Selective estrogen receptor modulators (SERMs) enhance neurogenesis and spine density following focal cerebral ischemia. Issue 146 (February 2015)

• Record Type: Journal Article
• Authors: Khan, Mohammad M.; Wakade, Chandramohan; de Sevilla, Liesl; Brann, Darrell W.
• Is Part Of: Journal of steroid biochemistry and molecular biology. Issue 146(2015)
• Page Start: 38
• Page End: 47
• Publication Date: 2015-02
• Subjects: BrdU 5-bromo-2′-deoxyuridine -- CNS central nervous system -- DCX doublecortin -- E2 17β-estradiol -- ER estrogen receptor -- MCAO middle cerebral artery occlusion -- NPCs neural progenitor cells -- PBS phosphate buffered saline -- SERM selective estrogen receptor modulator -- SVZ subventricular zone -- TTC 3, 5-triphenyltetrazolium chloride; Raloxifene -- Tamoxifen -- Estrogen -- Cerebral cortex -- Neurogenesis -- Plasticity -- Cerebral ischemia; Steroid hormones -- Periodicals; Biochemistry -- Periodicals; Hormones -- Periodicals; Molecular Biology -- Periodicals; Hormones stéroïdes -- Périodiques; Steroid hormones; Periodicals; 572.579
• DOI: 10.1016/j.jsbmb.2014.05.001
• Languages: English
• ISSNs: 0960-0760

Abstract

Highlights: Estradiol and raloxifene enhanced neurogenesis in the subventricular zone after focal cerebral ischemia. Tamoxifen did not enhance neurogenesis after focal cerebral ischemia. Estradiol, raloxifene and tamoxifen all enhanced spine density in the cerebral cortex after focal cerebral ischemia. The study demonstrates a profound structural remodeling potential of estradiol and SERMs in the brain following cerebral ischemia. Abstract: Selective estrogen receptor modulators (SERMs) have been reported to enhance synaptic plasticity and improve cognitive performance in adult rats. SERMs have also been shown to induce neuroprotection against cerebral ischemia and other CNS insults. In this study, we sought to determine whether acute regulation of neurogenesis and spine remodeling could be a novel mechanism associated with neuroprotection induced by SERMs following cerebral ischemia. Toward this end, ovariectomized adult female rats were either implanted with pellets of 17β-estradiol (estrogen) or tamoxifen, or injected with raloxifene. After one week, cerebral ischemia was induced by the transient middle-cerebral artery occlusion (MCAO) method. Bromodeoxyuridine (BrdU) was injected to label dividing cells in brain. We analyzed neurogenesis and spine density at day-1 and day-5 post MCAO. In agreement with earlier findings, we observed a robust induction of neurogenesis in the ipsilateral subventricular zone (SVZ) of both the intact as well as ovariectomized female rats following MCAO. Interestingly, neurogenesis in the ipsilateral SVZ following ischemia was significantly higher in estrogen and raloxifene-treated animals compared to placebo-treated rats. In contrast, this enhancing effect on neurogenesis was not observed in tamoxifen-treated rats. Finally, both SERMs, as well as estrogen significantly reversed the spine density loss observed in the ischemic cortex at day-5 post ischemia. Taken, together these results reveal a profound structural remodeling potential of SERMs in the brain following cerebral ischemia. This article is part of a Special Issue entitled "Sex steroids and brain disorders".