Chromosomal phylogeny of the primates.
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The contribution of hepatic apolipoprotein (apo) B-100 lipoproteins to plasma low-density lipoprotein (LDL) metabolic heterogeneity was examined in African green monkeys. Hepatic 3H-labeled very low-density lipoproteins (VLDL) (d less than 1.006, where d is density in g/ml) or hepatic 131I-labeled LDL (1.030 less than d less than 1.063) were isolated from perfused livers and injected simultaneously with autologous plasma 125I-LDL into African green monkeys. Serial blood samples were taken, and the distribution of radioactivity among various subfractions of apo B-100 lipoproteins was determined using density-gradient ultracentrifugation. Compartmental models were developed to describe simultaneously the kinetics of hepatic lipoproteins and plasma LDL. In five of seven studies, the metabolic behavior of LDL derived from radiolabeled hepatic lipoprotein precursors differed from the metabolic behavior of radiolabeled autologous plasma LDL. These differences could be described by different models supporting two hypotheses with different physiological interpretations: 1) lipoproteins of donor and recipient animals are kinetically distinct, and/or 2) plasma LDL derived from various potential sources are kinetically distinct. Compartmental modeling was used to test these hypotheses, which were not accessible to testing by conventional experimental methodologies. The kinetic analyses of these studies suggest that plasma LDL may be derived from a variety of precursors, including hepatic VLDL and hepatic LDL, with each source giving rise to metabolically distinct plasma LDL.
1. In the infragranular layers of the striate cortex of three monkeys, we studied tangential neuronal interactions by analyzing cross-correlograms calculated from spike trains recorded with 30 closely spaced microelectrodes. 2. There are two major types of correlogram structures--"narrow" peaks a few milliseconds wide, sometimes accompanied by small lateral troughs, and "broad" peaks approximately 30- to 100-ms wide. Isolated troughs are rare. Both types of structures are superimposed in the same correlograms; they are not due to shared optical stimulation. 3. In layer VI, narrow peaks are largest in a short lateral range of approximately 220 micron, and they depend on ocularity. In layer V, the lateral range is greater, and the dependency on ocularity is weak. 4. In addition, narrow peaks are largest at distances of 160 micron if the angles of preferred orientation are similar. In layer VI, however, at tangential distances of 300-400 micron, peaks are smaller, and troughs are found more often, for neuron pairs with parallel orientations compared with those with orthogonal orientations. From the agreement of this finding with a cooperative theory, we conclude that orientation selectivity is shaped by collective interactions. 5. Broad peaks always depend on ocularity, and the associated lateral interaction range exceeds the maximum of 1 mm investigated. Their size sharply decreases with receptive-field distance. 6. Average mutual delays of spikes of neuron pairs, manifest as lateral displacements of broad peaks, are interdependent; the delay between neurons 1 and 3 is the sum of that of neurons 1 and 2 and of neurons 2 and 3. This feature permits to rank the neurons on a "delay scale." 7. We conclude from 5 and 6 above that broad peaks partly result from intraretinal interactions whose effects are transmitted to the cortex via slow and fast pathways. 8. Lateral troughs adjacent to narrow peaks provide evidence that neurons at the "slow" end of the delay scale inhibit those at the "fast" end, and to a lesser extent, nondirectional neurons inhibit directional ones.
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Resting tremor and hypokinesia of unilateral limbs were produced in monkeys after making a lesion in the mesencephalic tegmentum. The administration of L-dopa or dopamine agonists relieved them and followingly induced dyskinesias. The same effects were produced by the direct injection of dopamine or its agonists into the dorsomedial part of caudate nucleus ipsilateral to the lesion, where spiroperidol binding to the D2 receptor was increased in the affinity. These results suggest that denervation supersensitivity at the postsynaptic D2 receptor is a basic condition for the development of dyskinesias, though they were slightly suppressed by the intracaudate injection of GABA, serotonin and met-enkephalin.
Japanese macaques (Macaca fuscata) and control species (vervet, pigtailed macaque, bonnet macaque) were trained for food to respond to one class of recorded fuscata vocalizations and do not respond to a second class. A measure of neural lateralization was obtained by presenting the stimuli randomly to the right or the left ear, and comparing performance in the two ears (ear advantage method). Vocalizations were from Steven Green's field tapes. In experiment I, the two classes were Green's 'smooth early high coos' (SE) and 'smooth late high coos' (SL). Experiment II utilized the same vocalizations, but sorted into a high-pitched and a low-pitched class, i.e., orthogonally to the communication-relevant dimension. We found that (a) Japanese macaques learned the SE-SL discrimination faster than the pitch discrimination; (b) the reverse was true for the controls; (c) Japanese macaques showed a right-ear advantage (presumed left hemisphere advantage) for the SE-SL distinction, but not for the pitch discrimination, and (d) controls (with one exception) showed no ear advantage for either discrimination. These demonstrations of selective attention to communication-relevant parameters of conspecific vocalizations, and neural lateralization in the perception of these vocalizations, parallel similar findings in human speech perception.
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10 monkeys (macaques) received adriamycin by monthly intravenous injections at 12 mg/m2 (1 mg/kg). 8 of the 10 monkeys developed congestive heart failure at an average cumulative adriamycin dose (310 mg/m2) well below that considered the safe upper limit (550 mg/m2) in man. Histologically, the myocardial lesions resembled those found in human anthracycline-induced cardiomyopathy. 1 of the 10 monkeys developed acute myeloblastic leukemia after receiving 324 mg/m2 of adriamycin; the 10th monkey is alive and well 26 months after the last dose of drug. Our results suggest that adriamycin is a more potent cardiotoxin in monkeys than in man, and that leukemia may be a consequence of prolonged treatment with this drug.
Multivariate statistical analysis, based upon a number of dimensions, showed significant contrasts in dental arch form between four primate groups, which was difficult to identify from subjective visual inspection. Furthermore, analysis of dental arch size was shown to differ from dental arch shape, although whether this reflected predominantly genetic or environmental factors, requires further research.
We have studied the morphology of the anatomical structures that permit communication between the anterior chamber and the sinus venosus sclerae. Examination of the posterior or inner wall of this canal, represented by the sclerocorneal trabecula, in 15 species of primates and 5 adult humans, has enabled us to observe the existence of some small orifices or stomata that are the outermost part of the so-called Sondermann's canals, which in our opinion are made by the successive confluence of the interstices worked in the interior of the sclerocorneal trabecula by means of contraction of the longitudinal portion of the ciliary muscle.
Multivariate morphometric analyses of the wrist morphology of monkeys, apes and humans indicated that there is a fundamental difference between cercopithecoids and hominoids which can be related to functional and behavioral differences. The wrists of the Miocene fossil hominoids (Dryopithecus africanus and Pliopithecus vindobonensis) are almost completely monkey-like in their structure.
The onset of puberty in males is indicated by a strong increase of weight, appearance of specific displays and changes in the vocal repertoire. Male social maturity follows sexual maturity, but does not depend only on age; it results also from behavioural interactions with the male leader within the one-male group.