TY - JOUR
T1 - Gender- and region-specific changes in estrogen signaling in aging rat brain mitochondria
AU - Evola, Christopher M
AU - Hudson, Tanner L
AU - Huang, Luping
AU - Corbett, Adrian M
AU - Mayes, Debra A
PY - 2018/8/31
Y1 - 2018/8/31
N2 - Recently epidemiological studies suggest females lose neuroprotection from neurodegenerative diseases as they go through menopause. It has been hypothesized that this neuroprotection is hormone-dependent. The current study characterized cell signaling molecules downstream of estrogen receptor beta that are known to play a role in memory, PKC, ERK, and connexin-43, in regions of the brain associated with memory decline in an attempt to elucidate significant changes that occur post-estrus. Total whole cell lysates were compared to isolated mitochondrial protein because mitochondrial function is known to be altered during aging. As hypothesized, protein concentrations differed depending on age, gender, and brain region. Additionally, many of these changes occurred within mitochondria but not within whole cell lysates indicating that these are epigenetic alterations. These findings accentuate the complexity of aging and provide insight into the gender-specific cellular processes that occur throughout this process.
AB - Recently epidemiological studies suggest females lose neuroprotection from neurodegenerative diseases as they go through menopause. It has been hypothesized that this neuroprotection is hormone-dependent. The current study characterized cell signaling molecules downstream of estrogen receptor beta that are known to play a role in memory, PKC, ERK, and connexin-43, in regions of the brain associated with memory decline in an attempt to elucidate significant changes that occur post-estrus. Total whole cell lysates were compared to isolated mitochondrial protein because mitochondrial function is known to be altered during aging. As hypothesized, protein concentrations differed depending on age, gender, and brain region. Additionally, many of these changes occurred within mitochondria but not within whole cell lysates indicating that these are epigenetic alterations. These findings accentuate the complexity of aging and provide insight into the gender-specific cellular processes that occur throughout this process.
UR - https://www.scopus.com/pages/publications/85052601719
UR - https://www.scopus.com/inward/citedby.url?scp=85052601719&partnerID=8YFLogxK
U2 - 10.18632/aging.101538
DO - 10.18632/aging.101538
M3 - Article
C2 - 30169330
SN - 0394-9532
VL - 10
SP - 2148
EP - 2169
JO - Aging
JF - Aging
IS - 8
ER -