2023
DOI: 10.3390/ijms241512115
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Antioxidant Activity of a Sicilian Almond Skin Extract Using In Vitro and In Vivo Models

Alessia Arangia,
Agnese Ragno,
Marika Cordaro
et al.

Abstract: Almond skins are known for their antioxidative and anti-inflammatory properties, which are mainly due to the presence of polyphenols. The aim of the present study was to evaluate the antioxidant and anti-inflammatory effects of almond skin extract (ASE) obtained from the Sicilian cultivar “Fascionello” and to evaluate the possible mechanisms of action using an in vitro model of human monocytic U937 cells as well as an in vivo model of carrageenan (CAR)-induced paw edema. The in vitro studies demonstrated that … Show more

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Cited by 2 publications
(4 citation statements)
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“…The almond (Prunus amygdalus L.) belongs to the Rosaceae family, and it is cultivated in east Mediterranean countries, Australia and Africa [25]. The skin of the nut has antiinflammatory and antioxidant activities due to the presence of nutrients, such as lipids, fatty acids, proteins, amino acids, vitamins, carbohydrates and minerals [26]. The sphingolipids isolated from nuts are capable of inhibiting the development of colon cancer and also decreasing the proportion of adenocarcinomas in mice [25].…”
Section: Almond (Prunus Amygdalus L)mentioning
confidence: 99%
“…The almond (Prunus amygdalus L.) belongs to the Rosaceae family, and it is cultivated in east Mediterranean countries, Australia and Africa [25]. The skin of the nut has antiinflammatory and antioxidant activities due to the presence of nutrients, such as lipids, fatty acids, proteins, amino acids, vitamins, carbohydrates and minerals [26]. The sphingolipids isolated from nuts are capable of inhibiting the development of colon cancer and also decreasing the proportion of adenocarcinomas in mice [25].…”
Section: Almond (Prunus Amygdalus L)mentioning
confidence: 99%
“…A rapid HPLC-UV method was applied to investigate the DSA lio polyphenolic profile [25]. Nine unknown compounds within acid phenolic, flavanol, and flavonol classes were observed: gallic acid (1), procyanidin B3 (2), procyanidin B1 (3), catechin (4), epicatechin (5), procyanidin C1 (6), kaempferol 3-O-rutinoside (7), isorhamnetin-3-Orutinoside (8), and quercetin (9) (Figure S1). The compounds were identified by comparing their retention time (Figure S1) and mass spectral data (Table 1 and Figure S2) with those of pure standards.…”
Section: Dsa Preliminary Chemical Characterization and Markers Choosingmentioning
confidence: 99%
“…The following supporting information can be downloaded: https://www. mdpi.com/article/10.3390/molecules28237913/s1, Figure S1: HPLC-UV profile of DSA: Gallic acid (1) procyanidin B3 (2), procyanidin B1 (3), catechin (4), epicatechin (5), procyanidin C1 (6), kaempferol 3-O-rutinoside (7), isorhamnetin-3-O-rutinoside (8), and quercetin (9); Figure S2: MS/MS spectra of phenolic compounds in DSA; Figure S3: Cell vitality on A375 (A), A549 (B), and HaCaT (C) cells was calculated as: % vitality = [100 × (OD treated/OD control)]. Results were analyzed using the nonparametric Mann-Whitney U test; Table S1: %RH ± SD (n = 3) of processed (40 • C ± 2 • C) and unprocessed skin almond samples.…”
Section: Supplementary Materialsmentioning
confidence: 99%
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