Effect of Sex and Age Interactions on Functional Outcome after Stroke

被引:51
作者
Kim, Tae-Hee [1 ,2 ]
Vemuganti, Raghu [1 ,2 ]
机构
[1] Univ Wisconsin, Dept Neurol Surg, Sch Med & Publ Hlth, Madison, WI 53792 USA
[2] Univ Wisconsin, Neurosci Training Program, Sch Med & Publ Hlth, Madison, WI 53792 USA
关键词
Aging; Cerebral ischemia; Hormones; microRNAs; Neuroprotection; Sex differences; Thrombolytic agents; CEREBRAL-ARTERY OCCLUSION; TRANSIENT FOCAL ISCHEMIA; RECEPTOR MODULATORS DECREASE; BLOOD-BRAIN-BARRIER; PLASMINOGEN-ACTIVATOR; 17-BETA-ESTRADIOL PROTECTS; INFLAMMATORY RESPONSE; ATRIAL-FIBRILLATION; GLUTAMATE RELEASE; HYPOXIA-ISCHEMIA;
D O I
10.1111/cns.12346
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Stroke is one of the leading causes of death and disability worldwide. Experimental and clinical studies showed that sex and age play an important role in deciding the outcome after stroke. At younger ages, males were shown to have a higher risk for stroke than females. However, this trend reverses in older ages particularly when females reach menopause. Many preclinical studies indicate that steroid hormones modulate the age-dependent differential stroke outcome. In addition, patterns of cell death pathways activated following cerebral ischemia are distinct between males and females, but independent of steroid hormones. Recent studies also indicate that microRNAs play important roles in mediating sex-specific stroke outcome by regulating stroke-related genes. This review discusses the contribution of sex and age to outcome after stroke with particular emphasis on the experimental studies that examined the effects of steroid hormones, differential cell death pathways, and involvement of sex-specific microRNAs following cerebral ischemia. Current understanding of the role of thrombolytic agents in stroke therapy is also discussed.
引用
收藏
页码:327 / 336
页数:10
相关论文
共 148 条
[1]   The Poly(ADP-ribose) polymerases (PARPs): New roles in intracellular transport [J].
Abd Elmageed, Zakaria Y. ;
Naura, Amarjit S. ;
Errami, Youssef ;
Zerfaoui, Mourad .
CELLULAR SIGNALLING, 2012, 24 (01) :1-8
[2]   Testosterone protects cerebellar granule cells from oxidative stress-induced cell death through a receptor mediated mechanism [J].
Ahlbom, E ;
Prins, GS ;
Ceccatelli, S .
BRAIN RESEARCH, 2001, 892 (02) :255-262
[3]   Gender-linked brain injury in experimental stroke [J].
Alkayed, NJ ;
Harukuni, I ;
Kimes, AS ;
London, ED ;
Traystman, RJ ;
Hurn, PD .
STROKE, 1998, 29 (01) :159-165
[4]  
[Anonymous], OBSTET GYNECOL INT
[5]  
[Anonymous], 2014, CIRCULATION, DOI DOI 10.1161/01.cir.0000441139.02102.80
[6]   Selective Oestrogen Receptor Modulators Decrease the Inflammatory Response of Glial Cells [J].
Arevalo, M. A. ;
Diz-Chaves, Y. ;
Santos-Galindo, M. ;
Bellini, M. J. ;
Garcia-Segura, L. M. .
JOURNAL OF NEUROENDOCRINOLOGY, 2012, 24 (01) :183-190
[7]   Erythropoietin exerts neuroprotective effect in neonatal rat model of hypoxic-ischemic brain injury [J].
Aydin, A ;
Genç, K ;
Akhisaroglu, M ;
Yorukogluc, K ;
Gokmen, N ;
Gonullu, E .
BRAIN & DEVELOPMENT, 2003, 25 (07) :494-498
[8]   Role of estrogen in angiogenesis in cardiovascular diseases [J].
Barnabas, Oche ;
Wang, Hong ;
Gao, Xiu-Mei .
JOURNAL OF GERIATRIC CARDIOLOGY, 2013, 10 (04) :377-382
[9]   Estrogen and selective estrogen receptor modulators exert neuroprotective effects and stimulate the expression of selective Alzheimer's disease indicator-1, a recently discovered antiapoptotic gene, in human neuroblast long-term cell cultures [J].
Benvenuti, S ;
Luciani, P ;
Vannelli, GB ;
Gelmini, S ;
Franceschi, E ;
Serio, M ;
Peri, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (03) :1775-1782
[10]   Pathophysiology of perinatal brain damage [J].
Berger, R ;
Garnier, Y .
BRAIN RESEARCH REVIEWS, 1999, 30 (02) :107-134