Showing posts with label GST. Show all posts
Showing posts with label GST. Show all posts

Monday, 15 September 2025

Investigation of the Role of Oxidative Stress-Related Genetic Variants in Type 2 Diabetes Mellitus-associated Nephropathy | Chapter 9 | Recent Developments in Chemistry and Biochemistry Research Vol. 3

The present study investigates the role of oxidative stress-related genetic variants in type 2 diabetes mellitus-associated nephropathy. Type 2 diabetes is thought to be associated with microvascular complications that comprise retinopathy, nephropathy, and neuropathy. Oxidative stress is a predominant factor involved in the pathogenesis of DN and alters metabolic endeavour and its hemodynamic pathways, which have varied correlations with renal problems, one of which is diabetic nephropathy, which leads to end-stage renal disease. Renal injury in DN occurs primarily through oxidative stress, which disrupts metabolic and hemodynamic pathways. Hyperglycemia is regarded as a hallmark feature of diabetes that increases reactive oxygen species generation, which eventually leads to increased oxidative stress, and this is considered the most essential event in the onset of DN. To prevent tubular injury in DN, antioxidants can be used to combat oxidative stress, which is primarily caused by several pathways. The most significant antioxidative enzymes are superoxide dismutase, catalase, glutathione-S-transferase, and glutathione peroxidase. As a result, this chapter emphasizes antioxidant gene polymorphisms and hypothesizes that these antioxidant genes may be an essential component of DN pathogenesis. Moreover, this chapter also retorts to the research questions raised by the physicians and illustrates the importance of regional population studies on detecting the SNPs of antioxidant genes and targeting therapeutic approaches aiding to lessen the severity of the disease at its initial stages.

 

 

Author(s) Details

Farhana Begum

Department of Biochemistry, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Kelambakkam, Tamil Nadu 603103, India.

Karpagavel Lakshmanan

Research and Education, Kelambakkam, Tamil Nadu 603103, India.

Please see the book here:- https://doi.org/10.9734/bpi/rdcbr/v3/297

Thursday, 25 July 2024

Investigation of the Role of Oxidative Stress-Related Genetic Variants in Type 2 Diabetes Mellitus-associated Nephropathy | Chapter 9 | Recent Developments in Chemistry and Biochemistry Research Vol. 3

The present study investigates the role of oxidative stress-related genetic variants in type 2 diabetes mellitus-associated nephropathy. Type 2 diabetes is thought to be associated with microvascular complications that comprise retinopathy, nephropathy, and neuropathy. Oxidative stress is a predominant factor involved in the pathogenesis of DN and alters metabolic endeavour and its hemodynamic pathways, which have varied correlations with renal problems, one of which is diabetic nephropathy, which leads to end-stage renal disease. Renal injury in DN occurs primarily through oxidative stress, which disrupts metabolic and hemodynamic pathways. Hyperglycemia is regarded as a hallmark feature of diabetes that increases reactive oxygen species generation, which eventually leads to increased oxidative stress, and this is considered the most essential event in the onset of DN. To prevent tubular injury in DN, antioxidants can be used to combat oxidative stress, which is primarily caused by several pathways. The most significant antioxidative enzymes are superoxide dismutase, catalase, glutathione-S-transferase, and glutathione peroxidase. As a result, this chapter emphasizes antioxidant gene polymorphisms and hypothesizes that these antioxidant genes may be an essential component of DN pathogenesis. Moreover, this chapter also retorts to the research questions raised by the physicians and illustrates the importance of regional population studies on detecting the SNPs of antioxidant genes and targeting therapeutic approaches aiding to lessen the severity of the disease at its initial stages.


Author(s) Details:

Farhana Begum,
Department of Biochemistry, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Kelambakkam, Tamil Nadu 603103, India.

Dr. Karpagavel Lakshmanan
Department of Biochemistry, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Kelambakkam, Tamil Nadu 603103, India.

Please see the link here: https://doi.org/10.9734/bpi/rdcbr/v3/297

Friday, 26 November 2021

Elevation of Glutathione-S-transferase and Inhibition of Cholinesterase Activity as a Biomarkers of Fungicide Toxicity in Mosquitofish Gambusia affinis: Experimental Investigation | Chapter 3 | New Visions in Biological Science Vol. 6

 Due to their longevity in the environment and possible impacts, pesticides have become a serious environmental problem. As a result of the effects of these chemicals, aquatic populations are vanishing all over the world. Water, in particular, is a key contamination carrier. In this study, the toxicity of ARTEA 330EC, a systemic fungicide that is being used for the first time in Algeria to combat grain pests, is assessed using two biochemical parameters: glutathione-S-transferase and cholinesterase. Gambusia affinis specimens were treated with ARTEA 330EC doses of 25, 50, 75, and 100 ppm. The average weight and size of exposed specimens have both fallen dramatically, according to the findings. Parallel to a decrease in the average rate of GSH, biochemical parameter monitoring revealed a considerable stimulating protein (Synthesis) connected with GST activity stimulation. The three fungicide concentrations show a considerable increase of acetylcholinesterase activity (25, 50 and 75ppm). Finally, our data imply that the rise in GST observed in connection with acetylcholinesterase inhibition could be used as toxicity indicators. Fungicide ARTEA 330EC in Gambusia affinis


Author(S) Details

N. Bourenane Bouhafs
Laboratoire de toxicologie cellulaire, faculté des sciences, Département de biologie, Université Badji Mokhtar, Annaba, 23000. Algérie.

M. R. Djebbar
Laboratoire de toxicologie cellulaire, faculté des sciences, Département de biologie, Université Badji Mokhtar, Annaba, 23000. Algérie.

H. Berebbeh
Laboratoire de toxicologie cellulaire, faculté des sciences, Département de biologie, Université Badji Mokhtar, Annaba, 23000. Algérie.

View Book:- https://stm.bookpi.org/NVBS-V6/article/view/4857