These results demonstrate that mRNA and protein for TRPM8 exist in multiple genitourinary organs in the rat and human, and it may be considered a possible new target, as is TRPV1, for the pharmacological treatment of detrusor overactivity or other urological disorders.

Minnery, Brandon S. and Daniel J. Simons. Response properties of whisker-associated trigeminothalamic neurons in rat nucleus principalis. J Neurophysiol 89: 40 -56, 2003; 10.1152/jn.00272.2002. Nucleus principalis (PrV) of the brain stem trigeminal complex mediates the processing and transfer of low-threshold mechanoreceptor input en route to the ventroposterior medial nucleus of the thalamus (VPM). In rats, this includes tactile information relayed from the large facial whiskers via primary afferent fibers originating in the trigeminal ganglion (NV). Here we describe the responses of antidromically identified VPM-projecting PrV neurons (n ϭ 72) to controlled rampand-hold deflections of whiskers. For comparison, we also recorded the responses of 64 NV neurons under identical experimental and stimulus conditions. Both PrV and NV neurons responded transiently to stimulus onset (ON) and offset (OFF), and the majority of both populations also displayed sustained, or tonic, responses throughout the plateau phase of the stimulus (75% of NV cells and 93% of PrV cells). Average ON and OFF response magnitudes were similar between the two populations. In both NV and PrV, cells were highly sensitive to the direction of whisker deflection. Directional tuning was slightly but significantly greater in NV, suggesting that PrV neurons integrate inputs from NV cells differing in their preferred directions. Receptive fields of PrV neurons were typically dominated by a "principal" whisker (PW), whose evoked responses were on average threefold larger than those elicited by any given adjacent whisker (AW; n ϭ 197). However, of the 65 PrV cells for which data from at least two AWs were obtained, most (89%) displayed statistically significant ON responses to deflections of one or more AWs. AW response latencies were 2.7 Ϯ 3.8 (SD) ms longer than those of their corresponding PWs, with an inner quartile latency difference of 1-4 ms (Ϯ25% of median). The range in latency differences suggests that some adjacent whisker responses arise within PrV itself, whereas others have a longer, multi-synaptic origin, possibly via the spinal trigeminal nucleus. Overall, our findings reveal that the stimulus features encoded by primary afferent neurons are reflected in the responses of VPMprojecting PrV neurons, and that significant convergence of information from multiple whiskers occurs at the first synaptic station in the whisker-to-barrel pathway.

Many studies of bottom-up visual attention have focused on identifying which features of a visual stimulus render it salient-i.e., make it "pop out" from its background-and on characterizing the extent to which salience predicts eye movements under certain task conditions. However, few studies have examined the relationship between salience and other cognitive functions, such as memory. We examined the impact of visual salience in an object-place working memory task, in which participants memorized the position of 3-5 distinct objects (icons) on a two-dimensional map. We found that their ability to recall an object's spatial location was positively correlated with the object's salience, as quantified using a previously published computational model (Itti et al., 1998). Moreover, the strength of this relationship increased with increasing task difficulty. The correlation between salience and error could not be explained by a biasing of overt attention in favor of more salient icons during memorization, since eye-tracking data revealed no relationship between an icon's salience and fixation time. Our findings show that the influence of bottom-up attention extends beyond oculomotor behavior to include the encoding of information into memory.

To understand how the lemniscal trigeminothalamic circuit (PrV --> VPM) of the rodent whisker-to-barrel pathway transforms afferent signals, we applied ramp-and-hold deflections to individual whiskers of lightly narcotized rats while recording the extracellular responses of neurons in either the ventroposterior medial (VPM) thalamic nucleus or in brain stem nucleus principalis (PrV). In PrV, only those neurons antidromically determined to project to VPM were selected for recording. We found that VPM neurons exhibited smaller response magnitudes and greater spontaneous firing rates than those of their PrV inputs, but that both populations were similarly well tuned for stimulus direction. In addition, fewer VPM (74%) than PrV neurons (93%) responded with sustained, or tonic, discharges during the plateau phase of the stimulus. Neurons in both populations responded most robustly to deflections of a single, "principal whisker" (PW), and the majority of cells in both PrV (90%) and VPM (73%) also responded to deflections of at least one adjacent whisker (AW). AW responses in both nuclei occurred on average at longer latencies and were more temporally dispersed than PW responses. Lateral inhibition, as evidenced by AW-evoked activity suppression, was rare in PrV but prevalent in VPM. In both nuclei, however, suppression was weak, with AW responses being on average excitatory. Our results suggest that the receptive-field structures and response properties of individual VPM neurons can be explained in large part by input from one or a small number of PrV neurons, but that intrathalamic mechanisms act to further transform the afferent signal.

No abstract