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At least 397 records · Page 22Linked to original sources
PubMed2007

Evaluation of dentin permeability after light activated internal dental bleaching.

The aim of this in vitro study was to assess quantitatively the dentin permeability of human teeth after intracoronal bleaching therapy with 35% hydrogen peroxide activated by LEDs, halogen lamp or using the walking bleach technique. Forty human maxillary central incisors had standard access cavities performed and the cervical thirds of the canals were prepared with Gates-Glidden drills up to a size 130. Roots were resected between the coronal and middle thirds and the apical portions were discarded. A glass ionomer, 2 mm thick cervical plug was placed inside the canal, at the cement-enamel junction level. Group I received 35% hydrogen peroxide gel activated by LEDs. Group II was submitted to 35% hydrogen peroxide gel activated by halogen lamp. Group III received 35% hydrogen peroxide gel and the walking bleach technique was followed. Group IV (control) received a dry cotton pellet inside the pulp chamber with temporary restoration. Dentinal permeability was quantified by copper ion penetration. Linear measurements were obtained by analysis of digital images under x 5 magnification. Mean values and SD for the experimental groups were: I, 7.1% (+/-3.2%); II, 8.4% (+/-3.0%); III, 9.1% (+/-3.0%); IV, 1.3% (+/-2.8%). One-way ANOVA was used to analyze the results. Results showed an increase of permeability values for groups I, II and III when compared to group IV (control); however, no statistical differences were found between the three tested bleaching techniques. It can be concluded that 35% hydrogen peroxide activated by LED, halogen lamp or used following the walking bleach technique produced similar increase in dentinal permeability.

Dental Pulp Cavity↗
PubMedDate not supplied

Palmar cutaneous nerve recording and clarification of median premotor potential generators.

In this study of the median nerve, serial bipolar and referential recordings from the thenar eminence show that the median premotor potential actually consists of two distinct negative waves, an early (N-I) and a late premotor potential (N-II). Anesthetic block of the palmar cutaneous branch of the median nerve eliminated the early premotor potential in all subjects. This suggests that the early premotor potential (N-I) is the sensory nerve action potential of the palmar cutaneous branch of the median nerve. Local anesthesia of the palmar cutaneous branch of the median nerve also defined its area of innervation as circumscribed in our subjects. No normative data concerning the sensory nerve action potential of the palmar cutaneous branch of the median nerve is currently available, because previous studies apparently recorded the late premotor potential. The late premotor potential (N-II) is a negative far field potential seen only on referential recordings. It seems unlikely that the late premotor potential (N-II) can be completely explained as a junctional potential from the thumb as some have proposed. This study demonstrates a positive far field potential (P-I) at the palm-thumb junction, having a latency inconsistent with that of the late premotor potential. The late premotor potential can also be recorded with the reference electrode at an electrically neutral site, questioning previous explanations for its generator. A second traveling wave (N-III) was recorded distal to the area of the palmar cutaneous branch of the median nerve innervation continuing into the thumb. N-III is most likely the median digital sensory nerve action potential.

Action Potentials↗
PubMed1994

Optical measurements of activity-dependent membrane recycling in motor nerve terminals of mammalian skeletal muscle.

Motor nerve terminals in a variety of rat and mouse skeletal muscles were stained in an activity-dependent fashion using the styryl dyes FM1-43 or FM2-10. Low-light video microscopy and digital image processing techniques were used to evaluate destaining of the preparations during application of depolarizing stimuli. Best results were obtained with the mouse triangularis sterni muscle. Quantitative analysis of the destaining of dye-loaded terminals supports the suggestion that FM1-43 stains a recycling membrane compartment, most probably synaptic vesicles. However, the pattern of staining and destaining were not the same as those reported previously for frog neuromuscular junctions. The pattern of nerve terminal staining was less punctate and the rate and amount of activity-dependent destaining were less than in frog muscle. Part of the explanation may be a more acute susceptibility of mammalian terminals to phototoxicity.

Animals↗
PubMed1995

Computer-assisted three-dimensional reconstruction of human dermal dendrocytes.

We attempted to characterize the three-dimensional structure of dermal dendrocytes and to clarify the spatial relationships between dermal dendrocytes and mast cells, macrophages, and nerves. Normal human adult skin (breast, n = 2) was routinely processed for electron microscopy. Every other section (about 50 per data set) was collected at 80-nm intervals traversing about 8 microns of tissue. Grids showing the same cells were photographed by electron microscopy at a magnification of 4000x. Based on the 10-20 photographs per data set, cell outlines were digitized into the reconstruction program at appropriate layers and aligned. Thin, elongated cytoplasmic "dendrites" of dermal dendrocytes in two-dimensional micrographs proved to be thin, membrane-bound flaps in three-dimensional reconstruction. For dermal dendrocytes concentrated about superficial vessels (perivascular dendrocytes), the flaps enshrouded the vessel wall, and for dermal dendrocytes directly beneath the epidermis (subepidermal dendrocytes), these flaps were aligned parallel to the dermal-epidermal junction. The three-dimensional feature of dermal dendrocytes (perivascular and subepidermal) is quite similar to that of perivascular adventitial veil cells, suggesting ultrastructurally identified perivascular dendrocytes and veil cells must be identical cells. In conventional ultrathin sections, 20-40% of perivascular dendrocytes and occasional subepidermal dendrocytes were closely associated with mast cells. When viewed by computer-assisted three-dimensional reconstruction, membrane flaps of dermal dendrocytes consistently shrouded mast cell membranes for 50-90% of their perimeter; mast cells resembled a ball in a baseball glove (dermal dendrocytes). Occasional dermal dendrocytes surrounded non-myelinated nerves in the superficial dermis. Membrane flaps also enabled dermal dendrocytes to present extensive areas to the plasma membranes of adjacent monocyte/macrophages. These findings indicate that dermal dendrocytes are non-dendritic cells that are spatially related to mast cells, monocyte/macrophages, microvessels, and nerves by their membranous flaps. This suggests the need for further study of functional interactions between these cells.

Adult↗
PubMed1988

Increase in intracellular calcium induced by the polycation-coated latex bead, a stimulus that causes postsynaptic-type differentiation in cultured Xenopus muscle cells.

The polycation-coated latex bead is a potent stimulus for the induction of postsynaptic-type differentiation in cultured Xenopus myotomal muscle cells. Specializations characteristic of the neuromuscular junction, such as clusters of acetylcholine receptors and other postsynaptic-specific proteins, develop at the bead-muscle contact. Previous studies have shown that a deprivation of extracellular calcium inhibits the effect of the beads in causing the development of these specializations. This suggests that an increase in intracellular Ca2+ is a necessary condition for the development of this specialization. In this study, we tested whether an increase in intracellular calcium is observable upon the bead-muscle contact. The measurement was carried out on cells loaded with the fluorescent calcium indicator fura-2 AM by digitized video microscopy. When polycation-coated beads were added to cells, an increase in intracellular calcium concentration in the range of 5 to 57% of the resting level was observed within 10 sec after bead-muscle contact. Afterward, the calcium level gradually returned to the resting level with a time course of about 3 min. Uncoated beads, which do not induce the formation of acetylcholine receptor clustering, failed to elicit this calcium transient. Removal of extracellular calcium as well as blocking calcium channels with 50 microM verapamil also suppressed this transient induced by the polycation-coated beads. Both treatments are known to suppress the formation of receptor clusters by these beads. These results suggest that the polycation-coated beads cause an influx of calcium by increasing the membrane conductance to this ion. This process may underlie the signaling of the postsynaptic differentiation.

Animals↗
PubMed2003

Finger interactions studied with transcranial magnetic stimulation during multi-finger force production tasks.

OBJECTIVE: We used transcranial magnetic stimulation (TMS) to investigate interactions among neuromuscular complexes involved in force production by individual fingers of a hand during single- and multi-finger tasks. METHODS: Subjects were asked to press with the fingertips at various levels of force using different finger combinations. TMS was applied over the M1 cortical hand area during constant force production. TMS-induced increments in fingertip forces were analyzed, as well as motor evoked potentials (MEPs) in flexor digitorum superficialis. RESULTS: Both MEP size and individual force increments had inverted U-shaped dependences on the background force (peak responses were seen at about 50% of the maximal force). Similar relationships were obtained when subjects were asked to produce different forces with the same finger combination or the same total force with different finger combinations. The relationships were similar when the force was produced by explicitly instructed fingers or by other fingers of the hand. Effects of TMS on the force of a finger showed a strong dependence on the background force produced by this finger and minimal or no dependence on forces produced by other fingers of the hand. CONCLUSIONS: Overall, TMS applied over M1 revealed little interaction among fingers. This supports the notion of digit-specific compartments in multi-digit extrinsic muscles of the hand and suggests that these compartments possess a high degree of physiological independence.

Adult↗
PubMed1992

Accuracy of visual inspection, fiber-optic transillumination, and various radiographic image modalities for the detection of occlusal caries in extracted non-cavitated teeth.

Occlusal caries lesions may progress into the dentin without this resulting in a macroscopic breakdown of the enamel surface. Imaging methods may therefore be needed to aid in the visual detection of occlusal caries. It was the aim of this study to evaluate diagnostic accuracy in a laboratory set-up of visual inspection (VI), fiber-optic-transillumination (FOTI), conventional radiography (CR), and two digital radiographic image modalities (DRm and DRr) for detection of occlusal caries in clinically non-cavitated teeth. Eighty-one extracted third molars from 18-20-year-old males were assessed by four observers on a five-rank confidence scale by the five methods. Ground sections (500-600 microns) served as validation for true state of disease: 1 = no caries in dentin, 2 = caries just beyond dentino-enamel junction, or 3 = deep dentinal caries, halfway or more to the pulp. ROC analysis was performed on the basis of the confidence rank scale data on two diagnostic thresholds, T1 = caries in dentin (disease state 2+3) and T2 = caries deep in dentin (state 3). On the T1 level, use of the FOTI method gave on average the most accurate diagnosis, closely followed by VI, both performing better than use of radiography. On the T2 level, all five diagnostic methods performed equally well.

Adolescent↗
PubMed1989

The extracellular matrix architecture relating to myotendinous pattern formation in the distal part of the developing chick limb: an ultrastructural, histochemical and immunocytochemical analysis.

In the later developmental stages (Hamburger and Hamilton, 25-34) the distal part of the chick leg possesses a distinctive extracellular matrix (ECM) architecture which relates to myotendinous patterning. There are two components: firstly, a system of dorsoventrally oriented fibrils which link the two ectodermal surfaces through the undifferentiated distal mesenchyme and secondly, a 'mesenchyme lamina' originates at the basement membrane distally, but proximally runs through the mesoderm, subjacent and parallel to the basement membrane. The 'mesenchyme lamina' appears to be a precursor of developing tendons and is spatially related to the distal tips of the myogenic blocks. As developing tendons form on the inner surface of the lamina at its proximal end, it becomes less distinct and disappears. Further dorsoventral fibrils run from the 'mesenchyme lamina' into the developing condensations and chondrogenic elements of the phalanges. The architecture of the ECM was revealed by silver and lectin staining (peanut and Ricinus communis agglutinins, PNA and RCA I), by immunocytochemistry (for fibronectin, tenascin, collagen type I) and by ultrastructural analysis. Both components stain with silver, PNA following neuraminidase digestion, RCA I, tenascin and collagen type I. However, the dorsoventral fibrils are positive for fibronectin and negative for PNA, while conversely the mesenchyme lamina is positive for PNA but much less so for fibronectin. Tenascin has been shown to be a specialized mesenchyme component of tendons and myotendinous junctions (Chiquet and Fambrough, 1984). Such a basement membrane forming a 'mesenchyme lamina' appears to be unique in epithelial-mesenchymal developing systems and points to an ectodermal role in tendon pattern formation within the mesenchyme. We discuss the possible role of mechanical force in converting the dorsoventral tenascin-positive fibrils into the localized pattern of tendon insertions into the proximal parts of the phalanges. Distally the dorsoventral fibrils may shape the digital plate by pulling together the two ectodermal surfaces. A similar ECM architecture is found in corresponding stages in the developing wing.

Animals↗
PubMed2001

The surgical anatomy of the dorsomedial cutaneous nerve of the hallux.

Most techniques described for the correction of hallux valgus require exposure of the distal aspect of the first metatarsal. A dorsomedial incision is often recommended. Texts counsel against damaging the dorsal digital nerve, as a painful neuroma is an unwelcome surgical complication. Our study on cadavers aimed to investigate the anatomy of the dorsomedial cutaneous nerve in the metatarsophalangeal region, with special reference to surgical incisions. A constant, previously unrecognised branch of the nerve was identified. This branch is likely to be damaged if a dorsomedial approach is used. It is recommended that a mid-medial incision be used instead, i.e. at the junction of the plantar and dorsal skin.

Cadaver↗
PubMed2002

Organization of Ca2+ stores in vascular smooth muscle: functional implications.

Much evidence suggests that caffeine/ryanodine (Caf/Ry)-releasable and inositol-1,4,5-trisphosphate (InsP3)-releasable Ca2+ stores in the sarcoplasmic reticulum (SR) of smooth muscles are at least partially distinct. We directly visualized SR stores in primary-cultured rat mesenteric artery myocytes with high-resolution digital imaging and the low-affinity Ca2, indicator, Furaptra (Kd = 75.6 microM). The SR appears to be a continuous tubular network. Nevertheless, SR Ca2+ stores are organized into small, separate, functionally independent compartments. Cyclopiazonic acid (CPA; inhibits SR (Ca2+ pump) and Caf (or Ry) release Ca2+ from different, spatially distinct compartments. Similar heterogeneity is seen with serotonin (acts via InsP3), which unloads only the CPA-sensitive compartments. Some of the SR ('junctional' SR; jSR) lies within 12-15 nm of the plasmalemma (PL). The jSR, the overlying PL microdomains, and the intervening, tiny volume of cytosol form junctional complexes ('PLasmERosomes'). Na+ pumps with high-ouabain-affinity alpha2 or alpha3 subunits, Na+/Ca2+ exchangers, and store-operated channels are confined to these PL microdomains, whereas Na+ pumps with low-ouabain-affinity alpha1 subunits and plasma membrane Ca2+ pumps are uniformly distributed. As a result of this organization, low-dose ouabain can selectively modulate Na+ and Ca2+ concentrations in the PLasmERosomes and jSR Ca2+ stores, and can thereby regulate Ca2+ signalling.

Adenosine Triphosphatases↗
PubMed2006

The clinical relevance and correlation between the initial straight length to the first curvature in human second maxillary premolars.

The aim of this study was to evaluate the straight lengths of the root canal of human second maxillary premolars using standardized radiological techniques in vitro. The distances were examined starting from the cemento-enamel junction (CEJ) to the appearance of a curvature. In particular recommendations which may facilitate decision making with regard to the length of post systems after successful endodontic treatment should be available. Extracted human second maxillary premolars (n = 210) were used; teeth with root caries, artificial crowns, extensive fillings or with previous endodontic treatment were excluded from this investigation. The teeth were fixed in a specially developed device with standardized and reproducible distances and digital radiographs using the parallel technique were made. A descriptive statistical analysis and the calculation of the cumulative frequencies were made. The values for the distance starting from the CEJ to a first curvature were as follows: a) For right second premolars: median value=10.3 mm (min.: 5 mm; max.: 15.8 mm) and mean value= 10.4 SD+/- 2.6 mm; b) left second premolars: median value =10.2 mm (min.: 5 mm; max.: 17 mm) and mean value =10.3 mm SD +/-2.2 mm. Based on our data, high number of second maxillary premolars showed a curvature (30.4%) 9 mm apically from the CEJ. These findings should be taken into consideration for endodontic treatments and post insertions.

Bicuspid↗
PubMed1991

[Statistical analysis of mediator release from the cyto-neural junction of the posterior canal of the labyrinth isolated from the frog].

The transmitter release mechanism was investigated at the cyto-neural junction of the frog labyrinth posterior canal. Low frequency (less than 100/s) non overlapping EPSPs were intracellularly recorded both at rest and during inhibitory mechanical stimulation of the canal (2-8 deg/s2). Recordings were obtained: in control solution; in the presence of increased external Ca2+ (9 mM); in Ca-free EGTA (5 mM) solution and during electrical activation at 50 Hz of the posterior canal inhibitory efferent system. Individual synaptic potentials were digitized and their peak amplitudes, their time integrals as well as the time intervals between them were evaluated. The time intervals proved to be exponentially distributed, suggesting a random EPSP occurrence. The analytical reconstruction of the EPSP waveform indicated that a gamma- function fitted reasonably well both the single and averaged events. As regards the averaged event, despite the scatter in the values of the gamma-function exponential factor (range 1.1-2.2), in the EPSP time-to-peak (0.6-1.2 ms) and peak amplitude (0.9-2.7 mV) displayed by the units, no significant differences were observed in the same fibre between control and test conditions. Moreover, the event peak amplitude distribution represented by cumulative plots or amplitude histograms was fitted by a lognormal function. The distributions obtained for the same unit in control solution proved to be not significantly different from those successively obtained under test conditions. The unimodal and continuous EPSP distributions, together with the unvarying characteristics of the single events, strongly suggest that the observed potentials are true mEPSPs due to the release of single quanta of transmitter.(ABSTRACT TRUNCATED AT 250 WORDS)

Action Potentials↗
PubMed1998

No evidence for cell-to-cell coupling in rat colonic crypts: studies with Lucifer Yellow and with photobleaching.

Epithelial cells of exocrine glands (pancreas, lacrimal glands, salivary glands, sweat glands and gastric glands) are intimately linked together by gap junctions. Due to this close junctional coupling exocrine secretion occurs as the well concerted effort of a cell population. Colonic crypts have, on the one hand, anatomical and functional properties resembling those of exocrine glands (mostly crypt base cells) and, on the other hand, properties of absorbing cells (mostly surface cells). In the mid-crypt, depending on the functional status, absorption and secretion can occur. The present study was aimed at examining whether rat distal colonic crypt cells co-ordinate their functional status by cell-to-cell coupling. Two types of measurements were performed: as an independent assessment of cell viability the membrane voltage (Vm) was measured with the fast whole-cell patch-clamp technique; to investigate cellular coupling simultaneously Lucifer Yellow (LY) (mol. wt. 443) distribution was visualized using digital video imaging. LY (500 micromol/l) was included into the patch pipette filling solution. The recorded Vm was -73.4+/-2.3 mV in crypt base cells (n=15), -63.7+/-2.1 mV in mid-crypt cells (n=17) and -52.3+/-2. 9 mV in crypt surface cells. All cells tested reversibly responded to carbachol (100 micromol/l) with a persistent hyperpolarization, as previously shown. Activation of Cl- secretion by elevation of the cAMP concentration with forskolin (5 micromol/l) led to a reversible depolarization. Throughout the duration of each individual experiment [mean experimental time in basal cells: 18.3+/-2.5 min (n=15), in mid-crypt cells: 19.6+/-3.4 min (n=17) and in crypt surface cells: 11.7+/-3.4 min (n=13)] LY dye distribution was solely confined to the patched cell. In addition bleaching of calcein fluorescence in laser scan microscopy was not followed by dye back diffusion, whereas this was clearly the case in pancreatic acini (n=5). These data indicate that colonic crypt cells are not coupled by gap junctions under resting conditions or in the presence of secretagogues.

Animals↗
PubMed1995

Immunolocalization of triadin, DHP receptors, and ryanodine receptors in adult and developing skeletal muscle of rats.

The dihydropyridine receptors (DHPR) and the ryanodine receptors (RyR) are well-characterized proteins of the triad junctions of skeletal muscle fibers. Recently, a newly discovered 95-kDa protein, triadin, has been purified from rabbit skeletal muscle heavy sarcoplasmic reticulum (SR) vesicles. WE have used indirect immunogold EM to localize triadin to the junctional face of the SR in isolated triads. In addition, we have used indirect immunofluorescence to localize triadin in relation to the DHPR and the RyR in adult and developing rat skeletal muscle. In double immunolabelling experiments of longitudinally oriented adult rat skeletal muscle tissue, triadin-specific and RyR-specific antibodies resulted in a characteristic striated staining pattern. The staining arising from these antibodies completely overlapped when examined by computer analysis of digitized laser scanning confocal microscopy images. A similar result was obtained in double staining experiments using antibodies raised against the DHPR and the RyR suggesting that all three proteins are located in the triads in situ. The developmental expression of the three triad proteins was examined using double labeling of skeletal muscle tissue from several fetal and early postnatal ages. The staining patterns of triadin, RyR, and DHPR antibodies were overlapping throughout development, suggesting that from their earliest appearance the three proteins are components of the triads.

Aging↗
PubMed2007

The proximal origin of the hamstrings and surrounding anatomy encountered during repair. A cadaveric study.

BACKGROUND: Avulsion of the proximal origin of the hamstrings has become a more frequently recognized athletic injury. Most orthopaedic surgeons rarely operate in this anatomic area. The purpose of the present study was to define the anatomy of the proximal origin of the hamstrings and its relationship to neurovascular and muscular structures encountered during a repair of a complete avulsion. METHODS: Fourteen fresh-frozen hip-to-foot human cadaveric specimens were dissected in the prone position. The proximal origin of the hamstrings and its relationship to the surrounding neurologic and muscular structures were documented and measured with use of digital calipers. RESULTS: Six of the fourteen specimens were from female donors. The average age of the donors at the time of death was 68 +/- 13 years. The average height of the donors was 66 +/- 3.5 in (167 +/- 8.9 cm), and the average weight was 142 +/- 39 lb (64 +/- 17.7 kg). The semitendinosus and biceps femoris have a common tendinous site of origin on the ischium. A number of measurements were obtained. The musculotendinous junctions of the semitendinosus and biceps femoris separated at an average of 9.9 +/- 1.5 cm from the most proximal origin site on the ischium. The average distance from the proximal border of the semitendinosus/biceps femoris origin to the inferior border of the gluteus maximus was 6.3 +/- 1.3 cm. At the lateral border of the ischium, the average distance from the inferior gluteal nerve and artery to the inferior border of the gluteus maximus was 5.0 +/- 0.8 cm. The sciatic nerve was an average of 1.2 +/- 0.2 cm from the most lateral aspect of the ischial tuberosity. The site of origin of the semitendinosus/biceps femoris was oval, with average measurements of 2.7 +/- 0.5 cm from proximal to distal and of 1.8 +/- 0.2 cm from medial to lateral. The site of origin of the semimembranosus was crescent-shaped, with average measurements of 3.1 +/- 0.3 cm from proximal to distal and of 1.1 +/- 0.5 cm from medial to lateral. CONCLUSIONS: The semitendinosus and biceps femoris have a common tendon of origin on the ischium, and the semimembranosus originates just laterally. The proximal origin of the hamstrings has intimate relationships with the inferior gluteal nerve and artery and the sciatic nerve, which may be at risk during surgical dissection and retraction.

Aged↗
PubMed1975

The ultrastructure of the sensory cells in the chemoreceptor of the ommatophore of Helix pomatia L.

Most of the sensory cells found in the chemoreceptor of the ommatophore of Helix pomatia are typical bipolar cells. The chemoreceptor is deveded by a furrow into two parts; within the ventral subdivision the layer of sensory cell bodiesis thicker than in the dorsal part. According to the differentiations of the apical surface of the dendrites, it is possible to distinguish six different classes: a) dendrites with one cilium and 75 nm thick cytofila (sometimes dendrites of identical appearance posses more than one cilium); b)dendrites with several cilial and 150 nm thick cytofila; c) dendrites with several cilia, 50 nm thick cytofila, and long, striated rootlets; d) dendrites with several cilia bur without cytofila; e) dendrites with 130 nm thick cytofila but without cilia; and f) dendrites with 65 nm thick cytofila but without cilia; dendrites of this class are the only ones with a cytoplasm more electron dense than that of the surrounding supporting cells. All these dendrites are connected to the surrounding supporting cells by terminal bars, each consisting of zonula adhaerens, aonula intermedia and zonula septata. The perikarya of the sensory cells measure approximately 15 mum by 8 mum and enclose 10 mum by 6 mum large nuclei. Axons, originating from these perikarya, extend to the branches of the digital ganglion. In the distal part of this gangloin the axons come into synaptic contact with interneurons, but in our electron micrography it was not possible to coordinate processes and synapses with the corresponding neurons.

Axons↗
PubMed2000

Fluoroscopic landmark for SVC-RA junction for central venous catheter placement in children.

BACKGROUND: Vascular access devices are commonly placed under image guidance. The usual aim is to place the tip at the superior vena cava-right atrial junction (SVC-RA). OBJECTIVE: To identify a radiographic landmark for the SVC-RA junction that would be useful for accurate central venous catheter tip placement in children. MATERIALS AND METHODS: Images from 56 children undergoing contrast studies of their upper limb venous systems were examined for location of the SVC-RA in relation to a radiographic landmark. RESULTS: Most patients (92.5%) showed the SVC-RA junction to lie at the sixth thoracic vertebral level or the interspace above or below. The SVC-RA junction lay lower than the right main bronchus and the notch on the right cardiomediastinal contour. CONCLUSION: The vertebral body provides a useful and radiographically visible landmark for accurate central catheter tip placement.

Adolescent↗
PubMed1997

Uniqueness of the S-cone pedicle in the human retina and consequences for color processing.

The purpose of this study was to investigate more fully the shape and content of ribbons and synapses to second-order neurons in the short-wavelength cone (S-cone, blue cone) pedicle and to learn more concerning the uniqueness of the S-cone system in the primate retina. A piece of well-fixed peripheral human retina (10 mm, 35 degrees nasal to the fovea) was serially thick sectioned in the tangential plane from the level of the outer segments to the tops of the cone pedicles. Then serial electron microscope (EM) sections were collected through the whole depth of the pedicle-occupying region into the neuropil of the outer plexiform layer (OPL). The resultant EM micrograph montages of a large field of cone pedicles were perused, and S-cone pedicles were identified. Serial micrographs of a single S-cone pedicle, picked out of the montages, were digitized and reconstructed by computer three-dimensional methods. The S-cone pedicle arose from a slightly oblique axon and projected 0.5-1 microm more vitread in the OPL than other cone pedicles. It was bilobed in shape, with synaptic invaginations and ribbons in both lobes. No cone-contacting telodendria projected from the S-cone pedicle itself, but a small number of neighboring cones sent telodendria to its surface to make small gap junctions. Neighboring rod spherules also made small gap junctions. Four robust bipolar cell dendrites, most likely from S-cone-specific bipolar cells, made synapses at ribbons and basal (distal) junctions. A small number of other bipolar cell dendrites made narrow-cleft basal junction only. The majority of lateral elements were thought to be from HII horizontal cells, and a minority from HI horizontal cells. We conclude that the S-cone pedicle has a unique morphology and connectivity to second-order neurons that makes it quite different from the other two longer wavelength cone systems, and we speculate on the consequences for color processing in the visual system in general.

Adult↗