Lack of association between atopic asthma and polymorphisms of the histamine H1 receptor, histamine H2 receptor, and histamine N-methyltransferase genes

被引:28
作者
Sasaki, Y
Ihara, K
Ahmed, S
Yamawaki, K
Kusuhara, K
Nakayama, H
Nishima, S
Hara, T
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 8128582, Japan
[2] Beppu Natl Hosp, Dept Pediat, Oita, Japan
[3] Natl Minami Fukuoka Chest Hosp, Fukuoka, Japan
关键词
histamine H1 receptor; histamine H2 receptor; histamine N-methyltransferase; polymorphism; atopic asthma;
D O I
10.1007/s002510050037
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Histamine functions as one of the major mediators in allergic diseases such as rhinitis, asthma, urticaria, and anaphylaxis when released from mast cells and basophils after cross-linking surface-bound IgE by allergen, The effects of histamine are mediated through three types of receptors, the H1 receptor (HRH1), H2 receptor (HRH2) and H3 receptor (Hill 1990). HRH1 mediates the proinflammatory actions of histamine in the cytokine release and adhesion process (Bachert 1998; Banu and Watanabe 1999), while HRH2 suppresses the production of the Th1-inducing cytokine interleukin-12, resulting in a shift of the Th1/Th2 balance toward Th2 dominance (van der Pouw Kraan et al. 1998). Furthermore, a linkage study identified Chromosome 3p25, where HRH1 is localized, as a candidate gene region for atopy in the Japanese population (Yokouchi et al. 1999).
引用
收藏
页码:238 / 240
页数:3
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