Andersson P, Bergstrand H
Br J Pharmacol. 1981 Nov;74(3):601-9. doi: 10.1111/j.1476-5381.1981.tb10470.x.
1 The effects of long-term treatment with sodium cromoglycate (SCG) and aminophylline on antigen-induced bronchoconstriction have been studied in guinea-pigs actively sensitized according to two different regimens (one producing IgE- and IgG-like antibodies and the other producing exclusively IgG-like antibodies). 2 Treatment for three weeks with SCG (10 mg/kg) and aminophylline (10, 30 or 60 mg/kg) led to a decreased bronchial response capacity which persisted even three days after treatment ceased. In this respect SCG was effective only in guinea-pigs sensitized to produce at least partly IgE-like antibodies; aminophylline was effective in guinea-pigs sensitized to produce both IgE and/or IgG antibodies. 3 The results in vivo with SCG were reflected in vitro by a reduced capacity of chopped lung tissue to release histamine at antigen challenge; lungs from animals treated with aminophylline did not show reduced histamine releasing capacity. 4 Acute treatment with atropine was shown to reduce significantly the antigen-induced bronchial contraction in guinea-pigs sensitized to produce both IgE- and IgG-antibodies. No effect of atropine was seen on an IgG-mediated anaphylaxis. 5 Increased reactivity to methacholine but not to histamine was seen in guinea-pigs sensitized to produce both IgG- and IgE-antibodies. Long-term treatment with SCG did not affect this hyperreactivity to methacholine. 6 Decreased reactivity to isoprenaline was found in isolated tracheae taken from guinea-pigs sensitized to produce both IgE- and IgG-like antibodies compared to unsensitized guinea-pigs. Long-term treatment with SCG, but not with aminophylline, reversed this decreased reactivity.
已在豚鼠身上研究了色甘酸钠(SCG)和氨茶碱长期治疗对抗原诱导的支气管收缩的影响,这些豚鼠按照两种不同方案进行主动致敏(一种产生IgE和IgG样抗体,另一种仅产生IgG样抗体)。
用SCG(10mg/kg)和氨茶碱(10、30或60mg/kg)治疗三周导致支气管反应能力下降,即使在治疗停止三天后仍持续存在。在这方面,SCG仅对致敏产生至少部分IgE样抗体的豚鼠有效;氨茶碱对致敏产生IgE和/或IgG抗体的豚鼠有效。
SCG的体内结果在体外表现为切碎的肺组织在抗原攻击时释放组胺的能力降低;用氨茶碱治疗的动物的肺未显示组胺释放能力降低。
已表明,对致敏产生IgE和IgG抗体的豚鼠,阿托品急性治疗可显著降低抗原诱导的支气管收缩。未观察到阿托品对IgG介导的过敏反应有影响。
在致敏产生IgG和IgE抗体的豚鼠中,观察到对乙酰甲胆碱的反应性增加,但对组胺的反应性未增加。SCG长期治疗不影响对乙酰甲胆碱的这种高反应性。
与未致敏的豚鼠相比,从致敏产生IgE和IgG样抗体的豚鼠分离的气管中发现对异丙肾上腺素的反应性降低。SCG长期治疗可逆转这种降低的反应性,但氨茶碱不能。