1. Academic Validation
  2. Maackiain is a novel antiallergic compound that suppresses transcriptional upregulation of the histamine H1 receptor and interleukin-4 genes

Maackiain is a novel antiallergic compound that suppresses transcriptional upregulation of the histamine H1 receptor and interleukin-4 genes

  • Pharmacol Res Perspect. 2015 Oct;3(5):e00166. doi: 10.1002/prp2.166.
Hiroyuki Mizuguchi 1 Yuki Nariai 1 Shuhei Kato 1 Tomohiro Nakano 1 Tomoyo Kanayama 1 Yoshiki Kashiwada 2 Hisao Nemoto 3 Kazuyoshi Kawazoe 4 Yoshihisa Takaishi 2 Yoshiaki Kitamura 5 Noriaki Takeda 5 Hiroyuki Fukui 6
Affiliations

Affiliations

  • 1 Department of Molecular Pharmacology, Institute of Biomedical Sciences, Tokushima University Graduate School 1-78-1 Sho-machi, Tokushima, 770-8505, Japan.
  • 2 Department of Pharmacognosy, Institute of Biomedical Sciences, Tokushima University Graduate School 1-78-1 Sho-machi, Tokushima, 770-8505, Japan.
  • 3 Department of Pharmaceutical Chemistry, Institute of Biomedical Sciences, Tokushima University Graduate School 1-78-1 Sho-machi, Tokushima, 770-8505, Japan.
  • 4 Department of Clinical Pharmacy, Institute of Biomedical Sciences, Tokushima Tokushima University Graduate School 3-18-15 Kuramoto, Tokushima, 770-8503, Japan.
  • 5 Department of Otolaryngology, Institute of Biomedical Sciences, Tokushima University Graduate School 3-18-15 Kuramoto, Tokushima, 770-8503, Japan.
  • 6 Department of Molecular Studies for Incurable Diseases, Institute of Biomedical Sciences, Tokushima University Graduate School 3-18-15 Kuramoto, Tokushima, 770-8503, Japan.
Abstract

Kujin contains antiallergic compounds that inhibit upregulation of histamine H1 receptor (H1R) and interleukin (IL)-4 gene expression. However, the underlying mechanism remains unknown. We sought to identify a Kujin-derived antiallergic compound and investigate its mechanism of action. The H1R and IL-4 mRNA levels were determined by real-time quantitative RT-PCR. To investigate the effects of maackiain in vivo, toluene-2,4-diisocyanate (TDI)-sensitized rats were used as a nasal hypersensitivity animal model. We identified (-)-maackiain as the responsible component. Synthetic maackiain showed stereoselectivity for the suppression of IL-4 gene expression but not for H1R gene expression, suggesting distinct target proteins for transcriptional signaling. (-)-Maackiain inhibited of PKCδ translocation to the Golgi and phosphorylation of Tyr(311) on PKCδ, which led to the suppression of H1R gene transcription. However, (-)-maackiain did not show any antioxidant activity or inhibition of PKCδ enzymatic activity per se. Pretreatment with maackiain alleviated nasal symptoms and suppressed TDI-induced upregulations of H1R and IL-4 gene expressions in TDI-sensitized rats. These data suggest that (-)-maackiain is a novel antiallergic compound that alleviates nasal symptoms in TDI-sensitized allergy model rats through the inhibition of H1R and IL-4 gene expression. The molecular mechanism underlying its suppressive effect for H1R gene expression is mediated by the inhibition of PKCδ activation.

Keywords

Allergic disease sensitive gene; IL-4 gene; Kujin; PKC δ; histamine H1 receptor gene; maackiain.

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