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1.
Int J Phytoremediation ; : 1-9, 2024 May 27.
Article in English | MEDLINE | ID: mdl-38800998

ABSTRACT

2,4-Dichlorophenoxyacetic acid (2,4-D) is an herbicide widely used in crops against broadleaf weeds. However, 2,4-D residues are considered an environmental pollutant in bodies of water. Phytoremediation with Plectranthus neochilus is a substantial strategy to remove 2,4-D from the aquatic environment. The objective of this study was to verify the efficiency of the association of the photostimulus by Light Emitting Diodes (LED) with P. neochilus to improve phytoremediation of 2,4-D in water. Phytoremediation was evaluated with the following samples: natural light, white LED, blue LED, and red LED, with and without the plant as controls. The data corresponding to the validation of the method were in accordance with the required parameters: R2: 0.9926; RSD: 1.74%; LOD: 0.075 mg.L-1; LOQ: 0.227 mg.L-1 and recovery by SPE was 76.57%. The efficiency of the association of LED with P. neochilus in the 28 days was: ambient light + plant (47.0%); white light + plant (37.10%); blue light + plant (26.80%); red light + plant (3.32%). This study demonstrated, for the first time, the efficiency of using LEDs light in association with P. neochilus for the phytoremediation of 2,4-D in water.


Phytoremediation of organic compounds in water is a time-consuming process and generally unfavorable to the plant. This study demonstrated that the photostimulation with blue and red LED lights can accelerate the phytoremediation of the herbicide by P. neochilus, decreasing the t1/2 of 2,4-D in water by 2 and 5 times, respectively. We equate the time of this process to physical-chemical degradation methods, but without the use of reagents, creating a green strategy to accelerate the decontamination of water resources contaminated with pesticides.

2.
Br J Nutr ; 131(11): 1827-1840, 2024 Jun 14.
Article in English | MEDLINE | ID: mdl-38410884

ABSTRACT

The purpose of this study was to investigate the effect of an egg white hydrolysate (EWH) to protect white adipose tissue damage from cardiometabolic changes induced by severe hypertension. Male Wistar rats were uninephrectomised and divided: SHAM (weekly subcutaneous vehicle (mineral oil + propylene glycol, 1:1)), SHAM + EWH (subcutaneous vehicle plus EWH via gavage, 1 g/kg per day), DOCA (deoxycorticosterone acetate diluted in vehicle subcutaneously weekly in subsequent doses of 20 mg/kg -1st week, 12 mg/kg - 2­3th week, and 6 mg/kg -4­8th week, respectively, plus 1 % NaCl and 0·2 % KCl in drinking water), and DOCA + EWH. Body weight gain, food and water intake, glucose and lipid metabolism were evaluated. Oxidative stress was assessed by biochemical assay and immunofluorescence for NOX-1, nuclear factor kappa B (NFκB), and caspase-3 in retroperitoneal white adipose tissue (rtWAT). Proinflammatory cytokines (IL-6 and 1ß), CD163+ macrophage infiltration, and immunohistochemistry for TNFα and uncoupling protein-1 were evaluated, as well as histological analysis on rtWAT. Glutathione peroxidase and reductase were also determined in plasma. EWH showed hypocholesterolemic, antioxidant, anti-inflammatory, and anti-apoptotic properties in the arterial hypertension DOCA-salt model. The results demonstrated the presence of functional changes in adipose tissue function by a decrease in macrophage infiltration and in the fluorescence intensity of NFκB, NOX-1, and caspase-3. A reduction of proinflammatory cytokines and restoration of antioxidant enzymatic activity and mitochondrial oxidative damage by reducing uncoupling protein-1 fluorescence intensity were also observed. EWH could be used as a potential alternative therapeutic strategy in the treatment of cardiometabolic complications associated with malignant secondary arterial hypertension.


Subject(s)
Adipose Tissue, White , Desoxycorticosterone Acetate , Egg White , Oxidative Stress , Rats, Wistar , Animals , Male , Adipose Tissue, White/metabolism , Adipose Tissue, White/drug effects , Oxidative Stress/drug effects , Egg White/chemistry , Rats , Hypertension/metabolism , Hypertension/chemically induced , Protein Hydrolysates/pharmacology , Lipid Metabolism/drug effects , Uncoupling Protein 1/metabolism , Intra-Abdominal Fat/metabolism , Intra-Abdominal Fat/drug effects
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