S1 S3 Research Articles

Amount of sympathetic sprouting in the dorsal root ganglia is not correlated to the level of sympathetic dependence of neuropathic pain in a rat model

Incomplete peripheral nerve injury often leads to neuropathic pains, some of which are relieved by sympathectomy, and results in sympathetic postganglionic nerve fiber sprouting in the dorsal root ganglion (DRG). This study was performed to see whether the sprouting in the DRG plays a key role in the sympathetic dependence of neuropathic pain. To this aim, we compared two groups of rats, both of which were subjected to unilateral transection of the inferior and superior caudal trunks at the levels between the S1 and S2, S2 and S3, and S3 and S4 spinal nerves, with respect to sympathetic fiber sprouting; one group showed neuropathic pain behaviours (i.e. mechanical and cold allodynia signs) which were very sensitive to phentolamine, alpha adrenergic blocker, and the other group exhibited no sensitivity. Immuno-histochemical staining with tyrosine hydroxylase antibody of the S1–S3 DRGs was not correlated with the sensitivity to phentolamine. These results suggest that the degree of sympathetic dependence of neuropathic pain is not a function of the extent of the sympathetic postganglionic nerve fiber sprouting in the DRG.

Immunodissection of the human proximal nephron: Flow sorting of S1S2S3, S1S2 and S3 proximal tubular cells

We report on the use of several proximal tubular cell (PTC) surface markets and corresponding antibodies in fluorescence-activated cell sorting (FACS), and their ability to identify and flow sort cells of defined proximal tubular origin (S1S2S3) or of defined proximal subsegmental origin (S1S2 only/S3 only). We tested monoclonal/polyclonal antibodies directed against five different surface peptidases [leucine aminopeptidase (LAP), neutral endopeptidase 24.11 (NEP), dipeptidyl peptidase IV (DPPIV), aminopeptidase A (APA) and gamma-glutamyl transferase (gamma-GT)], the S3 segment-specific marker intestinal type alkaline phosphatase (iAP) and an S1S2 marker (TN20-antigen), originally proposed as a surface marker for interstitial fibroblasts. Segmental (proximal tubular vs. distal tubular) and proximal subsegmental (S1S2 vs. S3) expression of all five surface peptidases and TN20 antigen were first assessed by comparing immunohistochemical staining on normal human kidney tissue with staining for well-known segment-specific differentiation markers (intestinal type alkaline phosphatase, Tamm-Horsfall protein) on adjacent sections. All five peptidases were found to be expressed to a certain degree in all subsegments (S1 S2 and S3) of the proximal nephron, whereas expression was never seen in the more distal parts of the nephron. Flow cytometry was performed on cells obtained following gradient purification of collagenase-digested human renal tissue. Labeling cells for expression of LAP, NEP or DPPIV resulted in high yields of specifically labeled PTC (S1S2S3 origin). Labeling with anti-LAP resulted in the clearest distinction between positive and negative cell subpopulations, and therefore LAP was considered the best PTC marker for use in FACS. iAP histochemical staining on sorted cells showed that flow sorting with monoclonal antibody (moAb) 250 (anti-intestinal type alkaline phosphatase) allowed sorting of S3 cells with > 90% purity. Likewise, moAb TN20 enabled us to obtain a highly purified S1S2 population as confirmed by the absence of iAP on sorted cells.

Chronic lymphocytic leukemia and hairy-cell leukemia--diagnosis and treatment: results of a consensus meeting of the German CLL Cooperative Group.

(1997) 74:291–294 after it had been originally published in Leukemia (1997) 11, Suppl. 2, S1–S3. By an error during the production process the source was omitted. The publisher apologizes for this error.

Localization of NADPH diaphorase in the thoracolumbar and sacrococcygeal spinal cord of the dog

The distribution of NADPH-d activity and NOS-immunoreactivity in the spinal cord of the dog was studied to evaluate the role of nitric oxide in lumbosacral afferent and spinal autonomic pathways. At all levels of the spinal cord examined, NADPH-d staining and NOS-immunoreactivity were present in neurons and fibers in the superficial dorsal horn, dorsal commissure and in neurons around the central canal. Sympathetic preganglionic neurons in the rostral lumbar segments identified by choline acetyl transferase (ChAT) immunoreactivity exhibited prominent NADPH-d and NOS-immunoreactive staining; whereas the ChAT-immunoreactive parasympathetic preganglionic neurons in the sacral segments were not stained. The most prominent NADPH-d activity in the sacral segments occurred in fibers extending from Lissauer's tract through lamina I along the lateral edge of the dorsal horn to the region of the sacral parasympathetic nucleus. These fibers were prominent in the S1–S3 segments but not in adjacent segments (L5–L7 and Cx1) or in thoracolumbar segments. The NADPH-d fibers were not NOS-immunoreactive, but did overlap with a prominent fiber bundle containing vasoactive intestinal polypeptide immunoreactivity in the sacral spinal cord. These results indicate that nitric oxide may function as a transmitter in thoracolumbar sympathetic preganglionic neurons, but not in sacral parasympathetic preganglionic neurons. The functional significance of the NADPH-d positive, NOS-negative fiber bundle on the lateral edge of the sacral dorsal horn remains to be determined. However, based on anatomical studies in other species it seems reasonable to speculate that the fiber tract represents, in part, visceral afferent projections to the sacral parasympathetic nucleus.

Characterization of La1 −x Sr1 +x Cu5 −x Fe x O12 + δ (0 ≤x ≤ 1·0) by dc electrical conductivity, magnetic susceptibility and EPR measurements(0 ≤x ≤ 1·0) by dc electrical conductivity, magnetic susceptibility and EPR measurements

The DC electrical resistivity results of La4 −x Sr1 +x Cu5 −x Fe x O12 + δ (0 ≤x ≤ 1·0) showed that for S1 (x = 0) and S2 (x = 0·25) the temperature coefficient of resistivity (TCR), dρ/dT, is positive and slightly increases with increasing temperature in the range 20–270 K. This shows the metallic nature of S1 and S2. For the samples S3(x = 0·5) and S4 (x = 0·75), TCR slightly increases in the range 20–270 K, with change in sign from negative to positive at ∼ 80 K and ∼ 130 K, respectively. These results show the metal-insulator type transition in S3 and S4. For the sample S5 (x = 1·0), the TCR is negative and gradually increases in the range 20–270 K, which shows its semiconductor-like behaviour. The activation energy for S5 is found to be 0·21 × 10−2 eV. Furthermore, the DC resistivity results of S1–S5 in the range 350–660 K are in conformity with the low temperature results. The very weak temperature dependence of magnetic susceptibility results of S1–S3 show Pauli-paramagnetic behaviour in the range 77K–400 K, while S4 and S5 exhibit Pauli-paramagnetic behaviour in the range 77–850 K. Long-range antiferromagnetic interaction is observed in S5 (x = 1·0) belowT c ∼ 100 K. The room temperature EPR lineshapes gradually improve from metallic S1 (x = 0) to semiconductor-like S5(x = 1·0). Negativeg-shift is observed in the samples S2–S5 with increasing trend ing iso-values of 1·880 in S2 to 1·961 in S5. However, theg iso-value for S1 could not be observed due to very poor lineshape.

Location of external anal sphincter motoneurons in the sacral cord of the female domestic pig

The location of the striated external anal sphincter motoneurons in the spinal cord was investigated in 12, between 3 and 4 months old, female domestic pigs using the retrograde tracer horseradish peroxidase (HRP). Their motoneuronal cell bodies were found in the spinal segments S1–S3, and were not located in the ventral horn, but dorsolateral to the central canal. This location within the spinal gray matter strongly differs from the location of the external anal sphincter motoneurons in rat, cat, dog, monkey and humans, but is similar to that in the Mongolian gerbil. The possible relevance of this ‘aberrant’ location is discussed.

Location of external anal sphincter motoneurons in the sacral cord of the female domestic pig

The location of the striated external anal sphincter motoneurons in the spinal cord was investigated in 12, between 3 and 4 months old, female domestic pigs using the retrograde tracer horseradish peroxidase (HRP). Their motoneuronal cell bodies were found in the spinal segments S1–S3, and were not located in the ventral horn, but dorsolateral to the central canal. This location within the spinal gray matter strongly differs from the location of the external anal sphincter motoneurons in rat, cat, dog, monkey and humans, but is similar to that in the Mongolian gerbil. The possible relevance of this ‘aberrant’ location is discussed.

Segmental distribution of afferent neurons innervating the canine testis

To clarify the afferent innervation of the canine scrotal contents, retrograde labeling of neurons in the dorsal root ganglia (DRG) has been carried out using two methods: (1) horseradish peroxidase (HRP) injection into the surface of the testis and epididymis; and (2) exposure of the superior spermatic nerve to a fluorescent dye (Fast blue; FB). Injections of HRP resulted in labeling of DRG cells located predominantly from T10 to L4 (87%) and, to a lesser extent, at S1–S3 (13%). Transection of the vas deferens previous to testicular injections eliminated labeling in the S1-S3 DRG, but not at thoracolumbar levels. These findings indicated that primary afferent fibers of the testis and epididymis project mainly to the DRG at higher than L4 through the superior spermatic nerve, but an additional population of the fibers also projects the sacral level through the inferior spermatic nerve. Exposure of the superior spermatic nerve to FB resulted in a similar distribution of labeled cells as compared with testicular injections of HRP after vasectomy. Labeled cells (8.1%) were also observed in the contralateral T13-L3 DRG. In both FB and HRP groups, the major part of the labeled cells was located in Ll and L2. The sizes of HRP- and FB-labeled cells were smaller than those of unlabeled cells in the Ll and L2 DRG. The cumulative frequency distribution histogram for the diameter of HRP- and FB-labeled cells could be fitted by a normal distribution.

Shock features in iron‐nickel metal and troilite of L‐group ordinary chondrites

Abstract— Shock metamorphic features in opaque minerals (FeNi metal and troilite) of 22 L chondrites have been studied petrographically and geochemically in an attempt to establish a connection between the present silicate‐based shock classification scheme (Stöffler et al., 1991) and the peak‐shock and postshock thermal history recorded in these minerals. Unshocked to weakly shocked (S1–S3) L chondrites contain FeNi metal and troilite that display textures related to normal, slow cooling. They may also contain rare disequilibrium shock features, which suggest localized departures from equilibrium shock conditions. Above shock stage S3, selected melting of FeNi metal and troilite produces melt droplets whose composition and abundance correspond to the maximum equilibrium shock state achieved by the sample. At these higher shock levels, the abundance of other shock‐induced features, such as polycrystalline kamacite, sheared and fizzed troilite, coarse‐grained pearlitic plessite, polycrystalline troilite, and polymineralic melt veins serve as textural criteria that can be used to establish peak‐shock conditions. Minimum postshock temperatures obtained from analyses of plessite components show a systematic increase in temperature with an increase in shock stage, thereby providing additional information about the postshock thermal histories of L chondrites. At the highest shock levels recorded in L chondrites (S6 and above), melting and chemical homogenization of FeNi metal produces flattened Ni profiles that may partially to completely obscure any evidence for an earlier, slow‐cooling history. All of these features serve as aids for shock classifying L chondrites as well as for quantifying minimum peak temperatures that resulted during shock metamorphism.

Immunohistochemical study on the immunocompetent cells of the pulp in human non-carious and carious teeth

The condition of the pulp tissue was classified into seven groups according to the depth of carious lesions from stage (S) 0 (non-carious teeth) to S6 (exposed pulp). A substantial change in the infiltration of immunocompetent cells occurred between S3 and S4; all types were markedly increased in S4 as compared to S3, with a remarkable increase in the number of helper T lymphocytes, B-lineage cells, neutrophils and macrophages. Therefore, the pulpal immune reaction to carious stimuli could be classified into early (S1–S3) and advanced phases (S4–S6). In the early phase a cellular immunoresponse would be induced by T-lineage cells, and in the advanced phase the humoral immunoresponse is furthered by B-lineage cells concomitant with the destruction of pulp tissue by proteolytic enzymes released from infiltrating neutrophils and macrophages. Human dental pulp is thus equipped with a functional immune response that is sufficient as a biodefensive mechanism. Dental caries should be treated before S4.

Multiple protracted cauda equina constrictions cause deep derangement in the lumbosacral spinal cord circuitry in the dog

Neuropathological changes of the neuronal pools and spinal cord circuitry in the lumbosacral segments were studied in a canine model of multiple protracted cauda equina constrictions. Anterograde degeneration of all sacrococcygeal and L7 dorsal root fibers was detected in S1–S3 and lower lumbar segments. A narrow degenerated gracile fascicle was found in all thoracic and cervical segments terminating in the gracile nucleus. Transneuronal degeneration of middle-sized and large neurons, located in S1–S3 and sporadically in L7 segments, was noted. Identical transneuronal degeneration was seen in a group of small neurons located in the ventralmost part of lamina VII in S1–S3 segments. Simultaneously, a terminal degeneration was detected in the lateral cervical nucleus and in the ventral posterior lateral nucleus of the ventrobasal thalamic complex. Concomitantly, a fully developed retrograde degeneration affecting motoneurons in the ventrolateral portion of the anterior horn in S1–S3 segments appeared.

Intravesical Electrical Stimulation—An Experimental Analysis of The Mechanism of Action

The working mechanism of intravesical electrical stimulation (IVES) was evaluated in α-chloralose anaesthetized cats and rats. IVES involved a direct activation of bladder mechanoreceptor afferents of the Aδ type and as a consequence a central reflex activation of the detrusor. The detrusor response was abolished by bilateral transection of the S1–S3 dorsal roots and by intravesical instillation of lidocaine. The optimal stimulation frequency was 20Hz. The results offer a theoretical rationale for the use of IVES as treatment of weak detrusor contractility in man.

Can enzymes adopt a self-inhibited form? results of X-ray crystallographic studies of chymosin

Chymosin molecules in the crystal lattice have Tyr77 occluding the S1 S3 substrate binding pockets suggesting that the enzyme is self-inhibited. An analysis of this structure in conjunction with its comparison with pepsin has shown that this is most probably an intrinsic property of the enzyme. It also indicates that chymosin's substrate specificity may be dependent upon the ability of the substrate to displace the tyrosine ring from the binding pockets. This analysis also implies that active and self-inhibited forms of other aspartic proteinases can exist in solution helping to explain the results of kinetic studies of these enzymes.

Protective activities in mice of monoclonal antibodies against pertussis toxin

Pertussis toxin (PT) protein, which is the most important protective antigen of Bordetella pertussis, has a hexameric structure composed of five subunits, designated S1 through S5. Immunoprotective activity of 20 different mouse monoclonal antibodies (MAbs) against pertussis toxin, 10 anti-S1, 1 anti-S2, 2 anti-S3, 4 anti-S23, and 3 anti-S4 antibodies, were investigated by aerosol and intracerebral challenges with virulent B. pertussis organisms in mice. Four anti-S1, named 1B7, 1D7, 3F11, and 10D6, and three anti-S23 antibodies, named 11E6, 10B5, and 10C9, showed the highest, and almost complete, protectivity against the aerosol challenge. Mouse protectivity against the intracerebral challenge was significant for these four anti-S1 MAbs but not for any of the three anti-S23 MAbs. Four anti-S1 and two anti-S4 MAbs did not protect the mice against either challenge. The other seven MAbs also showed dose-dependent moderate but significant protection against the aerosol challenge. In the aerosol challenge system, bacterial numbers and amounts of PT detected in the lung and the number of peripheral leukocytes were lower in the mice given the protective MAbs. All mice surviving 5 weeks after the infection produced high titers of antibodies against PT, filamentous hemagglutinin (FHA), and agglutinogens from the challenge organisms. A combination of the protective MAbs 1B7 and 11E6 strongly suppressed the disease and mortality of the mice at smaller amounts than with the anti-PT polyclonal antibody. Although combinations of one of the protective MAb and anti-FHA or anti-agglutinogen 2 also showed extremely high mouse protection without development of symptoms of the disease, antibody titers of the survivors against PT, FHA, and agglutinogens were significantly low. The foregoing results suggest that some important protective epitopes should be in S1 and S2 and/or S3, although there are both differences and similarities in the protective roles between anti-S1 and anti-S23 antibodies and also in the pathogenic mechanisms between aerosol and intracerebral infections. Furthermore, it was suggested that although not only FHA and agglutinogen 2 but also PT have roles as attachment factors, the processes of infection and protection are different between mice immunized with antibody against FHA or agglutinogen 2 and that against PT because the latter mice are also able to neutralize toxicity of PT diffused into the mice.

Deposition of Potash‐Magnesium Salts in the Qarhan Playa, Qaidam Basin

Abstract The Qarhan potash‐magnesium salt deposit, which consists from east to west of four playa districts, namely Huobuxun, Qarhan, Dabuxun and Bieletan, may be divided from bottom to top into three salt beds (S1 S2 and S3), with potash salts mainly occurring in S3 The paper lays emphasis on the evolutionary history of the deposition of Salt Bed S3 and the modes of formation of potash salts in the Qarhan playa.The analysis of the data obtained from more than 170 boreholes and the geochemical studies on bromine, magnesium and calcium reveal the existence of four concentration stages and three dilution stages during the formation of the Upper Salt Bed S3. In the process of concentration, evaporation of brine and precipitation of salt minerals dominated, which obeyed the regularity indicated by the phase diagram of the quaternary system Mg‐Na‐K/Cl−H2O. In the dilution stages, however, mixing of brines, dissolution of salts (especially the playa) and mechanical clastic deposition played the leading role. The prerequisite for mixing in the Qarhan salt deposit lies in that chloride type brine of the northeastern part coexists with magnesium sulfate type brine of the southwestern part in the same salt lake. The appearance of bassanite has verified the process of mixing. The dissolution refers to the partial dissolution of the salt beds originally deposited. Particularly in the last dilution process, approximately 200 km2 of the playa north of the Tuanjie Lake had been dissolved before a new‐born lake took form.Solid potash salts were formed in three ways: (1) The surficial brine of the Dabuxun lake coexistent with the playa had an intercompensational relationship with the intercrystalline brine in the playa. As a result, K+ ions were collected into the lake, and layered carnallite precipitated from lake brine during the seasons of evaporation, which was accelerated by the action of wind. (2) Disseminated potash‐magnesium salts were formed by further concentration of intercrystalline brine. (3) Dissolution and reformation of the playa resulted in the formation of a new‐born salt lake, in the drying of which brine collected the potash‐magnesium salts originally dispersed over the playa into local low‐lying areas, forming finally stratoid potash‐magnesium salts.

Spinal and far-field components of human somatosensory evoked potentials to posterior tibial nerve stimulation analysed with oesophageal derivations and non-cephalic reference recording

Somatosensory evoked potentials (SEPs) were elicited by stimulation of the right posterior tibial nerve at the ankle in 20 experiments on 18 normal adults. A non-cephalic reference on the left knee was used throughout (with triggering of averaging cycles from the ECG), except for recording the peripheral nerve potentials. The responses were recorded along the spine, from oesophageal probes and from the scalp. The peripheral nerve volley propagated at a mean maximum conduction velocity (CV) of 59.2 m/sec served to identify the spinal entry time (mean 19.7 msec) at spinal segments S1–S3, under the D12 spine. This entry time coincided with the onset of the N21 component which was interpreted as the dorsal column volley and considered equivalent to the neck N11 of the median nerve SEP. The large voltage of the spinal response at the D12 spine probably results from summation of N21 with a fixed latency N24 potential that phase reverses at oesophageal recording sites into a P24. The N24-P24 reflects a horizontal dipole in the dorsal horn and is equivalent to the N13-P13 of the neck SEP to median nerve stimulation. Spinal conduction between D12-C7 spines was spuriously overestimated because the true length of the dorsal spinal cord is shorter by about 13% than the distance measured on the skin over the dorsal convexity. This correction should be applied routinely and it leads to a mean maximum spinal CV of 57 m/sec. Several positive far fields with widespread scalp distribution and stationary latencies have been identified. The P17 (over spine and head) reflects the peripheral nerve volley at the upper buttock. The P21 is synchronous with the N21 at the D12 spine and reflects the initial volley in the dorsal column. No far-field equivalent has been found for the N24-P24, due to the horizontal axis of the corresponding dipole. The P26 far field reflects the ascending volley at spinal levels D10-D4. The P31 reflects the initial volley in the medial lemniscus. The P40 at Cz represents the cortical response of the foot projection. Average central CVs were calculated and discussed.

Theory of motion of saturn's coorbiting satellites

A simple analytic theory describing the 1:1 orbital resonance is presented and applied to Saturn's coorbiting pair, 1980S1 and 1980S3. These satellites are very small and can approach to within 15,000 km, but are prevented from passing each other by their mutual gravitational interaction. The long-term stability of the S1–S3 orbital configuration is discussed in this paper, and a tie between the 1966 and 1980 observations is establised.

Gowdy S1(X)S2and S3inhomogeneous cosmological models

The ADM-type Hamiltonian formulation of Gowdy (1971, 1974, 1975) S1(X)S2 and S3 vacuum inhomogeneous cosmological models is given. The canonical and constraint equations are explicitly solved and the asymptotic behaviour of the most general solution in the neighbourhood of the initial and final inhomogeneous scalar singularities is shown to be of the generalised Kasner type.

Nicotine receptors do not modulate the 3H-noradrenaline release from the isolated rat heart evoked by sympathetic nerve stimulation.

Isolated rat hearts with the right sympathetic nerves attached were perfused at a constant flow rate of 7 ml/min with Tyrode's solution. (-)-3H-Noradrenaline (final concentration 10–13.9 nM) was infused for 10 min to label the noradrenaline stores. After wash-out the sympathetic nerves were stimulated electrically (3 Hz, 180 impulses, 1 ms, 20–30 mA) three times (S1–S3) at intervals of 15 min. 3H-Noradrenaline and its metabolites were determined by liquid scintillation counting according to Graefe et al. (1973).

Unusual cell wall layers in elm parenchyma of secondary xylem

Multilayering of secondary wall layers in American elm parenchyma cells is described. This includes one additional layer like S1–S3 and protective layers each in vasicentric parenchyma and up to two additional such layers in ray parenchyma. These extra layers are comparable with those mentioned by a few other workers, but they are not necessarily related to tylosis formation as implied by some of these.