Stimulation of bursting in pre-Bötzinger neurons by Epac through calcium release and modulation of TRPM4 and K-ATP channels

The exchange factor directly activated by cAMP (Epac) can couple cAMP production to the activation of particular membrane and cytoplasmic targets. Using patch-clamp recordings and calcium imaging in organotypic brainstem slices, we examined the role of Epac in pre-B?tzinger complex, an essential part of the respiratory network. The selective agonist 8-(4-chlorophenylthio)-2'-O-methyl-cAMP (8-pCPT) sensitized calcium mobilisation from inositol-1,4,5-trisphosphate-sensitive internal stores that stimulated TRPM4 (transient receptor potential cation channel, subfamily M, Melastatin) channels and potentiated the bursts of action potentials. 8-pCPT actions were abolished after inhibition of phospholipase C with U73122 and depletion of calcium stores with thapsigargin. Caffeine-sensitive release channels were not modulated by 8-pCPT. Epac inhibited ATP-sensitive K(+) channels that also led to the enhancement of bursting by 8-pCPT. Bursting activity, spontaneous calcium transients and activity of TRPM4 and ATP-sensitive K(+) channels were potentiated after brief exposures to bradykinin and incubation with wortmannin produced opposite effects that can be explained by changes in phosphatidylinositol 4,5-bisphosphate levels. 8-pCPT stimulated the respiratory motor output in functionally intact preparations and the effects of bradykinin and wortmannin were identical to those observed in organotypic slices. The data thus indicate a novel pathway of controlling bursting activity in pre-B?tzinger complex neurons through Epac that can involved in reinforcement of the respiratory activity by cAMP.     

Relationship between cyanogenesis and latex stability on tapping panel dryness in rubber trunk girth

The presence of high cyanogenic glycoside concentrations may predispose plant to the tapping panel dryness (TPD). This study aimed to verify the involvement of cyanogenesis in the reduction of latex stability and in the establishment of TPD. The following parameters were evaluated in rubber tree trunk bark: concentration of cyanogenic glycosides with determination of cyanogenic potential (HCNp) and latex stability with lutoid bursting index (LBI). The study of the relationship between cyanogenesis and TPD was performed by semiquantitative comparison of hydrogen cyanide (HCN) gas released from the trunk bark under the following conditions: without (0%) and with (100%) TPD. The positive correlations between HCNp values and LBI indicate that cyanogenic glycosides present in the bark reduce latex stability, resulting in low yield due to the short duration of flow during tapping. The largest amount of HCN released by trunk bark tissues when the plant exhibits TPD symptoms strengthens the evidence of the involvement of this compound in the establishment of this condition.     

Synchronous Bursting Can Arise from Mutual Excitation, Even When Individual Cells are not Endogenous Bursters

Mutual excitation between two neurons is generally thought to raise the excitation level of each neuron or, if they are both bursty, to act to synchronize their bursts. If only one is bursty, it can induce synchronized bursts in the other cell. Here we show that two nonbursty cells can be induced to burst in synchrony by mutual excitatory synaptic connections, provided the presynaptic threshold for graded synaptic transmission ateach synapse is at a different level. This mechanism may operate in a recently discovered network in the lobster Homarus gammarus.By a duality between presynaptic threshold and injected current, we also show that two identical, nonbursty, mutual excitatory cells could be induced to burst in synchrony by injecting differing amounts of current inthe two cells. Finally we show that differential oscillations betweentwo mutual excitatory cells could be stopped by a slow-tailedhyperpolarizing current pulse into one cell or a slow-taileddepolarizing pulse into the other.     

TTX sensitive plateau potentials in the crayfish slowly adapting stretch receptor neuron

Summary Electrophysiological experiments showed that a tetrodotoxin (TTX) sensitive slowly inactivating Na⁺ current contributed to the excitability of the sensory neuron (SN1) that innervates the slow receptor muscle in the abdominal muscle receptor (MR1) of crayfish, Procambarus clarkii. Following either tetraethylammonium (TEA) blockage of the K⁺ delayed rectifier currents or exposure to high temperature, a depolarizing plateau potential was evoked by the slow Na⁺ current. Ca⁺⁺ substitution by other divalent cations had no effect on the plateau potential, demonstrating that Ca⁺⁺ is not involved in plateau potential genesis. Simultaneous intrasomatic and extraaxonic recordings coupled with 4-aminopyridine (4-AP) exposure indicated that the slowly inactivating Na⁺ current is primarily somatic, and does not contribute significantly to spiking.Abbreviations 4-AP 4-aminopyridine - HAP hyperpolarizing after-potential - MR1 slowly adapting muscle receptor organ - SR1 sensory neuron of MR1 - TEA tetraethylammonium - TTX tetrodotoxin     

UV microirradiation implicates F-actin in reinforcing growing hyphal tips

Summary The cell walls of plants and fungi are thought to provide the strength required to resist turgor and thus maintain the integrity and morphology of these cells. However, during growth, walls must undergo rapid expansion which requires them to be plastic and therefore weak. In most tip-growing cells there is an apical concentration of F-actin associated with the rapidly expanding cell wall. Disruption of F-actin in the growing tips of hyphae ofSaprolegnia ferax by a localized irradiation, beginning 2–6 m behind the apex, with actin-selective 270 nm uv light caused the hyphae to burst, suggesting that actin supports the weak apical wall against turgor pressure. Bursting was pH dependent and Ca²⁺ independent at neutral pH. Hyphae burst in the very tip, where the cell wall is expected to be weakest and actin is most concentrated, as opposed to the lower part of the apical taper where osmotic shock induces bursting when actin is intact. When hyphae were irradiated with a wavelength of light that is less effective at disrupting actin, growth was slowed but they failed to burst, demonstrating that bursting was most likely due to F-actin damage. We conclude that F-actin reinforces the expanding apical wall in growing hyphae and may be the prime stress bearing structure resisting turgor pressure in tip growing cells.Abbreviations RP rhodamine phalloidin - F-actin filamentous actin - EGTA ethylene-glycol-bis-(-amino-ethyl ether) N,N-tetra-acetic acid - PIPES piperazine-N,N-bis-(2-ethanesulfonic acid) - uv ultraviolet     

在大鼠受损坐骨神经上由藜芦碱诱发的抛物线簇放电

在大鼠受损坐骨神经上加入 5 μmol L藜芦碱溶液 ,观察到了抛物线簇放电的现象。根据Plant模型 ,发生抛物线簇放电的前提条件必须有两个慢变量所支配的慢振荡过程。结合实验模型 ,从离子通道活动的角度揭示了抛物线簇放电发生的生物物理机制。由藜芦碱诱发的慢变钠内流和钙依赖钾外流被认为是引发实验所观察到的抛物线簇放电的两个慢变量。进而阐明了藜芦碱引起这一放电形式所起的作用 ,即抑制钠通道失活引发慢变钠内流。这种利用非线性动力学理论的分析方法可能会为分析药物的药物动力学提供一种新的途径。     

Enhancer Histone Acetylation Modulates Transcriptional Bursting Dynamics of Neuronal Activity-Inducible Genes

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The role of extracellular potassium dynamics in the different stages of ictal bursting and spreading depression: A computational study

Experimental evidences point out the participation of nonsynaptic mechanisms (e.g., fluctuations in extracellular ions) in epileptiform bursting and spreading depression (SD). During these abnormal oscillatory patterns, it is observed an increase of extracellular potassium concentration [K⁺]_o and a decrease of extracellular calcium concentration [Ca²⁺]_o which raises the neuronal excitability. However, whether the high [K⁺]_o triggers and propagates these abnormal neuronal activities or plays a secondary role into this process is unclear. To better understand the influence of extracellular potassium dynamics in these oscillatory patterns, the experimental conditions of high [K⁺]_o and zero [Ca²⁺]_o were replicated in an extended Golomb model where we added important regulatory mechanisms of ion concentration as Na⁺-K⁺ pump, ion diffusion and glial buffering. Within these conditions, simulations of the cell model exhibit seizure-like discharges (ictal bursting). The SD was elicited by the interruption of the Na⁺−K⁺ pump activity, mimicking the effect of cellular hypoxia (an experimental protocol to elicit SD, the hypoxia-induced SD). We used the bifurcation theory and the fast-slow method to analyze the interference of K⁺ dynamics in the cellular excitability. This analysis indicates that the system loses its stability at a high [K⁺]_o, transiting to an elevated state of neuronal excitability. Effects of high [K⁺]_o are observed in different stages of ictal bursting and SD. In the initial stage, the increase of [K⁺]_o creates favorable conditions to trigger both oscillatory patterns. During the neuronal activity, a continuous growth of [K⁺]_o by outward K⁺ flow depresses K⁺ currents in a positive feedback way. At the last stage, due to the depression of K⁺ currents, the Na⁺-K⁺ pump is the main mechanism in the end of neuronal activity. Thus, this work suggests that [K⁺]_o dynamics may play a fundamental role in these abnormal oscillatory patterns.