Visual physiology of the lateral geniculate nucleus in two species of new world monkey: Saimiri sciureus and Aotus trivirgatis. (9/180)

1. Visual responses were recorded from neurones in the magnocellular and parvocellular layers of the lateral geniculate nucleus (LGN) of the thalamus in two species of New World monkeys - the diurnal squirrel monkey (Saimiri sciureus) and the nocturnal owl monkey (Aotus trivirgatis). Recording sites were reconstructed in postmortem tissue and comparisons were made between the response properties of magnocellular and parvocellular neurones. 2. Receptive fields were characterized with both white noise and drifting gratings. We found that most of the differences between magnocellular and parvocellular neurones that have been described in the macaque monkey hold for the squirrel monkey and owl monkey. In squirrel monkey and owl monkey, receptive fields of magnocellular neurones were larger than those of parvocellular neurones at similar eccentricities. Although visual responses in the owl monkey were significantly slower than in the squirrel monkey, in both species magnocellular neurones differed from parvocellular neurones in that their responses (1) had higher contrast gains, (2) tended to peak at higher temporal frequencies (but with considerable overlap), (3) had shorter response latencies, and (4) were more transient. 3. The strength of a neurone's receptive-field surround was assessed by comparing neuronal responses to gratings of optimal spatial frequency with responses to gratings of low spatial frequency. Using this approach, receptive-field surrounds were found to be equally strong on average for magnocellular and parvocellular neurones. 4. Spatial summation, as measured by a null test, was linear for all magnocellular and parvocellular cells tested; that is, Y cells were not observed in either species. Finally, most magnocellular neurones showed a contrast gain control mechanism, although this was not seen for parvocellular neurones.  (+info)

Growth of new brainstem connections in adult monkeys with massive sensory loss. (10/180)

Somatotopic maps in the cortex and the thalamus of adult monkeys and humans reorganize in response to altered inputs. After loss of the sensory afferents from the forelimb in monkeys because of transection of the dorsal columns of the spinal cord, therapeutic amputation of an arm or transection of the dorsal roots of the peripheral nerves, the deprived portions of the hand and arm representations in primary somatosensory cortex (area 3b), become responsive to inputs from the face and any remaining afferents from the arm. Cortical and subcortical mechanisms that underlie this reorganization are uncertain and appear to be manifold. Here we show that the face afferents from the trigeminal nucleus of the brainstem sprout and grow into the cuneate nucleus in adult monkeys after lesions of the dorsal columns of the spinal cord or therapeutic amputation of an arm. This growth may underlie the large-scale expansion of the face representation into the hand region of somatosensory cortex that follows such deafferentations.  (+info)

Protection of Aotus monkeys by Plasmodium falciparum EBA-175 region II DNA prime-protein boost immunization regimen. (11/180)

Aotus monkeys received 4 doses of Plasmodium falciparum EBA-175 region II vaccine as plasmid DNA (Dv-Dv) or recombinant protein in adjuvant (Pv-Pv) or as 3 doses of DNA and 1 dose of protein (Dv-Pv). After 3 doses, antibody titers were approximately 10(4) in DNA-immunized monkeys and 10(6) in protein-immunized monkeys. A fourth dose did not significantly boost antibody responses in the Dv-Dv only or Pv-Pv only groups, but titers were boosted to approximately 10(6) in monkeys in the Dv-Pv group. Four weeks after the last immunization, the animals were challenged with 10(4) P. falciparum-parasitized erythrocytes. Peak levels of parasitemia were lower in the 16 monkeys that received region II-containing plasmids or proteins than in the 16 controls (geometric mean: 194,178 and 410,110 parasites/microL, respectively; P=.013, Student's t test). Three of 4 monkeys in the Dv-Pv group did not require treatment. These data demonstrate that immunization with EBA-175 region II induces a significant antiparasite effect in vivo.  (+info)

M and P retinal ganglion cells of the owl monkey: morphology, size and photoreceptor convergence. (12/180)

We have estimated photoreceptor convergence to M and P retinal ganglion cells of two closely related nocturnal (owl monkey, Aotus) and diurnal (capuchin monkey, Cebus) anthropoids. Rod convergence is higher in the owl monkey retina while cone convergence to both M and P cells are very similar in the retinas of the owl monkey and the capuchin monkey. These results indicate that during evolution, the owl monkey retina has undergone changes compatible with a more nocturnal lifestyle, but kept a cone to ganglion cell relation similar to that found in diurnal primates.  (+info)

Cyclic changes in the circulating and urinary levels of ovarian steroids in the adult female owl monkey (Aotus trivirgatus). (13/180)

Circulating levels of oestrone and progesterone were measured by radioimmunoassays in plasma samles from 5 female owl monkeys on 60 consecutive days. Both steroids exhibited cyclic fluctuations and based on nadir to nadir intervals the ovarian cycle was estimated to be 15.92 +/- 0.26 days. Levels of oestrone and pregnanediol-3 alpha-glucuronide were also measured in daily urine samples. The fluctuations of urinary steroids reflected those observed in plasma. Ketamine sedation had no effect on the length of the cycle. Peak values of plasma progesterone and oestrone were 250.48 +/- 11.37 and 3.59 +/- 0.066 ng/ml respectively. There was no clear hormonal distinction between the follicular and luteal phase of the cycle in these owl monkeys.  (+info)

Repeated infection of Aotus monkeys with Plasmodium falciparum induces protection against subsequent challenge with homologous and heterologous strains of parasite. (14/180)

We evaluated repeated blood-stage infections with Plasmodium falciparum in eight Aotus lemurinus lemurinus monkeys. Over the course of seven infections with 10(4) P. falciparum (the Vietnam Oak Knoll [FVO] strain), the pre-patent period lengthened from 8.2 to 30.8 days; the peak parasitemia decreased from 4.5 x 10(5) to 0 parasites/microl (Challenges 6 and 7), and the requirement for treatment decreased from 100% to 0% (Challenges 3 to 7). Five weeks after the seventh FVO challenge, the eight immune and three naive monkeys received 10(4) parasitized erythrocytes infected with P. falciparum (CAMP strain). The three control animals experienced uncontrolled parasitemias reaching between 4.8 and 7.7 x 10(5) parasites/microl (pre-patency = 6.3 days) and all required drug treatment; six of the eight immune monkeys became parasitemic (pre-patency = 8.8 days), but self-cured. Two of three of the monkeys having the greatest reductions in hematocrit (50-60%) also had the highest parasitemias (approximately 10(4) parasites/microl) before self-curing. Repeated homologous infections induced sterile immunity to homologous challenge; during heterologous challenge the monkeys developed clinically relevant, but not life-threatening, parasitemias and anemia.  (+info)

Oriented axon projections in primary visual cortex of the monkey. (15/180)

One important aspect of the functional architecture of primary visual cortex is the circuitry that accounts for the receptive field properties of neurons. The anatomy that underlies retinotopy and ocular dominance is well known, but no anatomical structure related to orientation selectivity has been found in primates. We examined whether the arrangement of local axon systems projecting within the cortical layers might be correlated with orientation preference in New World monkeys. We found that axons in layer 3 spread out from the site of a tracer injection in an anisotropic manner and that this elongated distribution is aligned with the preferred orientation recorded at each site. Moreover, within a few degrees of the foveal representation, the majority of the axon terminals fall within or just outside of the limits of the cortical mapping of the classical receptive field. Thus local axons produce a field of monosynaptic excitation that aligns with orientation axes and reaches neurons that have receptive fields which are adjacent in visual space.  (+info)

Functional retinotopy of monkey visual cortex. (16/180)

The operations of primary visual cortex generate continuous representations of orientation, ocular dominance, and retinotopy that, to fit in two dimensions, organize at separate but overlapping scales (e.g., 20-500 microm, 200 microm to 5 mm, and 2-33 mm). Where their scales overlap, these organizations interact; iso-orientation contours cross ocular dominance columns at right angles, and ocular dominance columns distort retinotopy near the V1/V2 border. To explore these interactions, we developed an optical technique for visualizing retinotopy in vivo that allows us to analyze it in relation to ocular dominance and orientation patterns. Our results show local retinotopic distortions in every region of macaque V1 that we examine, including regions far from the V1/V2 border. They also show a consistent relation between local axes of distortion and ocular dominance slabs, which they intersect at angles of approximately 90 degrees. A further correlation is provided by retinotopic maps from New World primates that show less distortion (9 vs 60%) in two species characterized by an absence of pronounced ocular dominance columns. Retinotopic maps from these New World primates also revealed an unexpected tilt of the vertical midline representation that diverged from the V1/V2 border by an angle of approximately 20 degrees. Overall, these results suggest a general tendency for slab-based organizations to distort retinotopy by representing the same part of space more than once in adjacent slabs.  (+info)