45-Ca uptake by pinched-off nerve terminals (synaptosomes) of rat brain incubated in standard physiological saline (including 132 mM-Na + 5mM-K + 1-2 mM-Ca) at 30 degrees C averages about 0-5 mumole Ca per g protein per minute. This may be equivalent to a Ca influx of about 0-03 p-mole/cm-2 sec. 2. The rate of 45-Ca uptake is increased when the concentration of K in the medium is increased above 15-20 mM, K replacing Na isosmotically. Maximum stimulation, a three- to six-fold increase in the rate of Ca uptake, occurs when [K]o is about 60 mM. The effect of increased [K]o is reversible. 3. The K-stimulated Ca uptake is associated primarily with the nerve terminal fraction of brain homogenates. The entering Ca is not accompanied by extracellular markers such as mannitol or inulin. Replacement of external chloride by methylsulphate or sulphate does not prevent the stimulation by K. 4. The effects of external K are quantitatively mimicked by Rb. Caesium also stimulates Ca uptake, but is only about one fifth as effective as K or Rb; Li is ineffective. 5. Two other depolarizing agents also stimulate Ca uptake by synaptosomes: veratridine (7-5 times 10- minus 6 to 7-5 times 10- minus 5 M) and scorpion (Leirus quinquestriatus) venom (6-7 times 10- minus 7 to 6-7 times 10- minus g/ml.). The stimulatory effects of veratridine and scorpion venom, but not of increased [K] are blocked by 2 times 10- minus 7 M tetrodotoxin. 6. Internal K also influences the rate of 45-Ca uptake by synaptosomes: lowering [K]i reduces the stimulatory effect of external K and veratridine. 7. Replacement of external Na by choline markedly inhibits the response to veratridine, but has a much smaller effect on the response to increased [K]o. 8. The Ca uptake mechanism has an apparent dissociation constant for Ca (KCa) of about 0-8 mM. Increasing [K]o increases the maximal rate of Ca uptake, but has no effect on KCa. The K-induced 45-Ca uptake is competitively inhibited by Mg-2+, Mn-2+ and La-3+. 9. The release of acetylcholine and noradrenaline was also studied. Increasing [K]o stimulates external Ca-dependent acetylcholine release. Scorpion venom stimulates noradrenaline release from synaptosomes; this effect could be prevented by adding tetrodotoxin or removing external Ca. 10. These results indicate that synaptosomes may increase their permeability to Ca, accumulate Ca and release neural transmitter substances, when stimulated by depolarizing agents under appropriate physiological conditions.
摘要
在30℃下,将大鼠脑的切断神经末梢(突触体)置于标准生理盐水中(含132 mM - Na + 5 mM - K + 1 - 2 mM - Ca)孵育,其对45 - Ca的摄取平均约为每分钟每克蛋白质0 - 5微摩尔钙。这可能相当于约0 - 03皮摩尔/平方厘米·秒的钙内流。2. 当培养基中钾的浓度增加到15 - 20 mM以上,钾等渗替代钠时,45 - Ca的摄取速率增加。当[K]o约为60 mM时,刺激达到最大,钙摄取速率增加三至六倍。[K]o增加的作用是可逆的。3. 钾刺激的钙摄取主要与脑匀浆的神经末梢部分有关。进入的钙不伴有细胞外标记物如甘露醇或菊粉。用甲基硫酸根或硫酸根替代外部氯离子并不能阻止钾的刺激作用。4. 外部钾的作用在数量上可被铷模拟。铯也刺激钙摄取,但效果仅约为钾或铷的五分之一;锂无效。5. 另外两种去极化剂也刺激突触体对钙的摄取:藜芦碱(7.5×10⁻⁶至7.5×10⁻⁵ M)和蝎毒(Leirus quinquestriatus)(6.7×10⁻⁷至6.7×10⁻⁶ g/ml)。藜芦碱和蝎毒的刺激作用,但不是[K]增加的刺激作用,可被2×10⁻⁷ M河豚毒素阻断。6. 内部钾也影响突触体对45 - Ca的摄取速率:降低[K]i会降低外部钾和藜芦碱的刺激作用。7. 用胆碱替代外部钠会显著抑制对藜芦碱的反应,但对[K]o增加的反应影响小得多。8. 钙摄取机制对钙的表观解离常数(KCa)约为0 - 8 mM。增加[K]o会增加钙摄取的最大速率,但对KCa无影响。钾诱导的45 - Ca摄取受到Mg²⁺、Mn²⁺和La³⁺的竞争性抑制。9. 还研究了乙酰胆碱和去甲肾上腺素的释放。增加[K]o刺激外部钙依赖性乙酰胆碱释放。蝎毒刺激突触体释放去甲肾上腺素;添加河豚毒素或去除外部钙可阻止这种作用。10. 这些结果表明,在适当的生理条件下,当受到去极化剂刺激时,突触体可能会增加其对钙的通透性,积累钙并释放神经递质物质。