rat model;
auditory brainstem response (ABR);
vesicular transport proteins;
presbyacusis;
hearing loss;
cochlear nucleus;
AUDITORY BRAIN-STEM;
VESICULAR GLUTAMATE TRANSPORTERS;
CALCIUM-BINDING PROTEINS;
GROWTH-FACTOR-I;
UNILATERAL COCHLEAR REMOVAL;
CNS STRUCTURAL ELEMENTS;
INFERIOR COLLICULUS;
RESPONSE ABR;
SUPERIOR COLLICULUS;
CENTRAL NUCLEUS;
D O I:
10.3389/fnagi.2014.00029
中图分类号:
R592 [老年病学];
C [社会科学总论];
学科分类号:
03 ;
0303 ;
100203 ;
摘要:
Age-related hearing loss (ARHL) is one of the most frequent sensory impairments in senescence and is a source of important socio-economic consequences. Understanding the pathological responses that occur in the central auditory pathway of patients who suffer from this disability is vital to improve its diagnosis and treatment. Therefore, the goal of this study was to characterize age-related modifications in auditory brainstem responses (ABR) and to determine whether these functional responses might be accompanied by an imbalance between excitation and inhibition in the cochlear nucleus of Wistar rats. To do so, ABR recordings at different frequencies and immunohistochemistry for the vesicular glutamate transporter 1 (VGLUT1) and the vesicular GABA transporter (VGAT) in the ventral cochlear nucleus (VCN) were performed in young, middle-aged and old male Wistar rats. The results demonstrate that there was a significant increase in the auditory thresholds, a significant decrease in the amplitudes and an increase in the latencies of the ABR waves as the age of the rat increased. Additionally, there were decreases in VGLUT1 and VGAT immunostaining in the VCN of older rats compared to younger rats. Therefore, the observed age-related decline in the magnitude of auditory evoked responses might be due in part to a reduction in markers of excitatory function; meanwhile, the concomitant reduction in both excitatory and inhibitory markers might reflect a common central alteration in animal models of ARLH. Together, these findings highlight the suitability of the Wistar rat as an excellent model to study ARHL.
机构:
Harvard Med Sch, Massachusetts Eye & Ear Infirm, Boston, MA 02114 USA
Univ Texas San Antonio, San Antonio, TX USAHarvard Med Sch, Massachusetts Eye & Ear Infirm, Boston, MA 02114 USA
Valero, M. D.
Ratnam, R.
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机构:
Univ Texas San Antonio, San Antonio, TX USA
Univ Illinois, Urbana, IL 61801 USAHarvard Med Sch, Massachusetts Eye & Ear Infirm, Boston, MA 02114 USA
机构:
Univ Michigan, Dept Otolaryngol, Kresge Hearing Res Inst, Med Sci I Bldg,Rm 5315,1150 West Med Ctr Dr, Ann Arbor, MI 48109 USA
Chang Gung Univ, Coll Med, Kaohsiung Chang Gung Mem Hosp, Div Otol,Dept Otolaryngol, Kaohsiung, TaiwanUniv Michigan, Dept Otolaryngol, Kresge Hearing Res Inst, Med Sci I Bldg,Rm 5315,1150 West Med Ctr Dr, Ann Arbor, MI 48109 USA
Yang, Chao-Hui
Schrepfer, Thomas
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Univ Michigan, Dept Otolaryngol, Kresge Hearing Res Inst, Med Sci I Bldg,Rm 5315,1150 West Med Ctr Dr, Ann Arbor, MI 48109 USAUniv Michigan, Dept Otolaryngol, Kresge Hearing Res Inst, Med Sci I Bldg,Rm 5315,1150 West Med Ctr Dr, Ann Arbor, MI 48109 USA
Schrepfer, Thomas
Schacht, Jochen
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机构:
Univ Michigan, Dept Otolaryngol, Kresge Hearing Res Inst, Med Sci I Bldg,Rm 5315,1150 West Med Ctr Dr, Ann Arbor, MI 48109 USAUniv Michigan, Dept Otolaryngol, Kresge Hearing Res Inst, Med Sci I Bldg,Rm 5315,1150 West Med Ctr Dr, Ann Arbor, MI 48109 USA