4.7 Article

Clitoria ternatea L. petal bioactive compounds display antioxidant, antihemolytic and antihypertensive effects, inhibit α-amylase and α-glucosidase activities and reduce human LDL cholesterol and DNA induced oxidation

Journal

FOOD RESEARCH INTERNATIONAL
Volume 128, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.foodres.2019.108763

Keywords

Principal component analysis; Response surface methodology; Anthocyanins; Unconventional foods; Antihypertensive activity; Inhibitor of DNA strand scission

Funding

  1. PROAP/CAPES
  2. Fundacao Araucaria
  3. Conselho Nacional de Desenvolvimento Cientffico e Tecnologico (CNPQ) [302763/2014-7, 305804/2017-0, 303188/2016-2]
  4. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior - Brasil (CAPES) [001]

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The purpose of this study was to use a statistical approach to optimise the experimental conditions regarding the extraction of bioactive compounds, and to analyse the in vitro functional properties of crude lyophilized extracts (CLE) and partially purified (PPE) extracts of Clitoria ternatea petals. The results showed that the factors of temperature and time influenced the extraction of phenolic compounds, antioxidant activity and the physicochemical parameters. Simultaneous optimisation showed that the same levels of bioactive compounds were extracted when using temperatures from 11.7 to 68.3 degrees C and times from 8.47 to 51.12 min. Principal component analysis revealed the experimental conditions that provided the extraction producing the highest level of phenolic content (40 degrees C/30 min). The CLE showed antimicrobial activity; protective effect against hemolysis of erythrocytes; inhibition of alpha-amylase, alpha-glucosidase and angiotensin-I-converting (ACE-D enzymes; and inhibition of lipid peroxidation. The CLE and PPE demonstrated oxygen radical absorption capacity; inhibition of DNA strand scission; inhibition of LDL cholesterol oxidation; intracellular antioxidant activity against reactive oxygen species ( > 100 mu g/mL); and no cytotoxicity (IC50, GI(50) and LC50 > 900 mu g/mL) against A549, HCT8 and IMR90 cell lines.

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