W16-P-068 The unsaponifiable fraction and molecular species of triglycerides from virgin olive oil affect chylomicron composition of healthy subjects

2005 ◽  
Vol 6 (1) ◽  
pp. 118
Author(s):  
J.S. Perona ◽  
F. Rivas-Garcia ◽  
J.M. Sanchez-Dominguez ◽  
E. Montero ◽  
V. Ruiz-Gutierrez
2000 ◽  
Vol 55 (9-10) ◽  
pp. 814-819 ◽  
Author(s):  
Rocío de la Puerta ◽  
Eugenia Martínez-Domínguez ◽  
Valentina Ruíz-Gutiérrez

Abstract Interest in the health-promoting effects of virgin olive oil, an important part of the “Mediterranean diet”, prompted us to determine the antiinflammatory effects of erythrodiol, β-sitosterol and squalene, identified as major components of the so-called “unsaponifiable fraction” of virgin olive oil, as well as of the phenolic compounds from the “polar fraction”: oleuropein, tyrosol, hydroxytyrosol and caffeic acid. Their activities were compared to those of both, total unsaponifiable and polar fractions. This study was designed to analyse the antiinflammatory effect of these specific compounds from virgin olive oil on edema in mice induced by either arachidonic acid (AA ) or 12-O-tetradecanoylphorbol acetate (TPA). The inhibition of the myeloperoxidase (MPO), marker enzyme of the accumulation of neutrophils in the inflamed tissue, was also investigated by the TPA model. The topical application of the olive oil compounds (0.5 mg/ear) produced a variable degree of antiinflammatory effect with both assays. In the auricular edema induced by TPA, β-sitosterol and erythrodiol from the unsaponifiable fraction of the oil showed a potent antiedematous effect with a 61.4% and 82.1% of inhibition respectively, values not very different to that of the reference indomethacin (85.6%) at 0.5 mg/ear. The four phenolics exerted a similar range of inhibition (33- 45%). All compounds strongly inhibited the enzyme myeloperoxidase, indicating a reduction of the neutrophil influx in the inflamed tissues. The strongest inhibitor of AA edema was the total unsaponifiable fraction which inhibition was 34%, similar to that obtained by the reference drug dexamethasone at 0.05 mg/ear. Among the phenolics, oleuropein also produced an inhibition of about 30% with the same dose, but all the other components were found less active in this assay. The anti-inflammatory effects exerted by both unsaponifiable and polar compounds might contribute to the potential biological properties reported for virgin olive oil against different pathological processess.


2018 ◽  
Vol 84 (7) ◽  
pp. 1566-1574 ◽  
Author(s):  
Roberto Carnevale ◽  
Romano Silvestri ◽  
Lorenzo Loffredo ◽  
Marta Novo ◽  
Vittoria Cammisotto ◽  
...  

2013 ◽  
Vol 65 (6) ◽  
pp. 908-918 ◽  
Author(s):  
Ana Cárdeno ◽  
Marina Sánchez-Hidalgo ◽  
Amparo Cortes-Delgado ◽  
Catalina Alarcón de la Lastra

2015 ◽  
Vol 5 (7) ◽  
pp. e172-e172 ◽  
Author(s):  
F Violi ◽  
L Loffredo ◽  
P Pignatelli ◽  
F Angelico ◽  
S Bartimoccia ◽  
...  

Il Farmaco ◽  
1998 ◽  
Vol 53 (6) ◽  
pp. 448-449 ◽  
Author(s):  
M.T. Saenz ◽  
M.D. Garcia ◽  
M.C. Ahumada ◽  
V. Ruiz

2006 ◽  
Vol 95 (5) ◽  
pp. 889-897 ◽  
Author(s):  
Javier S. Perona ◽  
Michael Avella ◽  
Kathleen M. Botham ◽  
Valentina Ruiz-Gutierrez

The fatty acid composition of dietary oils can modulate the incorporation of triacylglycerol-rich lipoproteins (TRL) into hepatocytes, thus affecting the atherogenicity of these particles. However, nothing is known about the effect of the unsaponifiable fraction of the oils. In the present study, we evaluated the influence of these components on the uptake of TRL by rat primary hepatocytes. TRL were isolated from human serum after the intake of meals enriched in high-oleic sunflower oil (HOSO), virgin olive oil (VOO) or VOO enriched in its own unsaponifiable fraction (EVO). HOSO and HOSO-TRL differed from VOO and EVO and their corresponding TRL in the composition of triacylglycerol molecular species and of the unsaponifiable fraction. Furthermore, the increase in the unsaponifiable fraction of VOO led to changes in the triacylglycerol molecular species in the EVO-TRL. On incubation with hepatocytes, HOSO-TRL were taken up at a faster rate than VOO-TRL or EVO-TRL. In addition, in comparison to VOO-TRL, HOSO-TRL increased the expression of mRNA for the LDL receptor-related protein receptor, which plays an important role in the internalisation of remnant lipoproteins. EVO-TRL also increased LDL receptor-related protein mRNA expression in comparison with VOO-TRL, but this change was not accompanied by a rise in the uptake rate, suggesting that the unsaponifiable fraction of VOO may inhibit LDL receptor-related protein expression or activity post-transcriptionally. In conclusion, TRL from dietary oils with differing triacylglycerol molecular species and unsaponifiable fraction content are taken up by liver cells at different rates, and this may be important in the atherogenicity of these particles.


2016 ◽  
Vol 23 (19) ◽  
pp. 19397-19408 ◽  
Author(s):  
Imen Ghorbel ◽  
Mariem Chaâbane ◽  
Ons Boudawara ◽  
Naziha Grati Kamoun ◽  
Tahia Boudawara ◽  
...  

2013 ◽  
Vol 48 (3) ◽  
pp. 572-581 ◽  
Author(s):  
S. Sánchez-Fidalgo ◽  
A. Cárdeno ◽  
M. Sánchez-Hidalgo ◽  
M. Aparicio-Soto ◽  
I. Villegas ◽  
...  

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