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Anchietea pyrifolia A. St.-Hil. as a Cardiovascular-Endowed Species: A Whole-Biological Investigation.
Lima Tolouei, Sara Emilia; Palozi, Rhanany Alan Calloi; Tirloni, Cleide Adriane Signor; Marques, Aline Aparecida Macedo; Schaedler, Maysa Isernhagen; Guarnier, Lucas Pires; Silva, Aniely Oliveira; de Almeida, Valter Paes; Budel, Jane Manfron; Souza, Roosevelt Isaias Carvalho; Dos Santos, Ariany Carvalho; Nocchi, Samara Requena; Silva, Denise Brentan; Dalsenter, Paulo Roberto; Gasparotto Junior, Arquimedes.
Afiliação
  • Lima Tolouei SE; 1 Laboratory of Reproductive Toxicology, Federal University of Paraná, Curitiba, Paraná, Brazil.
  • Palozi RAC; 2 Laboratory of Electrophysiology and Cardiovascular Pharmacology (LEFaC), Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Tirloni CAS; 2 Laboratory of Electrophysiology and Cardiovascular Pharmacology (LEFaC), Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Marques AAM; 2 Laboratory of Electrophysiology and Cardiovascular Pharmacology (LEFaC), Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Schaedler MI; 2 Laboratory of Electrophysiology and Cardiovascular Pharmacology (LEFaC), Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Guarnier LP; 2 Laboratory of Electrophysiology and Cardiovascular Pharmacology (LEFaC), Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Silva AO; 2 Laboratory of Electrophysiology and Cardiovascular Pharmacology (LEFaC), Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • de Almeida VP; 3 Program of Post-Graduation in Pharmaceutical Sciences, State University of Ponta Grossa, Ponta Grossa, Paraná, Brazil.
  • Budel JM; 3 Program of Post-Graduation in Pharmaceutical Sciences, State University of Ponta Grossa, Ponta Grossa, Paraná, Brazil.
  • Souza RIC; 2 Laboratory of Electrophysiology and Cardiovascular Pharmacology (LEFaC), Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Dos Santos AC; 2 Laboratory of Electrophysiology and Cardiovascular Pharmacology (LEFaC), Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
  • Nocchi SR; 4 Laboratory of Natural Products and Mass Spectrometry (LaPNEM), Faculty of Pharmaceutical Sciences, Food and Nutrition (FACFAN), Federal University of Mato Grosso do Sul, Campo Grande, Mato Grosso do Sul, Brazil.
  • Silva DB; 4 Laboratory of Natural Products and Mass Spectrometry (LaPNEM), Faculty of Pharmaceutical Sciences, Food and Nutrition (FACFAN), Federal University of Mato Grosso do Sul, Campo Grande, Mato Grosso do Sul, Brazil.
  • Dalsenter PR; 1 Laboratory of Reproductive Toxicology, Federal University of Paraná, Curitiba, Paraná, Brazil.
  • Gasparotto Junior A; 2 Laboratory of Electrophysiology and Cardiovascular Pharmacology (LEFaC), Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
J Med Food ; 22(4): 393-407, 2019 Apr.
Article em En | MEDLINE | ID: mdl-30990753
ABSTRACT
Although leaves of Anchietea salutaris are used in Brazilian traditional medicine, there is no available data in the literature proving its efficacy and safety. Thus, the aim of the study was to perform a meticulous botanical, phytochemical, toxicological, and pharmacological investigation of A. salutaris in Wistar rats. At first, a morphoanatomical characterization of Anchietea pyrifolia leaves and stems was performed. Then, a purified infusion (ethanol-soluble fraction obtained from A. pyrifolia [ESAP]) was obtained followed by its chemical profile elucidation. Furthermore, an acute toxicity test was performed, and the acute and prolonged diuretic and hypotensive effects were also evaluated in Wistar rats. Finally, the vasodilatory responses of ESAP in mesenteric vascular beds were investigated. The main secondary metabolites identified from ESAP were O-glycosylated flavonoids, chlorogenic acids, and phenylpropanoic acid derivatives. ESAP did not promote any toxic effects in female rats nor increased urinary excretion in male rats after a single exposure. However, ESAP significantly reduced renal elimination of sodium, potassium, and chloride after prolonged treatment. An ESAP highest dose promoted significant acute hypotension without affecting blood pressure levels after prolonged use. Furthermore, its cardiovascular effects seem to be related with the calcium-activated potassium channel activation in resistance vessels.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Extratos Vegetais / Violaceae / Hipertensão / Anti-Hipertensivos Limite: Animals / Female / Humans / Male País/Região como assunto: America do sul / Brasil Idioma: En Revista: J Med Food Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Extratos Vegetais / Violaceae / Hipertensão / Anti-Hipertensivos Limite: Animals / Female / Humans / Male País/Região como assunto: America do sul / Brasil Idioma: En Revista: J Med Food Ano de publicação: 2019 Tipo de documento: Article