Ear Of Guinea Pig Research Articles

Changes in auditory function associated with 2‐cyano‐butyl‐acrylate adhesive implanted in the middle ear of experimental animals

The effects on auditory function caused by the implantation of 2-cyano-butyl-acrylate adhesive in the middle ear was investigated in experimental animals. Auditory brainstem responses to click stimuli were used to measure hearing thresholds prior to and following implantation of 2-cyano-butyl-acrylate adhesive in the middle ear of guinea pigs. A permanent and deep threshold shift observed at 2 months in 62% of the examined animals, suggested that this tissue adhesive is an ototoxic middle ear implant material and should not be considered in reconstructive middle ear surgery. The functional data correlate well with some of the previous morphological observations.

Right–Left Correlation in Guinea Pig Ears After Noise Exposure

In order to investigate whether experimental material consisting of noise-exposed animals should be regarded as 'ears' or 'animals', a comparison was made between the permanent threshold shifts in the right and left ears in 53 groups of noise-exposed guinea-pigs, with 5 animals in each group. The action potential (N1) thresholds were measured at fourteen frequencies in both ears. In the noise-exposed animals, the threshold elevations were up to 40 dB. The average right-left correlation coefficient within each group was about 0.79, regardless of noise energy. The degree of correlation was significantly greater after impact noise than after continuous noise. As a consequence of the high right-left correlation, the informative value of measuring a second ear in the same animal was, in our experiments, only 11% of that of the first one. No correlation could be found between the degree of skin pigmentation and the threshold elevation.

Frequency variation in spontaneous sound emissions from guinea pig and human ears

Spontaneous acoustic emissions were recorded from 7 of 15 human ears at frequencies between 900 and 4000 Hz and just above 1000 Hz in a guinea pig. The constancy or changes in the frequency composition of these emissions is of particular interest in the light of current models which implicate outer hair cell activity in their generation. In our present study, most emissions underwent continuous fluctuations in frequency over a bandwidth of 0.5-10 Hz in humans and more than 20 Hz in a young guinea pig. Jumps in frequency of emission by as much as 20 Hz occurred during test sessions in some of the human ears. Changes in emission frequency were also observed during suppression by an externally delivered tone. The frequency of the emissions at successive test sessions also varied in some human ears and in the guinea pig between the ages of 6 and 9 weeks. The guinea pig emission also underwent an increase of 50 Hz in frequency and a reduction of 25 dB in level during recovery from anaesthesia. Neely's model for the role of hair cells in the generation of spontaneous emissions suggests that changes in hair cell conductance could influence the frequency of spontaneous oscillation. The small, but continuous changes in spontaneous emission frequency seen in all ears may reflect changes in conductance at the hair cell level due to synaptic and transducer channel activity.

Long-Term Effects of Intense Sound on Hair Cells of Corti's Organ and Endocochlear DC Potential

Cochleograms of guinea pig ears were made 30-40 days after exposure to intense pure tones of 300 Hz, 500 Hz, 2 kHz, or 4 kHz at 130-150 dB SPL for 4-24 h. At 4 kHz, hair cells in the basal turn disappeared totally, in the second turn moderately, and were relatively undamaged in the third and apical turns. At 500 Hz, hair cells in the second and third turns were almost completely injured and at 300 Hz moderately damaged in the third and apical turns although the basal turn remained undamaged. At 2 kHz for 9 h, hair cells were almost completely injured in all turns. Negative endocochlear DC potential (negative EP) induced by furosemide was observed in the basal turn but not in the third turn of animals exposed to 300 Hz. Contrarily, negative EP was observed in the third turn but not in the basal turn of animals exposed to 4 kHz. We conclude that the hair cells of Corti's organ play an essential role in the production of negative EP.

Histamine H1-receptor of vascular endothelial cells cultured from guinea pig skin

In this study, a new procedure for the cultivation of dermal vascular endothelial cells from guinea pig ear lobe was established, and specific binding of [3H]mepyramine to the cultured cell membranes was demonstrated. The vascular endothelial cells were successfully isolated from the dermis of guinea pig ear lobes by the intravenous injection of dispase. Guinea pig serum, as a supplementary component in culture medium, is more suitable for the culture of guinea pig dermal vascular endothelial cell than is fetal calf serum. The [3H]mepyramine binding study indicated the presence of a large number of H1-receptors on the membrane of dermal vascular endothelial cells of guinea pigs, suggesting the important role of endothelial cells in cutaneous reactions to histamine.

Melanin in the inner ear. An experimental study with control and kanamycin-intoxicated colored guinea-pigs.

Following several studies on the effects of kanamycin toxicity on the inner ears of guinea pigs, we have studied the importance of melanin in this phenomenon. Transmission electron microscopy showed that, under the influence of kanamycin, the intermediate strial cells developed a secretory aspect similar to that seen in skin melanocytes. This aspect as yet has never been described for the inner ear cells. A planimetric, morphometric method was also used to determine the strial cell melanin status in control animals. Additional findings in the study confirmed an increase in the number of melanosomes during kanamycin poisoning. Statistical data are discussed.

Type II Collagen Distribution in the Ear of the Guinea Pig Fetus

By using monoclonal antibodies to type II collagen and immunohistochemical techniques, we studied the distribution of type II collagen in the developing guinea pig ear. Type II collagen appearance and disappearance corresponded to cartilage development and resorption. Type II collagen was identified in Meckel's and Reichert's cartilages, the cartilage plate of the auricle and external acoustic meatus, the ossicles, eustachian tube cartilage, and the otic capsule. Type II collagen also appeared with the development of structures in noncartilaginous parts including the tympanic membrane, tympanic annulus, basilar membrane, spiral limbus, spiral ligament, and osseous spiral lamina, Rosenthal's canal, the maculae of the utricle and saccule, and the semicircular canal membrane, crista ampullaris, and endolymphatic duct. Type II collagen is distributed widely in the ear after the early stages of development. Thus, type II collagen should be considered an important structural component of the ear.

Mucociliary disease of the middle ear during experimental otitis media with effusion induced by bacterial endotoxin.

Lipopolysaccharide (10 micrograms/mL) derived from Klebsiella pneumoniae was injected into the middle ear of guinea pigs. The animals were killed painlessly on days 1, 3, and 7 after inoculation, and the mucosal samples from two sites within the tympanic cavity, close to the tympanic orifice and distal to the orifice, were examined for ciliary activity and epithelial morphology. At day 1 and day 3 serous effusion was observed and deterioration of ciliary activity and morphologic changes were observed. No effusion was recognized at day 7, when the ciliary activity in the distal mucosa was still diminished and that in the proximal mucosa had recovered to a normal level. Our data have shown that lipopolysaccharide extracted from K pneumoniae can produce otitis media with effusion in laboratory animals, and dysfunction of cilia due to lipopolysaccharide probably is responsible for the accumulation of middle ear effusion. The mucociliary system is indeed an important defense system and failure of such a system, especially in the mucosa close to the tympanic orifice, can cause the buildup of effusions.

L-663,536 (MK-886) (3-[1-(4-chlorobenzyl)-3-t-butyl-thio-5-isopropylindol-2-yl]-2,2-dimethylpropanoic acid), a novel, orally active leukotriene biosynthesis inhibitor

L-663,536 (3-[1-(4-chlorobenzyl)-3-t-butyl-thio-5-isopropylindol-2-yl]-2, 2-dimethylpropanoic acid) is a potent inhibitor of leukotriene (LT) biosynthesis in intact human polymorphonuclear leukocytes (PMN) (IC50, 2.5 nM). Similarly, L-663,536 inhibited A23187-induced LTB4 formation by rat peripheral blood and elicited PMN. At concentrations where inhibition of leukotriene biosynthesis occurred in human whole blood (1.1 microM), no effect was seen on cyclooxygenase or 12-lipoxygenase, an effect also observed in washed human platelets. The compound had no effect on rat or porcine 5-lipoxygenase indicating that L-663,536 is not a direct 5-lipoxygenase inhibitor. When administered in vivo L-663,536 was a potent inhibitor of antigen-induced dyspnea in inbred rats pretreated with methysergide (ED50, 0.036 mg/kg p.o.) and of Ascaris-induced bronchoconstriction in squirrel monkeys (1 mg/kg p.o.). The compound inhibited leukotriene biosynthesis in vivo in a rat pleurisy model (ED50, 0.2 mg/kg p.o.), an inflamed rat paw model (ED50, 0.8 mg/kg), a model of leukotriene excretion in rat bile following antigen provocation, and a model in the guinea-pig ear where leukotriene synthesis was induced by topical challenge with ionophore A23187 (ED50, 2.5 mg/kg p.o. and 0.6 micrograms topically). The results indicate that L-663,536 is a potent inhibitor of leukotriene biosynthesis both in vitro and in vivo indicating that the compound is suitable for studying the role of leukotrienes in a variety of pathological situations.

Effect of gentamicin on the carbohydrates of the vestibular end organs: An investigation by the use of FITC-lectins

The effect of gentamicin on the glycoconjugates in the vestibular end organs is demonstrated using FITC-lectins. Five milligrams of gentamicin dissolved in 0.1 ml. saline was injected in a single dose into the middle ear of adult guinea pigs. Seven days after the injection, the fluorescent reactivity of Wheat germ agglutinin (WGA), Abrus precatorius agglutinin (APA), Concanavaline A (Con A), and Latyrus odoratus agglutinin (LOA) was decreased in the apical epithelial cell surface as well as in the gelatinous layer of the otolithic membrane of the maculae. In the cupula of the crista ampullaris, the reactivity for WGA and Con A was reduced. The otoconia, however, showed no detectable changes. This indicates that gentamicin may induce an altered carbohydrate metabolism resulting in a decrease of N-acetyl-glucosamine, mannose, galactose and glucose in the glycocalyx lining the epithelial cells as well as in the gelatinous layer of the otolithic membrane or cupula in the vestibular end organs.

Effect of static magnetic fields on the acoustic action potential of the cochlea in guinea pigs

Several experiments carried out during the past years indicate that strong magnetic fields induce disturbed blood circulation in capillaries and arterioles. When exposed to a magnetic field, disturbed blood circulation was found in the capillaries in frog webs as well as changes in skin temperature in several kinds of species. In our experiments we assessed the influence of a 8.5 T static magnetic field on the function of the inner ear of guinea pigs by monitoring the cochlea action potential. When blood circulation is disturbed in this organ it shows a rapid decline in function. Even when exposed to the magnetic field for 3 h, we could find no change in the function of the inner ear of the guinea pigs.

Maintenance of hydrostatic pressure gradients in the membranous labyrinth.

In normal guinea pig ears, hydrostatic perilymphatic pressure is equal to endolymphatic pressure. Alterations of perilymphatic pressure induced, for example, by laceration of the round window membrane are transmitted immediately to the endolymphatic compartment, probably via Reissner's membrane. In guinea pigs with experimental endolymphatic hydrops, however, pressure gradients between the endolymph and perilymph remained preserved after rupture of the round window membrane. This is considered as further evidence that after long-standing distention of Reissner's membrane the membranous labyrinth loses its ability to equalize endolymphatic and perilymphatic pressure.

Sound-evoked acoustic responses from the ears of guinea pigs

Sound-evoked acoustic responses from the ears of guinea pigs

Localization of the Atrial Natriuretic Peptide Binding Sites in the Inner Ear Tissue—Possibly an Additional Regulating System

Specific high affinity atrial natriuretic peptide (ANP) binding sites were identified and localized by autoradiography (125J-ANP 1-28) in the inner ear of guinea pigs. ANP is a cardiac hormone known to mediate increased capillary permeability, vasodilation, and natriuresis. Since specific receptors for ANP exist in both eye and brain, possibly playing a role in regulation of fluid and pressure (14, 15), we hypothetized that ANP might be involved also in inner ear fluid dynamics via interaction with other volume/electrolyte balance regulating hormones including vasopressin, renin, and aldosteron. The distribution of ANP receptor in the inner ear tissue appears unequal, which may play a significant role in view of some functional disturbances such as Meniere's disease.

Immunohistochemical Demonstration of Neuroactive Substances in the Inner Ear of Rat and Guinea Pig

The presence and localization of different neuropeptides and other putative neurotransmitters or -modulators were examined by immunohistochemistry in the cochleovestibular end organs and in neurons innervating them in rats and guinea pigs. In the organ of Corti neural elements beneath inner hair cells showed immunoreactivity for enkephalin (ENK), calcitonin gene-related peptide (CGRP), L-glutamate decarboxylase (GAD), substance P (SP) and tyrosine hydroxylase (TH). Nerve chalices of type I vestibular hair cells contained SP and GAD, but not consistently. SP was only occasionally observed in neuronal cell bodies of the 8th cranial nerve but fine fibers with different neuroactive substances were seen in the nerve trunk in the following relative numbers: TH greater than SP greater than CGRP greater than ENK. The present data demonstrate the presence of several different neuroactive substances in the rat and guinea pig inner ear suggesting a multiplicity of neurotransmitters or -modulators in this system.

ゲンタマイシンの前庭器・神経節におよぼす影響

Morphological changes in the vestibular sensory epithelial cells and the vestibular ganglia following gentamicin (GM) intoxication were demonstrated three dimensionally by scanning electron microscopy.A single dose of 4mg (0.1ml) of GM was injected into the middle ears of guinea pigs through the tympanic membrane. The vestibular organs and ganglia were observed from one day to 6 months after the treatment. Four days after the injection, fusion, ballooning and disappearance of sensory cilia were observed in the vestibular sensory epithelium. These changes were more marked in type I than in type II hair cells. Earlier morphological signs of degeneration were observed in the mitochondria of the supranuclear portion of type I hair cells.Eater dilatation of the cisterns in the Golgi apparatus as well as of the endoplasmic reticulum were noted. Nerve chalices also revealed disintegration in the earlier phase of degeneration. The changes of the sensory cell progressed and extended from the central toward the peripheral area of the crista and the macula.These findings suggest that GM may induce some metabolic changes in the vestibular sensory cells which result in fusion or loss of sensory hairs and later complete disappearance of sensory cells.Changes in the vestibular ganglia were first observed seven days after the treatment. The degenerative process started with destruction of the mitochondrial cristae of the Schwann cells and the ganglion cells. These changes were followed by dissociation of the myelin sheath around the ganglion cells. The cytoplasmic organelles in the ganglion cells gradually deteriorated. At a later stage, the myelin sheath around the ganglion cell disappeared and the number of cells was reduced.The changes in the ganglia are direct effects of GM.

モルモット耳における誘発耳音響放射の薬剤負荷による変化について

モルモット耳における誘発耳音響放射の薬剤負荷による変化について

Acoustic responses recorded from the saccular bundle on the eighth nerve of the guinea pig

Previous studies have demonstrated the existence of acoustic responses from the saccule in guinea pigs for stimulus intensities above 75 dB SPL. It is well known that the saccule receives a double afferent innervation: a bundle of the superior branch of the eighth nerve reaches its anterior part and another bundle of the inferior branch innervates its posterior part. These two bundles join just at the exit of the internal auditory meatus. An electrophysiological experiment was performed to investigate whether saccular acoustic responses could be similarly recorded from both bundles. Recordings from an electrode tip of 0.2 mm diameter were obtained in normal animals and also in animals with a complete and selective destruction of the cochlear sensory epithelium induced by treatment with an ototoxic antibiotic combined with a loop diuretic. In both normal and treated animals acoustic responses with the peculiar very short latency were specifically recorded in the area of the junction of the two bundles, they were of maximal amplitude on the bundle of the inferior branch. These data confirm in a more direct way the saccular origin of the short latency acoustic responses and indicate that they are probably conveyed in both saccular nerve bundles but mostly in that of the inferior branch of the eighth nerve. Finally these data show unequivocally that saccular acoustic responses exist in normal guinea pig ears.

Immunolocalization of beta-lipotropin in the inner ear of the guinea pig.

The occurrence of beta-lipotropin (beta-LTH) immunoreactive material was investigated in the inner ear of newborn and juvenile guinea pigs by means of Sternberger's PAP technique. Unlike met5-enkephalin and endorphin, beta-LTH could not be found in the organ of Corti but was identified in the spiral ganglion and the neuroepithelium of the crista ampullaris.

Functional disorder of eustachian tube in experimental otitis media with effusion following inoculation of bacterial endotoxin.

A 10-micrograms/mL solution of lipopolysaccharide derived from Klebsiella pneumoniae was inoculated into the middle ears of guinea pigs. The animals were killed painlessly on the first, third, or seventh day after inoculation, and the mucosal samples from the bony portion of the eustachian tube were examined for ciliary activity and epithelial morphology. On the first and third days, when middle ear effusions were present, deterioration of ciliary activity and morphologic changes in the mucociliary system were observed. On the seventh day, when middle ear effusions were absent, the ciliary activity had recovered to normal. Our data show that endotoxin extracted from K pneumoniae can produce otitis media with effusion and that dysfunction of cilia caused by endotoxin is a factor responsible for the manifestation of otitis media.