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依那普利增强体内抗卵清蛋白IgG2c的产生。

Enhancement of anti-OVA IgG2c production in vivo by enalapril.

作者信息

Almeida L C, Muraro L S, Albuquerque D A

机构信息

Departamento de Biomedicina, Centro Universitário Cândido Rondon, Cuiabá, MT, Brasil.

Departamento de Patologia Clínica e Parasitologia, Faculdade de Medicina Veterinária, Universidade de Cuiabá, Cuiabá, MT, Brasil.

出版信息

Braz J Med Biol Res. 2016 Jul 11;49(8). doi: 10.1590/1414-431X20165215.

Abstract

Angiotensin-converting enzyme (ACE) inhibitors have non-hemodynamic, pleiotropic effects on the immune response. The effects of ACE inhibitors on the production of cytokines and T-cell functions are well established. However, little is known on the effects of these medicines on humoral response to foreign antigens. In this study, we investigated the effect of enalapril treatment on ovalbumin (OVA)-specific IgG1 and IgG2c production in mice determined by ELISA. Two groups of 8-week-old C57BL/6 females mice (3-4/group) were subcutaneously immunized with OVA (10 μg/animal) in presence of Alhydrogel (1 mg/mouse) and boosted at day 21. The mice were treated with enalapril (5 mg/kg daily, po) or were left without treatment for one month. The animals were bled from the orbital plexus on days 0, 7, 14, 21, and 28 after the first immunization and the sera were stored at -20°C until usage. OVA-specific serum IgG1 and IgG2c were determined by ELISA using serum from each individual animal. The results showed that enalapril significantly increased anti-OVA serum IgG2c in the secondary response without affecting IgG1 synthesis. These data expand our understanding on the properties of enalapril on the immune response, including antibody production.

摘要

血管紧张素转换酶(ACE)抑制剂对免疫反应具有非血流动力学的多效性作用。ACE抑制剂对细胞因子产生和T细胞功能的影响已得到充分证实。然而,对于这些药物对外源抗原体液反应的影响却知之甚少。在本研究中,我们通过酶联免疫吸附测定(ELISA)研究了依那普利治疗对小鼠卵清蛋白(OVA)特异性IgG1和IgG2c产生的影响。将两组8周龄的C57BL/6雌性小鼠(每组3 - 4只)在氢氧化铝佐剂(1毫克/小鼠)存在的情况下皮下注射OVA(10微克/只动物),并在第21天进行加强免疫。小鼠接受依那普利治疗(每日5毫克/千克,口服)或不接受治疗持续1个月。在首次免疫后的第0、7、14、21和28天从眼眶丛采血,血清储存在-20°C直至使用。使用每只动物的血清通过ELISA测定OVA特异性血清IgG1和IgG2c。结果显示,依那普利在二次反应中显著增加了抗OVA血清IgG2c,而不影响IgG1的合成。这些数据扩展了我们对依那普利在免疫反应(包括抗体产生)方面特性的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/141e/4954734/bdd3e1111fdb/1414-431X-bjmbr-1414-431X20165215-gf001.jpg

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