Effect of haemin on growth, protein content and the antioxidant defence system in Trypanosoma cruzi

Parasitology ◽  
2007 ◽  
Vol 134 (7) ◽  
pp. 959-965 ◽  
Author(s):  
A. CICCARELLI ◽  
L. ARAUJO ◽  
A. BATLLE ◽  
E. LOMBARDO

SUMMARYA nutritional characteristic of trypanosomatid protozoa is that in vitro they need a haem-compound as a growth factor, which is supplied as haemoglobin, haematin or haemin. Because haemin and related porphyrins are an important source of oxidative stress in biological systems, the effect of haemin on growth, protein content and the antioxidant defence system in Trypanosoma cruzi was evaluated. We have observed that, in epimastigotes grown under different haemin concentrations in the culture medium (0–30 mg/l), 5 mg/l was the haemin concentration yielding optimum growth. Above 15 mg/l there was a clear decrease in growth rate, producing the epimastigote to amastigote transformation. Such morphological change was observed together with a marked injury of the enzymatic machinery of the parasite, leading to diminished protein synthesis as well as lower activity of the antioxidant enzymes (superoxide dismutase, ascorbate peroxidase and trypanothione reductase), reduced total thiol content and a marked increase in the HaemOx-1 activity and expression. The current work demonstrates that there is a correlation between higher haemin concentrations in the culture medium and oxidative damage in the cells. Under these conditions induction of HaemOx-1 would indicate the important role of this enzyme as an antioxidant defence response in Trypanosoma cruzi.

2017 ◽  
Vol 121 ◽  
pp. 153-160 ◽  
Author(s):  
Judit Dobránszki ◽  
Georgina Asbóth ◽  
Dávid Homoki ◽  
Piroska Bíró-Molnár ◽  
Jaime A. Teixeira da Silva ◽  
...  

Author(s):  
Augustine Apiamu ◽  
Samuel Ogheneovo Asagba ◽  
Nyerhovwo J. Tonukari

Abstract Background Cadmium (Cd) toxicity, which runs across the food chain, is chiefly regulated by in vivo antioxidant defence system or through antioxidant supplementation of biological systems predisposed to this environmental stressor. The present study was designed to examine the role of Anthocleista vogelii leaves in Cd-induced oxidative stress in the serum of Wistar rats through the application of response surface methodology (RSM) and biomonitoring of selective responses: malondialdehyde (MDA), catalase (CAT), superoxide dismutase (SOD), glutathione-s-transferase (GST) and peroxidase (POD) activities, respectively. The cold macerated plant leaves were subjected to fractionation process using methanol-hexane-chloroform (3:2:1 v/v) solvent system such that n-hexane fraction with ample antioxidant levels in terms of total phenolic content (TPC) and total flavonoid content (TFC) among others at p <  0.05 was selected for the study. The study employed central composite design (CCD) with twenty experimental “runs” of male Wistar rats for twenty-eight days, following a week of acclimatization, where n-hexane fraction of A. vogelii (NFAV), cadmium chloride (CdCl2) and body weights of rats were considered input factors in the study. Results The study generated five quadratic models, which differed significantly at p <  0.05 for MDA levels as well as CAT, SOD, GST and POD activities in the sera of Wistar rats. The study revealed that exposure to Cd toxicity caused a marked increase (p <  0.05) in serum MDA levels, but a significant inhibition (p <  0.05) of serum SOD, CAT, GST and POD activities. However, Cd interaction with NFAV showed marked amelioration of Cd-induced oxidative stress, which was confirmed by significant decrease in serum MDA levels, but significant increase in serum SOD, CAT, GST and POD activities at p <  0.05 via the response surface plots. The study also confirmed the reliability and adequacy of the models for accurate prediction of the responses since R-squared (R2) values obtained were greater than 90%. Conclusion It was inferred from the present study that the adequacy of the models validated the potency of A. vogelii leaves graphically in the amelioration of Cd-induced oxidative stress in the serum of Wistar rats. Hence, the plant was considered a rich source of bioactive compounds with significant antioxidant properties.


1996 ◽  
Vol 28 (6) ◽  
pp. 336-342 ◽  
Author(s):  
Yoshiji Ohta ◽  
Takashi Yamasaki ◽  
Takafumi Niwa ◽  
Katsuhiko Niimi ◽  
Yoshinao Majima ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
Rumyana Simeonova ◽  
Vessela Vitcheva ◽  
Magdalena Kondeva-Burdina ◽  
Ilina Krasteva ◽  
Vassil Manov ◽  
...  

The hepatoprotective potential of saponarin, isolated fromGypsophila trichotoma, was evaluatedin vitro/in vivousing a hepatotoxicity model of paracetamol-induced liver injury. In freshly isolated rat hepatocytes, paracetamol (100 μmol) led to a significant decrease in cell viability, increased LDH leakage, decreased levels of cellular GSH, and elevated MDA quantity. Saponarin (60–0.006 μg/mL) preincubation, however, significantly ameliorated paracetamol-induced hepatotoxicity in a concentration-dependent manner. The beneficial effect of saponarin was also observedin vivo. Rats were challenged with paracetamol alone (600 mg/kg, i.p.) and after 7-day pretreatment with saponarin (80 mg/kg, oral gavage). Paracetamol toxicity was evidenced by increase in MDA quantity and decrease in cell GSH levels and antioxidant defence system. No changes in phase I enzyme activities of AH and EMND and cytochrome P 450 quantity were detected. Saponarin pretreatment resulted in significant increase in cell antioxidant defence system and GSH levels and decrease in lipid peroxidation. The biochemical changes are in good correlation with the histopathological data. Protective activity of saponarin was similar to the activity of positive control silymarin. On the basis of these results, it can be concluded that saponarin exerts antioxidant and hepatoprotective activity against paracetamol liver injuryin vitro/in vivo.


2020 ◽  
Vol 69 ◽  
pp. 105001
Author(s):  
Mattia Acito ◽  
Desirée Bartolini ◽  
Maria Rachele Ceccarini ◽  
Carla Russo ◽  
Samuele Vannini ◽  
...  

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