In vivo and in vitro toxicological evaluations of aqueous extract from Cecropia pachystachya leaves.
Erminiana Damiani de Mendonça PereiraJuliana da SilvaPatrícia da Silva CarvalhoIvana GrivicichJaqueline Nascimento PicadaIlton Batista Salgado JúniorGabriela Jouglard VasquesMário Augusto da Silva PereiraFlavio Henrique ReginattoAlexandre de Barros Falcão FerrazPublished in: Journal of toxicology and environmental health. Part A (2020)
leaves are popularly used to treat asthma and diabetes. Despite the widespread consumption of this plant, there are few scientific studies regarding its toxicological potential. In order to conduct a thorough study concerning the potential adverse effects, the aim of this study was to assess acute and subacute toxicity tests of crude aqueous extract from C. pachystachya leaves (CAE-Cp) using in vivomodel, as well as in vitro cytotoxicity, genotoxicity and antioxidant activity. In addition, genotoxicity, and cytotoxicity of chlorogenic acid (CGA) and cytotoxicity of isoorientin (ISOO) were also evaluated. The antioxidant activity was verified by DPPH, cytotoxicity using sulforhodamine B (SRB) assay and genotoxicity by comet assay on V79 cells. The phytochemical analysis of CAE-Cp detected flavonoids and tannins, CGA and ISOO as the major compounds utilizing HPLC. The total flavonoid content (6.52 mg/g EQ) and antioxidant activity (EC50 = 62.15 µg/ml) of CAE-Cp were determined. In vitro evaluations with CAE-Cp showed genotoxic effects at 0.31 to 2.5 mg/ml and an expressive cytotoxicity on HT-29 (IC50 = 4.43 µg/ml) cells. CGA was genotoxic against V79 cells at 0.07 mg/ml and cytotoxic against to HT-29 (IC50 = 71.70 µg/ml), OVCAR-3 (IC50 = 80.07 µg/ml), MCF-7 (IC50 = 45.58 µg/ml) and, NCI-H460 (IC50 = 71.89 µg/ml) cancer cell lines. Wistar rats treated with a single dose (2,000 mg/kg) CAE-Cp decreased hemoglobin levels after 14 days, although no significant toxicity was observed in animals after 28 days. In view of the in vitro cytotoxicity and genotoxicity detected, further studies are necessary to establish the safe use of CAE-Cp.
Keyphrases
- induced apoptosis
- oxidative stress
- cell cycle arrest
- oxide nanoparticles
- type diabetes
- ms ms
- endoplasmic reticulum stress
- high throughput
- squamous cell carcinoma
- liver failure
- chronic obstructive pulmonary disease
- cell death
- intensive care unit
- risk assessment
- cardiovascular disease
- young adults
- metabolic syndrome
- high resolution
- papillary thyroid
- single cell
- adipose tissue
- lung function
- breast cancer cells
- acute respiratory distress syndrome
- drug induced