Biogenesis
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No Reports |
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Mitochondrial Genome
|
Increased mtDNA copy number |
Mouse |
Controlled-release DHT pellet implant |
90 days (2.75 μg/day) |
qPCR (mtCO1:tubulin) |
|
[69] |
No difference in mtDNA copy number |
Mouse—offspring |
DHT injection in dam post-coitus, assessed post-pubertal pup oocytes |
GD 16.5, 17.5, 18.5 |
qPCR (mtCO1:tubulin) |
|
[58] |
Ultrastructure
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Disorganized cristae, vacuoles, less electron-dense |
Mouse—offspring |
DHT injection in dam post-coitus, assessed post-pubertal pup oocytes |
GD 16.5, 17.5, 18.5 |
TEM |
|
[58] |
Mitochondria with malformed cristae with concentric circles, swollen or loss of cristae |
Mouse |
Controlled-release DHT pellet implant |
90 days (2.75 μg/day) |
SEM |
|
[69] |
Mitochondria have swollen cristae, no electron-dense contents, and are vacuolated |
Mouse—offspring |
DHT injection in dams post-coitus, assessed post-pubertal pup oocytes |
GD 16.5, 17.5, 18.5 |
TEM |
|
[70] |
Abnormal mitochondria distribution |
Human/Mouse |
EVs isolated from PCOS patients with non-hyperandrogenic phenotype were co-cultured with control murine oocytes |
|
Mitochondrial Red Fluorescent Probe |
|
[72] |
Metabolism
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Increased glucose, pyruvate consumption |
Human |
Rotterdam |
|
Ultra-microfluorometric assay |
|
[73] |
Increased ATP levels |
Mice |
Controlled-release DHT pellet implant |
90 days (2.75 μg/day) |
ATP assay |
|
[69] |
No difference in ATP levels |
Mouse—offspring |
DHT injection in dams post-coitus, assessed post-pubertal pup oocytes |
GD 16.5, 17.5, 18.5 |
|
[70] |
Decreased mitochondrial Complex I genes (ND1, ND2, ND5) |
Mice |
Controlled-release DHT pellet implant |
90 days (2.75 μg/day) |
qPCR |
|
[69] |
Increased mitochondrial Complexes I and IV genes (ND1, ND6 and CO1, CO2, CO3) |
Mouse—offspring |
DHT injection in dams post-coitus, assessed post-pubertal pup oocytes |
GD 16.5, 17.5, 18.5 |
|
[70] |
Decreased MMP |
Mice |
Controlled-release DHT pellet implant |
90 days (2.75 μg/day) |
JC-1 staining |
|
[69] |
Rat |
DHEA injection (interscapular region) |
20 days |
Rat-to-mouse BAT xenotransplant increased MMP |
[74] |
Mice—offspring |
DHT injection in dams post-coitus, assessed post-pubertal pup oocytes |
GD 16.5, 17.5, 18.5 |
|
[70] |
ROS and Repair
|
Increased ROS |
Rat |
DHEA injection (interscapular region) |
20 days |
ROS assay using DCFH-DA |
Rat-to-mouse BAT xenotransplant decreased ROS level |
[74] |
Human |
EVs isolated from PCOS patients with non-hyperandrogenic phenotype were co-cultured with control murine oocytes |
|
DCHF-DA staining |
|
[72] |
Mice—offspring |
DHT injection in dams post-coitus, assessed post-pubertal pup oocytes |
GD 16.5, 17.5, 18.5 |
CellROX staining |
|
[70] |
No differences in ROS |
Mice |
Controlled-release DHT pellet implant |
90 days (2.75 μg/day) |
|
[69] |
No differences in lipid peroxidation |
Mice |
Controlled-release DHT pellet implant |
90 days (2.75 μg/day) |
BODIPYC11® 581/591 staining |
|
[69] |
Increased CAT |
Human |
EVs isolated from PCOS patients with non-hyperandrogenic phenotype were co-cultured with control murine oocytes |
|
qPCR |
|
[72] |
Increased GSS |
Human |
EVs isolated from PCOS patients with non-hyperandrogenic phenotype were co-cultured with control murine oocytes |
|
qPCR |
|
[72] |