A subscription to JoVE is required to view this content. Sign in or start your free trial.

Research Article

Bibliometric Analysis of Pharmacological Research on Salidroside Based on CiteSpace: Trends, Hotspots and Future Prospects

133 views

DOI:

10.3791/71630

July 31st, 2026

In This Article

Summary

This study mapped global salidroside research from 2000 to 2025 using CiteSpace, identified publication trends, leading authors and institutions, major research hotspots, and emerging directions in its pharmacological applications.

Abstract

Salidroside exerts a broad spectrum of pharmacological activities and represents a promising drug candidate for multiple ailments, including myocardial ischemia-reperfusion injury, acute lung injury, and Alzheimer’s disease; nonetheless, quantitative and systematic overviews mapping its full research landscape remain inadequate. In this study, relevant publications from 2000 to 2025 were retrieved from the Web of Science Core Collection. Bibliometric and visual analyses were conducted using CiteSpace and Microsoft Excel. A total of 1400 eligible papers were included. Annual publication output increased gradually before 2010 and accelerated thereafter. Investigators across 62 countries have contributed to this field, with core research clusters centered at institutions such as China Pharmaceutical University. Keyword co‑occurrence analysis reveals that research hotspots center on salidroside’s anti-inflammatory, antioxidant, and anti-apoptotic properties, and research has increasingly focused on respiratory, neurological, and cardiovascular disorders through modulation of NF-κB, HIF-1α, and NLRP3 signaling cascades. Meanwhile, salidroside production has evolved from conventional herbal extraction toward industrial fermentation, and its pharmacological exploration has expanded beyond anti‑aging and anti‑hypoxia bioactivity to encompass anti‑tumor efficacy and multi‑organ protection.

Introduction

Salidroside is a phenylethanoid glycoside derived from a range of medicinal plants, including the traditional Chinese medicine herb Rhodiola crenulata (Dahuahongjingtian), Ligustrum lucidum (Nüzhenzi), Cistanche deserticola (Roucongrong), Eleutherococcus senticosus (Ciwujia), Sargentodoxa cuneata (Daxueteng), as well as Acer tegmentosum Maxim (Qingjieqi)1,2,3,4. It exhibits prominent pharmacological effects encompassing antioxidant, anti‑inflammatory, anti‑hypoxic, anti‑fatigue, and neuroprotective activities, and has been incorporated into multiple traditional Chinese medicinal preparations such as Nodikang Capsules, Jinlian Capsules, and Zhenqi Fuzheng Capsules5,6,7. Salidroside has shown tremendous potential in combating central nervous system disorders (such as Alzheimer's disease, Parkinson's disease, and ischemic stroke), managing metabolic diseases, and delaying senescence, thus emerging as a research hotspot in the field of natural product research and new drug development. With the advancement of molecular biology techniques, the molecular mechanisms of salidroside in regulating key signaling pathways, including nuclear factor erythroid 2-related factor (Nrf2), NOD‑like receptor pyrin domain‑containing protein 3 (NLRP3), and Nuclear Factor Kappa B (NF-κB), ameliorating mitochondrial function and modulating autophagy have been continuously elucidated, with a massive volume of relevant literature accumulated to date8,9,10,11,12,13,14,15,16,17.

Bibliometrics, initially categorized as statistical bibliography, is a discipline applying mathematical and statistical methods to bibliographic documents. It quantitatively analyzes a massive body of literature to reveal development trajectories, research hotspots, frontiers, and academic collaboration networks. Early on, librarians used it to identify core journals, optimize collections, and support acquisition decisions18. CiteSpace visualizes the evolution of specific knowledge domains through text mining. Compared with another bibliometric visualization tool based on VOSviewer, it offers unique features such as Timezone View and Timeline View, which clearly display the rise and fall, division, and integration of research topics over the years. Using co-occurrence, co-citation, and cluster analysis, it generates knowledge maps to pinpoint key literature, authors, institutions, and emerging fronts, earning it the title of “scientific knowledge mapping radar”19.

Research on traditional Chinese medicine (TCM) boasts a long history, backed by abundant archival literature. However, existing studies span a wide range of research themes, from the natural plant extraction and bioengineering synthesis of salidroside to investigations of its pharmacological mechanisms against diverse diseases, as well as extensive research on its combined medication regimens.

To date, research concerning salidroside has yielded substantial progress. Although numerous reviews have summarized salidroside's pharmacological activities, quantitative assessments of publication trends, collaboration patterns, research hotspots, and emerging topics remain limited. Accordingly, this study uses CiteSpace 6.4.R1 to conduct a visual analysis of publication output, focusing on the authors, affiliated institutions, and keywords of salidroside-related papers published between 2000 and 2025. It characterizes the evolution of research trends and hot topics over the past 25 years and identifies emerging research directions and potential future hotspots (Figure 1).

Access restricted. Please log in or start a trial to view this content.

Protocol

Data sources and retrieval strategy

All raw data used in this study were retrieved from the Web of Science Core Collection database20,21. The study period spans from January 1, 2000, to December 31, 2025, and the literature search was conducted on May 27, 2026. The specific search formula was set as:

TS=(Salidroside OR Rhodioloside OR Rhodosin OR "2-(4-Hydroxyphenyl)ethyl β-D-glucopyranoside" OR "p-Hydroxyphenethyl glucopyranoside" OR Tyrosol β-D-glucopyranoside OR Sallidroside) AND FPY=2000-2025.

Literature inclusion and exclusion criteria

In this study, only articles and reviews from the Web of Science Core Collection were included in the analysis, with English as the language restriction. Other document types, including Meeting Abstract, Retracted Publication, Correction, Retraction, Proceeding Paper, Editorial Material, Early Access, Letter, and Publication with Expression of Concern, were excluded from further analysis.

Data processing and visualization

All retrieved literature was exported in RefWorks format as a download.txt file, which was subsequently imported into CiteSpace 6.4.R1 for data conversion and analysis22. Prior to analysis, two researchers conducted manual screening to eliminate duplicate records. We compared basic metadata to spot duplicates and thoroughly checked entries with discrepant information for accurate identification.

To ensure accurate identification by the software, keyword unification was applied to the retrieved entries. For instance, variants including “nf kappa b” and “nuclear factor-kappab” were standardized to “NF-κB”, while “interleukin‑6” and “il 6” were consolidated as “IL-6”; further standardized items are listed in the supplementary table. After manual screening, all institutions are presented with their current official names, with no outdated names or secondary affiliated units involved. No authors have alternative names. Sovereign states are taken as the criterion for counting national publications. All records originally marked as “Taiwan” were reclassified under “China”23.

Detailed parameter configurations are as follows: the research time span was set from 2000 to 2025 with a 2-year slicing interval, and no publications were identified for the year 2000. Node types were selected as author, institution, and keyword, alongside a fixed g-index value of 25. The g-index threshold of 25 was adopted in line with common practices in bibliometric studies. This threshold effectively excludes scattered low-impact nodes while retaining core research entities and major cooperative relationships. The Link Retaining Factor was set to 2.5, and Maximum Links Per Node was limited to 10. For burst detection of visualized keywords, γ was assigned as 0.724,25. This coefficient ranges from 0 to 1; higher γ values impose stricter screening criteria, retaining only keywords with extremely strong burst strength. Meanwhile, Minimum Duration was set to 2, meaning a keyword is marked as a valid burst term only if its research hot spot persists for at least 2 consecutive years. All literature screening was performed manually by two reviewers independently, and discrepancies were resolved through discussion to reach consensus.

Access restricted. Please log in or start a trial to view this content.

Results

Analysis of publication trends

A total of 1468 publications were retrieved spanning 2000 to 2025. After document screening, only 1293 original Articles and 107 Review Articles were retained. Publications remained scarce from 2000 to 2010, indicating preliminary and sporadic exploration of salidroside research. No relevant papers were published in 2000, 2004, 2005, and 2009, and no stable research communities had formed during this period, with only a small number of researcher...

Access restricted. Please log in or start a trial to view this content.

Discussion

This study adopted bibliometric approaches based on publications retrieved from the Web of Science Core Collection spanning 2000 to 2025. Through systematic quantitative visualization, we mapped global research output, institutional collaboration landscapes, and shifting research hotspots surrounding salidroside, delineating stage-specific developmental trajectories across the 25-year analytical window. The field has advanced in distinct progressive phases. Prior to 2011, overall publication volume remained low, research...

Access restricted. Please log in or start a trial to view this content.

Disclosures

The authors have no conflicts of interest to declare.

Acknowledgements

This work is supported by the Natural Science Foundation of Sichuan Province (2024NSFSC0697).

Access restricted. Please log in or start a trial to view this content.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
CiteSpace 6.4.R1Drexel University, Philadelphia, PA, USAhttps://citespace.podia.comBibliometric visualization software
Microsoft Excel 2021Microsoft Corporation, Redmond, WA, USAhttps://www.microsoft.com/microsoft-365/excelSoftware for manual screening and merging of keywords, institutions and other items
Web of Science Core Collection databaseClarivate, Philadelphia, PA, USAhttps://www.webofscience.comOnline citation database

References

  1. Sutula M, Gubaidullin N, Rakhimzhanova A, Manabayeva S. Stress-induced secondary metabolite profiling in Cistanche deserticola callus cultures: insights from GC-MS and HPLC-MS analysis. Int J Mol Sci. 2025 Jun 25;26(13):6091.
  2. Molina CN, Gasparre N, Mañes Vinuesa J. Chemical profiling and processing effects on bioactive compounds in Rhodiola rosea and Eleutherococcus senticosus. Int J Food Sci Technol. 2025;60(1):vvaf049.
  3. Chun ZL, Xiao X, Zhang Y. Simultaneous determination of 8 chemical components in Sargentodoxa cuneata by ultra-high performance liquid chromatography-electrochemical detector. Phys Test Chem Anal Chem Part. 2022;58(7):752-759.
  4. Wang MM, Xiong YJ. Salidroside alleviates atopic dermatitis-like responses by inhibiting MAPKs and NF-κB signaling pathways. Arch Dermatol Res. 2025;317(1):666.
  5. Zhang J, et al. Salidroside alleviates early-stage MASH through the PPARγ-mediated inflammatory signaling pathway. J Ethnopharmacol. 2026;358:121045.
  6. Weng J, et al. Pharmacokinetic changes and mechanisms of salidroside in hypobaric hypoxic environment: A LC-MS and proteomics study. J Ethnopharmacol. 2026;360:121205.
  7. Deng M, et al. Rational Construction of a Lipid Droplet-Targeted Redox-Responsive Ratiometric Probe for Screening of Antioxidant Drugs and Its Application in Parkinson's Disease. Anal Chem. 2026;98(1):809-817.
  8. Wu Y, et al. Salidroside shows anticonvulsant and neuroprotective effects by activating the Nrf2-ARE pathway in a pentylenetetrazol-kindling epileptic model. Brain Res Bull. 2020;164:14-20.
  9. Wang N, et al. Salidroside alleviates simulated microgravity-induced bone loss by activating the Nrf2/HO-1 pathway. J Orthop Surg Res. 2024;19(1):531.
  10. Gao Z, et al. Salidroside alleviates acetaminophen-induced hepatotoxicity via Sirt1-mediated activation of Akt/Nrf2 pathway and suppression of NF-κB/NLRP3 inflammasome axis. Life Sci. 2023;327:121793.
  11. Wang Y, et al. Salidroside postconditioning attenuates ferroptosis-mediated lung ischemia-reperfusion injury by activating the Nrf2/SLC7A11 signaling axis. Int Immunopharmacol. 2023;115:109731.
  12. Li JH, et al. Salidroside Ameliorates Polycystic Ovary Syndrome in Mice by Regulating the AKT/NF-κB/NLRP3-HAS2 Axis. Food Sci Nutr. 2026;14(4):e71692.
  13. Li R, et al. Salidroside prevents tumor necrosis factor-α-induced vascular inflammation by blocking mitogen-activated protein kinase and NF-κB signaling activation. Exp Ther Med. 2019;18(5):4137-4143.
  14. Li S, Wang B. Anti-Inflammatory, Anti-Colitis, and Antioxidant Effects of Salidroside against Dextran Sodium Sulfate Induced Ulcerative Colitis in Rats via Inhibition of NF-κB-INOS-No and TLR4-NF-κB Signaling Pathways. J Biochem Mol Toxicol. 2025;39(10):e70520.
  15. Magani SK, et al. Salidroside-can it be a multifunctional drug?. Curr Drug Metab. 2020;21(7):512-524.
  16. Bai XL, et al. Rhodiola and salidroside in the treatment of metabolic disorders. Mini Rev Med Chem. 2019;19(19):1611-1626.
  17. Liang K, et al. Salidroside: An Overview of Its Promising Potential and Diverse Applications. Pharmaceuticals (Basel). 2024 Dec 17;17(12):1703.
  18. Lawani SM. Bibliometrics: Its theoretical foundations, methods and applications. Libri. 1981;31:294.
  19. Gross PL, Gross EM. College libraries and chemical education. Science. 1927;66(1713):385-389.
  20. Guo GY, et al. Visualized analysis of licorice research hotspots and trends in the field of traditional Chinese medicine resources based on VOSviewer and CiteSpace knowledge maps. Food Med Homol. 2024;1(2):9420011.
  21. Yao JL, et al. A bibliometric analysis of lipid peroxidation in alcoholic liver disease from 2001 to 2024. Food Med Homol. 2024;1:9420009.
  22. Xu WW, et al. Construction and visualization of knowledge map of Astragalus resources research hotspots. Food Med Homol. 2026;3(3):9420113.
  23. Zhang Y, et al. Bibliometric and Visual Analysis of the Immune System in Osteomyelitis (1990-2024). J Vis Exp. 2026;(229).
  24. Yang L, et al. Visualization analysis of research progress and trends in coexistence of lung cancer and pulmonary tuberculosis using bibliometrics. Med Adv. 2024;2(2):144-164.
  25. Wang Z, et al. A Bibliometric Analysis of Botulinum Toxin Type A in the Treatment of Lower Urinary Tract Dysfunction: Current Research Trends and Perspectives. Med Adv. 2025;3(4):268-286.
  26. Price DDS. A general theory of bibliometric and other cumulative advantage processes. J Am Soc Inf Sci. 1976;27(5):292-306.
  27. Chang X, et al. Cardioprotective effects of salidroside on myocardial ischemia-reperfusion injury in coronary artery occlusion-induced rats and Langendorff-perfused rat hearts. Int J Cardiol. 2016;215:532-544.
  28. Jin H, et al. Therapeutic Intervention of Learning and Memory Decays by Salidroside Stimulation of Neurogenesis in Aging. Mol Neurobiol. 2016;53(2):851-866.
  29. Zhu L, et al. Salidroside ameliorates arthritis-induced brain cognition deficits by regulating Rho/ROCK/NF-κB pathway. Neuropharmacology. 2016;103:134-142.
  30. Fu Y, et al. Integrated network pharmacology, bioinformatics, and experiment analysis to decipher the molecular mechanism of Salidroside on Gastric cancer via targeting NCOA4-mediated ferritinophagy. Chem Biol Interact. 2025;407:111368.
  31. Huang G, et al. Salidroside sensitizes Triple-negative breast cancer to ferroptosis by SCD1-mediated lipogenesis and NCOA4-mediated ferritinophagy. J Adv Res. 2025;74:589-607.
  32. Chen C. CiteSpace II: Detecting and visualizing emerging trends and transient patterns in scientific literature. J Am Soc Inf Sci Technol. 2006;57(3):359-377.
  33. Zhu R, et al. Comprehensive Review on Rhodiola crenulata: Ethnopharmacology, Phytochemistry, Pharmacological Properties and Clinical Applications. Chin J Integr Med. 2025;31(8):752-759.
  34. Goodwin J. Citation Indexing—Its Theory and Application in Science, Technology, and Humanities by Eugene Garfield. Technol Cult. 1980;21(4):714-715.
  35. Gan YN, Li DD, Robinson N, Liu JP. Practical guidance on bibliometric analysis and mapping knowledge domains methodology–A summary. Eur J Integr Med. 2022;56:102203.
  36. Chen C, Song M. Visualizing a field of research: A methodology of systematic scientometric reviews. PLoS One. 2019;14(10):e0223994.
  37. Gu C, et al. Salidroside Ameliorates Mitochondria-Dependent Neuronal Apoptosis after Spinal Cord Ischemia-Reperfusion Injury Partially through Inhibiting Oxidative Stress and Promoting Mitophagy. Oxid Med Cell Longev. 2020;2020:3549704.
  38. Song WT, Cao H, Zhang YH, Zheng XY, Liu JX. Protection of salidroside on endothelial cell barrier in cerebral ischemia-reperfusion model rats. Zhongguo Zhong Yao Za Zhi. 2022;47(19):5284-5291.
  39. Wang H, Li Q, Sun S, Chen S. Neuroprotective Effects of Salidroside in a Mouse Model of Alzheimer's Disease. Cell Mol Neurobiol. 2020;40(7):1133-1142.
  40. Xie Z, et al. Salidroside attenuates cognitive dysfunction in senescence-accelerated mouse prone 8 (SAMP8) mice and modulates inflammation of the gut-brain axis. Front Pharmacol. 2020;11:568423.
  41. Zhang X, et al. Salidroside ameliorates Parkinson's disease by inhibiting NLRP3-dependent pyroptosis. Aging (Albany NY). 2020;12(10):9405-9426.
  42. Wu Q, et al. Salidroside ameliorates neuroinflammation in autistic rats by inhibiting NLRP3/Caspase-1/GSDMD signal pathway. Brain Res Bull. 2025;220:111132.
  43. Cai Y, et al. Salidroside Ameliorates Alzheimer's Disease by Targeting NLRP3 Inflammasome-Mediated Pyroptosis. Front Aging Neurosci. 2022;13:809433.
  44. Liu J, et al. Salidroside protects mice from high-fat diet-induced obesity by modulating the gut microbiota. Int Immunopharmacol. 2023;120:110278.
  45. Gao J, et al. Salidroside suppresses inflammation in a D-galactose-induced rat model of Alzheimer's disease via SIRT1/NF-κB pathway. Metab Brain Dis. 2016;31(4):771-778.
  46. Xing SS, et al. Salidroside improves endothelial function and alleviates atherosclerosis by activating a mitochondria-related AMPK/PI3K/Akt/eNOS pathway. Vascul Pharmacol. 2015;72:141-152.
  47. Chai Y, et al. Mechanism of salidroside regulating autophagy based on network pharmacology and molecular docking. Anticancer Drugs. 2024;35(6):525-534.
  48. Jin L, Lu Y, Huang G. The potential targets of salidroside in the treatment of pediatric epilepsy are revealed by network pharmacology, molecular docking, and cell experiments. Lett Drug Des Discov. 2026;100230.
  49. Van Eck N, Waltman L. Software survey: VOSviewer, a computer program for bibliometric mapping. Scientometrics. 2010;84(2):523-538.

Access restricted. Please log in or start a trial to view this content.

Reprints and Permissions

Tags

Salidroside ResearchPharmacological ActivitiesCiteSpace VisualizationAnti InflammatoryAntioxidant PropertiesAnti ApoptoticCardiovascular DisordersNF KappaB SignalingIndustrial Fermentation