Karine Faucher

Damage and functional recovery of the Atlantic cod (Gadus morhua) inner ear hair cells following local injection of gentamicin

This study addresses the ultrastructural and functional damage and subsequent recovery of the inner ear in the Atlantic cod following intrasaccular gentamicin injection. Inner ear damage was assessed using SEM and measurements of AEP following 250-Hz pure-tone stimuli. Data from gentamicin-treated fish were compared with control (no injection) and sham (injection of saline) fish. Control fish had normal response thresholds associated with well-developed hair cell bundles in their macula sacculi. Sham fish had higher response thresholds compared with control fish during the first week post-intervention, but response thresholds were subsequently normal. Treated fish displayed significant inner ear damage associated with an increased average AEP threshold on the third day following treatment. Thereafter, inner ear tissue displayed signs of progressive regeneration until it was comparable to controls from the 14th day. Response thresholds were similar to those of control fish from the 17th day following treatment. These observations suggest that the macula sacculi of Atlantic cod can regenerate towards a near-complete functional and ultrastructural recovery within 17–21 days following ototoxic gentamicin treatment.

Spatial Distribution and Morphological Characteristics of the Trunk Lateral Line Neuromasts of the Sea Bass (Dicentrarchus labrax, L.; Teleostei, Serranidae)

The morphology and spatial distribution of the different types of neuromasts encountered on the trunk lateral line of the sea bass (Dicentrarchus labrax) were examined using scanning electron microscopy. The sea bass trunk lateral line exhibits a complete straight pattern. In their basic features, the two types of neuromasts present, canal and superficial, resemble what has been described in other fishes. They are similar in their general cellular organization but differ in sizes, and shapes, as well as in the densities and lengths of their hair bundles. However, the sea bass trunk lateral line distinguishes itself in several ways. For instance, the pores of the canal segments are partially obstructed due to the overlap of scales throughout the trunk. Moreover, based on the density and length of the hair bundles, two distinct areas, central and peripheral, could be distinguished within the maculae of canal neuromasts. Their cupulae are also peculiar as they possess two wing-like extensions and that their central core appears to be organized in layers instead of columns. In addition, the superficial neuromasts, up to 6 per scale, are either round or elliptical and seem to be distributed serendipitously. Finally, within the maculae of both types of neuromasts, a significant number of hair bundles do not follow the two-directional polarity pattern usually described. Although some hypotheses are proposed, the influence of these characteristics in terms of signal encoding and fish behavior is yet to be understood.

Quantitative Aspects of the Spatial Distribution and Morphological Characteristics of the Sea Bass (Dicentrarchus labrax L.; Teleostei, Serranidae) Trunk Lateral Line Neuromasts

The results presented herein report quantitative data relative to the distribution and morphological characteristics of both types of neuromasts encountered on the trunk lateral line of the sea bass (Dicentrarchus labrax, L.). These data were obtained from scanning electron micrographs. They indicate that, as expected, each modified scale of the sea bass possessed a single canal neuromast with long axis oriented parallel to the fish’s long axis. In contrast to several fish species, two thirds of superficial neuromasts observed herein were oriented perpendicular to the fish’s long axis. However, whatever the main orientation of superficial neuromasts, two thirds of their hair bundles were oriented parallel to the long axis of the animal with approximately half of them in the direction of the head. Similar ratios were observed for canal neuromasts whatever the area of the maculae: central or peripheral. For both types of neuromasts it was not possible to clearly distinguish a paired organization of hair bundles with opposing polarities. Superficial neuromasts on each trunk canal scale were located on either the dorsal or ventral side of the canal and appeared to be distributed along the trunk lateral line with a higher probability to be encountered closer to the operculum. The frequency of presence and the average number of superficial neuromasts per scale increased with fish size. We observed a size gradient for canal neuromasts between the operculum and caudal peduncle. This gradation was correlated with a reduction of the width of the central area of the canal segment. Canal neuromasts were always localized in the larger portions of the canal segments. Taken together, these results point out some specific features associated with the sea bass trunk lateral line. With the previous report, they establish the first full description of the trunk lateral line of sea bass and will be useful for upcoming experiments regarding the function of the two types of neuromasts.

Effects of systemic versus local gentamicin on the inner ear in the Atlantic cod, Gadus morhua (L.), relevance for fish hearing investigations.

UNLABELLED Fish models are increasingly being used for hearing research investigations. Aminoglycoside antibiotics that are used for damaging the inner ear hair cells can have systemic side effects leading to death of study animals. This study aimed to compare two methods: (i) systemic (intravenous) and (ii) local (intrasaccular) gentamicin administration for induction of inner ear hair cell damage in the Atlantic cod, Gadus morhua (L.). Hair cell damage was assessed using scanning electron microscopy; hair cell density, prevalence of immature hair cells and kinocilia length were measured. Gentamicin-treated fish were compared with control and sham fish. Intravenous gentamicin led to dose-dependent mortality caused by nephrotoxicity. The only visible effect after treatment was more immature hair cells and shorter kinocilia, the effect on hair cell density was equivocal. Following intrasaccular gentamicin treatment, fish mortality was negligible, and hair cells were damaged regardless of dose. Here, we observed decreased hair cell density, high prevalence of immature hair cells, and significantly shortened kinocilia. CONCLUSION intrasaccular injection is preferable to intravenous injection of gentamicin for the study of ototoxicity in the Atlantic cod.