17β-estradiol is protective in spinal cord injury in post- and pre-menopausal rats
The neuroprotective effects of 17β-estradiol have been shown in models of central nervous system injury, including ischemia, brain injury, and more recently, spinal cord injury (SCI). Recent epidemiological trends suggest that SCIs in elderly women are increasing; however, the effects of menopause o...
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th-mahidol.237342018-08-20T14:16:11Z 17β-estradiol is protective in spinal cord injury in post- and pre-menopausal rats Pimonporn Chaovipoch Karen A.Bozak Jelks Lynnette M. Gerhold Eric J. West Sukumal Chongthammakun Candace L. Floyd University of California, Davis Mahidol University Medicine The neuroprotective effects of 17β-estradiol have been shown in models of central nervous system injury, including ischemia, brain injury, and more recently, spinal cord injury (SCI). Recent epidemiological trends suggest that SCIs in elderly women are increasing; however, the effects of menopause on estrogen-mediated neuroprotection are poorly understood. The objective of this study was to evaluate the effects of 17β-estradiol and reproductive aging on motor function, neuronal death, and white matter sparing after SCI of post- and pre-menopausal rats. Two-month-old or 1-year-old female rats were ovariectomized and implanted with a silastic capsule containing 180 μg/mL of 17β-estradiol or vehicle. Complete crush SCI at T8-9 was performed 1 week later. Additional animals of each age group were left ovary-intact but were spinal cord injured. The Basso, Beattie, Bresnahan (BBB) locomotor test was performed. Spinal cords were collected on post-SCI days 1, 7, and 21, and processed for histological markers. Administration of 17β-estradiol to ovariectomized rats improved recovery of hind-limb locomotion, increased white matter sparing, and decreased apoptosis in both the post- and pre-menopausal rats. Also, ovary-intact 1-year-old rats did worse than ovary-intact 2-month-old rats, suggesting that endogenous estrogen confers neuroprotection in young rats, which is lost in older animals. Taken together, these data suggest that estrogen is neuroprotective in SCI and that the loss of endogenous estrogen-mediated neuroprotective seen in older rats can be attenuated with exogenous administration of 17β-estradiol. © Mary Ann Liebert, Inc. 2018-08-20T07:16:11Z 2018-08-20T07:16:11Z 2006-06-01 Article Journal of Neurotrauma. Vol.23, No.6 (2006), 830-852 10.1089/neu.2006.23.830 08977151 2-s2.0-33745501785 https://repository.li.mahidol.ac.th/handle/123456789/23734 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33745501785&origin=inward |
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Medicine Pimonporn Chaovipoch Karen A.Bozak Jelks Lynnette M. Gerhold Eric J. West Sukumal Chongthammakun Candace L. Floyd 17β-estradiol is protective in spinal cord injury in post- and pre-menopausal rats |
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The neuroprotective effects of 17β-estradiol have been shown in models of central nervous system injury, including ischemia, brain injury, and more recently, spinal cord injury (SCI). Recent epidemiological trends suggest that SCIs in elderly women are increasing; however, the effects of menopause on estrogen-mediated neuroprotection are poorly understood. The objective of this study was to evaluate the effects of 17β-estradiol and reproductive aging on motor function, neuronal death, and white matter sparing after SCI of post- and pre-menopausal rats. Two-month-old or 1-year-old female rats were ovariectomized and implanted with a silastic capsule containing 180 μg/mL of 17β-estradiol or vehicle. Complete crush SCI at T8-9 was performed 1 week later. Additional animals of each age group were left ovary-intact but were spinal cord injured. The Basso, Beattie, Bresnahan (BBB) locomotor test was performed. Spinal cords were collected on post-SCI days 1, 7, and 21, and processed for histological markers. Administration of 17β-estradiol to ovariectomized rats improved recovery of hind-limb locomotion, increased white matter sparing, and decreased apoptosis in both the post- and pre-menopausal rats. Also, ovary-intact 1-year-old rats did worse than ovary-intact 2-month-old rats, suggesting that endogenous estrogen confers neuroprotection in young rats, which is lost in older animals. Taken together, these data suggest that estrogen is neuroprotective in SCI and that the loss of endogenous estrogen-mediated neuroprotective seen in older rats can be attenuated with exogenous administration of 17β-estradiol. © Mary Ann Liebert, Inc. |
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University of California, Davis |
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University of California, Davis Pimonporn Chaovipoch Karen A.Bozak Jelks Lynnette M. Gerhold Eric J. West Sukumal Chongthammakun Candace L. Floyd |
format |
Article |
author |
Pimonporn Chaovipoch Karen A.Bozak Jelks Lynnette M. Gerhold Eric J. West Sukumal Chongthammakun Candace L. Floyd |
author_sort |
Pimonporn Chaovipoch |
title |
17β-estradiol is protective in spinal cord injury in post- and pre-menopausal rats |
title_short |
17β-estradiol is protective in spinal cord injury in post- and pre-menopausal rats |
title_full |
17β-estradiol is protective in spinal cord injury in post- and pre-menopausal rats |
title_fullStr |
17β-estradiol is protective in spinal cord injury in post- and pre-menopausal rats |
title_full_unstemmed |
17β-estradiol is protective in spinal cord injury in post- and pre-menopausal rats |
title_sort |
17β-estradiol is protective in spinal cord injury in post- and pre-menopausal rats |
publishDate |
2018 |
url |
https://repository.li.mahidol.ac.th/handle/123456789/23734 |
_version_ |
1763489480878063616 |