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神经周微管抑制剂可诱导脊髓后角胶状质中中枢伤害性感受终末发生退行性萎缩。

Perineural microtubule inhibitors induce degenerative atrophy of central nociceptive terminals in the Rolando substance.

作者信息

Csillik B, Knyihár E, Jójárt I, Elshiekh A A, Pór I

出版信息

Res Commun Chem Pathol Pharmacol. 1978 Sep;21(3):467-84.

PMID:705025
Abstract

Short-term perineural application of a microtubule inhibitor around a peripheral nerve induces degenerative atrophy of primary central nociceptive terminals in the Rolando substance. Consequences of the local microtubule inhibitor treatment are identical, both at light- and electron microscopic levels, with those that follow transection of a peripheral nerve. Degenerative atrophy in the Rolando substance is due to arrested axoplasmic transport in, and not to Wallerian degeneration of, the peripheral axons since (1) locally applied vinblastine and vincristone do not induce peripheral degeneration at all and (2) even though local colchicine treatment may cause Wallerian degeneration of thick myelinated axons, thin Adelta and C fibers do not undergo degeneration after colchicine treatment. The intriguing possibility to use this approach in the treatment of intractable pain is discussed.

摘要

在周围神经周围短期应用微管抑制剂会导致脊髓后角原发性中枢伤害性感受神经元终末发生退行性萎缩。局部微管抑制剂治疗的结果,在光学显微镜和电子显微镜水平上,与周围神经横断后的结果相同。脊髓后角的退行性萎缩是由于外周轴突内轴浆运输停滞,而非外周轴突的华勒氏变性,因为:(1)局部应用长春花碱和长春新碱根本不会诱导外周变性;(2)尽管局部秋水仙碱治疗可能会导致粗大的有髓轴突发生华勒氏变性,但细的Aδ纤维和C纤维在秋水仙碱治疗后不会发生变性。文中讨论了使用这种方法治疗顽固性疼痛的有趣可能性。

相似文献

1
Perineural microtubule inhibitors induce degenerative atrophy of central nociceptive terminals in the Rolando substance.神经周微管抑制剂可诱导脊髓后角胶状质中中枢伤害性感受终末发生退行性萎缩。
Res Commun Chem Pathol Pharmacol. 1978 Sep;21(3):467-84.
2
Effects of perineurally applied cytostatic, cytotoxic and chelating agents upon peripheral and central processes of primary nociceptive neurons.经神经周应用细胞抑制剂、细胞毒素和螯合剂对初级伤害性神经元外周和中枢突的影响。
Z Mikrosk Anat Forsch. 1980;94(3):531-44.
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Functional impairment of the primary nociceptive analyser in the course of transganglionic degenerative atrophy.经神经节变性萎缩过程中初级伤害性感受器的功能损害。
Acta Biol Hung. 1983;34(2-3):267-73.
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Reversibility of microtubule inhibitor-induced transganglionic degenerative atrophy of central terminals of primary nociceptive neurons.微管抑制剂诱导的初级伤害感受神经元中枢终末跨神经节变性萎缩的可逆性
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Axonal labyrinths in the rat spinal cord: a consequence of degenerative atrophy.大鼠脊髓中的轴突迷路:退行性萎缩的结果。
Acta Biol Acad Sci Hung. 1976;27(4):299-308.
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Iontophoretically applied microtubule inhibitors induce transganglionic degenerative atrophy of primary central nociceptive terminals and abolish chronic autochtonous pain.离子电渗法应用的微管抑制剂可诱导原发性中枢伤害性感受器终末的跨神经节变性萎缩,并消除慢性自发性疼痛。
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Light and electron microscopic localization of B-50 (GAP43) in the rat spinal cord during transganglionic degenerative atrophy and regeneration.经神经节变性萎缩和再生过程中大鼠脊髓中B-50(GAP43)的光镜和电镜定位
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Molecular plasticity of primary nociceptive neurons: relations of the NGF-c-jun system to neurotomy and chronic pain.
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Blockade of retrograde axoplasmic transport induces transganglionic degenerative atrophy of central terminals of primary nociceptive neurons.逆行轴浆运输的阻断会诱导初级伤害性神经元中枢终末的跨节段性变性萎缩。
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Transient loss of terminals from non-peptidergic nociceptive fibers in the substantia gelatinosa of spinal cord following chronic constriction injury of the sciatic nerve.坐骨神经慢性压迫损伤后脊髓胶状质中非肽能伤害性纤维终末的短暂丢失。
Neuroscience. 2006;138(2):675-90. doi: 10.1016/j.neuroscience.2005.11.051. Epub 2006 Jan 19.

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Depletion of substance P and somatostatin in the upper dorsal horn after blockade of axoplasmic transport.轴浆运输阻断后上背角中P物质和生长抑素的耗竭。
Histochemistry. 1984;81(4):391-400. doi: 10.1007/BF00514335.
3
Transneuronal degeneration in the Rolando substance of the primate spinal cord evoked by axotomy-induced transganglionic degenerative atrophy of central primary sensory terminals.
轴突切断术诱发的中枢初级感觉末梢跨神经节变性萎缩所引起的灵长类脊髓罗兰多质中的跨神经元变性。
Cell Tissue Res. 1989 Dec;258(3):515-25. doi: 10.1007/BF00218863.
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Fine structure of growth cones in the upper dorsal horn of the adult primate spinal cord in the course of reactive synapto-neogenesis.成年灵长类脊髓上背角中反应性突触新生过程中生长锥的精细结构
Cell Tissue Res. 1985;239(3):633-41. doi: 10.1007/BF00219242.