Mechanisms of estrogens' dose-dependent neuroprotective and neurodamaging effects in experimental models of cerebral ischemia - PubMed (original) (raw)
Review
Mechanisms of estrogens' dose-dependent neuroprotective and neurodamaging effects in experimental models of cerebral ischemia
Jakob O Strom et al. Int J Mol Sci. 2011.
Abstract
Ever since the hypothesis was put forward that estrogens could protect against cerebral ischemia, numerous studies have investigated the mechanisms of their effects. Despite initial studies showing ameliorating effects, later trials in both humans and animals have yielded contrasting results regarding the fundamental issue of whether estrogens are neuroprotective or neurodamaging. Therefore, investigations of the possible mechanisms of estrogen actions in brain ischemia have been difficult to assess. A recently published systematic review from our laboratory indicates that the dichotomy in experimental rat studies may be caused by the use of insufficiently validated estrogen administration methods resulting in serum hormone concentrations far from those intended, and that physiological estrogen concentrations are neuroprotective while supraphysiological concentrations augment the damage from cerebral ischemia. This evidence offers a new perspective on the mechanisms of estrogens' actions in cerebral ischemia, and also has a direct bearing on the hormone replacement therapy debate. Estrogens affect their target organs by several different pathways and receptors, and the mechanisms proposed for their effects on stroke probably prevail in different concentration ranges. In the current article, previously suggested neuroprotective and neurodamaging mechanisms are reviewed in a hormone concentration perspective in an effort to provide a mechanistic framework for the dose-dependent paradoxical effects of estrogens in stroke. It is concluded that five protective mechanisms, namely decreased apoptosis, growth factor regulation, vascular modulation, indirect antioxidant properties and decreased inflammation, and the proposed damaging mechanism of increased inflammation, are currently supported by experiments performed in optimal biological settings.
Keywords: administration methods; animal experiments; cerebral ischemia; estrogen; stroke.
Figures
Figure 1.
A simplified map of suggested pathways and mechanisms for estrogens’ effects in stroke. Orange and blue rectangles mark plausibly detrimental and protective effects, respectively. The balance in the background symbolizes that depending on the circumstances, such as the dose of estrogen, either the protective or detrimental mechanisms may dominate. The “E” in the middle of the figure is short for “Estrogens” (other abbreviations are detailed above the Introduction). Depicted pathways and mechanisms have previously been reviewed in numerous publications [,,,–43]. Each part of the figure is matched with exact citations in respective sections throughout the article.
Similar articles
- Different methods for administering 17beta-estradiol to ovariectomized rats result in opposite effects on ischemic brain damage.
Strom JO, Theodorsson E, Holm L, Theodorsson A. Strom JO, et al. BMC Neurosci. 2010 Mar 17;11:39. doi: 10.1186/1471-2202-11-39. BMC Neurosci. 2010. PMID: 20236508 Free PMC article. - Dose-related neuroprotective versus neurodamaging effects of estrogens in rat cerebral ischemia: a systematic analysis.
Strom JO, Theodorsson A, Theodorsson E. Strom JO, et al. J Cereb Blood Flow Metab. 2009 Aug;29(8):1359-72. doi: 10.1038/jcbfm.2009.66. Epub 2009 May 20. J Cereb Blood Flow Metab. 2009. PMID: 19458604 Review. - Molecular mechanisms mediating the neuroprotective role of the selective estrogen receptor modulator, bazedoxifene, in acute ischemic stroke: A comparative study with 17β-estradiol.
Jover-Mengual T, Castelló-Ruiz M, Burguete MC, Jorques M, López-Morales MA, Aliena-Valero A, Jurado-Rodríguez A, Pérez S, Centeno JM, Miranda FJ, Alborch E, Torregrosa G, Salom JB. Jover-Mengual T, et al. J Steroid Biochem Mol Biol. 2017 Jul;171:296-304. doi: 10.1016/j.jsbmb.2017.05.001. Epub 2017 May 4. J Steroid Biochem Mol Biol. 2017. PMID: 28479229 - Neuroprotective effects of estrogens following ischemic stroke.
Suzuki S, Brown CM, Wise PM. Suzuki S, et al. Front Neuroendocrinol. 2009 Jul;30(2):201-11. doi: 10.1016/j.yfrne.2009.04.007. Epub 2009 May 3. Front Neuroendocrinol. 2009. PMID: 19401209 Free PMC article. Review. - Estrogens as neuroprotectants against ischemic stroke.
Alonso de Leciñana M, Egido JA. Alonso de Leciñana M, et al. Cerebrovasc Dis. 2006;21 Suppl 2:48-53. doi: 10.1159/000091703. Epub 2006 May 2. Cerebrovasc Dis. 2006. PMID: 16651814 Review.
Cited by
- Menopausal hormone therapy and dementia: nationwide, nested case-control study.
Pourhadi N, Mørch LS, Holm EA, Torp-Pedersen C, Meaidi A. Pourhadi N, et al. BMJ. 2023 Jun 28;381:e072770. doi: 10.1136/bmj-2022-072770. BMJ. 2023. PMID: 37380194 Free PMC article. - Involvement of baroreflex deficiency in the age-related loss of estrogen efficacy against cerebral ischemia.
Wang L, Wang J, Shan Q, Shu H, Guo JM. Wang L, et al. Front Aging Neurosci. 2023 May 2;15:1167170. doi: 10.3389/fnagi.2023.1167170. eCollection 2023. Front Aging Neurosci. 2023. PMID: 37205058 Free PMC article. - Immune regulation based on sex differences in ischemic stroke pathology.
Niu P, Li L, Zhang Y, Su Z, Wang B, Liu H, Zhang S, Qiu S, Li Y. Niu P, et al. Front Immunol. 2023 Jan 30;14:1087815. doi: 10.3389/fimmu.2023.1087815. eCollection 2023. Front Immunol. 2023. PMID: 36793730 Free PMC article. Review. - Neuroprotective Mechanism of Icariin on Hypoxic Ischemic Brain Damage in Neonatal Mice.
Wang M, Yang X, Zhou Q, Guo Y, Chen Y, Song L, Yang J, Li L, Luo L. Wang M, et al. Oxid Med Cell Longev. 2022 Nov 15;2022:1330928. doi: 10.1155/2022/1330928. eCollection 2022. Oxid Med Cell Longev. 2022. PMID: 36425058 Free PMC article. - Targeting 17β-estradiol biosynthesis in neural stem cells improves stroke outcome.
Patkar S, Uwanogho D, Modo M, Tate RJ, Plevin R, Carswell HVO. Patkar S, et al. Front Cell Neurosci. 2022 Jul 22;16:917181. doi: 10.3389/fncel.2022.917181. eCollection 2022. Front Cell Neurosci. 2022. PMID: 35936502 Free PMC article.
References
- Hall ED, Pazara KE, Linseman KL. Sex differences in postischemic neuronal necrosis in gerbils. J. Cereb. Blood Flow Metab. 1991;11:292–298. - PubMed
- Simpkins JW, Rajakumar G, Zhang YQ, Simpkins CE, Greenwald D, Yu CJ, Bodor N, Day AL. Estrogens may reduce mortality and ischemic damage caused by middle cerebral artery occlusion in the female rat. J. Neurosurg. 1997;87:724–730. - PubMed
- Hurn PD, Littleton-Kearney MT, Kirsch JR, Dharmarajan AM, Traystman RJ. Postischemic cerebral blood flow recovery in the female: Effect of 17beta-estradiol. J. Cereb. Blood Flow Metab. 1995;15:666–672. - PubMed
- Lobo RA. The risk of stroke in postmenopausal women receiving hormonal therapy. Climacteric. 2009;12(Suppl 1):81–85. - PubMed
- Rossouw JE, Anderson GL, Prentice RL, LaCroix AZ, Kooperberg C, Stefanick ML, Jackson RD, Beresford SA, Howard BV, Johnson KC, Kotchen JM, Ockene J. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: Principal results from the Women’s Health Initiative randomized controlled trial. Jama. 2002;288:321–333. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources