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降钙素基因相关肽可增加大鼠膝关节的血流量并增强血浆蛋白外渗。

Calcitonin gene-related peptide increases blood flow and potentiates plasma protein extravasation in the rat knee joint.

作者信息

Cambridge H, Brain S D

机构信息

Biomedical Sciences Division, King's College, London.

出版信息

Br J Pharmacol. 1992 Jul;106(3):746-50. doi: 10.1111/j.1476-5381.1992.tb14404.x.

Abstract
  1. The effects of calcitonin gene-related peptide (CGRP) and other vasoactive mediators of inflammation on blood flow in the synovial vessels and plasma protein extravasation into the knee (femoro-tibial) joint of the pentobarbitone-anaesthetized rat were measured. 2. Changes in synovial blood flow were estimated by 133xenon clearance from the synovial cavity. CGRP (0.1 pmol and 10 pmol) and prostaglandin E1 (PGE1; 3 pmol and 300 pmol) significantly increased clearance from the knee joint measured 5 min after intra-articular injection. Substance P (10 pmol) had no effect on synovial blood flow. 3. Intra-articular perfusion of the rat knee with CGRP at concentrations up to 0.1 mM, or PGE1 at concentrations up to 10 microM, did not increase plasma extravasation into the synovial cavity measured by accumulation of intravenously injected 125I-albumin in the perfusate. 4. Plasma extravasation into the knee was significantly increased by infusion of bradykinin (0.1 microM), 5-hydroxytryptamine (1 microM) and histamine (0.1 mM), compared with the contralateral joints in the same animals which were perfused with Tyrode solution. 5. Perfusion of the knee joint with substance P did not specifically induce 125I-labelled albumin accumulation in the synovial cavity even at doses that had systemic effects as observed by marked plasma extravasation into other tissues. 6. The increase in plasma extravasation induced by histamine (0.1 mM) was potentiated by co-infusion with CGRP (0.1 microM) and PGE1 (3 microM). However the response to a submaximal dose (0.1 microM) of bradykinin, which induced similar plasma extravasation to histamine (0.1 mM), was not increased by co-infusion with CGRP or PGE1.7. These results show that CGRP is a potent vasodilator in the rat knee. CGRP released from sensory nerves may act synergistically with mediators of increased vascular permeability to modify the inflammatory response in this site.
摘要
  1. 测量了降钙素基因相关肽(CGRP)和其他炎症性血管活性介质对戊巴比妥麻醉大鼠滑膜血管血流以及血浆蛋白渗入膝关节(股骨 - 胫骨关节)的影响。2. 通过133氙从滑膜腔清除率估算滑膜血流变化。关节内注射后5分钟测量,CGRP(0.1皮摩尔和10皮摩尔)和前列腺素E1(PGE1;3皮摩尔和300皮摩尔)显著增加膝关节清除率。P物质(10皮摩尔)对滑膜血流无影响。3. 以高达0.1毫摩尔的浓度向大鼠膝关节内灌注CGRP,或以高达10微摩尔的浓度灌注PGE1,通过灌注液中静脉注射的125I - 白蛋白积累量测量,并未增加血浆渗入滑膜腔的量。4. 与用台氏液灌注的同一动物的对侧关节相比,缓激肽(0.1微摩尔)、5 - 羟色胺(1微摩尔)和组胺(0.1毫摩尔)的输注显著增加血浆渗入膝关节的量。5. 即使给予能产生全身效应(如明显血浆渗入其他组织)的剂量,向膝关节灌注P物质也不会特异性诱导125I标记的白蛋白在滑膜腔积累。6. 组胺(0.1毫摩尔)诱导的血浆渗出增加可通过与CGRP(0.1微摩尔)和PGE1(3微摩尔)共同输注而增强。然而,与组胺(0.1毫摩尔)诱导相似血浆渗出的次最大剂量(0.1微摩尔)缓激肽的反应,不会因与CGRP或PGE1共同输注而增加。7. 这些结果表明,CGRP是大鼠膝关节中的一种强效血管舒张剂。感觉神经释放的CGRP可能与血管通透性增加的介质协同作用,以改变该部位的炎症反应。

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引用本文的文献

本文引用的文献

1
Intraneuronal substance P contributes to the severity of experimental arthritis.
Science. 1984 Nov 2;226(4674):547-9. doi: 10.1126/science.6208609.
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Calcitonin gene-related peptide is a potent vasodilator.
Nature. 1985;313(5997):54-6. doi: 10.1038/313054a0.
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Capsaicin suppresses substance P-induced joint inflammation in the rat.
Neurosci Lett. 1989 Oct 23;105(1-2):155-8. doi: 10.1016/0304-3940(89)90028-1.
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Peptide neuroanatomy of adjuvant-induced arthritic inflammation in rat.
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Substance P activation of rheumatoid synoviocytes: neural pathway in pathogenesis of arthritis.
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