TY - JOUR
T1 - Responses and afferent pathways of C1-C2 spinal neurons to gastric distension in rats
AU - Qin, Chao
AU - Chandler, Margaret J.
AU - Miller, Kenneth E.
AU - Foreman, Robert D.
N1 - Funding Information:
The authors thank Dr. C.J. Jou and D. Holston for excellent technical assistance. This study was supported by National Institute of Neurological Disorders and Stroke grant NS-35471.
PY - 2003/3/28
Y1 - 2003/3/28
N2 - Some evidence shows that the upper cervical spinal cord might play an important role in propriospinal processing as a sensory filter and modulator for visceral afferents. The aims of this study were to determine (1) the responses of C1-C2 spinal neurons to gastric distension and (2) the relative contribution of vagal and spinal visceral afferent pathways for transmission of gastric input to the upper cervical spinal cord. Extracellular potentials of single C1-C2 spinal neurons were recorded in pentobarbital anesthetized male rats. Graded gastric distension (20-80 mm Hg) was produced by air inflation of a latex balloon surgically placed in the stomach. Sixteen percent of the neurons (32/198) responded to gastric distension; 17 neurons were excited and 15 neurons were inhibited by gastric distension. Spontaneous activity of neurons with inhibitory responses was higher than those neurons with excitatory responses (18.1±2.7 vs. 3.8±1.7 impulses s-1, p<0.001). Twenty-eight of thirty-two (87.5%) neurons responded to mechanical stimulation of somatic fields on head, neck, ears or shoulder. Most lesion sites of neurons with excitatory responses were found in laminae V, VII; however, neurons with inhibitory responses were in laminae III, IV. Bilateral cervical vagotomy abolished responses of 4/8 neurons tested. Spinal transection at C6-C7 abolished responses of the other four neurons that still responded to gastric distension after bilateral vagotomy. Results of these data supported the concept that a group of C1-C2 spinal neurons might play a role in processing sensory information from the stomach that travels in vagal and spinal visceral afferent fibers.
AB - Some evidence shows that the upper cervical spinal cord might play an important role in propriospinal processing as a sensory filter and modulator for visceral afferents. The aims of this study were to determine (1) the responses of C1-C2 spinal neurons to gastric distension and (2) the relative contribution of vagal and spinal visceral afferent pathways for transmission of gastric input to the upper cervical spinal cord. Extracellular potentials of single C1-C2 spinal neurons were recorded in pentobarbital anesthetized male rats. Graded gastric distension (20-80 mm Hg) was produced by air inflation of a latex balloon surgically placed in the stomach. Sixteen percent of the neurons (32/198) responded to gastric distension; 17 neurons were excited and 15 neurons were inhibited by gastric distension. Spontaneous activity of neurons with inhibitory responses was higher than those neurons with excitatory responses (18.1±2.7 vs. 3.8±1.7 impulses s-1, p<0.001). Twenty-eight of thirty-two (87.5%) neurons responded to mechanical stimulation of somatic fields on head, neck, ears or shoulder. Most lesion sites of neurons with excitatory responses were found in laminae V, VII; however, neurons with inhibitory responses were in laminae III, IV. Bilateral cervical vagotomy abolished responses of 4/8 neurons tested. Spinal transection at C6-C7 abolished responses of the other four neurons that still responded to gastric distension after bilateral vagotomy. Results of these data supported the concept that a group of C1-C2 spinal neurons might play a role in processing sensory information from the stomach that travels in vagal and spinal visceral afferent fibers.
KW - Spinal visceral afferent
KW - Stomach
KW - Upper cervical spinal cord
KW - Vagal afferent
UR - http://www.scopus.com/inward/record.url?scp=0037470856&partnerID=8YFLogxK
U2 - 10.1016/S1566-0702(03)00002-X
DO - 10.1016/S1566-0702(03)00002-X
M3 - Article
C2 - 12648614
AN - SCOPUS:0037470856
SN - 1566-0702
VL - 104
SP - 128
EP - 136
JO - Autonomic Neuroscience: Basic and Clinical
JF - Autonomic Neuroscience: Basic and Clinical
IS - 2
ER -