4.5 Article

Polysaccharides from Laminaria japonica protect memory abilities and neurogenesis in mice after cranial irradiation through ameliorating neuroinflammation and collagen IV degradation

期刊

INTERNATIONAL JOURNAL OF RADIATION BIOLOGY
卷 98, 期 11, 页码 1609-1618

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/09553002.2022.2063961

关键词

Polysaccharides from laminaria japonica; cognitive function; neurogenesis; microglia; collagen IV; radiation-induced brain injury

资金

  1. National Nature Science Foundation of China [81460479]
  2. Natural Science Foundation of Guangxi Zhuang [2018GXNSFAA281299]

向作者/读者索取更多资源

Laminaria japonica polysaccharides (LJP) have a neuroprotective effect on radiation-induced brain injury mice by preventing neurogenesis damage and alleviating neuroinflammation and collagen IV degradation.
Background Radiation-induced brain injury (RIBI) is one of the most common long-term complications for patients with malignant brain tumors after radiotherapy. At present, there is no effective treatment for RIBI. Recent studies have also confirmed that polysaccharides from laminaria japonica (LJP) display potential neuroprotective function. However, its mechanisms of neuroprotection remain unclear. Aim In this study, we aimed to explore the effect and underlying mechanism of LJP on neurogenesis in radiation-induced brain injury mice. Methods SPF two-month-old male mice were randomly divided into control group (Con), LJP treatment group (LJP), irradiation group (IR), and irradiation with LJP treatment group (IR + LJP). LJP (40 mg/kg/day) was intraperitoneally injected at one day before radiation for seven consecutive days (once daily). The mice were exposed to 10 Gy x 2 fractionated doses, once every other day, with a total dose of 20 Gy. Changes in cognitive function of mice following radiation were evaluated by the Morris water maze test. Furthermore, body weight and general status of mice were measured throughout the experiment. Immunohistochemical staining for neural proliferating cells (Ki67+ cells) and immature neurons (DCX + cells) was utilized to assay changes of neurogenesis in hippocampus. Microglial activation and collagen IV deposition within the neurogenic microenvironment were observed respectively by immunohistochemical staining for Iba-1 and Collagen IV in the hippocampus. Levels of pro-inflammatory cytokines (TNF-alpha and IL-1 beta) in the hippocampus were detected by ELISA kits post-radiation. Results Morris water maze test showed that LJP therapy markedly reduced the escape latency and increased the times of crossing platform and percent time of the target quadrant in the radiated mice. In addition, the decrease of the neural proliferating cells (Ki67+ cells) and immature neurons (DCX + cells) in the hippocampus of mice following irradiation was significantly mitigated by the LJP treatment, suggesting that LJP could prevent from neurogenesis damage after irradiation. LJP injection significantly attenuated degradation of collagen IV, activation of microglia, and increase of pro-inflammatory cytokines (TNF-alpha and IL-1 beta) levels in the neurogenic microenvironment of the hippocampus after radiation. Conclusion These findings suggest that LJP early treatment may mitigate radiation-induced cognitive impairments and that its mechanism may relate to its protection of neurogenesis by alleviating neuroinflammation and collagen IV degradation within the neurogenic microenvironment.

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