首页> 美国卫生研究院文献>BioMed Research International >Danggui Buxue Tang Attenuates Tubulointerstitial Fibrosis via Suppressing NLRP3 Inflammasome in a Rat Model of Unilateral Ureteral Obstruction
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Danggui Buxue Tang Attenuates Tubulointerstitial Fibrosis via Suppressing NLRP3 Inflammasome in a Rat Model of Unilateral Ureteral Obstruction

机译:当归补血汤通过抑制单侧输尿管梗阻大鼠模型中的NLRP3炎性小体减轻肾小管间质纤维化

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摘要

Inflammation significantly contributes to the progression of chronic kidney disease (CKD). This study aimed to characterize Danggui Buxue Tang (DBT) renoprotection and relationship with NOD-like receptors family pyrin domain-containing 3 (NLRP3) inflammasome expression in rats with unilateral ureteral obstruction (UUO). Sprague-Dawley rats were subjected to UUO and randomly assigned to untreated UUO, enalapril-treated (10 mg/kg/day), and DBT-treated (9 g/kg/day) groups. Sham-operated rats served as controls, with 8 rats in each group. All rats were sacrificed for blood and renal specimen collection at 14 days after UUO. Untreated UUO rats exhibited azotemia, intense tubulointerstitial collagen deposition, upregulations of tubulointerstitial injury index, augmentation levels of collagen I (Col I), α-smooth muscle actin (α-SMA), NLRP3, apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC), pro-caspase-1, caspase-1, IL-1β, and pro-IL-1β. DBT treatment significantly attenuated interstitial collagen deposition and tubulointerstitial injury, lowering Col I and α-SMA levels. Synchronous expressions of NLRP3, ASC, pro-caspase-1, caspase-1, pro-IL-1β, and IL-1β decreased in renal tissue. In comparison to enalapril, DBT significantly reduced tubulointerstitial injury, interstitial collagen deposition, and expressions of Col I and IL-1β. Thus, DBT offers renoprotection in UUO rats, which was associated with suppressing NLRP3 inflammasome expression and following reduction of the secretion of cytokine IL-1β. The mechanisms of multitargets of traditional Chinese medicine can be better used for antifibrotic treatment.
机译:炎症明显促进了慢性肾脏病(CKD)的发展。这项研究旨在表征当归补血汤(DBT)的肾脏保护作用以及与单侧输尿管梗阻(UUO)大鼠中NOD样受体家族含吡啶域3(NLRP3)炎性小体表达的关系。将Sprague-Dawley大鼠接受UUO处理,并随机分为未经治疗的UUO,依那普利治疗(10μg/ kg /天)和DBT治疗(9μg/ kg /天)组。假手术大鼠为对照组,每组8只。 UUO后第14天,处死所有大鼠以收集血液和肾脏标本。未经治疗的UUO大鼠表现出氮缺乏症,肾小管间质胶原沉积严重,肾小管间质损伤指数上调,胶原I(Col I)增强水平,α平滑肌肌动蛋白(α-SMA),NLRP3,与凋亡相关的斑点样蛋白(含胱天蛋白酶)募集域(ASC),前胱天蛋白酶-1,胱天蛋白酶-1,IL-1β和前IL-1β。 DBT治疗可显着减轻间质胶原沉积和肾小管间质损伤,降低Col I和α-SMA水平。肾组织中NLRP3,ASC,caspase-1,caspase-1,IL-1β和IL-1β的同步表达降低。与依那普利相比,DBT显着降低了肾小管间质损伤,间质胶原沉积以及Col I和IL-1β的表达。因此,DBT在UUO大鼠中提供了肾脏保护作用,这与抑制NLRP3炎性小体表达以及减少细胞因子IL-1β的分泌有关。中药多靶点的机制可以更好地用于抗纤维化治疗。

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