Catalpol alleviates the lipopolysaccharide-induced inflammatory response of BV2 cells

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DOI:

https://doi.org/10.3329/bjp.v19i3.76556

Keywords:

BV2 cell, Catalpol , Immunofluorescence detection, Inflammation, Lipopolysaccharide, Microglia, Neuroinflammation

Abstract

This study aimed to investigate the effect of catalpol on the inflammatory response of murine microglial cell line (BV2 cells) induced by lipopolysaccharide. Cell proliferation activity was detected by CCK-8 assay. The morphology of BV2 was observed by an optical microscope. The inflammatory factors interleukin-1β (IL-1β), IL-6, and tumor necrosis factor-α (TNF-α) were detected by enzyme‐linked immunosorbent assay (ELISA). Reactive oxygen species (ROS) were detected by flow cytometry. Induced nitric oxide synthase (iNOS) level was detected by immunofluorescence. The results showed that 5 μg/mL catalpol did not effect the proliferation of BV2 cells, while 10 μg/mL catalpol significantly decreased the viability of BV2 cells. Then the experiment was carried out with 5 μg/mL catalpol. Catalpol can improve the morphology of lipopolysaccharide-induced BV2 cells, decrease the level of inflammatory factors, and reduce the production of iNOS and ROS. Therefore, catalpol can inhibit the lipopolysaccharide-induced activation of BV2 cells and has anti-inflammatory effects.  

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References

Alsbrook DL, Di Napoli M, Bhatia K, Biller J, Andalib S, Hinduja A, Rodrigues R, Rodriguez M, Sabbagh SY, Selim M, Farahabadi MH, Jafarli A, Divani AA. Neuroinflammation in acute ischemic and hemorrhagic stroke. Curr Neurol Neurosci Rep. 2023; 23: 407-31.

Bhusal A, Afridi R, Lee WH, Suk K. Bidirectional communication between microglia and astrocytes in neuroinflammation. Curr Neuropharmacol. 2023; 21: 2020-29.

Bao Y, Zhu Y, He G, Ni H, Liu C, Ma L, Zhang L, Shi D. Dexmedetomidine attenuates neuroinflammation in LPS-stimulated BV2 microglia cells through up-regulation of miR-340. Drug Des Devel Ther. 2019; 13: 3465-75.

Bhattamisra SK, Yap KH, Rao V, Choudhury H. Multiple biological effects of an iridoid glucoside, catalpol and its underlying molecular mechanisms. Biomolecules 2019; 10: 32.

Estes ML, McAllister AK. Alterations in immune cells and mediators in the brain: It's not always neuroinflammation! Brain Pathol. 2014; 24: 623-30.

Fei B, Dai W, Zhao S. Efficacy, safety, and cost of therapy of the traditional Chinese medicine, catalpol, in patients following surgical resection for locally advanced colon cancer. Med Sci Monit. 2018; 24: 3184-92.

Gao C, Jiang J, Tan Y, Chen S. Microglia in neurodegenerative diseases: Mechanism and potential therapeutic targets. Signal Transduct Target Ther. 2023; 8: 359.

Guo S, Wang H, Yin Y. Microglia polarization from M1 to M2 in neurodegenerative diseases. Front Aging Neurosci. 2022; 14: 815347.

Henn A, Lund S, Hedtjarn M, Schrattenholz A, Porzgen P, Leist M. The suitability of BV2 cells as alternative model system for primary microglia cultures or for animal experiments examining brain inflammation. ALTEX. 2009; 26: 83-94.

Jurcau A, Simion A. Neuroinflammation in cerebral ischemia and ischemia/reperfusion injuries: From pathophysiology to therapeutic strategies. Int J Mol Sci. 2021; 23: 14.

Jiang T, Zhang A, Zhao R. Protective effect of catalpol in mice injuries induced by rotenone and evaluation of the safety of catalpol. Prog Mod Biomed. 2008; 8: 1039-41.

Leng F, Edison P. Neuroinflammation and microglial activation in Alzheimer disease: where do we go from here? Nat Rev Neurol. 2021; 17: 157-72.

Li G, Liu S, Chen Y, Zhao J, Xu H, Weng J, Yu F, Xiong A, Udduttula A, Wang D, Liu P, Chen Y, Zeng H. An injectable liposome-anchored teriparatide incorporated gallic acid grafted gelatin hydrogel for osteoarthritis treatment. Nat Commun. 2023; 14: 3159.

Liu Y, Xue Q, Li X, Zhang J, Fu Z, Feng B, Chen Y, Xu X. Amelioration of stroke-induced neurological deficiency by lyophilized powder of catalpol and puerarin. Int J Biol Sci. 2014; 10: 448-56.

Ni Chasaide C, Lynch MA. The role of the immune system in driving neuroinflammation. Brain Neurosci Adv. 2020; 4: 2398212819901082.

Nam HY, Nam JH, Yoon G, Lee JY, Nam Y, Kang HJ, Cho HJ, Kim J, Hoe HS. Ibrutinib suppresses LPS-induced neuroinflammatory responses in BV2 microglial cells and wild-type mice. J Neuroinflammation. 2018; 15: 271.

Stansley B, Post J, Hensley K. A comparative review of cell culture systems for the study of microglial biology in Alzheimer's disease. J Neuroinflammation. 2012; 9: 115.

Savage JC, Carrier M, Tremblay ME. Morphology of microglia across contexts of health and disease. Methods Mol Biol. 2019; 2034: 13-26.

Simpson DSA, Oliver PL. ROS generation in microglia: Understanding oxidative stress and inflammation in neuro-degenerative disease. Antioxidants (Basel). 2020; 9: 743.

Thakur S, Dhapola R, Sarma P, Medhi B, Reddy DH. Neuroinflammation in Alzheimer's disease. Current pro-gress in molecular signaling and therapeutics. Inflammation 2023; 46: 1-17.

Wang Z, Liu Q, Zhang R, Liu S, Xia Z, Hu Y. Catalpol ameliorates beta amyloid–induced degeneration of cholinergic neurons by elevating brain-derived neurotrophic factors. Neuroscience 2009; 163: 1363-72.

Wu Q, Zou C. Microglial dysfunction in neurodegenerative diseases via RIPK1 and ROS. Antioxidants (Basel). 2022; 11: 2201.

Xu G, Xiong Z, Yong Y, Wang Z, Ke Z, Xia Z, Hu Y. Catalpol attenuates MPTP induced neuronal degeneration of nigral-striatal dopaminergic pathway in mice through elevating glial cell derived neurotrophic factor in striatum. Neuroscience 2010; 167: 174-84.

Xia DY, Yuan JL, Jiang XC, Qi M, Lai NS, Wu LY, Zhang XS. SIRT1 promotes M2 microglia polarization via reducing ROS-mediated NLRP3 inflammasome signaling after sub-arachnoid hemorrhage. Front Immunol. 2021; 12: 770744.

You L, Peng H, Liu J, Cai M, Wu H, Zhang Z, Bai J, Yao Y, Dong X, Yin X, Ni J. Catalpol protects ARPE-19 cells against oxidative stress via activation of the Keap1/Nrf2/ARE pathway. Cells 2021; 10: 2635.

Zhang Z, Dai Y, Xiao Y, Liu Q. Protective effects of catalpol on cardio-cerebrovascular diseases: A comprehensive review. J Pharm Anal. 2023; 13: 1089-101.

Zhang LQ, Chen KX, Li YM. Bioactivities of natural catalpol derivatives. Curr Med Chem. 2019; 26: 6149-73.

Zhang M, Shao W, Yang T, Liu H, Guo S, Zhao D, Weng Y, Liang XJ, Huang Y. Conscription of immune cells by light-activatable silencing NK-derived exosome (LASNEO) for synergetic tumor eradication. Adv Sci (Weinh). 2022; 9: e2201135.

Zhao Z, Ning J, Bao XQ, Shang M, Ma J, Li G, Zhang D. Fecal microbiota transplantation protects rotenone-induced Parkinson's disease mice via suppressing inflammation mediated by the lipopolysaccharide-TLR4 signaling pathway through the microbiota-gut-brain axis. Microbiome 2021; 9: 226.

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Published

2024-12-13

How to Cite

Liu, S., J. Zhu, H. Huang, J. Xu, B. Zhang, and Y. Luo. “Catalpol Alleviates the Lipopolysaccharide-Induced Inflammatory Response of BV2 Cells”. Bangladesh Journal of Pharmacology, vol. 19, no. 3, Dec. 2024, pp. 88-94, doi:10.3329/bjp.v19i3.76556.

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Research Articles