Postnatal expression of neurotransmitters, receptors, and cytochrome oxidase in the rat pre-Bötzinger complex

2002 ◽  
Vol 92 (3) ◽  
pp. 923-934 ◽  
Author(s):  
Qiuli Liu ◽  
Margaret T. T. Wong-Riley

The pre-Bötzinger complex (PBC) is postulated as the center of respiratory rhythmogenesis. Previously, we found a reduction or plateau of cytochrome oxidase (CO) activity in the PBC and other respiratory nuclei at postnatal days 3–4, despite a general increase of CO with age, suggesting a period of synaptic readjustment. The present study examined the expression of CO and a number of neurochemicals in the PBC at closer time intervals. At postnatal days 3–4 and, more prominently, at postnatal day 12, expression of CO, glutamate, and N-methyl-d-aspartate receptor subunit 1 was reduced, whereas expression of GABA, GABABreceptor, glycine receptor, and α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptor subunit 2 was increased. These findings are consistent with our hypothesis that decreased CO activity is associated with an increase in inhibitory drive (mediated by GABA and glycine, their receptors, and possibly blockage of Ca2+ entry by glutamate receptor subunit 2) and a decrease in excitatory drive (mediated by glutamate and its receptors). Our findings point to two critical periods during postnatal development of the rat when their respiratory system may be more vulnerable to respiratory insults.

2003 ◽  
Vol 94 (3) ◽  
pp. 1115-1121 ◽  
Author(s):  
Qiuli Liu ◽  
Judy Kim ◽  
Jamye Cinotte ◽  
Patricia Homolka ◽  
Margaret T. T. Wong-Riley

Previously, we found that the rat pre-Bötzinger complex (PBC) exhibited reduced cytochrome oxidase (CO) activity on postnatal days (P) 3–4 and especially on P12, with a concomitant decrease in glutamate and N-methyl-d-aspartate receptor subunit 1, and an increase in GABA, GABAB, glycine recptor, and glutamate subunit 2. We hypothesized that the PBC would be more affected by carotid body denervation (CBD) during the two critical windows than at other times. Pairs of CBD and sham animals at each postnatal day from P2 to P14 and at P21 were operated on and survived for 3 days. Brain stems were processed for CO and neurokinin-1 receptor for the identification of PBC. Results indicate that CBD caused a significant loss in body weight in all animals and a reduction in PBC somal size when the surgery was between P2 and P7. CBD also induced a significant decrease in CO activity of the PBC in most animals and a distinct delay, as well as prolongation of the maturational process, especially when induced close to P3 and P11–P13.


2004 ◽  
Vol 96 (5) ◽  
pp. 1825-1831 ◽  
Author(s):  
Qiuli Liu ◽  
Margaret T. T. Wong-Riley

Previously, we reported that the pre-Bötzinger complex (PBC) exhibited a dramatic reduction in cytochrome oxidase activity at postnatal day (P) 12. This coincided in time with decreases in glutamate and NMDA receptor subunit 1 and increases in GABA, GABAB, glycine receptor, and glutamate receptor GluR2. To test our hypothesis that various α-subunits of GABAAreceptors also undergo changes in their expression during postnatal development, as they do in other brain regions, we undertook an in-depth immunohistochemical study of GABAAreceptor subunits α1, α2, and α3 in the PBC of P0 to P21 rats. We found that 1) GABAAα3-subunit was expressed at relatively high levels at P0, which then declined with age; 2) GABAAα1-subunit was expressed at relatively low levels at P0 but increased with age; 3) the developmental trends of subunits α1 and α3 intersected at P12; and 4) GABAAα2-subunit expression was moderate to light at P0 and remained quite constant during development, being lowest at P21. These findings suggest that the apparent switch in relative expressions of subunits α3 and α1 during development and the intersection of slopes around P12 may be associated with possible changes in GABAAreceptor subtypes that would mediate different functional properties of GABA transmission, such as primarily a less efficient inhibitory transmission before P12 and a more mature inhibitory effect at P12 and thereafter, as suggested by the kinetics of distinct postsynaptic potentials. This mechanism may contribute partially to the dramatic reduction in cytochrome oxidase activity within the PBC at P12, as shown previously.


Author(s):  
Clemens R. Scherzer ◽  
G. Bernhard Landwehrmeyer ◽  
Julie A. Kerner ◽  
Timothy J. Counihan ◽  
Christoph M. Kosinski ◽  
...  

2010 ◽  
Vol 14 (5) ◽  
pp. 496-502 ◽  
Author(s):  
XiaoPing Gu ◽  
Juan Zhang ◽  
ZhengLiang Ma ◽  
JunHua Wang ◽  
XiaoFang Zhou ◽  
...  

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