Merck
CN
  • Daikenchuto, a traditional Japanese herbal medicine, ameliorates postoperative ileus by anti-inflammatory action through nicotinic acetylcholine receptors.

Daikenchuto, a traditional Japanese herbal medicine, ameliorates postoperative ileus by anti-inflammatory action through nicotinic acetylcholine receptors.

Journal of gastroenterology (2013-07-13)
Mari Endo, Masatoshi Hori, Hiroshi Ozaki, Tetsuro Oikawa, Toshihiko Hanawa
摘要

Daikenchuto (DKT), a gastrointestinal prokinetic Japanese herbal medicine, is prescribed for patients with postoperative ileus (POI) and adhesive bowel obstruction following abdominal surgery. Several mechanisms for the amelioration of POI by DKT have been suggested; however, it has remained unclear whether DKT shows anti-inflammatory effects in POI. In the present study, we investigated the effects of DKT in a mouse POI model and attempted to clarify the detailed mechanisms of action. Intestinal manipulation (IM) was applied to the distal ileum of mice. DKT was administered orally to the animals 4 times before and after IM. Gastrointestinal transit in vivo, leukocyte infiltration, cytokine mRNA expression and gastrointestinal motility were analyzed. We also investigated the effects of the α7nAChR antagonist methyllycaconitine citrate (MLA) on the DKT-mediated ameliorative action against POI, and we studied the effects of DKT on inflammatory activity in α7nAChR knockout mice. DKT treatment led to recovery of the delayed intestinal transit induced by IM. DKT significantly inhibited the infiltration of neutrophils and CD68-positive macrophages, and inhibited mRNA expressions of TNF-α and MCP-1. MLA significantly reduced the anti-inflammatory action of DKT, and the amelioration of macrophage infiltration by DKT was partially suppressed in α7nAChR knockout mice. In conclusion, in addition to the gastrointestinal prokinetic action, DKT serves as a novel therapeutic agent for POI characterized by its anti-inflammatory potency. The DKT-induced anti-inflammatory activity may be partly mediated by activation of α7nAChR.

材料
货号
品牌
产品描述

Sigma-Aldrich
乙酸钠, anhydrous, ReagentPlus®, ≥99.0%
Sigma-Aldrich
乙酸钠, anhydrous, for molecular biology, ≥99%
Sigma-Aldrich
乙酸钠, ACS reagent, ≥99.0%
Sigma-Aldrich
乙酸钠, puriss. p.a., ACS reagent, reag. Ph. Eur., anhydrous
Sigma-Aldrich
乙酸钠, >99%, FG
Sigma-Aldrich
乙酸钠 溶液, BioUltra, for molecular biology, ~3 M in H2O
Sigma-Aldrich
乙酸钠, anhydrous, BioUltra, for luminescence, for molecular biology, ≥99.0% (NT)
Sigma-Aldrich
乙酸钠, 99.995% trace metals basis
Sigma-Aldrich
乙酸钠, powder, BioReagent, suitable for electrophoresis, suitable for cell culture, suitable for insect cell culture, ≥99%
Sigma-Aldrich
乙酸钠, anhydrous, free-flowing, Redi-Dri, ACS reagent, ≥99.0%
Sigma-Aldrich
乙酸钠, meets USP testing specifications, anhydrous
Sigma-Aldrich
乙酸钠, BioXtra, ≥99.0%
异氟醚, European Pharmacopoeia (EP) Reference Standard
USP
乙酸钠, United States Pharmacopeia (USP) Reference Standard
Sigma-Aldrich
乙酸钠, Vetec, reagent grade, 98%