首页> 外文期刊>British Journal of Pharmacology >P2X receptor-mediated excitation of nociceptive afferents in the normal and arthritic rat knee joint.
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P2X receptor-mediated excitation of nociceptive afferents in the normal and arthritic rat knee joint.

机译:P2X受体介导的正常和关节炎大鼠膝关节伤害感受传入的兴奋。

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摘要

1. We tested the hypothesis that functional P2X receptors are present on peripheral terminals of primary afferent articular nociceptors in the rat knee joint. Neural activity was recorded extracellularly from the medial articular nerve innervating the knee joint in rats anaesthetized with pentobarbitone. 2. The selective P2X receptor agonist, alphabeta methylene ATP (alphabetameATP), and the endogenous ligand, ATP, caused a rapid short-lasting excitation of a sub-population of C and Adelta nociceptive afferent nerves innervating normal knee joints when injected intra-arterially or intra-articularly, and this effect was antagonized by the non-selective P2 receptor antagonist PPADS. 3. Induction of a chronic (14-21 days) unilateral inflammatory arthritis of the knee joint using locally injected Freund's adjuvant neither increased or decreased responsiveness of joint nociceptors to alphabetameATP or ATP. 4. Our results support the hypothesis that alphabetameATP-sensitive P2X receptors are expressed on peripheral nociceptive afferents in the rat knee joint suggesting that they may be involved in the initiation of nociception and pain.
机译:1.我们测试了一种假设,即功能性P2X受体存在于大鼠膝关节初级传入关节伤害感受器的外周末端。在戊巴比妥麻醉的大鼠中,神经支配来自膝关节内侧神经的细胞外神经活动。 2.当通过动脉内注射时,选择性的P2X受体激动剂,字母亚甲基ATP(alphabetameATP)和内源性配体ATP引起C和Adelta伤害感受性传入神经的短时快速兴奋,支配正常膝关节。或关节内,非选择性P2受体拮抗剂PPADS拮抗了这种作用。 3.使用局部注射的弗氏佐剂诱导膝关节慢性(14-21天)慢性单侧炎性关节炎既不会增加也不会减少关节伤害感受器对字母ATP或ATP的反应性。 4.我们的研究结果支持以下假设:在大鼠膝关节的外周伤害感受性传入神经上表达对字母ATP敏感的P2X受体,这表明它们可能参与伤害感受和疼痛的发作。

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