Journal of Traditional Chinese Medicine ›› 2026, Vol. 46 ›› Issue (2): 509-516.DOI: 10.19852/j.cnki.jtcm.2026.02.022
• Reviews • Previous Articles
Masoumeh Amiri1, Mozafar Khazaei2,3, Tayebeh Sadat Tabatabai4, Leila Rezakhani2,3
Received:2025-07-22
Accepted:2025-12-06
Online:2026-04-15
Published:2026-04-04
Contact:
Dr. Leila Rezakhani, Fertility and Infertility Research Center, Health Technology Institute, Kermanshah University of Medical Sciences, Kermanshah 6715847141, Iran; Department of Tissue Engineering, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah 6715847141, Iran
Supported by:Masoumeh Amiri, Mozafar Khazaei, Tayebeh Sadat Tabatabai, Leila Rezakhani. Therapeutic potential of garlic-derived exosome like nanovesicles: challenge and opportunity[J]. Journal of Traditional Chinese Medicine, 2026, 46(2): 509-516.
| Nanoparticle Source | Application | Characteristics and effects | Tested on | Referenece |
|---|---|---|---|---|
| GaELNVs | Alleviation of brain inflammation | Reduces expression of inflammatory cytokines in microglia cells, decreases neuronal cell death, enhances memory function, improves glucose tolerance, and insulin sensitivity | Microglia cells, primary neuronal cells, mice | |
| GaELNVs | Treatment of ulcerative colitis | Particle size: 79.60 nm. Normalized production of proinfla-mmatory cytokines. Contents: functional proteins and microRNAs | Mice with DSS-induced colitis | |
| GaELNVs | Investigating the effects on mammalian cancer cells and normal cells | Exosome size: 30-100 nm. Contents: proteins, RNA, DNA, mRNA, and miRNA | Malignant cell lines Normal cells | |
| GaELNVs | Inhibition of systemic and brain inflammatory activity. Reversal of high-fat diet induced obesity in mice | GaELNs were isolated and orally administered to HFD-fed mice | Mice fed a high-fat diet | |
| GaELNVs | Training gut microbiota to release healthy outer membrane vesicles. Reversal of high-fat diet-induced type 2 diabetes and brain inflammation in mice | Gut microbiota can be trained by diet-derived exosome-like nanoparticles. Specific application: outer membrane vesicles released from GaELNs trained Akkermansia muciniphila in human gut | - | |
| SEVs | Investigating the effect on cancer cell progression, particularly in inducing apoptosis | Methods used: nanoparticle tracking analysis, electron microscopy, SEV surface antibody analysis | - | |
| GaELNVs | Investigation into how plant-derived nanovesicles is taken up by cells | GaELNVs isolated and digested with trypsin to remove surface proteins Comparison: digested GaELNVs showed reduced uptake compared to undigested GaELNVs, indicating the role of surface proteins in endocytosis | Contributes to understanding GaELNVs intern-alization mechanisms and their cellular anti-inflammatory effects | |
| GaELNVs | Therapeutic potential for ameliorating liver injury induced by LPS/D-GalN in mice. Delivery vehicle to inhibit inflammatory responses and reduce inflammatory cell infiltration | GaELNVs administered to mice with liver injury induced by LPS/ D-GalN/. | GaELNVs proposed as a novel therapeutic agent for clinical management of liver disease | |
| GaELNVs | Pharmacological potential in alleviating diseases. Maintenance of intestinal health through gut microbiome manipulation. Targeted therapy and drug delivery applications. Development into dietary supplements | ELNs are lipid bilayer membrane-bound vesicular structures, 30-150 nm in size. Similar features to exosomes derived from eukaryotic animal cells. | - |
Table 1 GaELNVs application in diseases
| Nanoparticle Source | Application | Characteristics and effects | Tested on | Referenece |
|---|---|---|---|---|
| GaELNVs | Alleviation of brain inflammation | Reduces expression of inflammatory cytokines in microglia cells, decreases neuronal cell death, enhances memory function, improves glucose tolerance, and insulin sensitivity | Microglia cells, primary neuronal cells, mice | |
| GaELNVs | Treatment of ulcerative colitis | Particle size: 79.60 nm. Normalized production of proinfla-mmatory cytokines. Contents: functional proteins and microRNAs | Mice with DSS-induced colitis | |
| GaELNVs | Investigating the effects on mammalian cancer cells and normal cells | Exosome size: 30-100 nm. Contents: proteins, RNA, DNA, mRNA, and miRNA | Malignant cell lines Normal cells | |
| GaELNVs | Inhibition of systemic and brain inflammatory activity. Reversal of high-fat diet induced obesity in mice | GaELNs were isolated and orally administered to HFD-fed mice | Mice fed a high-fat diet | |
| GaELNVs | Training gut microbiota to release healthy outer membrane vesicles. Reversal of high-fat diet-induced type 2 diabetes and brain inflammation in mice | Gut microbiota can be trained by diet-derived exosome-like nanoparticles. Specific application: outer membrane vesicles released from GaELNs trained Akkermansia muciniphila in human gut | - | |
| SEVs | Investigating the effect on cancer cell progression, particularly in inducing apoptosis | Methods used: nanoparticle tracking analysis, electron microscopy, SEV surface antibody analysis | - | |
| GaELNVs | Investigation into how plant-derived nanovesicles is taken up by cells | GaELNVs isolated and digested with trypsin to remove surface proteins Comparison: digested GaELNVs showed reduced uptake compared to undigested GaELNVs, indicating the role of surface proteins in endocytosis | Contributes to understanding GaELNVs intern-alization mechanisms and their cellular anti-inflammatory effects | |
| GaELNVs | Therapeutic potential for ameliorating liver injury induced by LPS/D-GalN in mice. Delivery vehicle to inhibit inflammatory responses and reduce inflammatory cell infiltration | GaELNVs administered to mice with liver injury induced by LPS/ D-GalN/. | GaELNVs proposed as a novel therapeutic agent for clinical management of liver disease | |
| GaELNVs | Pharmacological potential in alleviating diseases. Maintenance of intestinal health through gut microbiome manipulation. Targeted therapy and drug delivery applications. Development into dietary supplements | ELNs are lipid bilayer membrane-bound vesicular structures, 30-150 nm in size. Similar features to exosomes derived from eukaryotic animal cells. | - |
| 1. |
Banerjee S, Mukherjee PK, Maulik S. Garlic as an antioxidant: the good, the bad and the ugly. Phytother Res 2003; 17: 97-106.
DOI PMID |
| 2. |
Lanzotti V. The analysis of onion and garlic. J Chromatogr A 2006; 1112: 3-22.
DOI PMID |
| 3. |
Teng Y, Ren Y, Sayed M, et al. Plant-derived exosomal microRNAs shape the gut microbiota. Cell Host Microbe 2018; 24: 637-52.e638.
DOI PMID |
| 4. |
Zhang M, Wang X, Han MK, Collins JF, Merlin D. Oral administration of ginger-derived nanolipids loaded with siRNA as a novel approach for efficient siRNA drug delivery to treat ulcerative colitis. Nanomedicine 2017; 12: 1927-43.
DOI URL |
| 5. |
Deng Z, Rong Y, Teng Y, et al. Broccoli-derived nanoparticle inhibits mouse colitis by activating dendritic cell AMP-activated protein kinase. Mol Ther 2017; 25: 1641-54.
DOI PMID |
| 6. |
Fang Z, Liu K. Plant-derived extracellular vesicles as oral drug delivery carriers. J Control Release 2022; 350: 389-400.
DOI URL |
| 7. | Warnecke A, Harre J, Staecker H, et al. Extracellular vesicles from human multipotent stromal cells protect against hearing loss after noise trauma in vivo. Clin Transl Med 2020; 10: e262. |
| 8. |
Hadidi M, Karimabadi K, Ghanbari E, Rezakhani L, Khazaei M. Stem cells and exosomes: as biological agents in the diagnosis and treatment of polycystic ovary syndrome (PCOS). Front Endocrinol 2023; 14: 1269266.
DOI URL |
| 9. |
Rahmati S, Khazaei M, Abpeikar Z, Soleimanizadeh A, Rezakhani L. Exosome-loaded decellularized tissue: opening a new window for regenerative medicine. J Tissue Viability 2024; 33: 332-44.
DOI PMID |
| 10. |
Rahmati S, Karimi H, Alizadeh M, et al. Prospects of plant-derived exosome-like nanocarriers in oncology and tissue engineering. Hum Cell 2024; 37: 121-38.
DOI |
| 11. |
Amiri M, Kaviari MA, Rostaminasab G, Barimani A, Rezakhani L. A novel cell-free therapy using exosomes in the inner ear regeneration. Tissue Cell 2024; 88: 102373.
DOI URL |
| 12. |
Mu J, Zhuang X, Wang Q, et al. Interspecies communication between plant and mouse gut host cells through edible plant derived exosome-like nanoparticles. Mol Nutr Food Res 2014; 58: 1561-73.
DOI PMID |
| 13. |
Zhuang X, Teng Y, Samykutty A, et al. Grapefruit-derived nanovectors delivering therapeutic miR17 through an intranasal route inhibit brain tumor progression. Mol Ther 2016; 24: 96-105.
DOI PMID |
| 14. |
Wang B, Zhuang X, Deng ZB, et al. Targeted drug delivery to intestinal macrophages by bioactive nanovesicles released from grapefruit. Mol Ther 2014; 22: 522-34.
DOI PMID |
| 15. |
Farhat Z, Scheving T, Aga DS, et al. Antioxidant and antiproliferative activities of several garlic forms. Nutrients 2023; 15: 4099.
DOI URL |
| 16. |
Zheng X, Zhu Y, Zhao Z, Chu Y, Yang W. The role of amino acid metabolism in inflammatory bowel disease and other inflammatory diseases. Front Immunol 2023; 14: 1284133.
DOI URL |
| 17. |
Zhao X, Yin F, Fu L, et al. Garlic-derived exosome-like nanovesicles as a hepatoprotective agent alleviating acute liver failure by inhibiting CCR2/CCR5 signaling and inflammation. Biomater Adv 2023; 154: 213592.
DOI URL |
| 18. | Meza-Rios A, Velazquez-Juarez G, Castellanos-Huerta I, et al. The beneficial effects of components of garlic (Allium sativum L.) in the poultry industry. Food Nutr Sci 2024; 15: 27-57. |
| 19. |
Talib WH, Baban MM, Azzam AO, et al. Allicin and cancer hallmarks. Molecules 2024; 29: 1320.
DOI URL |
| 20. |
Ankri S, Mirelman D. Antimicrobial properties of allicin from garlic. Microbes Infect 1999; 1: 125-9.
DOI PMID |
| 21. | Strika I, Bašić Halilović A, Halilović N. Antimicrobial effects of garlic (Allium sativum L.). Bull Chem Technol Bosnia Herzeg 2016; 47: 17-20. |
| 22. |
Agarwal KC. Therapeutic actions of garlic constituents. Med Res Rev 1996; 16: 111-24.
DOI PMID |
| 23. |
Choo S, Chin VK, Wong EH, et al. Antimicrobial properties of allicin used alone or in combination with other medications. Folia Microbiol 2020; 65: 451-65.
DOI |
| 24. |
Martins N, Petropoulos S, Ferreira IC. Chemical composition and bioactive compounds of garlic (Allium sativum L.) as affected by pre- and post-harvest conditions: a review. Food Chem 2016; 211: 41-50.
DOI PMID |
| 25. | Wallock-Richards D, Doherty CJ, Doherty L, et al. Garlic revisited: antimicrobial activity of allicin-containing garlic extracts against Burkholderia cepacia complex. PLoS One 2014; 9: e112726. |
| 26. |
Amagase H, Milner JA. Impact of various sources of garlic and their constituents on 7,12-dimethylbenz[α]anthracene binding to mammary cell DNA. Carcinogenesis 1993; 14: 1627-31.
PMID |
| 27. |
Hussain S, Jannu L, Rao A. Chemopreventive action of garlic on methylcholanthrene-induced carcinogenesis in the uterine cervix of mice. Cancer Lett 1990; 49: 175-80.
PMID |
| 28. |
Sumiyoshi H, Wargovich MJ. Chemoprevention of 1,2-dimethylhydrazine-induced colon cancer in mice by naturally occurring organosulfur compounds. Cancer Res 1990; 50: 5084-7.
PMID |
| 29. |
Sarvizadeh M, Hasanpour O, Naderi Ghale-Noie Z, et al. Allicin and digestive system cancers: from chemical structure to its therapeutic opportunities. Front Oncol 2021; 11: 650256.
DOI URL |
| 30. |
Catanzaro E, Canistro D, Pellicioni V, Vivarelli F, Fimognari C. Anticancer potential of allicin: a review. Pharmacol Res 2022; 177: 106118.
DOI URL |
| 31. |
Țigu AB, Moldovan CS, Toma V A, et al. Phytochemical analysis and in vitro effects of Allium fistulosum L. and Allium sativum L. extracts on human normal and tumor cell lines: a comparative study. Molecules 2021; 26: 574.
DOI URL |
| 32. |
Tu G, Zhang YF, Wei W, et al. Allicin attenuates H2O2 induced cytotoxicity in retinal pigmented epithelial cells by regulating the levels of reactive oxygen species. Mol Med Rep 2016; 13: 2320-6.
DOI URL |
| 33. |
Wang S, Ren D. Allicin protects traumatic spinal cord injury through regulating the HSP70/Akt/iNOS pathway in mice. Mol Med Rep 2016; 14: 3086-92.
DOI PMID |
| 34. |
Wang W, Du Z, Nimiya Y, Sukamtoh E, Kim D, Zhang G. Allicin inhibits lymphangiogenesis through suppressing activation of vascular endothelial growth factor (VEGF) receptor. J Nutr Biochem 2016; 29: 83-9.
DOI PMID |
| 35. |
Chen L, Hong JY, So E, Hussin AH, Cheng WF, Yang CS. Decrease of hepatic catalase level by treatment with diallyl sulfide and garlic homogenates in rats and mice. J Biochem Mol Toxicol 1999; 13: 127-34.
PMID |
| 36. |
Hirata R, Matsushita S. Reducing activity level of alliin. Biosci Biotechnol Biochem 1996; 60: 484-5.
DOI URL |
| 37. |
Ide N, Lau BH. Garlic compounds minimize intracellular oxidative stress and inhibit nuclear factor-κB activation. J Nutr 2001; 131: 1020S-6S.
DOI PMID |
| 38. | Maslin DJ, Brown CA, Das I, Zhang XH. Nitric oxide — a mediator of the effects of garlic? Biochem Soc Trans 1997; 25: 408S. |
| 39. | Popov I, Blumstein A, Lewin G. Antioxidant effects of aqueous garlic extract. Arzneim-Forsch 1994; 44: 602-4. |
| 40. | Akullo JO, Kiage-Mokua BN, Nakimbugwe D, Kinyuru J. Phytochemical profile and antioxidant activity of various solvent extracts of two varieties of ginger and garlic. Heliyon 2023; 9: e18643. |
| 41. | Stabler SN, Tejani AM, Huynh F, Fowkes C. Garlic for the prevention of cardiovascular morbidity and mortality in hypertensive patients. Cochrane Database Syst Rev 2012; CD007653. |
| 42. |
Schwingshackl L, Missbach B, Hoffmann G. An umbrella review of garlic intake and risk of cardiovascular disease. Phytomedicine 2016; 23: 1127-33.
DOI PMID |
| 43. |
Chiavarini M, Minelli L, Fabiani R. Garlic consumption and colorectal cancer risk in man: a systematic review and meta-analysis. Public Health Nutr 2016; 19: 308-17.
DOI PMID |
| 44. |
Lee YM, Gweon OC, Seo YJ, et al. Antioxidant effect of garlic and aged black garlic in animal model of type 2 diabetes mellitus. Nutr Res Pract 2009; 3: 156.
DOI URL |
| 45. |
Jelodar Gholamali A, Maleki M, Motadayen M, Sirus S. Effect of fenugreek, onion and garlic on blood glucose and histopathology of pancreas of alloxan-induced diabetic rats. Indian J Med Sci 2005; 59: 64-9.
PMID |
| 46. |
Eidi A, Eidi M, Esmaeili E. Antidiabetic effect of garlic (Allium sativum L.) in normal and streptozotocin-induced diabetic rats. Phytomedicine 2006; 13: 624-9.
DOI PMID |
| 47. |
Liu CT, Sheen LY, Lii CK. Does garlic have a role as an antidiabetic agent? Mol Nutr Food Res 2007; 51: 1353-64.
DOI URL |
| 48. |
Wang J, Zhang X, Lan H, Wang W. Effect of garlic supplement in the management of type 2 diabetes mellitus (T2DM): a Meta-analysis of randomized controlled trials. Food Nutr Res 2017; 61: 1377571.
DOI URL |
| 49. |
Sundaram K, Mu J, Kumar A, et al. Garlic exosome-like nanoparticles reverse high-fat diet induced obesity via the gut/brain axis. Theranostics 2022; 12: 1220.
DOI PMID |
| 50. |
Wang X, Liu Y, Dong X, et al. peu-MIR2916-p3-enriched garlic exosomes ameliorate murine colitis by reshaping gut microbiota, especially by boosting the anti-colitic Bacteroides thetaiotaomicron. Pharmacol Res 2024; 200: 107071.
DOI URL |
| 51. |
Zhou S, Huang P, Cao Y, Hua X, Yang Y, Liu S. Garlic-derived exosome-like nanovesicles-based wound dressing for Staphylococcus aureus infection visualization and treatment. ACS Appl Bio Mater 2024; 7: 1888-98.
DOI URL |
| 52. |
Ünsal N, Koçak Denizci P, Yilmaz H, Şahin F, Yildirim Canpolat M. The apoptotic effect of garlic (Allium sativum) derived SEVs on different types of cancer cell lines in vitro. Turk J Biol 2024; 48: 182-91.
DOI PMID |
| 53. |
Liu B, Li X, Yu H, et al. Therapeutic potential of garlic chive-derived vesicle-like nanoparticles in NLRP3 inflammasome-mediated inflammatory diseases. Theranostics 2021; 11: 9311.
DOI PMID |
| 54. |
Zhu Z, Liao L, Gao M, Liu Q. Garlic-derived exosome-like nanovesicles alleviate dextran sulphate sodium-induced mouse colitis via the TLR4/MyD88/NF-κB pathway and gut microbiota modulation. Food Funct 2023; 14: 7520-34.
DOI URL |
| 55. |
Özkan İ, Koçak P, Yıldırım M, et al. Garlic (Allium sativum)-derived SEVs inhibit cancer cell proliferation and induce caspase mediated apoptosis. Sci Rep 2021; 11: 14773.
DOI PMID |
| 56. |
Anusha R, Priya S. Dietary exosome-like nanoparticles: an updated review on their pharmacological and drug delivery applications. Mol Nutr Food Res 2022; 66: 2200142.
DOI URL |
| 57. |
Sha A, Luo Y, Xiao W, et al. Plant-derived exosome-like nanoparticles: a comprehensive overview of their composition, biogenesis, isolation, and biological applications. Int J Mol Sci 2024; 25: 12092.
DOI URL |
| 58. | Markam R, Bajpai J, Bajpai A. Synthesis of ginger derived nanocarriers (GDNC) and study of in vitro release of 5-amino salicylic acid (5-ASA) as an anti inflammatory drug. J Drug Deliv Sci Technol 2019; 50: 355-64. |
| 59. |
Liu Y, Nie M, Li X, et al. Garlic-derived exosomes alleviate osteoarthritis through inhibiting the MAPK signaling pathway. Appl Biochem Biotechnol 2025; 197: 518-33.
DOI |
| 60. |
Ju S, Mu J, Dokland T, et al. Grape exosome-like nanoparticles induce intestinal stem cells and protect mice from DSS-induced colitis. Mol Ther 2013; 21: 1345-57.
DOI PMID |
| 61. |
Song H, Canup BS, Ngo VL, Denning TL, Garg P, Laroui H. Internalization of garlic-derived nanovesicles on liver cells is triggered by interaction with CD98. ACS Omega 2020; 5: 23118-28.
DOI PMID |
| 62. |
Yu C, Liu Y, Yu X, et al. Garlic derived exosome like nanovesicles: a promising natural nanotherapy for periodontitis via PHGDH/PI3K/AKT mediated metabolic and inflammatory regulation. Int J Nanomedicine 2025; 20: 5551-72.
DOI URL |
| 63. |
Sharma V, Sinha ES, Singh J. Investigation of in vitro anti-cancer and apoptotic potential of garlic-derived nanovesicles against prostate and cervical cancer cell lines. Asian Pac J Cancer Prev 2024; 25: 575.
DOI URL |
| 64. |
Rezakhani L, Fekri K, Rostaminasab G, Rahmati S. Exosomes: special nano-therapeutic carrier for cancers, overview on anticancer drugs. Med Oncol 2022; 40: 31.
DOI PMID |
| 65. |
Sundaram K, Teng Y, Mu J, et al. Outer membrane vesicles released from garlic exosome-like nanoparticles (GaELNs) train gut bacteria that reverse type 2 diabetes via the gut-brain axis. Small 2024; 20: 2308680.
DOI URL |
| 66. |
Dad HA, Gu TW, Zhu AQ, Huang LQ, Peng LH. Plant exosome-like nanovesicles: emerging therapeutics and drug delivery nanoplatforms. Mol Ther 2021; 29: 13-31.
DOI PMID |
| 67. |
Chai M, Gao B, Wang S, et al. Leveraging plant derived nanovesicles for advanced nucleic acid based gene therapy. Theranostics 2025; 15: 324-39.
DOI URL |
| 68. |
Barzin M, Bagheri AM, Ohadi M, Abhaji AM, Salarpour S, Dehghannoudeh G. Application of plant-derived exosome-like nanoparticles in drug delivery. Pharm Dev Technol 2023; 28: 383-402.
DOI URL |
| 69. |
Shang A, Cao SY, Xu XY, et al. Bioactive compounds and biological functions of garlic (Allium sativum L.). Foods 2019; 8: 246.
DOI URL |
| 70. |
Mu N, Li J, Zeng L, et al. Plant derived exosome like nanovesicles: current progress and prospects. Int J Nanomedicine 2023; 18: 4987-5009.
DOI URL |
| [1] | WANG Xuehui, SUN Yuxin, Birling Yoann, LI Xun, ZHAO Ruotong, ZHENG Youyou, SONG Zhenmei, ZHANG Yanli, DU Hongbo, WANG Jianyun, LI Yinqing, LIU Zhaolan, LIU Jianping. A Meta-analysis of Traditional Chinese Medicine constitution distribution in people with functional constipation [J]. Journal of Traditional Chinese Medicine, 2026, 46(2): 261-273. |
| [2] | LI Kexin, YANG Jinzu, XIAO Kunlin, DUAN Shaojie, XIAO Kunmin. Tongue-coating microbiome as a predictor of solid tumors: an updated scoping review of clinical studies [J]. Journal of Traditional Chinese Medicine, 2026, 46(2): 501-508. |
| [3] | LIN Lixia, LI Xin, LI Ling, YANG Pu, LU Liming, LIU Buping, SU Shengyong. Multiple acupuncture and moxibustion therapies for allergic rhinitis in adults: a network Meta-analysis of randomized controlled trials [J]. Journal of Traditional Chinese Medicine, 2026, 46(1): 1-13. |
| [4] | YANG Wu, LI Yinghui, LIAO Heng, XIONG Shangbin. Molecular landscape of Berberine's therapeutic potential in gastrointestinal disorders [J]. Journal of Traditional Chinese Medicine, 2026, 46(1): 245-256. |
| [5] | Hyungsun Jun, Nahyun Cho, Wonbae Ha, Junghan Lee, Mi Mi Ko, Young-Eun Kim, Jeeyoun Jung, Jungtae Leem. Key elements for screening kidney deficiency pattern in Traditional Chinese and Korean Medicine: a systematic review and Delphi study [J]. Journal of Traditional Chinese Medicine, 2025, 45(6): 1169-1177. |
| [6] | WANG Ci, CAO Yawen, WANG Jiaying, CHEN Jixin, MA Xue, WANG Xianliang, MAO Jingyuan. Efficacy and safety of acupuncture for arrythmias: an overview of systematic reviews and Meta-analyses [J]. Journal of Traditional Chinese Medicine, 2025, 45(6): 1178-1190. |
| [7] | KONG Lingyao, ZHANG Xiaowen, WANG Xuehui, WANG Zhijie, Robinson Nicola, LIU Jianping. Moxibustion for human immunodeficiency virus and acquired immunodeficiency syndrome and its complications: a systematic review of randomized controlled trials [J]. Journal of Traditional Chinese Medicine, 2025, 45(6): 1201-1214. |
| [8] | ZHANG Gedi, WEN Xiaoli, TAO Tianming, YAN Ziyou, LIU Hongning. Exploration of constructing a relatively comprehensive syndrome differentiation and treatment system based on dialectical materialism principles [J]. Journal of Traditional Chinese Medicine, 2025, 45(5): 1164-1168. |
| [9] | JIANG Jinglei, YU Tao, QIAN Yulin, WANG Meng. Understanding the role of microglia in Alzheimer's disease: insights into mechanisms, acupuncture, and potential therapeutic targets [J]. Journal of Traditional Chinese Medicine, 2025, 45(4): 922-936. |
| [10] | ZHANG Yang, LYU Wang, XU Xin, LI Jie, HU Shengli, WANG Ying. Clinical effect of Shugan Jieyu San (疏肝解郁散) for improving liver function and alleviating depression in patients with triple negative breast cancer [J]. Journal of Traditional Chinese Medicine, 2025, 45(3): 633-638. |
| [11] | WANG Yiying, DONG Shuai, LI Bo, HAN Mei, CAO Huijuan. Update evidence of effectiveness on pain relieving of cupping therapy: a systematic review and Meta-analysis of randomized controlled trials [J]. Journal of Traditional Chinese Medicine, 2025, 45(2): 234-253. |
| [12] | ZHANG Dingshan, CHEN Li, MARYAM Mazhar, XUE Jinyi, LIU Ping, LIU Mengnan. Application of promoting blood circulation and resolving blood stasis in intracerebral hemorrhage: a traditional method gradually being reconsidered [J]. Journal of Traditional Chinese Medicine, 2025, 45(2): 458-472. |
| [13] | DONG Yingying, GUO Qin, GAO Yuan, WANG Huanhuan, BAI Dong. Revealing the scientific connotation of compatibility of Chinese medicine medica based on self-assembly technology [J]. Journal of Traditional Chinese Medicine, 2024, 44(6): 1288-1295. |
| [14] | XI Hanqing, LI Xia, ZHANG Ziyi, CUI Xiang, JING Xianghong, ZHU Bing, GAO Xinyan. Neuro- and immuno-modulation mediated by the cardiac sympathetic nerve: a novel insight into the anti-ischemic efficacy of acupuncture [J]. Journal of Traditional Chinese Medicine, 2024, 44(5): 1058-1066. |
| [15] | XU Yingshan, WU Chunxiao, YU Wei, GUO Hongji, LU Liming, XU Nenggui, TANG Chunzhi. Systematic review and Meta-analysis of brain plasticity associated with electroacupuncture in experimental ischemic stroke [J]. Journal of Traditional Chinese Medicine, 2024, 44(5): 859-870. |
| Viewed | ||||||
|
Full text |
|
|||||
|
Abstract |
|
|||||
Sponsored by China Association of Chinese Medicine
& China Academy of Chinese Medical Sciences
16 Nanxiaojie, Dongzhimen Nei, Beijing, China. 100700 Email: jtcmen@126.com
Copyright 2020 Journal of Traditional Chinese Medicine. All rights reserved.
