

43 Mice were trained for 6 weeks by treadmill and voluntary wheel running or housed normally

44 proteins had dynamics consistent with actin treadmilling and microvillar lifetimes.

45 Microtubule treadmilling and protein synthesis have been estimated t

46 on (CHAIR), constrained locomotion in space (TREADMILL), and unconstrained locomotion (WALK).

47 We estimate forces in the actin treadmill, and we demonstrate that measured G-actin dist

48 bjects with simulated amputation walked on a treadmill at 1.25 m . s(-1).

49 HSA-/-) , mice were able to acutely run on a treadmill at an intensity sufficient to increase hippoca

50 healthy, young, male lowlanders walked on a treadmill at seven gait speeds (0.67-1.83 m s(-1)) on a

51 ase chain reaction, and CRF assessed using a treadmill-based exercise test.

52 blood and brain of normal rats, as well as a treadmill-based maximum capacity test (MCT).

53 Primary clinical outcomes included objective treadmill-based walking performance and subjective quali

54 rea CA1 of head-fixed mice actively moving a treadmill belt rich with visual-tactile stimuli.

55 hindlimb stepping-like movements on a moving treadmill belt, but with no rhythmic activity in the for

56 The present study findings indicate that (1) treadmill-calibrated heart rate recordings can be used a

57 including 2.5-fold greater speed in a forced treadmill challenge.

58 FtsAZ filaments treadmilled circumferentially around the division ring a

59 rats that underwent endurance training on a treadmill compared with those that performed RT by climb

60 al adhesions and the velocity of microtubule treadmilling compared with GDC-0941, suggesting that mec

61 lar fluid with contractility throughout, but treadmilling connected to a thin layer near the supporti

62 models of leading-edge protrusion rely on a treadmilling dendritic actin network that undergoes cont

63 Polymer treadmilling did not occur.

64 coordinated stepping movements at different treadmill directions.

65 Each 1-minute decline in treadmill duration between baseline and Year 20 was asso

66 e used age- and sex-specific distribution of treadmill duration from the overall Cooper Center Longit

67 Linear regression models regressed the treadmill duration on food groups and dietary scores and

68 nd wine) were positively associated with the treadmill duration overall; whole fruit (not juices), or

69 eak lung function, each additional minute of treadmill duration was associated with 1.00 ml/yr less d

70 The treadmilling dynamics direct the processive movement of

71 heir the C-tails may facilitate the coherent treadmilling dynamics of membrane-associated FtsZ bundle

72 stance on the 6-minute walk: lower-intensity treadmill exercise (12% increase; P=.001), stretching an

73 INTERVENTIONS; (1) A higher-intensity treadmill exercise (30 minutes at 70%-80% of heart rate

74 f heart rate reserve), (2) a lower-intensity treadmill exercise (50 minutes at 40%-50% of heart rate

75 s (9% increase; P<.02), and higher-intensity treadmill exercise (6% increase; P=.07), with no between

76 Supervised exercise consisted of treadmill exercise 3 times weekly for 6 months.

77 tes mediates part of the PGC-1a induction by treadmill exercise and its downstream effects on mitocho

78 mentally-set metabolic deficits, we compared treadmill exercise and NMN injection in offspring of obe

79 After 45 min of treadmill exercise at 70% of the peak oxygen uptake, par

80 ice exhibited poorer cardiac function, worse treadmill exercise capacity, and greater myocardial scar

81 Treadmill exercise capacity, forelimb grip strength, and

82 Thus, treadmill exercise does not affect muscle (18)F-FDG upta

83 In the SKM-D2KO mice, acute treadmill exercise failed to induce PGC-1a fully in sole

84 Female offspring weaned onto HFD were given treadmill exercise for 9 weeks, or NMN injection daily f

85 mine whether GM-CSF combined with supervised treadmill exercise improves 6-minute walk distance, comp

86 r studies reveal that 6 weeks of swimming or treadmill exercise improves heart pump function and redu

87 on of m. extensor digitorum longus (EDL) and treadmill exercise increased muscle and whole-body insul

88 extensor digitorum longus (EDL) and treadmill exercise increased muscle and whole-body insul

89 In conclusion, acute treadmill exercise increases SKM D2 expression through a

90 We report the effects of treadmill exercise on (18)F-FDG uptake in skeletal muscl

91 Treadmill exercise performance was also studied.

92 This study indicates that treadmill exercise reduces brain injury in stroke.

93 The lower-intensity treadmill exercise resulted in the greatest improvement

94 An acute treadmill exercise session (20 min at 70-75% of maximal

95 Among patients with PAD, supervised treadmill exercise significantly improved 6-minute walk

96 ular risk factor assessment, and incremental treadmill exercise test to evaluate CRF.

97 CRF was quantified by a maximal treadmill exercise test.

98 Fitness was measured by a maximal treadmill exercise test.

99 pacity in CHF as assessed by symptom-limited treadmill exercise testing and measurement of peak oxyge

100 dults study aged 18-30 in 1985 who underwent treadmill exercise testing at baseline visit, and 2,735

101 ex and CRF quantified as duration of maximal treadmill exercise testing.

102 underwent symptom-limited Naughton protocol treadmill exercise tests.

103 e in skeletal muscle is upregulated by acute treadmill exercise through a beta-adrenergic receptor-de

104 sitive lipase (HSL) knockout (KO) mice after treadmill exercise to stimulate the accumulation of DAGs

105 of the animals also performed low intensity treadmill exercise training.

106 related with reduced brain injury induced by treadmill exercise, in rats after cerebral ischemia.

107 diameter and density in response to physical treadmill exercise, whereas in Mkx(-/-) mice, tendons fa

108 eficient mice underwent echocardiography and treadmill exercise.

109 in the ischemic penumbra of rat brains after treadmill exercise.

110 olism in mice subjected to acute and chronic treadmill exercise.

111 y decreased fatty acid (FA) oxidation during treadmill exercise.

112 vels quantified by peak oxygen uptake during treadmill exercise.

113 used alone or when combined with supervised treadmill exercise.

114 was to investigate the role of caveolin-1 in treadmill-exercise-induced angiogenesis in the ischemic

115 Both the higher- and lower-intensity treadmill exercises improved cardiovascular fitness.

116 Both treadmill exercises improved peak $$ VO2 (7%-8% increase

117 s ST, 79 completed the 18-month clinical and treadmill follow-up assessment.

118 ontrol while 4 of 9 cats were trained on the treadmill for 20 min, 5 d a week for 3 weeks.

119 e walking protocol, participants walked on a treadmill for 5.5 h at approximately 3x resting energy e

120 ly cats) are often assessed on a simple flat treadmill (FTM), which imposes little demands on suprasp

121 ement on the rungs fixed to an ordinary flat treadmill (FTM).

122 Thus, FtsZ treadmilling guides the progressive insertion of new cel

123 arily on a running wheel, whereas HIT on the treadmill had a smaller, statistically non-significant e

124 Although the biochemical kinetics of treadmilling has been well characterized, the atomistic

125 for high- and low-capacity for running on a treadmill (HCR; LCR) also differ in wheel-running behavi

126 es, 22-35 years old) attempting to walk on a treadmill in synchrony with a series of pacing cue tones

127 motor deficits, they can walk on a circular treadmill in the direction ipsilateral to their lesion.

128 que and essential role in accelerating actin treadmilling in filamentous actin (F-actin) in a nucleot

129 hether adaptation to walking on a split-belt treadmill leads to a more economical walking pattern.

130 n which tethered bees walking on a spherical treadmill learn to discriminate visual stimuli video pro

131 in the spinal state by interventions such as treadmill locomotor training started within a few days a

132 ace the paws on the rungs of a moving ladder treadmill (LTM); (2) to assess the capability of cats af

133 EMENT This paper introduces a method (ladder treadmill [LTM]) to study the locomotor ability of cats

134 PLC, suggesting that increased actin network treadmilling may be a widespread mechanism for promoting

135 ectively; for FT: normal, mild=late positive treadmill, moderate=early positive treadmill or single-v

136 Different directions of the treadmill motion relative to the body axis were used (0,

137 are actively repositioned at the synapse by treadmilling of the actin cytoskeleton, an influence whi

138 h our robot rehabilitation paradigm, whereas treadmill-only trained do not.

139 ther continually renewed every 24-48 h via a treadmill or are stable, exceptionally long-lived struct

140 positive treadmill, moderate=early positive treadmill or single-vessel ischemia, and severe=large is

141 ilaments grow in a helical fashion following treadmilling or dynamic instability, although the underl

142 Treadmill organization requires myosin-2-powered contrac

143 ere measured when the subjects walked on the treadmill over three periods: baseline (1 min), adaptati

144 Secondary end points included treadmill pain-free walking distance, vascular quality o

145 Adapting this discrimination to the treadmill paradigm with a tethered, walking bee was succ

146 Furthermore, the ladder treadmill permits to train cats repetitively for weeks a

147 uniform density, whereas the rest forms the treadmilling polymer network.

148 ow that crawling uses a combination of actin treadmilling (polymerization), which pushes the front of

149 scherichia coli cells, FtsZ exhibits dynamic treadmilling predominantly determined by its guanosine t

150 eocilia occurs only at the tips and not by a treadmilling process.

151 ss levels, assessed using the modified Balke treadmill protocol between 1971 and 2009, and incident a

152 Thus, FtsZ treadmilling provides a mechanism for achieving uniform

153 The FtsZ treadmilling rate controlled both the rate of peptidogly

154 high intensity, short duration (HISD) forced treadmill regimen.

155 rty-two female C57BL/6 mice performed 1 h of treadmill running (18 m min(-1) ; 5 degrees grade), 1 h

156 e infusions) were measured during submaximal treadmill running (20 m min(-1), 5% grade).

157 were determined during supra-critical speed treadmill running (critical speed + 15%, 52.5 +/- 1.3 m

158 ction vs. O-SED) or exercise training (O-EX; treadmill running 20 m min(-1) with a 15% incline, 60 mi

159 vascular conductance (VC) during high-speed treadmill running above critical speed (asymptote of the

160 scent patients, we monitored activity during treadmill running aiming to detect presymptomatic change

161 to the same regimen but with 45 min of daily treadmill running at 70% of maximum oxygen uptake (SUR+E

162 of the animal to either awake immobility or treadmill running by using a head-fixed setup while simu

163 mized obese mice to either aerobic exercise (treadmill running for 30 min per day, 5 days a week, for

164 Here, we show that acute treadmill running in mice causes mitochondrial oxidative

165 ed before and after 10 weeks of a horizontal treadmill running protocol.

166 n both speed and endurance capacity in acute treadmill running tests (P < 0.05).

167 ells exhibited multiple firing fields during treadmill running, parallel to the periodic firing field

168 AT (atATGL-KO) were challenged with chronic treadmill running.

169 corticostriatal axis in rats during rest and treadmill running.

170 at hindlimb skeletal muscle during low-speed treadmill running.

171 effects of nNOS-derived NO during high-speed treadmill running.

172 they also outperformed original mdx mice on treadmill running.

173 om human subjects during cycle ergometry and treadmill running.

174 the skeletal muscles of mice after 30 min of treadmill running.

175 iary metabolism fluxes in both sedentary and treadmill-running mice.

176 Six rats performed three high-speed treadmill runs to exhaustion to determine critical speed

177 lower functional capacity, and a lower Duke Treadmill Score.

178 cs using other tools in women (0.70 for Duke Treadmill Score; 0.74 for Lauer nomogram) and men (0.72

179 4 for Lauer nomogram) and men (0.72 for Duke Treadmill Score; 0.75 for Lauer nomogram).

180 All mice were subjected to twice-weekly treadmill sessions, and functional and behavioral parame

181 pattern kinematics; and (5) are sensitive to treadmill speed and lesion severity, suggesting a role f

182 " behavior and location, while we varied the treadmill speed to distinguish time elapsed from distanc

183 nd finally after a complete SCI at different treadmill speeds.

184 s, and lateral gastrocnemius muscles at four treadmill speeds: 0.2, 0.4, 0.6, and 0.8 m/s.

185 8 versus 7.9+/-2.9 minutes; P<0.001) or peak treadmill stage (2.6+/-0.9 versus 3.1+/-1.0; P<0.001), p

186 ged simultaneously with the hindlimbs during treadmill step-training as opposed to training only the

187 16) use calcium imaging in mice performing a treadmill task to reveal differences in space-coding dyn

188 test (Ex 8), 45 patients within 48 h after a treadmill test (Ex 48), and 34 patients without prior ex

189 48 patients underwent PET within 8 h after a treadmill test (Ex 8), 45 patients within 48 h after a t

190 visit, and 2,735 participants with a second treadmill test 20 years later.

191 h cardiorespiratory fitness (CRF) based on a treadmill test and body mass index (BMI) (weight (kg)/he

192 ompleted at least 1 symptom-limited exercise treadmill test between 1977 and 2001 were included.

193 reduction in FEV(1) (%) after a standardized treadmill test were used for BHR assessment.

194 nderwent physiological examination, stepwise treadmill test with blood lactate analysis, and contrast

195 th syndrome X (chest pain, abnormal exercise treadmill test, normal coronary angiogram without other

196 Actual CRF was measured by a maximal treadmill test.

197 ttery of 3 mental stress tests followed by a treadmill test.

198 alking times were recorded during a standard treadmill test.

199 CRF was assessed by using a graded exercise treadmill test.

200 Fitness was determined by using a maximal treadmill test.

201 y were to (1) examine how data from exercise treadmill testing (ETT) can identify patients who have c

202 ercise-induced abnormalities during exercise treadmill testing (ETT) were initially compared in 60 su

203 xcept a suggestion of myocardial ischemia on treadmill testing and mild atherosclerosis noted on caro

204 rs in 263 HL survivors referred for exercise treadmill testing at a median interval of 19 years after

205 le; 64% white) without AF underwent exercise treadmill testing at a tertiary care center.

206 Risk assessment tools for exercise treadmill testing may have limited external validity.

207 onstrating an arrhythmia burden on Holter or treadmill testing received beta-blocker therapy (17%).

208 higher metabolic equivalent achieved during treadmill testing was associated with a 7% lower risk of

209 ht loss and improved fitness (as assessed on treadmill testing) were significant mediators of this ef

210 racial cohort that underwent graded exercise treadmill testing.

211 ere 18 years or older and underwent exercise treadmill testing.

212 te mortality in patients undergoing exercise treadmill testing.

213 rs, medications, and indication for exercise treadmill testing: odds ratio: 3.96 (95% confidence inte

214 results of downstream testing after exercise treadmill tests (ETTs).

215 assays (P < 0.05) and exercise tolerance in treadmill tests (P < 0.05), whereas miR-126 up-regulatio

216 associated with ischemic changes on exercise treadmill tests independent of traditional cardiac risk

217 stered PTSD Scale, and standardized exercise treadmill tests were performed to detect myocardial isch

218 unction on forced tasks, such as rotarod and treadmill tests, caused by substantia nigra lesioning in

219 performed incremental and run-to-exhaustion treadmill tests.

220 rats on the ketone diet ran 32% further on a treadmill than did control rats that ate an isocaloric d

221 to the substrate creates a stationary actin treadmill that allows leading-edge protrusion when adhes

222 cant increases in gait speed, incline on the treadmill, the maximal voluntary dorsiflexion torque, th

223 c conditions, with the subjects walking on a treadmill, the rasterstereographically-measured side len

224 In FtsZ mutants with severely reduced treadmilling, the spatial distribution of septal synthes

225 al firing patterns as rats ran in place on a treadmill, thus "clamping" behavior and location, while

226 ic quintiles (Q) according to Balke protocol treadmill time with Q1 as low fitness.

227 metabolic equivalents (METs) calculated from treadmill time.

228 imated in metabolic equivalents according to treadmill time.

229 c fitness levels were derived from the Balke treadmill times and categorized into low, intermediate,

230 ot low fit," based on age- and sex- adjusted treadmill times, and were followed for mortality, determ

231 high fit according to age- and sex-specific treadmill times.

232 fixed mice running or resting on a spherical treadmill to study the oscillation-dependent discharges

233 n to map motor cortex in two NTX groups: (1) treadmill trained (control group); and (2) robot-assiste

234 ined (control group); and (2) robot-assisted treadmill trained (improved function group).

235 Cats were not treadmill trained during the hemispinal period.

236 t rate did not decrease significantly in the treadmill training alone group (8.27 [5.55-12.31] falls

237 treadmill training plus VR group (n=154) or treadmill training alone group (n=148).

238 roups (10.7 [SD 35.6] falls per 6 months for treadmill training alone vs 11.9 [39.5] falls per 6 mont

239 s VR led to reduced fall rates compared with treadmill training alone.

240 eeks of either treadmill training plus VR or treadmill training alone.

241 obility would lead to fewer falls than would treadmill training alone.

242 ing remote mechanisms of inflammation, acute treadmill training can harness endogenous spinal plastic

243 Treadmill training could not rescue the regeneration int

244 Because treadmill training evokes broad responses not limited to

245 treadmill training plus VR group than in the treadmill training group (incident rate ratio 0.58, 95%

246 otor plasticity, we delivered lumbar-focused treadmill training in WT and KO mice during early (2-9 d

247 To address this question, we used a treadmill training paradigm in which mice were exposed t

248 adults were randomly assigned to either the treadmill training plus VR group (n=154) or treadmill tr

249 of falls was also significantly lower in the treadmill training plus VR group than in the treadmill t

250 incident rate was significantly lower in the treadmill training plus VR group than it had been before

251 roup of older adults at high risk for falls, treadmill training plus VR led to reduced fall rates com

252 ased allocation to receive 6 weeks of either treadmill training plus VR or treadmill training alone.

253 alone vs 11.9 [39.5] falls per 6 months for treadmill training plus VR).

254 Nerve regeneration was enhanced by treadmill training posttransection, regardless of the BD

255 Treadmill training prevented hippocampal microgliosis, a

256 central pattern generator activity, and that treadmill training promoted the appropriate inhibitory m

257 udy we investigated whether 4 weeks of daily treadmill training with an incline may facilitate cortic

258 he hypothesis that an intervention combining treadmill training with non-immersive virtual reality (V

259 ter 8 (Ex8) and 16 (Ex16) weeks of daily 1-h treadmill training, along with 4 and 8 weeks after exerc

260 ations secondary to both transplantation and treadmill training, and the two therapies combined, with

261 However, after 8 weeks of treadmill training, low responders failed to improve the

262 for running capacity in response to aerobic treadmill training.

263 kill usually acquired after several weeks of treadmill training.

264 exhaustion, accomplished in a non-motorized treadmill using a tethered system.

265 mPFC and MEC in mice running on a spherical treadmill, using two-photon laser-scanning microscopy an

266 mponent analysis to EEG data recorded during treadmill walking allowed us to uncover two distinct bet

267 activity in the VM became more robust during treadmill walking and more coherent with LFP activity in

268 y subjects with right-foot preference during treadmill walking at speeds of 1.1, 1.4 and 1.7 m/s.

269 mary end point was the difference in maximum treadmill walking distance at 12 months between the grou

270 y with GM-CSF 3 times a week did not improve treadmill walking performance at the 3-month follow-up.

271 tudy uses hemiparkinsonian rats performing a treadmill walking task to compare synchronized STN local

272 We studied split-belt treadmill walking that drives people to learn a new gait

273 5 [95% CI, 33.2 to 73.8]; P < .001), maximal treadmill walking time (intervention, 7.91 to 9.44 minut

274 The primary outcome was peak treadmill walking time (PWT) at 3 months.

275 Six-month mean (SE) changes in maximal treadmill walking time were 0.5 (2.3) minutes for the 12

276 the secondary outcomes was change in maximal treadmill walking time.

277 gnificant increases in pain-free and maximum treadmill walking times compared with placebo.

278 cs were recorded by 3D video analysis during treadmill walking with a velocity chosen by the child at

279 the changes of cortical involvement in human treadmill walking with and without BCI control of a walk

280 In contrast, during treadmill walking, marked increases in both motor cortex

281 econdary outcomes included 6-month change in treadmill walking, physical activity, the Walking Impair

282 During overground or treadmill walking, the stance phase and cycle durations

283 d hemisphere of hemiparkinsonian rats during treadmill walking.

284 tex (MCx) in the hemiparkinsonian rat during treadmill walking.

285 reased power output necessary on an inclined treadmill was important in revealing altered activity in

286 course in SOD1G93A mice, especially when the treadmill was inclined, including intermuscular phase, b

287 l coordinated stepping movements only if the treadmill was moving in the front-to-rear direction.

288 Exercise on a treadmill was used as the source of stress in the animal

289 y stereocilia tips had rapid turnover and no treadmilling was observed.

290 fast binding turnover, which we refer to as 'treadmilling', was linked to low transcriptional output.

291 Using a split-belt treadmill, we show that vestibular influence on locomoto

292 ext of adaptation to walking on a split-belt treadmill, which can impose a left-right asymmetry in st

293 t that FtsZ polymers move around the ring by treadmilling, which guides and regulates the inward grow

294 aining involved 30 min of walking daily on a treadmill with an incline for 30 days.

295 Here, human subjects walked on a split-belt treadmill with one belt moving at 0.4 m s(-1) and the ot

296 ecovered function in these rats persisted on treadmill with the robot both actuated and nonactuated,

297 reported their choice by moving a horizontal treadmill with their front limbs.

298 performed on decerebrate cats walking on the treadmill with their hindlimbs, whereas the head and tru

299 l stability in decerebrate cats walking on a treadmill with their hindlimbs.

300 sensus exists on the energetic cost of actin treadmilling, with estimates ranging from < 1% of the br