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急性和慢性给予硝基咪唑后小鼠神经传导速度的变化

Changes in nerve conduction velocity in the mouse after acute and chronic administration of nitroimidazoles.

作者信息

Hirst D G, Vojnovic B, Hobson B

出版信息

Br J Cancer. 1979 Feb;39(2):159-67. doi: 10.1038/bjc.1979.26.

DOI:10.1038/bjc.1979.26
PMID:435365
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2009849/
Abstract

The effect of the nitroimidazoles misonidazole, Ro-05-9963, RGW-608 and metronidazole on nerve conduction velocity (NCV) were measured in the anaesthetized mouse. The compounds were administered by i.p. injection either as a single dose of 1 mg/g (only 0.5 mg/g for RGW-608) or in 36 fractions of 0.15 mg/g over 18 days (only 4 fractions in 2 days for RGW-608). After single doses a reduction in nerve conduction velocity was seen with all the compounds except metronidazole, which had no significant effect. During chronic exposure, a reduction in NCV occurred towards the end of the course of injections. All compounds produced an effect, although RGW-608 was the most neurotoxic, giving the largest reduction in NCV after only 4 injections. After the end of chronic exposure to misonidazole, Ro-05-9963 and metronidazole, recovery to normal took 2-3 weeks.

摘要

在麻醉小鼠中测定了硝基咪唑类药物米索硝唑、Ro-05-9963、RGW-608和甲硝唑对神经传导速度(NCV)的影响。这些化合物通过腹腔注射给药,单次剂量为1 mg/g(RGW-608仅为0.5 mg/g),或在18天内分36次注射,每次0.15 mg/g(RGW-608在2天内仅分4次注射)。单次给药后,除甲硝唑无显著影响外,所有化合物均使神经传导速度降低。在慢性暴露期间,注射过程接近尾声时神经传导速度出现下降。所有化合物均产生了影响,尽管RGW-608神经毒性最大,仅4次注射后神经传导速度下降幅度最大。在慢性暴露于米索硝唑、Ro-05-9963和甲硝唑结束后,恢复正常需要2至3周。

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Changes in nerve conduction velocity in the mouse after acute and chronic administration of nitroimidazoles.急性和慢性给予硝基咪唑后小鼠神经传导速度的变化
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引用本文的文献

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A biochemical method for assessing the neurotoxic effects of misonidazole in the rat.一种评估米索硝唑对大鼠神经毒性作用的生化方法。
Br J Cancer. 1980 Dec;42(6):890-9. doi: 10.1038/bjc.1980.337.
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Effect of acute and chronic misonidazole administration on peripheral-nerve electrophysiology in mice.急性和慢性给予米索硝唑对小鼠周围神经电生理学的影响。
Br J Cancer. 1980 Apr;41(4):523-8. doi: 10.1038/bjc.1980.94.
3
In vivo assessment of basic 2-nitroimidazole radiosensitizers.2-硝基咪唑类基础放射增敏剂的体内评估
Br J Cancer. 1982 Jul;46(1):127-37. doi: 10.1038/bjc.1982.174.
4
Quantitative cytochemical assessment of the neurotoxicity of misonidazole in the mouse.米索硝唑对小鼠神经毒性的定量细胞化学评估
Br J Cancer. 1982 Apr;45(4):582-7. doi: 10.1038/bjc.1982.95.
5
Evoked potentials in rats with misonidazole neurotoxicity. I. Brain stem auditory evoked potentials.米索硝唑神经毒性大鼠的诱发电位。I. 脑干听觉诱发电位。
J Neurooncol. 1983;1(2):115-23. doi: 10.1007/BF00182956.

本文引用的文献

1
Hypoxic cell radiosensitizers: comparative tests of some electron affinic compounds using epidermal cell survival in vivo.缺氧细胞放射增敏剂:使用体内表皮细胞存活率对某些亲电子化合物进行的对比试验。
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Electron affinic sensitization. V. Radiosensitization of hypoxic bacteria and mammalian cells in vitro by some nitroimidazoles and nitropyrazoles.亲电子致敏作用。V. 某些硝基咪唑和硝基吡唑对缺氧细菌和哺乳动物细胞的体外放射致敏作用
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Electron affinic sensitization. II. Para-nitroacetophenone: a radiosensitizer for anoxic bacterial and mammalian cells.
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Nitrofurans as radiosensitizers of hypoxic mammalian cells.硝基呋喃作为缺氧哺乳动物细胞的放射增敏剂。
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Phase 1 study of high-dose metronidazole: a specific in vivo and in vitro radiosensitizer of hypoxic cells.大剂量甲硝唑的1期研究:一种低氧细胞特异性的体内外放射增敏剂。
Radiology. 1975 Oct;117(1):129-33. doi: 10.1148/117.1.129.
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In vivo testing of hypoxic radiosensitizers using the KHT murine tumour assayed by the lung-colony technique.使用肺集落技术通过KHT小鼠肿瘤对缺氧放射增敏剂进行体内测试。
Br J Radiol. 1975 Mar;48(567):209-20. doi: 10.1259/0007-1285-48-567-209.
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Mammalian cell toxicity of nitro compounds : dependence upon reduction potential.
Biochem Biophys Res Commun. 1976 Oct 4;72(3):824-9. doi: 10.1016/s0006-291x(76)80207-0.
8
Electron-affinic sensitization. VII. A correlation between structures, one-electron reduction potentials, and efficiencies of nitroimidazoles as hypoxic cell radiosensitizers.亲电子致敏作用。VII. 硝基咪唑类作为乏氧细胞放射增敏剂的结构、单电子还原电位与效率之间的相关性。
Radiat Res. 1976 Jul;67(1):9-20.
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Clinical testing of the radiosensitizer Ro 07-0582: experience with multiple doses.放射增敏剂Ro 07-0582的临床试验:多次给药的经验
Br J Cancer. 1977 May;35(5):567-79. doi: 10.1038/bjc.1977.90.
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Radiology. 1977 Mar;122(3):801-4. doi: 10.1148/122.3.801.