首页> 外文期刊>Journal of neurotrauma >Combined Treatment with Neurotrophin-3 and LSD Facilitates Behavioral Recovery from Double-Hemisection Spinal Injury in Neonatal Rats.
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Combined Treatment with Neurotrophin-3 and LSD Facilitates Behavioral Recovery from Double-Hemisection Spinal Injury in Neonatal Rats.

机译:Neurotrophin-3和LSD的联合治疗可促进新生大鼠双半横断脊髓损伤的行为恢复。

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We explored functional recovery in two spinal cord injury models following a novel combination treatment (NT-3 + LSD). One group of rats received a staggered double hemisection (DH) at postnatal day 2 (P2) of the left hemicord at T11 and the right hemicord at T12. Another group received complete transection (CT) at T11 on P2. A third group was sham operated. Each of these groups was also treated with the drug combination. Drugs were administered intrathecally above the lesion during surgery, and again s.c. at P4, P6, P8, and P10. Intracellular recording in an in vitro spinal cord preparation at P10-P12 in DH rats revealed weak polysynaptic connections to lumbar motoneurons through the injury region, but only in those receiving NT-3 + LSD; NT-3 or LSD alone had no effect. In behavioral experiments, the frequency of rearing in an open field and hindlimb kicks during swimming was assessed every 3-4 days from P9 to P58. Both CT and DH injury severely impaired rearing and hindlimb kicking during swimming. DH rats treated with NT-3 + LSD showed significantly more kicks during swimming than untreated DH or CT rats and treated CT rats beginning as early as P9 and lasting through the duration of testing. Rearing behavior was also improved by treatment but beginning only in the 3rd postnatal week, the time at which it normally develops. Rearing frequency reached sham control levels by P40. Our results suggest this combination treatment may be a promising new strategy for facilitating recovery from moderate spinal cord injury.
机译:我们探讨了两种新型联合治疗(NT-3 + LSD)后脊髓损伤模型中的功能恢复。一组大鼠在出生后第2天(P2)在T11处的左半球和在T12处的右半球进行了交错双半切(DH)。另一组在P2的T11接受了完全横切(CT)。第三组是假手术。这些组中的每一个也都用药物组合治疗。在手术过程中,在病变上方鞘内注射药物,然后再次进行皮下注射。在P4,P6,P8和P10。在DH大鼠的P10-P12体外脊髓制剂中进行的细胞内记录显示,通过损伤区域与腰部运动神经元的多突触连接较弱,但仅在接受NT-3 + LSD的患者中。仅NT-3或LSD无效。在行为实验中,从P9到P58每3-4天评估一次在游泳场中在露天场所饲养和后肢踢腿的频率。 CT和DH损伤均严重影响游泳期间的饲养和后肢踢腿。用NT-3 + LSD治疗的DH大鼠在游泳过程中表现出比未治疗的DH或CT大鼠显着更多的踢动,并且治疗的CT大鼠早于P9开始并持续到测试期间。通过治疗也可改善饲养行为,但仅在产后第3周开始,即正常发育的时间开始。饲养频率达到了P40的假控制水平。我们的结果表明,这种联合治疗可能是促进中度脊髓损伤恢复的有希望的新策略。

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