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响尾蛇毒素对大鼠行为的影响。

Crotoxin-induced behavioral effects in rats.

作者信息

Moreira E G, Nascimento N, Rosa G J, Rogero J R, Vassilieff V S

机构信息

Departamento de Farmacologia, Universidade Estadual Paulista, Botucatu, Brasil.

出版信息

Braz J Med Biol Res. 1996 May;29(5):629-32.

PMID:9033813
Abstract

Crotoxin is the major component of Crotalus durissus terrificus venom. In view of the presence of high-affinity specific binding sites for crotoxin in the brain, the objective of this work was to investigate whether crotoxin induces behavioral effects in the open-field and hole-board tests. Adult male Wistar rats (180-220 g) treated with crotoxin, 100, 250 and 500 micrograms/kg, ip, administered 2 h before the test, presented statistically significant behavioral alterations (ANOVA for one-way classification complemented with Dunnet test, P < 0.05). In the open-field test, 250 and 500 micrograms/kg of crotoxin increased freezing (from 3.22 sec to 10.75 sec and 11.2 sec) and grooming (from 13.44 sec to 22.75 sec and 21.22 sec) and decreased ambulation (from 64.8 to 39.38 and 45.8). The dose of 500 micrograms/kg also decreased rearing (from 24.9 to 17.5). In the hole-board test, 500 micrograms/kg of crotoxin decreased head-dip count (from 6.33 to 4.00). All the crotoxin-induced behavioral effects were antagonized by an anxiolytic dose of diazepam (1.5 mg/kg, ip. 30 min before the tests). These results show that crotoxin reduced open-field activity and exploratory behavior as well. We suggest that these effects express an increased emotional state induced by this toxin.

摘要

响尾蛇毒素是南美巨蝮蛇毒的主要成分。鉴于大脑中存在响尾蛇毒素的高亲和力特异性结合位点,本研究的目的是调查响尾蛇毒素在旷场试验和洞板试验中是否会诱发行为效应。成年雄性Wistar大鼠(180 - 220克)在试验前2小时腹腔注射100、250和500微克/千克的响尾蛇毒素,出现了具有统计学意义的行为改变(单向分类方差分析并辅以Dunnet检验,P < 0.05)。在旷场试验中,250和500微克/千克的响尾蛇毒素增加了静止时间(从3.22秒增加到10.75秒和11.2秒)和理毛时间(从13.44秒增加到22.75秒和21.22秒),并减少了行走距离(从64.8减少到39.38和45.8)。500微克/千克的剂量还减少了竖尾次数(从24.9减少到17.5)。在洞板试验中,500微克/千克的响尾蛇毒素减少了探洞次数(从6.33减少到4.00)。所有响尾蛇毒素诱导的行为效应都被抗焦虑剂量的地西泮(1.5毫克/千克,腹腔注射,试验前30分钟)所拮抗。这些结果表明,响尾蛇毒素降低了旷场活动和探索行为。我们认为这些效应表明这种毒素诱发了情绪状态的增加。

相似文献

1
Crotoxin-induced behavioral effects in rats.响尾蛇毒素对大鼠行为的影响。
Braz J Med Biol Res. 1996 May;29(5):629-32.
2
Gabaergic-benzodiazepine system is involved in the crotoxin-induced anxiogenic effect.γ-氨基丁酸能-苯二氮䓬系统参与了响尾蛇毒素诱导的致焦虑效应。
Pharmacol Biochem Behav. 2000 Jan 1;65(1):7-13. doi: 10.1016/s0091-3057(99)00177-x.
3
Lipoxygenase-derived eicosanoids are involved in the inhibitory effect of Crotalus durissus terrificus venom or crotoxin on rat macrophage phagocytosis.脂氧合酶衍生的类花生酸参与了杜氏响尾蛇毒液或响尾蛇毒素对大鼠巨噬细胞吞噬作用的抑制效应。
Toxicon. 2006 Mar;47(3):313-21. doi: 10.1016/j.toxicon.2005.11.008. Epub 2005 Dec 20.
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Actions of Crotalus durissus terrificus venom and crotoxin on the isolated rat kidney.杜氏剑尾蝮蛇毒液及响尾蛇毒素对离体大鼠肾脏的作用。
Braz J Med Biol Res. 2001 Oct;34(10):1347-52. doi: 10.1590/s0100-879x2001001000017.
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Effects of Crotalus durissus collilineatus venom in the isolated rat kidney.杜氏侏膨蝰蛇毒对离体大鼠肾脏的影响。
Toxicon. 2006 Mar;47(3):260-4. doi: 10.1016/j.toxicon.2005.10.007. Epub 2006 Jan 20.
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Opiate and acetylcholine-independent analgesic actions of crotoxin isolated from crotalus durissus terrificus venom.从南美巨蝮蛇毒中分离出的响尾蛇毒素的阿片样物质和乙酰胆碱非依赖性镇痛作用。
Toxicon. 2006 Aug;48(2):175-82. doi: 10.1016/j.toxicon.2006.04.008. Epub 2006 Apr 28.
7
Crotoxin from Crotalus durissus terrificus snake venom induces the release of glutamate from cerebrocortical synaptosomes via N and P/Q calcium channels.来自南美巨蝮蛇毒的响尾蛇毒素通过N型和P/Q型钙通道诱导大脑皮质突触体释放谷氨酸。
Toxicon. 2014 Jul;85:5-16. doi: 10.1016/j.toxicon.2014.04.008. Epub 2014 Apr 19.
8
Antinociceptive activity of crotoxin in the central nervous system: a functional Magnetic Resonance Imaging study.crotoxin 在中枢神经系统中的抗伤害活性:一项功能磁共振成像研究。
Toxicon. 2013 Nov;74:44-55. doi: 10.1016/j.toxicon.2013.07.019. Epub 2013 Aug 3.
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Contribution of crotoxin for the inhibitory effect of Crotalus durissus terrificus snake venom on macrophage function.响尾蛇毒素对杜氏响尾蛇蛇毒抑制巨噬细胞功能的贡献。
Toxicon. 2003 Jun;41(7):899-907. doi: 10.1016/s0041-0101(03)00069-2.
10
Effect of gamma irradiation on the behavioral properties of crotoxin.γ射线辐照对响尾蛇毒素行为特性的影响。
Braz J Med Biol Res. 1997 Feb;30(2):245-9. doi: 10.1590/s0100-879x1997000200014.

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