Caldwell-Violich M, Requena J
J Gen Physiol. 1979 Dec;74(6):739-52. doi: 10.1085/jgp.74.6.739.
The Mg content of axons freshly dissected from living specimens of the tropical squid Doryteuthis plei was determined by atomic absorption spectroscopy to be 4.2 +/- 0.2 mmol/kg axoplasm. The axon's ability to maintain this physiological content of total intracellular Mg([Mg]i) was studied. Mgi was shown to be a linear function of Mgo when Mgo of incubating fluid was varied between 0 and 250 mM. When Mgo = 15 mM, Mgi was found to be the same in incubated fibers as in fibers freshly dissected. Mgi levels were unaffected by depolarization of the membrane by high Ko. Stimulation resulted in an extra influx of Mg of 0.05 pmol/(cm2 . impulse) when Mgo = 55 mM. Mgi was found to be a complicated function of the concentration of extracellular Na or Li (Xo), which was substituted for Tris. With 385 mM Lio the Mgi level was found to be 2.5-fold larger than the level observed with 385 mM Nao after incubation for 3 h. The function relating Mgo to Xo was qualitatively unaffected in axons poisoned with the mitochondrial uncoupler carbonyl cyanide, p-trifluorome-thoxy-phenylhydrazone (FCCP) and the inhibitor of glycolysis, iodoacetic acid (IAA); the absolute levels of Mgi, however, were some 30% higher in the poisoned axons at all [X]o explored. 2 h incubation of axons in a 333 mM Mg, 40 mM Li solution increased Mgi 3.5-fold in control axons and 5-fold in poisoned axons. These Mg-loaded axons were able to recover physiological levels of Mgi with a half-time of 3-5 h only if kept in a solution which contained Na (220 mM) regardless of whether the axons had been inhibited with FCCP + IAA. Therefore, it may be concluded that the physiological Mgi concentration can be maintained by the Na electrochemical gradient, even when the axon is metabolically poisoned.
采用原子吸收光谱法测定了从热带鱿鱼杜氏枪乌贼(Doryteuthis plei)活体标本中新鲜分离的轴突的镁含量,结果为4.2±0.2 mmol/kg轴浆。研究了轴突维持这种细胞内总镁([Mg]i)生理含量的能力。当孵育液中的MgO在0至250 mM之间变化时,发现[Mg]i是MgO的线性函数。当MgO = 15 mM时,发现孵育纤维中的[Mg]i与新鲜分离的纤维中的[Mg]i相同。高钾引起的膜去极化不影响[Mg]i水平。当MgO = 55 mM时,刺激导致额外的镁流入量为0.05 pmol/(cm2·冲动)。发现[Mg]i是细胞外钠或锂(Xo)浓度的复杂函数,Xo替代了Tris。孵育3小时后,发现用385 mM LiO时的[Mg]i水平比用385 mM NaO时观察到的水平高2.5倍。在用线粒体解偶联剂羰基氰化物对三氟甲氧基苯腙(FCCP)和糖酵解抑制剂碘乙酸(IAA)中毒的轴突中,MgO与Xo的关系在定性上未受影响;然而,在所有探索的[X]o下,中毒轴突中的[Mg]i绝对水平约高30%。在333 mM Mg、40 mM Li溶液中孵育轴突2小时,对照轴突中的[Mg]i增加3.5倍,中毒轴突中的[Mg]i增加5倍。只有将这些负载镁的轴突保存在含有钠(220 mM)的溶液中,它们才能在3 - 5小时的半衰期内恢复[Mg]i的生理水平,无论轴突是否已被FCCP + IAA抑制。因此,可以得出结论,即使轴突发生代谢中毒,生理[Mg]i浓度也可通过钠电化学梯度维持。