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 Recordings are first obtained from
anesthetized or awake head-fixed rats.
180 ally, using in vivo two-photon microscopy in
anesthetized or awake-behaving mice, we document for the
181 t moderate local cortical cooling of lightly
anesthetized or naturally sleeping mice disrupts thalamo
182 Based largely on experimentation in
anesthetized or reduced preparations, a rostrally locate
183 Anesthetized,
ovariectomized mice had optical fibers imp
184 layers of the OT were recorded from lightly
anesthetized owls confronted with arrays of bars in whic
185 In
anesthetized,
paralyzed and ventilated rats, moderate AI
186 implanted in the superficial layers of V1 in
anesthetized,
paralyzed macaque monkeys.
187 The
anesthetized-
patched version can be completed in approxi
188 However, its role in
anesthetized patients undergoing major surgery is not kn
189 We studied 6
anesthetized pigs (mean body weight, 37 +/- 4 kg).
190 Our data demonstrate that in
anesthetized pigs INS infusion did not exert an anabolic
191 The present experiments were performed in
anesthetized pigs subjected to a transient or stable BP
192 Anesthetized pigs were subjected to RIPC (4x5/5 minutes
193 graphy (CT) to analyze regional inflation in
anesthetized pigs with lung injury.
194 From 4 other
anesthetized pigs, 64-lead body surface potential maps w
195 vivo by dynamic (11)C-metformin PET/CT in 6
anesthetized pigs, and renal clearance of (11)C-metformi
196 nnas were then characterized in vivo in five
anesthetized pigs, by placing one antenna outside the bo
197 selective stimulant for TRPV1 receptors, in
anesthetized preparation; 2) immunoreactivity and mRNA o
198 s, which would not be possible using current
anesthetized preparations.
199 S was also improved during alert compared to
anesthetized procedures.
200 rginal conjunctiva under the lower eyelid of
anesthetized rabbits at various time points via a microl
201 Four
anesthetized rabbits, ventilated in pressure controlled
202 aging of primary somatosensory cortex in the
anesthetized rat in response to deflections of the facia
203 trical stimulation of the whisker pad in the
anesthetized rat to identify components of the neural re
204 ., during a spreading depression event in an
anesthetized rat).
205 into the ventrolateral medulla (VLM) of the
anesthetized rat, suggesting selective expression of SST
206 cation of ACh modulates SSA in the IC of the
anesthetized rat.
207 ion of the somatosensory cortex (SSFP) of an
anesthetized rat.
208 controlled changes in inhalation flow in the
anesthetized rat.
209 lations of neurons in the auditory cortex of
anesthetized rats across different brain states.
210 Spatial discrimination of electric fields in
anesthetized rats allowed us to compare the pathway-spec
211 We found that CA3 AACs in
anesthetized rats and AACs in freely moving rats stopped
212 matics and recording single Vg units in both
anesthetized rats and awake, body restrained rats.
213 pontaneous cortical population activity from
anesthetized rats and found that UP and DOWN durations w
214 ssure microinjection of KCl, was recorded in
anesthetized rats and mice.
215 ssing basket cells in the CA1 hippocampus of
anesthetized rats and simultaneously detected layer-spec
216 capacity to generate phrenic motor output in
anesthetized rats at disease end stage was: (1) transien
217 In vivo recordings from the DANA platform in
anesthetized rats demonstrated the ability of the system
218 placing the biosensor in the hippocampus of
anesthetized rats demonstrated the feasibility of contin
219 Extracellular recordings were made in
anesthetized rats from the inferior colliculus (IC), the
220 in-expressing basket cells in areas CA2/3 of
anesthetized rats in relation to CA3 putative pyramidal
221 concentration was continuously monitored in
anesthetized rats in response to intravenous injections
222 Removal of polySia in the NTS of
anesthetized rats increased sympathetic nerve activity,
223 LTF and spinal inflammation were assessed in
anesthetized rats pretreated with IH-1 (2 min hypoxia, 2
224 In
anesthetized rats pretreated with intrathecal A2A recept
225 Anesthetized rats received one gastric fluid instillatio
226 Intravenous injection of S1P in
anesthetized rats reduced renal blood flow dose dependen
227 lar single-unit recordings of CeA neurons in
anesthetized rats showed that 5-HT2CR knockdown blocked
228 ied trigeminothalamic tract (VTT) neurons in
anesthetized rats that are differentially affected by mo
229 ked spike activity was monitored in urethane-
anesthetized rats using in vivo extracellular recordings
230 g neural responses in the auditory cortex of
anesthetized rats using stimulus-response models.
231 In vivo extracellular recording in
anesthetized rats was used to monitor single dLGN neuron
232 efrontal cortex (PFC; electrocorticogram) in
anesthetized rats were assessed.
233 al area representing the frontobuccal pad in
anesthetized rats while presenting moving textures of va
234 n nerve terminals, homogenate, and cortex of
anesthetized rats with and without bicuculline-induced s
235 us TRPC6 wild type and knockout mice, and in
anesthetized rats with and without in vivo knockdown of
236 ed to monitor stimulated dopamine release in
anesthetized rats with high sensitivity.
237 y and late phase LTP in the dentate gyrus of
anesthetized rats, and immunoblotting was used to measur
238 ined with electrophysiological recordings in
anesthetized rats, and this response compared with the e
239 In the
anesthetized rats, optogenetic and electrical stimulatio
240 In
anesthetized rats, we demonstrate that pLTF requires act
241 ions of the basal forebrain (BF) in urethane-
anesthetized rats, we investigated state-dependent spont
242 In
anesthetized rats, we measured with the same array a sig
243 decoupling odor sampling from respiration in
anesthetized rats, we show that M/T cell responses to ar
244 ound effects on the cardiovascular system of
anesthetized rats, whereas CfTX-A/B elicited only minor
245 EMG) and electroneurogram (ENG) signals from
anesthetized rats.
246 ced inhibition of midbrain DA cell firing in
anesthetized rats.
247 athway with extracellular unit recordings in
anesthetized rats.
248 ucleus releasing norepinephrine) in urethane-
anesthetized rats.
249 activity in somatosensory cortex of urethane
anesthetized rats.
250 neurons were reversibly silenced by light in
anesthetized rats.
251 occurred during periods of theta activity in
anesthetized rats.
252 spontaneously breathing vagotomized urethane-
anesthetized rats.
253 elicited by artificial (fictive) whisking in
anesthetized rats.
254 s activity of the bladder detrusor muscle in
anesthetized rats.
255 ts using in vivo intracellular recordings in
anesthetized rats.
256 l PET studies were performed with isoflurane-
anesthetized rats.
257 beled individual cholinergic interneurons in
anesthetized rats.
258 -transduced neurons to light was examined in
anesthetized rats.
259 plied on the left hind limb of pentobarbital-
anesthetized rats.
260 neurons in the spinal trigeminal nucleus of
anesthetized rats.
261 sessed by MRI and cardiac catheterization in
anesthetized rats.
262 lly defined slow calcium waves in isoflurane
anesthetized rats.
263 ilateral intrahippocampal infusion of ZIP in
anesthetized rats.
264 gle units in the inferior colliculus (IC) of
anesthetized rats.
265 ke, aged awake, young anesthetized, and aged
anesthetized rats.
266 in the midbrain dopamine system of awake and
anesthetized rats.
267 frequency tuning was found in both awake and
anesthetized recordings.
268 deling to quantify CSF-ISF exchange rates in
anesthetized rodents' brains in supine, prone, or latera
269 e on brainwide transport of inert tracers of
anesthetized rodents.
270 ed sustained improvements in O2 delivery; in
anesthetized sheep, decrements in hemodynamic status, re
271 piratory distress syndrome was induced in 10
anesthetized,
spontaneously breathing pigs.
272 onal connectivity within the spinal cords of
anesthetized squirrel monkeys at rest and show that the
273 ngoing spontaneous activity in the awake and
anesthetized state, and the role of cholinergic neurotra
274 cient to induce arousal from an unconscious,
anesthetized state.
275 compare neuronal responses between awake and
anesthetized state.
276 n is processed by the brain during awake and
anesthetized states and, crucially, during the transitio
277 y collected from humans in the conscious and
anesthetized states.
278 e once thought to only occur in sleeping and
anesthetized states.
279 ctures than the MAF method, as compared with
anesthetized studies.
280 were compared with those from a motion-free
anesthetized study.
281 In rats,
anesthetized subjects had significantly lower recollecti
282 Eleven deeply
anesthetized swine (weight 46.2 +/- 6.2 kg).
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