4.3 Article

Resolvin D1 protects against cadmium chloride-induced memory loss and hippocampal damage in rats: A comparison with docosahexaenoic acid

期刊

HUMAN & EXPERIMENTAL TOXICOLOGY
卷 40, 期 12_SUPPL, 页码 S215-S232

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SAGE PUBLICATIONS LTD
DOI: 10.1177/09603271211038739

关键词

Docosahexaenoic acid; resolvin D1; hippocampus; memory; Nrf2; Cadmium; NF-kB

资金

  1. King Khalid University, Abha, KSA [R.G.P.1/88/41]

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The study showed that DHA-rich diet or RVD1 treatment significantly increased the levels of DHA and RVD1 in the hippocampus of CdCl2-treated rats, improving memory function and hippocampal structure while decreasing levels of oxidative stress markers. RVD1 was more effective than DHA in preventing CdCl2-induced memory loss and hippocampal damage in rats.
Background Intoxication with cadmium (Cd) ions leads to hippocampal damage and cognitive impairment. However, omega-3 polyunsaturated fatty acids (n-3 PUFAs) exert neuroprotective effects in different animal models of neurodegeneration. Purpose This study compared the neuroprotective effect of the n-3 PUFA, docosahexaenoic acid (DHA), and its downstream metabolite, resolvin D1 (RVD1), on hippocampal damage and memory deficits in cadmium chloride (CdCl2)-treated rats. Research design Control or CdCl2 (0.5 mg/kg)-treated rats were subdivided into three groups (n = 18/each) and treated for 6 weeks as follows: (1) fed control diet, (2) fed DHA-rich diets (0.7 g/100 g), or (3) treated with RVD1 (0.2 mu g/kg, i.p). Results Treatment with a DHA-rich diet or RVD1 significantly increased the levels of docosahexaenoic acid and RVD1, respectively, in the hippocampal of CdCl2-treated rats without affecting the reduction in the expression of the 15-lipooxygenase-1 (ALOX15). These effects were associated with improvements in rats' memory function and hippocampal structure, as well as a redction in the hippocampal levels of reactive oxygen species (ROS), malondialdehyde (MDA), tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6), nuclear localization of the nuclear factor-kappa beta p65 (NF-kappa B p65), and expression of cleaved caspase-3. Concomitantly, hippocampi of both groups of rats showed significantly higher levels of Bcl-2, superoxide dismutase (SOD), and glutathione (GSH), as well as enhanced nuclear levels of the nuclear factor erythroid 2-related factor 2 (Nrf-2). The effects of RVD1 on all these markers in the CdCl2-induced rats were more profound than those of DHA. Also, the increase in the nuclear protein levels of Nrf-2 and the decrease in the levels of Bax and nuclear protein levels of NF-kappa B p65 were only seen in the hippocampal of CdCl2 + RVD1-treated rats. Conclusion RVD1 is more powerful than DHA in preventing CdCl2-induced memory loss and hippocampal damage in rats.

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