ACE and ACE2 catalytic activity in the fecal content along the gut

Author:

Ferreira‐Duarte Mariana12ORCID,Oliveira Lilian Caroline Gonçalves3ORCID,Quintas Clara1ORCID,Esteves‐Monteiro Marisa124ORCID,Duarte‐Araújo Margarida24ORCID,Sousa Teresa5ORCID,Casarini Dulce Elena3ORCID,Morato Manuela12ORCID

Affiliation:

1. Laboratory of Pharmacology, Department of Drug Sciences Faculty of Pharmacy of the University of Porto (FFUP) Porto Portugal

2. LAQV@REQUIMTE University of Porto Porto Portugal

3. Department of Medicine, Discipline Nephrology Universidade Federal de São Paulo (UNIFESP/EPM) São Paulo Brazil

4. Department of Immuno‐Physiology and Pharmacology, School of Medicine and Biomedical Sciences (ICBAS) University of Porto Porto Portugal

5. Department of Biomedicine‐Unit of Pharmacology and Therapeutics, Faculty of Medicine University of Porto (FMUP), Porto, Portugal, & Centro de Investigação Farmacológica e Inovação Medicamentosa, University of Porto (MedInUP) Porto Portugal

Abstract

AbstractBackgroundAngiotensin‐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.MethodsPortions 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.Key ResultsACE 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 & InferencesThis 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.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Fundação para a Ciência e a Tecnologia

Publisher

Wiley

Subject

Gastroenterology,Endocrine and Autonomic Systems,Physiology

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