游离大黄总蒽醌通过抑制 NLRP3/caspase-1/GSDMD 焦亡途径保护 SAP 大鼠肠黏膜屏障。
Free total rhubarb anthraquinones protect intestinal mucosal barrier of SAP rats via inhibiting the NLRP3/caspase-1/GSDMD pyroptotic pathway.
机构信息
Department of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, Sichuan, 646000, China; Department of Pharmacy, People's Hospital of Zhongjiang County, Deyang, Sichuan, 618000, China.
Department of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, Sichuan, 646000, China.
出版信息
J Ethnopharmacol. 2024 May 23;326:117873. doi: 10.1016/j.jep.2024.117873. Epub 2024 Feb 10.
ETHNOPHARMACOLOGICAL RELEVANCE
Rhubarb is the peeled and dried roots of Rheum palmatum L. and Rheum tanguticum Maxim. ex Balf. or Rheum officinale Baill. Free total rhubarb anthraquinones (FTRAs) were isolated and extracted from rhubarb. Previous studies have revealed that the early administration of FTRAs protects the intestinal mucosal barrier in rats with severe acute pancreatitis (SAP), the mechanism of which is not yet clear. However, we observed an enhanced expression of intestinal pyroptotic factors in rats treated with SAP, which may be related to the mechanism of intestinal barrier protection by FTRAs.
AIM OF THE STUDY
The main objective of this study was to investigate the mechanism by which FTRAs protect the intestinal mucosal barrier in SAP rats, focusing on the classical pyroptosis pathway.
MATERIALS AND METHODS
SAP was induced in rats through retrograde injection of sodium taurocholate via the pancreaticobiliary duct. Subsequently, FTRAs (22.5, 45, and 90 mg/kg), rhubarb (900 mg/kg, positive control), and saline (control) were administered at 0 h (immediately), 12 h, and 24 h post-surgery. Pancreatic and intestinal tissue injury, positive PI staining rate, and expression levels of various factors in intestinal tissues were compared across different groups. These factors include diamine oxidase (DAO), lactate dehydrogenase (LDH), high mobility group box chromosomal protein 1(HMGB1) and pro-inflammatory factors in intestinal and serum, pyroptosis-associated factors, toll-like receptor 4 (TLR-4), nuclear factor kappa-B (NF-kB), apoptosis-associated speck-like protein (ASC), NOD-like receptor protein 3 (NLRP3), cysteine protease-1 (caspase-1) and Gasdermin (GSDMD).
RESULTS
The findings indicated that FTRAs protected the damaged intestine and pancreas and restored the expression of intestinal epithelial junction proteins in SAP rats. Additionally, it reduced intestinal and serum levels of DAO, interleukin 1, interleukin 18, HMGB1, and LDH, attenuated intestinal Positive PI staining rate, and significantly decreased the expressions of TLR-4, NF-kB, ASC, NLRP3, caspase-1 and GSDMD in SAP rats.
CONCLUSIONS
The results suggest that FTRAs inhibited pyroptosis through down-regulation of the NLRP3-Caspase-1-GSDMD and TLR-4- NF-kB signaling pathways of intestinal tissues., thereby protecting the intestinal barrier of SAP rats.
民族药理学相关性
大黄是掌叶大黄、唐古特大黄或药用大黄的去皮和干燥的根。游离总大黄蒽醌(FTRA)从大黄中分离和提取出来。先前的研究表明,FTRA 的早期给药可保护重症急性胰腺炎(SAP)大鼠的肠黏膜屏障,但其机制尚不清楚。然而,我们观察到 SAP 大鼠中肠细胞焦亡相关因子的表达增强,这可能与 FTRA 保护肠屏障的机制有关。
研究目的
本研究的主要目的是研究 FTRA 通过经典的细胞焦亡途径保护 SAP 大鼠肠黏膜屏障的机制。
材料和方法
通过逆行胰胆管注射牛磺胆酸钠诱导大鼠 SAP。随后,在术后 0 h(即刻)、12 h 和 24 h 时给予 FTRA(22.5、45 和 90 mg/kg)、大黄(900 mg/kg,阳性对照)和生理盐水(对照)。比较不同组大鼠的胰腺和肠道组织损伤、阳性 PI 染色率以及肠道组织中各种因子的表达水平。这些因子包括二胺氧化酶(DAO)、乳酸脱氢酶(LDH)、高迁移率族蛋白 1(HMGB1)和肠道及血清中的促炎因子、细胞焦亡相关因子、Toll 样受体 4(TLR-4)、核因子 kappa-B(NF-kB)、凋亡相关斑点样蛋白(ASC)、NOD 样受体蛋白 3(NLRP3)、半胱氨酸蛋白酶-1(caspase-1)和 Gasdermin(GSDMD)。
结果
结果表明,FTRA 可保护 SAP 大鼠受损的肠和胰腺,并恢复肠上皮细胞连接蛋白的表达。此外,它降低了 SAP 大鼠的肠道和血清中 DAO、白细胞介素 1、白细胞介素 18、HMGB1 和 LDH 的水平,减轻了肠道的阳性 PI 染色率,并显著降低了 SAP 大鼠中 TLR-4、NF-kB、ASC、NLRP3、caspase-1 和 GSDMD 的表达。
结论
研究结果表明,FTRA 通过下调肠道组织的 NLRP3-Caspase-1-GSDMD 和 TLR-4-NF-kB 信号通路抑制细胞焦亡,从而保护 SAP 大鼠的肠屏障。