Squid ink polysaccharide reduces cyclophosphamide-induced testicular damage via Nrf2/ARE activation pathway in mice

نویسندگان

  • Huazhong Liu College of Science, Guangdong Ocean University, Zhanjiang, China
  • Ping Luo College of Science, Guangdong Ocean University, Zhanjiang, China
  • Xiaoyan Le College of Science, Guangdong Ocean University, Zhanjiang, China
  • Yexing Tao College of Science, Guangdong Ocean University, Zhanjiang, China
  • Yipeng Gu College of Science, Guangdong Ocean University, Zhanjiang, China
چکیده مقاله:

Objective(s):Cyclophosphamide (CP) toxicity on testis was hampered by squid ink polysaccharide (SIP) via restoration of antioxidant ability in our previous investigations. This study investigated roles of Nrf2/ARE signal pathway in testis of treated mice. Materials and Methods: Male Kunming mice were employed to undergo treatment with SIP and/or CP. Protein levels of Nrf2, keap-1, histone deacetylase 2 (HDAC2), quinone oxidoreductase 1 (NQO-1), and heme oxygenase 1 (HO-1) and phosphorylation level of protein kinase C (PKC) in testis were evaluated by Western blotting. Results: Data showed that SIP elevated expressions of NQO-1 and HO-1 genes, two downstream target molecules of Nrf2, via activating Nrf2 to play preventive roles on CP-treated testis, and further discovered that upstream regulators of Nrf2, keap-1, HDAC2, and PKC, were concerned with the regulation of Nrf2. Conclusion: These results suggest that SIP could effectively weaken CP-associated testicular damage via Nrf2/ARE signal pathway.

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squid ink polysaccharide reduces cyclophosphamide-induced testicular damage via nrf2/are activation pathway in mice

objective(s):cyclophosphamide (cp) toxicity on testis was hampered by squid ink polysaccharide (sip) via restoration of antioxidant ability in our previous investigations. this study investigated roles of nrf2/are signal pathway in testis of treated mice. materials and methods: male kunming mice were employed to undergo treatment with sip and/or cp. protein levels of nrf2, keap-1, histone deace...

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عنوان ژورنال

دوره 18  شماره 8

صفحات  827- 831

تاریخ انتشار 2015-08-01

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