Attenuation of Potassium Bromate-Induced Nephrotoxicity by Coumarin (1,2-Benzopyrone) in Wistar Rats: Chemoprevention Against Free Radical-Mediated Renal Oxidative Stress and Tumor Promotion Response

2005 ◽  
Vol 174 (6) ◽  
pp. 2145-2145 ◽  
Author(s):  
Fray F. Marshall
2012 ◽  
Vol 13 (9) ◽  
pp. 4393-4402 ◽  
Author(s):  
Oday O. Hamiza ◽  
Muneeb U. Rehman ◽  
Mir Tahir ◽  
Rehan Khan ◽  
Abdul Quaiyoom Khan ◽  
...  

2001 ◽  
Vol 88 (6) ◽  
pp. 294-299 ◽  
Author(s):  
Naghma Khan ◽  
Sonia Sharma ◽  
Aftab Alam ◽  
Mohammad Saleem ◽  
Sarwat Sultana

2019 ◽  
Vol 2019 ◽  
pp. 1-15 ◽  
Author(s):  
Anna Zalewska ◽  
Dominika Ziembicka ◽  
Małgorzata Żendzian-Piotrowska ◽  
Mateusz Maciejczyk

Oxidative stress plays a crucial role in the salivary gland dysfunction in insulin resistance; however, the cause of increased free radical formation in these conditions is still unknown. Therefore, the aim of the study was to investigate the effect of high-fat diet (HFD) on the mitochondrial respiratory system, prooxidant enzymes, ROS production, and nitrosative/oxidative stress in the submandibular and parotid glands of rats. The experiment was performed on male Wistar rats divided into two groups (n=10): control and HFD. The 8-week feeding of HFD affects glucose metabolism observed as significant increase in plasma glucose and insulin as well as HOMA-IR as compared to the control rats. The activity of mitochondrial Complex I and Complex II+III was significantly decreased in the parotid and submandibular glands of HFD rats. Mitochondrial cytochrome c oxidase (COX) activity and the hydrogen peroxide level were significantly increased in the parotid and submandibular glands of the HFD group as compared to those of the controls. HFD rats also showed significantly lower reduced glutathione (GSH) and reduced : oxidized glutathione (GSH : GSSG) ratio, as well as a higher GSSG level in the parotid glands of HFD rats. The activity of NADPH oxidase, xanthine oxidase, and levels of oxidative/nitrosative stress (malonaldehyde, nitric oxide, nitrotyrosine, and peroxynitrite) and inflammation/apoptosis (interleukin-1βand caspase-3) biomarkers were statistically elevated in the HFD group in comparison to the controls. HFD impairs mitochondrial function in both types of salivary glands by enhancing ROS production, as well as stimulating inflammation and apoptosis. However, free radical production, protein nitration, and lipid peroxidation were more pronounced in the parotid glands of HFD rats.


2001 ◽  
Vol 88 (6) ◽  
pp. 294-299 ◽  
Author(s):  
Naghma Khan ◽  
Sonia Sharma ◽  
Aftab Alam ◽  
Mohammad Saleem ◽  
Sarwat Sultana

Author(s):  
Adeola Temitope Salami ◽  
Gloria Enevwo Okotie ◽  
Precious Nekachi Echendu ◽  
Akapmu Uwaifoh ◽  
Samuel Babafemi Olaleye

Potassium bromate (KBrO3) present in consumed ozonised water was recently documented to exacerbate experimental gastric ulcer. Report is however vague as regards its effects in the colon; where water reabsorption occurs. In this study, we observed the possible effects of KBrO3 on oxidative stress and inflammatory biomarkers in NaOH induced crohn’s colitis. Wistar rats (180-200g) were divided into 6 groups (n=10); 1-control, 2-untreated crohn’s colitis (induced by 1.4% NaOH; intra-rectal administration) and 3-6: crohn’s colitis treated with vitamin E, KBrO3, vitamin E+KBrO3 and sulphazalazine respectively for seven days. Body weight and stool score were monitored daily. By 3 and 7, excised colon was evaluated for ulcer scores, biochemical and histological analysis. Collected blood samples on days 3 and 7 were assayed for haematological indices using standard methods. Data were subjected to ANOVA and p ≤0.05 considered significant. Platelet/lymphocyte ratio, colonic ulcer score, , malondialdehyde and mast cells were significantly decreased while colonic sulfhydryl, Ca2+ and Na+/K+ ATPase activities were increased following KBrO3 treatment compared with crohn’s colitis untreated. Findings suggest that KBrO3 may mitigate against NaOH induced crohn’s colitis via inhibiting mast cell population, oxidative and inflammatory content but stimulating colonic sulfhydryl, Ca2+ and Na+/K+ ATPase activities.


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