Safflower Extract Mitigates MIRI in Rats by Modulating TLR-4/NF-κB Signaling Pathway, Demonstrating Protective Effects.

IF 2.2 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mingling Deng, Jing Yang, Aimaiti Julaiti, Yue Dong, Yunfang Deng, Zhaoju Wang
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引用次数: 0

Abstract

Background: Myocardial ischemia-reperfusion injury (MIRI) exacerbates tissue damage following the restoration of coronary blood flow after ischemia. The TLR-4/NF-κB signaling pathway plays a crucial role in the pathogenesis of MIRI. This study investigated the therapeutic efficacy of safflower extract in mitigating MIRI and its modulation of TLR-4/NF-κB signaling in rats.

Methods: Adult male Sprague-Dawley rats were subjected to 30 minutes of myocardial ischemia followed by 2 h of reperfusion. Safflower extract was administered intravenously at doses of 2, 4, and 8 mg/kg 15 minutes before ischemia and 1 minute before reperfusion. Infarct size was assessed using TTC staining. Serum levels of creatine kinase (CK) and lactate dehydrogenase (LDH) were measured. Pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α) were quantified using ELISA. TLR-4 and NF-κB mRNA and protein expression were evaluated using qRT-PCR and western blotting, respectively. Histopathological changes were assessed using H&E staining.

Results: Safflower extract effectively reduced myocardial infarct size in a dose-dependent manner, with the highest dose providing the greatest benefit. Treatment with safflower extract significantly lowered the elevated levels of serum CK and LDH caused by ischemia-reperfusion (I/R) injury, bringing these biochemical markers closer to normal values. In addition, safflower extract decreased the levels of pro-inflammatory cytokines IL-1β, IL-6, and TNF-α in myocardial tissue, showing a clear dose-response relationship. Analysis through qRT-PCR and western blot confirmed that safflower extract downregulated the expression of TLR4 and NF-κB at both the transcriptional and protein levels. Histological studies further supported these findings, demonstrating that safflower extract improved myocardial tissue architecture, maintained cardiomyocyte structure, and reduced inflammatory cell infiltration.

Conclusions: Safflower extract provides significant cardioprotection against MIRI by modulating the TLR-4/NF-κB-mediated inflammatory response. These findings suggest that safflower extract may be a potential therapeutic agent for mitigating the effects of myocardial ischemiareperfusion injury.

红花提取物通过调节TLR-4/NF-κB信号通路减轻大鼠MIRI,显示保护作用。
背景:心肌缺血-再灌注损伤(MIRI)加重了缺血后冠状动脉血流恢复后的组织损伤。TLR-4/NF-κB信号通路在MIRI的发病中起着至关重要的作用。本研究探讨红花提取物对大鼠MIRI的缓解作用及其对TLR-4/NF-κB信号通路的调节作用。方法:成年雄性Sprague-Dawley大鼠心肌缺血30min,再灌注2h。红花提取物分别在缺血前15分钟和再灌注前1分钟静脉注射,剂量分别为2、4和8 mg/kg。TTC染色评估梗死面积。测定血清肌酸激酶(CK)和乳酸脱氢酶(LDH)水平。采用ELISA法定量检测促炎因子(IL-1β、IL-6、TNF-α)。采用qRT-PCR和western blotting分别检测TLR-4和NF-κB mRNA和蛋白的表达。H&E染色评估组织病理学变化。结果:红花提取物能有效减小心肌梗死面积,且呈剂量依赖性,最大剂量效果最大。红花提取物显著降低了缺血再灌注(I/R)损伤引起的血清CK和LDH水平升高,使这些生化指标接近正常值。红花提取物降低心肌组织中促炎因子IL-1β、IL-6、TNF-α水平,呈明显的量效关系。通过qRT-PCR和western blot分析证实红花提取物在转录和蛋白水平下调TLR4和NF-κB的表达。组织学研究进一步支持了这些发现,表明红花提取物改善心肌组织结构,维持心肌细胞结构,减少炎症细胞浸润。结论:红花提取物通过调节TLR-4/NF-κ b介导的炎症反应,对MIRI具有显著的心脏保护作用。这些结果提示红花提取物可能是一种潜在的治疗心肌缺血再灌注损伤的药物。
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来源期刊
Current pharmaceutical biotechnology
Current pharmaceutical biotechnology 医学-生化与分子生物学
CiteScore
5.60
自引率
3.60%
发文量
203
审稿时长
6 months
期刊介绍: Current Pharmaceutical Biotechnology aims to cover all the latest and outstanding developments in Pharmaceutical Biotechnology. Each issue of the journal includes timely in-depth reviews, original research articles and letters written by leaders in the field, covering a range of current topics in scientific areas of Pharmaceutical Biotechnology. Invited and unsolicited review articles are welcome. The journal encourages contributions describing research at the interface of drug discovery and pharmacological applications, involving in vitro investigations and pre-clinical or clinical studies. Scientific areas within the scope of the journal include pharmaceutical chemistry, biochemistry and genetics, molecular and cellular biology, and polymer and materials sciences as they relate to pharmaceutical science and biotechnology. In addition, the journal also considers comprehensive studies and research advances pertaining food chemistry with pharmaceutical implication. Areas of interest include: DNA/protein engineering and processing Synthetic biotechnology Omics (genomics, proteomics, metabolomics and systems biology) Therapeutic biotechnology (gene therapy, peptide inhibitors, enzymes) Drug delivery and targeting Nanobiotechnology Molecular pharmaceutics and molecular pharmacology Analytical biotechnology (biosensing, advanced technology for detection of bioanalytes) Pharmacokinetics and pharmacodynamics Applied Microbiology Bioinformatics (computational biopharmaceutics and modeling) Environmental biotechnology Regenerative medicine (stem cells, tissue engineering and biomaterials) Translational immunology (cell therapies, antibody engineering, xenotransplantation) Industrial bioprocesses for drug production and development Biosafety Biotech ethics Special Issues devoted to crucial topics, providing the latest comprehensive information on cutting-edge areas of research and technological advances, are welcome. Current Pharmaceutical Biotechnology is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the latest and most important developments.
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