4.7 Article

3,3′-Diindolylmethane Supplementation Maintains Oocyte Quality by Reducing Oxidative Stress and CEP-1/p53-Mediated Regulation of Germ Cells in a Reproductively Aged Caenorhabditis elegans Model

期刊

ANTIOXIDANTS
卷 11, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/antiox11050950

关键词

3,3 '-diindolylmethane; antioxidant; reproductive aging; oocyte quality; CEP-1/p53; germ cell apoptosis; germ cell proliferation; mitochondrial function; oxidative stress; Caenorhabditis elegans

资金

  1. National Research Foundation of Korea (NRF) - Korean Ministry of Science and ICT [NRF-2021R1A2C1011658]
  2. KIST intramural grant [2Z06482, 2E31881]

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In this study, the effects of 3,3'-diindolylmethane (DIM) on oocyte quality and reproductive aging were investigated in a model organism. DIM was found to improve mitochondrial function, reduce oxidative stress, and decrease chromosomal aberrations in aged oocytes, leading to improved fertility. Additionally, DIM supplementation maintained proper levels of germ cell apoptosis and proliferation, further delaying the onset of reproductive aging.
In recent decades, maternal age at first birth has increased, as has the risk of infertility due to rapidly declining oocyte quality with age. Therefore, an understanding of female reproductive aging and the development of potential modulators to control oocyte quality are required. In this study, we investigated the effects of 3,3'-diindolylmethane (DIM), a natural metabolite of indole-3-cabinol found in cruciferous vegetables, on fertility in a Caenorhabditis elegans model. C. elegans fed DIM showed decreased mitochondrial dysfunction, oxidative stress, and chromosomal aberrations in aged oocytes, and thus reduced embryonic lethality, suggesting that DIM, a dietary natural antioxidant, improves oocyte quality. Furthermore, DIM supplementation maintained germ cell apoptosis (GCA) and germ cell proliferation (GCP) in a CEP-1 /p53-dependent manner in a reproductively aged C. elegans germ line. DIM-induced GCA was mediated by the CEP-1-EGL-1 pathway without HUS-1 activation, suggesting that DIM-induced GCA is different from DNA damage-induced GCA in the C. elegans germ line. Taken together, we propose that DIM supplementation delays the onset of reproductive aging by maintaining the levels of GCP and GCA and oocyte quality in a reproductively aged C. elegans.

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