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. 2023 Aug 23;24(17):13123. doi: 10.3390/ijms241713123

Table 1.

Effects of PCOS on mitochondrial function in the ovary.

Mitochondrial Function Effect of PCOS Condition on Mitochondrial Function Model—Species PCOS Model/Diagnosis Treatment Timeframe Method Therapeutic Intervention Reference
Biogenesis Decreased PGC1α Rat IP Letrozole + HFD 21 days, 21 days, 35 days, 12 weeks qPCR, WB Cangfudaotan (IG) and metformin (IG) increased PGC1α to control levels [52]
Rat IG Letrozole 21 days WB [53]
Mouse SQ DHT 35 days WB Overexpressing SIRT3 in vivo increased PGC1α back to control levels [56]
Mouse HF/HGD (58% kcal fat + sucrose) 12 weeks qPCR Neurokinin-B antagonist increased PGC1α back to control levels [54]
Decreased TFAM Mouse SQ DHEA 20 days WB (1) L-carnitine (LC) + acetyl-L-carnitine (ACL)
(2) LC and ACL plus propionyl-L-carnitine
Both formulations increased TFAM compared to DHEA alone and controls
[55]
Rat IG Letrozole 21 days WB [53]
Mouse HF/HGD (58% kcal fat + sucrose) 12 weeks qPCR Neurokinin-B antagonist increased TFAM back to control levels [54]
Decreased NRF1 Mouse HF/HGD (58% kcal fat + sucrose) 12 weeks qPCR Neurokinin-B antagonist increased NRF1 back to control levels [54]
Mitochondrial Genome Increased mtDNA fragmentation Rat On day 22 of HFD (46% fat), OG letrozole 21 days qPCR Cangfudaotan (IG) and metformin (IG) decreased mtDNA damage and fragmentation [52]
Ultrastructure Membrane swelling and ruptures Rat IP Letrozole + HFD 21 days EM % of total damaged mitochondria decreased with either metformin (IG) or cangfudaotan (IG) but were still higher than control levels [52]
Metabolism Increased basal, maximal and ATP-linked OCR, proton leak Mice—offspring DHT injection in dams post-coitus, assessed pup neonatal ovaries GD 16.5, 17.5, 18.5 XF (Agilent) of whole neonatal ovaries [58]
Decreased OCR, RCR Rat IP letrozole + HFD 21 days Oxytherm Clark-type electrode on isolated mitochondria Cangfudaotan (IG) increased OCR, RCR [52]
Decreased ATP Rat On day 22 of HFD (46% fat), OG letrozole 21 days Colorimetric ATP assay SeNP alone and in combination with metformin increased ATP (most increase in combination) [57]
Rat IP letrozole + HFD 21 days ATP assay Cangfudaotan (IG) increased ATP levels [52]
No difference in ATP Mice—offspring DHT injection in dams post-coitus, assessed pup neonatal ovaries GD 16.5, 17.5, 18.5 XF (Agilent) of whole neonatal ovaries [58]
Decreased activity of mitochondrial complex enzymes Rat IP letrozole + HFD 21 days Complex enzyme activity assays Cangfudaotan (IG) increased mitochondrial complex activity [52]
Decreased Complex I activity Rat On day 22 of HFD (46% fat), OG letrozole 21 days Complex I enzyme activity assay SeNP alone and in combination with metformin increased Complex 1 activity (most increase in combination) [57]
Rat SQ DHEA 20 days Bushen Huatan Granules (OG) increased activity of Complex I [51]
Decreased Complexes III, IV activity SQ DHEA 20 days Complexes III, IV enzyme activity assays Bushen Huatan Granules (OG) increased activity of Complexes III and IV [51]
Decreased Complex IV (Cox6a2 subunit) Mice—offspring DHT injection in dams post-coitus, assessed pup neonatal ovaries GD 16.5, 17.5, 18.5 RNAseq [58]
Decreased citrate synthase activity Rat OG letrozole 21 days Citrate synthase activity assay Metformin (OG) and sodium selenite (OG) increased mitochondrial citrate synthase activity but still lower than control group [59]
Decreased MMP Rat On day 22 of HFD (46% fat), OG letrozole 21 days JC-1 staining SeNP alone and in combination with metformin increased MMP (most increase in combination) [57]
Rat IP letrozole + HFD Cangfudaotan (IG) or metformin (IG) increased MMP [52]
Dynamics Decreased MFN1 Rat IP letrozole + HFD 21 days qPCR/WB Cangfudaotan (IG) or metformin (IG) increased MFN1 [52]
Rat IG Letrozole 21 days WB [53]
Decreased MFN2 Rat IP letrozole + HFD 21 days qPCR/WB Cangfudaotan (IG) or metformin (IG) increased MFN2 [52]
Rat OG letrozole (OG) 21 days qPCR/ELISA kit Metformin (OG) and sodium selenite (OG) increased MFN2 but still lower than control group [59]
Rat IG Letrozole 21 days WB [53]
Decreased OPA1 Rat IP letrozole + HFD 21 days qPCR/WB Cangfudaotan (IG) or metformin (IG) increased OPA1 [52]
Increased DRP1 Rat IP letrozole + HFD 21 days qPCR/WB Cangfudaotan (IG) or metformin (IG) decreased DRP1 [52]
Rat OG letrozole 21 days qPCR/ELISA kit Metformin (OG) and sodium selenite (OG) decreased DRP1 but still higher than control group [59]
Rat IG Letrozole 21 days WB [53]
Increased FIS1 Rat IP letrozole + HFD 21 days qPCR/WB Cangfudaotan (IG) or metformin (IG) decreased FIS1 [52]
Rat IG Letrozole 21 days WB [53]
ROS and Repair Increased ROS Rat IP letrozole + HFD 21 days DCF staining Cangfudaotan (IG) or metformin (IG) decreased ROS [52]
Rat IG Letrozole 21 days Activity to produce superoxide anion assay [53]
Increased mitochondrial superoxide Rat SQ DHEA 20 days MitoSOX staining Bushen Huatan Granules (OG) decreased mitochondrial superoxide [51]
Increased lipid peroxidation Rat On day 22 of HFD (46% fat), OG letrozole 21 days MDA assay SeNP alone or in combination with metformin decreased lipid peroxidation [57]
Rat OG letrozole 21 days Metformin (OG) and sodium selenite (OG) decreased lipid peroxidation but still higher than control group [59]
Rat SQ DHEA 21 days [60]
Rat IG Letrozole 21 days [53]
Mouse SQ DHEA 20 days Genistein decreased lipid peroxidation [61]
Increased protein oxidation Rat OG letrozole 21 days DNPH reaction assay Metformin (OG) and sodium selenite (OG) decreased protein oxidation but still higher than control group [59]
Increased DNA oxidation Mouse SQ DHEA 20 days 8-OHdG ELISA Genistein decreased DNA oxidation levels [61]
Decreased antioxidant capacity Rat OG letrozole 21 days Ferric-reducing antioxidant power assay Metformin (OG) and sodium selenite (OG) increased antioxidant capacity but still lower than control group [59]
Decreased SOD activity Rat On day 22 of HFD (46% fat), OG letrozole 21 days SOD enzyme activity assay SeNP alone or in combination with metformin increased SOD levels [57]
Rat SQ DHEA 21 days [60]
Mouse SQ DHEA 20 days Genistein increased SOD [61]
Decreased SOD1 Mouse HF/HGD (58% kcal fat + sucrose) 12 weeks qPCR Neurokinin-B antagonist increased SOD1 [54]
Increased SOD2 (MnSOD) Mouse SQ DHEA 20 days WB (1) LC + ACL and (2) LC, ACL + propionyl-L-carnitine both decreased SOD2 [55]
Rat IG Letrozole 21 days WB [53]
Decreased GSH Rat On day 22 of HFD (46% fat), OG letrozole 21 days GSH level SeNP alone or in combination with metformin increased GSH levels [57]
Decreased GSH-Px (GPx) Rat OG letrozole 21 days GPx enzyme activity assay Metformin (OG) and sodium selenite (OG) increased GPx activity but still lower than control group [59]
Mouse SQ DHEA 20 days GSH-Px level Genistein increased GSH-Px [61]
Increased GSH-Px Rat IG Letrozole 21 days GSH-Px enzyme activity assay [53]
Decreased GR Mouse SQ DHEA 20 days GR enzyme activity assay [61]
Decreased GSH:GSSG ratio Mouse SQ DHEA 20 days GSH and GSSG levels Genistein increased GSH:GSSG ratio [61]
Decreased CAT activity Mouse SQ DHEA 20 days CAT enzyme activity assay Genistein increased CAT activity [61]
Rat SQ DHEA 21 days [60]
Mouse HF/HGD (58% kcal fat + sucrose) 12 weeks qPCR Neurokinin-B antagonist increased CAT expression [54]
Increased opening of mPTP Rat IP letrozole + HFD 21 days Mitochondrial Membrane Pore-Channel Colorimetric Assay Canfudaton (IG) or metformin (IG) decreased opening of mPTP [52]
Increased levels of Cytochrome C in cytosol than in mitochondria Rat SQ DHEA 20 days WB Bushen Huatan Granules (OG) decreased levels of Cytochrome C in cytosol fraction compared to mitochondrial fraction [51]

Footnotes for Table 1, Table 2 and Table 3: GC: granulosa cell; PGC1α: peroxisome proliferator-activated receptor gamma coactivator 1-alpha; TFAM: mitochondrial transcription factor A; NRF1: nuclear respiratory factor 1; OCR: oxygen consumption rate; RCR: respiratory control ratio; MMP: mitochondrial membrane potential; MFN1: mitofusin 1; MFN2: mitofusin 2; OPA1: optic atrophy 1 mitochondrial dynamin-like GTPase; DRP1: dynamin-related protein 1; FIS1: fission 1; SOD: superoxide dismutase; SOD1: superoxide dismutase 1; SOD2: superoxide dismutase 2; MnSOD: manganese superoxide dismutase; GSH: reduced glutathione; GSH-Px: glutathione peroxidase; GPx: glutathione peroxidase; GR: glutathione reductase; GSSG: oxidized glutathione; CAT: catalase; mPTP: mitochondrial permeability transition pore; NDUFB8: NADH:Ubiquinone Oxidoreductase Subunit B8; ATP5j: ATP Synthase Peripheral Stalk Subunit F6; VDAC1: voltage-dependent anion-selective channel 1; TSPO: translocator protein; UPR-MT: mitochondrial unfolded protein response; ND1: NADH dehydrogenase 1; ND2: NADH dehydrogenase 2; ND5: NADH dehydrogenase 5; ND6: NADH dehydrogenase 6; CO1: cytochrome c oxidase subunit 1; CO2: cytochrome c oxidase subunit 2; CO3: cytochrome c oxidase subunit 3; IP: intraperitoneal; HFD: high-fat diet; IG: intragastric; SQ: subcutaneous; DHT: dihydrotestosterone; HGD: high-glucose diet; kcal: kilocalories; DHEA: dehydroepiandrosterone; OG: oral gavage; EV: extracellular vesicle; GD: gestational day; EM: electron microscopy; TEM: transmission electron microscopy; XF: extracellular flux analysis; JC-1: mitochondrial membrane potential probe; DCF: Dichlorofluorescein; DCHF-DA: 2′-7′-Dichlorodihydrofluorescein diacetate; MDA: malondialdehyde; BAT: brown adipose tissue; TMRE: Tetramethylrhodamine, ethyl ester; ICC: immunocytochemistry; SIRT3: sirtuin 3; SeNP: selenium nanoparticle; 8-OHdG: 8-hydroxy-2′-deoxyguanosine; si-NK3R: small interfering RNA targeting human NK3R; eCG: equine chorionic gonadotropin.