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1.
1.  An extracellular recording and staining technique has been used to study the structure of individual ventral-cord elements in the auditory pathway ofLocusta migratoria.
2.  Three groups of auditory ventral-cord neurons can be distinguished: (a) neurons ascending to the supraesophageal ganglion, (b) T-shaped neurons, and (c) neurons limited to the thoracic ventral cord.
3.  The ventral-cord neurons ascending to the supraesophageal ganglion link the auditory centers of the thorax to those of the supraesophageal ganglion. These are, at least in part, richly arborized neurons of large diameter.
4.  The ventral-cord neurons with T structure send equivalent signals along both arms of the T; they resemble the neurons of the first group in that they make synaptic connections in the supraesophageal ganglion, but they also conduct auditory information to caudal regions of the thorax via the descending trunk of the axon.
5.  In the supraesophageal ganglion there are several extensive projection areas of the auditory ventral-cord neurons. No direct connections to the mushroom bodies, the central body or the protocerebral bridge could be demonstrated.
6.  The thoracic ventral-cord neurons act as short segmental interneurons, providing a connection between the tympanal receptor fibers and the ascending and T-shaped ventral-cord neurons. They play a crucial role in auditory information processing.
7.  The possible functional properties of the various morphological sections of the auditory ventral-cord neurons are discussed, with reference to their connections with motor and other neuronal systems.
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2.
1.  With Helix pomatia intracerebral injections of ferritin were carried out (maximal incubation time: 45 min). First, the marker spreads with time via the extracellular space throughout the cerebral ganglia and, secondly, is transported out of the ganglia. Electron microscopical studies showed that all glial cell types take up great amounts of ferritin by endocytosis. The plasmatic glial cells at the periphery incorporate more of the marker than the filamentous glial cells in the centre. No uptake of ferritin by neurons or axons was observed. In vitro studies proved that ferritin can penetrate from the connective tissue capsule into the ganglia only after disruption of the neural lamella and damaging of the peripheral glial processes.
2.  3H-glutamate, a putative transmitter of the CNS of Helix pomatia, was injected into the hemocoel of active snails (incubation times: 15min, l h, 6h, 3d). Light microscopical evaluation of radioautographs showed that great quantities of the tracer penetrate into the ganglia. The bulk of it is taken up by glial cells, whereas the neurons exhibit only small amounts of the tracer.
The studies with ferritin as well as those with 3H-glutamate indicate that the glial cells of the cerebral ganglia of Helix pomatia act as a hemolymph-neuron barrier. A dominant role of the plasmatic glial cells according to these processes is discussed.  相似文献   

3.
The caudal photoreceptors (CPRs) of crayfish (Procambarus clarkii) can trigger walking and abdominal movements by their response to light.
1.  In a restrained, inverted crayfish, illumination of A6 evoked a CPR discharge followed by leg movements and bursting from the abdominal tonic flexor (TF) motoneurons. Intracellular electrical stimulation of a single CPR at high frequency (80 Hz) evoked similar responses.
2.  Responses only occurred when a single CPR axon was driven at 60 Hz or more and outlasted the stimulus.
3.  CPR stimulation also excites the pattern-initiating network (Moore and Larimer 1987) in the abdomen.
4.  The axon of the CPR projects from ganglion A6 to the brain. Terminal branches occur in the subesophageal ganglion and the brain. A small descending interneuron is dye-coupled to CPR in the subesophageal ganglion.
5.  In animals with cut circumesophageal connectives, the CPRs can evoke walking and the abdominal motor pattern.
6.  The relationship of the abdominal motor pattern to walking is altered by restraint and/or inversion. In freely moving crayfish, the cyclic abdominal motor pattern is only observed with backward walking. In restrained, inverted crayfish, the motor pattern occurs with both forward or backward walking.
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4.
1.  Normal activity in bilateral pairs of heart interneurons, from ganglia 3 or 4, in the medicinal leech (Hirudo medicinalis) is antiphasic due to their reciprocally inhibitory connections. However, Ca+-free Co+-containing salines lead to synchronous oscillations in these neurons.
2.  Internal TEA+ allows expression of full plateaus during Co++ induced oscillations in heart interneurons; these plateaus are not blocked by Cs+. Similar plateaus are also observed with internal TEA+ alone, but under these conditions activity in heart interneurons from ganglia 3 or 4 is antiphasic.
3.  Plateaus in heart interneurons induced by Co++ and internal TEA+ involve a conductance increase.
4.  A voltage-dependent inward current, IP, showing little inactivation, was isolated using single-electrode voltageclamp in heart interneurons. This current is carried at least in part by Na+; the current is reduced when external Na+ is reduced and is carried by Li+ when substituted for Na+.
5.  Calcium channel blockers such as La3+ and Co++ block neither the TEA+ induced plateaus nor IP, suggesting that Na+ is not using Ca++ channels. Moreover, IP is enhanced by Ca++-free Co++-containing salines. Thus, IP is correlated with the TEA+- and Co++-induced plateau behavior.
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5.
1.  The excitatory and inhibitory influences on the gill ofAplysia Juliana, which are mediated by the branchial nerve, were studied by means of electrophysiological techniques. Excitatory and inhibitory pathways in the nerve were stimulated simultaneously or selectively.
2.  The branchial nerve was found to contain both excitatory and inhibitory pathways which did not contain synapses in the branchial ganglion. The excitatory pathways caused longitudinal shortening of the gill along the efferent branchial vessel and the inhibitory pathways were modulatory, depressing the longitudinal shortening.
3.  Branchial nerve stimulation elicited two types of excitatory junctional potential (EJP), which were not mediated by the branchial ganglion, in a muscle cell of the efferent branchial vessel. One type was attributed to the central motor neuron and the other type to a motor neuron which is probably situated in the neural plexus of the gill periphery.
4.  Four inhibitory pathways from the central nervous system to the gill were found.
5.  Inhibitory junctional potentials (IJPs) recorded from muscle cells of the efferent branchial vessel in response to branchial nerve stimulation did not have monosynaptic characteristics. It is thought that inhibitory motor neurons which were activated by the branchial nerve might exist at the neural plexus of the gill.
6.  A single EJP which has been induced by a stimulus pulse applied to the excitatory pathway of the branchial nerve may be depressed in an all-or-none manner by a stimulus pulse applied to the inhibitory pathway, if this is done within a distinct short period prior to or after the stimulus inducing the EJP. This indicates that the central motor neuron receives presynaptic inhibition at its periphery.
7.  The motor neurons of the neural plexus seem to receive inhibitory innervation. Suppression of endogenous EJPs in the efferent vessel persisted for a long period even after cessation of stimulation.
8.  A certain branchioganglionic neuron (BGN) was found to receive inhibitory postsynaptic potential (IPSP) inputs from the branchial nerve.
9.  The multimodality of both the excitatory and the inhibitory pathways in the branchial nerve may explain the compound neural modulations of gill movements.
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6.
1.  Coupling mechanisms between ciliary beating and the membrane potential in Paramecium were investigated under voltage clamp applying intracellular pressure injection of cAMP, cGMP and Ca-EGTA buffer. Ciliary responses following step changes in membrane potential were recorded by high-speed video on magnetic tape.
2.  Injections of cAMP and cGMP up to millimolar concentrations caused no detectable changes in the frequency voltage relationship. A minor effect was that the ciliary reorientation towards the anterior cell end (reversal) tended to be inhibited with depolarization up to 10 mV.
3.  Injection of Ca2+ into the cell clamped at the resting potential caused a transient anteriad ciliary reorientation and a simultaneous increase in the beating frequency.
4.  Injection of EGTA (to buffer Ca2+ below 10–8 M) was ineffective in relation to frequency for several minutes. After this time, hyperpolarization- and depolarization activated frequency responses of EGTA-injected cells were increasingly inhibited. The ciliary reorientation following depolarization was not affected by EGTA.
5.  A posterior contraction of the cell diameter was noticed upon membrane hyperpolarization. The contraction coincided in time with the increase in beating frequency.
6.  The results support the view that the voltage-dependent augmentation of the ciliary beating rate is not directly mediated by an intracellular increase in either cAMP or cGMP.
7.  The role of Ca2+ as intracellular messenger in the ciliary and somatic compartments is discussed.
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7.
Conclusions  
(1)  The aminoesters inhibit glucose-stimulated proton extrusion by yeast cells.
(2)  The inhibitory activity depends on aliphatic carbon chain length.
(3)  The inhibition of proton extrusion is concentration-dependent.
(4)  The aminoesters stimulate quinacrine accumulation in vacuoles of yeast cells so they should possess affinities for lysosomes.
This work was supported byKBN grant no. 7 A203 013 07.  相似文献   

8.
Electron microscopic investigations of secretory ameloblasts from deciduous tooth germs of mini-pig foetuses and investigations of the ability of various fixatives to preserve these cells in tooth germs immersion-fixed in toto 5 min, 10 min, 15 min, 20 min and 40 min after death of the mother gave the following results:
1.  The ameloblasts exhibit ultrastructural characteristics typical of exocrine secretory cells of merocrine type.
2.  The localization of organelles is as in rodent secretory ameloblasts, but differs from the location in the human analogues.
3.  Fixation with 4% formaldehyde invariably gives unacceptable ameloblast preservation.
4.  Fixation with 2.5% glutaraldehyde gives fair preservation of the ameloblasts when the germs are fixed within 10 min of the death of the mother.
5.  Fixation with a fixative mixture 2% formaldehyde — 1.25% glutaraldehyde gives good preservation when the ameloblasts are fixed within 15 min of the death of the mother.
6.  Fixation with a fixative mixture 2% formaldehyde — 1% glutaraldehyde — 1% acrolein gives good ameloblast preservation when the germs are fixed within 15 min of the death of the mother.
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9.
Intracellular recordings were carried out on locust flight motoneurons after hemisection of individual thoracic ganglia. With the exception of minimal surgical manipulations, the animals were intact and able to perform tethered flight. Analysis of the synaptic drive recorded in the motoneurons during flight motor activity revealed the extent to which ganglion hemisection influenced the premotor rhythm generating network.
1.  Hemisection of the mesothoracic ganglion (Fig. 2) as well as hemisection of both the mesothoracic and the prothoracic ganglia (Fig. 3) had no significant effects on the pattern of synaptic input to the flight motoneurons. Thus the rhythm generating premotor network does not depend on commissural information transfer in the mesothoracic and the prothoracic ganglia. This conclusion was supported by experiments in which more extensive surgical isolations of thoracic ganglia were carried out (Fig. 5).
2.  Removal of input from wing receptors (deafferentation) in addition to hemisection of the mesothoracic ganglion (Fig. 4) resulted in rhythmic and coordinated oscillations of the motoneuron membrane potential which were indistinguishable from those observed in deafferented animals with all ganglia intact.
3.  Hemisection of the metathoracic ganglion had more pronounced effects on the patterns of synaptic drive to the flight motoneurons and their spike discharge. Rhythmic activity which was often subthreshold could, however, still be recorded following a metathoracic split (Fig. 6).
4.  No rhythmic synaptic input was observed after hemisection of both mesothoracic and metathoracic ganglia (Fig. 7).
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10.
1.  A retention time of 150 days in the storage reservoir leads to a quite considerable reduction in copper and lead concentration (around 75% for lead and 50% for copper), while a levelling-off in the marked variations in the water flowing in is also found.
2.  Copper concentrations in the storage reservoir and the model reservoirs show a less constant picture with time then lead concentrations. This may well be caused by the absorption of copper by e.g. phytoplankton.
3.  Treatment of the water with Fe++ or AVR seems to have no effect on the removal of lead or suspended matter.
4.  Because of the small number of measurements it is difficult to quantify these results.
5.  For statements about seasonal trends, measurements must be made over a period of at least three years; they must be made at least once a week and the sampling procedure as regards place and frequency must remain unchanged.
6.  The available data indicate that in spite of the effect of mobilisation the removal of the two metals is such that sudden drastic rises of concentration in the unfiltered surface water entering the purification installation is not to be expected.
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11.
Interleukin-1 stimulates the beta-amyloid precursor protein promoter   总被引：7，自引：0，他引：7  
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12.
1.  We have obtained a cDNA clone encoding a human retinal D2 dopamine receptor.
2.  The longest open reading frame (1242 bp) of this clone encodes a protein of 414 amino acids having a predicted molecular weight of 47,000 and a transmembrane topology similar to that of other G protein-coupled receptors.
3.  Transient transfection of COS-7 cells with an expression vector containing the clone resulted in expression of a protein possessing a pharmacological profile similar to that of the D2 dopamine receptor found in striatum and retina.
4.  Northern blot analysis indicated that, in rat brain and retina, the mRNA for this receptor was 2.9 kb in size.
5.  In situ hybridization was performed to examine the distribution of the mRNA for this receptor in human retina. Specific hybridization was detected in both the inner and the outer nuclear layers.
6.  These findings are consistent with prior physiological and autoradiographic studies describing the localization of D2 dopamine receptors in vertebrate retinas. Our observations suggest that photoreceptors as well as cells in the inner nuclear layer of human retinas may express the mRNA for this D2 dopamine receptor.
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13.
1.  We used laser vibrometry and free field sound stimulation to study the frequency responses of the eardrum and the lateral body wall of awake male Eleutherodactylus coqui.
2.  The eardrum snowed one of two distinct frequency responses depending on whether the glottis was open (GO response) or closed (GC response) during the measurement.
3.  The lateral body wall vibrated with a maximum amplitude close to that of the eardrum and in the same frequency range.
4.  Covering the frog's body wall with vaseline reduced the vibration amplitude of the GC response by up to 15 dB.
5.  When a closed sound delivery system was used to stimulate a local area of the body wall the eardrum also showed one of two types of responses.
6.  These results suggest that sound is transmitted via the lung cavity to the internal surface of the eardrum. This lung input has a significant influence on the vibrations of the eardrum even when the glottis is closed.
7.  The vibration amplitude of the eardrum changed with the angle of sound incidence. The directionality was most pronounced in a narrow frequency range between the two main frequencies of the conspecific advertisement call.
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14.
1.  In this commentary we discuss results obtained by a micromethod for the study of Cl– permeability across single nerve membranes from rabbit Deiters' neurons.
2.  These results showed the presence of GABAA receptors on the nerve cell membrane cytoplasmic side.
3.  We could show that these receptor complexes have a higher affinity for GABA than their extracellularly facing counterparts. Moreover, they present a phenomenon of desensitization. Another distinct property is that upon activation by GABA, they expose positive charges at their cytoplasmic mouths.
4.  We propose that these receptor complexes could functionin situ as a device for extruding Cl– anions from the nerve cell interior. This phenomenon would create an electrochemical gradient for Cl– penetration into the cell upon the action of extracellular GABA, after its presynaptic release.
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15.
Oncostatin M, a multifunctional cytokine   总被引：6，自引：0，他引：6  
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16.
1.  Paramecium bursaria was stimulated by a light spot of 10–15 m diameter, and the photosensitive site was searched by recording responses in swimming behavior and in membrane potential.
2.  Local stimulation to the anterior half of the cell caused an avoiding response.
3.  Stimulation to the cells deciliated by ethanol treatment elicited a depolarization of the membrane potential.
4.  Local stimulation to the anteroventral portion elicited a depolarization, but stimulation to the dorsal side induced no change in the membrane potential.
5.  The action spectrum of depolarization elicited by local stimulation to the anteroventral surface showed two main peaks at 420 nm and 560 nm, corresponding to those of light stimulation of the whole cell.
6.  It is concluded that a photosensitive site exists on the anteroventral surface ofParamecium, in particular within the oral groove of the cell. This local photosensitivity is discussed with respect to the mating reaction.
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17.
1.  Non-visual sensory systems are likely to be important in antarctic fish since these fish inhabit an area where low light levels occur for long periods. This study was undertaken to examine the suitability of the lateral line system for prey detection.
2.  Recordings were made from afferent fibres of the anterior lateral line in the antarctic fishPagothenia borchgrevinki.
3.  A vibrating probe was used to stimulate the lateral line at a range of frequencies between 10 and 100 Hz.
4.  Most units responded best at a stimulus frequency of 40 Hz. Below the best frequency the response typically declined steeply and at higher frequencies it was usually better sustained.
5.  Crustacea identified as major components of the diet ofPagothenia borchgrevinki were individually attached to a force transducer to determine the vibrations produced by swimming movements.
6.  The Fourier amplitude spectra of swimming crustaceans exhibited prominent low frequency peaks at 3–6 Hz and higher frequency peaks in the 30–40 Hz range.
7.  It is concluded that the overlap in the frequency response characteristics of the anterior lateral line and the frequencies produced by crustacean prey clearly establishes the suitability of the lateral line for prey detection.
8.  In several instances recordings were made from fish primary afferent neurons responding to a swimming amphipod. These recordings confirm that crustacean swimming is indeed a potent natural stimulus of the lateral line system.
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18.
Metabolic characteristics of experimental hepatoma cells include elevated rates of glycolysis and lipid synthesis. However, pyruvate derived from glucose is not redily oxidized, and the source of acetly CoA for lipid synthesis in As-39D cells has not been characterized. In this study ketone bodies were examined as a possible source of acetyl CoA in AS-30D hepatoma cells.The major findings were:
1.  Acetoacetate was utilized by AS-30D cells, with14C-lipid and14CO2 as major products of [3-14C] acetoacetate.
2.  Lipid synthesis from acetoacetate was dependent on the presence of glucose in the medium.
3.  Acetoacetate supported rapid respiration by AS-30D mitochondria in the presence of 0.1 mM malate.
4.  Succinly CoA acetoacetyl CoA transferase activity in AS-30D mitochondria was approximately 40 fold greater than that found in rat liver mitochondria.
5.  Addition of acetoacetate, but not -hydroxybutyrate decreased conversion of [1-14C] acetate to14CO2, presumably by diluting the specific radioactivity of the acetyl CoA derived from the acetate tracer.
6.  In the presence of glucose, approximately one fourth of acetoacetate utilized was converted to lipid. This result is consistent with elevated lipogenesis postulated by the truncated TCA cycle hypothesis. These data demonstrate for the first time the flux of acetoacetate carbon to lipid and CO2 in hepatoma cells and suggest that increases in the ambient concentration of acetoacetate, occurring in fasting or malignant cachexia, could produce increases in the utilization of this ketone body by hepatoma cells containing 3-oxyacid CoA transferase activity.
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19.
Twelve of the main European LCA software packages currently available are examined wirh the aim of establishing which are the most appropriate for LCAs on industrial processes. The packages performances are assessed in terms of
–  • Volume of Data
–  • WindowsTM environment
–  • Network Capabilities
–  • Impact Assessment
–  • Graphical representation of the inventory results
–  • Sensitivity analysis
–  • Units
–  • Cost
–  • User Support
–  • Flow Diagrams
–  • Burdens allocation
–  • Transparency of data
–  • Input & output parameters
–  • Demo version
–  • Quality of data
The review concludes with a Specification Table which summarises the facilities available on each software package. The general conclusion from this study is that for industrially based LCAs, there are four packages which may offer advantages over the rest. These are The Boustead Model, The Ecobilan Group’s TEAM™, PEMS 3.0 and SimaPro 3.1.  相似文献   

20.
1.  In Polyporus ciliatus (Polyporaceae) dikaryotic fruiting is controlled by the tetrapolar mechanism of homogenic incompatibility.
2.  The occurrence of subunits of the mating type factors A and B, known in other Holobasidiomycetidae, could not be proved. If subunits are present, their distance must be less than 0.2 map units.
3.  Monokaryotic fruiting occurs in a strictly haploid phase. Neither karyogamy nor meiosis is required in the fruit bodies for the development of basidia having two spores.
4.  Genetic analysis has revealed that for the initiation of monokaryotic fruting a single gene (fi +/fi) is responsible. Additional genes control the shape of the fruit bodies (fb +/fb) and its fertility (mod +/mod).
5.  Monokaryotic fruiting is closely correlated with dikaryotic fruiting in two ways. On the one hand the B factors, part of the controlling system for dikaryotic fruiting, block monokaryotic fruiting when both partners are heterogenic for the B factor. On the other hand, despite the fact that monokaryotic fruiting is suppressed in a dikaryon, the fi gene controls the formation of dikaryotic fruit bodies. The allele fi + enhances fruit body production whereas the allele fi may inhibit fruit body production completely.
6.  The action and interaction of the incompatibility factors, the genes responsible for monokaryotic fruiting and the genes causing heterogenic incompatibility is discussed with respect to evolution and concerted breeding of mushrooms.
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