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本文引用的文献

1
Mustard oil enhances spinal neuronal responses to noxious heat but not cooling.芥子油增强脊髓神经元对有害热刺激的反应,但对冷刺激无此作用。
Neurosci Lett. 2009 Sep 25;461(3):271-4. doi: 10.1016/j.neulet.2009.06.036. Epub 2009 Jun 21.
2
Pharmacological blockade of TRPA1 inhibits mechanical firing in nociceptors.TRPA1的药理学阻断可抑制伤害感受器的机械放电。
Mol Pain. 2009 Apr 21;5:19. doi: 10.1186/1744-8069-5-19.
3
TRPA1 acts as a cold sensor in vitro and in vivo.TRPA1在体外和体内均作为冷感受器发挥作用。
Proc Natl Acad Sci U S A. 2009 Jan 27;106(4):1273-8. doi: 10.1073/pnas.0808487106. Epub 2009 Jan 14.
4
HC-030031, a TRPA1 selective antagonist, attenuates inflammatory- and neuropathy-induced mechanical hypersensitivity.HC-030031,一种TRPA1选择性拮抗剂,可减轻炎症和神经病变引起的机械性超敏反应。
Mol Pain. 2008 Oct 27;4:48. doi: 10.1186/1744-8069-4-48.
5
Pronociceptive response elicited by TRPA1 receptor activation in mice.TRPA1受体激活在小鼠中引发的伤害感受性反应。
Neuroscience. 2008 Mar 18;152(2):511-20. doi: 10.1016/j.neuroscience.2007.12.039. Epub 2008 Jan 9.
6
A role of TRPA1 in mechanical hyperalgesia is revealed by pharmacological inhibition.药理学抑制揭示了TRPA1在机械性痛觉过敏中的作用。
Mol Pain. 2007 Dec 17;3:40. doi: 10.1186/1744-8069-3-40.
7
Cross-desensitization of responses of rat trigeminal subnucleus caudalis neurons to cinnamaldehyde and menthol.大鼠三叉神经尾侧亚核神经元对肉桂醛和薄荷醇反应的交叉脱敏
Neurosci Lett. 2008 Jan 3;430(1):29-33. doi: 10.1016/j.neulet.2007.10.008. Epub 2007 Oct 22.
8
Effects of TRPA1 agonists mustard oil and cinnamaldehyde on lumbar spinal wide-dynamic range neuronal responses to innocuous and noxious cutaneous stimuli in rats.TRPA1激动剂芥子油和肉桂醛对大鼠腰段脊髓广动力范围神经元对无害和有害皮肤刺激反应的影响。
J Neurophysiol. 2008 Feb;99(2):415-25. doi: 10.1152/jn.00883.2007. Epub 2007 Oct 17.
9
Modulation of oral heat and cold pain by irritant chemicals.刺激性化学物质对口腔冷热疼痛的调节作用。
Chem Senses. 2008 Jan;33(1):3-15. doi: 10.1093/chemse/bjm056. Epub 2007 Aug 29.
10
TRPA1 mediates formalin-induced pain.瞬时受体电位锚蛋白1介导福尔马林诱导的疼痛。
Proc Natl Acad Sci U S A. 2007 Aug 14;104(33):13525-30. doi: 10.1073/pnas.0705924104. Epub 2007 Aug 8.

肉桂醛皮内注射致大鼠热痛觉过敏和机械性触诱发痛的行为学证据。

Behavioral evidence of thermal hyperalgesia and mechanical allodynia induced by intradermal cinnamaldehyde in rats.

机构信息

Department of Neurophysiology, Beritashvili Inst. Physiology, Tbilisi, Georgia, USA.

出版信息

Neurosci Lett. 2010 Apr 12;473(3):233-6. doi: 10.1016/j.neulet.2010.02.056. Epub 2010 Feb 26.

DOI:10.1016/j.neulet.2010.02.056
PMID:20219630
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2853256/
Abstract

TRPA1 agonists cinnamaldehyde (CA) and mustard oil (allyl isothiocyanate=AITC) induce heat hyperalgesia and mechanical allodynia in human skin, and sensitize responses of spinal and trigeminal dorsal horn neurons to noxious skin heating in rats. TRPA1 is also implicated in cold nociception. We presently used behavioral methods to investigate if CA affects sensitivity to thermal and mechanical stimuli in rats. Unilateral intraplantar injection of CA (5-20%) induced a significant, concentration-dependent reduction in latency for ipsilateral paw withdrawal from a noxious heat stimulus, peaking (61.7% of pre-injection baseline) by 30 min with partial recovery at 120 min. The highest dose of CA also significantly reduced the contralateral paw withdrawal latency. CA significantly reduced mechanical withdrawal thresholds of the injected paw that peaked sooner (3 min) and was more profound (44.4% of baseline), with no effect contralaterally. Bilateral intraplantar injections of CA resulted in a significant cold hyperalgesia (cold plate test) and a weak enhancement of innocuous cold avoidance (thermal preference test). The data are consistent with roles for TRPA1 in thermal (hot and cold) hyperalgesia and mechanical allodynia.

摘要

TRPA1 激动剂肉桂醛(CA)和芥末油(丙烯基异硫氰酸酯=AITC)在人体皮肤上诱发热痛觉过敏和机械性痛觉过敏,并敏化大鼠脊髓和三叉神经背角神经元对有害皮肤加热的反应。TRPA1 也与冷觉过敏有关。我们目前使用行为方法研究 CA 是否会影响大鼠对热和机械刺激的敏感性。单侧足底内注射 CA(5-20%)可显著、浓度依赖性地降低对有害热刺激的同侧爪撤回潜伏期,在 30 分钟时达到峰值(相对于注射前基线的 61.7%),在 120 分钟时部分恢复。最高剂量的 CA 也显著降低了对侧爪撤回潜伏期。CA 显著降低了注射爪的机械撤回阈值,其峰值出现得更早(3 分钟),且更为明显(相对于基线的 44.4%),对侧则没有影响。双侧足底内注射 CA 导致明显的冷痛觉过敏(冷板试验)和轻微增强的无害冷回避(热偏好试验)。这些数据支持 TRPA1 在热(热和冷)痛觉过敏和机械性痛觉过敏中的作用。