Gold nanoparticles-conjugation of irisin enhances therapeutic effect by improving cardiac function and attenuating inflammation in sepsis.

IF 3.9 2区 化学 Q2 CHEMISTRY, APPLIED
Lijiang Wang, Supaporn Kulthinee, Nahiro Yano, Huai Wen, Ling X Zhang, Zachary S S L Saleeba, Na Jin, Ou Chen, Ting C Zhao
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引用次数: 0

Abstract

Irisin is considered to be a promising therapeutic approach for cardiac depression and inflammatory disorders. The short half-life of irisin impeded its use and drug efficacy in the treatment. This study aimed to examine if pegylated gold nanoparticles-conjugated to irisin would improve therapeutic effects in cecal ligation and puncture (CLP)-induced sepsis in mice. Recombinant irisin were conjugated to a pegylated gold nanoparticle, which was given to mice exposed to CLP. The cecal ligation procedure and sham on mice were operated and assigned to one of following five groups: (I) CLP group: The mouse models underwent the CLP surgical procedure and received only vehicle saline treatment (n = 5); (II) CLP + soluble Irisin: The mouse underwent the CLP and received an intramuscular injection (i.m) (TA) injection of 1 ug of soluble irisin into each tibialis anterior (TA) leg (n = 5); (III) CLP + Gold nanoparticle-conjugated to Irisin: The mouse models underwent the CLP and received an i.m (TA) injection of 1 µg of Gold nanoparticle-irisin via intramuscular injection (TA) into each leg (n = 5); (IV) CLP + Gold nanoparticles- conjugated to IgG: The mouse underwent the CLP and received an i.m (TA) injection of gold nanoparticles conjugated to IgG (n = 5). (V) Sham: The mouse underwent the surgical operation without conducting the CLP (n = 10). The post-operated animals were observed for one week, and survival rates were estimated. Echocardiography was performed to measure cardiac function at 12 h following CLP. TUNEL was employed to detect apoptosis in both cardiac and skeletal muscles; histology was conducted to assess tissue injury in muscles. Enzyme linked immunosorbent assay (ELISA) was conducted to examine release of interleukin 6 (IL6) and the tumor necrosis factor (TNF) alpha. Compared to the CLP control, soluble irisin treatment improved cardiac function recovery, as indicated by the fractional shortening (FS) and ejection fraction (EF). Irisin treatment exhibited reduced IL6 and TNF-alpha release in association with less apoptosis, lower muscle injury index and improved survival post-CLP. However, compared to soluble irisin treatment, gold nanoparticles-conjugated to irisin showed a significant improvement in cardiac function, suppression of apoptosis, reduced IL6 and TNF-alpha releases, decreased muscle injury and an improved survival rate of post-CLP. This study reveals that gold nanoparticles-conjugated irisin can serve to improve irisin's therapeutic effects over a longer course of treatment.

Abstract Image

金纳米粒子与鸢尾素结合可改善败血症患者的心脏功能并减轻炎症反应,从而增强治疗效果。
鸢尾素被认为是治疗心脏抑郁和炎症性疾病的一种很有前景的方法。鸢尾素的半衰期较短,阻碍了其在治疗中的使用和药效。本研究旨在探讨与鸢尾素结合的聚乙二醇化金纳米粒子是否能提高对小鼠盲肠结扎和穿刺(CLP)诱导的败血症的治疗效果。将重组鸢尾素与聚乙二醇化金纳米粒子结合在一起,然后给暴露于CLP的小鼠服用。对小鼠进行盲肠结扎手术和假结扎手术,并将其分为以下五组:(I) CLP 组:小鼠模型接受CLP手术治疗,仅接受载体生理盐水治疗(n = 5);(II)CLP + 可溶性鸢尾素组:小鼠模型接受CLP手术,每条胫骨前(TA)腿肌肉注射(i.m)(TA)1微克可溶性鸢尾素(n = 5);(III)CLP + 与鸢尾素结合的金纳米颗粒:(IV) CLP + 与 IgG 结合的金纳米颗粒:小鼠接受 CLP,并通过肌肉注射(TA)向每条腿肌内注射 1 µg 金纳米颗粒-鸢尾素(n = 5);(IV) CLP + 与 IgG 结合的金纳米颗粒:小鼠接受 CLP,并通过肌肉注射(TA)向每条腿肌内注射与 IgG 结合的金纳米颗粒(n = 5)。(五)假阴性:小鼠接受手术,但不进行 CLP(n = 10)。观察术后动物一周,估计存活率。在 CLP 术后 12 小时进行超声心动图检查以测量心脏功能。采用 TUNEL 检测心肌和骨骼肌的细胞凋亡;采用组织学方法评估肌肉组织损伤。酶联免疫吸附试验(ELISA)用于检测白细胞介素6(IL6)和肿瘤坏死因子(TNF)α的释放。与中性粒细胞白血病对照组相比,可溶性鸢尾素治疗改善了心脏功能的恢复,这体现在分数缩短率(FS)和射血分数(EF)上。鸢尾素治疗可减少IL6和TNF-α的释放,同时减少细胞凋亡,降低肌肉损伤指数,提高CLP后的存活率。然而,与可溶性鸢尾素治疗相比,与鸢尾素结合的金纳米粒子能显著改善心脏功能、抑制细胞凋亡、减少 IL6 和 TNF-α 的释放、减少肌肉损伤并提高 CLP 后的存活率。这项研究表明,金纳米颗粒与鸢尾素结合可在较长的治疗过程中提高鸢尾素的治疗效果。
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来源期刊
Molecular Diversity
Molecular Diversity 化学-化学综合
CiteScore
7.30
自引率
7.90%
发文量
219
审稿时长
2.7 months
期刊介绍: Molecular Diversity is a new publication forum for the rapid publication of refereed papers dedicated to describing the development, application and theory of molecular diversity and combinatorial chemistry in basic and applied research and drug discovery. The journal publishes both short and full papers, perspectives, news and reviews dealing with all aspects of the generation of molecular diversity, application of diversity for screening against alternative targets of all types (biological, biophysical, technological), analysis of results obtained and their application in various scientific disciplines/approaches including: combinatorial chemistry and parallel synthesis; small molecule libraries; microwave synthesis; flow synthesis; fluorous synthesis; diversity oriented synthesis (DOS); nanoreactors; click chemistry; multiplex technologies; fragment- and ligand-based design; structure/function/SAR; computational chemistry and molecular design; chemoinformatics; screening techniques and screening interfaces; analytical and purification methods; robotics, automation and miniaturization; targeted libraries; display libraries; peptides and peptoids; proteins; oligonucleotides; carbohydrates; natural diversity; new methods of library formulation and deconvolution; directed evolution, origin of life and recombination; search techniques, landscapes, random chemistry and more;
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