Gauldie S D, McQueen D S, Pertwee R, Chessell I P
Sensory Pharmacology Unit, Department of Neuroscience, University of Edinburgh, Edinburgh, EH8 9JZ.
Br J Pharmacol. 2001 Feb;132(3):617-21. doi: 10.1038/sj.bjp.0703890.
The effects of the endogenous cannabinoid anandamide were studied on peripheral, polymodal nociceptors recorded from normal and chronically inflamed (Freund's adjuvant) knee joint afferents in rats anaesthetized with pentobarbitone. Anandamide (860 nmol) caused a rapid, short lasting excitation of a sub-population of capsaicin-sensitive nociceptive afferents in normal knee joints (7.2+/-2.3 impulses s(-1); n=15 units from five animals). In arthritic joints there were 9.7+/-3.0 impulses s(-1) (n=11 from six animals), which was not significantly different from normal joints. The excitation was dose dependent (8.6 - 2900 nmol) and mediated by activation of the vanilloid receptor (VR(1)) as it was abolished by the VR1 antagonist capsazepine (1 mg kg(-1)). Our results show that anandamide, at high doses, can activate nociceptive afferents innervating the rat knee joints, in contrast with its widely described analgesic actions.
研究了内源性大麻素花生四烯乙醇胺(anandamide)对戊巴比妥麻醉的大鼠正常及慢性炎症(弗氏佐剂)膝关节传入神经中记录到的外周多模式伤害感受器的影响。花生四烯乙醇胺(860 nmol)可使正常膝关节中辣椒素敏感伤害性传入神经亚群产生快速、短暂的兴奋(7.2±2.3 个冲动·秒⁻¹;来自五只动物的 15 个单位)。在关节炎关节中,其兴奋频率为 9.7±3.0 个冲动·秒⁻¹(来自六只动物的 11 个单位),与正常关节无显著差异。这种兴奋呈剂量依赖性(8.6 - 2900 nmol),且由香草酸受体(VR(1))激活介导,因为 VR1 拮抗剂辣椒平(1 mg·kg⁻¹)可消除该兴奋。我们的结果表明,与广泛描述的镇痛作用相反,高剂量的花生四烯乙醇胺可激活支配大鼠膝关节的伤害性传入神经。