High-Na tissues exposed to a Na-free solution with dimethyldiethanol ammonium chloride (DDA) or sucrose replacing Na, develop an increase in membrane permeability to small ions and molecules such as Na, K, sucrose and CoEDTA. 2. The increase in permeability only occurs when the Na gradient across the cell membrane is reversed, and is not due to damaging effects of the Na-free solution. It does not occur in normal or high-K tissues, and 15 mM-[Na]0 is enough to prevent the permeability change in high-Na tissues. 3. Tissues with increased permeability maintain high levels of Ca and the increased permeability does not occur in Ca-free solutions, or in solutions containing 5 mM-La3+. The rate of development of membrane leakiness depends on the level of extracellular Ca. 4. Tissues exposed to iodoacetic acid (IAA) and dinitrophenol (DNP) also develop a membrane leakiness, dependent on extracellular Ca and blocked by La3+. 5. The time taken for development of the increase in membrane permeability in metabolically inhibited tissues can be affected by the Na gradient. With no gradient, or a slightly reversed gradient the membrane break-down occurs more rapidly. 6. It is concluded that the increase in permeability is caused by an increase in internal Ca ions, and that the Na gradient as well as the levels of ATP are important in controlling Ca movements. 7. Tension recordings also support the some form of Na--Ca exchange mechanism operating in the taenia, and this mechanism is not completely blocked by La3+ ions, although they suppress the break-down in membrane permeability.
摘要
暴露于用二甲基二乙醇氯化铵(DDA)或蔗糖替代钠的无钠溶液中的高钠组织,其对钠、钾、蔗糖和钴乙二胺四乙酸等小离子和分子的膜通透性会增加。2. 通透性增加仅在跨细胞膜的钠梯度反转时发生,并非无钠溶液的损伤作用所致。在正常或高钾组织中不会发生,且15 mM的[Na]0足以防止高钠组织中的通透性变化。3. 通透性增加的组织维持高水平的钙,且在无钙溶液或含5 mM La3+的溶液中不会发生通透性增加。膜渗漏的发展速率取决于细胞外钙的水平。4. 暴露于碘乙酸(IAA)和二硝基苯酚(DNP)的组织也会出现膜渗漏,这取决于细胞外钙并被La3+阻断。5. 代谢抑制组织中膜通透性增加的发展时间可受钠梯度影响。无梯度或略微反转的梯度时,膜破坏发生得更快。6. 得出的结论是,通透性增加是由细胞内钙离子增加引起的,钠梯度以及ATP水平在控制钙的移动中很重要。7. 张力记录也支持在绦虫中存在某种形式的钠钙交换机制,尽管La3+离子会抑制膜通透性的破坏,但该机制并未被其完全阻断。