Layer V pyramidal neurons in the cat parietal cortex (areas 5 and 7) were investigated with intracellular HRP staining. Antidromic responses were recorded intracellularly as well as extracellularly with pontine stimulation under Nembutal anesthesia. The relationship between the latency of antidromic responses and the morphology of HRP-stained neurons was analyzed. A total of 65 neurons were stained with HRP, and sixteen of these neurons were activated antidromically with pontine stimulation. Two distinct groups of layer V pyramidal neurons were detected morphologically by intracellular HRP staining; i.e., one (F type) consisted of neurons with relatively large somata (58.4 +/- 8.1 micron X 24.5 +/- 5.1 micron, N = 11) and aspiny or sparsely spinous apical dendrites, and the other (S type) consisted of neurons with smaller somata (44.6 +/- 7.6 micron X 19.3 +/- 3.9 micron, N = 22) and richly spinous apical dendrites. These two groups showed different electrophysiological properties; i.e., the former responded antidromically to pontine stimulation at a latency shorter than 1.5 ms (namely, with a conduction velocity faster than 18 m/second) and the latter responded at a latency longer than 1.5 ms. The two neuronal types in the parietal cortex corresponded respectively to fast and slow pyramidal tract neurons (PTNs) investigated in the sensorimotor cortex. Although their morphological features were almost similar to those of PTNs, the branching pattern of apical dendrites of the F-type pyramidal neuron seemed to be different from that of fast PTNs. In the parietal cortex, apical dendrites of F-type neurons showed rather frequent branching in layer I. This was similar to the pattern of branching in slow PTNs. Such a characteristic branching pattern suggested that, in the cat parietal cortex, layer V pyramidal neurons of both types are adapted to receive cerebellar inputs through the ventroanterior (VA) thalamic nucleus to the superficial cortical layers.