Anti-Inflammatory Effects of Velvet Bean Leaves Ethanolic Ointment (Mucuna pruriens L. (DC.)) on Mice Leukocytes Level

Fadilaturahmah Fadilaturahmah, Resti Rahayu, Putra Santoso

Abstract


Abstract

Inflammation is a serious problem that needs to be treated. The use of steroid and non-steroidal drugs can treat inflammation well, but long-term use causes many side effects. So, it is necessary to use effective natural medicinal ingredients, one of which is velvet bean leaves (Mucuna pruriens L. (DC.)). This study aims to analyze the effect of velvet bean leaf ointment on the level of leukocyte components in mice experiencing inflammation. This research method was an experiment with a completely randomized design consisting of 6 treatment groups (normal, negative control, positive control (ketoconazole ointment)), velvet bean leaf ointment treatment at doses of 200, 400, and 600 mg/kgBW. The results showed that the use of velvet bean leaf ointment at doses of 200 and 400 mg/kgBW was able to significantly reduce the quantity of total leukocytes and monocytes in mice compared to the negative control (P <0.05); ointment at a dose of 200 mg/kgBW was able to significantly reduce the quantity of granulocytes and lymphocytes in mice compared to the negative control (P <0.05). The ability of velvet bean leaf ointment at a dose of 200 mg/kgBW is better in reducing the leukocyte quantity component compared to commercial drugs (ketoconazole ointment). Therefore, velvet bean leaf ointment at a dose of 200 mg/kgBW has great potential to be developed into an effective standardized anti-inflammatory drug.

Abstrak

Inflamasi merupakan masalah serius yang perlu ditangani. Penggunaan obat steroid dan nonsteroid dapat mengatasi inflamasi dengan baik, namun penggunaan jangka panjang menimbulkan banyak efek samping. Maka dari itu perlu digunakan bahan obat alami yang efektif, salah satunya adalah daun kacang miang (Mucuna pruriens L. (DC.)). Penelitian ini bertujuan untuk menganalisis pengaruh salep daun kacang miang terhadap kadar komponen leukosit pada mencit yang mengalami inflamasi. Metode penelitian ini adalah eksperimen dengan rancangan acak lengkap yang terdiri dari 6 kelompok perlakuan (normal, kontrol negatif, kontrol positif (salep ketokonazol)), perlakuan salep daun kacang miang dosis 200, 400, dan 600 mg/kgBB. Hasil penelitian menunjukkan bahwa penggunaan salep daun kacang miang dosis 200 dan 400 mg/kgBB mampu menurunkan kuantitas total leukosit dan monosit mencit secara bermakna dibandingkan dengan kontrol negatif (P <0,05); Salep daun kacang miang dosis 200 mg/kgBB mampu menurunkan jumlah granulosit dan limfosit pada mencit secara signifikan dibandingkan dengan kontrol negatif (P <0,05). Kemampuan salep daun kacang miang dosis 200 mg/kgBB lebih baik dalam menurunkan komponen jumlah leukosit dibandingkan dengan obat komersial (salep ketokonazol). Oleh karena itu, salep daun kacang miang dosis 200 mg/kgBB memiliki potensi besar untuk dikembangkan menjadi obat antiinflamasi terstandar yang efektif.


Keywords


Granulocytes; Inflammation; Lymphocytes; Monocytes; Steroids; Granulosit; Inflamasi; Limfosit; Monosit; Steroid

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References


Agoes, G. (2006). Pengembangan sediaan farmasi. Bandung: ITB.

Bajgai, J., Xingyu, J., Fadriquela, A., Begum, R., Kim, D. H., Kim, C. S., Lee, K. J. (2021). Effects of mineral complex material treatment on 2,4- dinitrochlorobenzene-induced atopic dermatitis like-skin lesions in mice model. BMC complementary medicine and therapies, 21(1), 82. doi: 10.1186/s12906-021-03259-5.

Bala, V., Debnath, A., Shill, A. K., & Bose, U. (2011). Anti-inflammatory, diuretic and antibacterial activities of aerial parts of Mucuna pruriens Linn. International Journal of Pharmacology, 7(4), 498-503. doi: 10.3923/ijp.2011.498.503.

Chen L., Huidan D., & Hengmin C. (2018). Inflammatory responses and inflammation associated diseases in organs. Oncotarget, 9(6), 7204-7218.

Chovatiya R. (2023). Atopic dermatitis (eczema). JAMA, 329(3), 268. doi: 10.1001/jama.2022.21457.

De Siquueira. P. L. L., de Brito M. R, D., E Silva, M. G., Dos Santos, A. C. L. A., Silva, Y. A., Paiva, P. M. G., … Napoleão, T. H. (2022). Inhibition of carrageenan-induced acute inflammation in mice by the Microgramma vacciniifolia Frond Lectin (MvFL). Polymers, 14(8), 1609. doi: 10.3390/polym14081609.

Fadilaturahmah, F., Rahayu, R., & Santoso, P. (2023). Anti-inflammatory effects of velvet bean (Mucuna pruriens L. (DC.), Fabaceae) leaf ethanolic extract against carrageenan in male mice. Journal of Research in Pharmacy, 27(4). doi: 10.29228/jrp.438.

Ferrero-Miliani, L., Nielsen, O. H., Andersen, P. S., & Girardin, S. (2007). Chronic inflammation: Importance of NOD2 and NALP3 in interleukin-1β generation. Clinical & Experimental Immunology, 147(2), 227-235. doi: 10.1111/j.1365-2249.2006.03261.x.

Ghasemian, M., Owlia, S., & Owlia, M. B. (2016). Review of anti-inflammatory herbal medicines. Advances in Pharmacological and Pharmaceutical Sciences, 2016. doi: 10.1155/2016/9130979.

Ghlichloo, I., & Gerriets, V. (2023). Nonsteroidal anti-inflammatory drugs (NSAIDs). Treasure Island: StatPearls Publishing.

Hagemann, J. H., Haegele, H., Müller, S., & Anders, H. J. (2013). Danger control programs cause tissue injury and remodeling. International journal of molecular sciences, 14(6), 11319-11346. doi: 10.3390/ijms140611319.

Harirforoosh, S., Asghar, W., & Jamali, F. (2013). Adverse effects of nonsteroidal antiinflammatory drugs: an update of gastrointestinal, cardiovascular and renal complications. Journal of Pharmacy & Pharmaceutical Sciences, 16(5), 821-847. doi: 10.18433/j3vw2f.

Heo, J. H., Heo, Y., Lee, H. J., Kim, M., & Shin, H. Y. (2018). Topical anti-inflammatory and anti-oxidative effects of porcine placenta extracts on 2,4-dinitrochlorobenzene-induced contact dermatitis. BMC complementary and alternative medicine, 18(1), 331. doi: 10.1186/s12906-018-2396-1.

Kakel, S. J. (2013). The evaluation of traditional and automatic coulter method in estimation of haematological parameters in adult rats. Beni-Suef University Journal of Basic and Applied Sciences, 2(1), 31-35.

Kim, E. Y., Hong, S., Kim, J. H., Kim, M., Lee, Y., Sohn, Y., & Jung, H. S. (2021). Effects of chloroform fraction of Fritillariae thunbergii Bulbus on atopic symptoms in a DNCB-induced atopic dermatitis-like skin lesion model and in vitro models. Journal of Ethnopharmacology, 281, 114453. doi: 10.1016/j.jep.2021.114453.

Kim, S. R., Choi, H. S., Seo, H. S., Choi, Y. K., Shin, Y. C., & Ko, S. G. (2012). Topical application of herbal mixture extract inhibits ovalbumin-or 2, 4-dinitrochlorobenzene-induced atopic dermatitis. Evidence-Based Complementary and Alternative Medicine, 2012. doi: 10.1155/2012/545497.

Krishna, A. B., & Sharma, N. (2016). Acute oral toxicity study in rats with Mucuna pruriens seed extract. Asian Journal of Plant Science & Research. doi: 10.22159/ajpcr.2019.v12i2.29750.

Ku, J. M., Hong, S. H., Kim, S. R., Choi, H. S., Kim, H. I., Kim, D. U., & Ko, S. G. (2018). The prevention of 2, 4-dinitrochlorobenzene-induced inflammation in atopic dermatitis-like skin lesions in BALB/c mice by Jawoongo. BMC complementary and alternative medicine, 18, 1-15. doi: 10.1186/s12906-018-2280-z.

Kwon, B., Hong, S. Y., Kim, E. Y., Kim, J. H., Kim, M., Park, J. H., & Jung, H. S. (2021). Effect of cone of pinus densiflora on DNCB-induced allergic contact dermatitis-like skin lesion in Balb/c Mice. Nutrients, 13(3), 839. doi: 10.3390/nu13030839.

Leick, M., Azcutia, V., Newton, G., & Luscinskas, F. W. (2014). Leukocyte recruitment in inflammation: Basic concepts and new mechanistic insights based on new models and microscopic imaging technologies. Cell and tissue research, 355(3), 647-656. doi: 10.1007/s00441-014-1809-9.

Leung, L. S., Chu, L., Prado, M. A., & Prado, V. F. (2021). Forebrain acetylcholine modulates isoflurane and ketamine anesthesia in adult mice. Anesthesiology, 134(4), 588-606. doi: 10.1097/ALN.0000000000003713.

Mauersberger, C., Hinterdobler, J., Schunkert, H., Kessler, T., & Sager, H. B. (2022). Where the action is-leukocyte recruitment in atherosclerosis. Frontiers in cardiovascular medicine, 8, 813984. doi: 10.3389/fcvm.2021.813984.

Moelyono, L. A., Akhmad, I., & Neli, S. (2017). Pengaruh pemberian ekstrak daun sirih merah (Piper crocatum) terhadap gambaran limfosit darah pada mencit balb/c yang diinfeksi Salmonella typhimurium. Jurnal Kedokteran Diponegoro, 6(2), 748-757.

Olsen, A. S., Fosbol, E. L., & Lindhardsen, J. (2012). Long-term cardiovascular risk of nonsteroidal anti-inflammatory drug use according to time passed after first-time myocardial infarction. Circulation, 126(16), 1955-1963. doi: 10.1161/CIRCULATIONAHA.112.112607.

Pezhman, L., Tahrani, A., & Chimen, M. (2021). Dysregulation of leukocyte trafficking in type 2 diabetes: Mechanisms and potential therapeutic avenues. Frontiers in cell and developmental biology, 9, 624184. doi: 10.3389/fcell.2021.624184.

Pratiwi, D. (2016). Uji efek antiinflamasi topikal ekstrak etanol daun jambu biji (Psidium guajava Linn.) pada edema kulit punggung mencit galur swiss terinduksi karagenan (Undergraduate thesis). Sanata Dharma University, DIY Yogyakarta, Indonesia.

Pubchem. National library of medicine. (2022, August 18). Retrieved from https://pubchem.ncbi.nlm.nih.gov/.

Purwanto, D. S., Susanti, H., & Sugihartini, N. (2021). Molecular docking as potential anti-inflamed quersetin of moringa leaf (Moringaloifera L.) with autodck-vina. Jurnal Ilmiah Manusia dan Kesehatan, 4(2), 309-313. doi: 10.31850/makes.v4i2.818.

Sardjono, R. E., Iqbal, M., Sholihin., Atun, Q., & Rahmi, R. (2017). Acute toxicity of ethanol extract of Indonesian velvet bean. International Journal of Pharmacy and Pharmaceutical Sciences, 9(5), 161-165.

Schellack, N., & Fourie, J. (2015). A review of nonsteroidal anti-inflammatory drugs. SA Pharmaceutical Journal, 82(3), 8-18.

Sonnenberg, G. F., & Hepworth, M. R. (2019). Functional interactions between innate lymphoid cells and adaptive immunity. Nature reviews. Immunology, 19(10), 599-613. doi: 10.1038/s41577-019-0194-8.

Sousa, L. P., Alessandri, A. L., Pinho, V., & Teixeira, M. M. (2013). Pharmacological strategies to resolve acute inflammation. Current opinion in pharmacology, 13(4), 625-631.

Sriuttha, P., Sirichanchuen, B., & Permsuwan, U. (2018). Hepatotoxicity of nonsteroidal anti‐inflammatory drugs: A systematic review of randomized controlled trials. International journal of hepatology, 2018(1), 5253623.

Tamagawa-Mineoka, R., & Katoh, N. (2020). Atopic dermatitis: Identification and management of complicating factors. International journal of molecular sciences, 21(8), 2671. doi: 10.3390/ijms21082671.




DOI: https://doi.org/10.15408/kauniyah.v1i1.34979 Abstract - 0 PDF - 0

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