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1.
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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2.
1.  The oscillations of the tympanal membrane of Locusta migratoria were analysed by combined laser vibrometry and interferometry. Simultaneously the activity in the tympanal nerve was recorded extracellularly. The animal was stimulated by sound pulses and one of the hindlegs was passively moved in a sinusoidal manner simulating stridulation. These stimuli were applied separately and in combination.
2.  Sound stimulation elicited high-frequency membrane oscillations, whereas leg movements induced slow rhythmic membrane displacements. During combined sound and movement stimulation these two types of oscillations superimposed without mutual interference.
3.  The tympanal nerve responded to sound with well synchronized receptor activity. The leg movement elicited less synchronized, phase-coupled activity. During combined sound and movement stimulation the responses to the two types of stimuli interfered strongly.
4.  The activity patterns of single receptor fibres and auditory interneurons were reanalysed from this point of view. The extent of synchronization of the receptors is found to be the major difference between the sound-induced and the movement-induced activation of the auditory system. A filter mechanism is postulated, consisting in the activation of some higher order auditory interneurons only by well-synchronized presynaptic activity, such as is induced by steeply rising sound pulses.
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3.
1.  Stimulation to left and right vagi caused an almost equal amount of inhibitory, and occasionally excitatory, effects on pacemaker activity. Both inhibitory and excitatory effects were abolished by atropine. Vagal stimulation hyperpolarized the resting membrane potential of pacemaker fibers in the sino-atrial valve, but did not change their action potential profile.
2.  The atrial action potential showed a prominent decrease in the action potential amplitude and duration in response to vagal stimulation. The atrial region surrounding the sino-atrial valve was more sensitive to right vagal stimulation.
3.  The fibers in the atrio-ventricular ring muscle were less sensitive to vagal stimulation than the atrial fibers. Some fibers showed a decrease in the action potential amplitude and duration by vagal stimulation, and other fibers showed a decrease in the amplitude, but a prolongation of the duration as the result of a slowing of the rate of upstroke. The atrial-ventricular conduction delay or block by vagal stimulation may depend on these properties of the action potential of the atrio-ventricular ring muscle.
4.  The sino-atrial conduction block is explained by the fact that the atrial fibers are more sensitive to vagal stimulation than pacemaker fibers.
5.  The possible pathways for the sino-ventricular conduction during vagal stimulation are discussed.
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4.
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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5.
1.  The effects of potassium channel blockade on afferent axons and terminal regions in frog dorsal roots and spinal cords, respectively, were investigatedin vitro.
2.  A condition-test (C-T) protocol was used to assess the population relative refractory period. Characteristics of main axons were evaluated by stimulation at the proximal end of transected dorsal roots (DR). Characteristics of terminal regions were tested by stimulation at the base of the dorsal horn (DH).
3.  DH recovery of excitability was delayed by low concentrations of 4-aminopyridine (4-AP) and tetraethylammonium (TEA) alone or combined. The same treatments did not affect recovery to DR stimulation.
4.  DH recovery of excitability was not delayed by solutions suppressing terminal calcium influx.
5.  We conclude that sensitivity of the relative refractory period to potassium channel blocking agents differs between main axons and axon terminal regions. This may indicate differences between axon terminals and main axons in the mechanism of action potential repolarization.
6.  We hypothesize that rapid action potential repolarization by pharmacologically sensitive potassium channels in presynaptic terminal regions keeps terminal action potentials short. Terminal action potential brevity would limit calcium influx, thus preventing terminal calcium overload but contributing to transmission failures at spinal synapses.
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6.
1.  Muscles of the posterior cardiac plate (pcp) and pyloric regions in the stomach of Squilla are innervated by motoneurons located in the stomatogastric ganglion (STG). The pattern of innervation of various muscles in these regions was determined using electrophysiological methods.
2.  The dilator muscles are singly or doubly innervated by the pyloric dilator neurons (PDs). The constrictor muscles are singly or doubly innervated by the pcp neuron (PCP) or the pyloric neurons (PYs). These muscles are sequentially activated by pcp-pyloric motor outputs produced by the PCP, PY, and PD. All muscles can generate an all-or-nothing spike.
3.  The constrictor muscles generate spikes followed by depolarizing afterpotentials which lead to a sustained depolarization with repetitive spikes. The PYs can entrain rhythmic spike discharges of these muscles.
4.  The spike of muscles remains unchanged by bath application of tetrodotoxin (10-7 M) to suppress neuronal impulse activities, but it is blocked by Mn2+ (10 mM).
5.  The constrictor muscle isolated from the STG displays an endogenous property of spontaneous membrane oscillation that produces a train of spikes. Brief depolarizing or hyperpolarizing stimuli can trigger or terminate an oscillatory potential, respectively, and reset the subsequent rhythm.
6.  The possible functions of myogenicity under the control of discharges of motoneurons in the pyloric constrictor neuromuscular system are discussed.
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7.
1.  Properties of the membrane currents ofDidinium nasutum have been investigated under voltage clamp in different solutions and after deciliation.
2.  Theearly transient Ca2+ inward current activates in a voltage-dependent manner. Inactivation is both Ca2+ -dependent and voltage-dependent.
3.  Alate Ca2+ current rises with time to peak > 50 ms and decays in the order of seconds.
4.  Activation and inactivation of the late Ca2+ current is voltage-dependent.
5.  The delayed outward current is activated by voltage. The kinetics of this K+ current, but not its amplitude, are enhanced in the presence of intracellular EGTA.
6.  The two voltage-dependent Ca2+ channels are located in the cilia, whereas all K+ channels are restricted to the somatic membrane.
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8.
1.  Direct contact between intra-epithelial nerve endings and ciliated cells was observed in frog (Rana pipiens) palate epithelium.
2.  Electrical stimulation of the palatine nerve to the explant or the explant culture induced an increase in ciliary beat frequency in explant and outgrowth cells.
3.  Atropine inhibited electrically stimulated ciliary beat frequency increase in the explant and outgrowth cells.
4.  Gap junctional intercellular communication appears to be involved in the propagation of stimulated ciliary beat frequency increase from innervated to non-innervated ciliated cells.
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9.
1.  The uropod righting reaction of the crayfish,Procambarus clarkii, was investigated in response to stimulation of proprioceptors at the bases of the walking legs and to stimulation of the balance organs, the statocysts.
2.  Tilting a platform beneath the legs of crayfish elicited movements of the exopodites of the uropods in the horizontal plane. These were produced by activity only in the slow opener and closer muscles of the exopodites, the fast muscles not being involved in the formation of the uropod pattern. Platform tilts (±20°) with the axis of rotation parallel to the transverse axis of the body elicited a symmetrical closing of the exopodites when the anterior leg groups were depressed, and a symmetrical opening when the same leg groups were levated.
3.  Platform tilts parallel to the longitudinal axis of the body elicited asymmetrical movements of the uropods with the exopodite ipsilateral to the levated legs opening and the contralateral exopodite closing. In all experiments the responses of the uropods were only reliably elicited when accompanied by extension of the abdomen.
4.  The influence of input from various leg groups was examined by raising them from the oscillating platform in various combinations. The strongest reflex drive came from the 4th and 5th pairs of walking legs. The major source of input came from the coxo-basipodite (C-B) joint of the walking legs. Blocking other leg joints (mero-carpopodite (M-C) and carpo-propodite (C-P)) had no obvious effects on the normal response.
5.  Tilting animals in the roll plane (±20°), with no leg contact, produced an opening of the exopodite on the upward side and a closing of the exopodite on the downward side. Responses were again only reliably elicited when accompanied by abdominal extension, and were produced by activity only in the slow opener and closer muscles.
6.  Previously identified statocyst interneurones (C1 and C2) were recorded in the circumoesophageal commissures. No modulation of their spontaneous activity by leg input could be detected.
7.  Results suggest that separate pathways from the leg proprioceptors and the statocyst organs to the uropods exist and converge at a late stage in the pathway, within the terminal (6th) abdominal ganglion.
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10.
Thiolutin was found to inhibit the utilization of glucose and other growth substrates in Escherichia coli. The inhibition was detected by a sharp drop of the respiration rate after addition of the antibiotic. The actual function affected was allocated to the cytoplasmic membrane of the bacterial cells by the following evidence:
–  - spheroplasts were affected like intact cells,
–  - individual reactions of either the electron transport chain or the glycolytic pathway were not inhibited,
–  - glucose consumption in the culture stopped and the cells accumulated guanosine tetraphosphate as under starvation conditions,
–  - activation of the cell's apo-glucose dehydrogenase restored respiration via bypassing the glucose phosphotransferase system.
It was concluded that the transport of certain substrates across the membrane was inhibited.  相似文献   

11.
Müller  D. G.  Frenzer  K. 《Hydrobiologia》1993,(1):37-44
Culture studies with healthy and virus-infected isolates of Ectocarpus siliculosus, Feldmannia simplex and F. irregularis gave the following results:
–  Virus particles are produced in deformed reproductive organs (sporangia or gametangia) of the hosts and are released into the surrounding seawater.
–  Their infective potential is lost after several days of storage under laboratory conditions.
–  New infections occur when gametes or spores of the host get in contact with virus particles. The virus genome enters all cells of the developing new plant via mitosis.
–  Virus expression is variable, and in many cases the viability of the host is not impaired. Infected host plants may be partly fertile and pass the infection to their daughter plants.
–  Meiosis of the host can eliminate the virus genome and generate healthy progeny.
–  The genome of the Ectocarpus virus consists of dsDNA. Meiotic segregation patterns suggest an intimate association between virus genome and host chromosomes.
–  An extra-generic host range has been demonstrated for the Ectocarpus virus.
–  Field observations suggest that virus infections in ectocarpalean algae occur on all coasts of the world, and many or all Ectocarpus and Feldmannia populations are subject to contact with virus genomes.
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12.
1.  The actions of GABA on three classes of visual interneurons in crayfish, Procambarus clarkii, medulla externa are examined. The effect of GABA on the visual response is compared to GABA's action on agonist-elicited responses purported to mediate the visual response.
2.  GABA produces a shunting type of inhibition in medullary amacrine cells which is associated with a small depolarization (Figs. 2, 3), a large increase in input conductance (Gn) and a reversal potential close to rest (Fig. 4). GABA is a potent antagonist to the depolarizing action of acetylcholine (ACh) (Fig. 5).
3.  GABA depolarizes dimming fibers (Fig. 2), and the response is mediated by an increase in Gn (Fig. 6). GABA antagonizes the light-elicited IPSP and the hyperpolarizing action of ACh (Fig. 7).
4.  Sustaining fibers (SF) do not appear to have GABA receptors but GABA inhibits the excitatory visual input pathway to the SFs (Fig. 8). Conversely, the GABA antagonist, bicuculline, potentiates the SF light response (Fig. 9).
5.  GABA has at least three different modes of antagonist action in the medulla: i) Increased conductance and depolarization in dimming fibers and medullary amacrine neurons; ii) Decreased chloride conductance in tangential cells; and iii) An inhibitory action on the visual pathway which drives SFs.
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13.
1.  Some units in the lateral ocellar nerves of the locust,Locusta migratoria, are influenced transsynaptically by the activity of ascending fibres in the thoracic connectives and therefore may be efferent to the afferent ocellar system.
2.  A variety of sensory inputs excite the ocellar nerve units, including illumination of the compound eyes, active and passive movement of the wings, wind stimuli to the thorax and sound.
3.  Most ocellar interneurons are influenced transsynaptically by electrical stimulation of the cervical connectives. L-neurons are depolarized and the components of their response to a rectangular light pulse are changed in amplitude. Only a few S-neurons could be examined. All of them were excited directly or indirectly.
4.  The descending ocellar interneurons (DN's) are influenced by stimulation of the contralateral connective, perhaps via efference to the ocellus or to ocellar L-cells.
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14.
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15.
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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16.
1.  Most Purkinje neurons show ongoing spike activity. In approximately 75%, this activity disappeared after peduncle lesion and in some of these the activity stopped when water flow over the gills was interrupted. Approximately one-fourth of Purkinje cells (PC's) showed continuing ongoing activity after afferent input was abolished.
2.  Stimulation of spinal cord elicited both simple spikes, mainly in ipsilateral PC's, and some complex responses (via climbing fibers) usually contralateral and of longer latency than the simple spikes.
3.  Tactile stimulation of skin and flexion of tail or fins, also lateral line stimulation by a water stream, evoked bursts of spikes in PC-s. Input was by mossy fibers and mechanoreceptive fields were large.
4.  Stimulation of vestibular nerve produced both simple and complex responses in PC's. Auditory stimuli were most effective at 800–1200 Hz in eliciting responses via mossy fibers. Responses to sound were phasic changes in ongoing frequency, bursts followed by inhibition or on-off excitation.
5.  Responses to visual stimuli were recorded in granule cells and Purkinje cells, also in mossy axons. Many PC's showed excitatory-inhibitory sequences; a few climbing fiber responses were recorded. The mossy fiber visual input is from optic tectum relay.
6.  Some PC's were activated by two or three sensory modalities.
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17.
1.  The effect of outward and inward water flows through the membrane on outward potassium currents of dialyzedHelix pomatia neurons was studied.
2.  An outward water flow increased the peak and sustained outward potassium currents and accelerated the kinetics of their activation. An inward water flow had quite opposite effects—it decreased the peak and sustained potassium currents and delayed the kinetics of their activation.
3.  The analysis of the effect of water flow on the conductance of potassium channels showed that an outward water flow increased both the potassium conductance at a given potential (gk) and the maximum potassium conductance (g k max ). An inward water flow again had the opposite effect—it decreased the potassium conductance at given potential and the maximum potassium conductance.
4.  Neither an outward nor an inward water flow significantly affected the fraction of open potassium channels at a given potential [n (V)].
5.  These data suggest that in dialyzed neurons the changes of outward potassium current during water flow through the membrane are due mainly to the changes in single-channel conductance and the time constant of current activation.
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18.
1.  Up to 9 kHz, the tympanal membrane of the grasshopper Chorthippus biguttulus responds with equal sensitivity at the attachment sites of the low and the high-frequency receptors; at the latter site it is also particularly sensitive between 10 and 20 kHz.
2.  The frequency spectra of the songs of both sexes exhibit maxima at 7–8 kHz, to which the membrane is well matched. In the high-frequency region, where the male songs have a peak at 30 kHz, there is no corresponding maximum in the membrane oscillation.
3.  Because the tympanal membrane is immediately adjacent to air sacs in the tracheal system, it is deflected inward and outward by as much as 80 m during the respiratory cycle.
4.  Measurements by laser vibrometry show that acoustically induced membrane oscillations are attenuated severely due to the respiratory displacement of the membrane for frequencies up to 10–12 kHz. By contrast, at higher frequencies the membrane sensitivity is doubled or tripled.
5.  As a result of these membrane effects, the discharge in the tympanal nerve was profoundly reduced in the low-frequency range, whereas above 11 kHz there was a marked increase. This modulation of auditory sensitivity affects the animals' ability to detect conspecific songs.
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19.
The effects of temperature, over the range 10–40 °C, on properties of locust (Schistocerca gregaria) ocellar L-neurones and of their interconnections have been investigated. At cooler temperatures, a small change in temperature has a larger effect than an equivalent change at warmer temperatures. An increase in temperature leads to the following:
1.  A decrease in input resistance, which typically halves in value as temperature increases from 15 °C to 35 °C. When synaptic transmission between photoreceptor cells and L-neurones is blocked with cobalt, temperature still affects L-neurone resistance. The membrane time constant also decreases, but the resting potential is unaffected.
2.  An increase in the sizes of rebound spikes, which are produced when hyperpolarizing pulses end. Above 35 °C, the maximum size of rebound spike is smaller than that at cooler temperatures.
3.  A decrease in the latency to response to light, and an increase in the speeds of the transient responses to changes in light.
4.  A decrease in the latency of transmission at both excitatory and inhibitory synapses between L-neurones.
5.  At excitatory synapses between L-neurones, an increase in the postsynaptic current. This is compensated by a decrease in postsynaptic membrane resistance, so that there is little effect on the size of the postsynaptic potential.
6.  At inhibitory synapses between L-neurones, a decrease in the time for the postsynaptic potential to reach its peak. The time for recovery of transmission at inhibitory synapses is unaffected by temperature.
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20.
3DFS is a 3D flexible searching system for lead discovery. Version 1.0 of 3DFS was published recently (Wang, T.; Zhou, J. J. Chem. Inf. Comput. Sci., 1998, 38, 71–77). Here version 1.2 represents a substantial improvement over version 1.0. There are six major changes in version 1.2 compared to version 1.0.
1.  A new rule of aromatic ring recognition.
2.  The inclusion of multiple-type atoms and chains in queries.
3.  The inclusion of more spatial constraints, especially the directions of lone pairs.
4.  The improvement of the query file format.
5.  The addition of genetic search for flexible search.
6.  An output option for generating MOLfiles of hits.
Besides the above, this paper supplies:
1.  More query examples.
2.  A comparison between genetic search and Powell optimization.
3.  More detailed comparison between 3DFS and Chem-X.
4.  A preliminary application of 3DFS to K+ channel opener studies.
Supplementary material to this paper is available in electronic form at http://dx.doi.org/10.1007/s0089490050231  相似文献   

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