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天然存在的神经肽相互作用对大鼠膝关节血流的影响。

Effects of interactions of naturally-occurring neuropeptides on blood flow in the rat knee joint.

作者信息

Lam F Y, Ferrell W R

机构信息

Institute of Physiology, University of Glasgow.

出版信息

Br J Pharmacol. 1993 Mar;108(3):694-9. doi: 10.1111/j.1476-5381.1993.tb12863.x.

Abstract
  1. Changes of blood flow in the rat knee joint, measured by laser Doppler flowmetry, were produced by topical application of naturally-occurring neuropeptides to the joint capsule. 2. Substance P (SP), neurokinin A (NKA), and neurokinin B (NKB) all produced dose-dependent transient vasodilatation of the rat knee joint microvasculature. NKB showed significantly smaller vasodilator responses compared to SP and NKA which were similar in their potencies. 3. Calcitonin gene-related peptide (CGRP) produced dose-dependent vasodilatation which was more pronounced than that produced by the neurokinins. The rank order of potency was: CGRP > SP = NKA > NKB. The vasodilator effect of CGRP was also more prolonged and this extended phase was abolished by co-administration of SP. 4. Cross-tachyphylaxis was not observed with the different neurokinins, but SP and NKA showed novel antagonistic effects on NKB-induced vasodilatation. 5. Co-administration of 1 nmol of the specific NK1 receptor antagonist, CP-96345, with 1 nmol of each of the neurokinins produced significant inhibition of the vasodilator response to SP but did not affect vasodilator responses to NKA and NKB. Co-administration of CP-96345 with the neurokinins plus superfusion of the rat knee joint with a solution containing 0.1 mM CP-96345 further reduced the vasodilator responses to SP but again the vasodilator responses to NKA and NKB were not significantly altered. 6. The results suggest that multiple neurokinin receptor types may be present in the rat knee joint which could mediate the vasodilator responses of the different neurokinins. Co-release of neuropeptides from sensory nerve endings in the rat knee joint may have inter-regulatory actions on their individual responses on the microvasculature.
摘要
  1. 通过激光多普勒血流仪测量,向大鼠膝关节囊局部应用天然存在的神经肽可引起大鼠膝关节血流变化。2. P物质(SP)、神经激肽A(NKA)和神经激肽B(NKB)均可引起大鼠膝关节微血管剂量依赖性的短暂血管舒张。与SP和NKA相比,NKB的血管舒张反应明显较小,而SP和NKA的效力相似。3. 降钙素基因相关肽(CGRP)产生剂量依赖性血管舒张,比神经激肽产生的血管舒张更明显。效力顺序为:CGRP>SP = NKA>NKB。CGRP的血管舒张作用也更持久,且该延长阶段可通过同时给予SP而消除。4. 不同神经激肽之间未观察到交叉快速耐受性,但SP和NKA对NKB诱导的血管舒张表现出新型拮抗作用。5. 将1 nmol特异性NK1受体拮抗剂CP-96345与1 nmol每种神经激肽共同给药,可显著抑制对SP的血管舒张反应,但不影响对NKA和NKB的血管舒张反应。将CP-96345与神经激肽共同给药,并向大鼠膝关节灌注含0.1 mM CP-96345 的溶液,可进一步降低对SP的血管舒张反应,但对NKA和NKB的血管舒张反应同样未产生显著改变。6. 结果表明,大鼠膝关节中可能存在多种神经激肽受体类型,它们可介导不同神经激肽的血管舒张反应。大鼠膝关节感觉神经末梢神经肽的共同释放可能对它们在微脉管系统上的个体反应具有相互调节作用。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/689e/1908032/607a680a4a78/brjpharm00209-0131-a.jpg

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