Effect of intranasal administration of neurotrophic factors on regeneration of chemically degenerated olfactory epithelium in aging mice

被引:18
作者
Fukuda, Yuriko [1 ,2 ]
Katsunuma, Sayaka [1 ,3 ]
Uranagase, Atsuhiro [4 ]
Nota, Jumpei [5 ]
Nibu, Ken-ichi [1 ]
机构
[1] Kobe Univ, Grad Sch Med, Kobe, Hyogo, Japan
[2] Kobe Red Cross Hosp, Kobe, Hyogo, Japan
[3] Hyogo Prefectural Kobe Childrens Hosp, Kobe, Hyogo, Japan
[4] Shinko Mem Hosp, Kobe, Hyogo, Japan
[5] Ehime Univ, Grad Sch Med, Matsuyama, Ehime, Japan
关键词
aging; neurotrophic factors; olfactory epithelium; FIBROBLAST-GROWTH-FACTOR; NEURAL STEM-CELLS; PROLIFERATION; NEUROGENESIS; HIPPOCAMPUS; EXPRESSION;
D O I
10.1097/WNR.0000000000001125
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the mammalian olfactory epithelium (OE), neurogenesis continues throughout the lifetime, by replacing olfactory receptor neurons (ORNs) lost by normal turnover in the postnatal period. However, this ability decreases with age and/or because of various toxic factors. To date, no effective treatment for olfactory dysfunction' especially because of aging, is available in clinical practice. Here, we examined the effects of intranasal administration of fibroblast growth factor-2 and insulin-like growth factor-1 in gelatin hydrogel on the degenerated OE of aging mice induced by methimazole administration. These topical treatments led to increases in the number of olfactory marker protein-positive cells, which identified mature ORNs, resulting in the increased thickness of OE. These results indicate that both fibroblast growth factor-2 and insulin-like growth factor-1 promote the proliferation of basal cells and differentiation of immature ORNs into mature ORNs in the degenerated OE of aging mice. These agents might be promising candidates for the treatment of degenerated OE of aging humans.
引用
收藏
页码:1400 / 1404
页数:5
相关论文
共 22 条
[1]  
Bakari A., 2012, Archives of International Surgery, V2, P2
[2]   Identification and molecular regulation of neural stem cells in the olfactory epithelium [J].
Beites, CL ;
Kawauchi, S ;
Crocker, CE ;
Calof, AL .
EXPERIMENTAL CELL RESEARCH, 2005, 306 (02) :309-316
[3]  
Calof AL, 1998, J NEUROBIOL, V36, P190, DOI 10.1002/(SICI)1097-4695(199808)36:2<190::AID-NEU7>3.0.CO
[4]  
2-X
[5]   Olfaction and anosmia in rhinosinusitis [J].
Dalton, P .
CURRENT ALLERGY AND ASTHMA REPORTS, 2004, 4 (03) :230-236
[6]   GENESIS OF OLFACTORY RECEPTOR NEURONS IN-VITRO - REGULATION OF PROGENITOR-CELL DIVISIONS BY FIBROBLAST GROWTH-FACTORS [J].
DEHAMER, MK ;
GUEVARA, JL ;
HANNON, K ;
OLWIN, BB ;
CALOF, AL .
NEURON, 1994, 13 (05) :1083-1097
[7]   OLFACTORY NEUROGENESIS - GENETIC OR ENVIRONMENTAL CONTROLS [J].
FARBMAN, AI .
TRENDS IN NEUROSCIENCES, 1990, 13 (09) :362-365
[8]   Fibroblast growth factors in the developing central nervous system [J].
Ford-Perriss, M ;
Abud, H ;
Murphy, M .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2001, 28 (07) :493-503
[9]  
Gokoffski KK, 2010, NEUROBIOLOGY OLFACTI
[10]   Molecular signals regulating proliferation of stem and progenitor cells in mouse olfactory epithelium [J].
Kawauchi, S ;
Beites, CL ;
Crocker, CE ;
Wu, HH ;
Bonnin, A ;
Murray, R ;
Calof, AL .
DEVELOPMENTAL NEUROSCIENCE, 2004, 26 (2-4) :166-180