Nanocurcumin Restores Arsenic-Induced Disturbances in Neuropharmacological Activities in Wistar Rats

化学 谷胱甘肽 亚砷酸钠 谷胱甘肽过氧化物酶 超氧化物歧化酶 抗氧化剂 砷毒性 脂质过氧化 药理学 氧化应激 谷胱甘肽还原酶 过氧化氢酶 内科学 内分泌学 生物化学 医学 有机化学
作者
N. Nithyashree,N. Tejo Prakash,Prashantkumar Waghe,CR Santhosh,B. H. Pavithra,Rashmi Rajashekaraiah,M. L. Sathyanarayana,U. Sunilchandra,Kranthi Kumar Ch,Shilpa Manjunatha,Muralidhar Yegireddy,G. R. Shivaprasad
出处
期刊:Toxicology International [Medknow Publications]
卷期号:: 429-445
标识
DOI:10.18311/ti/2022/v29i3/30342
摘要

The present study was carried out to examine the ameliorative potential of nanocurcumin against arsenic induced (sub-chronic) alterations in central nervous system in male Wistar rats. Nanocurcumin was synthesised and the hydrodynamic diameter, zeta potential and particle size were~76.60 nm, (-) 30 mV and 95nm, respectively. Experimental rats sub-chronically exposed to sodium (meta) arsenite (As; 10 mg.kg-1; 70 days; p.o) induced significant (p<0.05) reduction in superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase, glutathione and favoured free radical generation and induced lipid peroxidation in brain tissue. The exposure resulted in significant (p<0.05) decrease in voluntary- and involuntary motor activities and enhanced anxiety levels. However, experimental rats receiving nanocurcumin (15 mg.kg-1; p.o) showed significant (p<0.05) recovery in enzymatic - and non-enzymatic antioxidant defence system and restoration of redox balance and overcome arsenic induced depression in motor activities and elevated anxiety levels. Further, Arsenic induced elevation in pro-inflammatory cytokines, cyclooxygenase-2 activity and prostaglandin-E2 in brain and angiotensin-II levels (plasma) was significantly (p<0.05) ameliorated by nanocurcumin. Additionally, quantitative real -time polymerase chain reaction revealed a fivefold decrease in Nox2 expression in brain following nanocurcumin administration. Thus, the study concludes that nanocurcumin can serve as a potential therapeutic candidate to counter arsenic induced redox imbalance and neuropharmacological disturbances and there exists a vast scope to exploit its utility after appropriate clinical modelling.
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