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                <identifier>oai:data.mendeley.com/kd7n8xdr3t.1</identifier>
                <datestamp>2025-03-03T00:43:29Z</datestamp>
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    <dc:creator>Zheng, Qian</dc:creator>
    <dc:title>Original Image of Guzhi Zengsheng Zhitong Decoction Mitigates Osteoarthritis via FOXO1-Mediated Autophagy and Apoptosis</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>figure 1 (B-D) Representative histological images of knee joints after 4 weeks of treating, including hematoxylin-eosin (HE), safranin-O fast green, and toluidine blue staining. 

figure 2 (A) Micro-CT images showing 3D reconstructions of the distal femur and transverse and sagittal views of the tibial plateau.

figure 6 (I, J) Immunohistochemical analysis and quantification of FoxO1, LC3B, Parkin and PINK1 expression in the rat articular cartilage following oral administration (n=4, scale bar: 200 μm).

figure 7 (A) Representative transmission electron microscopy images showing mitochondrial morphology (scale bars: 5 μm, 2 μm, 500 nm). (C) Fluorescence images of mitochondrial membrane potential (MMP) staining. Red fluorescence represents JC-1 aggregates, green fluorescence represents JC-1 monomers, and the red/green intensity ratio reflects MMP (scale bar: 100 μm). (D) Fluorescence images of mitochondrial permeability transition pore (MPTP) staining (scale bar: 200 μm). (E) Fluorescence images of reactive oxygen species (ROS) levels (scale bar: 200 μm). 

figure 8 (C) TUNEL staining to evaluate apoptosis in knee cartilage of OA rats after oral GZZD treatment. (scale bar: 100 μm). 

figure 10 (A) JC-1 staining showing mitochondrial membrane potential (MMP) in OA chondrocytes with and without FoxO1 silencing (scale bar: 200 μm). (C) Effects of FoxO1 silencing on mitochondrial MPTP permeability after GZZD treatment. (scale bar: 200 μm). (E) ROS levels visualized by fluorescence staining before and after FoxO1 silencing. (scale bar: 200 μm). 

Supplement figures
Figure S1. Representative anatomical images of rat knee joints at week 4 post-treatment.
Figure S2. Identification of primary chondrocytes. (A) Observation of cell morphology; (B) COL2A1 immunofluorescence staining.
Figure S5. Effects of GZZD on OA chondrocyte apoptosis observed via Annexin V-FITC/PI staining (in vitro).
Figure S8. Effects of oral GZZD on STAT3, FOXO1, P-P65, and P65 protein levels in OA rat chondrocytes analyzed by Western blot and quantitative analysis, in vivo

Western Blot Original Image.</dc:description>
    <dc:subject>Natural Sciences</dc:subject>
    <dc:contributor>Lu, Bocheng</dc:contributor>
    <dc:contributor>Chen, Yongfu</dc:contributor>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/kd7n8xdr3t.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/kd7n8xdr3t.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
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    <dc:date>2025-03-03T00:43:29Z</dc:date>
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