4.7 Article

5-HT precursor loading, but not 5-HT receptor agonists, increases motor function after spinal cord contusion in adult rats

期刊

EXPERIMENTAL NEUROLOGY
卷 221, 期 1, 页码 68-78

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.expneurol.2009.10.003

关键词

mCPP; Fenfluramine; DPAT; L-5-HTP; 5-HT transporter; 5-HT2C receptor; Spinal cord contusion

资金

  1. NIH [PO1 NS24707, PO1 NS055976]
  2. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [P50NS024707, P01NS024707, P01NS055976] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Serotonergic (5-HT) receptors are upregulated following spinal cord transection. Stimulation by administration of serotonergic receptor agonists has been successful in improving hindlimb function. We tested whether this strategy would be successful in incomplete injury models (moderate or severe thoracic contusion) where descending projections are partially spared which should produce less denervation-induced receptor upregulation. Adult rats received midthoracic moderate (MOD: 25 mm drop) or severe (SEV: 50 mm drop) contusion injuries. Distribution of 5-HT and its transporter and expression of 5-HT2C receptors were evaluated in lumbar spinal cord and motor response to 5-HT receptor activation was assessed using open field locomotion (BBB) score, percent weight supported treadmill stepping (%WS) and evaluation of hindlimb muscle activation (tremor and serotonin syndrome). 5-HT immunostaining 3 months post-contusion revealed few 5-HT fibers caudal to the severe contusion, and more spared caudal to the moderate contusion. The distribution of 5-HT transporter paralleled 5-HT staining, but was more greatly reduced. Thus serotonin reuptake may be less efficient in the injured spinal cord. Immunostaining for the 5-HT2C receptor in the dorsal and ventral horns at L5 showed significant upregulation in SEV, compared to sham or MOD rats. Neither 5-HT2C nor 5-HT1A receptor agonists, alone or in combination, nor the serotonin transporter inhibitor D-fenfluramine modified BBB scores or %WS in either group. Despite the increased sensitivity of postsynaptic targets, agonist treatment did not improve function in SEV rats. We conclude that selective 5-HT2C or 5-HT1A receptor activation was not effective in improving hindlimb function after incomplete lesions. In contrast, the 5-HT precursor 5-hydroxytryptophan (L-5-HTP), which leads to activation of all classes of 5-HT receptors, increased both %WS and hindlimb activity in the MOD group. While no side effects were observed in normal or MOD rats, SEV rats displayed hindlimb tremors and 33% mortality, indicating hypersensitivity to the precursor. (C) 2009 Elsevier Inc. All rights reserved.

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