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1 social integration has a direct influence on thermoregulatory ability: individual animals that form a
3 system mediates hypothalamic coordination of thermoregulatory activity and is a primary regulator of
8 it is hypothesized that cocaine also impairs thermoregulatory adjustments that mediate heat dissipati
11 ral basis for reduced air hunger perception, thermoregulatory and autonomic deficiencies in the syndr
12 eta-endorphin modulates the acute endocrine, thermoregulatory and behavioral response to a social con
16 how that the cathinone analog 4-MMC exhibits thermoregulatory and locomotor properties that are disti
17 diotelemetry probes simultaneously monitored thermoregulatory and locomotor responses to various dose
19 The present results suggest that the blunted thermoregulatory and ventilatory responses to hypoxia in
21 d, little is known about the extent to which thermoregulatory behavior can be influenced by BAT therm
23 findings indicate that the ability to adjust thermoregulatory behavior to compensate for enhanced met
24 motor and thermogenic capabilities influence thermoregulatory behavior under different task condition
25 ated the incidence of yawning to other avian thermoregulatory behaviors in budgerigars (e.g., panting
28 ctotherms can rely on water availability and thermoregulatory behaviour to buffer constraints along t
29 ctively during cold exposure, gaining little thermoregulatory benefit from the presence of multiple l
30 The hindbrain may be capable of considerable thermoregulatory capacity independent of the hypothalamu
31 roduction is predicted to influence maternal thermoregulatory capacity, as are the size and compositi
32 al subdivision of the medial preoptic area ('thermoregulatory center'), and the reticular thalamic nu
34 ergic (non-p5HT) cells recorded responded to thermoregulatory challenges that evoked an increase in B
35 xtracellularly from raphe cells during three thermoregulatory challenges that evoked an increase in B
36 rgetically costly; thus, it is critical that thermoregulatory circuits are modulated by signals of en
37 istent with the current understanding of BAT thermoregulatory circuits from the DMH/DHA and mPOA.
38 ospectra of sympathetic discharges supplying thermoregulatory circulation but not those influencing t
39 ical sympathetic motor rhythm regulating the thermoregulatory circulation of the rat tail (T-rhythm;
40 ere we investigated whether nerves supplying thermoregulatory circulations share common rhythmic disc
42 n of key neurons in the central pathways for thermoregulatory cold defense is sufficient to induce a
43 key area of the central nervous pathways for thermoregulatory cold defense, by means of repeated micr
45 spinal somatosensory neurons directly to the thermoregulatory command center, the preoptic area (POA)
50 Neuraxial anaesthesia also impairs central thermoregulatory control, and prevents vasoconstriction
52 diurnality under natural conditions reduces thermoregulatory costs in small burrowing mammals like m
54 bient temperatures and can be explained by a thermoregulatory defect that leads to an increase in mot
57 uscles and vital organs, because of enhanced thermoregulatory demand for skin blood flow coupled with
59 cacy in rat models of ovariectomized-induced thermoregulatory dysfunction and morphine dependent flus
60 lemetric rat model of ovariectomized-induced thermoregulatory dysfunction and were efficacious at ora
61 has suggested that mirtazapine can alleviate thermoregulatory dysfunction by blocking 5-HT(2A) recept
64 lemetric rat model of ovariectomized-induced thermoregulatory dysfunction, a mouse p-phenylquinone (P
71 growth in iron-depleted medium abrogated the thermoregulatory effect, with high-level expression at b
72 ween output of thermointegrative centers and thermoregulatory effector responses rather than processi
74 lation of body temperature, we evaluated the thermoregulatory effects of ablating KNDy neurons by inj
87 clear evidence that alpha-1 AR activation of thermoregulatory hypothalamic neurons will result in a r
89 Previously, we showed that activation of a thermoregulatory ion channel, transient receptor potenti
91 cool sensory signals from the skin is a core thermoregulatory mechanism within the POA that is essent
94 s produces effects on drinking and autonomic thermoregulatory mechanisms, providing a structural basi
98 sent study, we tested whether induction of a thermoregulatory-mediated increase in tissue blood flow,
101 ons regulate life-sustaining respiratory and thermoregulatory networks, and demonstrates a noninvasiv
104 of a TRPV1 receptor antagonist, A-889425, on thermoregulatory neurons in the medial preoptic area of
105 1 receptors indirectly modulates activity of thermoregulatory neurons in the mPOA in a manner that is
108 ch as the hypothalamus, which is the site of thermoregulatory neurons, is critical for the febrile re
109 on the brown adipose tissue activity through thermoregulatory nuclei such as the dorsomedial nucleus
116 In summary, Trpv1 KO mice possess a distinct thermoregulatory phenotype, which is coupled with a pred
117 skeletal muscle and brown adipose tissue, in thermoregulatory physiology is less well understood.
119 to those of MDMA and METH, direct effects on thermoregulatory processes and locomotor activity are li
122 during both central nervous system-mediated, thermoregulatory reflex responses to whole-body heat str
123 entially constitutes the afferent arm of the thermoregulatory reflex that is triggered by cutaneous s
124 e preoptic area and anterior hypothalamus, a thermoregulatory region that integrates central and peri
125 ing prostaglandin E(2) (PGE(2)) synthesis in thermoregulatory regions of the preoptic area and anteri
126 ntitative real-time PCR, we investigated the thermoregulatory response for representative genes in ea
127 solution of the van der Pol equation and the thermoregulatory response in the data that has a stochas
128 and EP4 receptors all may contribute to the thermoregulatory response to PGE2, but each may have a d
129 uclease protection analysis showed that this thermoregulatory response was rapid as evidenced by the
130 somal protein S5, were shown to disrupt this thermoregulatory response, allowing papBA transcription
131 degrees C) cold exposure did not affect the thermoregulatory responses (deep body and tail skin temp
133 POINTS: Visceral thermoreceptors that modify thermoregulatory responses are widely accepted in animal
141 s to manifest and integrate normal sleep and thermoregulatory responses to metabolic challenges.
142 of neural activity in the NRM should reduce thermoregulatory responses to peripheral thermal challen
143 ctivities under basal conditions, as well as thermoregulatory responses to severe heat and cold.
144 into the sweltering heat evokes a number of thermoregulatory responses, both autonomic (sweating) an
145 tructing 4 mouse chimeras and studying their thermoregulatory responses, we found that all 3 phases o
148 nd raise questions about the assumption of a thermoregulatory set point in humans, and our evolutiona
150 herefore, TRPV1-targeted compounds that lack thermoregulatory side effects may provide relief from pa
151 ally thought that the DMH contained a single thermoregulatory site that worked as a fever-hypothermia
152 unstudied and such factors as reproductive, thermoregulatory, social, and predator-avoidance behavio
153 Further, the reflex SSNA response to a non-thermoregulatory stimulus was preserved in older adults
156 gic, sudomotor and cardiovagal functions and Thermoregulatory Sweat Test (TST), from which the Compos
158 ion from skin thermoreceptors to the central thermoregulatory system is important for the defense of
160 ensors in this tiny ectotherm reminiscent of thermoregulatory systems in larger, endothermic animals.
162 omote surgical-wound infection by triggering thermoregulatory vasoconstriction, which decreases subcu
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