Carbon dots derived from Zingiber officinale Rosc (ginger) with hemostatic effects.

IF 4.4 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in Molecular Biosciences Pub Date : 2025-03-04 eCollection Date: 2025-01-01 DOI:10.3389/fmolb.2025.1530469
Wen-Jing Hu, Ai-Qi Yu, Hai-Zheng Bi, Zhao-Jiong Zhang, Zhi-Bin Wang, Meng Wang, Hai-Xue Kuang
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Abstract

Introduction: Ginger, as a traditional Chinese medicine (TCM), can be used in clinical practice to treat various diseases. The product of ginger processed at high temperatures is called carbonized ginger (CG), which has a hemostatic effect that ginger originally did not have. The purpose of this study is to investigate the hemostatic effect of CG and the substances that exert hemostatic effects.

Methods: CG was prepared and successfully obtained CG carbon dots (CG-CDs) from its aqueous solution. After fully characterizing its structural information, the hemostatic effect was evaluated using mouse tail bleeding and liver injury bleeding models, and the clotting time was evaluated using capillary coagulation experiments. In addition, the hemostatic mechanism of CG-CDs was explored.

Results: The average particle size of CG-CDs was observed to be 4.07 nm and the lattice spacing was 0.216 nm. It was mainly composed of graphite structured carbon, with the main constituent elements being C, N, and O, containing functional groups such as C=N, C=O, and C-OH. The FL spectrum showed that the maximum excitation wavelength of CG-CDs was 360 nm, and the maximum emission wavelength was 470 nm. The QY of CG-CDs was calculated to be 0.45%. CG-CDs shortened bleeding time, reduced bleeding volume, and also shortened the time for blood clotting. With the increase of CG-CDs, the values of FIB gradually increased, and the PT values gradually decreased. In addition, CG-CDs increased PLT count, increased PLT activating factor TXB2, decreased 6-keto-PGF1α , increased PAI-1, and decreased t-PA.

Conclusion: CG-CDs obtained from CG has hemostatic activity, mainly by activating exogenous coagulation and co-coagulation pathways, increasing PLT count, increasing PLT activating factor TXB2, reducing 6-keto-PGF1α , increasing PAI-1, and reducing t-PA, thereby affecting the fibrinolytic system and other pathways to exert hemostatic effects.

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从姜中提取的具有止血作用的碳点。
生姜作为一种传统中药,在临床上可以治疗多种疾病。生姜经过高温处理后的产物被称为碳化姜(CG),它具有生姜原本不具备的止血作用。本研究的目的是探讨CG的止血作用及发挥止血作用的物质。方法:制备CG,并成功地从其水溶液中获得CG碳点(CG- cds)。在充分表征其结构信息后,采用小鼠尾出血和肝损伤出血模型评价其止血效果,采用毛细管凝血实验评价其凝血时间。并对CG-CDs的止血机制进行了探讨。结果:gc - cds的平均粒径为4.07 nm,晶格间距为0.216 nm。它主要由石墨结构碳组成,主要组成元素为C、N、O,含有C=N、C=O、C- oh等官能团。荧光光谱显示,CG-CDs的最大激发波长为360 nm,最大发射波长为470 nm。计算CG-CDs的QY为0.45%。CG-CDs缩短了出血时间,减少了出血量,也缩短了凝血时间。随着CG-CDs的增加,FIB值逐渐升高,PT值逐渐降低。此外,CG-CDs增加PLT计数,增加PLT激活因子TXB2,降低6-酮- pgf1 α,增加PAI-1,降低t-PA。结论:CG提取的CG- cds具有止血活性,主要通过激活外源性凝血和共凝途径,增加PLT计数,增加PLT活化因子TXB2,降低6-酮- pgf1 α,增加PAI-1,降低t-PA,从而影响纤溶系统等途径发挥止血作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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