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响尾蛇毒素对神经性疼痛的镇痛作用是由中枢毒蕈碱受体和5-脂氧合酶衍生的介质介导的。

The analgesic effect of crotoxin on neuropathic pain is mediated by central muscarinic receptors and 5-lipoxygenase-derived mediators.

作者信息

Nogueira-Neto Francisco de Sousa, Amorim Renée L, Brigatte Patrícia, Picolo Gisele, Ferreira Wilson A, Gutierrez Vanessa P, Conceição Isaltino Marcelo, Della-Casa Maisa S, Takahira Regina K, Nicoletti José Luis M, Cury Yara

机构信息

Laboratory of Pathophysiology, Butantan Institute, Vital Brazil Av., 1500, 05503-900, Sao Paulo, SP, Brazil.

出版信息

Pharmacol Biochem Behav. 2008 Dec;91(2):252-60. doi: 10.1016/j.pbb.2008.08.016. Epub 2008 Aug 23.

Abstract

Crotoxin (CTX), a neurotoxin isolated from the venom of the South American rattlesnake Crotalus durissus terrificus, induces analgesia. In this study, we evaluated the antinociceptive effect of CTX in a model of neuropathic pain induced by rat sciatic nerve transection. Hyperalgesia was detected 2 h after nerve transection and persisted for 64 days. Immersion of proximal and distal nerve stumps in CTX solution (0.01 mM for 10 s), immediately after nerve transection, blocked hyperalgesia. The antinociceptive effect of CTX was long-lasting, since it was detected 2 h after treatment and persisted for 64 days. CTX also delayed, but did not block, neurectomy-induced neuroma formation. The effect of CTX was blocked by zileuton (100 mg/kg, p.o.) and atropine (10 mg/kg, i.p.), and reduced by yohimbine (2 mg/kg, i.p.) and methysergide (5 mg/kg, i.p.). On the other hand, indomethacin (4 mg/kg, i.v.), naloxone (1 mg/kg, i.p.), and N-methyl atropine (30 mg/kg, i.p.) did not interfere with the effect of CTX. These results indicate that CTX induces a long-lasting antinociceptive effect in neuropathic pain, which is mediated by activation of central muscarinic receptors and partially, by activation of alpha-adrenoceptors and 5-HT receptors. Eicosanoids derived from the lipoxygenase pathway modulate the action of crotoxin.

摘要

响尾蛇毒素(CTX)是从南美响尾蛇(Crotalus durissus terrificus)毒液中分离出的一种神经毒素,具有镇痛作用。在本研究中,我们评估了CTX在大鼠坐骨神经横断诱导的神经性疼痛模型中的抗伤害感受作用。神经横断后2小时检测到痛觉过敏,并持续64天。神经横断后立即将近端和远端神经残端浸入CTX溶液(0.01 mM,持续10秒)可阻断痛觉过敏。CTX的抗伤害感受作用持久,因为在治疗后2小时即可检测到,并持续64天。CTX还延迟了,但未阻断神经切除术诱导的神经瘤形成。齐留通(100 mg/kg,口服)和阿托品(10 mg/kg,腹腔注射)可阻断CTX的作用,育亨宾(2 mg/kg,腹腔注射)和甲基麦角新碱(5 mg/kg,腹腔注射)可减弱其作用。另一方面,吲哚美辛(4 mg/kg,静脉注射)、纳洛酮(1 mg/kg,腹腔注射)和N-甲基阿托品(30 mg/kg,腹腔注射)不影响CTX的作用。这些结果表明,CTX在神经性疼痛中诱导持久的抗伤害感受作用,这是由中枢毒蕈碱受体的激活介导的,部分是由α-肾上腺素能受体和5-羟色胺受体的激活介导的。源自脂氧合酶途径的类花生酸调节响尾蛇毒素的作用。

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