Research Progress on Pharmacological and Toxicological Effects of Bavachin

Authors

  • Yeqing Jiang Hangzhou Fuyang Hospital of Traditional Chinese Medicine, 311400 Hangzhou, Zhejiang, China Author
  • Shiyu Hu School of Pharmaceutical Sciences, Zhejiang Chinese Medical University, 310053 Hangzhou, Zhejiang, China Author
  • Jiaman Shen School of Pharmaceutical Sciences, Zhejiang Chinese Medical University, 310053 Hangzhou, Zhejiang, China Author
  • Dongling Shi Academy of Chinese Medical Sciences, Zhejiang Chinese Medical University, 310053 Hangzhou, Zhejiang, China Author

DOI:

https://doi.org/10.62767/jecacm504.2748

Keywords:

bavachin, estrogen-like, anti-inflammatory, anti-tumor, immunoregulatory, toxicology

Abstract

Objective: To analyze and summarize the latest research progress regarding pharmacological and toxicological effects of bavachin. Methods: Through retrieval of all bavachin-related reports on pubmed, CNKI, Wanfang database and other databases, the pharmacologic and toxicological effects of bavachin were sorted out and concluded accordingly. Results: The study showed that bavachin had a wide range of pharmacological activities, including estrogen-like, anti-inflammatory, anti-tumor, immunoregulatory, anti-diabetes and its complications effects. The toxicological effects of bavachin were mainly manifested in three aspects: hepatotoxicity, reproductive toxicity and nephrotoxicity. Conclusions: Bavachin has the characteristics of multi-function and multi-target monomer similar to traditional Chinese medicine, and broad application prospects, but also has certain toxicological effects. How to avoid toxicity, as well as enhance strengths and avoid weaknesses is the direction of development and utilization of bavachin. This review provides reference for further development and utilization of bavachin.

References

Basera IA, Shah MB. A validated high-performance thin-layer chromatography method for quantification of bavachin, bakuchiol, and psoralen from Psoralea corylifolia seeds. JPC - Journal of Planar Chromatography - Modern TLC 2020; 33(3): 293-300.

Dong Y, Yu X, Wu P, et al. Detection of bavachin based on nitrogen-doped carbon dots as a fluorescence probe. Chinese Journal of Analysis Laboratory 2022; 41(6): 698-703.

Dong X, Fan Y, Yu L, et al. Synthesis of four natural prenylflavonoids and their estrogen-like activities. Archiv der Pharmazie 2007; 340(7): 372-376.

Park J, Kim DH, Ahn HN, et al. Activation of estrogen receptor by bavachin from Psoralea corylifolia. Biomolecules & Therapeutics 2012; 20(2): 183-188.

Wang J, Pei Y, Xu H, et al. Effects of bavachin and its regulation of melanin synthesis in A375 cells. Biomedical Reports 2016; 5(1): 87-92.

Weng Z, Gao Q, Wang F, et al. Positive skeletal effect of two ingredients of Psoralea corylifolia L. on estrogen deficiency-induced osteoporosis and the possible mechanisms of action. Molecular and Cellular Endocrinology 2015; 417: 103-113.

Wang D, Li F, Jiang Z. Osteoblastic proliferation stimulating activity of Psoralea corylifolia extracts and two of its flavonoids. Planta Medica 2001; 67(8): 748-749.

Li W, Yan C, Wu Y, et al. Osteoblasts proliferation and differentiation stimulating activities of the main components of Fructus Psoraleae corylifoliae. Phytomedicine 2014; 21(4): 400–405.

Kong X, Zhai Y, Liu Y, et al. Effect of bavachin on proliferation and maturation of cranioaural osteoblast in neonatal rats. The Journal of Traditional Chinese Orthopedics and Traumatology 2013; 25(9): 10-15.

Lee GJ, Cho IA, Kang KR, et al. Biological effects of the herbal plant-derived phytoestrogen bavachin in primary rat chondrocytes. Biological & Pharmaceutical Bulletin 2015; 38(8): 1199-1207.

Cheng C, Chen Y, Chang W, et al. Phytoestrogen bavachin mediates anti-inflammation targeting Ikappa B kinase-I kappaB alpha-NF-kappaB signaling pathway in chondrocytes in vitro. European Journal of Pharmacology 2010; 636(1-3): 181-188.

Han Y, Peng Y, Yu Y. Effects of Bavachin on Regulating Differentiation of Bone Marrow MSC by Mediating cAMP/PKA/CREB Signaling Pathway. Chinese Archives of Traditional Chinese Medicine 2019; 37(7): 1597-1600.

Ji W, Fu Y, Lu W. Effect of Brain Injury and Bavachin on 5-HT and VEGF of Rats with Tibial Fracture. Journal of Emergency in Traditional Chinese Medicine 2014; 23(9): 1585-1588.

Liang Z, Luo Z, Chen J, et al. Bavachin inhibits IL-4 expression by downregulating STAT6 phosphorylation and GATA-3 expression and ameliorates asthma inflammation in an animal model. Immunobiology 2022; 227(2): 152182.

Guedes RP, Csizmadia E, Moll HP, et al. A20 deficiency causes spontaneous neuroinflammation in mice. Journal of Neuroinflammation 2014; 11: 122.

Wang Y, Yang Z, Wang Q, et al. Bavachin exerted anti-neuroinflammatory effects by regulation of A20 ubiquitin-editing complex. International Immunopharmacology 2021; 100: 108085.

Xu Q, Hu Y, Li G, et al. Multi-target anti-alzheimer activities of four prenylated compounds from Psoralea Fructus. Molecules 2018; 23(3): 614.

Zhang Z, Sun L, Guo Y, et al. Bavachin ameliorates neuroinflammation and depressive-like behaviors in streptozotocin-induced diabetic mice through the inhibition of PKCδ. Free Radical Biology and Medicine 2024; 213: 52-64.

Ban KY, Nam GY, Kim D, et al. Prevention of LPS-induced acute kidney injury in mice by bavachin and its potential mechanisms. Antioxidants 2022; 11(11): 2096.

Takeda T, Tsubaki M, Tomonari Y, et al. Bavachin induces the apoptosis of multiple myeloma cell lines by inhibiting the activation of nuclear factor kappa B and signal transducer and activator of transcription 3. Biomedicine & Pharmacotherapy 2018; 100: 486-494.

Lee JY, Lim W, Song G. Bavachin suppresses human placental choriocarcinoma cells by targeting electron transport chain complexes and mitochondrial dysfunction. Free Radical Biology and Medicine 2020; 156: 26-35.

Luo Y, Gao X, Zou L, et al. Bavachin induces ferroptosis through the STAT3/P53/SLC7A11 axis in osteosarcoma cells. Oxidative Medicine and Cellular Longevity 2021; 2021: 1783485.

Wang M, Tian B, Shen J, et al. Bavachin induces apoptosis in colorectal cancer cells through Gadd45a via the MAPK signaling pathway. Chinese Journal of Natural Medicines 2023; 21(1): 36-46.

Hodge DR, Hurt EM, Farrar WL. The role of IL-6 and STAT3 in inflammation and cancer. European Journal of Cancer 2005; 41(16): 2502-2512.

Lee SW, Yun BR, Kim MH, et al. Phenolic compounds isolated from Psoralea corylifolia inhibit IL-6-induced STAT3 activation. Planta Medica 2012; 78(9): 903-906.

Soto-nieves N, Puga I, Abe BT, et al. Transcriptional complexes formed by NFAT dimers regulate the induction of T cell tolerance. Journal of Experimental Medicine 2009; 206(4): 867-876.

Jin YH, Kim DE, Jang MS, et al. Bavachin produces immunoadjuvant activity by targeting the NFAT signaling pathway. Phytomedicine 2021; 93: 153796.

Lee H, Li H, Noh M, et al. Bavachin from Psoralea corylifolia improves insulin-dependent glucose uptake through insulin signaling and AMPK activation in 3T3-L1 adipocytes. International Journal of Molecular Sciences 2016; 17(4): 527.

Park J, Seo E, Jun HS. Bavachin alleviates diabetic nephropathy in db/db mice by inhibition of oxidative stress and improvement of mitochondria function. Biomedicine & Pharmacotherapy 2023; 161: 114479.

Yeon MH, Seo E, Lee JH, et al. Bavachin and corylifol a improve muscle atrophy by enhancing mitochondria quality control in type 2 diabetic mice. Antioxidants 2023; 12(1): 137.

Tao Y, Sun D, Ren X, et al. Bavachin suppresses alpha-hemolysin expression and protects mice from pneumonia infection by Staphylococcus aureus. Journal of Industrial Microbiology & Biotechnology 2022; 32(10): 1253-1261.

Chen C, Shen Y, Hu Y, et al. Highly efficient inhibition of spring viraemia of carp virus replication in vitro mediated by bavachin, a major constituent of psoralea corlifonia Lynn. Virus Research 2018; 255: 24-35.

Jung J, Bae J, Park JS, et al. In Vitro Anti-Rotaviral Activity of Bavachin Isolated from Psoralea corylifolia L. (Fabaceae). Veterinary Sciences 2024; 11(5): 188.

He HQ, Law BYK, Zhang N, et al. Bavachin protects human aortic smooth muscle cells against beta-glycerophosphate-mediated vascular calcification and apoptosis via activation of mTOR-dependent autophagy and suppression of beta-Catenin signaling. Frontiers in Pharmacology 2019; 10: 1427.

Wei X, Lin L, Yuan Q, et al. Bavachin protects against diet-induced hepatic steatosis and obesity in mice. Acta Pharmacologica Sinica 2023; 44(7): 1416-1428.

Wang X, Li W, Zhang H, et al. Effect of Psoraleae Fructus and its main components on human normal hepatocyte L02. Traditional Chinese Medicinal Research 2020; 33(4): 59-63.

Yang Y, Tang X, Hao F, et al. Bavachin induces apoptosis through mitochondrial regulated ER stress pathway in HepG2 cells. Biological & Pharmaceutical Bulletin 2018; 41(2): 198-207.

Qin N, Xu G, Wang Y, et al. Bavachin enhances NLRP3 inflammasome activation induced by ATP or nigericin and causes idiosyncratic hepatotoxicity. Frontiers of Medicine 2021; 15(4): 594-607.

Guo Z, Li P, Wang C, et al. Five Constituents Contributed to the Psoraleae Fructus-Induced Hepatotoxicity via Mitochondrial Dysfunction and Apoptosis. Frontiers in Pharmacology 2021; 12: 682823.

Miksys S, Lerman C, Shields PG, et al. Smoking, alcoholism and genetic polymorphisms alter CYP2B6 levels in human brain. Neuropharmacology 2003; 45(1): 122-132.

Li H, Wang Y, Ma Z, et al. Inductive effects of psoralen , isopsoralen, bavachin and isobavachalcone cytochrome on P450 2B6. Pharmacology and Clinics of Chinese Materia Medica 2017; 33(1): 15-19.

Lin M, Li Y, Cao B, et al. Bavachin combined with epimedin B induce idiosyncratic liver injury under immunological stress conditions. Chemico-Biological Interactions 2023; 386: 110774.

Shen P, Bai Z, Zhou L, et al. A Scd1-mediated metabolic alteration participates in liver responses to low-dose bavachin. Journal of Pharmaceutical Analysis 2023; 13(7): 806-816.

Huang C, Deng H, Zhou L, et al. Undesirable ER stress induced by bavachin contributed to follicular atresia in zebrafish ovary. Biomedicine & Pharmacotherapy 2023; 166: 115322.

Ni Y, Deng H, Zhou L, et al. Ginsenoside Rb1 ameliorated bavachin-induced renal fibrosis via suppressing Bip/eIF2α/CHOP signaling-mediated EMT. Frontiers in Pharmacology 2022; 13: 872474.

Published

2024-11-08

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Issue

Section

Review

Similar Articles

1-10 of 12

You may also start an advanced similarity search for this article.

Most read articles by the same author(s)

<< < 2 3 4 5 6 7 8 9 > >>