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本文引用的文献

1
Role of peptidases and NK1 receptors in vascular extravasation induced by bradykinin in rat nasal mucosa.肽酶和NK1受体在缓激肽诱导的大鼠鼻黏膜血管外渗中的作用
J Appl Physiol (1985). 1993 May;74(5):2456-61. doi: 10.1152/jappl.1993.74.5.2456.
2
NK2 receptors mediate plasma extravasation in guinea-pig lower airways.NK2受体介导豚鼠下呼吸道的血浆外渗。
Br J Pharmacol. 1993 Feb;108(2):383-6. doi: 10.1111/j.1476-5381.1993.tb12813.x.
3
A rapid capsaicin-activated current in rat trigeminal ganglion neurons.大鼠三叉神经节神经元中一种快速的辣椒素激活电流。
Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):738-41. doi: 10.1073/pnas.91.2.738.
4
Sensory neuropeptide release by bradykinin: mechanisms and pathophysiological implications.缓激肽引起的感觉神经肽释放:机制及病理生理学意义
Regul Pept. 1993 Aug 13;47(1):1-23. doi: 10.1016/0167-0115(93)90268-d.
5
Neuronal pathways to the rat conjunctiva revealed by retrograde tracing and immunocytochemistry.逆行追踪和免疫细胞化学揭示的大鼠结膜神经元通路
Exp Eye Res. 1994 Jan;58(1):117-26. doi: 10.1006/exer.1994.1201.
6
Characterization of the capsaicin-sensitive component of cyclophosphamide-induced inflammation in the rat urinary bladder.环磷酰胺诱导的大鼠膀胱炎症中辣椒素敏感成分的特征分析。
Br J Pharmacol. 1994 Apr;111(4):1017-22. doi: 10.1111/j.1476-5381.1994.tb14845.x.
7
Blockade by oral or parenteral RPR 100893 (a non-peptide NK1 receptor antagonist) of neurogenic plasma protein extravasation within guinea-pig dura mater and conjunctiva.口服或肠胃外给予RPR 100893(一种非肽类NK1受体拮抗剂)对豚鼠硬脑膜和结膜内神经源性血浆蛋白外渗的阻断作用。
Br J Pharmacol. 1994 Jul;112(3):920-4. doi: 10.1111/j.1476-5381.1994.tb13168.x.
8
Pharmacology of CP-99,994; a nonpeptide antagonist of the tachykinin neurokinin-1 receptor.CP-99,994的药理学;速激肽神经激肽-1受体的非肽类拮抗剂
J Pharmacol Exp Ther. 1993 Oct;267(1):472-9.
9
Role of kinins in the vascular extravasation evoked by antigen and mediated by tachykinins in guinea pig trachea.激肽在豚鼠气管中由抗原诱发并由速激肽介导的血管外渗中的作用。
J Immunol. 1993 Nov 1;151(9):4902-7.
10
Tachykinins and kinins in antigen-evoked plasma extravasation in guinea-pig nasal mucosa.速激肽和激肽在豚鼠鼻黏膜抗原诱发的血浆外渗中的作用
Eur J Pharmacol. 1994 Aug 11;261(1-2):127-32. doi: 10.1016/0014-2999(94)90310-7.

速激肽在豚鼠结膜中由缓激肽和低pH介质诱导的血浆外渗中的作用。

Involvement of tachykinins in plasma extravasation induced by bradykinin and low pH medium in the guinea-pig conjunctiva.

作者信息

Figini M, Javdan P, Cioncolini F, Geppetti P

机构信息

Institute of Internal Medicine and Therapeutics IV, University of Florence, Italy.

出版信息

Br J Pharmacol. 1995 May;115(1):128-32. doi: 10.1111/j.1476-5381.1995.tb16329.x.

DOI:10.1111/j.1476-5381.1995.tb16329.x
PMID:7544195
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1908761/
Abstract
  1. The effect of bradykinin, capsaicin, substance P and low pH medium on plasma extravasation in the guinea-pig conjunctiva has been studied. Evans blue dye was measured in the conjunctiva after local instillation of the agents into the conjunctival sac. 2. Bradykinin (2-50 nmol), capsaicin (20-50 nmol) and substance P (0.5-5 nmol) caused a dose-dependent increase in plasma extravasation with the following order of potency: substance P > bradykinin = capsaicin. The effect of capsaicin (50 nmol) and substance P (5 nmol) was abolished by the tachykinin NK1 receptor antagonist, CP-99,994 (8 mumol kg-1, i.v.) (P < 0.01), whereas CP-100,263 (8 mumol kg-1, i.v.) the inactive enantiomer of CP-99,994 was without effect. CP-99,994 inhibited by 70% (P < 0.01) the effect of bradykinin. 3. The kinin B2 receptor antagonist, Hoe 140 (icatibant, 10 nmol kg-1, i.v.) abolished the response to bradykinin (50 nmol) (P < 0.01), but did not affect the responses to capsaicin (50 nmol) or substance P (5 nmol). Plasma extravasation induced by low pH medium (pH 1) was abolished by CP-99,994 (P < 0.01) and by Hoe 140 (P < 0.01). 4. The present findings suggest that: endogenous or exogenous tachykinins increase plasma extravasation in the guinea-pig conjunctiva by activation of NK1 receptors; bradykinin-induced plasma extravasation is mediated by tachykinin release from sensory nerve endings; low pH media cause plasma extravasation via release of kinins that by activation of B2 receptors release tachykinins from sensory nerve endings.
摘要
  1. 研究了缓激肽、辣椒素、P物质和低pH培养基对豚鼠结膜血浆外渗的影响。将这些试剂局部滴入结膜囊后,测定结膜中的伊文思蓝染料含量。2. 缓激肽(2 - 50 nmol)、辣椒素(20 - 50 nmol)和P物质(0.5 - 5 nmol)引起血浆外渗呈剂量依赖性增加,效力顺序如下:P物质>缓激肽 = 辣椒素。速激肽NK1受体拮抗剂CP - 99,994(8 μmol kg-1,静脉注射)可消除辣椒素(50 nmol)和P物质(5 nmol)的作用(P < 0.01),而CP - 99,994的无活性对映体CP - 100,263(8 μmol kg-1,静脉注射)则无作用。CP - 99,994可抑制缓激肽作用的70%(P < 0.01)。3. 缓激肽B2受体拮抗剂Hoe 140(艾替班特,10 nmol kg-1,静脉注射)可消除对缓激肽(50 nmol)的反应(P < 0.01),但不影响对辣椒素(50 nmol)或P物质(5 nmol)的反应。低pH培养基(pH 1)诱导的血浆外渗可被CP - 99,994(P < 0.01)和Hoe 140(P < 0.01)消除。4. 目前的研究结果表明:内源性或外源性速激肽通过激活NK1受体增加豚鼠结膜的血浆外渗;缓激肽诱导的血浆外渗由感觉神经末梢释放速激肽介导;低pH培养基通过释放缓激肽导致血浆外渗,缓激肽通过激活B2受体从感觉神经末梢释放速激肽。