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Am J Hypertens ; 37(7): 477-484, 2024 06 14.
Artigo em Inglês | MEDLINE | ID: mdl-38459938

RESUMO

BACKGROUND: The effectiveness of renal denervation (RDN) in reducing blood pressure and systemic sympathetic activity in hypertensive patients has been established. However, the underlying central mechanism remains unknown. This study aimed to investigate the role of RDN in regulating cardiovascular function via the central renin-angiotensin system (RAS) pathway. METHODS: Ten-week-old spontaneously hypertensive rats (SHR) were subjected to selective afferent renal denervation (ADN) using capsaicin solution. We hypothesized that ADN would effectively reduce blood pressure and rebalance the RAS component of the paraventricular nucleus (PVN) in SHR. RESULTS: The experimental results show that the ADN group exhibited significantly lower blood pressure, reduced systemic sympathetic activity, decreased chronic neuronal activation marker C-FOS expression in the PVN, and improved arterial baroreflex function, compared with the Sham group. Furthermore, ACE and AT1 protein expression was reduced while ACE2 and MAS protein expression was increased in the PVN of SHR after ADN. CONCLUSIONS: These findings suggest that RDN may exert these beneficial effects through modulating the central RAS pathway.


Assuntos
Barorreflexo , Pressão Sanguínea , Hipertensão , Rim , Núcleo Hipotalâmico Paraventricular , Ratos Endogâmicos SHR , Sistema Renina-Angiotensina , Sistema Nervoso Simpático , Animais , Núcleo Hipotalâmico Paraventricular/metabolismo , Núcleo Hipotalâmico Paraventricular/fisiopatologia , Rim/inervação , Rim/metabolismo , Hipertensão/fisiopatologia , Hipertensão/cirurgia , Hipertensão/metabolismo , Sistema Nervoso Simpático/fisiopatologia , Sistema Nervoso Simpático/cirurgia , Sistema Nervoso Simpático/metabolismo , Masculino , Enzima de Conversão de Angiotensina 2/metabolismo , Modelos Animais de Doenças , Proteínas Proto-Oncogênicas c-fos/metabolismo , Proto-Oncogene Mas , Peptidil Dipeptidase A/metabolismo , Simpatectomia/métodos , Receptor Tipo 1 de Angiotensina/metabolismo , Capsaicina/farmacologia , Receptores Acoplados a Proteínas G/metabolismo , Ratos
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