Evidence map›Paper›PMID 33691255›Full record

ArticleHearing research2021

Development of a chronically-implanted mouse model for studies of cochlear health and implant function.

Deborah J Colesa, Jenna Devare, Donald L Swiderski, Lisa A Beyer, Yehoash Raphael, Bryan E Pfingst

Open access · greenAbstract read
In one paragraph

Article in Hearing research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Cochlear Health and Cochlear-implant Function.Journal of the Association for Research in Otolaryngology : JARO · 2023
    Review
  9. Article
  10. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Deborah J ColesaKresge Hearing Research Institute, Department of Otolaryngology - Head and Neck Surgery, 1150 West Medical Center Drive, University of Michigan, Ann Arbor 48109-5616, MI, USA.
Jenna DevareKresge Hearing Research Institute, Department of Otolaryngology - Head and Neck Surgery, 1150 West Medical Center Drive, University of Michigan, Ann Arbor 48109-5616, MI, USA.
Donald L SwiderskiKresge Hearing Research Institute, Department of Otolaryngology - Head and Neck Surgery, 1150 West Medical Center Drive, University of Michigan, Ann Arbor 48109-5616, MI, USA.
Lisa A BeyerKresge Hearing Research Institute, Department of Otolaryngology - Head and Neck Surgery, 1150 West Medical Center Drive, University of Michigan, Ann Arbor 48109-5616, MI, USA.
Yehoash RaphaelKresge Hearing Research Institute, Department of Otolaryngology - Head and Neck Surgery, 1150 West Medical Center Drive, University of Michigan, Ann Arbor 48109-5616, MI, USA.
Bryan E PfingstKresge Hearing Research Institute, Department of Otolaryngology - Head and Neck Surgery, 1150 West Medical Center Drive, University of Michigan, Ann Arbor 48109-5616, MI, USA. Electronic address: bpfingst@umich.edu.
University of Michigan · US

Funding

Scientific Synergy CoreP30DC005188 · NIDCD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCHACHT, JOCHEN · 2002 to 2016
$10.3M
Enhancing Atoh1 function in hair cell regenerationR01DC014832 · NIDCD · WASHINGTON UNIVERSITY · PI Gabriel Corfas, Andrew K Groves · 2016 to 2026
$6.7M
Advanced Research Training in OtolaryngologyT32DC005356 · NIDCD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CORFAS, GABRIEL · 2002 to 2021
$3.5M
Functionally Important Features of the Electrically Stimulated CochleaR01DC015809 · NIDCD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PFINGST, BRYAN E · 2017 to 2021
$3.2M
NIDCD NIH HHS P30 DC005188NIDCD NIH HHS R01 DC014832NIDCD NIH HHS R01 DC015809NIDCD NIH HHS T32 DC005356
6 · The paper itself

Abstract

Mice with chronic cochlear implants can significantly contribute to our understanding of the relationship between cochlear health and implant function because of the availability of molecular tools for controlling conditions in the cochlea and transgenic lines modeling human disease. To date, research in implanted mice has mainly consisted of short-term studies, but since there are large changes in implant function following implant insertion trauma, and subsequent recovery in many cases, longer-term studies are needed to evaluate function and perception under stable conditions. Because frequent anesthetic administration can be especially problematic in mice, a chronic model that can be tested in the awake condition is desirable. Electrically-evoked compound action potentials (ECAPs) recorded with multichannel cochlear implants are useful functional measures because they can be obtained daily without anesthesia. In this study, we assessed changes and stability of ECAPs, electrically-evoked auditory brainstem responses (EABRs), ensemble spontaneous activity (ESA), and impedance data over time after implanting mice with multichannel implants. We then compared these data to histological findings in these implanted cochleae, and compared results from this chronic mouse model to data previously obtained in a well-established chronically-implanted guinea pig model. We determined that mice can be chronically implanted with cochlear implants, and ECAP recordings can be obtained frequently in an awake state for up to at least 42 days after implantation. These recordings can effectively monitor changes or stability in cochlear function over time. ECAP and EABR amplitude-growth functions (AGFs), AGF slopes, ESA levels and impedances in mice with multichannel implants appear similar to those found in guinea pigs with long-term multichannel implants. Animals with better survival of spiral ganglion neurons (SGNs) and inner hair cells (IHCs) have steeper AGF slopes, and larger ESA responses. The time course of post-surgical ear recovery may be quicker in mice and can show different patterns of recovery which seem to be dependent on the degree of insertion trauma and subsequent histological conditions. Histology showed varying degrees of cochlear damage with fibrosis present in all implanted mouse ears and small amounts of new bone in a few ears. Impedance changes over time varied within and across animals and may represent changes over time in multiple variables in the cochlear environment post-implantation. Due to the small size of the mouse, susceptibility to stress, and the higher potential for implant failure, chronic implantation in mice can be challenging, but overall is feasible and useful for cochlear implant research.

Indexed as

Cochlear ImplantationCochlear ImplantsAnimalsCochleaDisease Models, AnimalElectric StimulationEvoked Potentials, AuditoryEvoked Potentials, Auditory, Brain StemGuinea PigsMiceAuditory prosthesisCochlear implantElectrically-evoked compound action potential (ECAP)Mouse

Identifiers

PMID33691255
PMCPMC8080901
OpenAlexW3131625463

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.