2012
DOI: 10.1016/j.etp.2010.08.020
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Effect of sex differences and gonadal hormones on kainic acid-induced neurodegeneration in the bed nucleus of the stria terminalis of the rat

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Cited by 5 publications
(5 citation statements)
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“…Also, the SE induced by intrahippocampal kainate in NMRI mice was more severe in male than female mice, which could have affected the epileptogenic processes induced by SE in both genders [101]. Several previous studies reported that male rodents are more susceptible to the convulsive and neurodegenerative effects of systemic kainate administration than females, and a proconvulsive effect of testosterone and neuroprotective effect of estrogen was demonstrated [208-212]. However, Scharfman and MacLusky [198] reported that the SE induced by kainate was indistinguishable in male and female SD rats, and no significant difference in stages of the estrous cycle was found.…”
Section: Role Of Sex For Inter- and Intrastrain Differencesmentioning
confidence: 99%
“…Also, the SE induced by intrahippocampal kainate in NMRI mice was more severe in male than female mice, which could have affected the epileptogenic processes induced by SE in both genders [101]. Several previous studies reported that male rodents are more susceptible to the convulsive and neurodegenerative effects of systemic kainate administration than females, and a proconvulsive effect of testosterone and neuroprotective effect of estrogen was demonstrated [208-212]. However, Scharfman and MacLusky [198] reported that the SE induced by kainate was indistinguishable in male and female SD rats, and no significant difference in stages of the estrous cycle was found.…”
Section: Role Of Sex For Inter- and Intrastrain Differencesmentioning
confidence: 99%
“…2006). It is likely that, at least in some cases, the neuroprotective effects of T are largely due to the conversion of T to E 2 by the enzyme aromatase (Pereno & Beltramino 2009; Pereno et al. 2010).…”
Section: Introductionmentioning
confidence: 99%
“…The active, supportive role of sex steroid hormones is echoed in the fact that several hormonesensitive brain areas regress in response to hormone withdrawal (Cooke et al 1999;Panzica et al 2001;Johansen et al 2004;MacLusky et al 2006). It is likely that, at least in some cases, the neuroprotective effects of T are largely due to the conversion of T to E 2 by the enzyme aromatase (Pereno & Beltramino 2009;Pereno et al 2010). Given the clinical ramifications of sex steroid hormone-mediated neuroprotection, there is a significant need for animal models to study this phenomenon, especially in species that undergo substantial neurodegeneration in response to the withdrawal of circulating hormones.…”
Section: Introductionmentioning
confidence: 99%
“…In women, the low risk of dementia can be explained by the protective effect of estrogen, which elicits an anti-inflammatory effect that decreases the damage caused by cytokine secretion; this hormone also functions against neurodegeneration. 20 , 29 , 42 , 46 , 48 , 53 , 57 In addition, surgery for a fracture induces sequential inflammatory processes. 24 , 54 , 58 Further studies should also be conducted to determine whether or not other aging processes, physical conditions, and inflammation mediate fractures and cognitive decline.…”
Section: Discussionmentioning
confidence: 99%