| Literature DB >> 26798038 |
Peng Zhou1,2,3, Xiaodan Yang1,2,3, Xiaoyi Jia1,2,3, Jun Yu1,2,3, James Asenso1,2,3, Feng Xiao1,2,3, Chun Wang4,5,6, Wei Wei7,8,9.
Abstract
Allergic contact dermatitis (ACD) is a classical experimental model of allergic inflammatory skin disease, which is a delayed-type hypersensitivity reaction that is mediated by hapten-specific T lymphocytes. The goal of this study was to investigate the pharmacokinetic profiles of 6'-acetylpaeoniflorin (6-AP) and the effect of 6-AP on the ACD model. 6-AP was synthesized from paeoniflorin (Pae) via acetylation, and the structure was confirmed. There were statistically significant differences in the pharmacokinetic parameters including t 1/2α , t 1/2β , AUC, MRT and C max among the animals that were orally administered Pae and 6-AP. An ACD model was induced using immunization with dinitrochlorobenzene (DNCB) in BALB/c mice. The mice were orally administered 6-AP (35, 70 and 140 mg/kg/d), Pae (70 mg/kg/d) and prednisone (Pre, 5 mg/kg/d) from day 1 to day 7 after immunization. The results indicated that the topical application of DNCB to the skin provoked obvious inflammatory responses. 6-AP significantly inhibited ear swelling and decreased inflammatory cell infiltration and epidermal keratinization. Additionally, 6-AP observably alleviated the hyperplasia of red pulp and germinal center appearance, decreased the spleen index and inhibited splenocyte proliferation in the ACD model compared to that of Pae. Furthermore, the study indicated that 6-AP could increase the IL-10 level, while simultaneously reducing the IL-17 level in splenocytes. In summary, these results suggest that 6-AP has a significantly higher anti-inflammatory effect than Pae and that 6-AP might be a candidate for the treatment of allergic skin diseases.Entities:
Keywords: 6′-Acetylpaeoniflorin (6-AP); Allergic contact dermatitis (ACD); Anti-inflammatory activity; Paeoniflorin (Pae); Pharmacokinetics
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Year: 2016 PMID: 26798038 DOI: 10.1007/s12026-016-8788-8
Source DB: PubMed Journal: Immunol Res ISSN: 0257-277X Impact factor: 2.829