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用抗P物质抗体进行被动免疫可预防P物质和神经激肽A在麻醉豚鼠中诱导的支气管痉挛。

Passive immunization with an anti-substance P antibody prevents substance P- and neurokinin A-induced bronchospasm in anesthetized guinea-pigs.

作者信息

Jafarian A, Suresh M R, Kreutz F T, Biggs D F

机构信息

Faculty of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, Canada.

出版信息

Life Sci. 1995;57(2):143-53. doi: 10.1016/0024-3205(95)00255-5.

Abstract

In a guinea-pig model of asthma, active immunization against substance P (SP) prevented the development of airways' hyperresponsiveness and reduced bronchospastic responses to SP (i.v.). The rat-mouse heterohybridoma NC1/34 secretes a specific, rat IgG1, anti-substance P antibody (alpha-SP Ab) which was isolated and purified by passing supernatant from cultures through thiophilic gel. Purity of antibody was about 50% (SDS-PAGE). The relative affinities of the alpha-SP Ab for SP, neurokinin A (NKA) and calcitonin gene-related peptide (CGRP) were estimated by ELISA using a constant amount of SP coupled (glutaraldehyde) to bovine serum albumin (BSA) to capture the antibody, alone and in the presence of increasing concentrations of the neuropeptides. At alpha-SP Ab dilutions of 1 in 5,000 to 1 in 32,000, CGRP did not prevent antibody binding to SP-BSA conjugate bound to the plates, but both SP and NKA prevented binding. In this system, the relative affinity of the alpha-SP Ab, at dilutions of 1 in 5,000 and 1 in 10,000, was about 50 times greater for SP than NKA. Whether passive immunization with alpha-SP Ab prevented bronchospastic responses to SP and NKA (i.v.), in vivo, was determined in groups of anesthetized guinea-pigs by recording pulmonary flow resistance (RL) and dynamic pulmonary elastance (EL). Injection of alpha-SP Ab (i.v., 5:1 molar ratio: alpha-SP Ab:SP total dose) did not alter baseline values of RL and EL, but markedly inhibited increases in RL and EL induced by SP and NKA (i.v.) without affecting responses to methacholine (i.v.). A control, "irrelevant" rat IgG-type antibody at a similar concentration had no effect on responses to SP or NKA. These findings indicate that passive immunization with a monoclonal alpha-SP Ab can prevent the bronchospastic effects of exogenous SP and NKA in guinea-pigs.

摘要

在豚鼠哮喘模型中,针对P物质(SP)进行主动免疫可预防气道高反应性的发展,并降低对静脉注射SP的支气管痉挛反应。大鼠-小鼠异种杂交瘤NC1/34分泌一种特异性的大鼠IgG1抗P物质抗体(α-SP Ab),该抗体通过使培养上清液通过嗜硫凝胶进行分离和纯化。抗体纯度约为50%(SDS-PAGE)。使用固定量的通过戊二醛偶联至牛血清白蛋白(BSA)的SP来捕获抗体,单独以及在存在递增浓度神经肽的情况下,通过ELISA估计α-SP Ab对SP、神经激肽A(NKA)和降钙素基因相关肽(CGRP)的相对亲和力。在α-SP Ab稀释度为1:5000至1:32000时,CGRP不会阻止抗体与结合在平板上的SP-BSA偶联物结合,但SP和NKA均可阻止结合。在该系统中,在稀释度为1:5000和1:10000时,α-SP Ab对SP的相对亲和力比对NKA大50倍左右。通过记录肺血流阻力(RL)和动态肺弹性(EL),在麻醉的豚鼠组中确定α-SP Ab被动免疫是否能在体内预防对静脉注射SP和NKA的支气管痉挛反应。静脉注射α-SP Ab(摩尔比5:1:α-SP Ab:SP总剂量)不会改变RL和EL的基线值,但能显著抑制静脉注射SP和NKA诱导的RL和EL增加,而不影响对静脉注射乙酰甲胆碱的反应。类似浓度的对照“无关”大鼠IgG型抗体对SP或NKA的反应没有影响。这些发现表明,用单克隆α-SP Ab进行被动免疫可预防豚鼠中外源性SP和NKA的支气管痉挛作用。

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