Effects of chinese formula jueyin granules on psoriasis in an animal model.
Tian MaWen-Cheng JiangXin LiJie ChenTie-Jun WuHua NianRong XuQian-Yuan HuangQing-Qing XiaoQiang JianFu-Lun LiBin LiPublished in: Evidence-based complementary and alternative medicine : eCAM (2014)
Although Traditional Chinese medicine (TCM) is known to be effective for psoriasis patients, the responsible mechanisms still remain poorly understood. In this study, we aimed to evaluate the effect of one formula, named Jueyin granules (JYG) in the mouse model of the vaginal epithelium and tail epidermis. Additionally, we also determined the anti-inflammatory effects of JYG in an imiquimod- (IMQ-) induced psoriasis-like skin mouse model. Our results show that JYG can attenuate the IMQ-induced psoriasis-like inflammation, accompanied with increased epidermal hyperplasia. We also measured estrogenic stage mitosis of vaginal epithelial cells and the formation of granular cell layers in male mouse tails per 100 scales, as well as the tissue nitric oxide (NO) and malondialdehyde (MDA) levels using the ELISA method. The results suggest that JYG significantly inhibited mitosis in mouse vaginal epithelial cells, promoted the formation of the squamous epidermal granular layer in mice tails, and reduced the levels of NO and MDA in an imiquimod-induced psoriasis-like skin mouse model after 14 d (P < 0.05). These results demonstrate that JYG might be an effective clinical treatment for psoriasis and the effects may be related to inhibited keratinocytes proliferation, improved parakeratotic epidermal cells, and reduced expression of NO and MDA.
Keyphrases
- mouse model
- wound healing
- high glucose
- nitric oxide
- diabetic rats
- cell cycle arrest
- atopic dermatitis
- breast cancer cells
- oxidative stress
- anti inflammatory
- drug induced
- induced apoptosis
- end stage renal disease
- poor prognosis
- signaling pathway
- prognostic factors
- stem cells
- ejection fraction
- single cell
- skeletal muscle
- endothelial cells
- mesenchymal stem cells
- preterm infants
- hydrogen peroxide
- bone marrow
- human milk
- cell therapy
- long non coding rna
- cell proliferation
- patient reported
- combination therapy
- high fat diet induced
- preterm birth