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1.
J Chem Phys ; 147(15): 154307, 2017 Oct 21.
Article in English | MEDLINE | ID: mdl-29055318

ABSTRACT

The geometries and electronic structures of small Ninz clusters (n = 8, 9, 10) (z = 0, ±1, 2) have been elucidated for a range of multiplicities for each cluster size and charge, using density functional theory methods. These clusters have been found to conform in part to the existing superatomic model, with each cluster having a filled superatomic S-orbital, filled or partially filled superatomic P-orbitals, and empty or partially filled superatomic D-orbitals. Despite local states of mixed symmetry being present in the immediate vicinity of the Fermi energy, the addition or removal of a single electron from these systems causes a significant shift in the relative energies of the superatomic orbitals. In addition, this study demonstrates the possibility for d-electrons to contribute into superatomic orbitals to a greater or lesser extent, depending on the local environment. In summary, these observations lead to the prospect of a predictive model for electronic shell closings in some transition metal cluster systems.

2.
Pharmacogenomics J ; 16(5): 430-8, 2016 10.
Article in English | MEDLINE | ID: mdl-27241058

ABSTRACT

The relationship between dopamine (DA) tone in the prefrontal cortex (PFC) and PFC-dependent cognitive functions (for example, working memory, selective attention, executive function) may be described by an inverted-U-shaped function, in which both excessively high and low DA is associated with impairment. In the PFC, the COMT val158met single nucleotide polymorphism (rs4680) confers differences in catechol-O-methyltransferase (COMT) efficacy and DA tone, and individuals homozygous for the val allele display significantly reduced cortical DA. Many studies have investigated whether val158met genotype moderates the effects of dopaminergic drugs on PFC-dependent cognitive functions. A review of 25 such studies suggests evidence for this pharmacogenetic effect is mixed for stimulants and COMT inhibitors, which have greater effects on D1 receptors, and strong for antipsychotics, which have greater effects on D2 receptors. Overall, COMT val158met genotype represents an enticing target for identifying individuals who are more likely to respond positively to dopaminergic drugs.


Subject(s)
Catechol O-Methyltransferase/genetics , Cognition/drug effects , Dopamine Agents/therapeutic use , Dopamine/metabolism , Pharmacogenomic Variants , Polymorphism, Single Nucleotide , Prefrontal Cortex/drug effects , Animals , Antipsychotic Agents/therapeutic use , Catechol O-Methyltransferase/metabolism , Catechol O-Methyltransferase Inhibitors/therapeutic use , Dopamine Agents/adverse effects , Dopamine Agonists/therapeutic use , Gene Frequency , Heterozygote , Homozygote , Humans , Patient Selection , Pharmacogenetics , Phenotype , Precision Medicine , Prefrontal Cortex/enzymology , Receptors, Dopamine D1/agonists , Receptors, Dopamine D1/metabolism , Receptors, Dopamine D2/agonists , Receptors, Dopamine D2/metabolism
3.
Cell Death Dis ; 6: e1763, 2015 May 14.
Article in English | MEDLINE | ID: mdl-25973683

ABSTRACT

Here we study links between aminoglycoside-induced mistranslation, protein misfolding and neuropathy. We demonstrate that aminoglycosides induce misreading in mammalian cells and assess endoplasmic reticulum (ER) stress and unfolded protein response (UPR) pathways. Genome-wide transcriptome and proteome analyses revealed upregulation of genes related to protein folding and degradation. Quantitative PCR confirmed induction of UPR markers including C/EBP homologous protein, glucose-regulated protein 94, binding immunoglobulin protein and X-box binding protein-1 (XBP1) mRNA splicing, which is crucial for UPR activation. We studied the effect of a compromised UPR on aminoglycoside ototoxicity in haploinsufficient XBP1 (XBP1(+/-)) mice. Intra-tympanic aminoglycoside treatment caused high-frequency hearing loss in XBP1(+/-) mice but not in wild-type littermates. Densities of spiral ganglion cells and synaptic ribbons were decreased in gentamicin-treated XBP1(+/-) mice, while sensory cells were preserved. Co-injection of the chemical chaperone tauroursodeoxycholic acid attenuated hearing loss. These results suggest that aminoglycoside-induced ER stress and cell death in spiral ganglion neurons is mitigated by XBP1, masking aminoglycoside neurotoxicity at the organismal level.


Subject(s)
DNA-Binding Proteins/genetics , Endoplasmic Reticulum Stress/drug effects , Gentamicins/pharmacology , Hearing Loss, High-Frequency , Taurochenodeoxycholic Acid/pharmacology , Transcription Factors/genetics , Animals , CCAAT-Enhancer-Binding Proteins/metabolism , Cell Line , DNA-Binding Proteins/metabolism , Endoplasmic Reticulum/pathology , Female , HEK293 Cells , Hair Cells, Auditory/pathology , Hearing Loss, High-Frequency/chemically induced , Hearing Loss, High-Frequency/genetics , Hearing Loss, High-Frequency/pathology , Humans , Male , Membrane Glycoproteins/metabolism , Mice , Mice, Inbred CBA , Neurons/pathology , Protein Biosynthesis/drug effects , Protein Folding , Proteostasis Deficiencies , RNA Splicing/genetics , Regulatory Factor X Transcription Factors , Spiral Ganglion/cytology , Spiral Ganglion/drug effects , Spiral Ganglion/pathology , Transcription Factors/metabolism , Unfolded Protein Response/genetics , Unfolded Protein Response/physiology , X-Box Binding Protein 1
4.
Neuroscience ; 292: 22-33, 2015 Apr 30.
Article in English | MEDLINE | ID: mdl-25665752

ABSTRACT

This study compared the timing of appearance of three components of age-related hearing loss that determine the pattern and severity of presbycusis: the functional and structural pathologies of sensory cells and neurons and changes in gap detection (GD), the latter as an indicator of auditory temporal processing. Using UM-HET4 mice, genetically heterogeneous mice derived from four inbred strains, we studied the integrity of inner and outer hair cells by position along the cochlear spiral, inner hair cell-auditory nerve connections, spiral ganglion neurons (SGN), and determined auditory thresholds, as well as pre-pulse and gap inhibition of the acoustic startle reflex (ASR). Comparisons were made between mice of 5-7, 22-24 and 27-29 months of age. There was individual variability among mice in the onset and extent of age-related auditory pathology. At 22-24 months of age a moderate to large loss of outer hair cells was restricted to the apical third of the cochlea and threshold shifts in the auditory brain stem response were minimal. There was also a large and significant loss of inner hair cell-auditory nerve connections and a significant reduction in GD. The expression of Ntf3 in the cochlea was significantly reduced. At 27-29 months of age there was no further change in the mean number of synaptic connections per inner hair cell or in GD, but a moderate to large loss of outer hair cells was found across all cochlear turns as well as significantly increased ABR threshold shifts at 4, 12, 24 and 48 kHz. A statistical analysis of correlations on an individual animal basis revealed that neither the hair cell loss nor the ABR threshold shifts correlated with loss of GD or with the loss of connections, consistent with independent pathological mechanisms.


Subject(s)
Aging/physiology , Auditory Perception/physiology , Cochlear Nerve/physiology , Evoked Potentials, Auditory, Brain Stem/physiology , Hair Cells, Auditory, Inner/physiology , Aging/pathology , Animals , Auditory Pathways/pathology , Auditory Pathways/physiology , Auditory Threshold/physiology , Brain-Derived Neurotrophic Factor/metabolism , Cell Count , Cochlear Nerve/pathology , Female , Glial Cell Line-Derived Neurotrophic Factor/metabolism , Hair Cells, Auditory, Inner/pathology , Hair Cells, Auditory, Outer/pathology , Hair Cells, Auditory, Outer/physiology , Mice , Random Allocation , Reflex, Startle/physiology , Spiral Ganglion/pathology , Spiral Ganglion/physiology
5.
Heredity (Edinb) ; 112(5): 552-61, 2014 May.
Article in English | MEDLINE | ID: mdl-24346498

ABSTRACT

The accuracy of genomic selection depends on the relatedness between the members of the set in which marker effects are estimated based on evaluation data and the types for which performance is predicted. Here, we investigate the impact of relatedness on the performance of marker-assisted selection for fungal disease resistance in hybrid wheat. A large and diverse mapping population of 1739 elite European winter wheat inbred lines and hybrids was evaluated for powdery mildew, leaf rust and stripe rust resistance in multi-location field trials and fingerprinted with 9 k and 90 k SNP arrays. Comparison of the accuracies of prediction achieved with data sets from the two marker arrays revealed a crucial role for a sufficiently high marker density in genome-wide association mapping. Cross-validation studies using test sets with varying degrees of relationship to the corresponding estimation sets revealed that close relatedness leads to a substantial increase in the proportion of total genotypic variance explained by the identified QTL and consequently to an overoptimistic judgment of the precision of marker-assisted selection.


Subject(s)
Disease Resistance/genetics , Plant Diseases/genetics , Quantitative Trait Loci/genetics , Triticum/genetics , Ascomycota/physiology , Basidiomycota/physiology , Chromosome Mapping/methods , Chromosomes, Plant/genetics , Genes, Plant/genetics , Genetic Markers/genetics , Genome-Wide Association Study/methods , Genotype , Host-Pathogen Interactions/genetics , Hybridization, Genetic , Inbreeding , Phenotype , Plant Diseases/microbiology , Polymorphism, Single Nucleotide , Reproducibility of Results , Triticum/microbiology
6.
Neuroscience ; 152(1): 146-50, 2008 Mar 03.
Article in English | MEDLINE | ID: mdl-18234425

ABSTRACT

Oxidative stress in the cochlea is considered to play an important role in noise-induced hearing loss. This study determined changes in superoxide dismutase (SOD), catalase, lipid peroxidation (LPO) and the auditory brainstem response (ABR) in the cochlea of C57BL/6 mice prior to and immediately, 1, 3, 7, 10, 14 and 21 days after noise exposure (4 kHz octave band at the intensity of 110 dB SPL for 4 h). A significant increase in SOD activity immediately and on 1st day after noise exposure, without a concomitant increase in catalase activity suggested a difference in the time dependent changes in the scavenging enzymes, which facilitates the increase in LPO observed on day 7. The ABR indicated significant noise-induced functional deficits which stabilized in 2 weeks with a permanent threshold shift (PTS) of 15 dB at both 4 kHz and 8 kHz. The antioxidant D-methionine (D-Met) reversed the noise-induced changes in LPO levels and enzyme activities. It also significantly reduced the PTS observed on the 14th day from 15 dB to 5 dB for 4 kHz. In summary, the findings indicate that time-dependent alterations in scavenging enzymes facilitate the production of reactive oxygen species and that D-met effectively attenuates noise-induced oxidative stress and the associated functional loss in the mouse cochlea.


Subject(s)
Cochlea/drug effects , Cochlea/pathology , Methionine/pharmacology , Noise/adverse effects , Oxidative Stress/drug effects , Oxidative Stress/physiology , Acoustic Stimulation , Animals , Catalase/drug effects , Catalase/metabolism , Evoked Potentials, Auditory, Brain Stem , Hearing Loss, Noise-Induced/metabolism , Lipid Peroxidation/drug effects , Mice , Mice, Inbred C57BL , Superoxide Dismutase/drug effects , Superoxide Dismutase/metabolism , Time
7.
Georgian Med News ; (146): 14-7, 2007 May.
Article in English | MEDLINE | ID: mdl-17595452

ABSTRACT

A randomized double-blind study was performed to check the protective efficacy of vitamin E against aminoglycoside ototoxicity. 52 patients scheduled for gentamicin therapy because of acute pulmonary infections have been tested. Volunteers were randomly assigned to receive additionally either vitamin E or placebo. The daily dosage of gentamicin amounted to 240 mg and that of vitamin E to 2800 mg. The treatment lasted 7 days. Hearing function was assessed before the start of medication and at the follow-up visit 6 to 8 weeks afterwards. Elevation of auditory thresholds occurred in similar number of patients in the vitamin-E and placebo groups and no statistically significant differences were found between. Vitamin E has been not confirmed thus to possess any protective action against gentamicin-induced ototoxicity.


Subject(s)
Anti-Bacterial Agents/antagonists & inhibitors , Gentamicins/antagonists & inhibitors , Hearing Loss/prevention & control , Vitamin E/therapeutic use , Adolescent , Adult , Aged , Anti-Bacterial Agents/adverse effects , Anti-Bacterial Agents/therapeutic use , Double-Blind Method , Female , Gentamicins/adverse effects , Gentamicins/therapeutic use , Hearing Loss/chemically induced , Humans , Male , Middle Aged , Placebos , Pneumonia, Bacterial/drug therapy
8.
Georgian Med News ; (144): 14-8, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17473326

ABSTRACT

Hearing thresholds were measured in 224 Tbilisi citizens, 128 females and 96 males, at the frequencies of 0.125-16 kHz. None of the subjects reported any job-related noise exposures or other potentially confounding history. Initial signs of age-related hearing impairments were detected in females and males of 40-49 and 30-39 years of age, respectively. In both genders they involved high frequencies. In the following age decades, 50-59, 60-69, and 70-79 years, the hearing losses increased in magnitudes and extended to lower frequencies. From the age of 30-39 years to that of 40-49 and 50-59 years the dynamics of threshold elevations appeared more rapid in males than in females. The gender differences in hearing acuity increased respectively in this age period. Thereafter, in the ages of 60-69 and 70-79 years, the hearing alterations became steeper in females than in males. As a result, the gender differences in hearing smoothed significantly.


Subject(s)
Aging/physiology , Presbycusis/epidemiology , Presbycusis/physiopathology , Adult , Aged , Aged, 80 and over , Auditory Threshold/physiology , Female , Hearing Loss, Bilateral/epidemiology , Hearing Loss, Bilateral/physiopathology , Humans , Male , Middle Aged , Prevalence , Sex Distribution , Temporal Bone/physiopathology
9.
Cell Death Differ ; 13(1): 20-30, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16021180

ABSTRACT

Cochlear and vestibular sensory cells undergo apoptosis when exposed to aminoglycoside antibiotics in organ culture, but mechanisms of chronic drug-induced hair cell loss in vivo are unclear. We investigated cell death pathways in a mouse model of progressive kanamycin-induced hair cell loss. Hair cell nuclei showed both apoptotic- and necrotic-like appearances but markers for classic apoptotic pathways (cytochrome c, caspase-9, caspase-3, JNK, TUNEL) were absent. In contrast, drug treatment caused EndoG translocation, activation of mu-calpain, and both the synthesis and activation of cathepsin D. Poly (ADP-ribose) polymerase 1 (PARP1) was decreased, but a caspase-derived 89 kDa PARP1 fragment was not present. The mRNA level of PARP1 remained unchanged. Thus, chronic administration of aminoglycosides causes multiple forms of cell death, without a major contribution by classic apoptosis. These results provide a better understanding of the toxic effects of aminoglycosides and are relevant to design protection from aminoglycoside-induced hearing loss.


Subject(s)
Anti-Bacterial Agents/toxicity , Cell Death/drug effects , Hair Cells, Auditory/drug effects , Hair Cells, Auditory/pathology , Kanamycin/toxicity , Animals , Apoptosis/drug effects , Calpain/metabolism , Caspases/metabolism , Cathepsin D/metabolism , Cochlea/drug effects , Cochlea/pathology , Evoked Potentials, Auditory, Brain Stem/drug effects , Hair Cells, Auditory/metabolism , Hair Cells, Auditory, Outer/drug effects , Hair Cells, Auditory, Outer/pathology , Male , Mice , Mice, Inbred CBA , Microscopy, Electron , Mitochondria/drug effects , Mitochondria/metabolism , Necrosis , Organ of Corti/drug effects , Organ of Corti/pathology , Poly (ADP-Ribose) Polymerase-1 , Poly(ADP-ribose) Polymerases/genetics , Poly(ADP-ribose) Polymerases/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism
10.
Neuroscience ; 134(2): 633-42, 2005.
Article in English | MEDLINE | ID: mdl-15961244

ABSTRACT

Reactive oxygen species (ROS) and reactive nitrogen species (RNS) are involved in sensory cell and neural death in the peripheral nervous system, including damage induced by noise trauma. Antioxidant administration prior to or concomitant with noise exposure can prevent auditory deficits, but the efficacy of a delayed treatment is not known. We have recently found continued reactive oxygen species/reactive nitrogen species formation in the ear for 7-10 days following noise exposure and reasoned that antioxidant intervention during this period should also reduce noise-induced hearing loss. Guinea-pigs were subjected to 4 kHz octave band noise at 120 decibels sound- pressure-level (dB SPL) for 5 hours and received treatment with ROS and RNS scavengers (salicylate and trolox) beginning 3 days prior, 1 hour, 1, 3, or 5 days after noise exposure. Auditory thresholds were assessed by sound-evoked auditory brainstem response at 4, 8, and 16 kHz, before and 10 days after noise exposure. Hair cell damage was analyzed by quantitative histology, and free radical activity was determined immunohistochemically via 4-hydroxynonenal and nitrotyrosine as markers of reactive oxygen species and reactive nitrogen species action. Delivered up to 3 days after noise exposure, salicylate and trolox significantly reduced auditory brainstem response deficits, reduced hair cell damage, and decreased reactive oxygen species and reactive nitrogen species formation. Earlier drug treatment was more effective than later treatment. Our results detail a window of opportunity for rescue from noise trauma, and provide evidence for both morphological and functional protection by delayed pharmacological intervention.


Subject(s)
Hearing Loss, Noise-Induced , Aldehydes/metabolism , Animals , Cochlea/physiology , Guinea Pigs , Immunohistochemistry , Male , Reactive Oxygen Species/metabolism , Sound , Time Factors , Tyrosine/analogs & derivatives , Tyrosine/metabolism
11.
Laryngorhinootologie ; 83(5): 317-23, 2004 May.
Article in German | MEDLINE | ID: mdl-15143449

ABSTRACT

Gentamicin and cisplatin are clinically widely used pharmacological agents which may induce irreversible hearing loss as a side effect. Concerning the pathomechanisms of ototoxicity as well as preventive strategies there are similarities but also some differences. In this review we focus on the role of reactive oxygen species, the antioxidant system, cellular iron and calcium as well as nitric oxide and neurotrophins on gentamicin- and cisplatin-ototoxicity. Furthermore we deal with apoptotic and necrotic cell death as well as the role of mitochondria in these cell injury processes.


Subject(s)
Aminoglycosides/toxicity , Anti-Bacterial Agents/toxicity , Antineoplastic Agents/toxicity , Cisplatin/toxicity , Deafness/chemically induced , Gentamicins/toxicity , Animals , Apoptosis/drug effects , Dose-Response Relationship, Drug , Guinea Pigs , Hair Cells, Auditory/drug effects , Humans , Reactive Oxygen Species/metabolism , Spiral Ganglion/drug effects
12.
Neuroscience ; 123(4): 1037-43, 2004.
Article in English | MEDLINE | ID: mdl-14751294

ABSTRACT

Changes in gene expression are part of the homeostatic machinery with which cells respond to external stimuli or assaults. The activity of the early response transcriptional factor activator protein-1 (AP-1) can be modulated by a variety of environmental stimuli including those that alter the cellular oxidation/reduction status. This study investigates the activation of AP-1/DNA binding in the guinea-pig cochlea in response to acoustic overstimulation which produces reactive oxygen species. Electrophoretic mobility shift assays revealed that binding of AP-1 to its radiolabeled oligonucleotide probe markedly changed in nuclear extracts of inner ear tissues following intense noise exposure (4 kHz octave band, 115 dB, 5 h). AP-1/DNA binding increased in the organ of Corti and the lateral wall tissues immediately after the exposure, returning to near-baseline levels 5 h later. At 15 h after noise, a second peak of binding activity occurred in the organ of Corti whereas stria vascularis showed a lesser but more sustained activity. Binding in nuclear extracts from the spiral ganglion did not change. Incubation of nuclear extracts with antibodies against Fos/Jun family proteins prior to a supershift assay showed Fra-2 as a major component of the AP-1 complex immediately after the noise exposure. In the organ of Corti, Fra-2 immunoreactivity was localized to the middle turn, i.e. the region which is most affected by the 4-kHz octave band exposure. The results suggest the modulation of gene expression via the activation of AP-1 as a consequence of noise trauma but also demonstrate differential responses in cochlear tissues.


Subject(s)
Acoustic Stimulation/methods , Cochlea/radiation effects , DNA/radiation effects , Transcription Factor AP-1/metabolism , Animals , Cochlea/anatomy & histology , Cochlea/metabolism , DNA/metabolism , DNA-Binding Proteins/metabolism , Electrophoretic Mobility Shift Assay/methods , Fos-Related Antigen-2 , Guinea Pigs , Immunohistochemistry/methods , Male , Organ of Corti/metabolism , Protein Binding/radiation effects , Time Factors , Transcription Factors/metabolism
13.
Noise Health ; 5(20): 1-17, 2003.
Article in English | MEDLINE | ID: mdl-14558888

ABSTRACT

There is increasing evidence that at least one function of both the medial and the lateral olivocochlear efferent systems is to provide adjustment of the set point of activity in their postsynaptic target, the outer hair cells and afferent processes, respectively. New results, summarized in this review, suggest that both efferent systems can provide protection from noise through this mechanism. There are also intracellular pathways that can provide protection from noise-induced cellular damage in the cochlea. This review also summarizes new results on the pathways that regulate and react to levels of reactive oxygen species in the cochlea as well as the role of stress pathways for the heat shock proteins and for neurotrophic factors in protection, recovery and repair.


Subject(s)
Acoustic Stimulation , Cochlea/physiology , Hearing Loss, Noise-Induced/prevention & control , Action Potentials , Animals , Cochlea/anatomy & histology , Heat-Shock Proteins/metabolism , Humans , Oxidative Stress/physiology , Reactive Oxygen Species/metabolism
15.
16.
Hear Res ; 158(1-2): 165-78, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11506949

ABSTRACT

The availability of genetic information, transgenic and knock-out animals make the mouse a primary model in biomedical research. Aminoglycoside ototoxicity, however, has rarely been studied in mature mice because they are considered highly resistant to the drugs. This study presents models for kanamycin ototoxicity in adult CBA/J, C57BL/6 and BALB/c mouse strains and a comparison to Sprague-Dawley rats. Five-week-old mice were injected subcutaneously twice daily with 400-900 mg kanamycin base/kg body weight for 15 days. Kanamycin induced dose-dependent auditory threshold shifts of up to 70 dB at 24 kHz as measured by auditory brain stem-evoked responses. Vestibular function was also affected in all strains. The functional deficits were accompanied by hair cell loss in both cochlear and vestibular neurosensory epithelia. Concomitant administration of the antioxidant 2,3-dihydroxybenzoate significantly attenuated the kanamycin-induced threshold shifts. In adult male Sprague-Dawley rats, doses of 1 x 500 mg or 2 x 300 mg kanamycin base/kg body weight/day x 14 days induced threshold shifts of approximately 50 dB at 20 kHz. These were accompanied by loss of outer hair cells. The order of susceptibility, BALB>CBA>C57, was not due to differences in the pharmacokinetics of kanamycin. It also did not correlate with the presence of Ahl/Ahl2 genes which predispose C57 and BALB strains, respectively, to accelerated age-related hearing loss. Pigmentation, however, paralleled this rank order suggesting an influence of melanin on cochlear antioxidant status.


Subject(s)
Aminoglycosides/poisoning , Ear, Inner/drug effects , Kanamycin/poisoning , Aminoglycosides/antagonists & inhibitors , Aminoglycosides/blood , Animals , Antioxidants/pharmacology , Auditory Threshold/drug effects , Cell Survival/drug effects , Cochlea/drug effects , Cochlea/pathology , Evoked Potentials, Auditory, Brain Stem/drug effects , Hair Cells, Auditory/drug effects , Hair Cells, Auditory/physiology , Hydroxybenzoates/pharmacology , Kanamycin/antagonists & inhibitors , Kanamycin/blood , Kidney/drug effects , Kidney/physiology , Male , Mice , Mice, Inbred Strains , Rats , Rats, Sprague-Dawley , Vestibule, Labyrinth/drug effects , Vestibule, Labyrinth/pathology
17.
Audiol Neurootol ; 6(3): 117-23, 2001.
Article in English | MEDLINE | ID: mdl-11474137

ABSTRACT

The participation of reactive oxygen species in aminoglycoside-induced ototoxicity has been deduced from observations that aminoglycoside-iron complexes catalyze the formation of superoxide radicals in vitro and that antioxidants attenuate ototoxicity in vivo. We therefore hypothesized that overexpression of Cu/Zn-superoxide dismutase (h-SOD1) should protect transgenic mice from ototoxicity. Immunocytochemistry confirmed expression of h-SOD1 in inner ear tissues of transgenic C57BL/6-TgN[SOD1]3Cje mice. Transgenic and nontransgenic littermates received kanamycin (400 mg/kg body weight/day) for 10 days beginning on day 10 after birth. Auditory thresholds were tested by evoked auditory brain stem responses at 1 month after birth. In nontransgenic animals, the threshold in the kanamycin-treated group was 45-50 dB higher than in saline-injected controls. In the transgenic group, kanamycin increased the threshold by only 15 dB over the respective controls. The effects were similar at 12 and 24 kHz. The protection by overexpression of superoxide dismutase supports the hypothesis that oxidant stress plays a significant role in aminoglycoside-induced ototoxicity. The results also suggest transgenic animals as suitable models to investigate the underlying mechanisms and possible strategies for prevention.


Subject(s)
Anti-Bacterial Agents/adverse effects , Copper/metabolism , Hearing Disorders/chemically induced , Hearing Disorders/prevention & control , Kanamycin/adverse effects , Superoxide Dismutase/metabolism , Zinc/metabolism , Animals , Anti-Bacterial Agents/blood , Auditory Threshold/drug effects , Blood Urea Nitrogen , Cochlea/drug effects , Cochlea/metabolism , Cochlea/pathology , Immunohistochemistry , Kanamycin/blood , Mice , Mice, Inbred C57BL , Reactive Oxygen Species/metabolism , Vestibule, Labyrinth/drug effects , Vestibule, Labyrinth/metabolism , Vestibule, Labyrinth/pathology
18.
Hear Res ; 155(1-2): 1-8, 2001 May.
Article in English | MEDLINE | ID: mdl-11335071

ABSTRACT

The base of the cochlea is more vulnerable to trauma than the apex as seen in the pattern of hair cell damage by cisplatin or aminoglycosides. The differential vulnerability is maintained in organotypic cultures exposed directly to these drugs, suggesting there may be an intrinsic difference in sensitivity to damage along the cochlear spiral. We therefore investigated the survival capacity of isolated outer hair cells and strips dissected from different turns of the guinea pig organ of Corti in short-term culture. Cells were stained with fluorescent indicators of viable or dead cells, calcein-AM and ethidium homodimer. After 5 h at room temperature, up to 90% of outer hair cells from the apex survived, but less than 30% from the base. In contrast, basal inner hair cells remained viable, and supporting cells survived for at least 20 h. The difference in survival capacity between basal and apical outer hair cells coincided with a significantly lower level of the antioxidant glutathione in basal outer hair cells compared with apical outer hair cells. This suggested that basal outer hair cells may be more vulnerable to free-radical damage than apical outer hair cells. The survival of basal outer hair cells was significantly improved by addition of the radical scavengers n-acetyl cysteine, p-phenylenediamine, glutathione, mannitol or salicylate. The protection by antioxidants implies that the accelerated death of basal outer hair cells is due to free-radical damage. The results support an intrinsic susceptibility to free radicals that differs among cochlear cell populations. This differential provides a rational explanation for base-to-apex gradients observed in various forms of cochlear pathology.


Subject(s)
Hair Cells, Auditory, Outer/drug effects , Animals , Cell Survival/drug effects , Free Radical Scavengers/pharmacology , Free Radicals/toxicity , Glutathione/metabolism , Glutathione/pharmacology , Guinea Pigs , Hair Cells, Auditory, Outer/injuries , Hair Cells, Auditory, Outer/pathology , In Vitro Techniques , Mannitol/pharmacology
19.
J Neurosci Res ; 63(3): 252-6, 2001 Feb 01.
Article in English | MEDLINE | ID: mdl-11170174

ABSTRACT

The medial efferent system innervates outer hair cells in the organ of Corti. Neurotransmission at this synapse is mediated by acetylcholine (ACh) acting on nicotinic ACh receptors containing the alpha9 subunit. In addition to the sensory cells, the supporting cells of the mammalian cochlea also receive efferent innervation but the neurotransmitter(s) at these synapses are not known. We show slow transient increases of intracellular calcium evoked by ACh in isolated Deiters' cells of the guinea pig cochlea. The antagonists atropine, d-tubocurarine and strychnine blocked the ACh-effect. Nicotine was an ineffective agonist. The pharmacologic profile and the kinetics of the calcium response suggest an alpha9-like ACh receptor on Deiters' cells similar but not identical to that on the outer hair cells.


Subject(s)
Acetylcholine/pharmacology , Calcium/metabolism , Hair Cells, Auditory, Outer/drug effects , Receptors, Nicotinic/drug effects , Synapses/drug effects , Acetylcholine/metabolism , Animals , Cholinergic Antagonists/pharmacology , Guinea Pigs , Hair Cells, Auditory, Outer/cytology , Hair Cells, Auditory, Outer/metabolism , Intracellular Fluid/drug effects , Intracellular Fluid/metabolism , Nicotinic Agonists/pharmacology , Receptors, Nicotinic/metabolism , Synapses/metabolism
20.
J Assoc Res Otolaryngol ; 2(4): 399-407, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11833612

ABSTRACT

Supporting cells in the mammalian cochlea have recently received attention as potential targets of neurotransmitters, neuromodulators, and neurohumoral agents. Calcium homeostasis in Deiters' and Hensen's cells, for example, is regulated by ATP and nitric oxide. We studied the intracellular calcium concentration [Ca2+]i in isolated pillar cells of the guinea pig cochlea in response to extracellular ATP and nitric oxide using the fluorescent indicator fluo-3. [Ca2+]i increased rapidly and significantly throughout the pillar cell in response to a bolus of ATP or 2-methylthio ATP while alpha,beta-methylene ATP was ineffective. The response to ATP was inhibited by suramin and Cibacron Blue but not by pyridoxal phosphate 6-azophenyl-2',4'-disulfonic acid. This pharmacological profile is consistent with a [Ca2+]i increase largely mediated by P2Y receptors. In Ca2+-free medium supplemented with EGTA, the response to extracellularATP was reduced by 33%, suggesting a contribution of calcium influx to the overall effect. The ATP-induced increase of [Ca2+] was attenuated by NO donors (sodium nitroprusside or diethylamine NONOate), and this attenuation was reversed by KT5823, an antagonist to protein kinase G. The results indicate the involvement of purinergic mechanisms and the nitric oxide/cyclic GMP/protein kinase G pathway in the regulation of [Ca2+]i in cochlear pillar cells.


Subject(s)
Adenosine Triphosphate/physiology , Calcium/metabolism , Cochlea/cytology , Cochlea/metabolism , Intracellular Membranes/metabolism , Nitric Oxide/physiology , Adenosine Triphosphate/pharmacology , Animals , Calcium/analysis , Cochlea/drug effects , Cyclic GMP/physiology , Guinea Pigs , Isotonic Solutions/chemistry , Isotonic Solutions/pharmacology , Male , Nitric Oxide Donors/pharmacology , Osmolar Concentration , Purinergic Agonists , Purinergic Antagonists
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