Kwak Tae-Kyung, Jang Hyung-Seok, Lee Mi-Gi, Jung Young-Sung, Kim Dae-Ok, Kim Yoon-Bum, Kim Jong-In, Kang Hee
Graduate School of East-West Medical Science, Kyung Hee University, Yongin 17104, Republic of Korea.
Jang Hyung-Seok Korean Medicine Clinic, Seoul 06524, Republic of Korea.
Evid Based Complement Alternat Med. 2018 Aug 7;2018:4041873. doi: 10.1155/2018/4041873. eCollection 2018.
The rhizome of Koidz (AM) is a constituent of various Qi booster compound prescriptions. We evaluated inflammatory responses in macrophages and T cells isolated from mice following oral administration of AM water extract (AME). Peritoneal exudate cells were isolated from thioglycollate-injected mice and alterations in scavenger receptors were examined. Peritoneal macrophages were stimulated with lipopolysaccharide (LPS). Serum cytokine responses to intraperitoneal LPS injection were also evaluated. Splenocytes were isolated and their composition and functional responses were measured. The content of atractylenolide I and atractylenolide III, known anti-inflammatory ingredients, in AME was 0.0338 mg/g extract and 0.565 mg/g extract, respectively. AME increased the number of SRA(+)CD11b(+) cells in response to thioglycollate. Peritoneal macrophages isolated from the AME group showed no changes in inflammatory markers such as tumor necrosis factor- (TNF-) , interleukin- (IL-) 6, inducible nitric oxide synthase, and cyclooxygenase-2 but exhibited a decrease in CD86 expression. Interestingly, AME decreased the serum levels of TNF- and IL-6 upon intraperitoneal injection of LPS. Regarding the adaptive immune system, AME increased the CD4(+) T cell population and major histocompatibility complex class II molecule expression in the spleen, and cultured splenocytes from the AME group showed increased production of IL-4 concurrent with decreased interferon- production during T cell activation. AME promoted the replenishment of peritoneal macrophages during the inflammatory response but its anti-inflammatory activity did not appear to be mediated by the modulation of macrophage activity. AME also altered the immune status of CD4 T cells, promoting the Th2 response.
小泽泻(AM)的根茎是各种补气复方制剂的组成成分。我们评估了口服AM水提取物(AME)后从小鼠分离出的巨噬细胞和T细胞中的炎症反应。从注射巯基乙酸盐的小鼠中分离出腹腔渗出细胞,并检测清道夫受体的变化。用脂多糖(LPS)刺激腹腔巨噬细胞。还评估了对腹腔注射LPS的血清细胞因子反应。分离脾细胞并测量其组成和功能反应。AME中已知的抗炎成分白术内酯I和白术内酯III的含量分别为0.0338mg/g提取物和0.565mg/g提取物。AME增加了对巯基乙酸盐反应的SRA(+)CD11b(+)细胞数量。从AME组分离出的腹腔巨噬细胞在肿瘤坏死因子-(TNF-)、白细胞介素-(IL-)6、诱导型一氧化氮合酶和环氧化酶-2等炎症标志物方面没有变化,但CD86表达降低。有趣的是,腹腔注射LPS后,AME降低了TNF-和IL-6的血清水平。关于适应性免疫系统,AME增加了脾脏中CD4(+)T细胞群体和主要组织相容性复合体II类分子的表达,并且AME组培养的脾细胞在T细胞活化期间显示IL-4产生增加,同时干扰素-产生减少。AME在炎症反应期间促进腹腔巨噬细胞的补充,但其抗炎活性似乎不是由巨噬细胞活性的调节介导的。AME还改变了CD4 T细胞的免疫状态,促进了Th2反应。