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Sodium butyrate ameliorates lipopolysaccharide‐induced cow mammary epithelial cells from oxidative stress damage and apoptosis
Author(s) -
Li Lin,
Wang HuanHuan,
Nie XinTian,
Jiang WanRu,
Zhang YuanShu
Publication year - 2019
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.27565
Subject(s) - protein kinase b , sodium butyrate , oxidative stress , superoxide dismutase , pi3k/akt/mtor pathway , ly294002 , apoptosis , lipopolysaccharide , chemistry , glutathione peroxidase , caspase 3 , microbiology and biotechnology , biology , biochemistry , endocrinology , programmed cell death , gene
Abstract This study investigated the molecular mechanism by which sodium butyrate (NaB) causes oxidative stress damage induced by lipopolysaccharide (LPS) on cow mammary epithelial cells (MAC‐T). We found that NaB significantly increased the activities of antioxidant enzymes, including superoxide dismutase, glutathione peroxidase, catalase, peroxidase, and total antioxidant capacity and decreased the reactive oxygen species production in LPS‐induced MAC‐T cells. NaB attenuated protein damage and reduced apoptosis in LPS‐induced MAC‐T cells. The messenger RNA (mRNA) levels of caspase‐3, caspase‐9, and Bax decreased, while the Bcl‐2 mRNA level increased in LPS‐induced MAC‐T cells treated with NaB. Our results showed that NaB treatment increased the phosphoinositide 3‐kinase (PI3K) and phospho‐AKT (P‐AKT) protein levels, whereas it decreased the Bax, caspase‐3, and caspase‐9 protein levels in LPS‐induced MAC‐T cells. However, the increase in PI3K and P‐AKT protein levels and the decrease in Bax, caspase‐3, and caspase‐9 protein levels induced by NaB treatment were reversed when the cells were pretreated with LY294002 (PI3K inhibitor). These results indicate that NaB ameliorates LPS‐induced oxidative damage by increasing antioxidative enzyme activities and ameliorating protein damage in MAC‐T cells. In addition, NaB decreased apoptosis by inhibiting caspase‐3, caspase‐9, and Bax protein levels, and this action was mainly achieved via activation of the PI3K/AKT signaling pathways in LPS‐induced MAC‐T cells. These results provide substantial information for NaB as a chemical supplement to treat oxidative stress and its related diseases in ruminants.