Leonurus japonicus Houtt in Traditional Chinese Medicine: A Review of Phytochemistry, Pharmacology, and Clinical Applications

Authors

  • HuSile Graduate School, Inner Mongolia Medical University, Hohhot, Inner Mongolia, China
    Competing Interests

    No

  • Changbao Zhao College of Mongolian Medicine, Inner Mongolia Medical University, Hohhot, Inner Mongolia, China
    Competing Interests

    No

  • Hubisihalatu College of Mongolian Medicine, Inner Mongolia Medical University, Hohhot, Inner Mongolia, China

Keywords:

White Leonurus japonicus, Traditional Chinese Medicine, Phytochemistry, Pharmacology, Clinical Applications

Abstract

Background: Leonurus japonicus Houtt. grass (white Leonurus japonicus grass) is a perennial herbaceous plant, which is widely used in traditional Chinese medicine to treat gynecological diseases, cardiovascular protection, and inflammation management. This review integrates current knowledge of plant chemistry, pharmacology, and clinical applications to promote the integration of evidence-based and contemporary medicine. Method: A detailed literature review was conducted using PubMed, Web of Science, CNKI, and Wan Fang Data, with the search extended to December 2025. The terms "Leonurus japonicus", "plant chemistry", "pharmacology", and "clinical application" are used. Of the 680 articles initially identified, 326 meet the criteria for full-text review because they address the applications and pharmacological mechanisms of traditional Chinese medicine. Results: Alkaloids, flavonoids, and diterpenes are only a few of the many bioactive compounds found in Leonurus japonicus. In traditional Chinese medicine (TCM), it is mostly used to treat hypertension, edema, menstrual problems, and to accelerate recovery after childbirth. Studies on drugs show that they can make the uterus contract, stop bleeding, protect the heart, reduce inflammation, and protect the nervous system. Preliminary clinical evidence shows that it has the effect of preventing postpartum bleeding and relieving dysmenorrhea. Conclusion: Although preclinical evidence supports traditional applications, clinical verification is still insufficient. Future research must prioritize standardized extracts, high-quality randomized controlled trials, and mechanistic studies to fully clarify its therapeutic potential in both traditional Chinese medicine and contemporary medicine.

Abstract
5
PDF
2

References

1. Witkowska, A., Gryn-Rynko, A., Syrkiewicz, P., Kitala-Tańska, K., Majewski, M. S. (2024). Characterizations of White Mulberry, Sea-Buckthorn, Garlic, Lily of the Valley, Leonurus japonicas wort, and Hawthorn as Potential Candidates for Managing Cardiovascular Disease-In Vitro and Ex Vivo Animal Studies. Nutrients. 16(9), 1313. https://doi.org/10.3390/nu16091313

2. Zhang, R., Ji, D., Zhang, Q., Jin, L. (2021).

Evaluation of Eleven Plant Species as Potential Banker Plants to Support Predatory Orius sauteri in Tea Plant Systems. Insects. 12(2), 162. https://doi.org/10.3390/insects12020162

3. Jia, Z., Gou, J., Sun, Y., Yuan, L., Tang, Q., Yang, X., Pei, Y., Luo, K. (2010). Enhanced resistance to fungal pathogens in transgenic Populus tomentosa Carr. by overexpression of an nsLTP-like antimicrobial protein gene from motherwort (Leonurus japonicus). Tree Physiol. 30(12), 1599–

1605. https://doi.org/10.1093/treephys/tpq093

4. Yang, K., A Ru, N., Zhou, X., Zhang, N., Zhu, D. (2022). Textual research on Mongolian medicine Baiyimucao. Chin. J. Tradit. Chin. Med. Pharm. 37(07), 4130-4132.

5. Wei, N., Dong, Z. H., Zhao, R. W. (2024).

Bioinformatics-based investigation of the pharmacological mechanisms of Panzeria alaschanica Kupr in treating endometriosis. Chem. Life. 45(08), 1503-1517.

https://doi.org/10.13488/j.smhx.20250150

6. Wang, J. J., Zhu, W., Wu, D., Jia, X., Yang, Y. F.

(2024). Research progress of Mongolian medicine Baiyimucao. J. Baotou Med. Coll. 20(10), 87-91. https://doi.org/10.16833/j.cnki.jbmc.2024.10.018

7. Hubis, H., Wang, Q. H., He, X., Bilige, T., Bao, W.

Q. (2022). Isolation and identification of phenolic glycosides from Panzeria alashanica Kupr. and evaluation of their antioxidant activities in vitro. Chin. J. Mod. Appl. Pharm. 39(03), 321-315. https://doi.org/10.13748/j.cnki.issn1007-7693

8. Jin, C. M. (2021). Research progress on chemical constituents and clinical application of Mongolian medicine motherwort. J. Med. Pharm. Chin. Minor. 27(01), 63-64.

https://doi.org/10.16041/j.cnki.cn15-1175

9. Sarina. (2020). Research on the chemical composition and clinical application progress of Mongolian medicine motherwort. Cardiovasc. Dis. Electron. J. Integr. Tradit. Chin. West. Med. 8(25), 174-181.

https://doi.org/10.16282/j.cnki.cn11-9336/r

10. Zheng, Y. F., Yin, W., Lin, L. I., Du, S. S., Shan, T.,

Wang, Y. (2027). Advances in studies on Panzeria alaschanica. Chin. Tradit. Herb. Drugs. 38, 1434-6.

11. Liu, X. F., Li, X. L., Zhu, D. (2013). Monthly and regional variability in effective components of Mongolian Baiyimucao. Chin. J. Tradit. Chin. Med. Pharm. 28(01), 256-258.

12. Yuan, Y., Si, Q. (2019). Investigating the quality standards and active ingredient activity of Mongolian White motherwort. World Latest Med. Inf. Dig. 19(56), 222-223. https://doi. org/10.19613/j.cnki.1671-3141.2019.56.136

13. Lei, Q. F., Zhao, X. P., Zhu, D. (2017). Progress of Mongolian herb Panzeria alaschanica Kupr. in chemical components and clinical application. Chin. J. Tradit. Chin. Med. Pharm. 32(07), 3083-3085.

14. Dong, Z., Yu, Q. H., Zhu, D. (2012). Investigation into the assessment of therapeutical effect of Mongolian Herba Baiyimucao on female subjects with dysmenorrhea. J. Minzu Univ. China Nat. Sci. Ed. 21(01), 63-66.

15. Agula, L. Y., Erdeng, Xu, C. (1999). Morphological and histological characters of Mongolian medicine, Alashan Panzeria (Panzeria alaschanica). Chin. Tradit. Herb. Drugs (2), 140-142.

16. Ibrahim, S. R. M., Mohamed, H. M., Murshid, S.

S. A., Nashawi, A. A., Mohamed, G. A. (2026). Recent advances in cassane diterpenoids: structural diversity and biological activities. RSC Adv. 16(3), 2062-2092. https://doi.org/10.1039/d5ra07088k

17. Xiong, J., Ge, Q., Fu, B., Li, J., Lin, Z., Zhu, Y. Z.

(2026). SCM-198 ameliorates pulmonary arterial hypertension by modulating gut microbiota in rats.

J. Thorac. Dis. 17(11), 9799-9812.

https://doi.org/10.21037/jtd-2025-1363

18. Marini, M., Landini, L., Coppi, E., Tesi, M., Bellantoni, E., Chieca, M., Croce, E. B., Bonacchi, L., Brancolini, G. (2025). Anti-nociceptive action of leonurine through TRPA1 and TRPV4 channels modulation. Br. J. Pharmacol. 182(22), 5469-5488. https://doi.org/10.1111/bph.70135

19. Chen, Y., Li, R., Chen, Y., Li, C., Pan, M., Chen,

P., Jiang, Y., Chen, J., Huang, Z., Feng, Y. (2026). Inhibitory effects of diterpenoids from Celastrus rosthornianus Lose. on lipid accumulation. Bioorg. Med. Chem. Lett. 133, 130538. https://doi.org/10.1016/j.bmcl.2026.130538

20. Liu, Y. Y., Liang, C. H., Cao, J. Y., Lu, G. Y., Zhao,

D. S., Zhao, P., Deng, Z. P., Wang, S. J. (2025). A

new jatrophane diterpenoid with anti-inflammatory activity from Euphorbia thymifolia. Zhongguo Zhong Yao Za Zhi. 50(18), 5190-5197.

https://doi.org/10.19540/j.cnki.cjcmm.20250531.201

21. Zhang, Y., Deng, S., Qu, L., An, Y. T., Wu, C. H., Han,

L. F., Gao, X. M., Wang, T. (2013). Rare syringyl acylated flavonol glycosides from the aerial parts of Leonurus japonicus Houtt. Molecules. 18(3), 2967–

2977. https://doi.org/10.3390/molecules18032967

22. Cao, K., Song, M., Yu, R., Zhao, Y., Chen, P.,

Wang, C., Guo, S., Li, Z., Li, Y., Dang, Y., He, J.,

Xu, Y. (2026). Oroxylin A Suppresses Pathological Vascular Smooth Muscle Cell Phenotypic Switching and Neointima Formation Through Hindering TSC2/mTORC1/HIF-1-Dependent Glycolysis. Phytother. Res. 40(3), 907-923. https://doi.org/10.1002/ptr.70145

23. Liu, Y., Lu, Y., Bao, W., Zhu, H., Yuan, G., Guo,

L., Li, H., Li, J., Wu, T., Shi, X., Chen, D. (2026).

Quercitrin Inhibits NETosis via Histone H3 to Alleviate the Severity of Viral Pneumonia With Drug-Resistant Bacteria Co-Infection in Mice. Phytother. Res. 40(3), 924-940. https://doi.org/10.1002/ptr.70190

24. Pasi, S., Aligiannis, N., Pratsinis, H., Skaltsounis,

A. L., Chinou, I. B. (2009). Biologically active triterpenoids from Cephalaria ambrosioides. Planta Med. 75(2), 163-167.

https://doi.org/10.1055/s-0028-1088391

25. Mihai, R. A., Vivanco Gonzaga, R. F., Silva Ayo,

F. A., López Mendoza, R. A., Nicolalde Padilla,

M. A., Calahorrano Cabrera, J. E., Chuma, A. R., Catana, R. D. (2026). Host-dependent variations in antioxidant activity, metabolic profile, and phenolic content of the parasitic plant Phoradendron nervosum Oliv. Sci. Rep. 16(1), 1556. https://doi.org/10.1038/s41598-025-27242-z

26. Cheng, Y., Chen, S., Cao, D., Cheng, H., Chen, S., Shu, Y., Wang, Y., Chen, Z. (2025). Stachydrine Ameliorates Uterine Hypercontractility in Primary Dysmenorrhea by Targeting the COX-2/PGF2α Pathway. Curr. Issues Mol. Biol. 47(11), 961. https://doi.org/10.3390/cimb47110961

27. Li, L., Zhu, Y., Deng, H., Xie, L., Zheng, C. B.,

Yao, J. N., Li, J. (2025). Recent Advances in Ent-Abietane Diterpenes: Natural Sources, Biological Activities and Total Synthesis. Molecules. 31(1),

98. https://doi.org/10.3390/molecules3101009

28. Skała, E., Makowczyńska, J., Wieczfinska, J., Kowalczyk, T., Sitarek, P. (2020). Caffeoylquinic Acids with Potential Biological Activity from Plant In vitro Cultures as Alternative Sources of Valuable Natural Products. Curr. Pharm. Des. 26(24), 2817-2842. https://doi.org/10.2174/1381612826666200212115826

29. Wu, G., Chen, X., Wang, W., Kou, Z., Mao, H., Wang,

Y., Dong, L., Lin, T., Tian, F. (2025). Stachydrine mitigates high glucose-induced apoptosis in human

lens epithelial cells by activating mitophagy. Exp. Eye Res. 260, 110568.

https://doi.org/10.1016/j.exer.2025.110568

30. Chen, C., Liu, Q., Lu, Y., Liu, C., Wang, W.,

Luo, Q., Ren, Y., Xiong, Y., Tan, J., Sun, X. (2025). Motherwort synergized with oxytocin for postpartum hemorrhage prevention: Integrated clinical efficacy and mechanism exploration. Phytomedicine. 145, 156951. https://doi.org/10.1016/j.phymed.2025.156951

31. Chen, H. H., Wang, S. N., Cao, T. T., Zheng,

J. L., Tian, J., Shan, X. L., Zhao, P., Guo, W.,

Xu, M., Zhang, C., Lu, R. (2020). Stachydrine hydrochloride alleviates pressure overload-induced heart failure and calcium mishandling on mice. J. Ethnopharmacol. 248, 112306. https://doi.org/10.1016/j.jep.2019.11230

32. Tian, T., Feng, H., Liao, X., Su, Q., Li, Y., Li, X.

(2022). The Efficacy of the Yasmin Ethinylestradiol-Drospirenone (0.03/3 mg) Treatment for Postoperative Abortion: A Protocol of Meta-Analysis. Front. Med. 9, 746668. https://doi.org/10.3389/fmed.2022.746668

33. Shikov, A. N., Pozharitskaya, O. N., Makarov, V. G., Demchenko, D. V., Shikh, E. V. (2011). Effect of Leonurus cardiaca oil extract in patients with arterial hypertension accompanied by anxiety and sleep disorders. Phytother. Res. 25(4), 540-543. https://doi.org/10.1002/ptr.3292

34. Koshovyi, O., Raal, A., Kireyev, I., Tryshchuk, N., Ilina, T., Romanenko, Y., Kovalenko, S. M., Bunyatyan, N. (2021). Phytochemical and Psychotropic Research of Motherwort (Leonurus cardiaca L.) Modified Dry Extracts. Plants. 10(2),

230. https://doi.org/10.3390/plants10020230

35. Nsuala, B. N., Enslin, G., Chen, W., Veale, C., Viljoen, A. (2024). Chemical profiling, anticonvulsant and anxiolytic effects of the smoke constituents isolated from Leonotis leonurus (L.) R.Br. J. Ethnopharmacol. 331, 118271. https://doi.org/10.1016/j.jep.2024.118271

36. Li, P., Yan, M. X., Liu, P., Yang, D. J., He, Z.

K., Gao, Y. (2024). Multiomics analyses of two Leonurus species illuminate leonurine biosynthesis and its evolution. Mol. Plant 17(1), 158-177. https://doi.org/10.1016/j.molp.2023.11.003

37. Sitarek, P., Kowalczyk, T., Santangelo, S., Białas, A. J., Toma, M., Wieczfinska, J., Śliwiński, T., Skała, E. (2018). The Extract of Leonurus sibiricus Transgenic Roots with AtPAP1 Transcriptional Factor Induces Apoptosis via DNA Damage and Down Regulation of Selected Epigenetic Factors in Human Cancer Cells. Neurochem. Res. 43(7), 1363-1370. https://doi.org/10.1007/s11064-018-2551-6

38. Yan, M., An, Y. T., Li, J., Wu, Z. Z., Wang, T.

(2014). Regulatory effect of Leonurus extracts on hyperuricemia in rats. Zhongguo Zhong Yao Za Zhi. 39(24), 4856-4859.

39. Cao, T., Wang, Y., Zhang, J., Song, W., Dai, W., Ji, G., Gurumallesh, P. (2025). Leonurine Alleviates DSS-Induced Colitis in Mice by Regulating Pancreatic Secretion Pathway and Gut Microbiota.

J. Immunol. Res. 6626309. https://doi.org/10.1155/jimr/6626309

40. Shi, X. K., Peng, T., Azimova, B., Li, X. L., Li,

S. S., Cao, D. Y., Fu, N. J., Zhang, G. L., Xiao,

W. L., Wang, F. (2024). Luteolin and its analog luteolin-7-methylether from Leonurus japonicus Houtt suppress aromatase-mediated estrogen biosynthesis to alleviate polycystic ovary syndrome by the inhibition of tumor progression locus 2. J. Ethnopharmacol. 331, 118279. https://doi.org/10.1016/j.jep.2024.118279

41. Cheng, F., Zhou, Y., Wang, M., Guo, C., Cao, Z., Zhang, R., Peng, C. (2020). A review of pharmacological and pharmacokinetic properties of stachydrine. Pharmacol. Res. 155, 104755. https://doi.org/10.1016/j.phrs.2020.104755

42. Shang, X., Pan, H., Wang, X., He, H., Li, M. (2014).

Leonurus japonicus Houtt.: ethnopharmacology, phytochemistry and pharmacology of an important traditional Chinese medicine. J. Ethnopharmacol. 152(1), 14-32.

https://doi.org/10.1016/j.jep.2013.12.052

43. Zhao, Z. H., Yao, Z. H., Lin, S. J., Chu, G., Mu, K.

Q., Wang, Y., Bi, K. S., Wang, T. J., Li, Q., Liu, R.

(2022). Leonurus japonicus Houtt. (Motherwort): Systematic research through chemical profiling, stability under controlled conditions and pharmacokinetic analysis on screening Q-markers for quality control. J. Pharm. Biomed. Anal. 213, 114707. https://doi.org/10.1016/j.jpba.2022.11470

44. Wu, M., Liu, H., Zhang, J., Dai, F., Gong, Y., Cheng, Y. (2023). The mechanism of Leonuri Herba in improving polycystic ovary syndrome was analyzed based on network pharmacology and molecular docking. J. Pharm. Pharm. Sci. 26, 11234. https://doi.org/10.3389/jpps.2023.11234

45. Dou, Y., Shu, L., Jia, X., Yao, Y., Chen, S., Xu, Y.,

Li, Y. (2023). Rapid classification and identification of chemical constituents in Leonurus japonicus Houtt based on UPLC-Q-Orbitrap-MS combined with data post-processing techniques. J. Mass Spectrom. 58(11), e4978. https://doi.org/10.1002/jms.4978

46. Brenyo, A., Aktas, M. K. (2014). Review of complementary and alternative medical treatment of arrhythmias. Am. J. Cardiol. 113(5), 897-903. https://doi.org/10.1016/j.amjcard.2013.11.044

47. Wang, C., Lv, X., Liu, W., Liu, S., Sun, Z. (2020).

Uncovering the pharmacological mechanism of motherwort (Leonurus japonicus Houtt.) for treating menstrual disorders: A systems pharmacology approach. Comput. Biol. Chem. 89, 107384. https://doi.org/10.1016/j.compbiolchem.2020.107384

48. Xiong, Y., Cao, X. Y., Liu, B. Y., Dai, Y. Q., Zhou,

H. J., He, J. J., Gong, Y., Wu, X. W., Tang, H. B.

(2021). Exploring the mechanism of Buxue Yimu Pill on hemorrhagic anemia through molecular docking, network pharmacology and experimental validation. Chin. J. Nat. Med. 19(12), 900-911. https://doi.org/10.1016/S1875-5364(21)60104-8

49. Miao, L. L., Zhou, Q. M., Peng, C., Liu, Z. H.,

Xiong, L. (2019). Leonurus japonicus (Chinese motherwort), an excellent traditional medicine for obstetrical and gynecological diseases: A comprehensive overview. Biomed. Pharmacother. 117, 109060.

https://doi.org/10.1016/j.biopha.2019.109060

50. Xiang, Y., Wang, X., Gong, Y., Xiang, J. (2023). The effectiveness of motherwort injection in preventing postabortion hemorrhage after induced abortion: A protocol for systematic review and meta-analysis. Medicine. 102(7), e32935. https://doi.org/10.1097/MD.0000000000032935

Downloads

Published

2026-07-30

Issue

Section

Review Articles

How to Cite

HuSile, Zhao, C., & Hubisihalatu. (2026). Leonurus japonicus Houtt in Traditional Chinese Medicine: A Review of Phytochemistry, Pharmacology, and Clinical Applications. Journal of Eastern - Western Pharmacology and Pharmacy, 7(1), 35-43. https://doi.org/10.64269/jewpp.v7i1.5787