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1 n the skin under the cathodal electrodes was anaesthetized.
2 of whether the animal was awake, behaving or anaesthetized.
5 as recorded simultaneously from both eyes of anaesthetized adult Brown-Norway rats (ketamine: xylazin
6 two age groups (8 and 12 weeks old) of young anaesthetized adult normal WKY and SHR were acquired in
8 umbar dorsal root ganglion (DRG) neurones in anaesthetized adult rats, classified from dorsal root co
13 t activities of 88 C-fibres were recorded in anaesthetized and artificially ventilated rats when the
18 rons in the primary visual cortex of lightly anaesthetized and awake mice, during sensory processing.
22 in the intrascapular subcutaneous region of anaesthetized and heparinized nondiabetic Sprague-Dawley
29 ented that neurons in the auditory cortex of anaesthetized animals generally display transient respon
32 riments were carried out on alpha-chloralose-anaesthetized, artificially ventilated and atenolol (1 m
34 ium and potassium excretion were examined on anaesthetized, artificially ventilated New Zealand White
36 ydrated (DH) (48 h water deprived) rats were anaesthetized, bilaterally vagotomized and underwent acu
38 e situations where the patient prefers to be anaesthetized but intubation may be difficult following
39 al ganglionated plexus was recorded in eight anaesthetized canines using a 16-channel linear microele
40 stimulation, the present experiments in the anaesthetized cat provide a physiological confirmation o
42 riments were carried out in alpha-chloralose anaesthetized cats to determine if these cardiac vagal p
43 rmoregulation, experiments were performed on anaesthetized cats to determine the quantitative respons
44 he left thoracic sympathetic chain (T1-5) of anaesthetized cats to identify the afferents' responses
47 We show here, in primary visual cortex of anaesthetized cats under neuromuscular blockade, that co
48 mesenteric lymph and portal venous plasma in anaesthetized cats was measured with an enzyme-linked im
49 n lamina I of the lumbosacral spinal cord of anaesthetized cats were characterized by recording their
50 ygen concentrations in the striate cortex of anaesthetized cats while using visual stimuli to activat
69 a were obtained in both in situ and in vivo (anaesthetized/conscious) rats and suggest that following
70 e conclude that MAP is largely maintained in anaesthetized DH rats by a PVN-driven component of sSNA
71 this study, we acquired diffusion data from anaesthetized dogs and created a DTI-based atlas for a c
73 ry intercostal muscles in all interspaces in anaesthetized dogs were severed so that the diaphragm wa
77 l muscles in all interspaces were severed in anaesthetized dogs, so that the diaphragm was the only m
78 reasing pulsatile perfusion were assessed in anaesthetized dogs, with the anterior descending coronar
79 control of LSNA and RSNA in alpha-chloralose anaesthetized female rats, but only during pro-oestrus.
81 and primary fields of the auditory cortex of anaesthetized ferrets, and comparing these responses wit
85 s from the ventral cochlear nucleus (VCN) of anaesthetized guinea-pigs in response to iterated ripple
86 ugh initiated from the trachea and larynx in anaesthetized guinea-pigs is mediated by capsaicin-insen
87 voked a cough when applied to the trachea of anaesthetized guinea-pigs, but they substantially reduce
90 group of capillaries in cremaster muscles of anaesthetized hamsters were electrically stimulated to c
93 sthesia in mice, 12 female C57Bl/6 mice were anaesthetized in a crossover protocol with the following
95 d nucleus raphe obscurus of nine adult cats, anaesthetized, injected with a neuromuscular blocking ag
97 mporal shifts of r and r are coordinated, 12 anaesthetized juvenile pigs had pairs of colours of aero
98 rhage in the gyrencephalic brain of propofol-anaesthetized juvenile swine using subdural electrode st
100 le units in the reticular formation of three anaesthetized macaque monkeys whilst TMS was performed o
105 tion of the pelvic nerve (PN) in 12 urethane-anaesthetized male rats were tested for responses to mec
107 f phenylephrine and sodium nitroprusside, in anaesthetized male Wistar rats at a core temperature (T(
109 s were performed on spontaneously breathing, anaesthetized, male Wistar rats undergoing short-term sy
113 tra-vascular sensor in the carotid artery of anaesthetized, mechanically ventilated pigs, without lun
114 e and changes in plasma volume in isoflurane-anaesthetized mice (C57BL/6J) pre-treated with rolipram
117 ellular electrophysiological recordings from anaesthetized mice we first show that simple light steps
120 proved ability to withstand heat exposure in anaesthetized mice, it protected the intestine from inju
122 in vivo extracellular recordings in urethane-anaesthetized mice, we demonstrate that single units and
127 show that the same phenomenon is present in anaesthetized monkeys even at anaesthetic levels known t
131 Seven days postsurgery, LTF was studied in anaesthetized, neuromuscularly blocked and ventilated ra
132 adectomized (GDX) male Fischer 344 rats were anaesthetized, neuromuscularly blocked and ventilated.
135 oth superficial and deep laminae in urethane-anaesthetized newborn rats aged 3, 6, 10 and 21 days, an
136 dly increases total peripheral resistance in anaesthetized non-human primates, a response associated
139 ic balloon catheters were passed through the anaesthetized nose, and an endotracheal tube occlusion d
142 hing on venous return have been derived from anaesthetized or reduced animal preparations, making an
143 silenced primary visual cortex (V1), in nine anaesthetized owl monkeys injected with a neuromuscular
144 ed by I.V. phenylephrine or nitroprusside in anaesthetized, paralysed and artificially ventilated rat
145 periments were performed in alpha-chloralose-anaesthetized, paralysed and artificially ventilated rat
146 ntophoresis were performed in pentobarbitone-anaesthetized, paralysed and artificially ventilated rat
149 equivalent of human childhood) and were then anaesthetized, paralysed, ventilated and prepared with p
150 esistance arterioles in cremaster muscles of anaesthetized (pentobarbital sodium, 65 mg kg(-1)) mice.
153 al potassium concentrations were measured in anaesthetized potassium-replete and potassium-depleted r
154 eadily detectable using electrophysiology in anaesthetized preparations and for which neural circuits
157 synovial lining of the knee joint cavity of anaesthetized rabbits at a constant rate, along with a f
158 on was infused into the knee joint cavity of anaesthetized rabbits for 30 min, with or without hyalur
160 n 3.6 mg ml-1 were infused into the knees of anaesthetized rabbits, with Ringer solution as control i
164 he release of beta-endorphin in the urethane anaesthetized rat following electrical stimulation of th
167 ydrokainate (DHK) was microinjected into the anaesthetized rat nTS or applied to rat nTS slices.
172 the posterior lobe of the ketamine/xylazine-anaesthetized rat to examine the relationship between co
173 air into the sealed pharyngeal airway of the anaesthetized rat while measuring nasal pressure under c
178 (LC) noradrenergic neurons was determined in anaesthetized rats (n = 15) by in vivo extracellular ele
179 in 5 microl) into the lateral ventricles of anaesthetized rats also induces spontaneous epileptiform
180 sure applied to the isolated upper airway in anaesthetized rats before and after microinjection of mu
181 loop of Henle (TALH) in vivo was examined in anaesthetized rats by perfusing loops of Henle of superf
182 ) was studied in the submandibular glands of anaesthetized rats by stimulating the nerve supplies wit
183 nhibitor, neostigmine (NEOS), in the rRPa of anaesthetized rats decreased cold-evoked BAT sympathetic
185 y (RSNA) and blood pressure were recorded in anaesthetized rats during epicardial application of brad
186 ge 12-50 nm) could be detected in the NTS in anaesthetized rats in response to electrical stimulation
187 nhibitor of pancreatic exocrine secretion in anaesthetized rats in vivo and in pancreatic lobules in
190 enous administration of Hcrt-1 (orexin-A) to anaesthetized rats on glutamate and GABA release in the
192 n in situ'isolated' spinal cord preparation (anaesthetized rats spinalized at T10-T11 and cauda equin
194 C and HC stimulation in awake and isoflurane-anaesthetized rats that were chronically implanted with
195 on on tongue movements and flow mechanics in anaesthetized rats that were prepared with an isolated u
197 ecordings using sharp electrodes in urethane-anaesthetized rats to elucidate the cellular dynamics of
198 Increased left ventricular contractility in anaesthetized rats was observed when DVMN neurones were
199 ents innervating the mid-jejunum of urethane-anaesthetized rats was recorded with extracellular micro
203 from hippocampal CA1 neurons was examined in anaesthetized rats with a unilateral common carotid arte
204 to the NTS reduced phrenic nerve activity of anaesthetized rats with an elevated arterial P(CO(2)) .
205 ein secretion was investigated in vivo using anaesthetized rats with pancreatic ductal cannulas, and
207 cellular space of the brain, demonstrated in anaesthetized rats, and hold promise for future in vivo
211 aintain SNA and arterial pressure at rest in anaesthetized rats, but this loss reduces the sympathoex
212 recorded from single SCN neurons in urethane-anaesthetized rats, categorized them by the statistical
213 ns, identified by juxtacellular labelling in anaesthetized rats, had a slow regular discharge, were v
215 ight chain in astrocytes) reduced the HVR in anaesthetized rats, indicating that exocytotic release o
216 During continuous bladder cystometry in anaesthetized rats, inhibition of pannexin 1 channels us
218 n of tetanus-evoked oscillations in urethane-anaesthetized rats, validate our observations in vitro,
220 le unit recordings obtained from 32 urethane-anaesthetized rats, when analysed in groups based upon h
221 tral artery (CVA) in spontaneously breathing anaesthetized rats, whilst simultaneously recording tail
243 lity was measured manometrically in urethane-anaesthetized recipient rats in response to intra-arteri
244 entrolateral medulla (RVLM) were recorded in anaesthetized sino-aortic denervated and vagotomized rat
245 These events were measured in cats that were anaesthetized, so that recovery of spindle afferent func
253 ences in VNS heart control between awake and anaesthetized states, the physiological expression of th
256 intercostal (IIC) muscles were studied in 11 anaesthetized, tracheotomized and spontaneously breathin
257 ng two series of experiments using a supine, anaesthetized, tracheotomized rat in which tongue muscle
261 Hg) were assessed in the following groups of anaesthetized, vagotomized adult Sprague-Dawley rats (ag
262 response to lung inflation, were recorded in anaesthetized, vagotomized and artificially ventilated r
263 gonist, AS-19 (10 muM, 5 mul; 3 x 5 min), in anaesthetized, vagotomized and ventilated male Sprague-D
264 crol) was administered intrathecally (C4) to anaesthetized, vagotomized and ventilated male Sprague-D
266 rated phrenic nerve activity was measured in anaesthetized, vagotomized, neuromuscularly blocked and
267 roximately 500 microA) stimulus intensity in anaesthetized, vagotomized, neuromuscularly blocked and
268 ue-Dawley rats (14-15 months old) which were anaesthetized, vagotomized, neuromuscularly blocked and
269 enic nerve activity was recorded in urethane-anaesthetized, vagotomized, paralysed and ventilated rat
270 tly controlled isocapnic hypoxia in urethane-anaesthetized, vagotomized, paralysed and ventilated rat
271 of the descending aorta in 14 Dial-urethane anaesthetized, vagotomized, paralysed, artificially vent
272 descending aorta in thirty-six Dial-urethane-anaesthetized, vagotomized, paralysed, artificially vent
277 tion to phrenic nerve activity in chloralose-anaesthetized, ventilated, neuromuscularly blocked, vago
279 ver an area of forearm skin that was locally anaesthetized via application of EMLA (2.5 % lidocaine (
282 distension of the urinary bladder in the dog anaesthetized with a mixture of chloralose and urethane.
283 s by sodium cyanide, were studied in the cat anaesthetized with a mixture of chloralose and urethane.
290 e recorded from adult wild-type C57/BL6 mice anaesthetized with ketamine (70 mg kg(-1)) and xylazine
296 atropine increases LV contractility in rats anaesthetized with urethane, but not in animals anaesthe
297 eased left ventricular contractility in rats anaesthetized with urethane, confirming the existence of
298 ged (13 month) male Sprague-Dawley rats were anaesthetized with urethane, vagotomized, paralysed and
299 A) and third-order (3A) MAs of pentobarbital-anaesthetized Young (3-6 months) and Old (24-26 months)
300 Studying the gluteus maximus muscle (GM) of anaesthetized young (4 months) and old (24 months) male
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