2009
DOI: 10.1002/ar.20881
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Neurochemistry of Olivocochlear Neurons in the Hamster

Abstract: The present study was conducted to characterize the superior olivary complex (SOC) of the lower brain stem in the pigmented Djungarian hamster Phodopus sungorus. Using Nissl-stained serial cryostat sections from fresh-frozen brains, we determined the borders of the SOC nuclei. We also identified olivocochlear (OC) neurons by retrograde neuronal tracing upon injection of Fluoro-Gold into the scala tympani. To evaluate the SOC as a putative source of neuronal nitric oxide synthase (nNOS), arginine-vasopressin (A… Show more

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Cited by 18 publications
(10 citation statements)
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“…Gel foam pellets (Gelita Tampon, Braun, Melsungen, Germany) were placed in the round window niche and moistened with 10 µL artificial perilymph. This method to localize OCN in the brainstem was used in a number of our previous studies (Reuss et al, , in press; Riemann and Reuss, ).…”
Section: Methodsmentioning
confidence: 99%
“…Gel foam pellets (Gelita Tampon, Braun, Melsungen, Germany) were placed in the round window niche and moistened with 10 µL artificial perilymph. This method to localize OCN in the brainstem was used in a number of our previous studies (Reuss et al, , in press; Riemann and Reuss, ).…”
Section: Methodsmentioning
confidence: 99%
“…We described altered expression of PAC1-R in PACAP-deficient mice cochlea compared to wild-type mice (Tamas et al 2012 ). The modulatory character of PACAP has also been reported in the superior olive, which is considered to be a major complex involved in multiple aspects of hearing (Reuss et al 2009 ).…”
Section: Discussionmentioning
confidence: 97%
“…For double-immunostaining experiments, selected sections were incubated in primary Cygb-antibody as described above and simultaneously, in either a polyclonal sheep antibody raised against (nNOS, 1:50, Abcam, Cambridge, UK) or a mouse monoclonal antibody raised against tyrosine hydroxylase (TH, 1:200, Chemicon, Temecula, CA, USA). Both antibodies were used and characterized in our laboratory previously (Reuss et al, 2009a , b ). The additional primary antibodies were visualized using Cy2-conjugated F(ab′)2-fragments of anti-sheep or anti-mouse IgG (Dianova) at 1:300 dilution.…”
Section: Methodsmentioning
confidence: 99%