Chemical responsiveness and histochemical phenotype of electrophysiologically classified cells of the adult rat dorsal root ganglion

JC Petruska, J Napaporn, RD Johnson, BY Cooper - Neuroscience, 2002 - Elsevier
JC Petruska, J Napaporn, RD Johnson, BY Cooper
Neuroscience, 2002Elsevier
Whole cell patch recordings were obtained from medium diameter (35–45 μm) dorsal root
ganglion neurons. Using electrophysiological parameters, we were able to subclassify
acutely dissociated dorsal root ganglion cells into three uniform (types 5, 6 and 9) and one
mixed class (type 8) of neurons. All subtypes (types 5, 6, 8 and 9) had broad action
potentials (7.0±0.2, 5.2±0.4, 7.3±0.5 and 6.0±0.4 ms) and exceptionally long
afterhyperpolarizations (112±9, 178±19, 124±31 and 204±33 ms). Long …
Whole cell patch recordings were obtained from medium diameter (35–45 μm) dorsal root ganglion neurons. Using electrophysiological parameters, we were able to subclassify acutely dissociated dorsal root ganglion cells into three uniform (types 5, 6 and 9) and one mixed class (type 8) of neurons. All subtypes (types 5, 6, 8 and 9) had broad action potentials (7.0±0.2, 5.2±0.4, 7.3±0.5 and 6.0±0.4 ms) and exceptionally long afterhyperpolarizations (112±9, 178±19, 124±31 and 204±33 ms). Long afterhyperpolarizations have been linked to mechanically insensitive (silent) nociceptors by other laboratories [Djouhri et al., J. Physiol. 513 (1998) 857–872]. Chemosensitivity varied among cell classes. Cell types 5, 8 and 9 were capsaicin sensitive (45±13, 87±30 and 28±13 pA/pF; 5 μM) groups, while the type 6 cell was capsaicin insensitive. All cell types expressed ASIC-like (acid sensing ion channel) amiloride sensitive, proton-activated currents with a threshold of pH 6.8 and a peak near pH 5.0. All medium sized cells were sensitive to ATP (50 μM) and exhibited the ‘mixed’ form of ATP-gated current [Burgard et al., J. Neurophysiol. 82 (1999) 1590–1598; Grubb and Evans, Eur. J. Neurosci. 11 (1999) 149–154]. Immunohistochemistry performed on individual cells indicated the expression of both P2X1 and P2X3 subunits. Electrophysiologically defined classes were histochemically uniform. All types were examined for the presence of substance P (SP), calcitonin gene related peptide (CGRP) and binding of isolectin B4 (IB4). All subtypes expressed CGRP immunoreactivity. Types 5 and 8 co-expressed SP and CGRP immunoreactivity and also bound IB4. Subtypes 6 and 9 were positive for neurofilament m. It is likely that these cells represent major classes of myelinated and unmyelinated peptide expressing nociceptors.
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