Papel dos nervos renais no diabetes mellitus experimental

Bibliographic Details
Main Author: Oliveira, Tales Lyra de [UNIFESP]
Publication Date: 2018
Format: Doctoral thesis
Language: por
Source: Repositório Institucional da UNIFESP
Download full: https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6979670
https://repositorio.unifesp.br/handle/11600/52229
Summary: Introduction: Diabetes mellitus (DM) promotes increased renal sympathetic nerve activity (rSNA), autonomic imbalance, cardiovascular, metabolic and renal dysfunction. Apparently, the rSNA increases is directly associated with development and maintenance of neuropathy diabetic and autonomic nephropathy condition. Recently, there has been an important interest in clinical and experimental studies about bilateral renal denervation (BRD) procedure as a therapeutic alternative in some diseases related with renal sympathoexcitation. Aims: Protocol CEUA – UNIFESP 1787250714. Therefore, the present study evaluated the role of renal nerves on the autonomic, cardiovascular, metabolic and renal balance in the streptozotocindiabetic animal model. Methods: 8weekold Wistar rats were separated into three experimental groups: control (CTR), diabetic (DM) and denervated diabetic (DM BRD), with n=68 animals per group. DM was induced by one dose of streptozotocin (STZ; 60 mg/kg, ip) 4 weeks prior to the final experiments while the surgical BRD was performed 2 weeks before final experiments. The results were expressed as mean ± SEM and were compared by analysis of variance (ANOVA), P<0.05 was considered as the significance level. Results: DM was confirmed by body weight reduction (CTR: 351.5 ± 4.1, DM: 242.1 ± 6.7 g) and glycemia increases (CTR: 100.3 ± 3.7, DM: 509.1 ± 14.4 mg/dL). BRD significantly reduced glycemia (410.5 ± 5.8 mg/dL) and increased body weight (302.4 ± 5.7 g) in diabetic animals. DM promoted impairment of renal function such as glycosuria and albuminuria (CTR: 0,01 ± 0,001 and 0,08 ± 0,008, DM: 2.7 ± 0.19 and 0,39 ± 0,04 g/kg/24h), however BRD significantly attenuated these parameters (1,3 ± 0,19 and 0,13 ± 0,04 g/kg/24h). The heart rate (HR) was decreased in the DM animals (CTR: 352 ± 13, DM: 292 ± 11 bpm), associated with reduction of arterial baroreceptor reflex sensitivity to HR control (bradycardic response: CTR: 2.17 ± 0.06, DM: 1.92 ± 0.04 bpm/mmHg and tachycardic response: CTR: 2.55 ± 0.04, DM: 2.09 ± 0.03 bpm/mmHg). Interestingly, BRD was able to normalized HR (372 ± 23 bpm) and improved baroreflex sensitivity to the HR control (bradycardic response: 2.09 ± 0.14 and tachycardic response: 3.13 ± 0.05 bpm/mmHg) in the DM model. The rSNA was significantly increased (CTR: 82.6 ± 3.93, DM: 124.8 ± 6.45 pps), while splanchnic SNA (sSNA) was decreased in the diabetic animals (CTR: 120.5 ± 4.76, DM: 72.3 ± 5.70 pps), however BRD normalized sSNA (100.0 ± 9.23 pps) in the diabetic animals. The Na+/glucose cotransporter 2 (SGLT2) gene expression and tumor necrosis factor (TNFα) concentration were increased in the kidneys of DM group (CTR: 1.00 ± 0.24 and 233.3 ± 17.54, DM: 12.33 ± 1.25 normalized HPRT1 and 244.1 ± 12.19 pg/mL), meanwhile BRD was able to normalize (1.53 ± 0.85 normalized HPRT1 and 190.9 ± 7.53 pg/mL) these parameters.. Acutely, insulin microinjection in the rostoventrolateral medulla area (RVLM) increased mean arterial pressure (MAP; CTR: 8.7 ± 2.26, DM: 23.9 ± 19.27, DM BRD: 12.8 ± 4.25 %) and sSNA (CTR: 14.2 ± 3.50, DM: 21.2 ± 9.41, DM BRD: 17.5 ± 3.80%) only in DM groups, however, the rSNA was increased in all groups evaluated (CTR: 25.7 ± 4.62, DM: 20.6 ± 3.33%), compared to baseline means. Conclusion: Taken together, our results suggest that the renal nerves have an important role in the autonomic balance, cardiovascular, metabolic and renal function in the DM model. Furthermore, the reduction of renal SGLT2 and TNFα appears to be mechanisms involved in the improvement of these parameters (cardiovascular, autonomic, metabolic and renal) induced by BRD in the experimental DM. Cardiovascular changes in DM can be achieved by central or peripheral differential actions of insulin.
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spelling Papel dos nervos renais no diabetes mellitus experimentalRole of renal nerves in experimental diabetes mellitusSympathetic nerve activityInsulinSympathetic nervous systemRenin angiotensin aldosterone systemRenal denervationDiabetes MellitusAtividade nervosa simpáticaInsulinaSistema nervoso simpáticoSistema renina angiotensina aldosteronaDenervação renalIntroduction: Diabetes mellitus (DM) promotes increased renal sympathetic nerve activity (rSNA), autonomic imbalance, cardiovascular, metabolic and renal dysfunction. Apparently, the rSNA increases is directly associated with development and maintenance of neuropathy diabetic and autonomic nephropathy condition. Recently, there has been an important interest in clinical and experimental studies about bilateral renal denervation (BRD) procedure as a therapeutic alternative in some diseases related with renal sympathoexcitation. Aims: Protocol CEUA – UNIFESP 1787250714. Therefore, the present study evaluated the role of renal nerves on the autonomic, cardiovascular, metabolic and renal balance in the streptozotocindiabetic animal model. Methods: 8weekold Wistar rats were separated into three experimental groups: control (CTR), diabetic (DM) and denervated diabetic (DM BRD), with n=68 animals per group. DM was induced by one dose of streptozotocin (STZ; 60 mg/kg, ip) 4 weeks prior to the final experiments while the surgical BRD was performed 2 weeks before final experiments. The results were expressed as mean ± SEM and were compared by analysis of variance (ANOVA), P<0.05 was considered as the significance level. Results: DM was confirmed by body weight reduction (CTR: 351.5 ± 4.1, DM: 242.1 ± 6.7 g) and glycemia increases (CTR: 100.3 ± 3.7, DM: 509.1 ± 14.4 mg/dL). BRD significantly reduced glycemia (410.5 ± 5.8 mg/dL) and increased body weight (302.4 ± 5.7 g) in diabetic animals. DM promoted impairment of renal function such as glycosuria and albuminuria (CTR: 0,01 ± 0,001 and 0,08 ± 0,008, DM: 2.7 ± 0.19 and 0,39 ± 0,04 g/kg/24h), however BRD significantly attenuated these parameters (1,3 ± 0,19 and 0,13 ± 0,04 g/kg/24h). The heart rate (HR) was decreased in the DM animals (CTR: 352 ± 13, DM: 292 ± 11 bpm), associated with reduction of arterial baroreceptor reflex sensitivity to HR control (bradycardic response: CTR: 2.17 ± 0.06, DM: 1.92 ± 0.04 bpm/mmHg and tachycardic response: CTR: 2.55 ± 0.04, DM: 2.09 ± 0.03 bpm/mmHg). Interestingly, BRD was able to normalized HR (372 ± 23 bpm) and improved baroreflex sensitivity to the HR control (bradycardic response: 2.09 ± 0.14 and tachycardic response: 3.13 ± 0.05 bpm/mmHg) in the DM model. The rSNA was significantly increased (CTR: 82.6 ± 3.93, DM: 124.8 ± 6.45 pps), while splanchnic SNA (sSNA) was decreased in the diabetic animals (CTR: 120.5 ± 4.76, DM: 72.3 ± 5.70 pps), however BRD normalized sSNA (100.0 ± 9.23 pps) in the diabetic animals. The Na+/glucose cotransporter 2 (SGLT2) gene expression and tumor necrosis factor (TNFα) concentration were increased in the kidneys of DM group (CTR: 1.00 ± 0.24 and 233.3 ± 17.54, DM: 12.33 ± 1.25 normalized HPRT1 and 244.1 ± 12.19 pg/mL), meanwhile BRD was able to normalize (1.53 ± 0.85 normalized HPRT1 and 190.9 ± 7.53 pg/mL) these parameters.. Acutely, insulin microinjection in the rostoventrolateral medulla area (RVLM) increased mean arterial pressure (MAP; CTR: 8.7 ± 2.26, DM: 23.9 ± 19.27, DM BRD: 12.8 ± 4.25 %) and sSNA (CTR: 14.2 ± 3.50, DM: 21.2 ± 9.41, DM BRD: 17.5 ± 3.80%) only in DM groups, however, the rSNA was increased in all groups evaluated (CTR: 25.7 ± 4.62, DM: 20.6 ± 3.33%), compared to baseline means. Conclusion: Taken together, our results suggest that the renal nerves have an important role in the autonomic balance, cardiovascular, metabolic and renal function in the DM model. Furthermore, the reduction of renal SGLT2 and TNFα appears to be mechanisms involved in the improvement of these parameters (cardiovascular, autonomic, metabolic and renal) induced by BRD in the experimental DM. Cardiovascular changes in DM can be achieved by central or peripheral differential actions of insulin.Introdução: O diabetes mellitus (DM) promove aumento da atividade nervosa simpática renal (ANSr), desbalanço autonômico, disfunção cardiovascular, metabólica e renal. O aumento da ANSr parece ter estreita relação com a instalação e manutenção da condição de nefropatia diabética e de neuropatia autonômica. Recentemente, a denervação renal bilateral (BRD) tem sido utilizada como alternativa terapêutica em patologias que cursam com hiperatividade nervosa simpática renal. Objetivos: A partir destas informações, a presente tese buscou avaliar o papel dos nervos renais sobre o balanço autonômico, cardiovascular, metabólico e renal em animais diabéticos. Materiais e Métodos: Protocolo CEUA UNIFESP 1787250714. Para isto, foram utilizados ratos Wistar com 8 semanas de idade separados em três grupos experimentais independentes: controle (CTR), diabético (DM) e diabético submetido à denervação renal (DM BRD), sendo n=68 animais por grupo. O DM foi induzido por uma única dose de estreptozotocina (STZ; 60 mg/kg, ip) 4 semanas antes dos experimentos e a BRD cirúrgica foi realizada 2 semanas antes das avaliações. Os resultados foram expressos como média ± EPM e comparados por meio do teste de análise de variância (ANOVA), utilizando nível de significância de P<0,05. Resultados: O DM foi confirmado pela redução do peso corporal (CTR: 351,5 ± 4,1; DM: 242,1 ± 6,7 g) e pelo aumento da glicemia (CTR: 100,3 ± 3,7; DM: 509,1 ± 14,4 mg/dL). Por sua vez, a BRD reduziu significativamente a glicemia (410,5 ± 5,8 mg/dL) e aumentou o peso corporal (302,4 ± 5,7 g). O DM promoveu prejuízo da função renal gerando glicosuria e albuminuria (CTR: 0,01 ± 0,001 e 0,08 ± 0,008; DM: 2,7 ± 0,19 e 0,39 ± 0,04 g/kg/24h), mas a BRD atenuou significativamente esses indicadores de lesão renal (1,3 ± 0,19 e 0,13 ± 0,04 g/kg/24h). Houve redução da frequência cardíaca (FC) basal no grupo DM (CTR: 352 ± 13; DM: 292 ± 11bpm) associada a uma redução da sensibilidade do reflexo barorreceptor arterial (resposta bradicárdica: CTR: 2,17 ± 0,06; DM: 1,92 ± 0,04 bpm/mmHg e resposta taquicárdica: CTR: 2,55 ± 0,04; DM: 2,09 ± 0,03 bpm/mmHg), mas a BRD normalizou significativamente a FC (372 ± 23 bpm) e melhorou a sensibilidade do reflexo barorreceptor arterial (resposta bradicárdica: 2,09 ± 0,14 e resposta taquicárdica: 3,13 ± 0,05 bpm/mmHg). A ANSr foi significativamente aumentada (CTR: 82,6 ± 3,93; DM: 124,8 ± 6,45 pps), enquanto que a ANS esplâncnica (ANSe) foi reduzida no grupo DM (CTR: 120,5 ± 4,76; DM: 72,3 ± 5,70 pps) e, a BRD foi capaz de normalizar a ANSe (100,0 ± 9,23 pps). A expressão gênica do cotransportador de Na+/glicose 2 (SGLT2) e a concentração do fator de necrose tumoral alfa (TNFα) renais estiveram aumentados no DM (CTR: 1,00 ± 0,24 e 233,3 ± 17,54; DM: 12,33 ± 1,25 normalizado HPRT1 e 244,1 ± 12,19 pg/mL), porém, a BRD normalizou esses parâmetros (1,53 ± 0,85 normalizado HPRT1 e 190,9 ± 7,53 pg/mL). Agudamente, a microinjeção de insulina na região rostroventrolateral do bulbo (RVLM) promoveu aumento significante da PA (CTR: 8,7 ± 2,26; DM: 23,9 ± 19,27; DM BRD: 12,8 ± 4,25 %) e da ANSe (CTR: 14,2 ± 3,50; DM: 21,2 ± 9,41; DM BRD: 17,5 ± 3,80 %) apenas nos grupos DM, contudo, aumentou a ANSr em todos os grupos avaliados (CTR: 25,7 ± 4,62; DM: 20,6 ± 3,33 %), em comparação às medias basais. Conclusão: Em conjunto, os resultados demonstram que os nervos renais estão envolvidos de forma significante no balanço autonômico, na função cardiovascular, metabólica e renal no modelo de DM. É possível que os mecanismos envolvidos na melhora desses parâmetros por meio da BRD sejam mediados pelo SGLT2 e TNFα renais. As alterações cardiovasculares no DM podem ser consequentes às ações diferenciais (centrais ou periféricas) da insulina.Dados abertos - Sucupira - Teses e dissertações (2018)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)FAPESP: 2014/263871Universidade Federal de São Paulo (UNIFESP)Campos, Ruy Ribeiro [UNIFESP]Bergamaschi, Cássia Marta de Toledo [UNIFESP]http://lattes.cnpq.br/1166526138293050http://lattes.cnpq.br/2520398649906832http://lattes.cnpq.br/9149137484863942Universidade Federal de São Paulo (UNIFESP)Oliveira, Tales Lyra de [UNIFESP]2020-03-25T11:43:35Z2020-03-25T11:43:35Z2018-09-27info:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/publishedVersion190 f.application/pdfhttps://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6979670OLIVEIRA, Tales Lyra de. Papel dos nervos renais no diabetes mellitus experimental. 2018. Tese (Doutorado) - Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, 2018.2018-0144.pdfhttps://repositorio.unifesp.br/handle/11600/52229porSão Pauloinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-02T13:36:58Zoai:repositorio.unifesp.br/:11600/52229Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-02T13:36:58Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Papel dos nervos renais no diabetes mellitus experimental
Role of renal nerves in experimental diabetes mellitus
title Papel dos nervos renais no diabetes mellitus experimental
spellingShingle Papel dos nervos renais no diabetes mellitus experimental
Oliveira, Tales Lyra de [UNIFESP]
Sympathetic nerve activity
Insulin
Sympathetic nervous system
Renin angiotensin aldosterone system
Renal denervation
Diabetes Mellitus
Atividade nervosa simpática
Insulina
Sistema nervoso simpático
Sistema renina angiotensina aldosterona
Denervação renal
title_short Papel dos nervos renais no diabetes mellitus experimental
title_full Papel dos nervos renais no diabetes mellitus experimental
title_fullStr Papel dos nervos renais no diabetes mellitus experimental
title_full_unstemmed Papel dos nervos renais no diabetes mellitus experimental
title_sort Papel dos nervos renais no diabetes mellitus experimental
author Oliveira, Tales Lyra de [UNIFESP]
author_facet Oliveira, Tales Lyra de [UNIFESP]
author_role author
dc.contributor.none.fl_str_mv Campos, Ruy Ribeiro [UNIFESP]
Bergamaschi, Cássia Marta de Toledo [UNIFESP]
http://lattes.cnpq.br/1166526138293050
http://lattes.cnpq.br/2520398649906832
http://lattes.cnpq.br/9149137484863942
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Oliveira, Tales Lyra de [UNIFESP]
dc.subject.por.fl_str_mv Sympathetic nerve activity
Insulin
Sympathetic nervous system
Renin angiotensin aldosterone system
Renal denervation
Diabetes Mellitus
Atividade nervosa simpática
Insulina
Sistema nervoso simpático
Sistema renina angiotensina aldosterona
Denervação renal
topic Sympathetic nerve activity
Insulin
Sympathetic nervous system
Renin angiotensin aldosterone system
Renal denervation
Diabetes Mellitus
Atividade nervosa simpática
Insulina
Sistema nervoso simpático
Sistema renina angiotensina aldosterona
Denervação renal
description Introduction: Diabetes mellitus (DM) promotes increased renal sympathetic nerve activity (rSNA), autonomic imbalance, cardiovascular, metabolic and renal dysfunction. Apparently, the rSNA increases is directly associated with development and maintenance of neuropathy diabetic and autonomic nephropathy condition. Recently, there has been an important interest in clinical and experimental studies about bilateral renal denervation (BRD) procedure as a therapeutic alternative in some diseases related with renal sympathoexcitation. Aims: Protocol CEUA – UNIFESP 1787250714. Therefore, the present study evaluated the role of renal nerves on the autonomic, cardiovascular, metabolic and renal balance in the streptozotocindiabetic animal model. Methods: 8weekold Wistar rats were separated into three experimental groups: control (CTR), diabetic (DM) and denervated diabetic (DM BRD), with n=68 animals per group. DM was induced by one dose of streptozotocin (STZ; 60 mg/kg, ip) 4 weeks prior to the final experiments while the surgical BRD was performed 2 weeks before final experiments. The results were expressed as mean ± SEM and were compared by analysis of variance (ANOVA), P<0.05 was considered as the significance level. Results: DM was confirmed by body weight reduction (CTR: 351.5 ± 4.1, DM: 242.1 ± 6.7 g) and glycemia increases (CTR: 100.3 ± 3.7, DM: 509.1 ± 14.4 mg/dL). BRD significantly reduced glycemia (410.5 ± 5.8 mg/dL) and increased body weight (302.4 ± 5.7 g) in diabetic animals. DM promoted impairment of renal function such as glycosuria and albuminuria (CTR: 0,01 ± 0,001 and 0,08 ± 0,008, DM: 2.7 ± 0.19 and 0,39 ± 0,04 g/kg/24h), however BRD significantly attenuated these parameters (1,3 ± 0,19 and 0,13 ± 0,04 g/kg/24h). The heart rate (HR) was decreased in the DM animals (CTR: 352 ± 13, DM: 292 ± 11 bpm), associated with reduction of arterial baroreceptor reflex sensitivity to HR control (bradycardic response: CTR: 2.17 ± 0.06, DM: 1.92 ± 0.04 bpm/mmHg and tachycardic response: CTR: 2.55 ± 0.04, DM: 2.09 ± 0.03 bpm/mmHg). Interestingly, BRD was able to normalized HR (372 ± 23 bpm) and improved baroreflex sensitivity to the HR control (bradycardic response: 2.09 ± 0.14 and tachycardic response: 3.13 ± 0.05 bpm/mmHg) in the DM model. The rSNA was significantly increased (CTR: 82.6 ± 3.93, DM: 124.8 ± 6.45 pps), while splanchnic SNA (sSNA) was decreased in the diabetic animals (CTR: 120.5 ± 4.76, DM: 72.3 ± 5.70 pps), however BRD normalized sSNA (100.0 ± 9.23 pps) in the diabetic animals. The Na+/glucose cotransporter 2 (SGLT2) gene expression and tumor necrosis factor (TNFα) concentration were increased in the kidneys of DM group (CTR: 1.00 ± 0.24 and 233.3 ± 17.54, DM: 12.33 ± 1.25 normalized HPRT1 and 244.1 ± 12.19 pg/mL), meanwhile BRD was able to normalize (1.53 ± 0.85 normalized HPRT1 and 190.9 ± 7.53 pg/mL) these parameters.. Acutely, insulin microinjection in the rostoventrolateral medulla area (RVLM) increased mean arterial pressure (MAP; CTR: 8.7 ± 2.26, DM: 23.9 ± 19.27, DM BRD: 12.8 ± 4.25 %) and sSNA (CTR: 14.2 ± 3.50, DM: 21.2 ± 9.41, DM BRD: 17.5 ± 3.80%) only in DM groups, however, the rSNA was increased in all groups evaluated (CTR: 25.7 ± 4.62, DM: 20.6 ± 3.33%), compared to baseline means. Conclusion: Taken together, our results suggest that the renal nerves have an important role in the autonomic balance, cardiovascular, metabolic and renal function in the DM model. Furthermore, the reduction of renal SGLT2 and TNFα appears to be mechanisms involved in the improvement of these parameters (cardiovascular, autonomic, metabolic and renal) induced by BRD in the experimental DM. Cardiovascular changes in DM can be achieved by central or peripheral differential actions of insulin.
publishDate 2018
dc.date.none.fl_str_mv 2018-09-27
2020-03-25T11:43:35Z
2020-03-25T11:43:35Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6979670
OLIVEIRA, Tales Lyra de. Papel dos nervos renais no diabetes mellitus experimental. 2018. Tese (Doutorado) - Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, 2018.
2018-0144.pdf
https://repositorio.unifesp.br/handle/11600/52229
url https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=6979670
https://repositorio.unifesp.br/handle/11600/52229
identifier_str_mv OLIVEIRA, Tales Lyra de. Papel dos nervos renais no diabetes mellitus experimental. 2018. Tese (Doutorado) - Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, 2018.
2018-0144.pdf
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 190 f.
application/pdf
dc.coverage.none.fl_str_mv São Paulo
dc.publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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