# β-Cryptoxanthin Confers Radioprotection against Intestinal Injury via NRF2-Mediated Antioxidant Response and Gut Microbiota Reprogramming

**Authors:** Manman Zhang, Yingshuang Liu, Wenbo Ma, Jinhan Wang, Ningning He, Huijuan Song, Yeqing Gu, Mengmeng Yang, Xinran Lu, Jingxing Sun, Chang Xu, Liqing Du, Yayi Yuan, Yan Wang, Kaihua Ji, Qiang Liu

PMC · DOI: 10.7150/ijbs.125307 · 2026-02-11

## TL;DR

β-cryptoxanthin protects the intestines from radiation damage by boosting antioxidants and improving gut bacteria.

## Contribution

This study reveals β-cryptoxanthin's dual mechanism of radioprotection via NRF2 activation and gut microbiota reprogramming.

## Key findings

- β-cryptoxanthin reduces intestinal injury by enhancing NRF2-mediated antioxidant response.
- It restores beneficial gut bacteria and protective metabolites like short-chain fatty acids.
- The AMPK-GSK3β signaling axis is crucial for β-cryptoxanthin's radioprotective effects.

## Abstract

Radiation-induced intestinal injury, a common complication of abdominal/pelvic radiotherapy for cancer patients and accidental irradiation, presents a major clinical challenge due to the lack of effective treatments. This study investigates the radioprotective potential of β-cryptoxanthin, a provitamin A carotenoid known for its antioxidant properties. In vivo, oral β-cryptoxanthin administration alleviated radiation-induced intestinal injury by enhancing the NRF2-mediated antioxidant response, which was confirmed by its lack of efficacy in Nrf2-/- mice. Additionally, it restored radiation-impaired microbiota by increasing beneficial bacterial populations and protective metabolites like short-chain fatty acids (SCFAs), thereby re-establishing a radioprotective gut ecosystem. At the cellular level, β-cryptoxanthin pretreatment significantly improved cell viability and proliferation while reducing reactive oxygen species (ROS), apoptosis, and DNA damage in irradiated MODE-K intestinal epithelial cells. Mechanistically, β-cryptoxanthin activated the AMPK-GSK3β signaling axis, which drove NRF2 nuclear translocation and upregulated NRF2-dependent cytoprotective genes. Knockdown of NRF2 or AMPK abolished the radioprotective effects, confirming the involvement of these pathways. Overall, this study demonstrates that β-cryptoxanthin protects against radiation-induced intestinal injury through dual mechanisms: activating the NRF2-mediated antioxidant response and reprogramming the gut microbiota to restore a radioprotective ecosystem. These findings position β-cryptoxanthin as a promising candidate for clinical radioprotection.

## Linked entities

- **Genes:** GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562], GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932]
- **Chemicals:** β-cryptoxanthin (PubChem CID 5281235)

## Full-text entities

- **Genes:** Gsk3b (glycogen synthase kinase 3 beta) [NCBI Gene 56637] {aka 7330414F15Rik, 8430431H08Rik, GSK-3, GSK-3beta, GSK3}, RBX1 (ring-box 1) [NCBI Gene 9978] {aka BA554C12.1, RNF75, ROC1}, H2ax (H2A.X variant histone) [NCBI Gene 15270] {aka H2A.X, H2afx, Hist5-2ax, gammaH2ax}, CST12P (cystatin 12, pseudogene) [NCBI Gene 106478911] {aka Cst, Ctes4, E2}, OLFM4 (olfactomedin 4) [NCBI Gene 10562] {aka GC1, GW112, OLM4, OlfD, UNQ362, bA209J19.1}, CUL3 (cullin 3) [NCBI Gene 8452] {aka CUL-3, NEDAUS, PHA2E}, Olfm4 (olfactomedin 4) [NCBI Gene 380924] {aka GC1, GW112, Gm296, Gm913, OlfD, pPD4}, PRKAB1 (protein kinase AMP-activated non-catalytic subunit beta 1) [NCBI Gene 5564] {aka AMPK, HAMPKb}, Sod2 (superoxide dismutase 2, mitochondrial) [NCBI Gene 20656] {aka MnSOD, Sod-2}, Anxa5 (annexin A5) [NCBI Gene 11747] {aka Anx5, CPB-I}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, Rnase1 (ribonuclease, RNase A family, 1 (pancreatic)) [NCBI Gene 19752] {aka Rib-1, Rib1}, Lmnb1 (lamin B1) [NCBI Gene 16906], GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932], HMOX1 (heme oxygenase 1) [NCBI Gene 3162] {aka HMOX1D, HO-1, HSP32, bK286B10}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, BACH1 (BTB domain and CNC homolog 1) [NCBI Gene 571] {aka BACH-1, BTBD24}, Sod1 (superoxide dismutase 1, soluble) [NCBI Gene 20655] {aka B430204E11Rik, Cu/Zn-SOD, CuZnSOD, Ipo-1, Ipo1, SODC}, Hmox1 (heme oxygenase 1) [NCBI Gene 15368] {aka D8Wsu38e, HO-1, HO1, Hemox, Hmox, Hsp32}, FYN (FYN proto-oncogene, Src family tyrosine kinase) [NCBI Gene 2534] {aka SLK, SYN, p59-FYN}, Il22 (interleukin 22) [NCBI Gene 50929] {aka IL-22, IL-22a, ILTIFa, If2b1, Iltif}, Nqo1 (NAD(P)H dehydrogenase, quinone 1) [NCBI Gene 18104] {aka Dia4, Dtd, Nmo-1, Nmo1, Nmor1, Ox-1}, Mki67 (antigen identified by monoclonal antibody Ki 67) [NCBI Gene 17345] {aka D630048A14Rik, Ki-67, Ki67}, Cat (catalase) [NCBI Gene 12359] {aka 2210418N07, Cas-1, Cas1, Cs-1}, Nfe2l2 (nuclear factor, erythroid derived 2, like 2) [NCBI Gene 18024] {aka Nrf2}, KEAP1 (kelch like ECH associated protein 1) [NCBI Gene 9817] {aka INrf2, KLHL19}
- **Diseases:** colon injury (MESH:D003108), tissue injury (MESH:D017695), RIII (MESH:D011832), ocular disorders (MESH:D005128), metabolic disorders (MESH:D008659), cardiovascular, ocular disorders (MESH:D018376), Intestinal Injury (MESH:D007410), lung inflammation (MESH:D011014), lung, gastric, and bladder cancers (MESH:D013274), abdominal and pelvic malignancies (MESH:D000007), cytotoxicity (MESH:D064420), weight loss (MESH:D015431), lung, gastric, and colon cancers (MESH:D008175), cardiovascular diseases (MESH:D002318), Dysbiosis (MESH:D064806), cancer (MESH:D009369), colorectal, cervical, and prostate cancers (MESH:D015179), skin damage (MESH:D012871), inflammation (MESH:D007249), rheumatoid arthritis (MESH:D001172)
- **Chemicals:** glucose (MESH:D005947), ethanol (MESH:D000431), formaldehyde (MESH:D005557), fucoxanthin (MESH:C025164), sodium propionate (MESH:C514135), 4',6-diamidino-2-phenylindole (MESH:C007293), DMSO (MESH:D004121), glycine (MESH:D005998), Nervonic acid (MESH:C013147), SCFA (MESH:D005232), aldehyde (MESH:D000447), ROS (MESH:D017382), beta-Cryptoxanthin (MESH:D000072743), Alcian blue (MESH:D000423), neomycin (MESH:D009355), Acetate (MESH:D000085), sodium acetate (MESH:D019346), eosin (MESH:D004801), PBS (MESH:D007854), SDS (MESH:D012967), H (MESH:D006859), astaxanthin (MESH:C005948), vancomycin (MESH:D014640), lipid (MESH:D008055), paraformaldehyde (MESH:C003043), beta-carotene (MESH:D019207), TRIzol (MESH:C411644), vitamin A (MESH:D014801), ampicillin (MESH:D000667), 137Cesium (MESH:C000614989), torularhodin (MESH:C078923), lycopene (MESH:D000077276), CCK-8 (MESH:D012844), water (MESH:D014867), Carotenoids (MESH:D002338), CO2 (MESH:D002245), F (MESH:D005461), sodium butyrate (MESH:D020148), Valproic acid (MESH:D014635), Triton X-100 (MESH:D017830), lithocholic acid (MESH:D008095), propionate (MESH:D011422), metronidazole (MESH:D008795), lutein (MESH:D014975), butyrate (MESH:D002087), FITC (MESH:D016650), corn oil (MESH:D003314), fluorescein (MESH:D019793), Apollo (MESH:C062106), reactive nitrogen species (MESH:D026361), phosphoric acid (MESH:C030242), nitrogen (MESH:D009584), sodium citrate (MESH:D000077559), acid (MESH:D000143), unsaturated fatty acids (MESH:D005231), K (MESH:D011188), PI (MESH:D010716), aminoacyl-tRNA (MESH:D012346), hematoxylin (MESH:D006416), 4-methylvalerate acid (-)
- **Species:** Phascolarctobacterium (genus) [taxon 33024], Akkermansia (genus) [taxon 239934], Parasutterella (genus) [taxon 577310], Mustela putorius furo (black ferret, subspecies) [taxon 9669], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Caenorhabditis elegans (species) [taxon 6239]
- **Cell lines:** CRL-2190 — Homo sapiens (Human), Huntington's disease, Transformed cell line (CVCL_1H58), CRL-3266 — Homo sapiens (Human), Turner syndrome, Transformed cell line (CVCL_9M78), S2889 — Homo sapiens (Human), Finite cell line (CVCL_9L46), HIEC-6 — Homo sapiens (Human), Finite cell line (CVCL_6C21), MODE-K — Mus musculus (Mouse), Transformed cell line (CVCL_B4FG), CCL-171 — Mus musculus (Mouse), Undefined cell line type (CVCL_M023), C57BL/6J — Mus musculus (Mouse), Transformed cell line (CVCL_C0MW), MRC-5 — Homo sapiens (Human), Finite cell line (CVCL_0440)

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12965244/full.md

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Source: https://tomesphere.com/paper/PMC12965244