Evaluation of the usefulness of three-dimensional optical coherence tomography in a guinea pig model of endolymphatic hydrops induced by surgical obliteration of the endolymphatic duct

Abstract. Optical coherence tomography (OCT) has advanced significantly over the past two decades and is currently used extensively to monitor the internal structures of organs, particularly in ophthalmology and dermatology. We used ethylenediamine tetra-acetic acid (EDTA) to decalcify the bony walls of the cochlea and investigated the inner structures by deep penetration of light into the cochlear tissue using OCT on a guinea pig model of endolymphatic hydrops (EH), induced by surgical obliteration of the endolymphatic duct. The structural and functional changes associated with EH were identified using OCT and auditory brainstem response tests, respectively. We also evaluated structural alterations in the cochlea using three-dimensional reconstruction of the OCT images, which clearly showed physical changes in the cochlear structures. Furthermore, we found significant anatomical variations in the EH model and conducted graphical analysis by strial atrophy for comparison. The physical changes included damage to and flattening of the organ of Corti—evidence of Reissner’s membrane distention—and thinning of the lateral wall. These results indicate that observation of EDTA-decalcified cochlea using OCT is significant in examination of gradual changes in the cochlear structures that are otherwise not depicted by hematoxylin and eosin staining.

[1]  K Kawamoto,et al.  Ultrastructural changes of the nerve elements following disruption of the organ of Corti. II. Nerve elements outside the organ of Corti. , 1979, Acta oto-laryngologica.

[2]  N. Sakai,et al.  Ultrastructural changes of the nerve elements following disruption of the organ of Corti. I. Nerve elements in the organ of Corti. , 1977, Acta oto-laryngologica.

[3]  D. Jackson,et al.  3-D optical coherence tomography of the laryngeal mucosa. , 2004, Clinical otolaryngology and allied sciences.

[4]  Tatsunori Sakamoto,et al.  In Vivo Imaging of Mouse Cochlea by Optical Coherence Tomography , 2014, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

[5]  R. Kimura,et al.  Animal models of endolymphatic hydrops. , 1982, American journal of otolaryngology.

[6]  E A Swanson,et al.  Micrometer-scale resolution imaging of the anterior eye in vivo with optical coherence tomography. , 1994, Archives of ophthalmology.

[7]  H. Wit,et al.  Two-phase endolymphatic hydrops: a new dynamic guinea pig model. , 1997, Acta oto-laryngologica.

[8]  Young Chul Kim,et al.  Expression of osmotic stress protein 94 in murine endolymphatic hydrops model , 2012, Acta oto-laryngologica.

[9]  Tatsuya Yamasoba,et al.  Evaluation of the Internal Structure of Normal and Pathological Guinea Pig Cochleae Using Optical Coherence Tomography , 2013, Audiology and Neurotology.

[10]  Jeehyun Kim,et al.  In vivo imaging of middle-ear and inner-ear microstructures of a mouse guided by SD-OCT combined with a surgical microscope. , 2014, Optics express.

[11]  J C Andrews,et al.  The surgical approach to the endolymphatic sac and the cochlear aqueduct in the guinea pig. , 1989, American journal of otolaryngology.

[12]  John S. Oghalai,et al.  Quantitative imaging of cochlear soft tissues in wild-type and hearing-impaired transgenic mice by spectral domain optical coherence tomography , 2011, Optics express.

[13]  John S. Oghalai,et al.  In vivo vibrometry inside the apex of the mouse cochlea using spectral domain optical coherence tomography , 2013 .

[14]  J. Welzel Optical coherence tomography in dermatology: a review , 2001, Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging.

[15]  Zhongping Chen,et al.  Optical Coherence Tomography of the Cochlea in the Porcine Model , 2008, The Laryngoscope.

[16]  Matti Anniko,et al.  A new animal model for Ménière's disease , 2008, Acta oto-laryngologica.

[17]  R. Kimura,et al.  LII Experimental Blockage of the Endolymphatic DUCT and SAC and ITS Effect on the Inner Ear of the Guinea Pig , 1967, The Annals of otology, rhinology, and laryngology.

[18]  B. Wong,et al.  Optical coherence tomography of the rat cochlea. , 2000 .

[19]  J. Fujimoto,et al.  High-precision, high-accuracy ultralong-range swept-source optical coherence tomography using vertical cavity surface emitting laser light source. , 2013, Optics letters.

[20]  Zhongping Chen,et al.  Imaging the internal structure of the rat cochlea using optical coherence tomography at 0.827 microm and 1.3 microm. , 2004, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

[21]  Zhongping Chen,et al.  Imaging the Internal Structure of the Rat Cochlea Using Optical Coherence Tomography at 0.827 μm and 1.3 μm , 2004 .

[22]  Hinrich Staecker,et al.  Optical Coherence Tomography Imaging of the Inner Ear: A Feasibility Study with Implications for Cochlear Implantation , 2008, The Annals of otology, rhinology, and laryngology.

[23]  Cliff A. Megerian,et al.  Surgical Induction of Endolymphatic Hydrops by Obliteration of the Endolymphatic Duct , 2010, Journal of visualized experiments : JoVE.

[24]  J. Fujimoto,et al.  High-resolution optical coherence tomographic imaging using a mode-locked Ti:Al2O3 laser source , 2001 .

[25]  Chen D. Lu,et al.  Retinal, anterior segment and full eye imaging using ultrahigh speed swept source OCT with vertical-cavity surface emitting lasers , 2012, Biomedical optics express.

[26]  J G Fujimoto,et al.  High-resolution optical coherence tomographic imaging using a mode-locked Ti:Al(2)O(3) laser source. , 1995, Optics letters.

[27]  Kenji Kondo,et al.  Supporting cell proliferation after hair cell injury in mature guinea pig cochlea in vivo , 2006, Cell and Tissue Research.