TY - JOUR
T1 - L-2-Oxothiazolidine-4-carboxylic acid mitigates the thromboembolic effects and systemic toxicity induced by sub-acute exposure to cadmium in mice
AU - Fahim, Mohamed Abdelmonem
AU - Nemmar, Abderrahim
AU - Singh, Sarabjit
AU - Shafiullah, Mohamed
AU - Yasin, Javed
AU - Hasan, Mohamed Yousif
N1 - Publisher Copyright:
© 2016, E-Century Publishing Corporation. All rights reserved.
PY - 2016/8/30
Y1 - 2016/8/30
N2 - Exposure to cadmium (Cd) as a result of its environmental pervasiveness poses deleterious health effects, which has been attributed to oxidative stress. Therefore, this study aims to examine the sub-acute (1 mg Cd/kg/day, i.p., for 3 weeks) systemic and thrombotic influence of Cd exposure in vivo, and to assess the protective effects of the antioxidant L-2-Oxothiazolidine-4-Carboxylic acid (OTC, 80 mg/kg/day, i.p.). Cd compared with control group significantly reduced both the time for the first platelet aggregate and until blood flow stopped in pial microvessels. OTC significantly increased both the time for the first aggregate and until flow stopped. Cd induced a significant increase in total WBC, CK, AST, and LDH. The antioxidants SOD and catalase activities significantly increased in mice treated with Cd. OTC, through its antioxidant actions, appeared to effectively protect Cd induced thrombosis in mice. Hence, OTC represents a potential protective candidate from the detrimental effect of Cd toxicity.
AB - Exposure to cadmium (Cd) as a result of its environmental pervasiveness poses deleterious health effects, which has been attributed to oxidative stress. Therefore, this study aims to examine the sub-acute (1 mg Cd/kg/day, i.p., for 3 weeks) systemic and thrombotic influence of Cd exposure in vivo, and to assess the protective effects of the antioxidant L-2-Oxothiazolidine-4-Carboxylic acid (OTC, 80 mg/kg/day, i.p.). Cd compared with control group significantly reduced both the time for the first platelet aggregate and until blood flow stopped in pial microvessels. OTC significantly increased both the time for the first aggregate and until flow stopped. Cd induced a significant increase in total WBC, CK, AST, and LDH. The antioxidants SOD and catalase activities significantly increased in mice treated with Cd. OTC, through its antioxidant actions, appeared to effectively protect Cd induced thrombosis in mice. Hence, OTC represents a potential protective candidate from the detrimental effect of Cd toxicity.
KW - Cadmium
KW - Kidney
KW - Liver
KW - OTC
KW - Thrombosis
KW - Toxicology
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M3 - Article
AN - SCOPUS:84985943053
SN - 1940-5901
VL - 9
SP - 15764
EP - 15771
JO - International Journal of Clinical and Experimental Medicine
JF - International Journal of Clinical and Experimental Medicine
IS - 8
ER -