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Antihistamines suppress upregulation of histidine decarboxylase gene expression with potencies different from their binding affinities for histamine H1 receptor in toluene 2,4-diisocyanate-sensitized rats

机译：抗组胺药抑制组氨酸脱羧酶基因表达的上调，其效力不同于对甲苯2,4-二异氰酸酯致敏的大鼠中组胺H1受体的结合亲和力

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Mizuguchi Hiroyuki; Das Asish K.; Maeyama Kazutaka; Dev Shrabanti; Shahriar Masum; Kitamura Yoshiaki; Takeda Noriaki; Fukui Hiroyuki;
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1. Repeated pre-treatment with antihistamines causes transcriptional up-regulations of histamine H(1) receptor and interleukin-4 genes in toluene-2,4-diisocyanate-sensitized rats. [J] . Mizuguchi H, Hatano M, Matsushita C, Journal of pharmacological sciences. . 2008,第4期

机译：反复用抗组胺药预处理会导致甲苯2,4-二异氰酸酯致敏大鼠中组胺H（1）受体和白细胞介素4基因的转录上调。
2. Suplatast Tosilate Inhibits Histamine Signaling by Direct and Indirect Down-Regulation of Histamine H1 Receptor Gene Expression through Suppression of Histidine Decarboxylase and IL-4 Gene Transcriptions [J] . Masum Shahriar, Hiroyuki Mizuguchi, Kazutaka Maeyama, The journal of immunology . 2009,第3期

机译：Suplatast Tosilate通过组氨酸脱羧酶和IL-4基因转录的抑制，通过直接和间接下调组胺H1受体基因表达来抑制组胺信号传导。
3. Suplatast tosilate inhibits histamine signaling by direct and indirect down-regulation of histamine H1 receptor gene expression through suppression of histidine decarboxylase and IL-4 gene transcriptions. [J] . Shahriar M, Mizuguchi H, Maeyama K The Journal of Immunology: Official Journal of the American Association of Immunologists . 2009,第3期

机译：Suplatast Tosilate通过抑制组氨酸脱羧酶和IL-4基因转录，通过直接和间接下调组胺H1受体基因表达来抑制组胺信号传导。
4. Pharmacodynamics of Latest Generation H_1.Antihistamines: Relevance of Drug Concentrations at Receptor Sites and of Affinity Values for H_1 Receptors [C] . M. Strolin Benedetti, M. Gillard, N. Frossard, Collegium Internationale Allergologicum . 2007

机译：最新一代H_1的药效学.AntiHistamines：H_1受体的受体位点和亲和力值的相关性的相关性
5. Synthesis, histamine H1 receptor pharmacology, and quantitative structure-affinity analysis of 2-dimethylamino-5-phenyl-1,2,3,4-tetrahydronaphthalenes. [D] . Legere, Jacqueline Anne. 2004

机译：2-二甲基氨基-5-苯基-1,2,3,4-四氢萘的合成，组胺H1受体药理学和定量结构亲和力分析。
6. Histamine H1 receptors on adherent rheumatoid synovial cells in culture: demonstration by radioligand binding and inhibition of histamine-stimulated prostaglandin E production by histamine H1 antagonists. [O] . D J Taylor, D E Woolley 1987

机译：培养的类风湿性滑膜细胞上的组胺H1受体：通过放射性配体结合和组胺H1拮抗剂抑制组胺刺激的前列腺素E产生来证明。
7. Antihistamines suppress upregulation of histidine decarboxylase gene expression with potencies different from their binding affinities for histamine H1 receptor in toluene 2,4-diisocyanate-sensitized rats [O] . Hiroyuki Mizuguchi, Asish K. Das, Kazutaka Maeyama, 2016

机译：抗组胺药抑制组氨酸脱羧酶基因表达上调，其效力不同于甲苯2,4-二异氰酸酯致敏大鼠对组胺H1受体的结合亲和力
8. Implication of Prostaglandins and Histamine H1 and H2 Receptors in Radiation-Induced Temperature Responses of Rats [R] . Kandasamy, S. B., Hunt, W. A., Mickley, G. A 1988

机译：前列腺素和组胺H1和H2受体在大鼠辐射诱导的温度反应中的意义

Antihistamines suppress upregulation of histidine decarboxylase gene expression with potencies different from their binding affinities for histamine H1 receptor in toluene 2,4-diisocyanate-sensitized rats

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