Importantly, this perspective suggests the immediate goal of determining how well each visual area has untangled the neuronal representation, which can be quantified via a simple summation decoding scheme (described above). It redirects emphasis toward determining the mechanisms that might contribute to http://www.selleckchem.com/screening/tyrosine-kinase-inhibitor-library.html untangling—and dictates what must be “explained” at the single-neuron level, rather than creating “just so” stories based on the phenomenologies of heterogenous single neurons. Decades of evidence argue that the primate ventral visual processing stream—a set of cortical areas arranged along the occipital and temporal lobes ( Figure 3A)—houses

key circuits that underlie object recognition behavior (for reviews, see Gross, 1994, Miyashita, 1993, Orban, 2008 and Rolls, 2000). Object recognition is not the only ventral stream function, and we refer the reader to others ( Kravitz et al., 2010, Logothetis and Sheinberg, 1996, Maunsell and Treue, 2006 and Tsao and Livingstone, 2008) Osimertinib in vitro for a broader discussion. Whereas lesions in the posterior ventral stream produce complete blindness in part of the visual field (reviewed by Stoerig and Cowey, 1997), lesions or inactivation of anterior regions,

especially the inferior temporal cortex (IT), can produce selective deficits in the ability to distinguish among complex objects (e.g.,  Holmes and Gross, 1984, Horel, 1996, Schiller, 1995, Weiskrantz and Saunders, 1984 and Yaginuma et al., 1982). While these deficits are not always severe, and sometimes not found at all ( Huxlin et al., 2000), this

variability probably depends on the type of object recognition task (and thus the alternative visual strategies available). For example, some ( Schiller, 1995 and Weiskrantz Oxymatrine and Saunders, 1984), but not all, primate ventral stream lesion studies have explicitly required invariance. While the human homology to monkey IT cortex is not well established, a likely homology is the cortex in and around the human lateral occipital cortex (LOC) (see Orban et al., 2004 for review). For example, a comparison of monkey IT and human “IT” (LOC) shows strong commonality in the population representation of object categories (Kriegeskorte et al., 2008). Assuming these homologies, the importance of primate IT is suggested by neuropsychological studies of human patients with temporal lobe damage, which can sometimes produce remarkably specific object recognition deficits (Farah, 1990). Temporary functional disruption of parts of the human ventral stream (using transcranial magnetic stimulation, TMS) can specifically disrupt certain types of object discrimination tasks, such as face discrimination (Pitcher et al., 2009). Similarly, artificial activation of monkey IT neurons predictably biases the subject’s reported percept of complex objects (Afraz et al., 2006).