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[吡哆醇对大鼠肥大细胞组胺释放和脱颗粒的影响]

[Effect of pyridoxine on histamine liberation and degranulation of rat mast cells].

作者信息

Garcia M, González R

出版信息

Allergol Immunopathol (Madr). 1979 Nov-Dec;7(6):427-32.

PMID:94242
Abstract

Pyridoxine, one of the B vitamins, has been shown to be useful in the treatment of childhood bronchial asthma by Collip et al. (1975). A double-blind study with 76 asthmatic children followed for five months indicated significant improvement in asthma following pyridoxine therapy (200 mg daily) and a reduction in dosage of bronchodilators and cortisone. Other reports have shown that nicotinamide, another B vitamin shows inhibitory activity in rat mast cell degranulation and histamine release (Bekier et al. 1974, Wiczolkowska and Maslinski, 1975, 1976). These results induced us to investigate if pyridoxine, like nicotinamide or disodium cromoglycate, exhibits pharmacological inhibitory activity in rat mast cell degranulation and histamine release induced by antigen or other non-immunological stimulants. We found that pyridoxine at concentrations of 10 (-3) M, or greater significantly inhibited rat mast cell degranulation and histamine release induced by phospholipase A, compound 48/80, antigen (egg albumin) or a mixture of dextran and phosphatidyl serine, respectively. In these experimental models, pyridoxine shows a pharmacological profile similar to nicotinamide and disodium cromoglycate, although weaker than the latter. In spite of this, the lack of toxicity of this vitamin at relatively high doses (1 or 1.5 g), the possibility that other mechanisms of action may be involved, such as the improvement in tryptophan metabolism reported by Collip following pyridoxine therapy, suggest that this vitamine merits additional research.

摘要

维生素B6是B族维生素之一,Collip等人(1975年)已证明它对儿童支气管哮喘的治疗有效。一项针对76名哮喘儿童进行的为期五个月的双盲研究表明,服用维生素B6(每日200毫克)后哮喘症状有显著改善,支气管扩张剂和可的松的用量减少。其他报告显示,另一种B族维生素烟酰胺对大鼠肥大细胞脱颗粒和组胺释放具有抑制活性(Bekier等人,1974年;Wiczolkowska和Maslinski,1975年、1976年)。这些结果促使我们研究维生素B6是否像烟酰胺或色甘酸钠一样,在抗原或其他非免疫刺激物诱导的大鼠肥大细胞脱颗粒和组胺释放中表现出药理抑制活性。我们发现,浓度为10(-3)M或更高的维生素B6分别显著抑制了磷脂酶A、化合物48/80、抗原(卵清蛋白)或葡聚糖与磷脂酰丝氨酸混合物诱导的大鼠肥大细胞脱颗粒和组胺释放。在这些实验模型中,维生素B6显示出与烟酰胺和色甘酸钠相似的药理特性,尽管比后者弱。尽管如此,这种维生素在相对高剂量(1或1.5克)时缺乏毒性,以及可能涉及其他作用机制,如Collip报道的维生素B6治疗后色氨酸代谢的改善,表明这种维生素值得进一步研究。

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