Introduction: Perivascular adipose tissue (PVAT) surrounds most of the blood vessels and modulates the contractile vascular response to stimulation with different agonists, the so-called anticontractile effect (AE). However, PVAT is dysfunctional in hypertension, with loss of this effect. Both ?- and ?-adrenergic receptors (AR) are present in PVAT and their effects in the vascular tone can be seen using phenylephrine (PHE), a selective ?1-AR agonist, and noradrenaline (NE), that acts at ?-AR and ?-AR, putting these agonists as keys to understand modulation of the vascular tone through PVAT – and for its dysfunction as well. The aim of the present study was to evaluate the AE of PVAT of the thoracic aorta of DOCA-salt animals when stimulated with PHE or NE. Methods: Uninefrectomized male Wistar rats (ICB-USP Animal Experimentation Ethics Committee, record nº 03/2016) were divided into SHAM and DOCA-salt groups. For 8 weeks, caudal blood pressure (BP) was accompanied by tail plethysmography. Afterwards, the rats were killed and aortic rings with (PVAT+) and without (PVAT-) PVAT were mounted on a wire myograph to analyze the vascular response to PHE or NE. Statistical analysis: t-test or ANOVA. Results: BP was 65% higher in DOCA-salt compared to SHAM. Contractile response to PHE or NE was reduced in aortic PVAT+ rings compared with PVAT- in both groups. In addition, the PVAT+ rings of DOCA-salt showed a loss of AE in response to PHE when compared to SHAM (-56% vs. SHAM). However, with NE this behavior was not observed, and there was no difference between responses of SHAM and DOCA-salt’s PVAT against this agonist. Conclusion: PVAT’s dysfunction found in DOCA-salt animals is not observed when stimulation is performed with a nonselective a- and b-AR agonist, demonstrating a protective effect, probably by b-AR, that prevents the loss of the PVAT AE in this condition.
Comissão Organizadora
José Wilson do Nascimento Corrêa
Simone Potje
Gabriel Tavares do Vale
Stêfany Cau
Roger Lyrio
Simone R Potje
Alice Valença Araújo
Ruth Cristina Albuquerque Santos
Lara Caroline Amaro
Ana Dária Cassoli da Silva
Pollyana Peixoto
Izabela Moreira Bonfim
Jocimar José Pitol
Sunamita Vaz Martins
Izabela Moreira Bonfim
Palloma Emanuelle Dornelas de Melo
Daniella Bonaventura
Tagana Rosa
Sarah Victory Santana Gomes
Priscila Cruz
André Lucas Borges
Jéssyca Aparecida Soares Giesen
Leticia Tinoco Gonçalves
Silvia Maria Luna Alves
NAYANA YARED BATISTA
Wellington Francisco Pereira da Silva
Natália Ferreira de Araújo
Leandro de Carvalho Gomes
Comissão Científica