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L G Montgomery

Publications and source records attributed to L G Montgomery.

5 recordsLinked to original sources

How body size affects middle-ear structure and function and auditory sensitivity in gekkonoid lizards.

Gekkonoid lizards increase in body size throughout life, and the present study investigates whether changes in auditory function accompany these increases. Middle-ear structures in four groups of animals, adults and juveniles of two gekkonoid species (Eublepharis macularius and Oedura marmorata), were examined. Tympanic membrane velocity and phase were also measured in all four groups. An indication of peripheral auditory function was obtained for each group by measuring compound action potentials (CAPs) from the round window membrane. The middle-ear contribution to CAP thresholds was obtained by comparing threshold levels of the CAP response with and without an intact middle-ear system. The results from these studies indicated that significant changes occurred in middle-ear structure, tympanic membrane velocity and CAP threshold between the younger and older animals. In addition, the adults of both species exhibited better auditory function when the acoustic stimulus was delivered to the tympanic membrane than when it was delivered to the columella footplate. The findings show clearly that increased body size (or age) is accompanied by functional changes in the auditory periphery.

Action Potentials↗

Predominance of the alpha1D subunit in L-type voltage-gated Ca2+ channels of hair cells in the chicken's cochlea.

The voltage-gated Ca2+ channels that effect tonic release of neurotransmitter from hair cells have unusual pharmacological properties: unlike most presynaptic Ca2+ channels, they are sensitive to dihydropyridines and therefore are L-type. To characterize these Ca2+ channels, we investigated the expression of L-type alpha1 subunits in hair cells of the chicken's cochlea. In PCRs with five different pairs of degenerate primers, we always obtained alpha1D products, but only once an alpha1C product and never an alpha1S product. A full-length alpha1D mRNA sequence was assembled from overlapping PCR products; the predicted amino acid sequence of the alpha1D subunit was about 90% identical to those of the mammalian alpha1D subunits. In situ hybridization confirmed that the alpha1D mRNA is present in hair cells. By using a quantitative PCR assay, we determined that the alpha1D mRNA is 100-500 times more abundant than the alpha1C mRNA. We conclude that most, if not all, voltage-gated Ca2+ channels in hair cells contain an alpha1D subunit. Furthermore, we propose that the alpha1D subunit plays a hitherto undocumented role at tonic synapses.

Amino Acid Sequence↗

Hair cell-specific splicing of mRNA for the alpha1D subunit of voltage-gated Ca2+ channels in the chicken's cochlea.

The L-type voltage-gated Ca2+ channels that control tonic release of neurotransmitter from hair cells exhibit unusual electrophysiological properties: a low activation threshold, rapid activation and deactivation, and a lack of Ca2+-dependent inactivation. We have inquired whether these characteristics result from cell-specific splicing of the mRNA for the L-type alpha1D subunit that predominates in hair cells of the chicken's cochlea. The alpha1D subunit in hair cells contains three uncommon exons: one encoding a 26-aa insert in the cytoplasmic loop between repeats I and II, an alternative exon for transmembrane segment IIIS2, and a heretofore undescribed exon specifying a 10-aa insert in the cytoplasmic loop between segments IVS2 and IVS3. We propose that the alternative splicing of the alpha1D mRNA contributes to the unusual behavior of the hair cell's voltage-gated Ca2+ channels.

Alternative Splicing↗