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雌二醇增强而他莫昔芬抑制大鼠肥大细胞的分泌。

Estradiol augments while tamoxifen inhibits rat mast cell secretion.

作者信息

Vliagoftis H, Dimitriadou V, Boucher W, Rozniecki J J, Correia I, Raam S, Theoharides T C

机构信息

Department of Pharmacology and Experimental Therapeutics, Tufts University School of Medicine, New England Medical Center, Boston, Mass 02111.

出版信息

Int Arch Allergy Immunol. 1992;98(4):398-409. doi: 10.1159/000236217.

Abstract

Mast cells have been studied extensively for their involvement in allergic reactions, where they secrete numerous powerful mediators in response to immunoglobulin E and specific antigens. However, they are also triggered by neuropeptides, they have been found in close contact with neurons, and they are activated in diseases such as angioedema, interstitial cystitis and irritable bowel disease, the prevalence of which is much higher in women. When tested on purified rat peritoneal mast cells, 17 beta-estradiol augmented secretion of histamine and serotonin, starting at 1 microM and in a dose-dependent manner, whether stimulated by the mast cell secretagogue compound 48/80 or the neuropeptide substance P. However, 17 beta-estradiol did not augment mast cell secretion stimulated by immunoglobulin E and specific antiserum indicating that immunologic stimulation is under different regulation. Testosterone inhibited secretion induced by compound 48/80. Tamoxifen, an estrogen receptor antagonist used in the treatment of breast cancer, inhibited serotonin and histamine release from purified rat peritoneal mast cells triggered by compound 48/80 or substance P. Tamoxifen also inhibited the increase in intracellular free Ca2+ originating from an influx of extracellular Ca2+ in response to compound 48/80. Moreover, tamoxifen antagonized the synergistic effect of phorbol myristate and the cation ionophore A23187 on mast cell secretion, suggesting that tamoxifen's inhibition may be due to regulation of protein kinase C activity. Tamoxifen may, therefore, have a beneficial effect in other neuroimmunoendocrine disorders both through estrogen receptor blockade and inhibition of mast cell secretion.

摘要

肥大细胞因其参与过敏反应而受到广泛研究,在过敏反应中,它们会响应免疫球蛋白E和特定抗原来分泌多种强效介质。然而,它们也会被神经肽触发,已发现它们与神经元密切接触,并且在诸如血管性水肿、间质性膀胱炎和肠易激综合征等疾病中被激活,这些疾病在女性中的患病率要高得多。在纯化的大鼠腹膜肥大细胞上进行测试时,17β-雌二醇会增加组胺和5-羟色胺的分泌,从1微摩尔开始且呈剂量依赖性,无论其是由肥大细胞促分泌剂化合物48/80还是神经肽P物质刺激。然而,17β-雌二醇不会增加由免疫球蛋白E和特异性抗血清刺激的肥大细胞分泌,这表明免疫刺激受不同的调节。睾酮抑制化合物48/80诱导的分泌。他莫昔芬是一种用于治疗乳腺癌的雌激素受体拮抗剂,它抑制由化合物48/80或P物质触发的纯化大鼠腹膜肥大细胞释放5-羟色胺和组胺。他莫昔芬还抑制因化合物48/80导致的细胞外Ca2+内流引起的细胞内游离Ca2+增加。此外,他莫昔芬拮抗佛波醇肉豆蔻酸酯和阳离子离子载体A23187对肥大细胞分泌的协同作用,这表明他莫昔芬的抑制作用可能是由于对蛋白激酶C活性的调节。因此,他莫昔芬可能通过阻断雌激素受体和抑制肥大细胞分泌,在其他神经免疫内分泌疾病中发挥有益作用。

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