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Biomedical subjects

P F Fahey

Publications and source records attributed to P F Fahey.

3 recordsLinked to original sources

Using acoustic distortion products to measure the cochlear amplifier gain on the basilar membrane.

Most models of the cochlea developed during the last decade have explained frequency selectivity and sensitivity of the cochlea at threshold by the use of power amplification of the acoustic wave on the basilar membrane. This power amplification has been referred to as the cochlear amplifier (CA). In this paper, a method to measure the cochlear amplifier gain as a function of position along the basilar membrane is derived from a simple model. Next, experimental evidence is presented that strongly restricts the properties of these proposed cochlear amplifier models. Specifically, it is shown that small signals generated by mechanical nonlinearities in the basilar membrane motion are not amplified during basilar membrane propagation, contrary to what would be expected from the cochlear amplifier hypotheses. This paper describes a method of measuring the cochlear power gain as a function of frequency and position, from the stapes to within 2 mm of the place corresponding to the frequency being measured. Experimental results in the cat indicate that the total gain of the cochlear amplifier, over the range of positions measured, must be less than 10 dB. The simplest interpretation of the experimental results is that there is no cochlear amplifier. The results suggest that the cochlea must achieve its frequency selectivity by some other means.

Animals

Lateral diffusion in phospholipid bilayer membranes and multilamellar liquid crystals.

The lateral-diffusion coefficients (D) of a fluorescent lipid analogue, 3,3'-dioctadecylindotricarbocyanine (diI), have been measured in black lipid membranes (BLMs), in large (20--50-micron diameter) solvent-free bilayer and multilayer membrane vesicles, and in multilamellar liquid crystals of dipalmitoylphosphatidylcholine, dimyristoylphosphatidylcholine, and egg lecithin. They show that D changes by several orders of magnitude at the liquid-crystal transformations of the solvent-free bilayers and multilayer. In all BLMs, D approximately 10(-7)cm2/s with only weak temperature dependence even near the putative phase-transformation temperatures, Tt. In the corresponding liquid crystals and large vesicles, D approximately 10(-8)cm2/s above Tt, decreasing by about two orders of magnitude to D approximately 10(-10)cm2/s below Tt. The changes of D in bilayer vesicles suggest that the expected liquid-crystal phase transitions from smectic A to a higher ordered state do persist in isolated bilayers. Retained solvent in black lipid membranes formed by both Mueller--Rudin and Montal--Mueller methods appears to enhance lateral diffusion. A simple method of forming small numbers of large solvent-free vesicles is described.

Crystallization

Lateral diffusion in planar lipid bilayers.

Direct measurements by fluorescence correlation spectroscopy of lateral diffusion coefficients of fluorescent lipid analogs in lipid bilaryer membranes indicate self-diffusion coefficients D greater than 10(-7) square centimeters per second for various lipid systems above their reported transition temperatures. Cholesterol in egg lecithin at mole ratio of 1 : 2 reduces D by about twofold, while retained hydrocarbon solvent can increase it by two- to threefold.

Cholesterol