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钠对体外分离神经末梢中钙通量的影响。

The influence of sodium on calcium fluxes in pinched-off nerve terminals in vitro.

作者信息

Blaustein M P, Oborn C J

出版信息

J Physiol. 1975 Jun;247(3):657-86. doi: 10.1113/jphysiol.1975.sp010951.

Abstract
  1. The influence of internal and external Na concentrations on Ca movements have been measured in pinch-off presynaptic nerve terminals (synaptosomes). Ca uptake is enhanced when external Na (Nao) is replaced by Li, choline or dextrose, in Na-loaded synaptosomes. Depletion of internal Na (Nai) abolishes the stimulatory effect of external Na removal. 2. Ca uptake from Na-depleted media is proportional to [Na]i -2, and averages about 1-5 mumole Ca/g synaptosome protein per minute when [Na]i is approximately 137 mM. This may correspond to a Ca influx of about 0-1 p-mole/cm-2 sec. 3. External Na is a competitive inhibitor of the Nai-dependent Ca uptake. The interrelationship between [Na]o, [Ca]o and Ca uptake indicate that two external Na ions may compete with one Ca at each uptake site. 4. The distribution of particles with Nai-dependent Ca uptake activity parallels the distribution of synaptosomes in the preparative sucrose gradient. Thus, this Ca uptake activity is probably a property of the pinched-off nerve terminals per se, and not of the mitochondria which may contaminate the synaptosome fraction. 5. The Nai-dependent Ca uptake mechanism requires an intact surface membrane, since synaptosomes subjected to osmotic lysis lose the ability to accumulate Ca by this route. 6. Ca efflux into Ca-free media is largely dependent upon the presence of external Na. The curve relating Ca efflux to [Na]o is sigmoid, and suggests that more than one external Na ion (perhaps 2 or 3) is needed to activate the efflux of each Ca ion. 7. The net Ca gain exhibited by Na-loaded synaptosomes incubated in Na-depleted media can be accounted for by the increased Ca uptake and decreased Ca loss observed under these conditions. 8. Treatment of synaptosomes with cyanide or 2,4-dinitrophenol decreases Ca uptake and enhances Ca efflux into Na-containing media. This results in a net loss of Ca from the terminals, even in the presence of external Ca. 9. In contrast to the Ca efflux from synaptosomes, the Ca efflux from brain mitochondria is not dependent upon external Na, and is reduced by succinate, a substrate which is known to fuel mitochondrial respiration. 10. The temperature coefficient (Q10) of the Nai-dependent Ca uptake is about 3. 11. The Nai-dependent Ca uptake is reduced at low pH. The relationship between this Ca uptake and pH approximates a titration curve with a pKa of about 5-6. 12. The data indicate that Ca transport in rat brain presynaptic terminals may involve a carrier-mediated Na-Ca exchange mechanism, and that some of the energy required for Ca extrusion may come from the Na electrochemical gradient across the surface membranes.
摘要
  1. 已在钳断的突触前神经末梢(突触体)中测量了细胞内外钠离子浓度对钙离子转运的影响。在钠离子负载的突触体中,当细胞外钠(Nao)被锂、胆碱或葡萄糖替代时,钙离子摄取增强。细胞内钠(Nai)的耗尽消除了细胞外钠去除的刺激作用。2. 从低钠培养基中摄取钙离子与[Nai] -2成正比,当[Nai]约为137 mM时,平均每分钟每克突触体蛋白摄取约1 - 5微摩尔钙离子。这可能对应于约0 - 1皮摩尔/平方厘米·秒的钙离子内流。3. 细胞外钠是Nai依赖性钙离子摄取的竞争性抑制剂。[Na]o、[Ca]o与钙离子摄取之间的相互关系表明,在每个摄取位点,两个细胞外钠离子可能与一个钙离子竞争。4. 具有Nai依赖性钙离子摄取活性的颗粒分布与制备蔗糖梯度中突触体的分布平行。因此,这种钙离子摄取活性可能本身就是钳断神经末梢的特性,而不是可能污染突触体组分的线粒体的特性。5. Nai依赖性钙离子摄取机制需要完整的表面膜,因为经历渗透裂解的突触体失去了通过该途径积累钙离子的能力。6. 钙离子向无钙培养基中的外流在很大程度上取决于细胞外钠的存在。钙离子外流与[Na]o的关系曲线呈S形,表明激活每个钙离子外流可能需要不止一个细胞外钠离子(可能2或3个)。7. 在低钠培养基中孵育的钠离子负载突触体所表现出的净钙离子增加可以由在这些条件下观察到的钙离子摄取增加和钙离子损失减少来解释。8. 用氰化物或2,4 -二硝基苯酚处理突触体可降低钙离子摄取并增强钙离子向含钠培养基中的外流。这导致即使在存在细胞外钙的情况下,末梢中的钙离子也会净损失。9. 与突触体中的钙离子外流不同,脑线粒体中的钙离子外流不依赖于细胞外钠,并且已知作为线粒体呼吸燃料的琥珀酸可使其减少。10. Nai依赖性钙离子摄取的温度系数(Q10)约为3。11. Nai依赖性钙离子摄取在低pH下降低。这种钙离子摄取与pH之间的关系近似于pKa约为5 - 6的滴定曲线。12. 数据表明,大鼠脑突触前末梢中的钙离子转运可能涉及载体介导的钠 - 钙交换机制,并且钙离子外流所需的一些能量可能来自跨表面膜的钠电化学梯度。

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