Ventral Prefrontal Cortex Is Not Essential for Working Memory

It is widely held that the prefrontal cortex is important for working memory. It has been suggested that the inferior convexity (IC) may play a special role in working memory for form and color (Wilson et al., 1993). We have therefore assessed the ability of monkeys with IC lesions to perform visual pattern association tasks and color-matching tasks, both with and without delay. In experiment 1, six monkeys were trained on a visual association task with delays of up to 2 sec. Conservative IC lesions that removed lateral area 47/12 in three animals had no effect on the task. Further experiments showed that these lesions had no effect on the postoperative new learning of a color-matching task with delays of up to 2 sec or versions of the visual association task involving delays of up to 8 sec. In experiment 2, larger lesions of both areas 47/12 and 45A were made in the three control animals. This lesion caused a profound deficit in the ability to relearn simultaneous color matching, but subsequent matching with delays of up to 8 sec was clearly unimpaired. We suggest that the IC may be more important for stimulus selection and attention as opposed to working memory.

[1]  R. Butler,et al.  Perseverative Interference in Monkeys Following Bilateral Removal of the Prefrontal Areas , 1956 .

[2]  M MISHKIN,et al.  Effects of small frontal lesions on delayed alternation in monkeys. , 1957, Journal of neurophysiology.

[3]  N Butters,et al.  Retention of Delayed-Alternation: Effect of Selective Lesions of Sulcus Principalis , 1969, Science.

[4]  H. E. Rosvold,et al.  Localization of function within the dorsolateral prefrontal cortex of the rhesus monkey. , 1970, Experimental neurology.

[5]  Richard Passingham,et al.  Delayed matching after selective prefrontal lesions in monkeys (Macaca mulatta) , 1975, Brain Research.

[6]  M. Mishkin,et al.  Non-spatial memory after selective prefrontal lesions in monkeys , 1978, Brain Research.

[7]  Joaquin M. Fuster,et al.  Single cell activity in ventral prefrontal cortex of behaving monkeys , 1981, Brain Research.

[8]  S. P. Wise,et al.  Set-related neuronal activity in the premotor cortex of rhesus monkeys: effects of changes in motor set , 1985, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[9]  M. Petrides Deficits in non-spatial conditional associative learning after periarcuate lesions in the monkey , 1985, Behavioural Brain Research.

[10]  R. Passingham,et al.  Premotor cortex and the conditions for movement in monkeys (Macaca fascicularis) , 1985, Behavioural Brain Research.

[11]  R E Passingham Memory of monkeys (Macaca mulatta) with lesions in prefrontal cortex. , 1985, Behavioral neuroscience.

[12]  H. Barbas Anatomic organization of basoventral and mediodorsal visual recipient prefrontal regions in the rhesus monkey , 1988, The Journal of comparative neurology.

[13]  P. Goldman-Rakic,et al.  Posterior parietal cortex in rhesus monkey: II. Evidence for segregated corticocortical networks linking sensory and limbic areas with the frontal lobe , 1989, The Journal of comparative neurology.

[14]  Mortimer Mishkin,et al.  The role of the inferior prefrontal convexity in performance of delayed nonmatching-to-sample , 1991, Neuropsychologia.

[15]  M. Corbetta,et al.  Selective and divided attention during visual discriminations of shape, color, and speed: functional anatomy by positron emission tomography , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  M. J. Eacott,et al.  Inferotemporal‐frontal Disconnection: The Uncinate Fascicle and Visual Associative Learning in Monkeys , 1992, The European journal of neuroscience.

[17]  Alan C. Evans,et al.  Dissociation of human mid-dorsolateral from posterior dorsolateral frontal cortex in memory processing. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[18]  P. Goldman-Rakic,et al.  Dissociation of object and spatial processing domains in primate prefrontal cortex. , 1993, Science.

[19]  P. Goldman-Rakic,et al.  Dorsolateral prefrontal lesions and oculomotor delayed-response performance: evidence for mnemonic "scotomas" , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[20]  R. Passingham The frontal lobes and voluntary action , 1993 .

[21]  Edward E. Smith,et al.  Spatial working memory in humans as revealed by PET , 1993, Nature.

[22]  Richard S. J. Frackowiak,et al.  Cortical control of saccades and fixation in man. A PET study. , 1994, Brain : a journal of neurology.

[23]  P. Goldman-Rakic,et al.  Functional magnetic resonance imaging of human prefrontal cortex activation during a spatial working memory task. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[24]  Leslie G. Ungerleider,et al.  The functional organization of human extrastriate cortex: a PET-rCBF study of selective attention to faces and locations , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[25]  M. Petrides Comparative architectonic analysis of the human and the macaque frontal cortex , 1994 .

[26]  J. Price,et al.  Architectonic subdivision of the orbital and medial prefrontal cortex in the macaque monkey , 1994, The Journal of comparative neurology.

[27]  E. Rolls,et al.  Gustatory, olfactory, and visual convergence within the primate orbitofrontal cortex , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[28]  S. Funahashi,et al.  Working memory and prefrontal cortex , 1994, Neuroscience Research.

[29]  Leslie G. Ungerleider,et al.  Connections of inferior temporal areas TEO and TE with parietal and frontal cortex in macaque monkeys. , 1994, Cerebral cortex.

[30]  S M Kosslyn,et al.  Identifying objects seen from different viewpoints. A PET investigation. , 1994, Brain : a journal of neurology.

[31]  P. Goldman-Rakic,et al.  Cytoarchitectonic definition of prefrontal areas in the normal human cortex: II. Variability in locations of areas 9 and 46 and relationship to the Talairach Coordinate System. , 1995, Cerebral cortex.

[32]  J. Kalaska,et al.  Deciding not to GO: neuronal correlates of response selection in a GO/NOGO task in primate premotor and parietal cortex. , 1995, Cerebral cortex.

[33]  G. C. Baylis,et al.  Afferent connections of the caudolateral orbitofrontal cortex taste area of the primate , 1995, Neuroscience.

[34]  Edward E. Smith,et al.  Spatial versus Object Working Memory: PET Investigations , 1995, Journal of Cognitive Neuroscience.

[35]  E. Halgren,et al.  Cortical metabolic activation in humans during a visual memory task. , 1995, Cerebral cortex.

[36]  M. Goldberg,et al.  Oculocentric spatial representation in parietal cortex. , 1995, Cerebral cortex.

[37]  Cheryl L. Grady,et al.  Hemispheric differences in neural systems for face working memory: A PET‐rCBF study , 1995 .

[38]  P. Goldman-Rakic,et al.  Activation of human prefrontal cortex during spatial and nonspatial working memory tasks measured by functional MRI. , 1996, Cerebral cortex.

[39]  Leslie G. Ungerleider,et al.  Effect of task difficulty on cerebral blood flow during perceptual matching of faces , 1996, Human brain mapping.

[40]  D. Pandya,et al.  Comparison of prefrontal architecture and connections. , 1996, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[41]  M. Hallett,et al.  Cerebral structures participating in motor preparation in humans: a positron emission tomography study. , 1996, Journal of neurophysiology.

[42]  E. Rolls,et al.  The Orbitofrontal Cortex , 2019 .

[43]  Leslie G. Ungerleider,et al.  Object and spatial visual working memory activate separate neural systems in human cortex. , 1996, Cerebral cortex.

[44]  R. Dolan,et al.  Active representation of shape and spatial location in man. , 1996, Cerebral cortex.

[45]  Alan C. Evans,et al.  Evidence for a two-stage model of spatial working memory processing within the lateral frontal cortex: a positron emission tomography study. , 1996, Cerebral cortex.

[46]  Leslie G. Ungerleider,et al.  Changes in limbic and prefrontal functional interactions in a working memory task for faces. , 1996, Cerebral cortex.

[47]  P. Goldman-Rakic The prefrontal landscape: implications of functional architecture for understanding human mentation and the central executive. , 1996, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[48]  M. Petrides,et al.  Specialized systems for the processing of mnemonic information within the primate frontal cortex. , 1996, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[49]  R. Desimone,et al.  Neural Mechanisms of Visual Working Memory in Prefrontal Cortex of the Macaque , 1996, The Journal of Neuroscience.