Safko M J, Chan S C, Cooper K D, Hanifin J M
J Allergy Clin Immunol. 1981 Sep;68(3):218-25. doi: 10.1016/0091-6749(81)90187-1.
Studies of mononuclear leukocytes from patients with atopic dermatitis showed depressed cyclic AMP (cAMP) responses after exposure to isoproterenol, histamine, and prostaglandin E1. Because plasma and tissue histamine levels are elevated in atopic dermatitis, we questioned whether histamine or other mediators might be responsible for cAMP abnormalities. We found that exposure of normal cells to low (10(-6)M) concentrations of histamine, isoproterenol, or prostaglandin E desensitized the cells to subsequent stimulatory concentrations of any of the agonists. This heterologous desensitization occurred within 15 min and persisted for days, with gradual recovery of cAMP responses roughly paralleling those of cells from patients with atopic dermatitis. These findings provide a possible explanation for Szentivanyi's beta adrenergic blockade theory and the depressed leukocyte cAMP response to multiple agonists in atopy.
对特应性皮炎患者的单核白细胞研究显示,在暴露于异丙肾上腺素、组胺和前列腺素E1后,其环磷酸腺苷(cAMP)反应受到抑制。由于特应性皮炎患者血浆和组织中的组胺水平升高,我们质疑组胺或其他介质是否可能是cAMP异常的原因。我们发现,将正常细胞暴露于低浓度(10⁻⁶M)的组胺、异丙肾上腺素或前列腺素E中,会使细胞对随后任何一种激动剂的刺激浓度产生脱敏作用。这种异源脱敏在15分钟内发生,并持续数天,cAMP反应逐渐恢复,大致与特应性皮炎患者的细胞相似。这些发现为森蒂瓦尼的β肾上腺素能阻滞理论以及特应性中白细胞对多种激动剂的cAMP反应降低提供了一种可能的解释。