<i>N</i>-Acetylcysteine Reverses Monocrotophos Exposure-Induced Hepatic Oxidative Damage via Mitigating Apoptosis, Inflammation and Structural Changes in Rats

Oxidative stress-mediated tissue damage is primarily involved in hepatic injuries and dysfunctioning. Natural antioxidants have been shown to exert hepatoprotective, anti-inflammatory and antiapoptotic properties. The present study evaluated the effect of <i>N</i>-acetylcysteine (NAC) ag...

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Main Authors: Jagjeet Singh (Author), Annu Phogat (Author), Chandra Prakash (Author), Sunil Kumar Chhikara (Author), Sandeep Singh (Author), Vinay Malik (Author), Vijay Kumar (Author)
Format: Book
Published: MDPI AG, 2021-12-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Jagjeet Singh  |e author 
700 1 0 |a Annu Phogat  |e author 
700 1 0 |a Chandra Prakash  |e author 
700 1 0 |a Sunil Kumar Chhikara  |e author 
700 1 0 |a Sandeep Singh  |e author 
700 1 0 |a Vinay Malik  |e author 
700 1 0 |a Vijay Kumar  |e author 
245 0 0 |a <i>N</i>-Acetylcysteine Reverses Monocrotophos Exposure-Induced Hepatic Oxidative Damage via Mitigating Apoptosis, Inflammation and Structural Changes in Rats 
260 |b MDPI AG,   |c 2021-12-01T00:00:00Z. 
500 |a 10.3390/antiox11010090 
500 |a 2076-3921 
520 |a Oxidative stress-mediated tissue damage is primarily involved in hepatic injuries and dysfunctioning. Natural antioxidants have been shown to exert hepatoprotective, anti-inflammatory and antiapoptotic properties. The present study evaluated the effect of <i>N</i>-acetylcysteine (NAC) against monocrotophos (MCP) exposure-induced toxicity in the rat liver. Albino Wistar rats were divided into four groups: (1) control, (2) NAC-treated, (3) MCP-exposure, (4) NAC and MCP-coexposure group. The dose of MCP (0.9 mg/kg b.wt) and NAC (200 mg/kg b.wt) were administered orally for 28 days. Exposure to MCP caused a significant increase in lipid peroxidation, protein oxidation and decreased glutathione content along with the depletion of antioxidant enzyme activities. Further MCP exposure increased pro-inflammatory cytokines levels and upregulated Bax and Caspase-3 expressions. MCP exposure also caused an array of structural alternations in liver tissue, as depicted by the histological and electron microscopic analysis. Thepretreatment of NAC improved glutathione content, restored antioxidant enzyme activities, prevented oxidation of lipids and proteins, decreased pro-inflammatory cytokines levels and normalized apoptotic protein expression. Treatment of NAC also prevented histological and ultrastructural alternations. Thus, the study represents the therapeutic efficacy and antioxidant potential of NAC against MCP exposure in the rat liver. 
546 |a EN 
690 |a <i>N</i>-acetylcysteine 
690 |a hepatic oxidative stress 
690 |a monocrotophos 
690 |a antioxidants 
690 |a apoptosis 
690 |a inflammation 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Antioxidants, Vol 11, Iss 1, p 90 (2021) 
787 0 |n https://www.mdpi.com/2076-3921/11/1/90 
787 0 |n https://doaj.org/toc/2076-3921 
856 4 1 |u https://doaj.org/article/792a044273954ec3b51a9a85c50cc4ed  |z Connect to this object online.