Selective Loss of Calretinin-Poor Cochlear Afferent Nerve Fibers in Streptozotocin-Induced Hyperglycemic Mice

2020 ◽  
Vol 20 (9) ◽  
pp. 5515-5519
Author(s):  
Kwon Woo Kang ◽  
Rudra Pangeni ◽  
JinWoo Park ◽  
Jaekwang Lee ◽  
Eunyoung Yi

Hearing loss is one of the major complications of diabetes mellitus and significantly lowers the quality of life of diabetic patients. In studies using diabetic animal models hearing loss have been frequently associated with damages to cochlear afferent fibers. Recent studies suggested that cochlear afferent neurons are composed of heterogeneous populations and a subgroup of neurons equipped with low level of calretinin might be more vulnerable to various noxious stimuli such as noise and neurotoxins. Here, we tested if cochlear afferent neurons deficient in the Ca2+-buffering protein calretinin are more vulnerable to hyperglycemic insults. Streptozotocin-induced (50 mg/kg, i.p.) hyperglycemic mice (>250 mg/dl) were tested. The expression patterns of calretinin in peripheral processes and the cell bodies of cochlear afferent nerve fibers were examined using immunohistochemistry and confocal microscopy. The proportion of calretinin-poor cochlear afferent fibers was much lower in hyperglycemic mice compared to the normoglycemic control group. (30.0 vs. 55.5% in the peripheral process; 15.7 vs. 24.4 % in spiral ganglion neuron). The results suggest that calretinin-poor cochlear nerve fibers may be selectively lost after the hyperglycemic insults. The finding also supports a calretinin’s neuroprotective role against diabetic neuropathy in cochlear afferent neurons.

2008 ◽  
Vol 104 (5) ◽  
pp. 1394-1401 ◽  
Author(s):  
David F. Donnelly

The mechanism by which action potentials (APs) are generated in afferent nerve fibers in the carotid body is unknown, but it is generally speculated to be release of an excitatory transmitter and synaptic depolarizing events. However, previous results suggested that Na+ channels in the afferent nerve fibers play an important role in this process. To better understand the potential mechanism by which Na+ channels may generate APs, a mathematical model of chemoreceptor nerve fibers that incorporated Hodgkin-Huxley-type Na+ channels with kinetics of activation and inactivation, as determined previously from recordings of petrosal chemoreceptor neurons, was constructed. While the density of Na+ channels was kept constant, spontaneous APs arose in nerve terminals as the axonal diameter was reduced to that in rat carotid body. AP excitability and pattern were similar to those observed in chemoreceptor recordings: 1) a random pattern at low- and high-frequency discharge rates, 2) a high sensitivity to reductions in extracellular Na+ concentration, and 3) a variation in excitability that increased with AP generation rate. Taken together, the results suggest that an endogenous process in chemoreceptor nerve terminals may underlie AP generation, a process independent of synaptic depolarizing events.


2019 ◽  
Vol 60 (2) ◽  
pp. 202-210 ◽  
Author(s):  
Judith M. Lionarons ◽  
Govert Hoogland ◽  
Ruben G. F. Hendriksen ◽  
Catharina G. Faber ◽  
Danique M. J. Hellebrekers ◽  
...  

1929 ◽  
Vol 26 (4) ◽  
pp. 288-289
Author(s):  
C. D. Leake ◽  
A. G. Kammer ◽  
J. B. Hitz

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