Norn S, Elmgreen J, Stahl Skov P, Holme Jorgensen P, Ankjaergaard N, Hagen Petersen S
Clin Exp Immunol. 1976 Oct;26(1):162-8.
Anaphylaxis in a glucose-free medium containing pyruvate caused a release of histamine and a significant decrease in the ATP level of rat mast cells. The fall was maximal after 10 min and it was found to reverse after 22 min. Glucose completely counteracted the ATP fall without changing the anaphylactic histamine release. Furthermore, the oxidative metabolism of exogenous pyruvate to CO2 was stimulated in the mast cell. A high level of protection of mast cells to antigen challenge was obtained following hyposensitization and only a small amount of the intracellular histamine was released in contrast to non-hyposensitized cells. Hyposensitization counteracted the ATP fall by antigen challenge but the increase in oxidative metabolism remained unchanged. The results indicate that hyposensitization exerts effects in the mast cell consistent with a reduced ATP utilization or with a reduced uncoupling of oxidative phosphorylation. The mechanism of the hyposensitization must be due to inhibition of one or more of the cellular steps leading to histamine release and subsequent morphological changes of the cell or to uncoupling of oxidative phosphorylation.
在含有丙酮酸的无葡萄糖培养基中发生过敏反应,会导致大鼠肥大细胞释放组胺,且其ATP水平显著降低。ATP水平在10分钟后降至最低,22分钟后开始回升。葡萄糖能完全抵消ATP水平的下降,同时不改变过敏反应性组胺的释放。此外,肥大细胞中外源丙酮酸向二氧化碳的氧化代谢受到刺激。在进行低敏治疗后,肥大细胞对抗原攻击具有高度保护作用,与未进行低敏治疗的细胞相比,只有少量细胞内组胺被释放。低敏治疗可对抗抗原攻击导致的ATP水平下降,但氧化代谢的增加保持不变。结果表明,低敏治疗在肥大细胞中发挥作用,这与ATP利用减少或氧化磷酸化解偶联减少一致。低敏治疗的机制必定是由于抑制了导致组胺释放以及随后细胞形态变化的一个或多个细胞步骤,或者抑制了氧化磷酸化解偶联。