Neurones in the ventrolateral pons are required for post-hypoxic frequency decline in rats.
about
Pontine mechanisms of respiratory controlEnhanced non-eupneic breathing following hypoxic, hypercapnic or hypoxic-hypercapnic gas challenges in conscious mice.Morphine has latent deleterious effects on the ventilatory responses to a hypoxic challenge.Hypoxic activation of arterial chemoreceptors inhibits sympathetic outflow to brown adipose tissue in rats.Respiratory and Mayer wave-related discharge patterns of raphé and pontine neurons change with vagotomy.Analysis and modeling of ensemble recordings from respiratory pre-motor neurons indicate changes in functional network architecture after acute hypoxia.Post-hypoxic recovery of respiratory rhythm generation is gender dependent.Neuroplasticity in respiratory motor control.Respiratory modulation of sympathetic activity is attenuated in adult rats conditioned with chronic hypobaric hypoxiaInvited review: Neural network plasticity in respiratory control.Vagal-dependent nonlinear variability in the respiratory pattern of anesthetized, spontaneously breathing rats.Impaired ventilatory and thermoregulatory responses to hypoxic stress in newborn phox2b heterozygous knock-out miceKölliker–Fuse neurons send collateral projections to multiple hypoxia-activated and nonactivated structures in rat brainstem and spinal cord.Cardiorespiratory control and cytokine profile in response to heat stress, hypoxia, and lipopolysaccharide (LPS) exposure during early neonatal period.Chapter 3--networks within networks: the neuronal control of breathing.Computational models and emergent properties of respiratory neural networks.Functional connectivity in the pontomedullary respiratory network.Time Domains of the Hypoxic Ventilatory Response and Their Molecular Basis.Lateral parabrachial nucleus mediates shortening of expiration during hypoxiaPhrenic motoneuron discharge patterns during hypoxia-induced short-term potentiation in rats.Breathing at high altitude.The ventilatory response to hypoxia in mammals: mechanisms, measurement, and analysis.Respiratory recovery following organophosphate poisoning in a rat model is suppressed by isolated hypoxia at the point of apnea.Evidence that ventilatory rhythmogenesis in the frog involves two distinct neuronal oscillators.Neurons of the A5 region are required for the tachycardia evoked by electrical stimulation of the hypothalamic defence area in anaesthetized rats.A5 cells are silenced when REM sleep-like signs are elicited by pontine carbachol.Consequences of in utero caffeine exposure on respiratory output in normoxic and hypoxic conditions and related changes of Fos expression: a study on brainstem-spinal cord preparations isolated from newborn rats.Nasal trigeminal inputs release the A5 inhibition received by the respiratory rhythm generator of the mouse neonate.Hypoxic ventilatory response in Tac1-/- neonatal mice following exposure to opioids.Integral-differential calculus computations by short-term potentiation and depression in NTS-pontine pathways.Time domains of the sympatho-respiratory response to hypoxia: plasticity in phrenic and sympathetic nerve activities.The Hypothalamic PVN Contributes to Acute Intermittent Hypoxia-Induced Sympathetic but not Phrenic Long-Term Facilitation.Specific carotid body chemostimulation is sufficient to elicit phrenic poststimulus frequency decline in a novel in situ dual-perfused rat preparation.Time-dependent modulation of carotid body afferent activity during and after intermittent hypoxia.Differences in time-dependent hypoxic phrenic responses among inbred rat strains.Entrainment pattern between sympathetic and phrenic nerve activities in the Sprague-Dawley rat: hypoxia-evoked sympathetic activity during expiration.Brainstem PCO2 modulates phrenic responses to specific carotid body hypoxia in an in situ dual perfused rat preparation.Integration-differentiation and gating of carotid afferent traffic that shapes the respiratory pattern.Pontine respiratory-modulated activity before and after vagotomy in decerebrate cats.The Kölliker-Fuse nucleus gates the postinspiratory phase of the respiratory cycle to control inspiratory off-switch and upper airway resistance in rat.
P2860
Q26866162-C5A61F1E-9E01-448E-92F5-272E9D064CB2Q30366078-940FC6B0-234A-4CBD-9756-06862009DB1BQ30411852-0C05F950-FD2D-48AE-8F98-45608C0E08BAQ31170930-406AED0E-F97C-4C5F-8D5A-F91F533747B3Q33995231-1AA0D8C8-C6D3-4315-B058-B9C36D02DB08Q34165748-ACCB90A6-163F-44E1-A3C1-37B7DAC283B7Q34673773-96EE2113-D822-4190-AC14-04551ABE03F0Q35027281-F7A85AF5-B928-4139-B463-9D3A4C244B06Q35040762-72AEEC5E-6C69-43AA-8ECC-50FFF7C51BA6Q35061542-E4DDC8E3-61E2-46E6-A13E-59C84A875B24Q35108731-EC8074E6-F63F-467D-BB2B-EF84674F7540Q35228564-7144A3EB-6499-4191-B3F5-88E2CF11DDB9Q36282221-20700E40-1CAD-4D67-9A32-533A655BD2A1Q36597668-20D91205-FE70-48A4-8177-DA863B15C542Q36838975-E550499F-FC6A-469F-8911-815E1527B73CQ36850940-812776F8-9183-4DD9-A0BE-EAC9703A69C6Q36956880-B9ECA57E-49E3-4463-94DC-ED49F600F355Q37069679-B42B0283-B132-42F4-BAE7-5A61BFA3E258Q37218642-CEDEE154-78AE-49BE-A6EA-C620481057AFQ37416707-8F62F0BE-27B4-4C37-B36B-F8844A9FEE27Q37597944-CD966996-E09F-4B28-AFD9-C14799748850Q37731210-9D631386-30A2-4612-A234-17604F4CEEBDQ42377276-6AEA658E-F747-4308-80A2-8950A395B703Q43961424-585182D6-242C-436A-8EB0-CE4318A1AF9EQ43976770-D9D147B2-CE9E-4C4C-B33A-32A78D79445BQ44138655-04C5A4E3-2177-4F49-B0DE-322B48E8EABAQ44285475-D289AEE7-7581-4239-A1B7-F7F0F483F8AAQ44619374-8C5CB2C7-2F51-40E8-AF96-4C5EA7EDC54BQ45201455-14BD4D5B-797A-4964-998F-FBFA072AE00AQ46375868-B909FC6C-0447-49A2-8340-85A032F620B8Q46376150-DB18CA8C-8023-4AB8-A20D-749E4EE2C790Q47650944-A46250BB-DEDB-4780-B557-17890C140286Q47822505-B4406EF4-D93D-4C70-B861-BE91E233E057Q47858575-31B2C439-B584-4E6B-AF97-B26964C06542Q47899240-4D65A5E3-F971-49DE-9950-E375C06D7F87Q48010803-0A68E326-3521-4E81-A861-66376653C204Q48379945-0CEFA637-5C1B-439B-A5FA-0626A71D3AD0Q48421173-35FEFC8B-24B8-4064-9C57-EA39E1875EF4Q48430091-8CCA7AC9-1C51-4275-B9B9-B7A004A799F2Q48438442-370E97F0-FD9C-43FF-95FA-A7814CE057AD
P2860
Neurones in the ventrolateral pons are required for post-hypoxic frequency decline in rats.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh-hant
name
Neurones in the ventrolateral ...... xic frequency decline in rats.
@en
Neurones in the ventrolateral ...... xic frequency decline in rats.
@nl
type
label
Neurones in the ventrolateral ...... xic frequency decline in rats.
@en
Neurones in the ventrolateral ...... xic frequency decline in rats.
@nl
prefLabel
Neurones in the ventrolateral ...... xic frequency decline in rats.
@en
Neurones in the ventrolateral ...... xic frequency decline in rats.
@nl
P1476
Neurones in the ventrolateral ...... xic frequency decline in rats.
@en
P2093
P356
10.1113/JPHYSIOL.1996.SP021751
P407
P478
497 ( Pt 1)
P577
1996-11-01T00:00:00Z