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When temperature (T) of skin decreases stepwise, cold fibers evoke transient afferent discharges, inducing cold sensation and heat-gain responses. Hence we have proposed that cold receptors at distal ends of cold fibers are thermostats to regulate skin T against cold. Here, with patch-clamp techniques, we studied the ionic basis of cold receptors in cultured dorsal root ganglion (DRG) neurons of rats, as a model of nerve endings. Cells that increased cytosolic Ca(2+) level in response to moderate cooling were identified as neurons with cold receptors. In whole-cell current-clamp recordings of these cells, in response to cooling, cold receptors evoked a dynamic receptor potential (RP), eliciting impulses briefly. In voltage-clamp recordings (-60 mV), step cooling induced an inward cold current (I(cold)) with inactivation, underlying the dynamic RP. Ca(2+) ions that entered into cells from extracellular side induced the inactivation. Analysis of the reversal potential implied that I(cold) was nonselective cation current with high Ca(2+) permeability. Threshold temperatures of cooling-induced Ca(2+) response and I(cold) were different primarily among cells. In outside-out patches, when T decreased, single nonselective cation channels became active at a critical T. This implies that a cold receptor is an ion channel and acts as the smallest thermostat. Because these thermal properties were consistent with that in cold fibers, we conclude that the same cold receptors exist at nerve endings and generate afferent impulses for cold sensation and heat-gain behaviors in response to cold.

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Cross-sectional areas and succinate dehydrogenase (SDH) activities of muscle fibers in the rat levator ani (LA) and bulbocavernosus (BC) were determined and compared with those of the soleus (SOL) and superficial (TAs) and deep (TAd) portions of the tibialis anterior (TA). In addition, cell body sizes and SDH activities of spinal motoneurons innervating the LA and BC were examined. Histochemical myofibrillar adenosine triphosphatase (mATPase) staining reactions following alkaline and acid preincubations revealed that all the muscle fibers in the LA and BC were type IIB. Gel electrophoresis, however, showed that the LA and BC contained 2.9 and 2.4% type IIx myosin heavy chain (MHC) isoform, respectively. Immunohistochemical analyses using MHC antibodies showed that the muscle fibers in the LA and BC had types IIx + IIa (–3%) or type lib MHC isoforms. The mean fiber cross-sectional areas in the LA and BC were significantly smaller than those in the SOL, TAs, or TAd. The mean fiber SDH activities in the LA and BC were significantly lower than those in the SOL or TAd, and similar to TAs. The population of alpha motoneurons innervating the LA and BC had similar SDH activities, irrespective of their cell body sizes. These data indicate that the LA and BC are comprised of a relatively homogeneous population of small, fast and low oxidative fibers innervated by a relatively homogeneous population of spinal motoneurons. These characteristics of the muscle fibers and motoneurons are consistent with their function in short, high-intensity activities.