Hofman J, Chyrek-Borowska S
Agents Actions. 1981 Apr;11(1-2):107-9. doi: 10.1007/BF01991473.
The effect of drugs applied in the treatment of allergic diseases such as hydrocortisone and disodium cromoglycate-Intal on the release of histamine during immediate allergic response was investigated. Experiments carried out on guinea-pigs showed that after hydrocortisone administration the blood histamine level fell, whereas the histamine concentration in the lung tissue varied, depending on the time of the drug administration in relation to the antigen challenge. Disodium cromoglycate give before induction of an asthma attack in guinea-pigs lowered the histamine level in the blood and in the lung tissue homogenates. Investigations were also carried out on isolated rat mast cells and human basophils. The stabilizing effect of hydrocortisone was much weaker than that of disodium cromoglycate especially regarding mastocytes. It was found that the extent of histamine release from mastocytes and basophils depends on the concentration of the drugs applied and on the type of antigen used for induction of cell degranulation.
研究了氢化可的松和色甘酸钠(咳乐钠)等用于治疗过敏性疾病的药物对速发型过敏反应期间组胺释放的影响。在豚鼠身上进行的实验表明,给予氢化可的松后,血液中的组胺水平下降,而肺组织中的组胺浓度则有所变化,这取决于给药时间与抗原激发时间的关系。在豚鼠诱发哮喘发作前给予色甘酸钠可降低血液和肺组织匀浆中的组胺水平。还对分离的大鼠肥大细胞和人嗜碱性粒细胞进行了研究。氢化可的松的稳定作用比色甘酸钠弱得多,尤其是对肥大细胞而言。发现肥大细胞和嗜碱性粒细胞释放组胺的程度取决于所用药物的浓度以及用于诱导细胞脱颗粒的抗原类型。