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钾离子诱导中枢神经节的运动增加。

Potassium-induced motion increase in a central nervous ganglion.

作者信息

Sattelle D B, Piddington R W

出版信息

J Exp Biol. 1975 Jun;62(3):753-70. doi: 10.1242/jeb.62.3.753.

Abstract
  1. By means of light-beating spectroscopy, a four-fold increase in the modulation of laser light scattered at right angles by a locust (Schistocerca gregaria, Forskål) ganglion is detected when potassium ions replace sodium ions in the Ringer solution. 2. This is interpreted as an increased level of motion of the scattering particles (size 0.3-3.0 mum, if viscosity is taken to be 0.01 poises). 3. The amplitude of the potassium-response is similar at all frequencies in the range 6.3-150 Hz and is reversible on return to normal (Na+) Ringer. 4. Desheathing the ganglion reduces the half-time of the potassium-response by 3-4 times. 5. By means of photon-correlation spectroscopy it was estimated that less than 10% of the tissue contributes to the motion detected. 6. Cyanide (1-2 mM) typically enhances the potassium-response and renders it irreversible, suggesting that the response is thermally rather than metabolically-driven. In addition, the dependence of both the correlation function and the power spectrum on the scattering angle is in the direction predicted for a diffusive process. 7. Cobaltous ions (2-10 mM), which block calcium entry into nerve cells, depress the potassium-response. 8. It is proposed that potassium-depolarization and the resultant calcium entry into the cells causes a partial liquefaction of the cytoplasms which is detected as an increase in the level of Brownian motion. This mechanism could be used in vesicular release or in growth.
摘要
  1. 通过光拍频光谱法,当林格氏液中的钾离子取代钠离子时,检测到蝗虫(飞蝗,福斯科尔)神经节以直角散射的激光光调制增加了四倍。2. 这被解释为散射颗粒(尺寸为0.3 - 3.0微米,假设粘度为0.01泊)的运动水平增加。3. 在6.3 - 150赫兹范围内的所有频率下,钾反应的幅度相似,并且在恢复到正常(钠)林格氏液时是可逆的。4. 去除神经节的鞘膜可使钾反应的半衰期缩短3 - 4倍。5. 通过光子相关光谱法估计,不到10%的组织对检测到的运动有贡献。6. 氰化物(1 - 2毫摩尔)通常会增强钾反应并使其不可逆,这表明该反应是由热驱动而非代谢驱动的。此外,相关函数和功率谱对散射角的依赖性与扩散过程预测的方向一致。7. 钴离子(2 - 10毫摩尔)可阻止钙进入神经细胞,从而抑制钾反应。8. 有人提出,钾去极化以及由此导致的钙进入细胞会引起细胞质的部分液化,这被检测为布朗运动水平的增加。这种机制可用于囊泡释放或生长过程。

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