Literature DB >> 23921373

Inhibitory effects of Diospyros kaki in a model of allergic inflammation: role of cAMP, calcium and nuclear factor-κB.

Hui-Hun Kim1, Duk-Sil Kim, Sung-Wan Kim, Se-Hyun Lim, Dae Keun Kim, Tae-Yong Shin, Sang-Hyun Kim.   

Abstract

Diospyros kaki (D. kaki) has been cultivated throughout Eastern Asia for hundreds of years. D. kaki contains various biological active compounds, such as amino acids, carotenoids, flavonoids, tannins, catechins and vitamin A. Previous studies have shown that D. kaki has beneficial effects on homeostasis, constipation, hypertension, atherosclerosis and allergic dermatitis and is a good source of antioxidants, polyphenols and dietary fiber. However, the anti-allergic and anti-inflammatory effects of D. kaki have not yet been elucidated. This study aimed to investigate the protective effects of the aqueous extract of Diospyros kaki (AEDK) on mast cell-mediated allergic inflammation and to determine its possible mechanisms of action by using in vitro and in vivo mast cell-based models. The cAMP and intracellular calcium levels were measured to clarify the mechanisms by which AEDK inhibits the release of histamine from mast cells. AEDK inhibited the release of histamine and β-hexosaminidase from mast cells by modulating cAMP and intracellular calcium levels. We also measured the expression of pro-inflammatory cytokines, such as tumor necrosis factor (TNF)-α and interleukin (IL)-1β. AEDK decreased gene expression and the secretion of the pro-inflammatory cytokines, TNF-α and IL-1β by inhibiting nuclear factor-κB. In addition, AEDK inhibited systemic and cutaneous allergic reaction. The inhibitory effects of AEDK on allergic reaction and the release of histamine were found to be similar to those of disodium cromoglycate, a known anti-allergic drug. To isolate the active component of AEDK, activity-guided fractionation was performed, based on the inhibitory effects on systemic anaphylaxis. Catechin was identified as an active compound. The present findings provide evidence that AEDK inhibits allergic inflammation and suggest the therapeutic application of AEDK in allergic inflammatory disorders.

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Year:  2013        PMID: 23921373     DOI: 10.3892/ijmm.2013.1465

Source DB:  PubMed          Journal:  Int J Mol Med        ISSN: 1107-3756            Impact factor:   4.101


  7 in total

1.  SG-HQ2 inhibits mast cell-mediated allergic inflammation through suppression of histamine release and pro-inflammatory cytokines.

Authors:  In-Gyu Je; Hui-Hun Kim; Pil-Hoon Park; Taeg Kyu Kwon; Seung-Yong Seo; Tae-Yong Shin; Sang-Hyun Kim
Journal:  Exp Biol Med (Maywood)       Date:  2014-10-27

2.  Diospyros kaki Extract Inhibits Alkali Burn-Induced Corneal Neovascularization.

Authors:  Sung Jae Yang; Hyoung Jo; Kyung-A Kim; Hong Ryul Ahn; Suk Woo Kang; Sang Hoon Jung
Journal:  J Med Food       Date:  2015-09-08       Impact factor: 2.786

3.  Protective effects of curcumin against rat intestinal inflammation‑related motility disorders.

Authors:  Yang Yao; Ranyuan Luo; Shu Xiong; Chang Zhang; Yukun Zhang
Journal:  Mol Med Rep       Date:  2021-03-24       Impact factor: 2.952

4.  The leaves of Diospyros kaki exert beneficial effects on a benzalkonium chloride-induced murine dry eye model.

Authors:  Kyung-A Kim; Lee Chung Hyun; Sang Hoon Jung; Sung Jae Yang
Journal:  Mol Vis       Date:  2016-04-02       Impact factor: 2.367

5.  Study of Antiobesity Effect through Inhibition of Pancreatic Lipase Activity of Diospyros kaki Fruit and Citrus unshiu Peel.

Authors:  Gyo-Nam Kim; Mi-Rae Shin; Sung Ho Shin; Ah Reum Lee; Joo Young Lee; Bu-Il Seo; Min Yeong Kim; Tae Hoon Kim; Jeong Sook Noh; Man Hee Rhee; Seong-Soo Roh
Journal:  Biomed Res Int       Date:  2016-07-27       Impact factor: 3.411

6.  Diospyros kaki calyx inhibits immediate-type hypersensitivity via the reduction of mast cell activation.

Authors:  Min-Jong Kim; Hae Ran Park; Tae-Yong Shin; Sang-Hyun Kim
Journal:  Pharm Biol       Date:  2017-12       Impact factor: 3.503

7.  Anti-cancer potential of persimmon (Diospyros kaki) leaves via the PDGFR-Rac-JNK pathway.

Authors:  Heon-Su Kim; Jung-Soo Suh; Yoon-Kwan Jang; Sang-Hyun Ahn; Ganesan Raja; Jin-Chul Kim; Youngmi Jung; Sang Hoon Jung; Tae-Jin Kim
Journal:  Sci Rep       Date:  2020-10-22       Impact factor: 4.379

  7 in total

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