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CN 34-1304/RISSN 1674-3679

Volume 27 Issue 4
Apr.  2023
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GUO Yaxin, XU Jiaying, WEI Wei, LI Deming, QIN Liqiang. Lactoferrin ameliorates radiation-induced intestinal injury in mice by regulating ferroptosis[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2023, 27(4): 465-470. doi: 10.16462/j.cnki.zhjbkz.2023.04.016
Citation: GUO Yaxin, XU Jiaying, WEI Wei, LI Deming, QIN Liqiang. Lactoferrin ameliorates radiation-induced intestinal injury in mice by regulating ferroptosis[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2023, 27(4): 465-470. doi: 10.16462/j.cnki.zhjbkz.2023.04.016

Lactoferrin ameliorates radiation-induced intestinal injury in mice by regulating ferroptosis

doi: 10.16462/j.cnki.zhjbkz.2023.04.016
Funds:

The National Natural Science Foundation of China 82073482

The National Natural Science Foundation of China 82173502

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  • Corresponding author: QIN Liqiang, E-mail: qinliqiang@suda.edu.cn
  • Received Date: 2022-09-08
  • Rev Recd Date: 2022-12-02
  • Available Online: 2023-04-28
  • Publish Date: 2023-04-10
  •   Objective  To explore the protective effect and mechanism of lactoferrin (Lf) on a radiation-induced intestinal injury.  Methods  Mice were randomly divided into the control group, 10 Gy group, and Lf+10 Gy group. On 7 d before irradiation, the Lf+10 Gy group was given 250 mg/kg Lf by gavage daily. Mice in the 10 Gy group and Lf+10 Gy group received 10 Gy abdominal irradiation. The mice were sacrificed 3.5 d after irradiation, and the samples were collected to determine the related indexes.  Results  Irradiation-induced intestinal injury. Lf intervention restored weight loss, hepatic oxidative stress, and pathological intestinal damage in mice. Lf significantly increased the number of Lgr5 and Ki67 positive cells, reflecting the proliferation and regeneration ability of small intestinal cells. Irradiation-induced ferroptosis in small intestinal tissue. Via the iron metabolism pathway, Lf intervention significantly downregulated the expression of intestinal divalent metal transporter (DMT1) and Fe2+ content; via the GSH/GPX4-lipid peroxidation pathway, Lf intervention significantly upregulated the intestinal solute carrier family 7 members (SLC7A11) and glutathione peroxidase 4 (GPX4) protein expression, downregulated acyl-CoA synthase long chain 4 (ACSL4) protein expression, and reduced malondialdehyde (MDA) levels.  Conclusions  Lf ameliorated radiation-induced intestinal injury, possibly due to the regulation of ferroptosis through iron metabolism and the GSH/GPX4-lipid peroxidation pathway.
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