Protective effects of lycorine against carbon tetrachloride induced hepatotoxicity in Swiss albino mice

2011 ◽  
Vol 26 (3) ◽  
pp. 393-401 ◽  
Author(s):  
S. Ilavenil ◽  
B. Kaleeswaran ◽  
S. Ravikumar
2011 ◽  
Vol 3 (8) ◽  
pp. 680-684 ◽  
Author(s):  
Faiza Rifat ◽  
◽  
Archana Sharma ◽  
Preeti Srivastava ◽  
Shikha Patni ◽  
...  

2017 ◽  
Vol 487 (1) ◽  
pp. 62-67 ◽  
Author(s):  
Hoda Aayadi ◽  
Smriti P.K. Mittal ◽  
Anjali Deshpande ◽  
Makarand Gore ◽  
Saroj S. Ghaskadbi

Nefrología ◽  
2016 ◽  
Vol 36 (6) ◽  
pp. 643-652 ◽  
Author(s):  
Badr Abdullah Aldahmash ◽  
Doaa Mohamed El-Nagar ◽  
Khalid Elfakki Ibrahim

Mutagenesis ◽  
2006 ◽  
Vol 21 (1) ◽  
pp. 61-66 ◽  
Author(s):  
R.M. Samarth ◽  
Meenakshi Panwar ◽  
Madhu Kumar ◽  
Ashok Kumar

2018 ◽  
Vol 10 (2) ◽  
pp. 548-552
Author(s):  
Mohammad Firoz Alam

The present study targeted the brain mitochondria dysfunction in Swiss albino mice through carbon tetrachloride intoxication and its treatment with Zingerone. It is proposed that brain mitochondria is the main organelle responsible for oxidative stress by producing  reactive oxygen species (ROS). Swiss albino mice were divided into four groups; Group-1 was control; Group-2 was carbon tetrachloride (CCl4) toxic (1.5mg kg-1 bm i.p two days in a week.); Group-3 was pretreated with Zingerone (100 mg kg-1 b.m)  a day before  the administration of CCl4 and Group-4 was only Zingerone (100 mg kg-1 bm) given orally for 15days once in a day. At the end of the experiment mice were sacrificed and mitochondria were isolated from brain. Isolated brain mitochondria were further analyzed for oxidative stress marker. Thiobarbituric acid reactive substance (TBARS) content was increased significantly by CCl4 administration in Group-II as compared to the control Group-I, while the antioxidant (GSH) and other antioxidant enzyme GPx , GR, and CAT was depleted significantly in CCl4 treated Group-II as compare to control Group-I. Zingerone protected the  toxicity of brain mitochondria by reducing the lipid peroxidation and enhancing the antioxidant enzyme in Group-III and there was no significant changes were noticed in Group-IV as  compared to Group-I. Overall results showed the potential effects of Zingerone in protecting the neuronal cell loss by oxidative stress. Thus, the  present study indicated that the Zingerone may be used as the potential therapeutic tools for the prevention of CCl4 induced brain mitochondrial toxicity.  


2003 ◽  
Vol 17 (6) ◽  
pp. 614-617 ◽  
Author(s):  
K. Premkumar ◽  
Suresh K. Abraham ◽  
S. T. Santhiya ◽  
A. Ramesh

2018 ◽  
Vol 2018 ◽  
pp. 1-7 ◽  
Author(s):  
Mohammed M. Safhi

The protective effects of Zingerone against CCl4 induced nephrotoxicity in Swiss albino mice via modulation of metabolizing enzyme, oxidative stress, inflammatory cytokines, and apoptosis. The biochemical estimation indicated that the BUN and creatinine were significantly increased in group 2 (CCl4) compared to group 1 (normal) which was significantly reduced after treatment with Zingerone in group 3 when compared with group 2. The CCl4 treatment has significantly increased TBARS levels and reduced the antioxidant enzyme such as GSH, GPx, GR, GST, CAT, and SOD in group 2 compared to group 1, while the Zingerone treatment showed significant reduction in TBARS levels and increased the antioxidant enzymes in group 3 (CCl4 + Zingerone) as compared to group 2. Similarly, it was observed that CCl4 significantly increased the cytokines such as IL-1β, IL-2, and TNFα levels in group 2 as compared to group 1. The treatment with Zingerone significantly attenuated the levels of IL-1β, IL-2, and TNFα in group 3 compared to group 2. Caspase 3 and caspase 9 were also significantly increased in CCl4-treated group 2, whereas Zingerone treatment significantly reduced the elevated levels of caspases 3 and 9 in group 3 compared to group 2.


2011 ◽  
Vol 50 (2) ◽  
pp. 271-280 ◽  
Author(s):  
Amit Kunwar ◽  
S. Jayakumar ◽  
H. N. Bhilwade ◽  
P. P. Bag ◽  
H. Bhatt ◽  
...  

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