Abstract
The present study was intended to explore the valuable effects of triptonide on inflammation, asthmatic, and nociceptive. Triptonide possesses numerous beneficial effects extensively managed in the treatment of inflammation disease condition. Initially, triptonide showed anti-inflammation properties over lipopolysaccharide-induced RAW 264.7 cells. Hence, the present study was directed to explore the protecting efficacy of triptonide in ovalbumin (OVA)-induced asthma in mice. Asthma was induced intraperitoneally administration (200μL) in female BALB/c mice with suspension which has ovalbumin (100 μg/mL) and aluminum hydroxide (10 mg/mL). Triptonide (30 mg/kg) over OVA-induced experimental animals altered lung mass, nitric oxide, myeloperoxidase, immunoglobulin E status, interleukins (4, 5, and 13) inflammatory cytokines status, and histological modifications. Animals were also managed with the standard drug dexamethasone (50 mg/kg) followed by the asthma induction, which is also efficient over OVA-induced experimental animals. The nociception was provoked in male Swiss mice by various chemicals (acetic acid, capsaicin, and glutamate). The animals were administered with triptonide (5, 10, and 15 mg/kg) and separate standard drugs like diclofenac sodium (10 mg/kg) and morphine (5 mg/kg) over chemical-induced nociceptive animals. The present outcome evidently established that the triptonide considerably reduced the various chemical-induced nociception in mice (Fig. 7A, B, and C). Ultimately, the present work explored the evident powerful anti-inflammation, antinociceptive, and anti-asthma properties of a diterpenoid, triptonide experimental animal models. And it is recommended that triptonide is an excellent compound in the management of asthma and its related diseases.
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Abbreviations
- OVA :
-
Ovalbumin
- TPN :
-
Triptonide
- MTT :
-
3-(4, 5-Dimethylthiazol-2-y1)-2, 5-diphenyltetrazolium bromide
- DMSO :
-
Dimethyl sulfoxide
- DMEM :
-
Dulbecco’s modified Eagle’s medium
- FBS :
-
Fetal bovine serum
- LPS :
-
Lipopolysaccharides
- MPO :
-
Myeloperoxidase
- NO :
-
Nitric oxide
References
Furman, D., Campisi, J., Verdin, E., Carrera-Bastos, P., Targ, S., Franceschi, C., Ferrucci, L., Gilroy, D. W., Fasano, A., Miller, G. W., Miller, A. H., Mantovani, A., Weyand, C. M., Barzilai, N., Goronzy, J. J., Rando, T. A., Effros, R. B., Lucia, A., Kleinstreuer, N., & Slavich, G. M. (2019). Chronic inflammation in the etiology of disease across the life span. Nature Medicine, 25(12), 1822–1832.
Sorriento, D., & Iaccarino, G. (2019). Inflammation and cardiovascular diseases: The most recent findings. International Journal of Molecular Sciences, 20(16), 3879.
Greten, F. R., & Grivennikov, S. I. (2019). Inflammation and cancer: Triggers, mechanisms, and consequences. Immunity, 51(1), 27–41.
Papi, A., Brightling, C., Pedersen, S. E., & Reddel, H. K. (2018). Asthma. Lancet, 391(10122), 783–800. https://doi.org/10.1016/S0140-6736(17)33311-1
Nunes, C., Pereira, A. M., & Morais-Almeida, M. (2017). Asthma costs and social impact. Asthma Research and Practice, 3, 1.
Burke, W., Fesinmeyer, M., Reed, K., Hampson, L., & Carlsten, C. (2003). Family history as a predictor of asthma risk. American Journal of Preventive Medicine, 24, 160–169.
Centers for Disease Control and Prevention (2013) Asthma facts—CDC’s national asthma control program grantees. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention. 8. Dr Green. Asthma. Retrieved from http://www.drgreene.com/211252.html
Suleyman, H., Albayrak, A., Bilici, M., Cadirci, E., & Halici, Z. (2010). Different mechanisms in formation and prevention of indomethacin-induced gastric ulcers. Inflammation, 33(4), 224–234.
Thompson, P. W., Tee, L., McBride, J., Quincey, D., & Liddiard, G. S. (2005). Long-term NSAID use in primary care: Changes over a decade and NICE risk factors for gastrointestinal adverse events. Rheumatology, 44(10), 1308–1310.
Jang, H. H., Cho, S. Y., Kim, M. J., Kim, J. B., Lee, S. H., Lee, M. Y., & Lee, Y. M. (2016). Anti-inflammatory effects of Salvia plebeia R Br extract in vitro and in ovalbumin-induced mouse model. Biological Research, 49, 41.
Bloechliger, M., Reinau, D., Spoendlin, J., Chang, S. C., Kuhlbusch, K., Heaney, L. G., Jick, S. S., & Meier, C. R. (2018). Adverse events profile of oral corticosteroids among asthma patients in the UK: Cohort study with a nested case-control analysis. Respiratory Research, 19, 75.
Amaral-Machado, L., Oliveira, W. N., Moreira-Oliveira, S. S., Pereira, D. T., Alencar, E. N., Tsapis, N., & Egito, E. S. T. (2020). Use of natural products in asthma treatment. Evid Based Complement Alternat Med., 2020, 1021258.
Shin, I. S., Lee, M. Y., Lim, H. S., Ha, H., Seo, C. S., Kim, J. C., et al. (2012). An extract of Crataegus pinnatifida fruit attenuates airway inflammation by modulation of matrix metalloproteinase-9 in ovalbumin induced asthma. PLoS ONE, 7(9), e45734.
Wang, S. S., Lv, Y., Xu, X. C., et al. (2019). Triptonide inhibits human nasopharyngeal carcinoma cell growth via disrupting Lnc-RNA THOR-IGF2BP1 signaling. Cancer Letters, 443, 13–24.
Zhang, M., Tan, S., Yu, D., et al. (2019). Triptonide inhibits lung cancer cell tumorigenicity by selectively attenuating the Shh-Gli1 signaling pathway. Toxicology and Applied Pharmacology, 365, 1–8.
**ang, S., Zhao, Z., Zhang, T., Zhang, B., Meng, M., Cao, Z., & Zhou, Q. (2020). Triptonide effectively suppresses gastric tumor growth and metastasis through inhibition of the oncogenic Notch1 and NF-κB signaling pathways. Toxicology and Applied Pharmacology, 388, 114870. https://doi.org/10.1016/j.taap.2019.114870
Ling, Y. J., Ding, T. Y., Dong, F. Y., Gao, Y. J., & Jiang, B. C. (2020). Intravenous administration of triptonide attenuates CFA-induced pain hypersensitivity by inhibiting DRG AKT signaling pathway in mice. Journal of Pain Research, 13, 3195–3206.
Chang, Z., Qin, W., Zheng, H., et al. (2021). Triptonide is a reversible non-hormonal male contraceptive agent in mice and non-human primates. Nature Communications, 12, 1253.
Dong, F., Yang, P., Wang, R., et al. (2019). Triptonide acts as a novel antiprostate cancer agent mainly through inhibition of mTOR signaling pathway. Prostate, 79(11), 1284–1293.
Dai, R., Niu, M., Wang, N., & Wang, Y. (2021). Syringin alleviates ovalbumin-induced lung inflammation in BALB/c mice asthma model via NF-κB signaling pathway. Environmental Toxicology, 36(3), 433–444. https://doi.org/10.1002/tox.23049
Gawade, S. P. (2012). Acetic acid induced painful endogenous infliction in writhing test on mice. Journal of Pharmacology and Pharmacotherapeutics, 3(4), 348.
Giorno, T. B. S., Ballard, Y. L. L., Cordeiro, M. S., Silva, B., Pinto, A. C., & Fernandes, P. D. (2015). Central and peripheral antinociceptive activity of 3-(2-oxopropyl)-3-hydroxy-2-oxindoles. Pharmacology Biochemistry and Behavior, 135, 13–19.
Liu, J., **ong, H., & Cheng, Y. (2013). Effects of taraxasterol on ovalbumin-induced allergic asthma in mice. Journal of Ethnopharmacology, 148, 787–793.
Murdoch, J. R., & Lloyd, C. M. (2010). Chronic inflammation and asthma. Mutation Research, 690(1–2), 24–39.
Gauthier, M., Ray, A., & Wenzel, S. E. (2015). Evolving concepts of asthma. American Journal of Respiratory and Critical Care Medicine, 192(6), 660–668.
Caubet, J. C., & Wang, J. (2011). Current understanding of egg allergy. Pediatric Clinics of North America, 58(2), 427–443.
Wu, C., Zhao, W., Zhang, X., & Chen, X. (2015). Neocryptotanshinone inhibits lipopolysaccharide-induced inflammation in RAW264.7 macrophages by suppression of NF-κB and iNOS signaling pathways. Acta Pharmaceutica Sinica B, 5(4), 323–329.
Fahy, J. V., & Dickey, B. F. (2010). Airway mucus function and dysfunction. New England Journal of Medicine, 363(23), 2233–2247.
Deepa, K., Ingawalea, M., Satish, K., Mandlik, B., & Snehal, S. (2020). Combination of sarsasapogenin and fluticasone attenuates ovalbumin-induced airway inflammation in a mouse asthma model. Immunopharmacology and Immunotoxicology, 3, 244–260.
Soodaeva, S., Klimanov, I., Kubysheva, N., Popova, N., & Batyrshin, I. (2020). The State of the Nitric oxide cycle in respiratory tract diseases. Oxidative Medicine and Cellular Longevity, 2020, 4859260.
Prasch, J., Bernhart, E., Reicher, H., Kollroser, M., Rechberger, G. N., Koyani, C. N., Trummer, C., Rech, L., Rainer, P. P., Hammer, A., Malle, E., & Sattler, W. (2020). Myeloperoxidase-derived 2-chlorohexadecanal is generated in mouse heart during endotoxemia and induces modification of distinct cardiomyocyte protein subsets in vitro. International Journal of Molecular Sciences, 21, 9235.
Zhang, L., **npeng, H., Devanathadesikan, S. V., Aziz, I. I. A., & Ou, L. (2022). Tilianin alleviates airway inflammation in ovalbumin-induced allergic asthma in mice through the regulation of Th2 cytokines and TGF-b1/Smad markers. Arabian Journal of Chemistry, 15, 103961.
Bao, K., & Lee, R. R. (2015). The differential expression of IL-4 and IL-13 and its impact on type-2 immunity. Cytokine, 75(1), 25–37.
Kim, D. I., Song, M. K., & Lee, K. (2019). Comparison of asthma phenotypes in OVA-induced mice challenged via inhaled and intranasal routes. BMC Pulmonary Medicine, 19, 241.
Gour, N., & Wills-Karp, M. (2015). IL-4 and IL-13 Signaling in allergic airway disease. Cytokine, 75(1), 68–78.
Lee, J. E., & Im, D. S. (2021). Suppressive effect of carnosol on ovalbumin-induced allergic asthma. Biomol Ther (Seoul)., 29(1), 58–63.
Doeing, D. C., & Solway, J. (2013). Airway smooth muscle in the pathophysiology and treatment of asthma. Journal of Applied Physiology (1985), 114(7), 834–43.
Kudo, M., Ishigatsubo, Y., & Aoki, I. (2013). Pathology of asthma. Frontiers in Microbiology, 4, 263.
Begnami, A. F., Spindola, H. M., Ruiz, A. L. T. G., de Carvalho, J. E., Groppo, F. C., & Rehder, V. L. G. (2018). Antinociceptive and anti-edema properties of the ethyl acetate fraction obtained from extracts of Coriandrum sativum Linn Leaves. Biomedicine & Pharmacotherapy, 103, 1617–1622.
Smart, T. G., & Paoletti, P. (2012). Synaptic neurotransmitter-gated receptors. Cold Spring Harbor Perspectives in Biology, 4(3), a009662.
Fattori, V., Hohmann, M. S. N., Rossaneis, A. C., Pinho-Ribeiro, F. A., & Verri, W. A. (2016). Capsaicin: Current understanding of its mechanisms and therapy of pain and other pre-clinical and clinical uses. Molecules, 21(7), 844.
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Li, Z., Geng, Y., Wu, Q. et al. Triptonide, a Diterpenoid Displayed Anti-Inflammation, Antinociceptive, and Anti-Asthmatic Efficacy in Ovalbumin-Induced Mouse Model. Appl Biochem Biotechnol 195, 1736–1751 (2023). https://doi.org/10.1007/s12010-022-04167-1
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DOI: https://doi.org/10.1007/s12010-022-04167-1