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  4. Identification of active thoracic spinal segments responsible for tonic and bursting sympathetic discharge in neonatal rats.
 
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Identification of active thoracic spinal segments responsible for tonic and bursting sympathetic discharge in neonatal rats.

Resource
Brain Res., 966: 288-299
Journal
Brain Res.
Journal Issue
966
Pages
288-299
Date Issued
2003
Date
2003
Author(s)
Su, Chun-Kuei
Phoon, Sau-Leong
CHEN-TUNG YEN  
DOI
10.1016/S0006-8993(02)04227-0
URI
http://ntur.lib.ntu.edu.tw//handle/246246/139879
Abstract
The isolated thoracic cord of a neonatal rat in vitro generates tonic sympathetic activities in the splanchnic nerves. This tonic sympathetic nerve discharge (SND) has a prominent quasi-periodic oscillation at approximately 1-2 Hz. Bath application of bicuculline and strychnine, which removes endogenous GABA(A) and glycine receptor activities, transforms the quasi-periodic tonic SND into synchronized bursts (bSND). Picrotoxin, another GABA(A) receptor antagonist, also induces bSND. Serial transections of the thoracic cord (T1-12) were performed to identify the cord segments responsible for these tonic and bursting SNDs. Removal of T1-5 did not affect tonic SND. Nerve-cord preparation with either T6-8 or T10-12 segments could generate a substantial amount of tonic SND that retained comparable oscillating patterns. On the other hand, removal of T1-5 significantly reduced bSND amplitude without affecting its rhythmicity. Either T6-8 or T10-12 segments alone could generate bSND. Mid-point transection of T6-12 at T9 might split bSND rhythmogenesis, leading to the occurrence of bSND that could be attributed to two independent oscillators. Our results demonstrated that three segments within the T6-12 cord were sufficient to generate a rudimentary tonic and bursting SNDs. The thoracic cord segments, however, are dynamically interacting so that a full size bSND could only be produced with the intact thoracic cord.
Type
journal article

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