Laboratory of Pharmacology, Department of Drug Sciences, Faculty of Pharmacy of the University of Porto (FFUP), Porto, Portugal.
LAQV@REQUIMTE, University of Porto, Porto, Portugal.
Neurogastroenterol Motil. 2023 Sep;35(9):e14598. doi: 10.1111/nmo.14598. Epub 2023 Apr 13.
Angiotensin-converting enzyme (ACE) and ACE2 are two major enzymes of the renin-angiotensin-aldosterone system (RAAS), which control the formation/degradation of angiotensin (Ang) II and Ang1-7, regulating their opposite effects. We aimed at evaluating the catalytic activity of ACE and ACE2 in the intestinal content and corresponding intestinal tissue along the gut of Wistar Han rats.
Portions of the ileum, cecum, proximal colon, and distal colon, and the corresponding intestinal content were collected from Wistar Han rats. Enzyme activity was evaluated by fluorometric assays using different substrates: Hippuryl-His-Leu for ACE-C-domain, Z-Phe-His-Leu for ACE-N-domain, and Mca-APK(Dnp) for ACE2. ACE and ACE2 concentration was assessed by ELISA. Ratios concerning concentrations and activities were calculated to evaluate the balance of the RAAS. Statistical analysis was performed using Friedman test followed by Dunn's multiple comparisons test or Wilcoxon matched-pairs test whenever needed.
ACE and ACE2 are catalytically active in the intestinal content along the rat gut. The ACE N-domain shows higher activity than the C-domain both in the intestinal content and in the intestinal tissue. ACE and ACE2 are globally more active in the intestinal content than in the corresponding intestinal tissue. There was a distal-to-proximal prevalence of ACE2 over ACE in the intestinal tissue.
CONCLUSIONS & INFERENCES: This work is the first to report the presence of catalytically active ACE and ACE2 in the rat intestinal content, supporting future research on the regulatory role of the intestinal RAAS on gut function and a putative link to the microbiome.
血管紧张素转换酶 (ACE) 和 ACE2 是肾素-血管紧张素-醛固酮系统 (RAAS) 的两个主要酶,控制血管紧张素 (Ang) II 和 Ang1-7 的形成/降解,调节它们的相反作用。我们旨在评估 Wistar Han 大鼠肠道的肠内容物和相应肠组织中 ACE 和 ACE2 的催化活性。
从 Wistar Han 大鼠中收集回肠、盲肠、近端结肠和远端结肠的部分以及相应的肠内容物。使用不同的底物通过荧光测定法评估酶活性:Hippuryl-His-Leu 用于 ACE-C 结构域,Z-Phe-His-Leu 用于 ACE-N 结构域,Mca-APK(Dnp) 用于 ACE2。通过 ELISA 评估 ACE 和 ACE2 的浓度。计算浓度和活性的比值,以评估 RAAS 的平衡。使用 Friedman 检验 followed by Dunn's multiple comparisons test 或 Wilcoxon matched-pairs test 进行统计分析,具体取决于需要。
ACE 和 ACE2 在大鼠肠道的肠内容物中具有催化活性。ACE-N 结构域在肠内容物和肠组织中的活性均高于 C 结构域。ACE 和 ACE2 在肠内容物中的活性总体上高于相应的肠组织。在肠组织中,ACE2 的活性从远端到近端超过 ACE。
这项工作首次报道了具有催化活性的 ACE 和 ACE2 存在于大鼠肠内容物中,支持了关于肠道 RAAS 对肠道功能的调节作用及其与微生物组之间可能存在联系的进一步研究。