Neurons in the cerebral cortex are not homogeneous. However, neuronal types have been ignored in most previous work studying neuronal processes in behaving monkeys. We propose a new method to identify neuronal types in extracellular recording studies of behaving monkeys. We classified neurons as either bursting or non-bursting, and then classified the bursting neurons into three types: (i) neurons displaying a burst of many spikes (maximum number of spikes within a burst; NSB max > or = 8) at a high discharge rate (maximum interspike interval; ISI max < 5 ms); (ii) neurons displaying a burst of fewer spikes (NSB max < or = 5) at a high discharge rate (ISI max < 5 ms); and (iii) neurons displaying a burst of a few spikes (NSB max < or = 7) at relatively long ISIs (ISI max > 5 ms). We found that the discharge patterns of the four groups corresponded to those of regular spiking (RS), fast spiking (FS), fast rhythmic bursting (FRB) and intrinsic bursting (IB) neurons demonstrated in intracellular recording studies using in vitro slice preparations, respectively. In addition, we examined correlations with the task events for neurons recorded in the frontal eye field and neuronal interactions for pairs of neurons recorded simultaneously from a single electrode. We found that they were substantially different between RS and FS types. These results suggest that neurons in the frontal cortex of behaving monkeys can be classified into four types based on their discharge patterns, and that these four types contribute differentially to cortical operations.
The retinas of macaque monkeys usually contain three types of photopigment, providing them with trichromatic color vision homologous to that of humans. However, we recently used molecular genetic analysis to identify several macaques with a dichromatic genotype. The affected X chromosome of these animals contains a hybrid gene of long-wavelength-sensitive (L) and middle-wavelength-sensitive (M) photopigments instead of separate genes encoding L and M photopigments. The product of the hybrid gene exhibits a spectral sensitivity close to that of M photopigment; consequently, male monkeys carrying the hybrid gene are genetic protanopes, effectively lacking L photopigment. In the present study, we assessed retinal expression of L photopigment in monkeys carrying the hybrid gene. The relative sensitivities to middlewavelength (green) and long-wavelength (red) light were measured by electroretinogram flicker photometry. We found the sensitivity to red light to be extremely low in protanopic male monkeys compared with monkeys with the normal genotype. In female heterozygotes, sensitivity to red light was intermediate between the genetic protanopes and normal monkeys. Decreased sensitivity to long wavelengths was thus consistent with genetic loss of L photopigment. T richromatic color vision in Old World primates originates from three types of retinal cone photoreceptors possessing differing spectral sensitivities. This difference arises from the selective expression of three genes respectively encoding longwavelength-sensitive (L), middle-wavelength-sensitive (M), and short-wavelength-sensitive photopigment. In humans, the genes encoding L and M photopigment are located in a head-to-tail tandem array on the X chromosome, and loss of one or the other-caused by unequal chromosome recombination-results in dichromatic color vision (1). Dichromatism in humans has been studied for the purposes of making clinical diagnoses and achieving a better understanding of the mechanisms responsible for trichromatic color vision; the roles of lost and retained photopigments become more apparent in dichromats. Macaque monkeys have trichromatic color vision homologous to that of humans (2) and have served as subjects in a variety of physiological and psychophysical studies of color vision. Therefore, the dichromatic macaque may be a useful animal model of dichromatism with which to conduct clinical studies and investigate the mechanisms underlying color vision.In many species of New World monkeys, both dichromatic and trichromatic animals are mixed within a species because of the alleles whose products exhibit different spectral sensitivities in a single cone photopigment locus on the X chromosome (3-8). On the other hand, dichromatic macaques were not recognized until recently (9, 10). However, our molecular genetic analysis showed the existence of a dichromatic genotype of the crab-eating macaque (11). By using PCR to specify genotype, we found male protanopes and female heterozygotes spread among some troops in Pangandaran National Par...
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