ライフサイエンスコーパス: thermoregulatory

1 ol: Physical and ecological traits influence thermoregulatory ability and population trends.

2 Finally, we tested whether thermoregulatory ability could explain species' demograp

3 We investigated which factors influence thermoregulatory ability in a subset of the Mediterranea

4 Thermoregulatory ability is impaired in persons with ele

5 social integration has a direct influence on thermoregulatory ability: individual animals that form a

6 The main thermoregulatory abnormality of Trpv1 KO mice was a diff

7 system mediates hypothalamic coordination of thermoregulatory activity and is a primary regulator of

8 central modulatory effect governing efferent thermoregulatory activity in humans.

9 aneous vasodilatation by inhibiting efferent thermoregulatory activity in humans.

10 ripheral (i.e. effector organ) modulation of thermoregulatory activity.

11 Although genetic selection for thermoregulatory adaptation is frequently presumed to be

12 and torpor, neurally regulated metabolic and thermoregulatory adaptations enable survival during peri

13 Although derived musculoskeletal and thermoregulatory adaptations for EPA in humans have been

14 it is hypothesized that cocaine also impairs thermoregulatory adjustments that mediate heat dissipati

15 sweat losses, and hypohydration negates the thermoregulatory advantages conferred by acclimation.

16 Notably, this 'thermoregulatory afferent' pathway exists in parallel wi

17 ral basis for reduced air hunger perception, thermoregulatory and autonomic deficiencies in the syndr

18 eta-endorphin modulates the acute endocrine, thermoregulatory and behavioral response to a social con

19 Experiment 1 addressed the thermoregulatory and cardiovascular concomitants of ultr

20 Ruling out thermoregulatory and immediate effects of social interac

21 ") prompted the current investigation of the thermoregulatory and locomotor effects of 4-MMC.

22 how that the cathinone analog 4-MMC exhibits thermoregulatory and locomotor properties that are disti

23 diotelemetry probes simultaneously monitored thermoregulatory and locomotor responses to various dose

24 rogen-sensitive MPA neurons in directing the thermoregulatory and metabolic responses to energy defic

25 n how trained women will respond from both a thermoregulatory and performance stand-point.

26 In experiment 1, the thermoregulatory and psychomotor responses produced by M

27 Percher vs. flier flight-style, a trait with thermoregulatory and signaling consequences, has not yet

28 nd can be harnessed to differentiate between thermoregulatory and sleep-wake-driven effects in experi

29 The present results suggest that the blunted thermoregulatory and ventilatory responses to hypoxia in

30 both critical sites to regulate sympathetic, thermoregulatory BAT circuits.

31 d, little is known about the extent to which thermoregulatory behavior can be influenced by BAT therm

32 parative research suggests that yawning is a thermoregulatory behavior in homeotherms.

33 ey uncertainty is understanding whether such thermoregulatory behavior occurs in natural forest canop

34 findings indicate that the ability to adjust thermoregulatory behavior to compensate for enhanced met

35 motor and thermogenic capabilities influence thermoregulatory behavior under different task condition

36 Through precise thermoregulatory behavior viviparous phrynosomatids are

37 blish a key link between neural activity and thermoregulatory behavior, elucidating the neural basis

38 itical neural mechanisms underlying flexible thermoregulatory behavior.

39 ated the incidence of yawning to other avian thermoregulatory behaviors in budgerigars (e.g., panting

40 This prediction was supported by thermoregulatory behaviors of lizards in outdoor arenas

41 ng was also positively correlated with other thermoregulatory behaviors.

42 and determine whether seasonal trade-offs in thermoregulatory behaviour shape thermal performance and

43 ctotherms can rely on water availability and thermoregulatory behaviour to buffer constraints along t

44 udy underscores the importance of individual thermoregulatory behaviours for understanding species' v

45 Species also differed in their thermoregulatory behaviours, with some - such as the Rin

46 ctively during cold exposure, gaining little thermoregulatory benefit from the presence of multiple l

47 honeybee (Apis mellifera) protrudes with its thermoregulatory capabilities, which enables a nearly wo

48 ecific differences in water requirements and thermoregulatory capacity and thus sensitivity to climat

49 ents, amphibious mammals have expanded their thermoregulatory capacity at the expense of their olfact

50 ities synchronously associated with gains in thermoregulatory capacity in amphibious taxa sampled fro

51 The hindbrain may be capable of considerable thermoregulatory capacity independent of the hypothalamu

52 roduction is predicted to influence maternal thermoregulatory capacity, as are the size and compositi

53 ponses to temperature driving differences in thermoregulatory capacity.

54 ntial for advancing evidence-based equitable thermoregulatory care.

55 al subdivision of the medial preoptic area ('thermoregulatory center'), and the reticular thalamic nu

56 dian subregion of the preoptic area (POA), a thermoregulatory centre.

57 controlling glucose homoeostasis under this thermoregulatory challenge.

58 ic and amphibious mammals face olfactory and thermoregulatory challenges not generally encountered by

59 ergic (non-p5HT) cells recorded responded to thermoregulatory challenges that evoked an increase in B

60 xtracellularly from raphe cells during three thermoregulatory challenges that evoked an increase in B

61 he brain-mediated mechanisms involved in the thermoregulatory changes observed during lipopolysacchar

62 DMH augment our understanding of the central thermoregulatory circuitry in non-torpid mammals.

63 iceptors, which transduce signals to central thermoregulatory circuits and release proinflammatory fa

64 rgetically costly; thus, it is critical that thermoregulatory circuits are modulated by signals of en

65 istent with the current understanding of BAT thermoregulatory circuits from the DMH/DHA and mPOA.

66 set as well as experiments designed to probe thermoregulatory circuits in zebrafish.

67 ospectra of sympathetic discharges supplying thermoregulatory circulation but not those influencing t

68 ical sympathetic motor rhythm regulating the thermoregulatory circulation of the rat tail (T-rhythm;

69 ere we investigated whether nerves supplying thermoregulatory circulations share common rhythmic disc

70 The central neural circuits of thermoregulatory cold defense have been recently unravel

71 n of key neurons in the central pathways for thermoregulatory cold defense is sufficient to induce a

72 key area of the central nervous pathways for thermoregulatory cold defense, by means of repeated micr

73 to the hypercapnic ventilatory response and thermoregulatory cold defense.

74 spinal somatosensory neurons directly to the thermoregulatory command center, the preoptic area (POA)

75 spinal somatosensory neurons directly to the thermoregulatory command center, the preoptic area.

76 s of top-down versus bottom-up processes and thermoregulatory constraints.

77 dissect brain-body interactions required for thermoregulatory control and examine how coordination be

78 e anterior hypothalamus (POAH), an important thermoregulatory control center in the brain.

79 ll mechanisms involved in cardiovascular and thermoregulatory control during SI, the present study sh

80 However, this refined thermoregulatory control is often challenged by external

81 Thermoregulatory control is sometimes impaired by seriou

82 The effect of opioids on normal thermoregulatory control is well established.

83 ly, men with a PFO appear to have a shift in thermoregulatory control to higher internal temperatures

84 Neuraxial anaesthesia also impairs central thermoregulatory control, and prevents vasoconstriction

85 serotonin (5-HT) neurons to respiratory and thermoregulatory control.

86 Here we quantify energy output and thermoregulatory costs in partially migratory common bla

87 diurnality under natural conditions reduces thermoregulatory costs in small burrowing mammals like m

88 ntributed to species' declines by simulating thermoregulatory costs in the Mojave Desert for 50 bird

89 Here, we explore the potential for thermoregulatory costs to underlie the community collaps

90 hicks (i.e., warmer temperatures that reduce thermoregulatory costs).

91 ding season, driven by a combination of high thermoregulatory costs, diving activity, colony attendan

92 the year in the UK when birds have elevated thermoregulatory costs.

93 Thermoregulatory cutaneous vasodilatation (VD) is attenu

94 bient temperatures and can be explained by a thermoregulatory defect that leads to an increase in mot

95 e protein--containing nerves or some central thermoregulatory defect.

96 The major thermoregulatory defences in humans are sweating, arteri

97 stically express REM sleep when the need for thermoregulatory defense is minimized.

98 uscles and vital organs, because of enhanced thermoregulatory demand for skin blood flow coupled with

99 This study reports testing of a thermoregulatory device-'Thermal Jacket' that includes a

100 is a more sensitive indicator for detecting thermoregulatory differences across biomes.

101 Here we leverage the thermoregulatory differences between mice and hibernatin

102 apeutic target for sympathetic hyperactivity thermoregulatory disorders.

103 Hypothalamic abnormalities and thermoregulatory dysfunction against a milieu of decreas

104 cacy in rat models of ovariectomized-induced thermoregulatory dysfunction and morphine dependent flus

105 lemetric rat model of ovariectomized-induced thermoregulatory dysfunction and were efficacious at ora

106 has suggested that mirtazapine can alleviate thermoregulatory dysfunction by blocking 5-HT(2A) recept

107 2A) receptor blockade appeared to exacerbate thermoregulatory dysfunction in OVX rats.

108 iol, alleviates hot flushes in rat models of thermoregulatory dysfunction of the brain.

109 lemetric rat model of ovariectomized-induced thermoregulatory dysfunction, a mouse p-phenylquinone (P

110 Menopause-associated thermoregulatory dysfunction, including hot flushes and

111 In the morphine-dependent model of thermoregulatory dysfunction, mirtazapine (10 mg/kg, i.p

112 us in animal models of depression, pain, and thermoregulatory dysfunction.

113 sed in two rat models of ovariectomy-induced thermoregulatory dysfunction.

114 in two rodent models of ovariectomy-induced thermoregulatory dysfunction.

115 interventions in subjects without underlying thermoregulatory dysfunction.

116 growth in iron-depleted medium abrogated the thermoregulatory effect, with high-level expression at b

117 ween output of thermointegrative centers and thermoregulatory effector responses rather than processi

118 es the thermosensory information and outputs thermoregulatory effector signals.

119 lation of body temperature, we evaluated the thermoregulatory effects of ablating KNDy neurons by inj

120 or activation plays a permissive role in the thermoregulatory effects of methanandamide.

121 109A, fully recapitulated the somnogenic and thermoregulatory effects of nicotinic acid suggesting th

122 n TAAR1 function in aversive, locomotor, and thermoregulatory effects that are important to consider

123 hat did not produce accompanying sedative or thermoregulatory effects that could concomitantly influe

124 y a dense array of triangular hairs with two thermoregulatory effects.

125 However, the thermoregulatory explanation for hair loss was supported

126 mals is not solely due to metabolic rate and thermoregulatory factors.

127 a profound effect on the development of the thermoregulatory febrile response.

128 This butterfly's wing melanization has a thermoregulatory function and changes seasonally.

129 However, thermoregulatory function during a controlled heat stres

130 ts a central and/or peripheral modulation of thermoregulatory function in humans.

131 To corroborate its thermoregulatory function, we also related the incidence

132 its hair-producing, protective, sensory, and thermoregulatory functions.

133 ory organs implicated in either olfactory or thermoregulatory functions.

134 considered delta(13)C-derived carbon source, thermoregulatory group, and season.

135 s mediated by high-protein crops, but not by thermoregulatory habitat at the scale examined.

136 ons receive the most attention in studies of thermoregulatory homeostasis, but we demonstrated here t

137 nd moonlight (a proxy for predation risk) on thermoregulatory homeostasis.

138 A thermodynamic model of thermoregulatory huddling interactions between endotherm

139 of ambient temperatures over which adaptive thermoregulatory huddling will emerge.

140 clear evidence that alpha-1 AR activation of thermoregulatory hypothalamic neurons will result in a r

141 val was not influenced by activity levels or thermoregulatory indices.

142 orpid rat, either exclusion of the canonical thermoregulatory integrator in the preoptic hypothalamus

143 x gene, ttx-3, functions in the antagonistic thermoregulatory interneuron AIY ().

144 a and help optimize allocation of additional thermoregulatory interventions.

145 nse is replaced by a new, emerging paradigm, thermoregulatory inversion (TI), an alternative homeosta

146 te has been identified - a phenomenon called thermoregulatory inversion.

147 Previous thermoregulatory investigations proposed that an endogen

148 Previously, we showed that activation of a thermoregulatory ion channel, transient receptor potenti

149 epRb neurons in the DMH/DHA and mPOA mediate thermoregulatory leptin action.

150 We posit that these newly identified thermoregulatory macrophages may broaden our view of imm

151 echniques opens up new pathways to realizing thermoregulatory materials and provides an innovative wa

152 Additional thermoregulatory measures may be needed to increase the

153 cool sensory signals from the skin is a core thermoregulatory mechanism within the POA that is essent

154 lations, and biochemical analyses unveil the thermoregulatory mechanisms and dynamics of increased re

155 Therefore, thermoregulatory mechanisms engaged during moderate cool

156 In menopausal women, dysregulation of thermoregulatory mechanisms leads to hot flushes and nig

157 y, and species' relative reliance on the two thermoregulatory mechanisms of wing adjustment versus mi

158 l for required cool housing temperatures and thermoregulatory mechanisms to influence the interpretat

159 s produces effects on drinking and autonomic thermoregulatory mechanisms, providing a structural basi

160 of pharmacologically induced hypothermia and thermoregulatory mechanisms.

161 block measures of METH neurotoxicity by non-thermoregulatory mechanisms.

162 n selection should drive local adaptation of thermoregulatory mechanisms.

163 d in the Tb setting through afferents to the thermoregulatory median preoptic nucleus (MnPO).

164 sent study, we tested whether induction of a thermoregulatory-mediated increase in tissue blood flow,

165 We test hypotheses of how thermoregulatory mode, environmental temperature, protec

166 These findings support a thermoregulatory model of vasomotor symptoms.

167 However, recent thermoregulatory models have postulated that increased a

168 ve sport and protective clothing, as well as thermoregulatory models.

169 ggshell pigmentation may have been shaped by thermoregulatory needs.

170 intain core body temperature in mammals, CNS thermoregulatory networks respond to cold exposure by in

171 ons regulate life-sustaining respiratory and thermoregulatory networks, and demonstrates a noninvasiv

172 to prevalent models, providing a new view on thermoregulatory neural circuits.

173 d is required for the function of AIZ in the thermoregulatory neural network.

174 of a TRPV1 receptor antagonist, A-889425, on thermoregulatory neurons in the medial preoptic area of

175 1 receptors indirectly modulates activity of thermoregulatory neurons in the mPOA in a manner that is

176 Thermoregulatory neurons in the preoptic area of the ant

177 Thermoregulatory neurons of the median preoptic nucleus

178 ch as the hypothalamus, which is the site of thermoregulatory neurons, is critical for the febrile re

179 on the brown adipose tissue activity through thermoregulatory nuclei such as the dorsomedial nucleus

180 ons that receive synaptic input from several thermoregulatory nuclei.

181 and release of selective constraints on the thermoregulatory-olfaction trade-off in amphibious speci

182 ion has a communicative function, not just a thermoregulatory one.

183 We don't know the limitations of the bear's thermoregulatory or swimming capabilities in Arctic wate

184 In humans, the dynamic thermoregulatory organ, comprised of 2-4 million sweat g

185 l insight for clinical trials evaluating the thermoregulatory outcomes of septic patients with hypert

186 hich is thought to contain neurons providing thermoregulatory output to effectors.

187 for the function of this interneuron in the thermoregulatory pathway.

188 induces the TI state through an alternative thermoregulatory pathway.

189 sory reflex circuit within the mammalian CNS thermoregulatory pathways and support the potential for

190 hough it is generally assumed that the major thermoregulatory pathways are well understood, here we d

191 king current concepts concerning the central thermoregulatory pathways based on the MnPO(EP3R) neuron

192 cyclooxygenase (COX)/prostaglandin E2 (PGE2) thermoregulatory pathways, observed in rodents, present

193 ext with a specific temperature by combining thermoregulatory Pavlovian conditioning with engram-labe

194 distribution of thermal resources constrains thermoregulatory performance over space and time.

195 To assess the thermoregulatory performance, this protocol uses non-inv

196 This study aimed at determining the thermoregulatory phenotype of mice lacking transient rec

197 In summary, Trpv1 KO mice possess a distinct thermoregulatory phenotype, which is coupled with a pred

198 is parameter can be used to characterize the thermoregulatory phenotypes of endotherms on a spectrum

199 Herein, we combined thermoregulatory physiology and cryoelectron microscopy

200 skeletal muscle and brown adipose tissue, in thermoregulatory physiology is less well understood.

201 s expand our knowledge on sex differences in thermoregulatory physiology.

202 optimal body temperatures, achieving greater thermoregulatory precision in spring and summer when env

203 performance were higher during seasons when thermoregulatory precision was high.

204 This biological solution for a thermoregulatory problem may lead to the development of

205 to those of MDMA and METH, direct effects on thermoregulatory processes and locomotor activity are li

206 pine is not a likely mechanism for restoring thermoregulatory processes in OVX rats.

207 eurons within a neural network dedicated for thermoregulatory processes.

208 developed a composite material with tunable thermoregulatory properties.

209 during both central nervous system-mediated, thermoregulatory reflex responses to whole-body heat str

210 entially constitutes the afferent arm of the thermoregulatory reflex that is triggered by cutaneous s

211 e preoptic area and anterior hypothalamus, a thermoregulatory region that integrates central and peri

212 c area (POA) of the hypothalamus, a critical thermoregulatory region.

213 ing prostaglandin E(2) (PGE(2)) synthesis in thermoregulatory regions of the preoptic area and anteri

214 tion, likely relating to colony segregation, thermoregulatory requirements, and foraging opportunitie

215 ntributed to meeting the elevated metabolic (thermoregulatory) requirements and fetal growth rates as

216 ntitative real-time PCR, we investigated the thermoregulatory response for representative genes in ea

217 solution of the van der Pol equation and the thermoregulatory response in the data that has a stochas

218 Most reported examples of this type of thermoregulatory response involve behavioral fevering.

219 er, in hibernation or torpor, this canonical thermoregulatory response is replaced by a new, emerging

220 and EP4 receptors all may contribute to the thermoregulatory response to PGE2, but each may have a d

221 uclease protection analysis showed that this thermoregulatory response was rapid as evidenced by the

222 somal protein S5, were shown to disrupt this thermoregulatory response, allowing papBA transcription

223 degrees C) cold exposure did not affect the thermoregulatory responses (deep body and tail skin temp

224 n addition, they indicate sex differences in thermoregulatory responses and will inform the design of

225 To test the hypothesis that thermoregulatory responses are attenuated in such patien

226 POINTS: Visceral thermoreceptors that modify thermoregulatory responses are widely accepted in animal

227 Visceral thermoreceptors that modify thermoregulatory responses are widely accepted in animal

228 ed the patterns of Fos distribution with the thermoregulatory responses elicited by the LPS.

229 s play a key role in mediating the sleep and thermoregulatory responses of nicotinic acid.

230 We studied thermoregulatory responses of ten well-trained ( VO2max

231 ABSTRACT: We studied thermoregulatory responses of ten well-trained [VO2 max

232 ore, humid heat affects both performance and thermoregulatory responses to a greater extent than OCP

233 e that TRPA1 channels do not drive autonomic thermoregulatory responses to cold in rodents.

234 the hypothesis that motion sickness affects thermoregulatory responses to cooling in humans.

235 heral leukocyte concentrations or behavioral thermoregulatory responses to infection.

236 of LPS inflammation, it should mediate both thermoregulatory responses to LPS.

237 s to manifest and integrate normal sleep and thermoregulatory responses to metabolic challenges.

238 of neural activity in the NRM should reduce thermoregulatory responses to peripheral thermal challen

239 ctivities under basal conditions, as well as thermoregulatory responses to severe heat and cold.

240 aglandins as mediators of the sleep-wake and thermoregulatory responses to various physiological chal

241 These thermoregulatory responses were associated with an incre

242 and (iii) the sudomotor but not behavioural thermoregulatory responses were impaired compared to mat

243 into the sweltering heat evokes a number of thermoregulatory responses, both autonomic (sweating) an

244 tructing 4 mouse chimeras and studying their thermoregulatory responses, we found that all 3 phases o

245 These data indicate a novel thermoregulatory role for both IGF-1R and neuronal insul

246 A thermoregulatory role for human scalp hair has been prev

247 The thermoregulatory role of hypothalamic excitatory neurons

248 with increases in temperature, supporting a thermoregulatory role of UV pigmentation.

249 nd raise questions about the assumption of a thermoregulatory set point in humans, and our evolutiona

250 ergy balance can lead to regulated shifts in thermoregulatory set-points that support physiological a

251 tters and to instability in the hypothalamic thermoregulatory setpoint.

252 The teleological 'reason' for this thermoregulatory shift is unclear, but the shift of ~0.5

253 herefore, TRPV1-targeted compounds that lack thermoregulatory side effects may provide relief from pa

254 ally thought that the DMH contained a single thermoregulatory site that worked as a fever-hypothermia

255 unstudied and such factors as reproductive, thermoregulatory, social, and predator-avoidance behavio

256 Further, the reflex SSNA response to a non-thermoregulatory stimulus was preserved in older adults

257 eing, SSNA can be further increased by a non-thermoregulatory stimulus.

258 ill increasingly need to rely on behavioural thermoregulatory strategies to regulate body temperature

259 strates that tropical species employ diverse thermoregulatory strategies, which is also reflected in

260 marine predators diverge systematically with thermoregulatory strategy and water temperature, reflect

261 s such as mobility, diet specialization, and thermoregulatory strategy are central to understanding a

262 chain (benthic, pelagic, benthopelagic) and thermoregulatory strategy on trophic total Hg (THg) dyna

263 ation pose challenges for collecting resting thermoregulatory sweat for non-invasive analysis of body

264 Autonomic reflex screens (77%) and thermoregulatory sweat test (67%) confirmed sudomotor dy

265 gic, sudomotor and cardiovagal functions and Thermoregulatory Sweat Test (TST), from which the Compos

266 lunteers were dehydrated (2.2-5.8% B(m)) via thermoregulatory sweating.

267 the predominant subtypes in pupillomotor and thermoregulatory symptoms.

268 The remarkable plasticity of the thermoregulatory system allowed mammals to thrive in var

269 Their thermoregulatory system demonstrates remarkable adaptive

270 ion from skin thermoreceptors to the central thermoregulatory system is important for the defense of

271 ral systems produces adaptive changes in the thermoregulatory system that enable survival.

272 volume and respiratory rate by affecting the thermoregulatory system, causing specific airway resista

273 s normally tightly regulated by an effective thermoregulatory system.

274 ensors in this tiny ectotherm reminiscent of thermoregulatory systems in larger, endothermic animals.

275 view will further promote development of the thermoregulatory textile field in both academia and indu

276 laborate on typical smart passive and active thermoregulatory textiles considering current working me

277 try for the sustainable development of smart thermoregulatory textiles.

278 discuss the latest technological advances in thermoregulatory textiles.

279 set of arteriolar smooth muscle cells within thermoregulatory tissues.

280 en exercising in the heat: (i) a performance-thermoregulatory trade-off occurred that required behavi

281 ndividuals of these species: acclimate their thermoregulatory traits to maintain stable leaf temperat

282 ndividuals of three species acclimated their thermoregulatory traits, and three species increased the

283 omote surgical-wound infection by triggering thermoregulatory vasoconstriction, which decreases subcu

284 nt of both smaller (capillaries) and larger (thermoregulatory) vessels.