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Short-latency projections to the cat's cerebral cortex from skin and muscle afferents in the contralateral forelimb.

1. The potentials evoked in the first sensorimotor area on stimulation of muscle and skin nerves in the contralateral forelimb were recorded in preparations with either the dorsal funiculus (DF) or the spinocervical tract (SCT) interrupted.2. The short-latency, surface-positive potentials in these preparations are mediated by the remaining path, either the DF or SCT.3. Cutaneous afferents project through both paths to two discrete areas which correspond to the classical sensory and motor cortices (Fig. 10 A and B). The projection areas are not identical: the DF path seems to activate most effectively the sensory cortex; and the SCT path, most effectively the motor cortex.4. The potentials evoked from cutaneous nerves have a similar latency in the two areas. On stimulation of the superficial radial nerve the latency was about 4.5 msec in preparations with intact DF, and about 5.3 msec in preparations with intact SCT.5. High threshold muscle afferents project to the same areas as the cutaneous afferents.6. Group I muscle afferents project, exclusively through the DF path, to an area distinct from the two cutaneous projection areas (Fig. 10C). It occupies a caudal part of the motor cortex and an intermediate zone between the sensory and motor cortices.7. The projection areas are compared with the recent cytoarchitectonic map of Hassler & Muhs-Clement (1964) (Fig. 10D).8. It is suggested that the afferent projections to the motor cortex and the intermediate zone are used in the integration of movements elicited from the cortex. The general similarity in the organization of afferent paths to the motor cortex and the cerebellum is pointed out.

Animals↗

Organization of climbing fibre projections to the cerebellar cortex from trigeminal cutaneous afferents and from the SI face area of the cerebral cortex in the cat.

1. In cats anaesthetized with pentobarbitone, the projection of climbing fibres (CFs) to the cerebellar cortex from trigeminal cutaneous branches and from the face area of the sensorimotor (SI) cortex was mapped, using the technique of laminar field potential analysis. 2. The CF projections from both the trigeminal nerve and the SI face area were found to be localized to the same cerebellar folia, viz. chiefly the ipsilateral lobule HVI, with a small overlap on to the adjacent folia of lobule V and crus Ia of HVIIA. Frequently a projection from the superficial radial nerve to part or all of this area, was also found. 3. A correspondence in the distribution and amplitudes of CF potentials evoked at most points by stimulation of the trigeminal nerve and the SI cortex was found. This implies a convergence of afferents from these two sources at or before the inferior olive. 4. In more than half of the cats, a small area of the cerebellar hemisphere was found, in which contralateral as well as ipsilateral trigeminal stimulation would evoke CF potentials. Usually inputs from the superficial radial nerve and the SI cortex also converged upon this area. 5. The organization of CF projections from trigeminal and superficial radial nerve afferents to the cerebellar hemisphere was found to occur in the same 'patchy' pattern of somatotopy that has been described for spinal nerve inputs to the anterior lobe. 6. One constant factor was found in the pattern of organization of CF projections to this area from cutaneous afferent nerves. That is, only the afferents from overlapping areas of skin projected to a given recording point: no instance of CF projections from trigeminal branches innervating discontinuous skin areas was observed.

Animals↗

Induction of compression in the re-established visual projections on to a rotated tectal reimplant that retains its original topographic polarity within the halved optic tectum of adult goldfish.

1. The topographic pattern of re-established retinotectal projections following various surgical manipulations of the optic tectum was studied in adult goldfish with neurophysiological mapping methods. 2. Immediately following excision of the caudal half of the tectum, a piece of the tectal tissue was dissected from the remaining rostral half-tectum, and then reimplanted to the same half-tectum after either 180 or 90 degrees anticlockwise rotation around the dorsoventral axis in the first experimental group. 3. A majority (twenty-one out of twenty-three) of these operated fish, in which the reimplanted tectal tissue degenerated, showed no sign of a field compression: only the nasal half of the visual field (with a localized partial scotoma corresponding to the area of the degenerated reimplant) projected on to the remaining intact area of the rostral half-tectum. 4. In seven fish, the re-established visual projections on to the 180 or 90 degrees rotated reimplants showed a corresponding localized 180 or 90 degrees rotation with reference to the other projections on to the surrounding intact area of the same half-tectum. Only one of these seven fish showed also a compression in the re-established projections from the entire visual field on to the operated half-tectum with the 90 degrees rotated reimplant. 5. When a field compression was induced first in the intact rostral half-tectum following excision of the caudal half, and then a piece of the 90 degrees rotated tectal tissue was reimplanted later within the rostral half-tectum, the previously induced field compression persisted, regardless of whether the reimplanted tissue degenerated or survived. In the latter case, the compression in the re-established visual projections on to the surviving reimplant occurred according to the original topographic polarity of the 90 degrees rotated tectal tissue. 6. A field compression could also be induced within a rotated tectal reimplant, which retained its original polarity, as follows. A piece of the tectal tissue was dissected from the central area of the whole tectum, and then reimplanted after either 180 or 90 degrees rotation. When the reimplanted tectal tissue became reinnervated later, the caudal half of the operated tectum (including the posterior half of the reimplant) was excised. The re-established visual projections on to the remaining part of the halved reimplant within the rostral half-tectum showed later a field compression in accordance with the original topographic polarity of the 180 or 90 degrees rotated tectal tissue. 7. These results provide direct evidence for the compatibility between the retention of original topographic polarity by a reimplanted tectal tissue and the capability of the same tectal tissue to readjust to a disparity in size. 8. Histological examination of the operated half-tectum with a reimplant, stained by a modified rapid Golai method, revealed that the reimplanted tectal tissues retained highly organized cytoarchitectonic structures...

Animals↗

Gastrointestinal-projecting neurones in the dorsal motor nucleus of the vagus exhibit direct and viscerotopically organized sensitivity to orexin.

Orexin (hypocretin)-containing projections from lateral hypothalamus (LH) are thought to play an important role in the regulation of feeding behaviour and energy balance. In rodent studies, central administration of orexin peptides increases food intake, and orexin neurones in the LH are activated by hypoglycaemia during fasting. In addition, administration of orexins into the fourth ventricle or the dorsal motor nucleus of the vagus (DMV) has been shown to stimulate gastric acid secretion and motility, respectively, via vagal efferent pathways. In this study, whole-cell recordings were obtained from DMV neurones in rat brainstem slices to investigate the cellular mechanism(s) by which orexins produce their gastrostimulatory effects. To determine whether responsiveness to orexins might be differentially expressed among distinct populations of preganglionic vagal motor neurones, recordings were made from neurones whose projections to the gastrointestinal tract had been identified by retrograde labelling following apposition of the fluorescent tracer DiI to the gastric fundus, corpus or antrum/pylorus, the duodenum or caecum. Additionally, the responses of neurones to orexins were compared with those produced by oxytocin, which acts within the DMV to stimulate gastric acid secretion, but inhibits gastric motor function. Bath application of orexin-A or orexin-B (30-300 nM) produced a slow depolarization, accompanied by increased firing in 47 of 102 DMV neurones tested, including 70 % (30/43) of those that projected to the gastric fundus or corpus. In contrast, few DMV neurones that supplied the antrum/pylorus (3/13), duodenum (4/18) or caecum (1/13) were responsive to these peptides. The depolarizing responses were concentration dependent and persisted during synaptic isolation of neurones with TTX or Cd2+, indicating they resulted from activation of postsynaptic orexin receptors. They were also associated with a small increase in membrane resistance, and in voltage-clamp recordings orexin-A induced an inward current that reversed near the estimated equilibrium potential for K+, indicating the depolarization was due in large part to a reduction in K+ conductance. Orexins did not affect synaptically evoked excitation, but did reduce membrane excitability in a subset of gastric-projecting DMV neurones by enhancing GABA-mediated synaptic input. Lastly, although many DMV neurones responded to orexins and oxytocin with excitation, for the most part these peptides modulated excitability of distinct populations of gastric-projecting vagal motor neurones. These results indicate that orexins act preferentially within the DMV to directly excite vagal motor neurones that project to gastric fundus and corpus. In this way, release of endogenous orexins from descending hypothalamic projections into the DMV may mediate the increase in gastric acid secretion and motor activity associated with the cephalic phase of feeding.

Action Potentials↗

Distinctive membrane and discharge properties of rat spinal lamina I projection neurones in vitro.

Most lamina I neurones with a projection to the brainstem express the neurokinin 1 receptor and thus belong to a small subgroup of lamina I neurones that are necessary for the development of hyperalgesia in rat models of persisting pain. These neurones are prone to synaptic plasticity following primary afferent stimulation in the noxious range while other nociceptive lamina I neurones are not. Here, we used whole-cell patch-clamp recordings from lamina I neurones in young rat spinal cord transverse slices to test if projection neurones possess membrane properties that set them apart from other lamina I neurones. Neurones with a projection to the parabrachial area or the periaqueductal grey (PAG) were identified by retrograde labelling with the fluorescent tracer DiI. The properties of lamina I projection neurones were found to be fundamentally different from those of unidentified, presumably propriospinal lamina I neurones. Two firing patterns, the gap and the bursting firing pattern, occurred almost exclusively in projection neurones. Most spino-parabrachial neurones showed the gap firing pattern while the bursting firing pattern was characteristic of spino-PAG neurones. The underlying membrane currents had the properties of an A-type K(+) current and a Ca(2+) current with a low activation threshold, respectively. Projection neurones, especially those of the burst firing type, were more easily excitable than unidentified neurones and received a larger proportion of monosynaptic input from primary afferent C-fibres. Intracellular labelling with Lucifer yellow showed that projection neurones had larger somata than unidentified neurones and many had a considerable extension in the mediolateral plane.

Animals↗

Automatic needle segmentation in three-dimensional ultrasound images using two orthogonal two-dimensional image projections.

In this paper, we describe an algorithm to segment a needle from a three-dimensional (3D) ultrasound image by using two orthogonal two-dimensional (2D) image projections. Not only is the needle more conspicuous in a projected (volume-rendered) image, but its direction in 3D lies in the plane defined by the projection direction and the needle direction in the projected 2D image. Hence, using two such projections, the 3D vector describing the needle direction lies along the intersection of the two corresponding planes. Thus, the task of 3D needle segmentation is reduced to two 2D needle segmentations. For improved accuracy and robustness, we use orthogonal projection directions (both orthogonal to a given a priori estimate of the needle direction), and use volume cropping and Gaussian transfer functions to remove complex background from the 2D projection images. To evaluate our algorithm, we tested it with 3D ultrasound images of agar and turkey breast phantoms. Using a 500 MHz personal computer equipped with a commercial volume-rendering card, we found that our 3D needle segmentation algorithm performed in near real time (about 10 fps) with a root-mean-square accuracy in needle length and endpoint coordinates of better than 0.8 mm, and about 0.5 mm on average, for needles lengths in the 3D image from 4.0 mm to 36.7 mm.

Algorithms↗

Diffuse lung disease: assessment with helical CT--preliminary observations of the role of maximum and minimum intensity projection images.

PURPOSE: To evaluate assessment of diffuse lung disease with helical computed tomography (CT) and maximum intensity projection (MIP) and minimum intensity projection images. MATERIALS AND METHODS: Six patients with suspected lung disease (the control group) and 20 patients with documented disease underwent axial helical CT through the upper and lower lung fields. Findings on the MIP and minimum intensity projection images of each helical data set were compared with findings on the thin-section scan obtained at the midplane of the series. RESULTS: Owing to markedly improved visualization of peripheral pulmonary vessels (n = 26) and improved spatial orientation, MIP images were superior to helical scans to help identify pulmonary nodules and characterize them as peribronchovascular (n = 2) or centrilobular (n = 7). Minimum intensity projection images were more accurate than thin-section scans to help identify lumina of central airways (n = 23) and define abnormal low (n = 15) and high (ground-glass) (n = 8) lung attenuation. Conventional thin-section scans depicted fine linear structures more clearly than either MIP or minimum intensity projection images, including the walls of peripheral, dilated airways (n = 3) and interlobular septa (n = 3). MIP and minimum intensity projection images added additional diagnostic findings to those on thin-section scans in 13 (65%) of 20 cases. CONCLUSION: MIP and minimum intensity projection images of helical data sets may help diagnosis of a wide spectrum of diffuse lung diseases.

Adult↗

Renal artery origins: best angiographic projection angles.

PURPOSE: To determine the best projection angles for imaging the renal artery origins in profile. MATERIALS AND METHODS: A mathematical model of the anatomy at the renal artery origins in the transverse plane was used to analyze the amount of aortic lumen that projects over the renal artery origins at various projection angles. Computed tomographic (CT) angiographic data about the location of 400 renal artery origins in 200 patients were statistically analyzed. RESULTS: In patients with an abdominal aortic diameter no larger than 3.0 cm, approximately 0.5 mm of the proximal part of the renal artery and origin may be hidden from view if there is a projection error of +/-10 degrees from the ideal image. A combination of anteroposterior and 20 degrees and 40 degrees left anterior oblique projections resulted in a 92% yield of images that adequately profiled the renal artery origins. Right anterior oblique projections resulted in the least useful images. CONCLUSION: An error in projection angle of +/-10 degrees is acceptable for angiographic imaging of the renal artery origins. Patients sex, site of interest (left or right artery), and local diameter of the abdominal aorta are important factors to consider.

Angiography↗

Antidromic activation reveals tonotopically organized projections from primary auditory cortex to the central nucleus of the inferior colliculus in guinea pig.

The inferior colliculus (IC) is highly modulated by descending projections from higher auditory and nonauditory centers. Traditionally, corticofugal fibers were believed to project mainly to the extralemniscal IC regions. However, there is some anatomical evidence suggesting that a substantial number of fibers from the primary auditory cortex (A1) project into the IC central nucleus (ICC) and appear to be tonotopically organized. In this study, we used antidromic stimulation combined with other electrophysiological techniques to further investigate the spatial organization of descending fibers from A1 to the ICC in ketamine-anesthetized guinea pigs. Based on our findings, corticofugal fibers originate predominantly from layer V of A1, are amply scattered throughout the ICC and only project to ICC neurons with a similar best frequency (BF). This strict tonotopic pattern suggests that these corticofugal projections are involved with modulating spectral features of sound. Along the isofrequency dimension of the ICC, there appears to be some differences in projection patterns that depend on BF region and possibly isofrequency location within A1 and may be indicative of different descending coding strategies. Furthermore, the success of the antidromic stimulation method in our study demonstrates that it can be used to investigate some of the functional properties associated with corticofugal projections to the ICC as well as to other regions (e.g., medial geniculate body, cochlear nucleus). Such a method can address some of the limitations with current anatomical techniques for studying the auditory corticofugal system.

Acoustic Stimulation↗

Long-term potentiation in direct perforant path projections to the hippocampal CA3 region in vivo.

The perforant path constitutes the primary projection system relaying information from the neocortex to the hippocampal formation. Long-term synaptic potentiation (LTP) in the perforant path projections to the dentate gyrus is well characterized. However, surprisingly few studies have addressed the mechanisms underlying LTP induction in the direct perforant path projections to the hippocampus. Here we investigate the role of N-methyl-D-aspartate (NMDA) and opioid receptors in the induction of LTP in monosynaptic medial and lateral perforant path projections to the CA3 region in adult pentobarbital sodium-anesthetized rats. Similar to LTP observed at the medial perforant path-dentate gyrus synapse, medial perforant path-CA3 synapses display LTP that is blocked by both local and systemic administration of the competitive NMDA receptor antagonist (+/-)-3-(2-carboxypiperazin-4-yl) propyl-1-phosphonic acid [(+/-)-CPP]. By contrast, LTP induced at the lateral perforant path-CA3 synapses is not blocked by either local or systemic administration of this NMDA receptor antagonist. The induction of LTP at lateral perforant path-CA3 synapses, which is blocked by the opioid receptor antagonist naloxone, is also blocked by the selective mu opioid receptor antagonist Cys(2)-Tyr(3)-Orn(5)-Pen(7)-amide (CTOP), but not the selective delta opioid receptor antagonist naltrindole (NTI). CTOP was without effect on the induction of medial perforant path-CA3 LTP. The selective sensitivity of lateral perforant path-CA3 LTP to mu-opioid receptor antagonists corresponds with the distribution of mu-opioid receptors within the stratum lacunosum-moleculare of area CA3 where perforant path projections to CA3 terminate. These data indicate that both lateral and medial perforant path projections to the CA3 region display LTP, and that LTP induction in medial and lateral perforant path-CA3 synapses are differentially sensitive to NMDA receptor and mu-opioid receptor antagonists. This suggests a role for opioid, but not NMDA receptors in the induction of LTP at lateral perforant path projections to the hippocampal formation.

Animals↗

Somatotopic organization of hindlimb cutaneous nerve projections to cat dorsal horn.

1. The dorsal horn lamina III-IV projections of 10 hindlimb nerves innervating most of the hindlimb have been studied in the cat using transganglionic transport of horseradish peroxidase (HRP). The somatotopic organization of whole cutaneous nerve projections was largely in register with the somatotopic organization of dorsal horn cells. That is, nerves projected to areas of dorsal horn where their innervation fields overlap the receptive fields of dorsal horn cells. 2. However, long-ranging projections were observed that were more extensive than predicted from the somatotopy of dorsal horn cells: these long-ranging projections may reflect the presence of normally ineffective synapses (synapses that do not cause postsynaptic discharge during receptive-field mapping of dorsal horn cells,) or a misconception of dorsal horn cell somatotopy in S2 and caudal segments, or the existence of a functionally separate cell group in ventral lamina IV and lamina V of these segments. 3. The cutaneous innervation fields of homologous nerves possessed high bilateral symmetry, as did their lamina III-IV projection fields. The degree of separation or overlap of two cutaneous nerves' projection fields was predictable from the degree of separation or overlap of their cutaneous innervation fields.

Animals↗

The spinal projection of individual identified A-delta- and C-fibers.

1. Recordings were made from individual sensory neurons with an A-delta peripheral conduction velocity, either intrasomally in the L7 dorsal root ganglion, or extracellularly in Lissauer's Tract or in the dorsal root close to the root entry zone. The spinal projection of these afferents was assessed by their antidromic response to stimulation of the dorsal columns (DC) or Lissauer's Tract (LT) at the L5/L6 border. The adequate stimulus was also ascertained. 2. A-delta-fibers could be divided into two groups: high-threshold mechanoreceptors from either skin or muscle (HTMRs) and low-threshold mechanoreceptors (LTMs), primarily Down Hairs. A third group of cells recorded intrasomally had broad spikes with shoulders on the downstroke characteristic of A-delta-nociceptors and were so classified provisionally, although no adequate stimulus could be identified. HTMRs and broad spike cells projected either in DC or LT, but LTMs projected only in DC, never in LT. About one-quarter of both groups failed to project rostrally as far as L5/L6. 3. Cells with unmyelinated axons recorded intrasomally were found to supply either low-threshold or high-threshold mechanoreceptors. Unlike A-delta-cells, all these cells had broad spikes with shoulders on the downstroke. Proportionally fewer C-fibers than A-delta-fibers projected as far as one segment rostral from their root entry zone. Of those that did, axons supplying low-threshold mechanoreceptors projected only in DC, whereas those innervating high-threshold mechanoreceptors could project either through LT or DC. 4. A-delta-fibers supplying LTMs and HTMRs exhibited a similar reduced conduction velocity was reduced even further in the spinal cord but much more for HTMRs than for LTMs. For C-fibers the conduction velocity decrease was more substantial in the dorsal root for HTMRs than for LTMs. 5. These findings suggest that axons innervating different peripheral receptors exhibit characteristic cellular properties. They confirm that the primary afferent component of Lissauer's Tract is specialized as a "pain pathway" but also indicate that the dorsal columns may play some role in the transmission of nociceptive information.

Afferent Pathways↗

Motor and somatosensory corticostriatal projection magnifications in the squirrel monkey.

1. Motor and somatosensory cortex project massively to the primate striatal matrix, terminating in distributed sets of overlapping projection zones (matrisomes) within the putamen. To study this system quantitatively, we have developed a computer-assisted estimation of the changes in magnification that occur as motor and somatosensory cortical body representations are projected onto the putamen. 2. Cortical and striatal body maps were assessed in squirrel monkeys by injecting anterograde tract tracers into electrophysiologically identified body-part representations in cortical areas 4, 3a, 3b, and 1. Relative projection magnification was defined as the ratio of the cortical injection site volume to the striatal projection site volume. 3. Magnification comparisons indicate that the tracers wheat germ agglutinin-conjugated horseradish peroxidase (WGA-HRP) and 35S-methionine have similar sensitivities. 4. The relative proportions of body-part representations in the striatal maps were not significantly different from those in cortical maps. Both had large representations of hand, foot, and mouth, and smaller representations of trunk. 5. The relative magnification of the motor cortex projection to the striatum was roughly twice as large as those of projections from individual somatosensory areas. 6. These findings suggest that, in the sensorimotor striatum, motor and somatosensory inputs may undergo different proportions of local processing at the borders of their distribution zones (striosomes and matrisomes).

Animals↗

Corticoreticular pathways in the cat. I. Projection patterns and collaterization.

This paper summarizes and compares the projection patterns and the receptive fields of cortical neurons in areas 4 and 6 that project to the pontomedullary reticular formation (PMRF). A total of 326 neurons were recorded in area 4 and 129 in area 6 in four awake, unrestrained cats that were chronically implanted with arrays of electrodes in the PMRF and the pyramidal tract (PT). In area 4, 47% of the neurons projected to the caudal PT but not to the PMRF (PTNs); 19% were activated only from the PMRF [corticoreticular neurons (CRNs)], whereas 27% were activated from both the PT and the PMRF (PTN/CRNs). More PTN/CRNs conducted at velocities >20 m/s (82%) than did CRNs (23%). In area 6, only 19% of the neurons were identified as PTNs, 12% were PTN/CRNs and 31% were CRNs; a further 38% could not be activated from either structure. Collateral branches within the PMRF conducted at maximum velocities of 20 m/s (average = 6.5 m/s). No significant differences in the conduction velocities of the collateral branches were found either between fast and slow PTNs or between area 4 and area 6 neurons. A large proportion of neurons in area 4 (85/173, 49%) were activated by passive manipulation of the more distal, contralateral forelimb, with approximately equal numbers being classed as PTNs, PTN/CRNs and CRNs. Most neurons in area 6 for which a receptive field could be found were excited by lightly touching or tapping the face and neck; a receptive field could not be determined for 39% of the area 6 neurons compared with only 5% of those in area 4. Finally, there was evidence that neurons in quite widespread areas of the pericruciate cortex, including both areas 4 and 6 projected onto similar, restricted regions of the PMRF. The fact that the cortical projection from area 4 to the PMRF includes a high percentage of fast PTNs with a receptive field on the distal forelimb is consistent with the view that this projection may serve to integrate movement and the dynamic postural adjustments that accompany them. The fact that the cortical projection from area 6 to the PMRF is primarily from slow PTNs with receptive fields on the face, neck and back is consistent with a role for this cortical area in adjusting the general posture of the animal on which movements are superimposed.

Animals↗

Convergence of thalamic and cholinergic projections in the 'dentate area' of lizards.

The small-celled part of the medial cortex (Cxms) in lizards is comparable to the hippocampal area dentata in mammals. As in mammals, most of the afferents to this cortical area are arranged in sharply delimited laminae. In reptiles this lamination pattern is species-specific. In the lizard Tupinambis nigropunctatus projections from the multisensory dorsolateral thalamic nucleus (Dla) terminate in the middle one-third of the outer plexiform layer throughout the whole rostrocaudal extent of Cxms. In Podarcis hispanica the thalamic projections terminate not only in the middle one-third of Cxms but also in the inner plexiform layer. To find out whether the species-related variation of thalamic projections to Cxms is a solitary phenomenon or is related to variations of other afferents of Cxms, we studied the relationships between the thalamic and cholinergic projections from the basal telencephalon in the medial cortex of three lizard families: the Lacertidae, the Teiidae and the Gekkonidae. In the gekkonid lizards Gekko gecko and Eublepharius macularius, Dla projections were studied with the anterograde tracer Phaseolus vulgaris-leucoagglutinin. Projections were found in only the rostral one-third of Cxms where the fibers terminate in the superficial half of the outer plexiform layer and in the deep half of the inner plexiform layer. From acetylcholinesterase staining in the Cxms of representatives of these three lizard families, it appeared that the main cholinergic afferents terminate in the same subregions and the same laminae as the Dla projections. Therefore, there seems to be a close association between thalamic and cholinergic afferents in the Cxms of lizards, irrespective of their precise location in the cortex of the various species. This suggests a functional relationship between these two afferents of the dentate area in lizards.

Acetylcholinesterase↗

Anterograde projections of the motorcortical tongue area in the saddle-back tamarin (Saguinus fuscicollis).

In the New World monkey Saguinus fuscicollis, the anterograde projections of the motorcortical tongue area were studied. Three animals were analyzed. In two, biotin dextran amine was used as tracer; in the third, Phaseolus vulgaris leucoagglutinin was used. Identification of the tongue area was carried out by electrical brain stimulation. Intracortical projections were found into the neighboring primary motor cortex, ventral premotor cortex, frontoopercular cortex, and primary and secondary somatosensory cortex. Projections also ended in the ventrolateral prefrontal cortex, orbital cortex, supplementary motor area, anterior cingulate cortex and agranular as well as granular insula. In addition, weaker labeling was found in the inferior and dorsal parietal cortex, and perirhinal and inferotemporal cortex. Subcortically, there was a heavy projection into the ventral putamen, a moderate projection into the caudate nucleus and claustrum, and a weak projection into the anterior, central and lateral amygdala. In the thalamus, terminal labeling was found in the nuclei ventralis posterior medialis, ventralis lateralis, reticularis, centralis lateralis, medialis dorsalis, pulvinaris oralis, centrum medianum, reuniens and suprageniculatus in an order of intensity. Subthalamically, weak projections could be traced into the zona incerta and lateral hypothalamus. In the midbrain, labeling was found in the deep layers of the colliculus superior, area praetectalis, dorsal reticular formation and, very sparsely, in the periaqueductal gray. In the lower brainstem, fibers ended in the griseum pontis, medial and lateral parabrachial nuclei, lateral pontine and medullary reticular formation, paramedian and dorsal reticular nuclei, solitary tract nucleus and principal as well as spinal trigeminal nuclei. No terminals were found in the hypoglossal nucleus itself; there were, however, terminals in the immediately bordering reticular formation.

Animals↗

Electrophysiological studies on the cerebellothalamocortical projections.

Electrophysiological studies on the cerebellothalamocortical projections of cats and monkeys are presented and discussed, referring mainly to the mechanisms of thalamocortical (TC) projections. Two types of TC projections, deep and superficial, were distinguished electrophysiologically. The former corresponds mostly to the 'specific' TC projection system which can be traced with conventional histological methods, whereas the latter constitutes the final direct TC pathway of the recruiting systme ('nonspecific' or 'diffuse' TC projection system). Superficial TC neurones were identified electrophysiologically in the thalamus and their distinctive responses were demonstrated in relation to cortical recruiting responses, spindling waves and desynchronized activation of the cortex due to the midbrain reticular formation. The characteristics of superficial TC projections and their cortical distributions appear to indicate that the superficial TC projections are much more developed in primates, probably most in the human, and that they convey the impulses responsible for more associative and elaborate integrations in the cerebral cortex.

Animals↗

Retinofugal and retinopetal projections in the green sunfish, Lepomis cyanellus.

The retinofugal and retinopetal connections in the green sunfish were studied by autoradiographic and horseradish peroxidase methods. All retinofugal fibers decussate in the optic chiasm. Some fibers project to contralateral preoptic and hypothalamic nuclei while others recross to project to the comparable ipsilateral nuclei. Contralaterally, the medial optic tract projects to the periventricular thalamic and pretectal nuclei and, sparsely, to the rostral optic tectum. The dorsal optic tract projects to the parvocellular portion of the superficial pretectal nucleus, the central pretectal nucleus, nucleus corticalis, and the rostral portion of the optic tectum. The ventral optic tract primarily projects to the caudal portion of the optic tectum, giving off fibers in route to innervate various nuclei, including the parvocellular superficial pretectal nucleus and the dorsal and ventral accessory optic nuclei. The axial optic tract projects to the dorsal accessory optic nucleus, the central pretectal nucleus, and the caudal optic tectum. Retinal fibers reach the ipsilateral thalamus, pretectum and other sites via a redecussation through the posterior commissure. From outgroup analysis it is concluded that such redecussating fibers are an independently derived character within actinopterygians and are homoplasous to nondecussating ipsilateral retinal projections in other vertebrates. Neurons retrogradely labeled with horseradish peroxidase were found to form a rostrocaudal column from the olfactory bulb and nerve through the ventral telencephalon to caudal diencephalic levels along the medial aspect of the optic tract. It is possible that all these neurons consist of one population of migrated ganglion cells of the nervus terminalis.

Animals↗