Siwu Paste protects bone marrow hematopoietic function in rats with blood deficiency syndrome by regulating TLR4/NF-κB/NLRP3 signaling pathway

骨髓 造血 TLR4型 医学 细胞因子 血细胞 免疫学 药理学 生物 炎症 干细胞 细胞生物学
作者
Qing Du,Dan He,Hongliang Zeng,Jian Liu,Hui Yang,Linben Xu,Hao Liang,Dan Wan,Chunyu Tang,Ping Cai,Jianhua Huang,Shuihan Zhang
出处
期刊:Journal of Ethnopharmacology [Elsevier BV]
卷期号:262: 113160-113160 被引量:21
标识
DOI:10.1016/j.jep.2020.113160
摘要

Siwu Paste (SWP) was recorded in the first national Pharmacopoeia of China, “Tai Ping Hui Min He Ji Ju Fang”, it showed excellent effects in regulating all syndromes relevant to blood. Aim of the study: This study aimed to investigate the protective effects of Siwu Paste (SWP) on bone marrow hematopoietic by using rats’ model with blood deficiency syndrome induced by chemotherapy. Animal model with blood deficiency syndrome was successfully established by evaluating their peripheral blood cell level and erythrocyte membrane energy metabolism enzyme activity. Serum hematopoietic cytokine levels were detected by using Enzyme-linked immunosorbent assay (ELISA). Hematoxylin-Eosin (HE) staining method was used to observe the pathological morphology of femur bone marrow, and the viability of BMSC was detected by Cell Counting Kit (CCK-8). Furthermore, the expression of toll-like receptor 4 (TLR4), nuclear transcription factor kB (NF-κB), and NOD-like receptor protein 3 (NLRP3) protein in femur bone marrow were detected by using Western-blotting and High-content cell imaging analysis system (HCA). Obtained results showed that SWP could significantly improve the status of anemia, regulate the expressions of serum hematopoietic cytokines, and protect bone marrow hematopoietic cells. Furthermore, the expressions of TLR4, NF-κB, and NLRP3 protein were inhibited in bone marrow hematopoietic cells. Siwu Paste (SWP) could recover the bone marrow hematopoietic functions in rats with blood deficiency syndrome. The therapeutic mechanism may be related to the regulation of serum hematopoietic cytokines, and inhibition of TLR4/NF-κB/NLRP3 signaling pathway.
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