Zhou S Y, Basura G J, Goshgarian H G
Department of Anatomy and Cell Biology, Wayne State University School of Medicine, 540 East Canfield Ave., Detroit, MI 48201, USA.
J Appl Physiol (1985). 2001 Dec;91(6):2665-73. doi: 10.1152/jappl.2001.91.6.2665.
The aim of the present study was to specifically investigate the involvement of serotonin [5-hydroxytryptamine (5-HT(2))] receptors in 5-HT-mediated respiratory recovery after cervical hemisection. Experiments were conducted on C(2) spinal cord-hemisected, anesthetized (chloral hydrate, 400 mg/kg ip), vagotomized, pancuronium- paralyzed, and artificially ventilated female Sprague-Dawley rats in which CO(2) levels were monitored and maintained. Twenty-four hours after spinal hemisection, the ipsilateral phrenic nerve displayed no respiratory-related activity indicative of a functionally complete hemisection. Intravenous administration of the 5-HT(2A/2C)-receptor agonist (+/-)-2,5-dimethoxy-4-iodoamphetamine hydrochloride (DOI) induced respiratory-related activity in the phrenic nerve ipsilateral to hemisection under conditions in which CO(2) was maintained at constant levels and augmented the activity induced under conditions of hypercapnia. The effects of DOI were found to be dose dependent, and the recovery of activity could be maintained for up to 2 h after a single injection. DOI-induced recovery was attenuated by the 5-HT(2)-receptor antagonist ketanserin but not with the 5-HT(2C)-receptor antagonist RS-102221, suggesting that 5-HT(2A) and not necessarily 5-HT(2C) receptors may be involved in the induction of respiratory recovery after cervical spinal cord injury.
本研究的目的是专门调查血清素[5-羟色胺(5-HT(2))]受体在颈髓半切术后5-羟色胺介导的呼吸恢复中的作用。实验在C(2)脊髓半切、麻醉(水合氯醛,400mg/kg腹腔注射)、迷走神经切断、泮库溴铵麻痹并人工通气的雌性Sprague-Dawley大鼠身上进行,监测并维持其二氧化碳水平。脊髓半切24小时后,同侧膈神经未显示出与呼吸相关的活动,表明半切功能完整。在二氧化碳水平保持恒定的条件下,静脉注射5-HT(2A/2C)受体激动剂(±)-2,5-二甲氧基-4-碘苯丙胺盐酸盐(DOI)可诱导半切同侧膈神经产生与呼吸相关的活动,并增强高碳酸血症条件下诱导的活动。发现DOI的作用具有剂量依赖性,单次注射后活动恢复可持续长达2小时。DOI诱导的恢复被5-HT(2)受体拮抗剂酮色林减弱,但未被5-HT(2C)受体拮抗剂RS-102221减弱,这表明5-HT(2A)而非5-HT(2C)受体可能参与颈脊髓损伤后呼吸恢复的诱导。