(A) Schematic representation of the tonotopic axis of the rat cochlea. Recordings were made at locations marked by black disks, corresponding to characteristic frequencies (in kHz) increasing from the apex to the base of the cochlea as indicated on the figure and to fractional distances from the apex of 5%, 10%, 20%, and 50%. We report measurements from both inner and outer hair cells at the 1‒4 kHz locations, but only from inner hair cells at the 15-kHz location. The rat cochlea was typically 10 mm long. Adapted from Viberg and Canlon (2004). (B) Schematic layout of the experimental pipettes around a given outer hair cell. We combined fluid-jet stimulation of single hair bundles, iontophoresis of a Ca2+ chelator (EDTA), patch-clamp recordings of transduction currents, and perfusion of low-Ca2+ saline. (C) Schematic representation of the fluid-jet pipette and of a hair bundle (left) and micrograph of a fluid-jet pipette ready to stimulate an outer hair cell of the rat cochlea (right). A positive (negative) deflection of the hair bundle, as defined on the drawing, was elicited by fluid suction (ejection) into (from) the pipette, promoting opening (closure) of the transduction channels. The horizontal projected distance between the mouth of the pipette (blue vertical line) and the hair bundle (green vertical line) was set at ~8 µm.