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1 r responses to chemoreceptor activation when anesthetized.
2 power of both slow oscillations (0.5-2 Hz in anesthetized, 0.5-4 Hz in behaving animals) and suprathe
3 behaving animals) and supratheta (6-10 Hz in anesthetized, 10-25 Hz in behaving animals) bands.
4                                The pigs were anesthetized, a medial sternotomy performed and miniatur
5                                   Isoflurane-anesthetized adult male wild-type C57B/6 or alpha-Syn mi
6  Finally, MBDs were implanted in the mPFC of anesthetized adult male Wistar rats for in vivo evaluati
7                          We conclude that in anesthetized adult rats active expiration is driven by t
8           In vivo recordings from the STN of anesthetized adult rats demonstrated that the spike firi
9 spontaneously breathing vagotomized urethane-anesthetized adult rats.
10 ons in response to cocaine administration in anesthetized adult rats.
11 recordings and two-photon calcium imaging in anesthetized adult zebra finches (Taeniopygia guttata) t
12 d binocular interactions in visual cortex of anesthetized amblyopic monkeys (female Macaca nemestrina
13 nes was state-dependent and apparent only in anesthetized and active awake animals, but not during qu
14  dLGN, and lateral posterior nucleus of both anesthetized and awake animals, using a common set of st
15                We recorded GCs in the MOB of anesthetized and awake mice and identified state-depende
16 d patch-clamp recordings in visual cortex of anesthetized and awake mice to measure intracellular act
17        We used two-photon calcium imaging in anesthetized and awake mice to visualize both odorant-ev
18 n dLGN, lateral posterior nucleus, and V1 in anesthetized and awake mice.
19 ion of odorants across these neuron types in anesthetized and awake mice.
20 both low and high odor concentrations and in anesthetized and awake mice.
21 of-view mesoscopic imaging of cortex in both anesthetized and awake mice.
22 y evoked dopamine release in the NAc of both anesthetized and awake rats.
23 mplitude as a function of irradiance in both anesthetized and awake, freely moving mice and at the le
24 frequency power in the prefrontal network of anesthetized and awakeTgDyrk1Amice.
25 n hippocampal local field potentials in both anesthetized and behaving mice.
26 ing of regional activity and connectivity in anesthetized and behaving mice; however, the kinetics of
27                         Pigs (35-40 kg) were anesthetized and bled to mean arterial pressure of 35-40
28                        Twenty-four pigs were anesthetized and cardiac arrest was induced using three
29 on of RVLM-CA neurons increased breathing in anesthetized and conscious mice.
30                                    Rats were anesthetized and cooled to 16 degrees C to 18 degrees C
31                                    Mice were anesthetized and exposed to 1) room air, no mechanical v
32 rding sites, into the CA1 pyramidal layer of anesthetized and freely moving mice.
33      Using an extracorporeal heat exchanger, anesthetized and instrumented animals were maintained at
34 tion of mean arterial pressure at 35 mm Hg), anesthetized and instrumented pigs were randomly assigne
35  34.7-49.9 kg) INTERVENTIONS: : Animals were anesthetized and intubated, and saline lung lavage was p
36                                  Forty-eight anesthetized and mechanically ventilated Balb/c mice.
37                                         Nine anesthetized and mechanically ventilated closed-chest La
38      We developed a model of CO poisoning in anesthetized and mechanically ventilated mice to assess
39                                     Thirteen anesthetized and mechanically ventilated pigs.
40                                With the pigs anesthetized and mechanically ventilated, 40 mL/kg of bl
41 ll-specific optogenetic manipulation in both anesthetized and non-anesthetized mice, we found that tw
42                     Two macaque monkeys were anesthetized and received a unilateral intravitreal inje
43                                    Rats were anesthetized and surgically prepared for controlled cort
44                             Thirty pigs were anesthetized and then randomized to cardiac arrest induc
45                             BALB/c mice were anesthetized and treated with calcium phosphate to induc
46         Male Sprague-Dawley rats (n=31) were anesthetized and treated with the (KOR) agonist salvinor
47                                    Mice were anesthetized and unilateral injections of dextran-amine
48                                              Anesthetized and ventilated adult female C57BL/6 wild-ty
49 teral phrenic nerve activity was recorded in anesthetized and ventilated adult male rats and a multie
50                                    Cats were anesthetized and ventilated.
51 ody (MGB)] of young awake, aged awake, young anesthetized, and aged anesthetized rats.
52                                 Animals were anesthetized, and injections of dextran-amine were made
53 , however, receptive field properties in the anesthetized animal remain a good model for those in the
54 ed at the same time and were present in both anesthetized animals and behavioral experiments in which
55 king and vigilance and is readily induced in anesthetized animals by stimulating the brainstem reticu
56           However, recent in vivo studies in anesthetized animals have questioned this simple model.
57         Using a similar approach in urethane-anesthetized animals in vivo, we found that photostimula
58  predominantly from experiments performed in anesthetized animals or reduced ex vivo preparations.
59 sured using voltage-sensitive dye imaging in anesthetized animals was combined with behavioral detect
60  awake animals, whereas coupling in urethane-anesthetized animals was slower, and in some cases inclu
61                                Compared with anesthetized animals, the temporal frequency that evoked
62                            In both awake and anesthetized animals, we found that activating either fa
63                       Conversely, units from anesthetized animals, with little top-down influences, s
64  imaging, have described receptive fields in anesthetized animals.
65 owing controlled intracisternal infusions in anesthetized animals.
66 serotonergic modulation has been observed in anesthetized animals.
67 udies of the primary auditory cortex (A1) in anesthetized animals.
68 n in single cells is based on experiments in anesthetized animals.
69 perties (receptive fields) were performed in anesthetized animals.
70                                Recordings in anesthetized birds show that FoxP2 knockdown interferes
71 erforming electrophysiological recordings in anesthetized birds, we found neurons in the auditory for
72 bservations of long-range correlation in the anesthetized brain and show that a rich functional dynam
73  resting-state hemodynamics in the awake and anesthetized brain are coupled to underlying patterns of
74                                              Anesthetized canines with (n = 7) and without (n = 7) in
75 ind that constant optogenetic stimulation of anesthetized cat area 21a produces gamma-band activity e
76 orded responses of geniculate X-cells in the anesthetized cat, we synthesized thalamic sub-population
77 vity of one to three nearby neurons in V1 of anesthetized cats during the presentation of drifting si
78 ratory demonstrated that cortical neurons in anesthetized cats exhibit spatial stream segregation (SS
79                        We recorded CINs from anesthetized cats.
80                                              Anesthetized CD-1 mice underwent orotracheal instillatio
81                                We found that anesthetized children had significantly lower recollecti
82 l potentials were recorded simultaneously in anesthetized closed-chest pigs (n=5) during sinus rhythm
83 pacts using two different weights to lightly anesthetized, completely unrestrained mice established a
84 onal networks were recruited in awake versus anesthetized conditions.
85 age quality was comparable between awake and anesthetized conditions.
86 tics of the lead compound were determined in anesthetized dogs as well as by a dosimetric analysis.
87  bolus+6-9 mug/kg per hour IV infusion) into anesthetized dogs for 7 hours, maintaining plasma levels
88 resonance imaging (MRI) studies of awake and anesthetized dogs have been reported.
89                    Studies were performed in anesthetized dogs with acute left bundle-branch block (L
90                                           In anesthetized dopamine-intact rats, molecularly identifie
91 valuated using wide-field imaging in lightly anesthetized Emx1-creXRosa26-GCaMP3 mice expressing calc
92  of 2-deoxy-D-glucose or 5-thio-D-glucose in anesthetized, euglycemic rats.
93 ort (<25 ms) laser pulses to kill or disable anesthetized female Anopheles stephensi mosquitoes, whic
94 ordings from principal neurons of the MSO of anesthetized female gerbils.
95  of multiunit firing activity during tACS in anesthetized ferrets (Mustela putoris furo), a model spe
96 ly manipulated the activity of CG neurons in anesthetized ferrets in vivo using a combined viral-infe
97                                       In the anesthetized FHM1 mouse model in vivo, we used two-photo
98  in the auditory cortex of urethane/xylazine-anesthetized Fmr1 KO mice in response to tones and frequ
99 ent cecal ligation and incision and remained anesthetized for evaluation of survival for 12 hours (ra
100 rage volume of opening 28% larger than prior anesthetized FUS procedures.
101                                              Anesthetized greyhounds underwent 30 minutes DCD by with
102                                           An anesthetized guinea pig model was used to elicit a SOF+A
103  neurons sensitive to either ITDs or ILDs in anesthetized guinea pig, before, during, and following r
104                                           In anesthetized guinea pigs intratracheal administration of
105 d in the primary auditory cortex of urethane-anesthetized guinea pigs.
106 ere observed on cardiovascular parameters in anesthetized guinea pigs.
107                                   In the non-anesthetized head-restrained mice, cooling also prevente
108 e analyzes were performed on tilapia fillets anesthetized in five concentrations between 5 and 15x10(
109                                   Sheep were anesthetized, insufflated with cooled cotton smoke via t
110                                    Seventeen anesthetized intubated control anesthesia patients were
111                                    Pigs were anesthetized, intubated, and mechanically ventilated.
112        Term newborn piglets (n=8/group) were anesthetized, intubated, instrumented, and exposed to 45
113 )I-ioflupane in mouse brain in the awake and anesthetized (isoflurane) states.
114 ge wing discs at regular intervals in living anesthetized larvae so as to follow the growth of the ti
115 o reveal that most neurons in area MT of the anesthetized macaque encode 3D motion information.
116 ientation tuning in primary visual cortex of anesthetized macaque monkeys, and how quickly responses
117 f V1 and V2 neurons recorded individually in anesthetized macaque monkeys.
118 e texture boundary responses in V1 and V2 in anesthetized macaque monkeys.
119 m neuronal populations in areas V1 and V2 of anesthetized macaque monkeys.
120 s to fit the model to LFPs recorded in V1 of anesthetized macaques (Macaca mulatta) during the presen
121 sly that a subpopulation of neurons in V2 in anesthetized macaques responds to orientation discontinu
122  neurons in the spinal trigeminal nucleus of anesthetized male and female rats.
123 tion-processing medial temporal (MT) area of anesthetized male marmosets.
124 de, pulse-like increments in LH secretion in anesthetized male mice.
125                                           In anesthetized male nonhuman primates (n = 3), we used pos
126 unit recording in the trigeminal ganglion of anesthetized male rats.
127 ainic acid (KA)-induced seizures in urethane anesthetized, male Sprague Dawley rats.
128                 Typical VVRs were induced in anesthetized, male, Long-Evans rats by sinusoidal galvan
129                               Studies in the anesthetized marmoset have detailed the anatomy and phys
130 electrode recordings from cerebral cortex in anesthetized marmoset monkeys.
131  We recorded single-cell activity in dLGN of anesthetized marmoset monkeys.
132                       We show that bees with anesthetized MBs distinguish odors and learn elemental o
133                              Fourteen fasted anesthetized mechanically ventilated domestic pigs.
134                                 Twenty-eight anesthetized, mechanically ventilated pigs.
135                                              Anesthetized, mechanically ventilated, and surgically in
136 tion of cholinergic MSDB neurons in urethane-anesthetized mice acts on hippocampal networks via two d
137 r recordings in somatosensory neocortex from anesthetized mice and awake monkeys supported these pred
138 rity of neuronal action in ketamine-xylazine-anesthetized mice and non-anesthetized mice to manipulat
139  the packaged devices in the intact brain of anesthetized mice co-expressing Channelrhodopsin-2 and A
140  to optically-control glucose homeostasis in anesthetized mice following delivery of blue light to th
141 to NH4(+) and in the somatosensory cortex of anesthetized mice in response to i.v. NH4(+).
142  was also observed in cortical astrocytes of anesthetized mice in response to local field stimulation
143 tion (LTP) and long-term depression (LTD) in anesthetized mice in vivo.
144 gs from primary somatosensory cortex (S1) in anesthetized mice indicated that optogenetic whisker pad
145 ent subdivisions of the auditory thalamus in anesthetized mice revealed a stimulus-specific, subdivis
146  ketamine-xylazine-anesthetized mice and non-anesthetized mice to manipulate the thalamocortical acti
147 ng resistance and dynamic compliance in live anesthetized mice using invasive plethysmography.
148                                              Anesthetized mice were subjected to myocardial ischemia
149                       To address this issue, anesthetized mice were suspended with the hindlimb allow
150                                              Anesthetized mice were ventilated with injurious high ti
151              In the primary visual cortex of anesthetized mice, activation of iChloC suppressed spiki
152                                           In anesthetized mice, after intragastric or intravenous sal
153                                In the deeply anesthetized mice, moderate cortical cooling was charact
154                              We show that in anesthetized mice, the physiological activation of olfac
155              Using high-speed videography in anesthetized mice, we characterize the amplitude of whis
156 ic manipulation in both anesthetized and non-anesthetized mice, we found that two major classes of in
157                            In both awake and anesthetized mice, we imaged an 8 x 8 mm field of view t
158 in vivo two-photon imaging of both awake and anesthetized mice, we recorded spontaneous, ongoing neur
159 w oscillation in the hippocampus of urethane-anesthetized mice, which couples to nasal respiration an
160 n in slices and at each respiration cycle in anesthetized mice.
161 o pancreatic ductal secretion was studied in anesthetized mice.
162 cies (2-4 Hz) in the hippocampus of urethane-anesthetized mice.
163 e of theta oscillations (2-6 Hz) in urethane-anesthetized mice.
164 se of global EEG signal in ketamine-xylazine anesthetized mice.
165 es following electrical stimulation of LC in anesthetized mice.
166 ina and in the cremaster microcirculation of anesthetized mice.
167  bulb using multiphoton imaging in awake and anesthetized mice.
168 cein isothiocyanate-fibrin labeled emboli in anesthetized mice.
169 ptogenetically silenced in awake, but not in anesthetized, mice.
170 s study, we used juxtacellular recordings in anesthetized Mongolian gerbils to assess the effect of a
171                          Previous studies in anesthetized monkeys found that inactivating feedback fr
172          Here, we examine fMRI datasets from anesthetized monkeys with simultaneous hippocampal elect
173 eptive heat stimulation of digits in lightly anesthetized monkeys.
174 al MRI during the resting state in awake and anesthetized monkeys.
175  that are sustained for several hours in the anesthetized mouse or rat and thus provides unprecedente
176 e molecular layer of the visual cortex of an anesthetized mouse.
177   Equilibrium analysis was used for both the anesthetized (n = 4) and the awake (n = 5) datasets to c
178  renal hemodynamics and tubular functions in anesthetized non-diabetic Sprague Dawley (SD) rats and 5
179               Isoflurane concentrations that anesthetize only Ndufs4(KO) mice (0.6%) decreased the fr
180           Recordings are first obtained from anesthetized or awake head-fixed rats.
181 ally, using in vivo two-photon microscopy in anesthetized or awake-behaving mice, we document for the
182 t moderate local cortical cooling of lightly anesthetized or naturally sleeping mice disrupts thalamo
183          Based largely on experimentation in anesthetized or reduced preparations, a rostrally locate
184                                              Anesthetized, ovariectomized mice had optical fibers imp
185  layers of the OT were recorded from lightly anesthetized owls confronted with arrays of bars in whic
186                                           In anesthetized, paralyzed and ventilated rats, moderate AI
187 implanted in the superficial layers of V1 in anesthetized, paralyzed macaque monkeys.
188                                          The anesthetized-patched version can be completed in approxi
189                         However, its role in anesthetized patients undergoing major surgery is not kn
190                                 We studied 6 anesthetized pigs (mean body weight, 37 +/- 4 kg).
191                 Our data demonstrate that in anesthetized pigs INS infusion did not exert an anabolic
192    The present experiments were performed in anesthetized pigs subjected to a transient or stable BP
193                                              Anesthetized pigs were subjected to RIPC (4x5/5 minutes
194 graphy (CT) to analyze regional inflation in anesthetized pigs with lung injury.
195                                 From 4 other anesthetized pigs, 64-lead body surface potential maps w
196  vivo by dynamic (11)C-metformin PET/CT in 6 anesthetized pigs, and renal clearance of (11)C-metformi
197 nnas were then characterized in vivo in five anesthetized pigs, by placing one antenna outside the bo
198  selective stimulant for TRPV1 receptors, in anesthetized preparation; 2) immunoreactivity and mRNA o
199 s, which would not be possible using current anesthetized preparations.
200 S was also improved during alert compared to anesthetized procedures.
201 rginal conjunctiva under the lower eyelid of anesthetized rabbits at various time points via a microl
202                                         Four anesthetized rabbits, ventilated in pressure controlled
203 aging of primary somatosensory cortex in the anesthetized rat in response to deflections of the facia
204 trical stimulation of the whisker pad in the anesthetized rat to identify components of the neural re
205 ., during a spreading depression event in an anesthetized rat).
206  into the ventrolateral medulla (VLM) of the anesthetized rat, suggesting selective expression of SST
207 cation of ACh modulates SSA in the IC of the anesthetized rat.
208 ion of the somatosensory cortex (SSFP) of an anesthetized rat.
209 controlled changes in inhalation flow in the anesthetized rat.
210 lations of neurons in the auditory cortex of anesthetized rats across different brain states.
211 Spatial discrimination of electric fields in anesthetized rats allowed us to compare the pathway-spec
212                    We found that CA3 AACs in anesthetized rats and AACs in freely moving rats stopped
213 matics and recording single Vg units in both anesthetized rats and awake, body restrained rats.
214 pontaneous cortical population activity from anesthetized rats and found that UP and DOWN durations w
215 ssure microinjection of KCl, was recorded in anesthetized rats and mice.
216 ssing basket cells in the CA1 hippocampus of anesthetized rats and simultaneously detected layer-spec
217 capacity to generate phrenic motor output in anesthetized rats at disease end stage was: (1) transien
218 In vivo recordings from the DANA platform in anesthetized rats demonstrated the ability of the system
219  placing the biosensor in the hippocampus of anesthetized rats demonstrated the feasibility of contin
220        Extracellular recordings were made in anesthetized rats from the inferior colliculus (IC), the
221 in-expressing basket cells in areas CA2/3 of anesthetized rats in relation to CA3 putative pyramidal
222  concentration was continuously monitored in anesthetized rats in response to intravenous injections
223             Removal of polySia in the NTS of anesthetized rats increased sympathetic nerve activity,
224 LTF and spinal inflammation were assessed in anesthetized rats pretreated with IH-1 (2 min hypoxia, 2
225                                           In anesthetized rats pretreated with intrathecal A2A recept
226                                              Anesthetized rats received one gastric fluid instillatio
227              Intravenous injection of S1P in anesthetized rats reduced renal blood flow dose dependen
228 lar single-unit recordings of CeA neurons in anesthetized rats showed that 5-HT2CR knockdown blocked
229 ied trigeminothalamic tract (VTT) neurons in anesthetized rats that are differentially affected by mo
230 ked spike activity was monitored in urethane-anesthetized rats using in vivo extracellular recordings
231 g neural responses in the auditory cortex of anesthetized rats using stimulus-response models.
232           In vivo extracellular recording in anesthetized rats was used to monitor single dLGN neuron
233 efrontal cortex (PFC; electrocorticogram) in anesthetized rats were assessed.
234 al area representing the frontobuccal pad in anesthetized rats while presenting moving textures of va
235 n nerve terminals, homogenate, and cortex of anesthetized rats with and without bicuculline-induced s
236 us TRPC6 wild type and knockout mice, and in anesthetized rats with and without in vivo knockdown of
237 ed to monitor stimulated dopamine release in anesthetized rats with high sensitivity.
238 y and late phase LTP in the dentate gyrus of anesthetized rats, and immunoblotting was used to measur
239 ined with electrophysiological recordings in anesthetized rats, and this response compared with the e
240                                       In the anesthetized rats, optogenetic and electrical stimulatio
241                                           In anesthetized rats, we demonstrate that pLTF requires act
242 ions of the basal forebrain (BF) in urethane-anesthetized rats, we investigated state-dependent spont
243                                           In anesthetized rats, we measured with the same array a sig
244 decoupling odor sampling from respiration in anesthetized rats, we show that M/T cell responses to ar
245 ound effects on the cardiovascular system of anesthetized rats, whereas CfTX-A/B elicited only minor
246 EMG) and electroneurogram (ENG) signals from anesthetized rats.
247 ced inhibition of midbrain DA cell firing in anesthetized rats.
248 athway with extracellular unit recordings in anesthetized rats.
249 ucleus releasing norepinephrine) in urethane-anesthetized rats.
250 activity in somatosensory cortex of urethane anesthetized rats.
251 neurons were reversibly silenced by light in anesthetized rats.
252 occurred during periods of theta activity in anesthetized rats.
253 spontaneously breathing vagotomized urethane-anesthetized rats.
254 elicited by artificial (fictive) whisking in anesthetized rats.
255 s activity of the bladder detrusor muscle in anesthetized rats.
256 ts using in vivo intracellular recordings in anesthetized rats.
257 l PET studies were performed with isoflurane-anesthetized rats.
258 beled individual cholinergic interneurons in anesthetized rats.
259 -transduced neurons to light was examined in anesthetized rats.
260 plied on the left hind limb of pentobarbital-anesthetized rats.
261  neurons in the spinal trigeminal nucleus of anesthetized rats.
262 sessed by MRI and cardiac catheterization in anesthetized rats.
263 lly defined slow calcium waves in isoflurane anesthetized rats.
264 ilateral intrahippocampal infusion of ZIP in anesthetized rats.
265 gle units in the inferior colliculus (IC) of anesthetized rats.
266 ke, aged awake, young anesthetized, and aged anesthetized rats.
267 in the midbrain dopamine system of awake and anesthetized rats.
268 frequency tuning was found in both awake and anesthetized recordings.
269 deling to quantify CSF-ISF exchange rates in anesthetized rodents' brains in supine, prone, or latera
270 e on brainwide transport of inert tracers of anesthetized rodents.
271 ed sustained improvements in O2 delivery; in anesthetized sheep, decrements in hemodynamic status, re
272 piratory distress syndrome was induced in 10 anesthetized, spontaneously breathing pigs.
273 onal connectivity within the spinal cords of anesthetized squirrel monkeys at rest and show that the
274 ngoing spontaneous activity in the awake and anesthetized state, and the role of cholinergic neurotra
275 cient to induce arousal from an unconscious, anesthetized state.
276 compare neuronal responses between awake and anesthetized state.
277 n is processed by the brain during awake and anesthetized states and, crucially, during the transitio
278 y collected from humans in the conscious and anesthetized states.
279 e once thought to only occur in sleeping and anesthetized states.
280 ctures than the MAF method, as compared with anesthetized studies.
281  were compared with those from a motion-free anesthetized study.
282                                     In rats, anesthetized subjects had significantly lower recollecti
283  patients with acute respiratory failure and anesthetized swine.
284 ously over the bilateral cortex of awake and anesthetized Thy1-GCaMP mice using wide-field optical ma
285           As the animal transitions from the anesthetized to awake state, spontaneous single neuron f
286  sufficient to induce the transition from an anesthetized, unconscious state to an awake state, sugge
287                  The majority (86%) of young anesthetized units preferred RAN SAM stimuli; significan
288                                 Animals were anesthetized, ventilated, and randomized into three grou
289 NP) were compared using 16.4 T in isoflurane anesthetized wild type (WT) and HD mice at 9 weeks.
290 ing were obtained for 4 groups of isoflurane-anesthetized Wistar rats: controls (n = 7); pretreated w
291                                    Rats were anesthetized with 1.5% isoflurane and 95% oxygen.
292                                         Rats anesthetized with isoflurane were given intravenous infu
293 ed directly into the VLPO of a mouse lightly anesthetized with isoflurane, dexmedetomidine increased
294                                 Animals were anesthetized with ketamine and xylazine (250 mg/kg and 1
295               New Zealand White rabbits were anesthetized with ketamine/medetomidine before tracer ad
296 Four or 10 days after the surgery, rats were anesthetized with urethane.
297 rtical, and olfactory bulb (OB) LFPs in rats anesthetized with urethane.
298 r recollection indices as rats that had been anesthetized without tissue injury.
299 -(11)C-methyl-JNJ-31020028 were conducted in anesthetized Yorkshire x Landrace pigs, concurrent with
300 ctional magnetic resonance imaging (fMRI) in anesthetized young monkeys and quietly resting children

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