School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
The Key Research Laboratory of "Exploring Effective Substance in Classic and Famous Prescriptions of Traditional Chinese Medicine". The State Administration of Traditional Chinese Medicine of the People's Republic of China, Beijing, China.
Pharm Biol. 2023 Dec;61(1):1374-1386. doi: 10.1080/13880209.2023.2243999.
Jiang-Zhi-Ning (JZN), a traditional Chinese medicinal formula, is used to treat hyperlipidemia in clinics.
To screen the hypolipidemic "bioequivalent substance system (BSS)" of JZN and elucidate the potential hypolipidemic mechanism.
, the TG content in HepG2 cells was determined after the intervention of the combination of advantageous components (CAC) by uniform design. , hyperlipidemia models were established by Triton WR-1339 (400 mg/kg; i.p.) in male ICR mice, and corresponding treatments were administered via oral administration once. The mice were divided into 12 groups (): control, hyperlipidemic model, simvastatin (positive control, 20 mg/kg), gradient doses of JZN granules (2, 4 and 8 g/kg) and the hypolipidemic effective extraction (HEE) of JZN (120, 240 and 480 mg/kg) and CAC groups (20, 40 and 160 mg/kg). Serum TC, TG, LDL-C and HDL-C were performed after 24 h. Transcriptomics and qRT-PCR technology were used to explore the mechanism of the "BSS" of JZN.
, the ratio of CAC was determined. CAC could reduce the TG content in HepG2 cells (77.21%). Compared with the model group, the high dose of CAC could markedly decrease the levels of TC (61.86%), TG (105.54%) and LDL-C (39.38%) and increase the level of HDL-C (232.67%). CAC was proved to be the "BSS". Transcriptomics and qRT-PCR analysis revealed CAC regulated non-alcoholic fatty liver disease, bile secretion, PPAR and adipocytokine signalling pathway.
These findings provided new feasible ideas and methods for the elucidation of the pharmacodynamic material basis.
降脂宁(JZN)是一种中药方剂,临床上用于治疗高脂血症。
筛选 JZN 的降脂“生物等效物质体系(BSS)”,并阐明潜在的降脂机制。
采用均匀设计法,考察优势组分组合(CAC)干预后 HepG2 细胞内 TG 含量的变化。雄性 ICR 小鼠腹腔注射 Triton WR-1339(400mg/kg)建立高脂血症模型,灌胃给予相应药物。实验共分为 12 组():对照组、高脂血症模型组、辛伐他汀(阳性对照,20mg/kg)组、JZN 颗粒(2、4、8g/kg)梯度剂量组和 JZN 降脂有效提取部位(HEE)(120、240、480mg/kg)组及 CAC 组(20、40、160mg/kg)。24h 后检测血清 TC、TG、LDL-C 和 HDL-C。采用转录组学和 qRT-PCR 技术探索 JZN“BSS”的作用机制。
确定了 CAC 的配比。CAC 可降低 HepG2 细胞内 TG 含量(77.21%)。与模型组比较,CAC 高剂量可显著降低 TC(61.86%)、TG(105.54%)和 LDL-C(39.38%)水平,升高 HDL-C(232.67%)水平。CAC 被证明是“BSS”。转录组学和 qRT-PCR 分析表明,CAC 调节非酒精性脂肪性肝病、胆汁分泌、PPAR 和脂肪细胞因子信号通路。
这些发现为阐明药效物质基础提供了新的可行思路和方法。