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1.
Hear Res ; 155(1-2): 82-90, 2001 May.
Artigo em Inglês | MEDLINE | ID: mdl-11335078

RESUMO

The C57BL/6J (B6) and DBA/2J (D2) inbred strains of mice exhibit an age-related hearing loss (AHL) due to a recessive gene (Ahl) that maps to Chromosome 10. The Ahl gene is also implicated in the susceptibility to noise-induced hearing loss (NIHL). The B6 mice (Ahl/Ahl) are more susceptible to NIHL than the CBA/CaJ (CB) mice (+(Ahl)). The B6xD2.F(1) hybrid mice (Ahl/Ahl) are more susceptible to NIHL than the CBxB6.F(1) mice (+/Ahl) [Erway et al., 1996. Hear. Res. 93, 181-187]. These genetic effects implicate the Ahl gene as contributing to NIHL susceptibility. The present study demonstrates segregation for the putative Ahl gene and mapping of such a gene to Chromosome 10, consistent with other independent mapping of Ahl for AHL in 10 strains of mice [Johnson et al., 2000. Genomics 70, 171-180]. The present study was based on a conventional cross between two inbred strains, CBxB6.F(1) backcrossed to B6 with segregation for the putative +/Ahl:Ahl/Ahl. These backcross progeny were exposed to 110 dB SPL noise for 8 h. All of the progeny were tested for auditory evoked brainstem responses and analyzed for any significant permanent threshold shift of NIHL. Cluster analyses were used to distinguish the two putative genotypes, the least affected with NIHL (+/Ahl) and most affected with PTS (Ahl/Ahl). Approximately 1/2 of the backcross progeny exhibited PTS, particularly at 16 kHz. These mice were genotyped for two D10Mit markers. Quantitative trait loci analyses (log of the odds=15) indicated association of the genetic factor within a few centiMorgan of the best evidence for Ahl [Johnson et al., 2000. Genomics 70, 171-180]. All of the available evidence supports a role for the Ahl gene in both AHL and NIHL among these strains of mice.


Assuntos
Perda Auditiva Provocada por Ruído/genética , Animais , Limiar Auditivo , Cruzamentos Genéticos , Potenciais Evocados Auditivos do Tronco Encefálico , Feminino , Genótipo , Perda Auditiva Provocada por Ruído/fisiopatologia , Hibridização Genética , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Endogâmicos CBA , Camundongos Endogâmicos DBA , Fenótipo , Especificidade da Espécie
2.
Invest Ophthalmol Vis Sci ; 26(3): 289-302, 1985 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-2579042

RESUMO

Intravitreal injection of some fluorescent and nonfluorescent tissue-reactive dyes results in selective intracellular staining of a specific population of cones of macaque retina that have been identified tentatively as blue-sensitive cones. This paper describes quantitative density profiles of these cones as a function of retinal eccentricity. These profiles were measured from 0 deg to about 60 deg eccentricity along the nasal and temporal segments of the horizontal meridian of macaque retina. Stained cones were found to be absent from the very center of the fovea. These cones reach peak densities at 0.75-1.50 deg eccentricity, and decrease with greater eccentricity, more rapidly on the temporal than on the nasal segment of the horizontal meridian. Peak densities were found to be slightly closer to the foveal center of the retinas of adult male than of adult female macaques. Packing patterns of stained and unstained cones are discussed as is the mathematic expression of stained cone distribution. The spatial properties of the retinal distribution of stained cones agree very closely with those obtained in psychophysical human studies and other anatomic simian studies of blue-sensitive cones.


Assuntos
Células Fotorreceptoras/citologia , Retina/citologia , Animais , Cor , Feminino , Fóvea Central/citologia , Macaca mulatta , Masculino , Retina/fisiologia , Coloração e Rotulagem , Acuidade Visual
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