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发育中大鼠脊髓运动神经元的轴突切断:细胞存活、胞体大小、肌肉恢复及睾酮的影响

Axotomy of developing rat spinal motoneurons: cell survival, soma size, muscle recovery, and the influence of testosterone.

作者信息

Lubischer J L, Arnold A P

机构信息

Program in Neuroscience, University of California, Los Angeles 90024-1563, USA.

出版信息

J Neurobiol. 1995 Feb;26(2):225-40. doi: 10.1002/neu.480260207.

Abstract

During the period of synapse elimination, motoneurons are impaired in their ability to generate or regenerate axonal branches: following partial denervation of their target muscle, young motoneurons do not sprout to nearby denervated fibers and after axonal injury, they fail to reinnervate the muscle. In the rat levator ani (LA) muscle, which is innervated by motoneurons in the spinal nucleus of the bulbocavernosus (SNB), synapse elimination ends relatively late in development and can be regulated by testosterone. We took advantage of this system to determine if the end of synapse elimination and the development of regenerative capabilities by motoneurons share a common mechanism, or, alternatively, if these two events can be dissociated in time. Axotomy on or before postnatal day 14 (P14) caused the death of SNB motoneurons. By P21, toward the end of synapse elimination in the LA muscle, SNB motoneurons had developed the ability to survive axonal injury. Altering testosterone levels by castration on P7 followed by 4 weeks of either testosterone propionate or control injections did not change the ability of SNB motoneurons to survive axonal injury during development, although these same treatments alter the time course of synapse elimination in the LA muscle. Thus, we dissociated the inability of SNB motoneurons to recover from axonal injury from their developmental elimination of synaptic terminals. We also measured the effect of early axotomy on motoneuronal soma size and on target muscle weight. Axotomy on P14 caused a long-lasting decrease in the soma size of surviving SNB motoneurons, whereas motoneurons axotomized on P28 recovered their normal soma size. Axotomy on or before P7 caused severe atrophy of the target muscles, matching the extensive loss of motoneurons. However, target muscle recovery after axotomy on P14 was as good as recovery after axotomy at later ages, despite greater motoneuronal death after axotomy on P14. This result may reflect an increase in motor unit size, a decrease in polyneuronal innervation by SNB motoneurons that survive axotomy on P14, or a combination of the two.

摘要

在突触消除期,运动神经元产生或再生轴突分支的能力受损:在其靶肌肉部分去神经支配后,年轻的运动神经元不会向附近去神经支配的纤维发出新芽,并且在轴突损伤后,它们无法重新支配肌肉。在大鼠球海绵体肌(LA)中,该肌肉由球海绵体核(SNB)中的运动神经元支配,突触消除在发育过程中结束得相对较晚,并且可以受睾酮调节。我们利用这个系统来确定突触消除的结束和运动神经元再生能力的发展是否共享一个共同机制,或者,这两个事件在时间上是否可以分离。出生后第14天(P14)或之前进行轴突切断会导致SNB运动神经元死亡。到P21时,接近LA肌肉突触消除结束时,SNB运动神经元已发展出在轴突损伤后存活的能力。在P7进行阉割,随后4周注射丙酸睾酮或对照注射来改变睾酮水平,并没有改变SNB运动神经元在发育过程中在轴突损伤后存活的能力,尽管这些相同的处理改变了LA肌肉中突触消除的时间进程。因此,我们将SNB运动神经元从轴突损伤中恢复的无能与它们在发育过程中对突触终末的消除分离开来。我们还测量了早期轴突切断对运动神经元胞体大小和靶肌肉重量的影响。P14进行轴突切断导致存活的SNB运动神经元胞体大小长期减小,而在P28进行轴突切断的运动神经元恢复了正常的胞体大小。P7或之前进行轴突切断会导致靶肌肉严重萎缩,这与运动神经元的大量损失相匹配。然而,尽管P14进行轴突切断后运动神经元死亡更多,但P14进行轴突切断后靶肌肉的恢复与后期进行轴突切断后的恢复一样好。这个结果可能反映了运动单位大小的增加、在P14进行轴突切断后存活的SNB运动神经元对多神经元支配的减少,或者两者的结合。

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