Chakravarty N
Agents Actions. 1985 Apr;16(3-4):133-7. doi: 10.1007/BF01983120.
The glycogen content of rat peritoneal mast cells (mean: 3 nmoles/10(6) cells) was increased 15% by incubation with glucose (1 mM) and reduced 35% when incubated without glucose at 37 degrees C for 15 min. The storage capacity for glycogen is thus low. Lactate production at 37 degrees C in a substrate-free medium was low (2.5-6.3 nmoles/10(6) cells in 40 min), but was stimulated 5-fold in the aerobic medium and 10-15 fold in the anaerobic medium by glucose. Both aerobic and anaerobic glycolysis in presence of glucose can thus provide energy for histamine secretion. The initial enzymes of the pentose phosphate pathway, glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase, have been demonstrated in mast cells. The enzyme activity in mast cells was, however, low compared to the high activity in the other peritoneal cells. The extent of the pentose cycle activity was determined from the conversion of 14C1- and 14C6-glucose to 14CO2, expressing the specific 14CO2 yields as fractions of the total glucose utilization. The normal pentose cycle activity with 1 mM glucose was 0.4% of the glucose metabolism. This was remarkably simulated by an electron acceptor, phenazine methosulfate. The pentose cycle was enhanced to 0.71% (80% stimulation) after exposure of the mast cells to compound 48/80, causing 68% histamine release. The stimulation of the pentose cycle by compound 48/80 seems to be due to the enhancement of biosynthetic processes during the regenerative phase.(ABSTRACT TRUNCATED AT 250 WORDS)
大鼠腹膜肥大细胞的糖原含量(平均:3 纳摩尔/10⁶ 个细胞)在与 1 毫摩尔葡萄糖一起孵育时增加了 15%,而在 37℃无葡萄糖孵育 15 分钟后减少了 35%。因此,糖原的储存能力较低。在无底物培养基中 37℃时乳酸生成量较低(40 分钟内为 2.5 - 6.3 纳摩尔/10⁶ 个细胞),但在有氧培养基中葡萄糖可使其刺激 5 倍,在厌氧培养基中刺激 10 - 15 倍。因此,在有葡萄糖存在时,有氧和无氧糖酵解都可为组胺分泌提供能量。已在肥大细胞中证实了磷酸戊糖途径的起始酶,即葡萄糖 -6-磷酸脱氢酶和 6-磷酸葡萄糖酸脱氢酶。然而,与其他腹膜细胞中的高活性相比,肥大细胞中的酶活性较低。通过将¹⁴C1-和¹⁴C6-葡萄糖转化为¹⁴CO₂来确定戊糖循环活性的程度,将特定的¹⁴CO₂产量表示为总葡萄糖利用量的分数。1 毫摩尔葡萄糖时的正常戊糖循环活性为葡萄糖代谢的 0.4%。这被电子受体硫酸吩嗪显著模拟。在肥大细胞暴露于化合物 48/80 导致 68%组胺释放后,戊糖循环增强至 0.71%(刺激 80%)。化合物 48/80 对戊糖循环的刺激似乎是由于再生阶段生物合成过程的增强。(摘要截短于 250 字)