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    Structured Review

    MedChemExpress pbs
    The influence of changes in glycolysis level on myopia. A-B. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, <t>LIM,</t> <t>LIM+2DG,</t> LIM + <t>PBS,</t> NC+2DG, NC + PBS group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. C-D. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. E-L. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). M-T. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). U. HK2, PFKL, LDHA, NRF2 and Keap1 immunofluorescence staining in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 6w.
    Pbs, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 99/100, based on 447 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/2+deoxy+d+glucose/pmc13092674-79-23-19?v=MedChemExpress
    Average 99 stars, based on 447 article reviews
    pbs - by Bioz Stars, 2026-07
    99/100 stars

    Images

    1) Product Images from "Quercetin improves retinal glycolysis to slow myopia progression through orchestrating the AKT/FOXO/HK2 axis"

    Article Title: Quercetin improves retinal glycolysis to slow myopia progression through orchestrating the AKT/FOXO/HK2 axis

    Journal: Redox Biology

    doi: 10.1016/j.redox.2026.104139

    The influence of changes in glycolysis level on myopia. A-B. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. C-D. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. E-L. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). M-T. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). U. HK2, PFKL, LDHA, NRF2 and Keap1 immunofluorescence staining in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 6w.
    Figure Legend Snippet: The influence of changes in glycolysis level on myopia. A-B. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. C-D. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. E-L. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). M-T. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). U. HK2, PFKL, LDHA, NRF2 and Keap1 immunofluorescence staining in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 6w.

    Techniques Used: Expressing, Western Blot, Derivative Assay, Immunofluorescence, Staining

    Glycolysis influences the effect of oxidative phosphorylation on myopia. A. Single-cell sequencing KEGG analysis. B. Mitochondrial membrane potential detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. C. ROS detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. D. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗∗∗P < 0.001, ∗P < 0.05). E. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗P < 0.05). F. Bar graphs of ROS analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗P < 0.05). G. Bar graphs of ROS analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). H. Bar graphs of LA analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). I. Mitochondrial respiratory function in the retina after 6 weeks of myopia induction. J. Bar graphs of basal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01, ∗P < 0.05). K. Bar graphs of maximal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). L. Glycolytic function in the retina after 6 weeks of myopia induction. M. Bar graphs of glycolytic capacity analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). N. Bar graphs of glycolytic reserve analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05) NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).
    Figure Legend Snippet: Glycolysis influences the effect of oxidative phosphorylation on myopia. A. Single-cell sequencing KEGG analysis. B. Mitochondrial membrane potential detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. C. ROS detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. D. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗∗∗P < 0.001, ∗P < 0.05). E. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗P < 0.05). F. Bar graphs of ROS analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗P < 0.05). G. Bar graphs of ROS analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). H. Bar graphs of LA analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). I. Mitochondrial respiratory function in the retina after 6 weeks of myopia induction. J. Bar graphs of basal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01, ∗P < 0.05). K. Bar graphs of maximal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). L. Glycolytic function in the retina after 6 weeks of myopia induction. M. Bar graphs of glycolytic capacity analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). N. Bar graphs of glycolytic reserve analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05) NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Techniques Used: Phospho-proteomics, Single Cell, Sequencing, Membrane, Control, Plasmid Preparation, Injection

    HK2 interacts with KEAP1 and regulates the development of myopia. A. KEAP1 and HK2 molecules docking. B. The protein interaction between KEAP1 and HK2 was analyzed by co-immunoprecipitation. C. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗∗P < 0.001). D. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups ((∗∗P < 0.01, ∗P < 0.05)). E. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗P < 0.01). F. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05). ROS: Reactive oxygen species, NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).
    Figure Legend Snippet: HK2 interacts with KEAP1 and regulates the development of myopia. A. KEAP1 and HK2 molecules docking. B. The protein interaction between KEAP1 and HK2 was analyzed by co-immunoprecipitation. C. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗∗P < 0.001). D. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups ((∗∗P < 0.01, ∗P < 0.05)). E. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗P < 0.01). F. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05). ROS: Reactive oxygen species, NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Techniques Used: Immunoprecipitation, Control, Plasmid Preparation, Injection



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    The influence of changes in glycolysis level on myopia. A-B. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, <t>LIM,</t> <t>LIM+2DG,</t> LIM + <t>PBS,</t> NC+2DG, NC + PBS group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. C-D. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. E-L. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). M-T. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). U. HK2, PFKL, LDHA, NRF2 and Keap1 immunofluorescence staining in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 6w.
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    The influence of changes in glycolysis level on myopia. A-B. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. C-D. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. E-L. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). M-T. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). U. HK2, PFKL, LDHA, NRF2 and Keap1 immunofluorescence staining in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 6w.

    Journal: Redox Biology

    Article Title: Quercetin improves retinal glycolysis to slow myopia progression through orchestrating the AKT/FOXO/HK2 axis

    doi: 10.1016/j.redox.2026.104139

    Figure Lengend Snippet: The influence of changes in glycolysis level on myopia. A-B. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. C-D. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. E-L. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). M-T. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). U. HK2, PFKL, LDHA, NRF2 and Keap1 immunofluorescence staining in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 6w.

    Article Snippet: Additionally, animals in the NC and LIM groups received intraperitoneal injections of 99.93% pure 2-Deoxy- d -glucose (2DG) (HY-13966, MedChemExpress, China) dissolved in PBS at a dose of 500 mg/kg [ , ]; these groups were designated the NC+2DG group and LIM+2DG group, respectively.

    Techniques: Expressing, Western Blot, Derivative Assay, Immunofluorescence, Staining

    Glycolysis influences the effect of oxidative phosphorylation on myopia. A. Single-cell sequencing KEGG analysis. B. Mitochondrial membrane potential detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. C. ROS detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. D. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗∗∗P < 0.001, ∗P < 0.05). E. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗P < 0.05). F. Bar graphs of ROS analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗P < 0.05). G. Bar graphs of ROS analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). H. Bar graphs of LA analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). I. Mitochondrial respiratory function in the retina after 6 weeks of myopia induction. J. Bar graphs of basal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01, ∗P < 0.05). K. Bar graphs of maximal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). L. Glycolytic function in the retina after 6 weeks of myopia induction. M. Bar graphs of glycolytic capacity analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). N. Bar graphs of glycolytic reserve analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05) NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Journal: Redox Biology

    Article Title: Quercetin improves retinal glycolysis to slow myopia progression through orchestrating the AKT/FOXO/HK2 axis

    doi: 10.1016/j.redox.2026.104139

    Figure Lengend Snippet: Glycolysis influences the effect of oxidative phosphorylation on myopia. A. Single-cell sequencing KEGG analysis. B. Mitochondrial membrane potential detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. C. ROS detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. D. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗∗∗P < 0.001, ∗P < 0.05). E. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗P < 0.05). F. Bar graphs of ROS analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗P < 0.05). G. Bar graphs of ROS analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). H. Bar graphs of LA analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). I. Mitochondrial respiratory function in the retina after 6 weeks of myopia induction. J. Bar graphs of basal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01, ∗P < 0.05). K. Bar graphs of maximal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). L. Glycolytic function in the retina after 6 weeks of myopia induction. M. Bar graphs of glycolytic capacity analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). N. Bar graphs of glycolytic reserve analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05) NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Article Snippet: Additionally, animals in the NC and LIM groups received intraperitoneal injections of 99.93% pure 2-Deoxy- d -glucose (2DG) (HY-13966, MedChemExpress, China) dissolved in PBS at a dose of 500 mg/kg [ , ]; these groups were designated the NC+2DG group and LIM+2DG group, respectively.

    Techniques: Phospho-proteomics, Single Cell, Sequencing, Membrane, Control, Plasmid Preparation, Injection

    HK2 interacts with KEAP1 and regulates the development of myopia. A. KEAP1 and HK2 molecules docking. B. The protein interaction between KEAP1 and HK2 was analyzed by co-immunoprecipitation. C. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗∗P < 0.001). D. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups ((∗∗P < 0.01, ∗P < 0.05)). E. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗P < 0.01). F. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05). ROS: Reactive oxygen species, NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Journal: Redox Biology

    Article Title: Quercetin improves retinal glycolysis to slow myopia progression through orchestrating the AKT/FOXO/HK2 axis

    doi: 10.1016/j.redox.2026.104139

    Figure Lengend Snippet: HK2 interacts with KEAP1 and regulates the development of myopia. A. KEAP1 and HK2 molecules docking. B. The protein interaction between KEAP1 and HK2 was analyzed by co-immunoprecipitation. C. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗∗P < 0.001). D. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups ((∗∗P < 0.01, ∗P < 0.05)). E. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗P < 0.01). F. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05). ROS: Reactive oxygen species, NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Article Snippet: Additionally, animals in the NC and LIM groups received intraperitoneal injections of 99.93% pure 2-Deoxy- d -glucose (2DG) (HY-13966, MedChemExpress, China) dissolved in PBS at a dose of 500 mg/kg [ , ]; these groups were designated the NC+2DG group and LIM+2DG group, respectively.

    Techniques: Immunoprecipitation, Control, Plasmid Preparation, Injection

    The influence of changes in glycolysis level on myopia. A-B. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. C-D. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. E-L. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). M-T. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). U. HK2, PFKL, LDHA, NRF2 and Keap1 immunofluorescence staining in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 6w.

    Journal: Redox Biology

    Article Title: Quercetin improves retinal glycolysis to slow myopia progression through orchestrating the AKT/FOXO/HK2 axis

    doi: 10.1016/j.redox.2026.104139

    Figure Lengend Snippet: The influence of changes in glycolysis level on myopia. A-B. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. C-D. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. E-L. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). M-T. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). U. HK2, PFKL, LDHA, NRF2 and Keap1 immunofluorescence staining in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 6w.

    Article Snippet: Additionally, animals in the NC and LIM groups received intraperitoneal injections of 99.93% pure 2-Deoxy- d -glucose (2DG) (HY-13966, MedChemExpress, China) dissolved in PBS at a dose of 500 mg/kg [ , ]; these groups were designated the NC+2DG group and LIM+2DG group, respectively.

    Techniques: Expressing, Western Blot, Derivative Assay, Immunofluorescence, Staining

    Glycolysis influences the effect of oxidative phosphorylation on myopia. A. Single-cell sequencing KEGG analysis. B. Mitochondrial membrane potential detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. C. ROS detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. D. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗∗∗P < 0.001, ∗P < 0.05). E. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗P < 0.05). F. Bar graphs of ROS analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗P < 0.05). G. Bar graphs of ROS analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). H. Bar graphs of LA analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). I. Mitochondrial respiratory function in the retina after 6 weeks of myopia induction. J. Bar graphs of basal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01, ∗P < 0.05). K. Bar graphs of maximal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). L. Glycolytic function in the retina after 6 weeks of myopia induction. M. Bar graphs of glycolytic capacity analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). N. Bar graphs of glycolytic reserve analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05) NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Journal: Redox Biology

    Article Title: Quercetin improves retinal glycolysis to slow myopia progression through orchestrating the AKT/FOXO/HK2 axis

    doi: 10.1016/j.redox.2026.104139

    Figure Lengend Snippet: Glycolysis influences the effect of oxidative phosphorylation on myopia. A. Single-cell sequencing KEGG analysis. B. Mitochondrial membrane potential detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. C. ROS detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. D. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗∗∗P < 0.001, ∗P < 0.05). E. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗P < 0.05). F. Bar graphs of ROS analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗P < 0.05). G. Bar graphs of ROS analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). H. Bar graphs of LA analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). I. Mitochondrial respiratory function in the retina after 6 weeks of myopia induction. J. Bar graphs of basal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01, ∗P < 0.05). K. Bar graphs of maximal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). L. Glycolytic function in the retina after 6 weeks of myopia induction. M. Bar graphs of glycolytic capacity analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). N. Bar graphs of glycolytic reserve analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05) NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Article Snippet: Additionally, animals in the NC and LIM groups received intraperitoneal injections of 99.93% pure 2-Deoxy- d -glucose (2DG) (HY-13966, MedChemExpress, China) dissolved in PBS at a dose of 500 mg/kg [ , ]; these groups were designated the NC+2DG group and LIM+2DG group, respectively.

    Techniques: Phospho-proteomics, Single Cell, Sequencing, Membrane, Control, Plasmid Preparation, Injection

    HK2 interacts with KEAP1 and regulates the development of myopia. A. KEAP1 and HK2 molecules docking. B. The protein interaction between KEAP1 and HK2 was analyzed by co-immunoprecipitation. C. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗∗P < 0.001). D. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups ((∗∗P < 0.01, ∗P < 0.05)). E. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗P < 0.01). F. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05). ROS: Reactive oxygen species, NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Journal: Redox Biology

    Article Title: Quercetin improves retinal glycolysis to slow myopia progression through orchestrating the AKT/FOXO/HK2 axis

    doi: 10.1016/j.redox.2026.104139

    Figure Lengend Snippet: HK2 interacts with KEAP1 and regulates the development of myopia. A. KEAP1 and HK2 molecules docking. B. The protein interaction between KEAP1 and HK2 was analyzed by co-immunoprecipitation. C. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗∗P < 0.001). D. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups ((∗∗P < 0.01, ∗P < 0.05)). E. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗P < 0.01). F. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05). ROS: Reactive oxygen species, NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Article Snippet: Additionally, animals in the NC and LIM groups received intraperitoneal injections of 99.93% pure 2-Deoxy- d -glucose (2DG) (HY-13966, MedChemExpress, China) dissolved in PBS at a dose of 500 mg/kg [ , ]; these groups were designated the NC+2DG group and LIM+2DG group, respectively.

    Techniques: Immunoprecipitation, Control, Plasmid Preparation, Injection

    The influence of changes in glycolysis level on myopia. A-B. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. C-D. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. E-L. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). M-T. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). U. HK2, PFKL, LDHA, NRF2 and Keap1 immunofluorescence staining in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 6w.

    Journal: Redox Biology

    Article Title: Quercetin improves retinal glycolysis to slow myopia progression through orchestrating the AKT/FOXO/HK2 axis

    doi: 10.1016/j.redox.2026.104139

    Figure Lengend Snippet: The influence of changes in glycolysis level on myopia. A-B. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. C-D. HK2, PFKL, PKM2, and LDHA expression detected by Western blot in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, group in 4w and 6w. Samples derived from the same experiment and that blots were processed in parallel. E-L. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). M-T. Bar graphs of Western blot analysis for HK2, PFKL, PKM2, and LDHA in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 4w and 6w. (∗∗∗P < 0.001, ∗P < 0.05). U. HK2, PFKL, LDHA, NRF2 and Keap1 immunofluorescence staining in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group in 6w.

    Article Snippet: Additionally, animals in the NC and LIM groups received intraperitoneal injections of 99.93% pure 2-Deoxy- d -glucose (2DG) (HY-13966, MedChemExpress, China) dissolved in PBS at a dose of 500 mg/kg [ , ]; these groups were designated the NC+2DG group and LIM+2DG group, respectively.

    Techniques: Expressing, Western Blot, Derivative Assay, Immunofluorescence, Staining

    Glycolysis influences the effect of oxidative phosphorylation on myopia. A. Single-cell sequencing KEGG analysis. B. Mitochondrial membrane potential detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. C. ROS detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. D. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗∗∗P < 0.001, ∗P < 0.05). E. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗P < 0.05). F. Bar graphs of ROS analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗P < 0.05). G. Bar graphs of ROS analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). H. Bar graphs of LA analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). I. Mitochondrial respiratory function in the retina after 6 weeks of myopia induction. J. Bar graphs of basal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01, ∗P < 0.05). K. Bar graphs of maximal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). L. Glycolytic function in the retina after 6 weeks of myopia induction. M. Bar graphs of glycolytic capacity analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). N. Bar graphs of glycolytic reserve analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05) NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Journal: Redox Biology

    Article Title: Quercetin improves retinal glycolysis to slow myopia progression through orchestrating the AKT/FOXO/HK2 axis

    doi: 10.1016/j.redox.2026.104139

    Figure Lengend Snippet: Glycolysis influences the effect of oxidative phosphorylation on myopia. A. Single-cell sequencing KEGG analysis. B. Mitochondrial membrane potential detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. C. ROS detection in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups at 6 weeks. D. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗∗∗P < 0.001, ∗P < 0.05). E. Bar graphs of Mitochondrial membrane potential analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗P < 0.05). F. Bar graphs of ROS analysis in NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl group (∗P < 0.05). G. Bar graphs of ROS analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). H. Bar graphs of LA analysis in NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS group (∗∗∗P < 0.001, ∗P < 0.05). I. Mitochondrial respiratory function in the retina after 6 weeks of myopia induction. J. Bar graphs of basal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01, ∗P < 0.05). K. Bar graphs of maximal mitochondrial respiration analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). L. Glycolytic function in the retina after 6 weeks of myopia induction. M. Bar graphs of glycolytic capacity analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗P < 0.01). N. Bar graphs of glycolytic reserve analysis in NC, LIM, HK2-5 μl, LIM+2DG, NC+2DG (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05) NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Article Snippet: Additionally, animals in the NC and LIM groups received intraperitoneal injections of 99.93% pure 2-Deoxy- d -glucose (2DG) (HY-13966, MedChemExpress, China) dissolved in PBS at a dose of 500 mg/kg [ , ]; these groups were designated the NC+2DG group and LIM+2DG group, respectively.

    Techniques: Phospho-proteomics, Single Cell, Sequencing, Membrane, Control, Plasmid Preparation, Injection

    HK2 interacts with KEAP1 and regulates the development of myopia. A. KEAP1 and HK2 molecules docking. B. The protein interaction between KEAP1 and HK2 was analyzed by co-immunoprecipitation. C. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗∗P < 0.001). D. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups ((∗∗P < 0.01, ∗P < 0.05)). E. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗P < 0.01). F. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05). ROS: Reactive oxygen species, NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Journal: Redox Biology

    Article Title: Quercetin improves retinal glycolysis to slow myopia progression through orchestrating the AKT/FOXO/HK2 axis

    doi: 10.1016/j.redox.2026.104139

    Figure Lengend Snippet: HK2 interacts with KEAP1 and regulates the development of myopia. A. KEAP1 and HK2 molecules docking. B. The protein interaction between KEAP1 and HK2 was analyzed by co-immunoprecipitation. C. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗∗P < 0.001). D. The mean values of refraction in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups ((∗∗P < 0.01, ∗P < 0.05)). E. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, Empty, HK2-1μl, HK2-3μl, HK2-5μl groups (∗∗P < 0.01). F. The mean values of axial length in the right eyes of the guinea pigs after myopia induction for 0, 4, and 6 weeks between the NC, LIM, LIM+2DG, LIM + PBS, NC+2DG, NC + PBS groups (∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05). ROS: Reactive oxygen species, NC: normal control, LIM: lens-induced myopia, Empty: (LIM + empty AAV vector), HK2-1μl: (LIM + AAV-HK2 1 μL intravitreal injection), HK2-3μl: (LIM + AAV-HK2 3 μL intravitreal injection), HK2-5μl: (LIM + AAV-HK2 5 μL intravitreal injection), LIM+2DG: (LIM + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), LIM + PBS: (LIM + PBS intraperitoneal injection), NC+2DG: (NC + 2-deoxy- d -glucose 500 mg/kg intraperitoneal injection), NC + PBS: (NC + PBS intraperitoneal injection).

    Article Snippet: Additionally, animals in the NC and LIM groups received intraperitoneal injections of 99.93% pure 2-Deoxy- d -glucose (2DG) (HY-13966, MedChemExpress, China) dissolved in PBS at a dose of 500 mg/kg [ , ]; these groups were designated the NC+2DG group and LIM+2DG group, respectively.

    Techniques: Immunoprecipitation, Control, Plasmid Preparation, Injection

    Changes in glycolysis-related molecules by depletion of HIF-1α. (A) Gene set enrichment heatmap of genes in the QI_HYPOXIA, REACTOME_STRIATED_MUSCLE_CONTRACTION and GOBP_CARBOHYDRATE_CATABOLIC_PROCESS sets shows reduced expression of these genes in HIF-KO samples when compared with that in the Mock control (n=1 each). Reverse transcription-quantitative PCR analysis of (B) Slc2a1 and (C) Hk2 mRNA in Mock and HIF-KO cells under adherent in normoxic or hypoxic (2% O 2 ) conditions for 20 h (n=3). Reverse transcription-quantitative PCR analysis of (D) Slc2a1 and (E) Hk2 mRNA collected as in (n=3). (F) Scheme showing how BAY-876 and 2-Deoxy-D-glucose (2-DG) affect Glut1 and Hexokinase function. Viability of Mock and HIF-KO cells treated for 2 days with the indicated concentrations of (G) BAY-876 or (H) 2-DG. Assays were performed in quadruplicate, and data are expressed as mean ± SD relative (−fold) to the corresponding control value for cells incubated in the absence of these agents. HIF-KO, hypoxia inducible factor knockout. *P<0.05 and **P<0.01.

    Journal: Oncology Reports

    Article Title: Depleting HIF-1α attenuates the progression of osteosarcoma, but tumorigenicity is sustained through HIF-independent pathways

    doi: 10.3892/or.2026.9099

    Figure Lengend Snippet: Changes in glycolysis-related molecules by depletion of HIF-1α. (A) Gene set enrichment heatmap of genes in the QI_HYPOXIA, REACTOME_STRIATED_MUSCLE_CONTRACTION and GOBP_CARBOHYDRATE_CATABOLIC_PROCESS sets shows reduced expression of these genes in HIF-KO samples when compared with that in the Mock control (n=1 each). Reverse transcription-quantitative PCR analysis of (B) Slc2a1 and (C) Hk2 mRNA in Mock and HIF-KO cells under adherent in normoxic or hypoxic (2% O 2 ) conditions for 20 h (n=3). Reverse transcription-quantitative PCR analysis of (D) Slc2a1 and (E) Hk2 mRNA collected as in (n=3). (F) Scheme showing how BAY-876 and 2-Deoxy-D-glucose (2-DG) affect Glut1 and Hexokinase function. Viability of Mock and HIF-KO cells treated for 2 days with the indicated concentrations of (G) BAY-876 or (H) 2-DG. Assays were performed in quadruplicate, and data are expressed as mean ± SD relative (−fold) to the corresponding control value for cells incubated in the absence of these agents. HIF-KO, hypoxia inducible factor knockout. *P<0.05 and **P<0.01.

    Article Snippet: 2-deoxy-D-glucose (3.3–30.0 mM; 2 days; Tokyo Chemical Industry Co., Ltd.), Farnesyl Diphosphate (FPP; 50 μM; 2 days) and Geranylgeranyl Diphosphate (GGPP; 50 μM; 2 days; Echelon) were dissolved in water.

    Techniques: Expressing, Control, Reverse Transcription, Real-time Polymerase Chain Reaction, Incubation, Knock-Out