Capsaicin is a pungent-tasting compound produced by plants in the Caps
ium family that activates a subset of primary afferent neurons associa
ted with pain and thermoreception. Previous studies from dorsal root g
anglion (DRGs) neurons suggest that many of capsaicin's physiological
responses are a consequence of its activating a cation-selective curre
nt, To further characterize the responses to capsaicin whole-cell patc
h-clamp measurements were performed on rat DRGs to which 0.1-10 mu M c
apsaicin was continuously applied. The capsaicin-activated currents ex
hibited marked variability in their thresholds, amplitude (to 15 nA),
rates of desensitization, and the number of distinct maxima in the evo
ked current. Similar responses were found in rat trigeminal ganglion c
ells. The heterogeneity in the magnitude of the currents evoked by 0.1
mu M capsaicin likely reflects different types of capsaicin-sensitive
neurons; a result consistent with in vitro extracellular recordings f
rom capsaicin-sensitive sensory afferents (Seno and Dray 1993).