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金属肽酶和激肽受体在猪口咽组织中的表达:血管紧张素I转换酶抑制和炎症的影响。

Expression of metallopeptidases and kinin receptors in swine oropharyngeal tissues: effects of angiotensin I-converting enzyme inhibition and inflammation.

作者信息

Moreau Marie Eve, Dubreuil Pascal, Molinaro Giuseppe, Chagnon Miguel, Müller-Esterl Werner, Lepage Yves, Marceau François, Adam Albert

机构信息

Université de Montréal, Faculté de Pharmacie, Room 3190, 2900 Blvd.Edouard-Montpetit, C.P. 6128, succ Centre-ville, Montréal, Québec H3C 3J7, Canada.

出版信息

J Pharmacol Exp Ther. 2005 Dec;315(3):1065-74. doi: 10.1124/jpet.105.088005. Epub 2005 Sep 15.

Abstract

Angiotensin I-converting enzyme inhibitors (ACEi) cause both chronic and acute side effects, including rare but potentially life-threatening angioedema (AE). The main hypothesis to be tested in this study was that metallopeptidases and kinin receptors are present in oropharyngeal tissues and that their expression is modulated by ACEi and inflammation. Novel real-time polymerase chain reaction analysis was developed and allowed the relative quantification of tissue's gene expression for neprilysin, membrane-bound aminopeptidase P (mAPP), and both B1 and B2 kinin receptor subtypes in tongue, parotid gland, and laryngeal tissue (areas especially involved in the gravest clinical forms of AE) and in kidney in a porcine model (single injection or 7-day ACEi oral treatments applied or lipopolysaccharide injected as a positive inflammatory control). The results provide evidence of the expression and activities of kininases in oropharyngeal tissues in the swine. ACEi treatment modulated the expression of neutral endopeptidase and mAPP mRNA, but the corresponding enzyme activities and that of angiotensin I-converting enzyme (ACE) were generally stable in tissues. The 7-day ACEi treatment up-regulated both kinin receptor mRNAs in the oropharynx and the B1 receptor mRNA in the lingual vascular endothelium (immunohistochemistry). The inhibition of ACE in plasma is responsible for an accumulation of bradykinin and des-arginine9-bradykinin generated during activation of the contact system with glass beads. The expression of critical components of the kallikrein-kinin system in the oropharyngeal tissues supports the role of kinins in ACEi-induced AE.

摘要

血管紧张素I转换酶抑制剂(ACEi)会引发慢性和急性副作用,包括罕见但可能危及生命的血管性水肿(AE)。本研究要检验的主要假设是,金属肽酶和激肽受体存在于口咽组织中,且它们的表达受ACEi和炎症调节。我们开发了新型实时聚合酶链反应分析方法,可对猪模型(单次注射或进行7天的ACEi口服治疗,或注射脂多糖作为阳性炎症对照)的舌头、腮腺、喉组织(尤其涉及最严重临床形式AE的区域)以及肾脏中的中性内肽酶、膜结合氨基肽酶P(mAPP)以及B1和B2激肽受体亚型进行组织基因表达的相对定量分析。结果提供了猪口咽组织中激肽酶表达和活性的证据。ACEi治疗调节了中性内肽酶和mAPP mRNA的表达,但相应的酶活性以及血管紧张素I转换酶(ACE)的活性在组织中通常是稳定的。7天的ACEi治疗上调了口咽中两种激肽受体mRNA以及舌血管内皮中B1受体mRNA的表达(免疫组织化学)。血浆中ACE的抑制导致在用玻璃珠激活接触系统过程中产生的缓激肽和去精氨酸9 - 缓激肽积累。口咽组织中激肽释放酶 - 激肽系统关键成分的表达支持了激肽在ACEi诱导的AE中的作用。

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