GSTA4 mediates reduction of cisplatin ototoxicity in female mice

説明

<jats:title>Abstract</jats:title><jats:p>Cisplatin is one of the most widely used chemotherapeutic drugs for the treatment of cancer. Unfortunately, one of its major side effects is permanent hearing loss. Here, we show that glutathione transferase α4 (GSTA4), a member of the Phase II detoxifying enzyme superfamily, mediates reduction of cisplatin ototoxicity by removing 4-hydroxynonenal (4-HNE) in the inner ears of female mice. Under cisplatin treatment, loss of<jats:italic>Gsta4</jats:italic>results in more profound hearing loss in female mice compared to male mice. Cisplatin stimulates GSTA4 activity in the inner ear of female wild-type, but not male wild-type mice. In female<jats:italic>Gsta4</jats:italic><jats:sup>−/−</jats:sup>mice, cisplatin treatment results in increased levels of 4-HNE in cochlear neurons compared to male<jats:italic>Gsta4</jats:italic><jats:sup>−/−</jats:sup>mice. In CBA/CaJ mice, ovariectomy decreases mRNA expression of<jats:italic>Gsta4</jats:italic>, and the levels of GSTA4 protein in the inner ears. Thus, our findings suggest that GSTA4-dependent detoxification may play a role in estrogen-mediated neuroprotection.</jats:p>

収録刊行物

  • Nature Communications

    Nature Communications 10 (1), 4150-, 2019-09-12

    Springer Science and Business Media LLC

被引用文献 (3)*注記

もっと見る

詳細情報 詳細情報について

問題の指摘

ページトップへ