Access the full text.
Sign up today, get DeepDyve free for 14 days.
G. Paxinos, Charles Watson (1983)
The Rat Brain in Stereotaxic Coordinates
G. Kumar, V. Rai, Suresh Sharma, D. Ramakrishnan, Ying‐Jie Peng, Dangjai Souvannakitti, N. Prabhakar (2006)
Chronic intermittent hypoxia induces hypoxia‐evoked catecholamine efflux in adult rat adrenal medulla via oxidative stressThe Journal of Physiology, 575
D. Kline (2010)
Chronic intermittent hypoxia affects integration of sensory input by neurons in the nucleus tractus solitariiRespiratory Physiology & Neurobiology, 174
Yuri Koutcherov, J. Mai, K. Ashwell, G. Paxinos (2000)
Organization of the human paraventricular hypothalamic nucleusJournal of Comparative Neurology, 423
D. Zoccal, Julian Paton, B. Machado (2009)
Frontiers in Research Review: In vitro Approaches to the Study of Neural Control of Autonomic and Respiratory Functions DO CHANGES IN THE COUPLING BETWEEN RESPIRATORYAND SYMPATHETIC ACTIVITIES CONTRIBUTE TO NEUROGENIC HYPERTENSION?
V. Braga, R. Soriano, B. Machado (2006)
Sympathoexcitatory response to peripheral chemoreflex activation is enhanced in juvenile rats exposed to chronic intermittent hypoxiaExperimental Physiology, 91
E. Gozal, L. Sachleben, M. Rane, Céline Véga, David Gozal (2005)
Mild sustained and intermittent hypoxia induce apoptosis in PC-12 cells via different mechanisms.American journal of physiology. Cell physiology, 288 3
Constancio González, L. Almaraz, A. Obeso, R. Rigual (1994)
Carotid body chemoreceptors: from natural stimuli to sensory discharges.Physiological reviews, 74 4
G. Bao, Naira Metreveli, Rena Li, Addison Taylor, E. Fletcher (1997)
Blood pressure response to chronic episodic hypoxia: role of the sympathetic nervous system.Journal of applied physiology, 83 1
N. Prabhakar, T. Dick, J. Nanduri, G. Kumar (2007)
Systemic, cellular and molecular analysis of chemoreflex‐mediated sympathoexcitation by chronic intermittent hypoxiaExperimental Physiology, 92
J. Büttner-Ennever (1997)
The Rat Brain in Stereotaxic Coordinates, 3rd edn. By George Paxinos and Charles Watson. (Pp. xxxiii+80; illustrated; £$69.95 paperback; ISBN 0 12 547623; comes with CD‐ROM.) San Diego: Academic Press. 1996.Journal of Anatomy, 191
D. Kline, T. King, J. Austgen, C. Heesch, E. Hasser (2010)
Sensory afferent and hypoxia-mediated activation of nucleus tractus solitarius neurons that project to the rostral ventrolateral medullaNeuroscience, 167
R. Perrot, R. Berges, A. Bocquet, J. Eyer (2008)
Review of the Multiple Aspects of Neurofilament Functions, and their Possible Contribution to NeurodegenerationMolecular Neurobiology, 38
M. Adams, Rosemary Brown, C. Gibson, C. Coulter, I. McMillen (2001)
Tyrosine hydroxylase protein content in the medulla oblongata of the foetal sheep brain increases in response to acute but not chronic hypoxiaNeuroscience Letters, 316
M. Gonzalez-Martin, M. Vega-Agapito, Silvia Conde, Silvia Conde, J. Castañeda, R. Bustamante, E. Olea, F. Pérez-Vizcaino, Constancio Gonzalez, Constancio Gonzalez, A. Obeso (2011)
Carotid body function and ventilatory responses in intermittent hypoxia. evidence for anomalous brainstem integration of arterial chemoreceptor inputJournal of Cellular Physiology, 226
S. Mahamed, G. Mitchell (2007)
Is there a link between intermittent hypoxia‐induced respiratory plasticity and obstructive sleep apnoea?Experimental Physiology, 92
M. Carden, J. Trojanowski, W. Schlaepfer, V. Lee (1987)
Two-stage expression of neurofilament polypeptides during rat neurogenesis with early establishment of adult phosphorylation patterns, 7
P. Guyenet (2006)
The sympathetic control of blood pressureNature Reviews Neuroscience, 7
J. Roux, J. Pequignot, S. Dumas, O. Pascual, G. Ghilini, J. Pequignot, J. Mallet, M. Denavit‐Saubié (2000)
O2‐sensing after carotid chemodenervation: hypoxic ventilatory responsiveness and upregulation of tyrosine hydroxylase mRNA in brainstem catecholaminergic cellsEuropean Journal of Neuroscience, 12
P. Pilowsky, C. Jiang, J. Lipski (1990)
An intracellular study of respiratory neurons in the rostral ventrolateral medulla of the rat and their relationship to catecholamine‐containing neuronsJournal of Comparative Neurology, 301
Rosario Pasaro, J. Ribas-Salgueiro, E. Matarredona, Manuel Sarmiento, Juan Ribas (2009)
Systemic inhibition of the Na(+)/H (+) exchanger type 3 in intact rats activates brainstem respiratory regions.Advances in experimental medicine and biology, 648
[Neural plasticity is defined as a persistent change in the morphology and/or function based on prior experiences. Plasticity is well evident when the triggering experience occurs early in life, but in the case of respiratory control plasticity, it also can be triggered in adult life. We have combined a 10 days postnatal hypoxic (PH) (0–10 days of age;11% O2) and a 15 days intermittent hypoxia (IH) exposures in the adulthood (90–105 days of age; 5% O2, 40 s/20% O2, 80 s; 8 h/day) to test if early PH interacts with IH of the adulthood to generate detrimental plastic changes. After recording of ventilatory parameters, the brains were studied immunocytochemically for localization of the organization pattern of non-phosphorylated subunit of neurofilament H (NFH) and tyrosine hydroxylase (TH) expression in the nucleus tractus solitarius (Sol) and caudal (CVL) and rostral ventrolateral reticular (RVL) nuclei, areas related to central cardio-respiratory regulation. In comparison to control, PH male rats (but not females) at 1 month of age hyperventilated at rest, in response to moderate hypoxia (12% O2) and 5% CO2, the effect being due to increased tidal volume. At 3.5 months sex differences in ventilation disappeared and it was indistinguishable between control and PH. IH tended to decrease ventilation in both control (C) and PH animals. PH augmented PENH values in air and in hypoxic conditions when compared with C group. IH in both groups, tended to decrease the PENH value, being statistically different in PH+IH. Results also show an increment of disorganization of NFH-positive labeled structures at the level of Sol and CVL/RVL nuclei in PH, IH and HP+HI groups. PH rats showed differences in the number of TH-positive neurons at the level of CVL/RVL nuclei, which was increased in the PH and PH+IH groups with respect to C one. In conclusion, PH alters the central morpho-physiological organization and the catecholaminergic components of cardio-respiratory nuclei, whose effects were enhanced after a period of IH in the adulthood.]
Published: Aug 8, 2012
Keywords: Neural plasticity; Nucleus tractus solitarius; Caudal ventrolateral reticular nucleus; Rostral ventrolateral reticular nucleus; Respiratory control plasticity; Carotid body chemoreflex
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.