Pattern of Mas expression in acute and post-acute stage of nerve injury in mice

•Mas receptor is differentially expressed in acute and post-acute phase after axotomy.•Antagonist of the Mas receptor (A779) causes worse result in sciatic functional test.•A779 affects the Schwann cell activity and the number of macrophages after axotomy. Angiotensin-(1–7) (Ang [1–7]) and its recep...

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Veröffentlicht in:Peptides (New York, N.Y. : 1980) N.Y. : 1980), 2017-10, Vol.96, p.15-19
Hauptverfasser: Assis, Alex Dias, de Assis Araújo, Fernanda, dos Santos, Robson Augusto Souza, Andrade, Silvia Passos, Zanon, Renata Graciele
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container_title Peptides (New York, N.Y. : 1980)
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creator Assis, Alex Dias
de Assis Araújo, Fernanda
dos Santos, Robson Augusto Souza
Andrade, Silvia Passos
Zanon, Renata Graciele
description •Mas receptor is differentially expressed in acute and post-acute phase after axotomy.•Antagonist of the Mas receptor (A779) causes worse result in sciatic functional test.•A779 affects the Schwann cell activity and the number of macrophages after axotomy. Angiotensin-(1–7) (Ang [1–7]) and its receptor Mas are involved in a number of physiological processes, including control of arterial pressure and modulation of nervous system actions. However, the involvement of the Ang-(1–7)/Mas axis in peripheral nerve injury has not been investigated. Using a model of sciatic nerve injury in mice, we demonstrated opposing changes in Mas receptor expression at days 2 and 14 post-injury. Mas receptor expression was more intense 2days after the nerve lesion, compared with the intensity of the intact nerve. At this time point, the sciatic nerve functional index was −20. At day 14 after the lesion, the intensity of the immunostaining labeling in longitudinal sections of the nerve was reduced (∼30%) and the functional index increased +36 (gait improvement). In the axotomized group treated with A779 (a Mas receptor antagonist), the functional recovery index decreased in relation to the untreated axotomized group. The Mas receptor inhibitor also altered the intensity of labeling of S-100, GAP43, and IBA-1 (morphological features compatible with delayed axon growth). This study demonstrated that Ang-(1–7)/Mas axis activity was differentially modulated in the acute and post-acute stages of nerve injury.
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Angiotensin-(1–7) (Ang [1–7]) and its receptor Mas are involved in a number of physiological processes, including control of arterial pressure and modulation of nervous system actions. However, the involvement of the Ang-(1–7)/Mas axis in peripheral nerve injury has not been investigated. Using a model of sciatic nerve injury in mice, we demonstrated opposing changes in Mas receptor expression at days 2 and 14 post-injury. Mas receptor expression was more intense 2days after the nerve lesion, compared with the intensity of the intact nerve. At this time point, the sciatic nerve functional index was −20. At day 14 after the lesion, the intensity of the immunostaining labeling in longitudinal sections of the nerve was reduced (∼30%) and the functional index increased +36 (gait improvement). In the axotomized group treated with A779 (a Mas receptor antagonist), the functional recovery index decreased in relation to the untreated axotomized group. The Mas receptor inhibitor also altered the intensity of labeling of S-100, GAP43, and IBA-1 (morphological features compatible with delayed axon growth). 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Angiotensin-(1–7) (Ang [1–7]) and its receptor Mas are involved in a number of physiological processes, including control of arterial pressure and modulation of nervous system actions. However, the involvement of the Ang-(1–7)/Mas axis in peripheral nerve injury has not been investigated. Using a model of sciatic nerve injury in mice, we demonstrated opposing changes in Mas receptor expression at days 2 and 14 post-injury. Mas receptor expression was more intense 2days after the nerve lesion, compared with the intensity of the intact nerve. At this time point, the sciatic nerve functional index was −20. At day 14 after the lesion, the intensity of the immunostaining labeling in longitudinal sections of the nerve was reduced (∼30%) and the functional index increased +36 (gait improvement). In the axotomized group treated with A779 (a Mas receptor antagonist), the functional recovery index decreased in relation to the untreated axotomized group. The Mas receptor inhibitor also altered the intensity of labeling of S-100, GAP43, and IBA-1 (morphological features compatible with delayed axon growth). This study demonstrated that Ang-(1–7)/Mas axis activity was differentially modulated in the acute and post-acute stages of nerve injury.</description><subject>Angiotensin II - analogs &amp; derivatives</subject><subject>Angiotensin II - pharmacology</subject><subject>Animals</subject><subject>Axon repair</subject><subject>Axotomy</subject><subject>GAP-43 Protein - metabolism</subject><subject>Male</subject><subject>Mas receptor</subject><subject>Mice</subject><subject>Peptide Fragments - pharmacology</subject><subject>Peripheral nerve</subject><subject>Peripheral Nerves - drug effects</subject><subject>Peripheral Nerves - metabolism</subject><subject>Peripheral Nerves - pathology</subject><subject>Proto-Oncogene Proteins - antagonists &amp; inhibitors</subject><subject>Proto-Oncogene Proteins - metabolism</subject><subject>Receptors, G-Protein-Coupled - antagonists &amp; inhibitors</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>S100 Proteins - metabolism</subject><subject>Sciatic Neuropathy - metabolism</subject><issn>0196-9781</issn><issn>1873-5169</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOwzAQRS0EoqXwC1WWbBL8SBxnB6p4SUVlAWvLsSfIUZsE26no35MoLVtWo5HOnas5CC0JTggm_K5OOuiCNeATikmeYJFgLM7QnIicxRnhxTmaY1LwuMgFmaEr72uMcZoW4hLNqBA5zgsxR5t3FQK4Jmqr6E35CH46B97btolsEyndB4hUY6Ku9SGeVh_UF4x8A24PA1b37jDSO6vhGl1Uauvh5jgX6PPp8WP1Eq83z6-rh3WsGRchNilXXAMxqqyoYCXRFS0NqXDGlBKa5SZTFAAU5QXFJTYqr1gKBkCwlArOFuh2utu59rsHH-TOeg3brWqg7b0kBcsEIWlKBpRPqHat9w4q2Tm7U-4gCZajTFnLk0w5ypRYyEHmEFweO_pyB-YvdrI3APcTAMOnewtOem2h0WCsAx2kae1_Hb8nnYph</recordid><startdate>201710</startdate><enddate>201710</enddate><creator>Assis, Alex Dias</creator><creator>de Assis Araújo, Fernanda</creator><creator>dos Santos, Robson Augusto Souza</creator><creator>Andrade, Silvia Passos</creator><creator>Zanon, Renata Graciele</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201710</creationdate><title>Pattern of Mas expression in acute and post-acute stage of nerve injury in mice</title><author>Assis, Alex Dias ; 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inhibitors</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>S100 Proteins - metabolism</topic><topic>Sciatic Neuropathy - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Assis, Alex Dias</creatorcontrib><creatorcontrib>de Assis Araújo, Fernanda</creatorcontrib><creatorcontrib>dos Santos, Robson Augusto Souza</creatorcontrib><creatorcontrib>Andrade, Silvia Passos</creatorcontrib><creatorcontrib>Zanon, Renata Graciele</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Peptides (New York, N.Y. : 1980)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Assis, Alex Dias</au><au>de Assis Araújo, Fernanda</au><au>dos Santos, Robson Augusto Souza</au><au>Andrade, Silvia Passos</au><au>Zanon, Renata Graciele</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pattern of Mas expression in acute and post-acute stage of nerve injury in mice</atitle><jtitle>Peptides (New York, N.Y. : 1980)</jtitle><addtitle>Peptides</addtitle><date>2017-10</date><risdate>2017</risdate><volume>96</volume><spage>15</spage><epage>19</epage><pages>15-19</pages><issn>0196-9781</issn><eissn>1873-5169</eissn><abstract>•Mas receptor is differentially expressed in acute and post-acute phase after axotomy.•Antagonist of the Mas receptor (A779) causes worse result in sciatic functional test.•A779 affects the Schwann cell activity and the number of macrophages after axotomy. 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subjects Angiotensin II - analogs & derivatives
Angiotensin II - pharmacology
Animals
Axon repair
Axotomy
GAP-43 Protein - metabolism
Male
Mas receptor
Mice
Peptide Fragments - pharmacology
Peripheral nerve
Peripheral Nerves - drug effects
Peripheral Nerves - metabolism
Peripheral Nerves - pathology
Proto-Oncogene Proteins - antagonists & inhibitors
Proto-Oncogene Proteins - metabolism
Receptors, G-Protein-Coupled - antagonists & inhibitors
Receptors, G-Protein-Coupled - metabolism
S100 Proteins - metabolism
Sciatic Neuropathy - metabolism
title Pattern of Mas expression in acute and post-acute stage of nerve injury in mice
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