Protective effect of glutathione S-transferase enzyme activity against aflatoxin B1 in poultry species: Relationship between glutathione S-transferase enzyme kinetic parameters, and resistance to aflatoxin B1

Abstract The expression of the allelic isovitexin 7-O-glycosylation genes gG (transfer of glucose) and gX (transfer of xylose) was studied in cotyledons, rosette leaves, stem leaves and petals of Silene plants. These studies revealed that gG is expressed in all ontogenetic stages, whereas its allele gX is only expressed in the petals. In the vegetative parts of gX individuals 7-O -xylosylation is replaced by 7-O-galactosylation. The possibility that gX encodes an enzyme activity that catalyzes different reactions in the petals and the vegetative parts resulting in the accumulation of the 7-O-xyloside and the 7-O-galactoside respectively, has been disproved. It is shown that there are two different enzymes catalyzing the biosynthesis of isovitexin 7-O-galactoside. These 7-O -galactosyl-transferase activities differ with respect to heat inactivation, pH optimum , flavone acceptor specificity and Michaelis-Menten enzyme kinetic parameters. The genes controlling these enzyme activities are regulated differentially, with gene O7g (described previously by Steyns et al. [11]), expressed in the cotyledons and the rosette leaves and Xgal in the stem leaves and petals.

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Chemoprotective Effects of Propolis on Aflatoxin B1-Induced Hepatotoxicity in Rats: Oxidative Damage and Hepatotoxicity by Modulating TP53, Oxidative Stress

Current Proteomics ◽

10.2174/1570164617666190925121720 ◽

2020 ◽

Vol 17 (3) ◽

pp. 191-199

Author(s):

Seval Yilmaz ◽

Fatih Mehmet Kandemir ◽

Emre Kaya ◽

Mustafa Ozkaraca

Keyword(s):

Oxidative Stress ◽

Gene Expression ◽

Oxidative Damage ◽

Aflatoxin B1 ◽

Tp53 Gene ◽

Control Group ◽

Glutathione S Transferase ◽

Gene Expressions ◽

Cat Gene ◽

Gst Activity

Objective: This study aimed to detect hepatic oxidative damage caused by aflatoxin B1 (AFB1), as well as to examine how propolis protects against hepatotoxic effects of AFB1. Method: Rats were split into four groups as control group, AFB1 group, propolis group, AFB1+ propolis group. Results: There was significant increase in malondialdehyde (MDA) level and tumor suppressor protein (TP53) gene expression, Glutathione (GSH) level, Catalase (CAT) activity, CAT gene expression decreased in AFB1 group in blood. MDA level and Glutathione-S-Transferase (GST) activity, GST and TP53 gene expressions increased in AFB1 group, whereas GSH level and CAT activity alongside CAT gene expression decreased in liver. AFB1+propolis group showed significant decrease in MDA level, GST activity, TP53 and GST gene expressions, GSH level and CAT activity and CAT gene expression increased in liver compared to AFB1 group. Conclusion: These results suggest that propolis may potentially be natural agent that prevents AFB1- induced oxidative stress and hepatotoxicity.

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Antioxidant Enzyme Levels Inversely Covary with Hearing Loss After Amikacin Treatment

Journal of the American Academy of Audiology ◽

10.1055/s-0040-1715718 ◽

2003 ◽

Vol 14 (03) ◽

pp. 134-143 ◽

Cited By ~ 6

Author(s):

James J. Klemens ◽

Robert P. Meech ◽

Larry F. Hughes ◽

Satu Somani ◽

Kathleen C.M. Campbell

Keyword(s):

Hearing Loss ◽

Enzyme Activity ◽

Antioxidant Enzyme ◽

Guinea Pigs ◽

Auditory Brainstem ◽

Antioxidant Enzyme Activity ◽

Control Group ◽

Glutathione S Transferase ◽

Brainstem Response ◽

The Difference

This study's purpose was to determine if a correlation exists between cochlear antioxidant activity changes and auditory function after induction of aminoglycoside (AG) ototoxicity. Two groups of five 250-350 g albino guinea pigs served as subjects. For 28 days, albino guinea pigs were administered either 200 mg/kg/day amikacin, or saline subcutaneously. Auditory brainstem response testing was performed prior to the first injection and again before sacrifice, 28 days later. Cochleae were harvested and superoxide dismutase, catalase, glutathione peroxidase, glutathione-S-transferase, glutathione reductase activities and malondialdehyde levels were measured. All antioxidant enzymes had significantly lower activity in the amikacin group (p ≤ 0.05) than in the control group. The difference in cochlear antioxidant enzyme activity between groups inversely correlated significantly with the change in ABR thresholds. The greatest correlation was for the high frequencies, which are most affected by aminoglycosides. This study demonstrates that antioxidant enzyme activity and amikacin-induced hearing loss significantly covary.

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Effect of Pseudomonas moorei KB4 Cells’ Immobilisation on Their Degradation Potential and Tolerance towards Paracetamol

Molecules ◽

10.3390/molecules26040820 ◽

2021 ◽

Vol 26 (4) ◽

pp. 820

Author(s):

Robert Surma ◽

Danuta Wojcieszyńska ◽

Jagna Karcz ◽

Urszula Guzik

Keyword(s):

Protective Effect ◽

Kinetic Parameters ◽

Toxicity Assessment ◽

Bacterial Cells ◽

Low Concentrations ◽

Toxicity Analysis ◽

Immobilised Cells ◽

Degradation Activity ◽

High Concentrations ◽

The Hill

Pseudomonas moorei KB4 is capable of degrading paracetamol, but high concentrations of this drug may cause an accumulation of toxic metabolites. It is known that immobilisation can have a protective effect on bacterial cells; therefore, the toxicity and degradation rate of paracetamol by the immobilised strain KB4 were assessed. Strain KB4 was immobilised on a plant sponge. A toxicity assessment was performed by measuring the concentration of ATP using the colony-forming unit (CFU) method. The kinetic parameters of paracetamol degradation were estimated using the Hill equation. Toxicity analysis showed a protective effect of the carrier at low concentrations of paracetamol. Moreover, a pronounced phenomenon of hormesis was observed in the immobilised systems. The obtained kinetic parameters and the course of the kinetic curves clearly indicate a decrease in the degradation activity of cells after their immobilisation. There was a delay in degradation in the systems with free cells without glucose and immobilised cells with glucose. However, it was demonstrated that the immobilised systems can degrade at least ten succeeding cycles of 20 mg/L paracetamol degradation. The obtained results indicate that the immobilised strain may become a useful tool in the process of paracetamol degradation.

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