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5-羟色胺对正常及关节炎大鼠关节感觉感受器的影响。

The effects of 5-HT on articular sensory receptors in normal and arthritic rats.

作者信息

Birrell G J, McQueen D S, Iggo A, Grubb B D

机构信息

Department of Pharmacology, University of Edinburgh Medical School.

出版信息

Br J Pharmacol. 1990 Nov;101(3):715-21. doi: 10.1111/j.1476-5381.1990.tb14146.x.

Abstract
  1. The effects of intra arterial (i.a.) injections of 5-hydroxytryptamine (5-HT, 1-100 micrograms) on the discharge of (a) identified articular high threshold mechanoreceptors and (b) unidentified chemosensitive receptors in the ankle joint have been studied electrophysiologically in anaesthetized normal and arthritic rats. Recordings were made from a fine branch of the medial plantar nerve. 2. 5-HT increased the mechanical responsiveness of high threshold nociceptive mechanoreceptors with C and A delta fibre afferents in both normal and adjuvant-arthritic rats. Receptors in arthritic joints were more sensitive to 5-HT than were those from normal joints. 3. 5-HT produced a complex response from both types of articular receptors following i.a. injection. Two separate components were identified: (a) a fast transient burst of activity was obtained within 10 s of this injection in 66% of units from normal animals and 45% from arthritics, followed by (b) a delayed slow longer-lasting excitation seen in 62% of the units examined from normals and 77% of units from arthritic rats. 4. Increased mechanoreceptor responsiveness produced by 5-HT was reduced or abolished by the 5-HT3 receptor antagonists studied (MDL 72222, ICS 205-930, or GR 38032F, in single doses of 100 micrograms kg-1, i.a.). 5. Fast excitation showed marked tachyphylaxis and was antagonized by MDL 72222, ICS 205-930 or GR 38032F. It was unaffected by ketanserin (100 micrograms kg-1, i.a.). Delayed excitation was reduced or abolished by ketanserin but was unaffected by the 5-HT3-receptor antagonists. 6. Administration of MDL 72222, ICS 205-930 or GR 38032F caused short lasting (< 5 min) reductions in background activity from both types of unit recorded in arthritic rats, as well as in normal rats in which activity had increased following administration of 5-HT. Ketanserin caused similar reductions in background activity in chemosensitive units, but had no effect on mechanoreceptors. 7. At least two types of receptor are involved in the actions of 5-HT on articular sensory receptors with fine afferent fibres. Increased mechano-responsiveness involves a 5-HT3-receptor as does fast excitation. Delayed excitation probably involves a 5-HT2-receptor. Endogenous 5-HT appears not to play a crucial role in sensitization of high threshold mechanoreceptors in this model of chronic inflammation and arthritis, although its local release may potentiate the actions of other inflammatory mediators on sensory receptors in the ankle joint.
摘要
  1. 采用电生理学方法,在麻醉的正常大鼠和关节炎大鼠中,研究了动脉内(i.a.)注射5-羟色胺(5-HT,1 - 100微克)对(a)已鉴定的关节高阈值机械感受器和(b)踝关节中未鉴定的化学敏感感受器放电的影响。记录取自足底内侧神经的一个细分支。2. 5-HT增强了正常大鼠和佐剂性关节炎大鼠中具有C和Aδ纤维传入的高阈值伤害性机械感受器的机械反应性。关节炎关节中的感受器对5-HT比正常关节中的感受器更敏感。3. 动脉内注射5-HT后,两种类型的关节感受器均产生复杂反应。鉴定出两个独立的成分:(a)在注射后10秒内,66%的正常动物单位和45%的关节炎动物单位出现快速短暂的活动爆发,随后(b)在62%的正常检查单位和77%的关节炎大鼠单位中出现延迟的缓慢持久兴奋。4. 所研究的5-HT3受体拮抗剂(MDL 72222、ICS 205 - 930或GR 38032F,动脉内单次剂量100微克/千克)可降低或消除5-HT引起的机械感受器反应性增加。5. 快速兴奋表现出明显的快速耐受,并被MDL 72222、ICS 205 - 930或GR 38032F拮抗。它不受酮色林(动脉内100微克/千克)影响。延迟兴奋被酮色林降低或消除,但不受5-HT3受体拮抗剂影响。6. 给予MDL 72222、ICS 205 - 930或GR 38032F可使关节炎大鼠记录的两种类型单位的背景活动短暂降低(<5分钟),在给予5-HT后活动增加的正常大鼠中也是如此。酮色林使化学敏感单位的背景活动产生类似降低,但对机械感受器无影响。7. 5-HT对具有细传入纤维的关节感觉感受器的作用至少涉及两种类型的受体。机械反应性增加涉及5-HT3受体,快速兴奋也是如此。延迟兴奋可能涉及5-HT2受体。内源性5-HT在这种慢性炎症和关节炎模型中对高阈值机械感受器的敏化似乎不发挥关键作用,尽管其局部释放可能增强其他炎症介质对踝关节感觉感受器的作用。

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