TY - JOUR

T1 - The time course of serotonin 2C receptor expression after spinal transection of rats

T2 - an immunohistochemical study

AU - Ren, Li-Qun

AU - Wienecke, Jacob

AU - Chen, Meng

AU - Møller, Morten

AU - Hultborn, Hans

AU - Zhang, Mengliang

N1 - CURIS 2013 NEXS 022

PY - 2013

Y1 - 2013

N2 - In the spinal cord 5-HT systems modulate the spinal network via various 5-HT receptors. 5-HT2A and 2C receptors are likely the most important 5-HT receptors for enhancing the motoneuron excitability by facilitating the persistent inward current, and thus play an important role for the pathogenesis of spasticity after spinal cord injury. In conjunction with our 5-HT2A receptor study, using a same sacral spinal transection rat model we have in this study examined 5-HT2C receptor immunoreactivity (5-HT2CR-IR) changes at seven different time intervals after spinal injury. We found that 5-HT2CR-IR was widely distributed in different regions of the spinal gray matter and was predominantly located in the neuronal somata and their dendrites although it seemed also present in axonal fibers in the superficial dorsal horn. 5-HT2CR-IR in different regions of the spinal gray matter was seen to be increased at 14 days after transection (with an average ~1.3-fold higher than in sham-operated group) but did not reach a significant level until at 21 days (~1.4-fold). The increase sustained thereafter and a plateau level was reached at 45 days (~1.7-fold higher), a value similar as that at 60 days. When 5-HT2CR-IR analysis was confined to the ventral horn motoneuron somata (including a proportion of proximal dendrites) a significant increase was not detected until 45 day post-operation. 5-HT2CR upregulation in the spinal gray matter is confirmed with Western blot in the rats 60 days post-operation. The time course of 5-HT2CR up-regulation in the spinal gray matter and motoneurons was positively correlated with the development of tail spasticity (clinical scores). This indicates that 5-HT2CR is probably an important factor underlying this pathophysiological development by increasing the excitability of both motoneurons and interneurons.

AB - In the spinal cord 5-HT systems modulate the spinal network via various 5-HT receptors. 5-HT2A and 2C receptors are likely the most important 5-HT receptors for enhancing the motoneuron excitability by facilitating the persistent inward current, and thus play an important role for the pathogenesis of spasticity after spinal cord injury. In conjunction with our 5-HT2A receptor study, using a same sacral spinal transection rat model we have in this study examined 5-HT2C receptor immunoreactivity (5-HT2CR-IR) changes at seven different time intervals after spinal injury. We found that 5-HT2CR-IR was widely distributed in different regions of the spinal gray matter and was predominantly located in the neuronal somata and their dendrites although it seemed also present in axonal fibers in the superficial dorsal horn. 5-HT2CR-IR in different regions of the spinal gray matter was seen to be increased at 14 days after transection (with an average ~1.3-fold higher than in sham-operated group) but did not reach a significant level until at 21 days (~1.4-fold). The increase sustained thereafter and a plateau level was reached at 45 days (~1.7-fold higher), a value similar as that at 60 days. When 5-HT2CR-IR analysis was confined to the ventral horn motoneuron somata (including a proportion of proximal dendrites) a significant increase was not detected until 45 day post-operation. 5-HT2CR upregulation in the spinal gray matter is confirmed with Western blot in the rats 60 days post-operation. The time course of 5-HT2CR up-regulation in the spinal gray matter and motoneurons was positively correlated with the development of tail spasticity (clinical scores). This indicates that 5-HT2CR is probably an important factor underlying this pathophysiological development by increasing the excitability of both motoneurons and interneurons.

U2 - 10.1016/j.neuroscience.2012.12.063

DO - 10.1016/j.neuroscience.2012.12.063

M3 - Journal article

C2 - 23337537

VL - 236

SP - 31

EP - 46

JO - Neuroscience

JF - Neuroscience

SN - 0306-4522

IS - 1

ER -