2019
DOI: 10.1016/j.bjp.2018.12.001
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Cytotoxic effects of Euterpe oleraceae fruit oil (açaí) in rat liver and thyroid tissues

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Cited by 15 publications
(6 citation statements)
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“…As depicted in Figure 2 A, our results showed that AHE did not exert cytotoxic effects at lower doses, but reduced almost 50% of mitochondrial activity at the highest concentration tested (75 mg/L), affecting cellular viability, in comparison to control group ( p = 0.0026). In accordance, it has been recently demonstrated that açaí oil induces hepatic and thyroid tissue toxicity in male Wistar rats, after the intake of oil doses higher than 100 mg/kg for 14 days [ 32 ]. In comparison, no genotoxic effects were reported for the same doses in leukocytes, liver, bone marrow and testicular rat cells [ 33 ].…”
Section: Resultsmentioning
confidence: 77%
See 1 more Smart Citation
“…As depicted in Figure 2 A, our results showed that AHE did not exert cytotoxic effects at lower doses, but reduced almost 50% of mitochondrial activity at the highest concentration tested (75 mg/L), affecting cellular viability, in comparison to control group ( p = 0.0026). In accordance, it has been recently demonstrated that açaí oil induces hepatic and thyroid tissue toxicity in male Wistar rats, after the intake of oil doses higher than 100 mg/kg for 14 days [ 32 ]. In comparison, no genotoxic effects were reported for the same doses in leukocytes, liver, bone marrow and testicular rat cells [ 33 ].…”
Section: Resultsmentioning
confidence: 77%
“…In comparison, no genotoxic effects were reported for the same doses in leukocytes, liver, bone marrow and testicular rat cells [ 33 ]. The toxic effects registered by histological and histochemical analysis were attributed to palmitic and oleic acids, major constituents of açaí oil, together with vanillic, g-linolenic, linoleic, cinnamic, caffeic, protocatechuic, ferulic, syringic acids, and flavonoids quercetin and kaempferol rutinoside [ 32 , 33 ]. For this reason, the further evaluation of the bioactive properties of AHE was assessed using non-toxic concentrations, in order to consider its pharmacological potential, since some of the compounds reported in fruit oil were also identified in AHE (e.g., protocatechuic acid and quercetin).…”
Section: Resultsmentioning
confidence: 99%
“…The ACP oil showed higher activity (2.1-fold) as an inhibitor against the proliferation of HT-29 human colon adenocarcinoma cells compared to the pulp extract obtained with ethyl acetate [182]. The cytotoxicity of ACP oil in rat liver and thyroid tissues [183] and its genotoxicity in mammalian cells in vivo were evaluated [184]. The results indicated that ACP oil did not present genotoxic effects in the animals' leukocytes, liver, bone marrow, and testicular cells.…”
Section: Bioactive Compoundsmentioning
confidence: 96%
“…However, Marques et al [ 186 ] used rat models to demonstrate that the oral administration of açaí oil at doses of 30, 100, and 300 mg/kg over a time period of 14 days resulted in altered thyroid cell follicular morphology and reduced size of follicular cells due to hypertrophy and unorganized growth. Interestingly, these doses of açaí oil also caused hepatocyte vacuolization, as well as a shift from eosinophilic to basophilic characteristics in the cells.…”
Section: Toxicity and Safety Studiesmentioning
confidence: 99%